quinazolines has been researched along with Experimental Neoplasms in 117 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 13 (11.11) | 18.7374 |
1990's | 8 (6.84) | 18.2507 |
2000's | 39 (33.33) | 29.6817 |
2010's | 51 (43.59) | 24.3611 |
2020's | 6 (5.13) | 2.80 |
Authors | Studies |
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Deng, J; Lei, F; Li, J; Liang, Z; Shi, T; Wang, Y; Wang, Z; Yang, X; Zhang, H | 1 |
Ahmed, AU; Balyasnikova, IV; Burga, R; Castro, B; Cordero, A; Fares, J; Kanojia, D; Lee-Chang, C; Lesniak, MS; Miska, J; Petrosyan, E; Ramsey, MD; Rashidi, A; Schwartz, CW; Xiao, T; Zhang, P | 1 |
Cui, H; Dong, Z; Hou, J; Ke, X; Wang, F; Yang, L; Yin, C; Zhang, K; Zhang, R; Zhong, X | 1 |
Benites, J; Buc Calderon, P; Muccioli, GG; Ríos, D; Valderrama, JA | 1 |
Fujiwara, Y; Hamada, A; Ohuchi, M; Ryu, S; Shimoi, T; Tamura, K; Yagishita, S; Yonemori, K | 1 |
Ahn, YG; Bae, I; Choi, J; Hyung Kim, H; Kim, D; Kim, DK; Kim, J; Kim, M; Kim, YH; Park, B | 1 |
Bi, K; Chen, S; Dong, G; Huang, Y; Li, Y; Sheng, C; Wu, S | 1 |
Shi, Y; Su, C; Zhao, L; Zheng, Y | 1 |
Balaji, KS; Devegowda, PS; Jayarama, S; Kameshwar, VH; Prasanna, DS; Rangappa, KS; Siddalingaiah, L; Swaroop, TR | 1 |
Kharbanda, A; Runkle, K; Wang, W; Witze, ES | 1 |
Babbar, A; Brehmer, D; Chen, JH; Chen, Y; Darjania, L; Deng, X; Dhanak, D; Ely, T; Feng, J; Firdaus, SJ; Guo, X; Hansen, R; Hu-Lowe, D; Janes, MR; Kessler, LV; Kucharski, JM; Li, LS; Li, S; Liu, Y; Long, YO; Lorenzi, MV; Patricelli, MP; Peters, U; Ren, P; Thach, C; Wang, Y; Wu, T; Yao, Y; Yu, K; Zarieh, A; Zarrinkar, PP; Zhang, J | 1 |
Ferrari, M; Gu, J; Hamilton, DJ; Jiang, S; Li, F; Li, Z; Pettigrew, RI; Qiu, Y; Yang, Z | 1 |
Anderson, J; Barone, G; Blackledge, MD; Carceller, F; Chesler, L; Clarke, M; Jamin, Y; Jerome, NP; Koers, A; Koh, DM; Marshall, LV; McErlean, CM; McHugh, K; Moreno, L; Pearson, ADJ; Poon, E; Robinson, SP; Sebire, N; Vaidya, SJ; Yuan, Y; Zormpas-Petridis, K | 1 |
Chern, JW; Hsin, LW; Hung, PY; Liu, JR; Yu, CW | 1 |
Duan, W; Feng, Y; Hei, YY; Mao, S; Sun, H; Wang, J; Xin, M; Zhang, H; Zhang, SQ | 1 |
Cai, G; Cai, J; Gao, R; Ji, Q; Li, C; Li, Q; Song, D; Sui, H; Teng, P; Wang, Y; Zhou, L | 1 |
Albanese, C; Alzani, R; Amboldi, N; Bungaro, S; Casolaro, A; Cazzaniga, G; Ceruti, R; Cribioli, S; Giussani, U; Golay, J; Introna, M; Losa, M; Marchesi, F; Patton, V; Pesenti, E; Pezzoni, A; Rambaldi, A; Texido, G; Valsasina, B | 1 |
Ishiguro, H; Ishiguro, Y; Miyamoto, H | 1 |
Chen, JQ; Giaccone, G; Goldsmith, PK; Heldman, MR; Herrmann, MA; Lee, JH; Park, KS; Wang, Y | 1 |
Fan, C; Guo, Z; Li, Y; Lin, D; Yang, S; Yang, Y; Zhang, L; Zhao, S; Zhu, J | 1 |
Döme, B; Fehniger, TE; Jansson, B; Laurell, T; Marko-Varga, G; Rezeli, M; Végvári, Á; Welinder, C | 1 |
Bull, CO; Fracasso, PR; Haegebarth, A; Hentemann, M; Liu, N; Mumberg, D; Rowley, BR; Schatz, CA; Schneider, C; Scott, WJ; Wilhelm, SM; Wilkie, DP; Ziegelbauer, K | 1 |
Biersack, B; Ficner, R; Mahal, K; Mueller, T; Resch, M; Schobert, R | 1 |
Bergbower, E; Dennis, PA; Dogan, I; Ekmekci, A; Gills, JJ; Kawabata, S; Rudin, CM; Wilson, W | 1 |
Deng, ZJ; Dreaden, EC; Hammond, PT; Lee, MJ; Morton, SW; Shah, NJ; Shopsowitz, KE; Siouve, E; Yaffe, MB | 1 |
Niessen, HG; Poot, AJ; Schuit, RC; Slobbe, P; Smit, EF; Solca, F; Stehle, G; Stigter-van Walsum, M; van Dongen, GA; Windhorst, AD | 1 |
Fu, LW; Huang, LY; Huang, ZC; To, KK; Wang, F; Wang, XK; Xu, JH; Yang, K; Ye, S | 1 |
Baumann, M; Ebert, N; Eicheler, W; Gurtner, K; Krause, M; Pfitzmann, D; Zips, D | 1 |
Chen, V; Crooks, DR; Ghosh, S; Krishna, MC; Liao, PJ; Linehan, WM; Mannes, PZ; Matsumoto, S; Merino, M; Mitchell, JB; Neckers, L; Pendergast, AM; Ricketts, CJ; Rouault, TA; Sourbier, C; Srinivasan, R; Srivastava, G; Vocke, CD; Wei, MH; Yang, Y | 1 |
Kang, BR; Li, Y; Lu, SM; Wang, XM; Xin, MH; Xu, J; Zhang, SQ | 1 |
Lin, J; Xue, L; Yin, S; Zhang, C; Zhou, L | 1 |
Chen, D; Fan, C; Li, Y; Yang, Y; Zhang, L; Zhao, S; Zheng, Q; Zheng, S; Zhou, H | 1 |
Cao, YX; He, YY; Mao, S; Xiao, X; Xie, XX; Xin, MH; Xuan, W; Zhang, S; Zhang, SQ; Zuo, SJ | 1 |
Cai, R; Chen, S; Cheng, Y; Du, L; Han, B; Li, M; Lin, Y; Ma, Z; Shi, B; Shi, X; Wu, W; Zhou, Y | 1 |
Amoozgar, Z; Batchelor, TT; Batista, A; Chatterjee, S; Datta, M; Duda, DG; Farrar, CT; Fukumura, D; Goveia, J; Huang, Y; Jain, RK; Jung, K; Kamoun, WS; Kirkpatrick, ND; Kloepper, J; Leow, CC; Marijt, KA; Muzikansky, A; Peterson, TE; Seano, G; Snuderl, M; Vardam, T; Xu, L | 1 |
Fang, W; Tian, Y; Xue, C; Zhan, J; Zhang, J; Zhang, L; Zhao, Y | 1 |
He, J; Huang, C; Li, J; Li, Z; Liu, C; Meng, X; Zhang, L | 1 |
Ohyashiki, K; Okabe, S; Sakuta, J; Tanaka, Y; Tauchi, T | 1 |
Chen, M; Guo, Y; Huang, J; Jiang, H; Li, M; Xie, Y; Yue, S; Zhang, F; Zhou, G | 1 |
Allen, DA; Baskaran, S; Bui, M; Elling, RA; Flanagan, WM; Fung, AD; Hanan, EJ; Harris, S; Heumann, SA; Hoch, U; Jacobs, JW; Lam, J; Lawrence, CE; Lew, W; McDowell, RS; Nannini, MA; O'Brien, T; Oslob, JD; Romanowski, MJ; Shen, W; Silverman, JA; Sopko, MM; Tangonan, BT; Teague, J; Yoburn, JC; Yu, CH; Zhong, M; Zimmerman, KM | 1 |
Curtin, NJ; Kyle, S; Mitchell, J; Thomas, HD | 1 |
Barr, S; Brown, E; Buck, E; Epstein, D; Eyzaguirre, A; Gibson, NW; Haley, JD; Iwata, KK; Ji, QS; Miglarese, M; Mulvihill, M; O'Connor, M; Pachter, J; Rosenfeld-Franklin, M; Thomson, S; Yao, Y | 1 |
Katayama, H; Kishino, D; Kiura, K; Kuyama, S; Ohashi, K; Okada, T; Sato, K; Takigawa, N; Tanimoto, M | 1 |
Gaballah, K; Hills, A; Oakley, R; Partridge, M; Ryan, A | 1 |
Cerniglia, GJ; Choe, R; Durduran, T; Evans, SM; Hahn, SM; Koch, CJ; Lee, WM; Maity, A; Mick, R; Pore, N; Quon, H; Schultz, S; Sehgal, CM; Tsai, JH; Xing, X; Yodh, AG | 1 |
Amornphimoltham, P; Chiorini, JA; Gutkind, JS; Schmidt, M; Weller, ML; Wilson, PA | 1 |
Chang, TH; Huang, CP; Lan, CC; Lin, SB; Shih, JY; Su, KY; Tsai, MF; Wu, CP; Wu, SG; Yang, CH; Yang, PC; Yu, SL; Yu, YL | 1 |
Asano, K; Ohkuma, H | 1 |
Aten, JA; Buist, MR; Eppink, B; Essers, J; Franken, NA; Kanaar, R; Krawczyk, PM; O'Connor, MJ; Odijk, H; Rens, J; Rodermond, H; Soullié, T; Stalpers, LJ; Stap, J; Ten Hagen, TL; van Bree, C; Verhagen, HJ; Zelensky, A | 1 |
Kachnic, LA; Powell, SN | 1 |
Gilmer, TM; Rusnak, D | 1 |
Alferez, D; Davies, BR; Heaton, SP; Heier, A; Holt, SV; Logié, A; Odedra, R; Smith, PD; Wilkinson, RW | 1 |
Collins, M; Gore, JC; Halliday, J; Huszar, D; Lawson, D; Loveless, ME; Nadella, MV; Reimer, C; Waterton, JC; Yankeelov, TE | 1 |
Farsaci, B; Greiner, JW; Sabzevari, H; Schlom, J; Takai, S | 1 |
Feng, ZH; Li, D; Liao, SJ; Shu, Y; Sun, R; Wang, Q; Wei, JJ; Yan, B; Yuan, Y; Zhang, GM; Zhou, YH; Zhu, JH | 1 |
Fung, AS; Jonkman, J; Tannock, IF | 1 |
Abe, M; Hashimoto, O; Inoue, K; Iwamoto, H; Koga, H; Masuda, H; Nakamura, T; Sata, M; Torimura, T; Ueno, T; Yano, H | 1 |
Bokacheva, L; Carlin, S; Halliday, J; Kotedia, K; Koutcher, JA; Le, CH; Reese, M; Ricketts, SA | 1 |
Davis, C; Ding, L; Hu, S; Hu, Y; Kang, X; Long, W; Tan, F; Wang, F; Wang, Y; Xie, G; Zhang, DX | 1 |
Chang, YL; Chen, HJ; Chen, KF; Cheng, AL; Liu, CY; Shiau, CW; Yu, HC | 1 |
Alapati, V; Manjula, SN; Noolvi, MN; Pallavi, KJ; Patel, HM; Satyanarayana, SV; Tippeswamy, BS | 1 |
Casanovas, O; Castillo-Ávila, W; Condom, E; Garcia Del Muro, X; Germà, JR; Graupera, M; Hernández-Losa, J; Juliachs, M; Pandiella, A; Piulats, JM; Teixidó, C; Vidal, A; Villanueva, A; Viñals, F | 1 |
Buechner, SA; Erne, P; Iezzi, G; Kyriakakis, E; Pfaff, D; Philippova, M; Resink, TJ; Schoenenberger, AW; Spagnoli, GC | 1 |
Ajaykumar, R; Babu, PA; Deevi, DS; Kumar, GS; Kumar, KB; Mamidi, NV; Narasimhulu, CP; Prasanna, P; Puranik, RC; Rajagopal, S; Rajagopalan, R; Rao, CS; Rao, CV; Renuka, B; Seshu, KV; Sharma, VM; Subramanyam, D; Venkateswarlu, A | 1 |
Bigley, AL; Boffey, SJ; Chester, R; Curry, B; Curwen, JO; Dukes, M; Graham, GA; Hennequin, LF; Hughes, GD; Jackson, JA; Kendrew, J; Musgrove, HL; Ogilvie, DJ; Richmond, GH; Stokes, ES; Thomas, AP; Valentine, PJ; Wadsworth, PF; Wedge, SR | 1 |
Ben-David, I; Chisin, R; Freedman, NM; Levitzki, A; Mishani, E; Ortu, G; Rozen, Y | 1 |
Bianco, AR; Bianco, C; Bianco, R; Caputo, R; Ciardiello, F; Damiano, V; Fontanini, G; Pepe, S; Raben, D; Tortora, G; Troiani, T; Veneziani, BM | 1 |
Affleck, K; Alligood, KJ; Gilmer, TM; Keith, BR; Knight, WB; Lackey, K; Mullin, RJ; Murray, DM; Rhodes, N; Rusnak, DW; Wood, ER | 1 |
Affleck, K; Cockerill, GS; Gaul, MD; Gilmer, TM; Griffin, RJ; Guntrip, S; Guo, Y; Keith, BR; Knight, WB; Lackey, K; Mullin, RJ; Murray, DM; Rusnak, DW; Smith, K; Tadepalli, S; Wood, ER | 1 |
Fredriksson, A; Stone-Elander, S | 1 |
Checkley, D; Curry, B; Dukes, M; Kendrew, J; Middleton, B; Tessier, JJ; Waterton, JC; Wedge, SR | 1 |
BALDWIN, RW; CUNNINGHAM, GJ; DEAN, HG; PARTRIDGE, MW; SURTEES, SJ; VIPOND, HJ | 1 |
Bruneteau, G; Clement, O; Cuenod, CA; de Bazelaire, C; Frija, G; Frouin, F; Pradel, C; Robert, PH; Siauve, N; Tessier, JL; Wedge, SR | 1 |
Checkley, D; Kendrew, J; Tessier, JJ; Waterton, JC; Wedge, SR | 1 |
Abbott, E; Brown, EN; Colagiovanni, DB; Desjardins, J; Drolet, DW; Emerson, DL | 1 |
Brousal, J; Cuneo, K; Fu, A; Geng, L; Hallahan, DE; Hayflick, JS; Himmelfarb, E; Kesicki, EA; Niermann, K; Schueneman, A; Tan, J; Treiberg, J | 1 |
Arribas, J; Baselga, J; Cassia, R; Di Cosimo, S; Guzmán, M; Matar, P; Moreno-Bueno, G; Palacios, J; Rodriguez, S; Rojo, F; Tabernero, J | 1 |
Brandt, R; Hynes, NE; Littlewood, A; O'Reilly, T; Schnell, C; Sini, P; Wood, J; Wyder, L | 1 |
Arao, T; Koizumi, F; Nishio, K; Shiratori, Y; Takeda, M; Takigahira, M; Yanagihara, K | 1 |
Ballard, P; Bradbury, RH; Hennequin, LF; Hickinson, DM; Johnson, PD; Kettle, JG; Klinowska, T; Morgentin, R; Ogilvie, DJ; Olivier, A | 1 |
Gibbs, DD; Henley, A; Jackman, AL; Raynaud, F; Wood, N; Workman, P | 1 |
Ajiki, T; Digiovanni, J; Kawamoto, T; Kiguchi, K; Ruffino, L | 1 |
Alvarez, JV; Bulmer, SE; Chen, TH; Feng, W; Frank, DA; Greulich, H; Hahn, WC; Jänne, PA; Meyerson, M; Sellers, WR; Zappaterra, M | 1 |
Ariazi, E; Bertucci, A; Grigg, R; Jordan, VC; Lee, ES; Meeke, K; Morris, C; O'Regan, RM; Osipo, C; Sarker, MA | 1 |
Goto, H; Matsumori, Y; Nakataki, E; Ryan, AJ; Sone, S; Wedge, SR; Yano, S | 1 |
Birle, DC; Hedley, DW | 1 |
Fujiwara, M; Ikehara, S; Ikehara, Y; Kodera, Y; Koike, M; Mochizuki, Y; Nakanishi, H; Nakao, A; Tatematsu, M; Yatabe, Y; Yokoyama, H | 1 |
Beroukhim, R; Cloughesy, T; DeBiasi, RM; Feng, WL; Gabriel, S; Getz, G; Glatt, KA; Greulich, H; Huang, JH; Kawaguchi, T; Khan, H; King, JC; Leahy, DJ; Lee, JC; Levine, RL; Liau, LM; Linhart, DJ; Mellinghoff, IK; Meyerson, M; Mischel, P; Nelson, SF; Nghiemphu, P; O'Neill, K; Onofrio, R; Paez, JG; Peck, TC; Pieper, RO; Rao, PN; Sawyers, CL; Sellers, WR; Thomas, RK; Vivanco, I; Xu, Q; Yoshimoto, K; Yuza, Y; Ziaugra, L | 1 |
Courtright, J; Gorlick, R; Houghton, PJ; Keir, ST; Kolb, EA; Lock, R; Maris, JM; Morton, CL; Reynolds, CP; Smith, MA; Tajbakhsh, M; Wu, J | 1 |
Barrass, NC; Bigley, A; Boyle, FT; Brady, MC; Brown, E; Byth, KF; Crafter, C; Foote, KM; Foster, JR; Green, S; Heaton, SP; Heron, NM; Jung, FH; Keen, NJ; Mortlock, AA; Mundt, KE; Odedra, R; Wedge, SR; Wilkinson, RW | 1 |
Acton, DG; Ballard, P; Barlaam, B; Bradbury, RH; Cross, D; Ducray, R; Germain, H; Hudson, K; Klinowska, T; Magnien, F; Ogilvie, DJ; Olivier, A; Ross, HS; Smith, R; Trigwell, CB; Vautier, M; Wright, L | 1 |
Cummings, J; Dive, C; Growcott, J; Heaton, SP; Hodgkinson, C; Hughes, A; Mundt, KE; Odedra, R; Sini, P; Ward, TH; Wilkinson, RW | 1 |
Amin, DN; Bielenberg, DR; Heymach, JV; Klagsbrun, M; Lifshits, E | 1 |
Bertino, JR; Cardenas, RM; Fernandes, DJ; Hynes, JB | 1 |
Betit-Yen, K; Gitterman, CO; Lee, G; Luell, S; Prendergast, JS; Skipski, VP; Stock, CC | 1 |
Amyx, H; Boytos, CM; Duch, DS; Ferone, R; Smith, GK; Wilson, HR | 1 |
Bacquet, RJ; Bartlett, CA; Booth, CL; Deal, J; Herrmann, SM; Howland, EF; Janson, CA; Johnston, A; Jones, TR; Kathardekar, V; Lewis, KK; Matthews, DA; Mazdiyasni, H; Morse, CA; Nguyen, D; Reddy, MR; Smith, WW; Varney, MD; Ward, RW; Webber, S; Webber, SE; Welsh, KM; White, J | 1 |
Bridges, AJ; Denny, WA; Dobrusin, EM; Doherty, A; Fry, DW; Greis, KD; Hicks, JL; Hook, KE; Keller, PR; Leopold, WR; Loo, JA; McNamara, DJ; Nelson, JM; Sherwood, V; Smaill, JB; Trumpp-Kallmeyer, S | 1 |
Carroll, ML; Discafani, CM; Floyd, MB; Greenberger, LM; Hollander, IJ; Husain, Z; Johnson, BD; Kitchen, D; Malo, MS; May, MK; Minnick, AA; Nilakantan, R; Shen, R; Wang, YF; Wissner, A | 1 |
Bridges, AJ; Dykes, DJ; Elliott, WL; Fry, DW; Leopold, WR; Patmore, SJ; Roberts, BJ; Rose, S; Sherwood, V; Vincent, PW; Zhou, H | 1 |
Bianco, AR; Bianco, R; Caputo, R; Ciardiello, F; Damiano, V; De Placido, S; Pomatico, G; Tortora, G | 1 |
Bianco, AR; Bianco, R; Caputo, R; Ciardiello, F; Cuccato, S; Damiano, V; De Placido, S; Fontanini, G; Tortora, G | 1 |
Ahmad, T; Anderson, NG; Bundred, NJ; Chan, K; Dobson, R | 1 |
Bertino, JR; Hynes, JB; Moroson, BA; Scanlon, KJ | 1 |
Bertino, JR; Cashmore, AR; Elslager, EF; Moroson, BA; Sawicki, WL | 1 |
Donsback, RC; Sirotnak, FM | 1 |
Gibson, W; Jackman, AL; Jodrell, DI; Stephens, TC | 1 |
Bertino, JR; Lin, JT | 1 |
Atassi, G; Baron, M; Bissery, MC; Cros, S; Gebel-Servolles, P; Giorgi-Renault, S; Lavelle, F; Paoletti, C; Renault, J | 1 |
Osada, Y; Tanaka, NG; Tohgo, A | 1 |
Bissery, MC; Corbett, TH; Luk, GD; Mucci-LoRusso, P; Plowman, J; Polin, L; Valeriote, F | 1 |
Griswold, DP; Hook, KE; Leopold, WR; Nelson, JM; Roberts, BJ | 1 |
Cradock, J; Grillo-Lopez, A; Leyland-Jones, B; O'Dwyer, PJ; Plowman, J; Shoemaker, DD | 1 |
Baldwin, RW; Chayen, J; Diengdoh, JV | 1 |
Maley, F; Maley, GF | 1 |
Carlin, SC; Friedkin, M; Rosenberg, RN; VandeVenter, L | 1 |
Marini, JL; Modest, EJ; Nadel, ME; Rosowsky, A | 1 |
2 review(s) available for quinazolines and Experimental Neoplasms
Article | Year |
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PET screening of anticancer drugs. A faster route to drug/target evaluations in vivo.
Topics: Animals; Antineoplastic Agents; Drug Evaluation; Drug Screening Assays, Antitumor; Enzyme Inhibitors; ErbB Receptors; Haplorhini; Humans; Image Processing, Computer-Assisted; Isotope Labeling; Neoplasm Proteins; Neoplasms; Neoplasms, Experimental; Quinazolines; Radiopharmaceuticals; Rats; Tomography, Emission-Computed; Xenograft Model Antitumor Assays | 2003 |
Update on trimetrexate, a folate antagonist with antineoplastic and antiprotozoal properties.
Topics: Adult; Aged; Animals; Antineoplastic Agents; Antiprotozoal Agents; Clinical Trials as Topic; Drug Resistance; Female; Folic Acid Antagonists; Humans; Male; Middle Aged; Neoplasms, Experimental; Quinazolines; Trimetrexate | 1991 |
3 trial(s) available for quinazolines and Experimental Neoplasms
Article | Year |
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The Polo-Like Kinase 1 (PLK1) inhibitor NMS-P937 is effective in a new model of disseminated primary CD56+ acute monoblastic leukaemia.
Topics: Adult; Animals; CD56 Antigen; Cell Cycle Proteins; Humans; Leukemia, Myeloid, Acute; Mice; Mice, Inbred NOD; Mice, SCID; Neoplasms, Experimental; Polo-Like Kinase 1; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Proto-Oncogene Proteins; Pyrazoles; Quinazolines; Tumor Cells, Cultured; Xenograft Model Antitumor Assays | 2013 |
Response of HT29 colorectal xenograft model to cediranib assessed with 18 F-fluoromisonidazole positron emission tomography, dynamic contrast-enhanced and diffusion-weighted MRI.
Topics: Animals; Antineoplastic Agents; Contrast Media; Fluorodeoxyglucose F18; Gadolinium DTPA; HT29 Cells; Humans; Neoplasms, Experimental; Positron-Emission Tomography; Quinazolines; Radiopharmaceuticals; Rats; Reproducibility of Results; Sensitivity and Specificity; Treatment Outcome; Xenograft Model Antitumor Assays | 2013 |
Trimetrexate: a new antifol entering clinical trials.
Topics: Animals; Biological Availability; Biological Transport; Cells, Cultured; Clinical Trials as Topic; DNA; Dogs; Drug Evaluation, Preclinical; Folic Acid Antagonists; Mice; Neoplasms, Experimental; Nucleosides; Quinazolines; Trimetrexate | 1985 |
112 other study(ies) available for quinazolines and Experimental Neoplasms
Article | Year |
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Design, synthesis and bioactivity evaluation of novel evodiamine derivatives with excellent potency against gastric cancer.
Topics: Animals; Antineoplastic Agents; Apoptosis; Cell Differentiation; Cell Proliferation; Cells, Cultured; Dose-Response Relationship, Drug; Drug Design; Drug Screening Assays, Antitumor; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; Molecular Structure; Neoplasms, Experimental; Quinazolines; Stomach Neoplasms; Structure-Activity Relationship | 2022 |
Combination of tucatinib and neural stem cells secreting anti-HER2 antibody prolongs survival of mice with metastatic brain cancer.
Topics: Animals; Antineoplastic Agents, Immunological; Brain Neoplasms; Cell Line, Tumor; Humans; Mice; Mice, Nude; Neoplasm Metastasis; Neoplasms, Experimental; Neural Stem Cells; Oxazoles; Pyridines; Quinazolines; Receptor, ErbB-2; Xenograft Model Antitumor Assays | 2022 |
G9a promotes cell proliferation and suppresses autophagy in gastric cancer by directly activating mTOR.
Topics: Animals; Autophagy; Azepines; Cell Cycle; Cell Line; Cell Proliferation; Cell Survival; Down-Regulation; Female; Histocompatibility Antigens; Histone-Lysine N-Methyltransferase; Histones; Humans; Mice, SCID; Neoplasms, Experimental; Quinazolines; Stomach Neoplasms; TOR Serine-Threonine Kinases | 2019 |
In Vitro Inhibition of Hsp90 Protein by Benzothiazoloquinazolinequinones Is Enhanced in The Presence of Ascorbate. A Preliminary In Vivo Antiproliferative Study.
Topics: Animals; Antineoplastic Agents; Ascorbic Acid; Cell Proliferation; HSP90 Heat-Shock Proteins; Humans; MCF-7 Cells; Mice; Neoplasm Proteins; Neoplasms, Experimental; Quinazolines; Xenograft Model Antitumor Assays | 2020 |
Visualization of the distribution of nanoparticle-formulated AZD2811 in mouse tumor model using matrix-assisted laser desorption ionization mass spectrometry imaging.
Topics: Acetanilides; Animals; Antineoplastic Agents; Cell Line, Tumor; Drug Carriers; Male; Mammary Neoplasms, Experimental; Mice; Mice, Inbred BALB C; Nanoparticles; Neoplasm Transplantation; Neoplasms; Neoplasms, Experimental; Quinazolines; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | 2020 |
Design, synthesis and biological evaluation of new bivalent quinazoline analogues as IAP antagonists.
Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Cell Survival; Dogs; Dose-Response Relationship, Drug; Drug Design; Drug Screening Assays, Antitumor; Humans; Inhibitor of Apoptosis Proteins; Mice; Molecular Structure; Neoplasms, Experimental; Quinazolines; Rats; Structure-Activity Relationship | 2021 |
Water-soluble derivatives of evodiamine: Discovery of evodiamine-10-phosphate as an orally active antitumor lead compound.
Topics: Administration, Oral; Animals; Antineoplastic Agents; Apoptosis; Cell Proliferation; DNA Topoisomerases, Type I; Dose-Response Relationship, Drug; Drug Discovery; Drug Screening Assays, Antitumor; Female; HCT116 Cells; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; Molecular Structure; Neoplasms, Experimental; Phosphates; Quinazolines; Solubility; Structure-Activity Relationship; Water | 2021 |
Chitosan nanoparticle-mediated co-delivery of shAtg-5 and gefitinib synergistically promoted the efficacy of chemotherapeutics through the modulation of autophagy.
Topics: A549 Cells; Animals; Antineoplastic Agents; Apoptosis; Autophagy; Autophagy-Related Protein 5; Cell Line, Tumor; Chitosan; Drug Delivery Systems; Female; Gefitinib; Gene Silencing; Humans; Mice, Inbred BALB C; Mice, Nude; Nanomedicine; Nanoparticles; Neoplasms, Experimental; Quinazolines; RNA, Small Interfering; Transfection | 2017 |
Synthesis, Characterization of 4-Anilino-6,7-Dimethoxy Quinazoline Derivatives as Potential Anti-Angiogenic Agents.
Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Cell Proliferation; Drug Screening Assays, Antitumor; Humans; Mice; Molecular Docking Simulation; Neoplasms, Experimental; Quinazolines; Receptors, Vascular Endothelial Growth Factor; Tumor Cells, Cultured; Vascular Endothelial Growth Factor Receptor-2 | 2018 |
Induced sensitivity to EGFR inhibitors is mediated by palmitoylated cysteine 1025 of EGFR and requires oncogenic Kras.
Topics: Antineoplastic Agents; Apoptosis; Cocarcinogenesis; Cysteine; Dose-Response Relationship, Drug; Drug Resistance, Neoplasm; ErbB Receptors; Gefitinib; Humans; Lipoylation; MCF-7 Cells; Membrane Proteins; Mutation; Neoplasms, Experimental; Proto-Oncogene Proteins p21(ras); Quinazolines | 2017 |
Targeting KRAS Mutant Cancers with a Covalent G12C-Specific Inhibitor.
Topics: Animals; Antineoplastic Agents; Cell Proliferation; Cells, Cultured; Female; HCT116 Cells; HEK293 Cells; Humans; Male; Mice; Mice, Inbred BALB C; Mice, Nude; Molecular Docking Simulation; Mutation; Neoplasms, Experimental; Piperazines; Protein Binding; Proto-Oncogene Proteins p21(ras); Quinazolines | 2018 |
Single-Molecule Force Measurement Guides the Design of Multivalent Ligands with Picomolar Affinity.
Topics: Animals; Antineoplastic Agents; Binding Sites; Cell Line, Tumor; Humans; Ligands; Mice; Molecular Structure; Neoplasms, Experimental; Optical Imaging; Piperidines; Positron-Emission Tomography; Protein Kinase Inhibitors; Quinazolines; Receptors, Vascular Endothelial Growth Factor | 2019 |
MRI Imaging of the Hemodynamic Vasculature of Neuroblastoma Predicts Response to Antiangiogenic Treatment.
Topics: Angiogenesis Inhibitors; Animals; Child; Child, Preschool; Contrast Media; Female; Humans; Infant; Magnetic Resonance Imaging; Male; Mice, Transgenic; N-Myc Proto-Oncogene Protein; Neoplasms, Experimental; Neuroblastoma; Prospective Studies; Protein Kinase Inhibitors; Quinazolines; Treatment Outcome | 2019 |
High-selective HDAC6 inhibitor promotes HDAC6 degradation following autophagy modulation and enhanced antitumor immunity in glioblastoma.
Topics: Animals; Antineoplastic Agents; Autophagy; Cell Line, Tumor; Cell Proliferation; Cell Survival; Gene Expression Regulation, Neoplastic; Glioblastoma; Histone Deacetylase 6; Histone Deacetylase Inhibitors; Humans; Male; Mice; Mice, Nude; Molecular Structure; Neoplasms, Experimental; Quinazolines | 2019 |
Alkylsulfonamide-containing quinazoline derivatives as potent and orally bioavailable PI3Ks inhibitors.
Topics: Administration, Oral; Animals; Antineoplastic Agents; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Female; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; Models, Molecular; Molecular Structure; Neoplasms, Experimental; Phosphatidylinositol 3-Kinases; Phosphoinositide-3 Kinase Inhibitors; Quinazolines; Structure-Activity Relationship; Sulfonamides; Tumor Cells, Cultured | 2019 |
Development of EGFR-targeted evodiamine nanoparticles for the treatment of colorectal cancer.
Topics: Animals; Antineoplastic Agents; Cell Proliferation; Cell Survival; Colorectal Neoplasms; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; ErbB Receptors; Humans; Male; Mice; Mice, Inbred ICR; Molecular Structure; Neoplasms, Experimental; Quinazolines; Structure-Activity Relationship; Tumor Cells, Cultured | 2019 |
Epidermal growth factor receptor tyrosine kinase inhibition up-regulates interleukin-6 in cancer cells and induces subsequent development of interstitial pneumonia.
Topics: Antibodies, Neutralizing; Antineoplastic Agents; Blotting, Western; Cell Line, Tumor; Enzyme-Linked Immunosorbent Assay; ErbB Receptors; Gefitinib; Humans; Interleukin-6; Lung Diseases, Interstitial; Neoplasms, Experimental; Phosphorylation; Protein Kinase Inhibitors; Quinazolines; Reverse Transcriptase Polymerase Chain Reaction; Signal Transduction; Tyrphostins; Up-Regulation | 2013 |
Capillary isoelectric-focusing immunoassays to study dynamic oncoprotein phosphorylation and drug response to targeted therapies in non-small cell lung cancer.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Benzimidazoles; Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Drug Resistance, Neoplasm; Erlotinib Hydrochloride; Extracellular Signal-Regulated MAP Kinases; Humans; Immunoassay; Lung Neoplasms; Lymphatic Metastasis; MAP Kinase Kinase 2; MAP Kinase Signaling System; Mice; Mice, Nude; Molecular Targeted Therapy; Neoplasms, Experimental; Oncogene Proteins; Phosphorylation; Protein Kinase Inhibitors; Quinazolines | 2013 |
Discovery of a potent dual EGFR/HER-2 inhibitor L-2 (selatinib) for the treatment of cancer.
Topics: Aniline Compounds; Animals; Antineoplastic Agents; Cell Proliferation; Dose-Response Relationship, Drug; Drug Discovery; Drug Screening Assays, Antitumor; ErbB Receptors; Female; Humans; Lapatinib; Male; Mice; Mice, Inbred BALB C; Molecular Structure; Neoplasms; Neoplasms, Experimental; Quinazolines; Rats; Rats, Wistar; Receptor, ErbB-2; Solubility; Structure-Activity Relationship | 2013 |
Experimental models to study drug distributions in tissue using MALDI mass spectrometry imaging.
Topics: Adenocarcinoma; Animals; Biological Transport; Cholinergic Antagonists; Erlotinib Hydrochloride; Gefitinib; Humans; Lung Neoplasms; Mice; Microtomy; Neoplasms, Experimental; Protein Kinase Inhibitors; Quinazolines; Scopolamine Derivatives; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Tiotropium Bromide; Tissue Culture Techniques; Tumor Microenvironment | 2013 |
BAY 80-6946 is a highly selective intravenous PI3K inhibitor with potent p110α and p110δ activities in tumor cell lines and xenograft models.
Topics: Administration, Intravenous; Animals; Apoptosis; Cell Line, Tumor; Drug Evaluation, Preclinical; Drug Resistance, Neoplasm; Gene Expression Regulation, Neoplastic; Humans; Mice; Mice, Nude; Molecular Targeted Therapy; Neoplasms; Neoplasms, Experimental; Phosphatidylinositol 3-Kinases; Phosphoinositide-3 Kinase Inhibitors; Protein Kinase Inhibitors; Pyrimidines; Quinazolines; Rats; Rats, Nude; Receptor, ErbB-2; TOR Serine-Threonine Kinases; Xenograft Model Antitumor Assays | 2013 |
Effects of the tumor-vasculature-disrupting agent verubulin and two heteroaryl analogues on cancer cells, endothelial cells, and blood vessels.
Topics: Animals; Antineoplastic Agents; Blood Vessels; Cell Count; Cell Cycle; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Endothelial Cells; HCT116 Cells; HT29 Cells; Humans; MCF-7 Cells; Mice; Mice, Nude; Models, Molecular; Molecular Structure; Neoplasms, Experimental; Neovascularization, Pathologic; Quinazolines; Structure-Activity Relationship | 2014 |
SOX2 expression is an early event in a murine model of EGFR mutant lung cancer and promotes proliferation of a subset of EGFR mutant lung adenocarcinoma cell lines.
Topics: Adenocarcinoma; Animals; Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Drug Resistance, Neoplasm; ErbB Receptors; Erlotinib Hydrochloride; Gene Expression; Humans; Lung Neoplasms; Mice, Transgenic; Mutation; Neoplasms, Experimental; Quinazolines; SOXB1 Transcription Factors | 2014 |
A nanoparticle-based combination chemotherapy delivery system for enhanced tumor killing by dynamic rewiring of signaling pathways.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Doxorubicin; Drug Carriers; Erlotinib Hydrochloride; Female; Liposomes; Mice; Mice, Inbred BALB C; Nanoparticles; Neoplasms, Experimental; Quinazolines | 2014 |
Development of [18F]afatinib as new TKI-PET tracer for EGFR positive tumors.
Topics: Afatinib; Animals; Cell Line, Tumor; ErbB Receptors; Fluorine Radioisotopes; Isotope Labeling; Metabolic Clearance Rate; Mice; Mice, Inbred BALB C; Mice, Nude; Neoplasms, Experimental; Organ Specificity; Positron-Emission Tomography; Quinazolines; Radiopharmaceuticals; Reproducibility of Results; Sensitivity and Specificity; Tissue Distribution | 2014 |
Afatinib circumvents multidrug resistance via dually inhibiting ATP binding cassette subfamily G member 2 in vitro and in vivo.
Topics: Afatinib; Animals; Antineoplastic Agents; ATP Binding Cassette Transporter, Subfamily G, Member 2; ATP-Binding Cassette Transporters; Blotting, Western; Cell Line, Tumor; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Female; Flow Cytometry; Humans; Immunohistochemistry; In Vitro Techniques; Male; Mice; Mice, Inbred BALB C; Neoplasm Proteins; Neoplasms, Experimental; Quinazolines; Real-Time Polymerase Chain Reaction; Topotecan; Xenograft Model Antitumor Assays | 2014 |
Effect of combined irradiation and EGFR/Erb-B inhibition with BIBW 2992 on proliferation and tumour cure in cell lines and xenografts.
Topics: Afatinib; Animals; Cell Line, Tumor; Chemoradiotherapy; Dose Fractionation, Radiation; ErbB Receptors; Female; Humans; Male; Mice; Mice, Nude; Neoplasms, Experimental; Quinazolines; Radiation-Sensitizing Agents; Transplantation, Heterologous; Xenograft Model Antitumor Assays | 2014 |
Targeting ABL1-mediated oxidative stress adaptation in fumarate hydratase-deficient cancer.
Topics: Animals; Cell Line, Tumor; Cell Nucleus; Fumarate Hydratase; Fumarates; Gene Expression Regulation, Neoplastic; Glycolysis; HEK293 Cells; Humans; Kidney Neoplasms; Mice; Neoplasms, Experimental; NF-E2-Related Factor 2; Oxidative Stress; Piperidines; Proto-Oncogene Mas; Proto-Oncogene Proteins c-abl; Quinazolines; Signal Transduction; Xenograft Model Antitumor Assays | 2014 |
Synthesis and antitumor activities evaluation of m-(4-morpholinoquinazolin-2-yl)benzamides in vitro and in vivo.
Topics: Animals; Antineoplastic Agents; Apoptosis; Benzamides; Cell Cycle; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; HCT116 Cells; Humans; MCF-7 Cells; Mice; Molecular Docking Simulation; Molecular Structure; Neoplasms, Experimental; Quinazolines; Structure-Activity Relationship; Tumor Cells, Cultured | 2015 |
Design, synthesis and biological activities of novel oxazolo[4,5-g]quinazolin-2(1H)-one derivatives as EGFR inhibitors.
Topics: Animals; Antineoplastic Agents; Benzoxazoles; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Design; Drug Screening Assays, Antitumor; ErbB Receptors; Humans; Mice; Mice, SCID; Neoplasms, Experimental; Quinazolines; Structure-Activity Relationship | 2015 |
Structure-activity study of quinazoline derivatives leading to the discovery of potent EGFR-T790M inhibitors.
Topics: Afatinib; Animals; Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Discovery; ErbB Receptors; Female; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; Molecular Structure; Neoplasms, Experimental; Protein Kinase Inhibitors; Quinazolines; Structure-Activity Relationship; Xenograft Model Antitumor Assays | 2015 |
Combination of 4-anilinoquinazoline, arylurea and tertiary amine moiety to discover novel anticancer agents.
Topics: Amines; Aniline Compounds; Animals; Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; ErbB Receptors; Humans; Mice; Mice, Nude; Molecular Structure; Neoplasms, Experimental; Protein Kinase Inhibitors; Quinazolines; Structure-Activity Relationship; Urea | 2016 |
Discovery of the First Environment-Sensitive Near-Infrared (NIR) Fluorogenic Ligand for α1-Adrenergic Receptors Imaging in Vivo.
Topics: Animals; Binding Sites; Carbocyanines; Cell Line, Tumor; CHO Cells; Cricetulus; Dose-Response Relationship, Drug; Drug Discovery; Fluorescence; Fluorescent Dyes; HEK293 Cells; Humans; Ligands; Mice; Molecular Structure; Neoplasms, Experimental; Piperazine; Piperazines; Quinazolines; Receptors, Adrenergic, alpha-1; Structure-Activity Relationship | 2016 |
Dual inhibition of Ang-2 and VEGF receptors normalizes tumor vasculature and prolongs survival in glioblastoma by altering macrophages.
Topics: Animals; Antibodies, Neoplasm; Cell Line, Tumor; Drug Screening Assays, Antitumor; Glioblastoma; Macrophages; Mice; Neoplasm Proteins; Neoplasms, Experimental; Neovascularization, Pathologic; Quinazolines; Receptors, Vascular Endothelial Growth Factor; Ribonuclease, Pancreatic | 2016 |
In vitro and in vivo efficacy of afatinib as a single agent or in combination with gemcitabine for the treatment of nasopharyngeal carcinoma.
Topics: Afatinib; Animals; Antineoplastic Agents; Carcinoma; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Proliferation; Deoxycytidine; Dose-Response Relationship, Drug; Gemcitabine; Humans; Male; Mice; Mice, Inbred BALB C; Mice, Nude; Nasopharyngeal Carcinoma; Nasopharyngeal Neoplasms; Neoplasms, Experimental; Quinazolines; Structure-Activity Relationship | 2016 |
Quinazoline derivative QPB-15e stabilizes the c-myc promoter G-quadruplex and inhibits tumor growth in vivo.
Topics: Animals; Antineoplastic Agents; Benzamides; Cell Line, Tumor; G-Quadruplexes; Genes, myc; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; Neoplasms, Experimental; Promoter Regions, Genetic; Proto-Oncogene Mas; Proto-Oncogene Proteins c-myc; Quinazolines; Xenograft Model Antitumor Assays | 2016 |
Combination therapy with copanlisib and ABL tyrosine kinase inhibitors against Philadelphia chromosome-positive resistant cells.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Cell Line, Tumor; Cell Proliferation; Drug Resistance, Neoplasm; Drug Synergism; Female; Fusion Proteins, bcr-abl; Humans; Imatinib Mesylate; Imidazoles; K562 Cells; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Mice; Mice, Inbred BALB C; Mice, Nude; Mutation; Neoplasms, Experimental; Phosphoinositide-3 Kinase Inhibitors; Protein Kinase Inhibitors; Pyridazines; Pyrimidines; Quinazolines | 2016 |
miR-200c enhances sensitivity of drug-resistant non-small cell lung cancer to gefitinib by suppression of PI3K/Akt signaling pathway and inhibites cell migration via targeting ZEB1.
Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; Cell Movement; Drug Resistance, Neoplasm; Gefitinib; Gene Expression Regulation; Gene Silencing; Humans; Mice; Mice, Nude; MicroRNAs; Neoplasms, Experimental; Phosphatidylinositol 3-Kinases; Proto-Oncogene Proteins c-akt; Quinazolines; Signal Transduction; Zinc Finger E-box-Binding Homeobox 1 | 2017 |
Discovery of a potent and selective aurora kinase inhibitor.
Topics: Animals; Antineoplastic Agents; Aurora Kinases; Drug Screening Assays, Antitumor; HCT116 Cells; Humans; Mice; Neoplasm Transplantation; Neoplasms, Experimental; Phenylurea Compounds; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Quinazolines; Structure-Activity Relationship; Thiazoles | 2008 |
Exploiting the Achilles heel of cancer: the therapeutic potential of poly(ADP-ribose) polymerase inhibitors in BRCA2-defective cancer.
Topics: Animals; Azulenes; Benzodiazepines; BRCA2 Protein; DNA Breaks, Double-Stranded; DNA Breaks, Single-Stranded; Enzyme Inhibitors; Female; Mice; Mice, Nude; Neoplasms, Experimental; Poly(ADP-ribose) Polymerase Inhibitors; Quinazolines; Recombination, Genetic | 2008 |
Feedback mechanisms promote cooperativity for small molecule inhibitors of epidermal and insulin-like growth factor receptors.
Topics: Adaptor Proteins, Signal Transducing; Animals; Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Dose-Response Relationship, Drug; Drug Synergism; ErbB Receptors; Erlotinib Hydrochloride; Feedback, Physiological; Female; Humans; Imidazoles; Insulin Receptor Substrate Proteins; MAP Kinase Signaling System; Mice; Mice, Nude; Neoplasms, Experimental; Phosphorylation; Proto-Oncogene Proteins c-akt; Pyrazines; Quinazolines; Receptor, IGF Type 1; Signal Transduction | 2008 |
Effect of gefitinib on N-nitrosamine-4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone induced lung tumorigenesis in A/J mice.
Topics: Animals; Antineoplastic Agents; Carcinogens, Environmental; Cell Growth Processes; Cell Line, Tumor; Cell Transformation, Neoplastic; ErbB Receptors; Female; Gefitinib; Lung; Lung Neoplasms; Mice; Mice, Inbred Strains; Neoplasms, Experimental; Nitrosamines; Pulmonary Fibrosis; Quinazolines; Smoking; Tumor Burden | 2009 |
The antiangiogenic agent ZD4190 prevents tumour outgrowth in a model of minimal residual carcinoma in deep tissues.
Topics: Angiogenesis Inhibitors; Animals; Disease Models, Animal; Female; Mice; Mice, Inbred C57BL; Neoplasm, Residual; Neoplasms, Experimental; Quinazolines; Triazoles; Vascular Endothelial Growth Factor A; Vascular Endothelial Growth Factor Receptor-2 | 2009 |
Epidermal growth factor receptor inhibition modulates the microenvironment by vascular normalization to improve chemotherapy and radiotherapy efficacy.
Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; ErbB Receptors; Erlotinib Hydrochloride; Female; Humans; Hypoxia-Inducible Factor 1, alpha Subunit; Mice; Mice, Nude; Neoplasms, Experimental; Oxygen; Quinazolines; Vascular Endothelial Growth Factor A | 2009 |
Epidermal growth factor receptor is a co-receptor for adeno-associated virus serotype 6.
Topics: Animals; Cell Line, Tumor; Dependovirus; ErbB Receptors; Female; Gefitinib; Gene Expression; Genetic Therapy; Genetic Vectors; Head and Neck Neoplasms; Isoantigens; Mice; Mice, Nude; Neoplasms, Experimental; Quinazolines; Receptors, Virus; Transduction, Genetic; Tyrphostins | 2010 |
Slug confers resistance to the epidermal growth factor receptor tyrosine kinase inhibitor.
Topics: Adenocarcinoma; Animals; Antineoplastic Agents; Apoptosis; Blotting, Western; Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Drug Resistance, Neoplasm; ErbB Receptors; Gefitinib; Gene Knockout Techniques; Humans; Lung Neoplasms; Mice; Neoplasms, Experimental; Quinazolines; Snail Family Transcription Factors; Transcription Factors | 2011 |
Epithelial growth factor receptor tyrosine kinase inhibitor prevents infiltration and cerebrospinal fluid dissemination in malignant glioma: an experimental study.
Topics: Animals; Antineoplastic Agents; Blotting, Western; Brain Neoplasms; Cadherins; Cell Line; Enzyme Inhibitors; ErbB Receptors; Glioma; Male; Neoplasms, Experimental; Quinazolines; Rats; Rats, Sprague-Dawley; Tyrphostins; Up-Regulation | 2011 |
Mild hyperthermia inhibits homologous recombination, induces BRCA2 degradation, and sensitizes cancer cells to poly (ADP-ribose) polymerase-1 inhibition.
Topics: Animals; Benzoquinones; BRCA2 Protein; Cell Line; Cell Line, Tumor; Cells, Cultured; DNA Repair; DNA-Binding Proteins; Embryonic Stem Cells; Female; HeLa Cells; Hot Temperature; Humans; Immunoblotting; Lactams, Macrocyclic; Mice; Mice, Nude; Neoplasms, Experimental; Phthalazines; Piperazines; Poly(ADP-ribose) Polymerase Inhibitors; Poly(ADP-ribose) Polymerases; Quinazolines; Rats; Recombination, Genetic; RNA Interference; Transplantation, Heterologous; Tumor Burden | 2011 |
Homologous recombination research is heating up and ready for therapy.
Topics: Animals; Benzoquinones; BRCA2 Protein; Cell Line, Tumor; DNA Repair; DNA-Binding Proteins; Hot Temperature; Humans; Immunoblotting; Lactams, Macrocyclic; Mice; Neoplasms, Experimental; Phthalazines; Piperazines; Poly(ADP-ribose) Polymerase Inhibitors; Poly(ADP-ribose) Polymerases; Quinazolines; Rats; Recombination, Genetic; RNA Interference; Transplantation, Heterologous; Tumor Burden | 2011 |
The discovery of lapatinib (GW572016).
Topics: Animals; Antineoplastic Agents; Cell Division; Enzyme Inhibitors; ErbB Receptors; Female; Furans; Humans; Neoplasms, Experimental; Quinazolines; Receptor, ErbB-2 | 2011 |
The MEK1/2 inhibitor, selumetinib (AZD6244; ARRY-142886), enhances anti-tumour efficacy when combined with conventional chemotherapeutic agents in human tumour xenograft models.
Topics: Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Benzimidazoles; Cell Line, Tumor; Cell Proliferation; Dacarbazine; Docetaxel; Female; Humans; MAP Kinase Kinase 1; MAP Kinase Kinase 2; MAP Kinase Signaling System; Mice; Mice, Nude; Mitogen-Activated Protein Kinase Kinases; Neoplasms, Experimental; Organophosphates; Protein Kinase Inhibitors; Quinazolines; Taxoids; Temozolomide; Xenograft Model Antitumor Assays | 2012 |
Comparisons of the efficacy of a Jak1/2 inhibitor (AZD1480) with a VEGF signaling inhibitor (cediranib) and sham treatments in mouse tumors using DCE-MRI, DW-MRI, and histology.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Biomarkers, Tumor; Cell Line, Tumor; Enzyme Inhibitors; Female; Humans; Janus Kinase 1; Janus Kinase 2; Magnetic Resonance Imaging; Mice; Mice, Nude; Neoplasms, Experimental; Pyrazoles; Pyrimidines; Quinazolines; Xenograft Model Antitumor Assays | 2012 |
Distinct effects of saracatinib on memory CD8+ T cell differentiation.
Topics: Animals; Antigens, Viral; Benzodioxoles; Cancer Vaccines; CD8-Positive T-Lymphocytes; Cell Differentiation; Cell Line, Tumor; Humans; Hyaluronan Receptors; Immunologic Memory; Influenza A virus; Influenza Vaccines; Interferon-gamma; L-Selectin; Mice; Mice, Transgenic; Neoplasms, Experimental; Quinazolines; src-Family Kinases; Viral Proteins | 2012 |
Targeting nuclear factor-κB suppresses the negative effect of toll-like receptor 4 signaling on antimetastasis therapy based on targeting αvβ3.
Topics: Animals; Antineoplastic Agents; Apoptosis; Blotting, Western; Cell Line, Tumor; Cell Movement; Female; Fibronectins; Integrin alphaVbeta3; Lipopolysaccharides; Mice; Mice, Inbred C57BL; Neoplasm Metastasis; Neoplasms, Experimental; NF-kappa B; Quinazolines; Recombinant Proteins; Reverse Transcriptase Polymerase Chain Reaction; RNA Interference; Signal Transduction; Survival Analysis; Toll-Like Receptor 4 | 2012 |
Quantitative immunohistochemistry for evaluating the distribution of Ki67 and other biomarkers in tumor sections and use of the method to study repopulation in xenografts after treatment with paclitaxel.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Biomarkers, Tumor; Cell Line, Tumor; Cell Proliferation; Female; Gefitinib; Humans; Immunohistochemistry; Ki-67 Antigen; Mice; Mice, Nude; Neoplasms, Experimental; Paclitaxel; Quinazolines; Xenograft Model Antitumor Assays | 2012 |
Vandetanib, an inhibitor of VEGF receptor-2 and EGF receptor, suppresses tumor development and improves prognosis of liver cancer in mice.
Topics: Animals; Apoptosis; Cell Line, Tumor; Cell Proliferation; ErbB Receptors; Human Umbilical Vein Endothelial Cells; Humans; Liver Neoplasms; Mice; Mice, Nude; Neoplasms, Experimental; Phosphorylation; Piperidines; Prognosis; Quinazolines; Vascular Endothelial Growth Factor Receptor-2 | 2012 |
Synthesis and biological evaluation of crown ether fused quinazoline analogues as potent EGFR inhibitors.
Topics: Animals; Antineoplastic Agents; Cell Proliferation; Crown Ethers; Dose-Response Relationship, Drug; ErbB Receptors; Humans; Mice; Models, Molecular; Molecular Structure; Neoplasms, Experimental; Protein Kinase Inhibitors; Quinazolines; Rats; Structure-Activity Relationship; Xenograft Model Antitumor Assays | 2012 |
Inhibition of CIP2A determines erlotinib-induced apoptosis in hepatocellular carcinoma.
Topics: Animals; Apoptosis; Autoantigens; Carcinoma, Hepatocellular; Cell Line, Tumor; Cell Survival; Dose-Response Relationship, Drug; Down-Regulation; Erlotinib Hydrochloride; Gene Expression Regulation, Neoplastic; Gene Knockdown Techniques; Humans; Intracellular Signaling Peptides and Proteins; Liver Neoplasms; Male; Membrane Proteins; Mice; Mice, Nude; Neoplasms, Experimental; Protein Kinase Inhibitors; Protein Phosphatase 2; Proto-Oncogene Proteins c-akt; Quinazolines; RNA, Small Interfering | 2013 |
In vivo anti-tumour activity of novel Quinazoline derivatives.
Topics: Animals; Antineoplastic Agents; Body Weight; Cell Line, Tumor; Female; Mice; Neoplasms, Experimental; Quinazolines | 2012 |
ErbBs inhibition by lapatinib blocks tumor growth in an orthotopic model of human testicular germ cell tumor.
Topics: Animals; Antibodies, Monoclonal, Humanized; Antineoplastic Agents; Blotting, Western; Carcinoma, Embryonal; Cell Survival; Cetuximab; Choriocarcinoma; Endodermal Sinus Tumor; ErbB Receptors; Gefitinib; Gene Expression Regulation, Neoplastic; Humans; Immunoprecipitation; Lapatinib; Male; Mice; Mice, Nude; Neoplasms, Experimental; Neoplasms, Germ Cell and Embryonal; Phosphorylation; Protein Kinase Inhibitors; Quinazolines; Real-Time Polymerase Chain Reaction; Receptor, ErbB-2; Receptor, ErbB-3; Teratocarcinoma; Testicular Neoplasms; Transplantation, Heterologous | 2013 |
T-cadherin loss promotes experimental metastasis of squamous cell carcinoma.
Topics: Animals; Cadherins; Carcinoma, Squamous Cell; Cell Adhesion; Cell Line, Tumor; Cells, Cultured; Coculture Techniques; Endothelial Cells; ErbB Receptors; Gefitinib; Human Umbilical Vein Endothelial Cells; Humans; Immunoblotting; Keratinocytes; Lung Neoplasms; Mice; Mice, Inbred NOD; Mice, SCID; Microscopy, Confocal; Neoplasms, Experimental; Protein Kinase Inhibitors; Quinazolines; RNA Interference; Skin Neoplasms; Transendothelial and Transepithelial Migration; Transplantation, Heterologous | 2013 |
Novel indolo[2,1-b]quinazoline analogues as cytostatic agents: synthesis, biological evaluation and structure-activity relationship.
Topics: Animals; Antineoplastic Agents; Biological Availability; Cell Division; Drug Screening Assays, Antitumor; Humans; Indoles; Male; Mice; Neoplasms, Experimental; Quinazolines; Structure-Activity Relationship; Transplantation, Heterologous; Tumor Cells, Cultured | 2002 |
ZD6474 inhibits vascular endothelial growth factor signaling, angiogenesis, and tumor growth following oral administration.
Topics: Administration, Oral; Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Cell Division; Endothelial Growth Factors; Enzyme Inhibitors; Female; Humans; Lymphokines; Male; Mice; Neoplasms, Experimental; Neovascularization, Pathologic; Piperidines; Quinazolines; Rats; Rats, Wistar; Receptor Protein-Tyrosine Kinases; Receptors, Growth Factor; Receptors, Vascular Endothelial Growth Factor; Signal Transduction; Tumor Cells, Cultured; Vascular Endothelial Growth Factor A; Vascular Endothelial Growth Factors; Xenograft Model Antitumor Assays | 2002 |
Labeled EGFr-TK irreversible inhibitor (ML03): in vitro and in vivo properties, potential as PET biomarker for cancer and feasibility as anticancer drug.
Topics: Acrylamides; Animals; Antineoplastic Agents; Blotting, Western; Carbon Radioisotopes; Disease Models, Animal; Enzyme Inhibitors; ErbB Receptors; Humans; Isotope Labeling; Liver; Male; Neoplasm Transplantation; Neoplasms, Experimental; Phosphorylation; Quinazolines; Rats; Receptor Protein-Tyrosine Kinases; Tissue Distribution; Tomography, Emission-Computed; Tumor Cells, Cultured | 2002 |
Enhancement of antitumor activity of ionizing radiation by combined treatment with the selective epidermal growth factor receptor-tyrosine kinase inhibitor ZD1839 (Iressa).
Topics: Animals; Antineoplastic Agents; bcl-X Protein; Blotting, Western; Combined Modality Therapy; Disease Models, Animal; Dose-Response Relationship, Drug; ErbB Receptors; Female; Gefitinib; Humans; Immunoenzyme Techniques; Mice; Mice, Inbred BALB C; Mice, Nude; Neoplasms, Experimental; Phosphorylation; Protein Serine-Threonine Kinases; Protein-Tyrosine Kinases; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-akt; Proto-Oncogene Proteins c-bcl-2; Quinazolines; Radiation, Ionizing; Survival Rate; Tumor Cells, Cultured | 2002 |
The effects of the novel, reversible epidermal growth factor receptor/ErbB-2 tyrosine kinase inhibitor, GW2016, on the growth of human normal and tumor-derived cell lines in vitro and in vivo.
Topics: Animals; Antineoplastic Agents; Apoptosis; Blotting, Western; Cell Cycle; Cell Division; Enzyme Inhibitors; Epidermal Growth Factor; ErbB Receptors; Female; Fibroblasts; Furans; Humans; Infant, Newborn; Mice; Mice, Nude; Mice, SCID; Neoplasms, Experimental; Phosphorylation; Precipitin Tests; Quinazolines; Receptor, ErbB-2; Signal Transduction; Skin; Tumor Cells, Cultured; Xenograft Model Antitumor Assays | 2001 |
Discovery and biological evaluation of potent dual ErbB-2/EGFR tyrosine kinase inhibitors: 6-thiazolylquinazolines.
Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; Enzyme Inhibitors; ErbB Receptors; Female; Humans; Inhibitory Concentration 50; Mice; Mice, Inbred Strains; Neoplasms, Experimental; Quinazolines; Receptor, ErbB-2; Structure-Activity Relationship; Transplantation, Heterologous | 2003 |
Dynamic contrast-enhanced MRI of vascular changes induced by the VEGF-signalling inhibitor ZD4190 in human tumour xenografts.
Topics: Animals; Contrast Media; Female; Gadolinium DTPA; Humans; Magnetic Resonance Imaging; Male; Mice; Mice, Nude; Neoplasm Transplantation; Neoplasms, Experimental; Quinazolines; Transplantation, Heterologous; Triazoles; Vascular Endothelial Growth Factor A | 2003 |
FURTHER STUDIES ON THE INFLUENCE OF PERIPHERAL RING SUBSTITUTION ON THE CARCINOGENICITY OF TRICYCLOQUINAZOLINE.
Topics: Carcinogens; Chemistry, Pharmaceutical; Heterocyclic Compounds; Mice; Neoplasms, Experimental; ortho-Aminobenzoates; Papilloma; Pharmacology; Quinazolines; Research; Skin Neoplasms; Toxicology | 1965 |
Reduced capillary perfusion and permeability in human tumour xenografts treated with the VEGF signalling inhibitor ZD4190: an in vivo assessment using dynamic MR imaging and macromolecular contrast media.
Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Capillary Permeability; Cell Line, Tumor; Contrast Media; Magnetic Resonance Angiography; Male; Mice; Mice, Nude; Neoplasm Transplantation; Neoplasms, Experimental; Neovascularization, Pathologic; Quinazolines; Triazoles; Vascular Endothelial Growth Factor A | 2003 |
Use of dynamic contrast-enhanced MRI to evaluate acute treatment with ZD6474, a VEGF signalling inhibitor, in PC-3 prostate tumours.
Topics: Adenocarcinoma; Animals; Capillary Permeability; Contrast Media; Dose-Response Relationship, Drug; Gadolinium DTPA; Humans; Magnetic Resonance Imaging; Male; Mice; Neoplasms, Experimental; Piperidines; Prostatic Neoplasms; Quinazolines; Reproducibility of Results; Signal Transduction; Transplantation, Heterologous; Vascular Endothelial Growth Factor A | 2003 |
Pharmacokinetics, safety, and efficacy of a liposome encapsulated thymidylate synthase inhibitor, OSI-7904L [(S)-2-[5-[(1,2-dihydro-3-methyl-1-oxobenzo[f]quinazolin-9-yl)methyl]amino-1-oxo-2-isoindolynl]-glutaric acid] in mice.
Topics: Animals; Antineoplastic Agents; Biological Availability; Carbon Radioisotopes; Disease Models, Animal; Drug Carriers; Drug Delivery Systems; Enzyme Inhibitors; Humans; Indoles; Isoindoles; Liposomes; Metabolic Clearance Rate; Mice; Mice, Inbred BALB C; Neoplasm Transplantation; Neoplasms, Experimental; Quinazolines; Thymidylate Synthase; Tissue Distribution; Treatment Outcome; Tumor Cells, Cultured; Xenograft Model Antitumor Assays | 2004 |
A specific antagonist of the p110delta catalytic component of phosphatidylinositol 3'-kinase, IC486068, enhances radiation-induced tumor vascular destruction.
Topics: Animals; Catalytic Domain; Cell Movement; Cell Survival; Cells, Cultured; Endothelium, Vascular; Enzyme Inhibitors; Humans; Mice; Neoplasms, Experimental; Neovascularization, Pathologic; Phosphoinositide-3 Kinase Inhibitors; Quinazolines; Radiation-Sensitizing Agents | 2004 |
Combined epidermal growth factor receptor targeting with the tyrosine kinase inhibitor gefitinib (ZD1839) and the monoclonal antibody cetuximab (IMC-C225): superiority over single-agent receptor targeting.
Topics: Animals; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Cell Proliferation; Cetuximab; Dose-Response Relationship, Drug; Drug Therapy, Combination; ErbB Receptors; Female; Gefitinib; Gene Expression Regulation, Neoplastic; Humans; Immunohistochemistry; In Situ Nick-End Labeling; Ki-67 Antigen; Mice; Mice, Inbred BALB C; Mice, Nude; Mitogen-Activated Protein Kinases; Neoplasms, Experimental; Oligonucleotide Array Sequence Analysis; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-akt; Quinazolines; Signal Transduction; Xenograft Model Antitumor Assays | 2004 |
The antitumor and antiangiogenic activity of vascular endothelial growth factor receptor inhibition is potentiated by ErbB1 blockade.
Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Apoptosis; Cell Line; Cell Line, Tumor; Coculture Techniques; Drug Synergism; Endothelial Cells; Enzyme-Linked Immunosorbent Assay; Epidermal Growth Factor; ErbB Receptors; Fluorescent Antibody Technique; Gefitinib; Humans; Immunoblotting; In Situ Nick-End Labeling; Mice; Mice, Inbred BALB C; Mice, Nude; Neoplasm Transplantation; Neoplasms, Experimental; Phthalazines; Platelet Endothelial Cell Adhesion Molecule-1; Protein Kinase Inhibitors; Pyridines; Quinazolines; Transplantation, Heterologous; Vascular Endothelial Growth Factor A | 2005 |
ZD6474 inhibits tumor growth and intraperitoneal dissemination in a highly metastatic orthotopic gastric cancer model.
Topics: Biomarkers, Tumor; Carcinoma, Signet Ring Cell; Gene Expression Profiling; Humans; Neoplasm Metastasis; Neoplasms, Experimental; Peritoneal Neoplasms; Piperidines; Quinazolines; Reverse Transcriptase Polymerase Chain Reaction; Stomach Neoplasms; Tumor Cells, Cultured | 2006 |
5-Substituted 4-anilinoquinazolines as potent, selective and orally active inhibitors of erbB2 receptor tyrosine kinase.
Topics: Administration, Oral; Animals; Antineoplastic Agents; Carrier Proteins; Enzyme Inhibitors; Inhibitory Concentration 50; Intracellular Signaling Peptides and Proteins; Mice; Neoplasms, Experimental; Quinazolines; Structure-Activity Relationship; Transplantation, Heterologous; Tumor Burden | 2005 |
A liquid chromatographic-tandem mass spectrometric method for the determination of two selective thymidylate synthase inhibitors, BGC945 and BGC638, in mouse plasma.
Topics: Animals; Calibration; Chromatography, Liquid; Enzyme Inhibitors; Humans; Injections, Intravenous; KB Cells; Mice; Mice, Inbred BALB C; Mice, Inbred ICR; Mice, Nude; Neoplasms, Experimental; Quinazolines; Reproducibility of Results; Spectrometry, Mass, Electrospray Ionization; Thymidylate Synthase | 2005 |
Chemopreventive and therapeutic efficacy of orally active tyrosine kinase inhibitors in a transgenic mouse model of gallbladder carcinoma.
Topics: Animals; Anticarcinogenic Agents; Antineoplastic Agents; Blotting, Western; Body Weight; Carcinoma; Cell Line, Tumor; Disease Models, Animal; Enzyme Inhibitors; ErbB Receptors; Gallbladder; Gallbladder Neoplasms; Gefitinib; Humans; In Situ Nick-End Labeling; MAP Kinase Signaling System; Mice; Mice, Transgenic; Microscopy, Fluorescence; Neoplasms, Experimental; Phosphorylation; Protein-Tyrosine Kinases; Quinazolines; Receptor, ErbB-2; Tolonium Chloride | 2005 |
Oncogenic transformation by inhibitor-sensitive and -resistant EGFR mutants.
Topics: Adaptor Proteins, Signal Transducing; Animals; Antineoplastic Agents; Cell Transformation, Neoplastic; Drug Resistance, Neoplasm; ErbB Receptors; Erlotinib Hydrochloride; Exons; Gefitinib; Genetic Therapy; Humans; Mice; Mice, Nude; Mutation; Neoplasms, Experimental; NIH 3T3 Cells; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-akt; Quinazolines; Shc Signaling Adaptor Proteins; Src Homology 2 Domain-Containing, Transforming Protein 1; STAT3 Transcription Factor; Transfection; Tumor Stem Cell Assay | 2005 |
Development and therapeutic options for the treatment of raloxifene-stimulated breast cancer in athymic mice.
Topics: Animals; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic Agents; Breast Neoplasms; Cell Proliferation; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Design; Drug Resistance, Neoplasm; Estradiol; Estrogen Receptor alpha; Female; Fulvestrant; Gefitinib; Gene Expression Regulation, Neoplastic; Genes, erbB-2; Humans; Mice; Mice, Inbred BALB C; Neoplasms, Experimental; Quinazolines; Raloxifene Hydrochloride; RNA, Messenger; Structure-Activity Relationship; Transplantation, Heterologous; Trastuzumab; Xenograft Model Antitumor Assays | 2006 |
ZD6474, an inhibitor of vascular endothelial growth factor receptor tyrosine kinase, inhibits growth of experimental lung metastasis and production of malignant pleural effusions in a non-small cell lung cancer model.
Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Cell Proliferation; Endothelium, Vascular; Enzyme-Linked Immunosorbent Assay; ErbB Receptors; Flow Cytometry; Gefitinib; Humans; Immunohistochemistry; Lung Neoplasms; Male; Mice; Mice, Inbred BALB C; Neoplasm Transplantation; Neoplasms, Experimental; Neovascularization, Pathologic; Piperidines; Pleural Effusion, Malignant; Quinazolines; Reverse Transcriptase Polymerase Chain Reaction; Vascular Endothelial Growth Factor Receptor-2 | 2006 |
Signaling interactions of rapamycin combined with erlotinib in cervical carcinoma xenografts.
Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Cell Line, Tumor; Cell Proliferation; Drug Interactions; Epidermal Growth Factor; Erlotinib Hydrochloride; Extracellular Signal-Regulated MAP Kinases; Female; Humans; Mice; Mice, SCID; Neoplasm Transplantation; Neoplasms, Experimental; Phosphorylation; Quinazolines; Ribosomal Protein S6; Signal Transduction; Sirolimus; Transplantation, Heterologous; Uterine Cervical Neoplasms | 2006 |
Molecular basis for sensitivity and acquired resistance to gefitinib in HER2-overexpressing human gastric cancer cell lines derived from liver metastasis.
Topics: Animals; Antineoplastic Agents; Blotting, Western; Cell Line, Tumor; Drug Resistance, Neoplasm; Enzyme-Linked Immunosorbent Assay; Flow Cytometry; Gefitinib; Humans; Immunohistochemistry; Liver Neoplasms; Male; Mice; Mice, Nude; Neoplasms, Experimental; Quinazolines; Receptor, ErbB-2; Stomach Neoplasms | 2006 |
Epidermal growth factor receptor activation in glioblastoma through novel missense mutations in the extracellular domain.
Topics: Animals; Astrocytes; Binding Sites; Cell Line, Tumor; Cell Survival; Cells, Cultured; ErbB Receptors; Erlotinib Hydrochloride; Gene Expression Regulation, Neoplastic; Glioblastoma; Humans; Mice; Mice, Nude; Models, Molecular; Mutation, Missense; Neoplasms, Experimental; NIH 3T3 Cells; Phosphorylation; Protein Binding; Protein Kinase Inhibitors; Protein Structure, Tertiary; Quinazolines; Reverse Transcriptase Polymerase Chain Reaction; Transfection | 2006 |
Initial testing of the VEGFR inhibitor AZD2171 by the pediatric preclinical testing program.
Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Cell Line, Tumor; Female; Humans; Leukemia, Experimental; Mice; Mice, Inbred BALB C; Mice, Inbred NOD; Mice, Nude; Mice, SCID; Neoplasm Proteins; Neoplasms, Experimental; Neovascularization, Pathologic; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-kit; Quinazolines; Random Allocation; Receptors, Vascular Endothelial Growth Factor; Xenograft Model Antitumor Assays | 2008 |
AZD1152, a selective inhibitor of Aurora B kinase, inhibits human tumor xenograft growth by inducing apoptosis.
Topics: Animals; Antineoplastic Agents; Apoptosis; Aurora Kinase B; Aurora Kinases; Cell Line, Tumor; Cell Proliferation; Flow Cytometry; Humans; Mice; Mice, Nude; Neoplasms, Experimental; Organophosphates; Protein Serine-Threonine Kinases; Quinazolines; Rats; Transplantation, Heterologous | 2007 |
Neutral 5-substituted 4-indazolylaminoquinazolines as potent, orally active inhibitors of erbB2 receptor tyrosine kinase.
Topics: Administration, Oral; Animals; Antineoplastic Agents; Breast Neoplasms; Cell Line, Tumor; Cell Proliferation; Dogs; Epidermal Growth Factor; ErbB Receptors; Ether-A-Go-Go Potassium Channels; Female; Hepatocytes; Humans; Indazoles; Keratinocytes; Lapatinib; Male; Metabolic Clearance Rate; Mice; Mice, Nude; Mice, SCID; Microsomes; Molecular Structure; Neoplasms, Experimental; Phosphorylation; Protein Kinase Inhibitors; Quinazolines; Rats; Rats, Wistar; Receptor, ErbB-2; Survival Rate; Xenograft Model Antitumor Assays | 2008 |
Preclinical evaluation of M30 and M65 ELISAs as biomarkers of drug induced tumor cell death and antitumor activity.
Topics: Animals; Antineoplastic Agents; Apoptosis; Biomarkers, Tumor; Enzyme-Linked Immunosorbent Assay; Keratin-18; Male; Neoplasms, Experimental; Organophosphates; Quinazolines; Rats; Rats, Nude | 2008 |
Targeting EGFR activity in blood vessels is sufficient to inhibit tumor growth and is accompanied by an increase in VEGFR-2 dependence in tumor endothelial cells.
Topics: Animals; Cell Line; Cell Line, Tumor; Cell Proliferation; Cinnamates; Endothelial Cells; Endothelium, Vascular; Enzyme Inhibitors; Epidermal Growth Factor; ErbB Receptors; Extracellular Signal-Regulated MAP Kinases; Gefitinib; Humans; Male; Mice; Mice, Nude; Neoplasms, Experimental; Neuropilin-1; Phosphorylation; Proto-Oncogene Proteins c-akt; Quinazolines; Receptor, ErbB-2; Signal Transduction; Transplantation, Heterologous; Tyrphostins; Vascular Endothelial Growth Factor Receptor-2 | 2008 |
Effects of 5,8-dideazaisopteroylglutamate and its possible tri-gamma-glutamyl metabolite (5,8-dideazaisoPteGlu3) on colon adenocarcinoma, and the folate dependent enzymes thymidylate synthase and dihydrofolate reductase.
Topics: Adenocarcinoma; Animals; Cell Line; Colonic Neoplasms; DNA Replication; Drug Resistance; Female; Humans; Kinetics; Leukemia; Methotrexate; Methyltransferases; Mice; Mice, Inbred C57BL; Neoplasms, Experimental; Peptide Synthases; Quinazolines; Tetrahydrofolate Dehydrogenase; Thymidylate Synthase | 1983 |
Possible relationship between glycosphingolipids and the formation of metastasis in certain human experimental tumors.
Topics: Animals; Carcinoma, Squamous Cell; Chick Embryo; Gangliosides; Glycosphingolipids; Humans; Neoplasm Metastasis; Neoplasms, Experimental; Quinazolines; Sarcoma; Thiazoles | 1980 |
Enhanced antitumor activity for the thymidylate synthase inhibitor 1843U89 through decreased host toxicity with oral folic acid.
Topics: Animals; Body Weight; Dogs; Dose-Response Relationship, Drug; Enzyme Inhibitors; Folic Acid; Humans; Indoles; Intestinal Diseases; Isoindoles; Leucovorin; Mice; Neoplasms, Experimental; Osteosarcoma; Quinazolines; Thymidylate Synthase; Tumor Cells, Cultured | 1995 |
Structure-based design of substituted diphenyl sulfones and sulfoxides as lipophilic inhibitors of thymidylate synthase.
Topics: Animals; Antineoplastic Agents; Cell Division; Crystallography, X-Ray; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Escherichia coli; Humans; Magnetic Resonance Spectroscopy; Mice; Models, Molecular; Molecular Conformation; Molecular Structure; Neoplasms, Experimental; Quinazolines; Structure-Activity Relationship; Sulfones; Sulfoxides; Thymidylate Synthase; Tumor Cells, Cultured | 1997 |
Specific, irreversible inactivation of the epidermal growth factor receptor and erbB2, by a new class of tyrosine kinase inhibitor.
Topics: Animals; Antineoplastic Agents; Binding Sites; Cell Line; Cysteine; Enzyme Inhibitors; ErbB Receptors; Humans; Mice; Mice, Nude; Models, Molecular; Mutagenesis, Site-Directed; Neoplasm Transplantation; Neoplasms, Experimental; Protein Conformation; Protein-Tyrosine Kinases; Quinazolines; Receptor, ErbB-2; Recombinant Fusion Proteins; Transplantation, Heterologous; Tumor Cells, Cultured | 1998 |
Irreversible inhibition of epidermal growth factor receptor tyrosine kinase with in vivo activity by N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-2-butynamide (CL-387,785).
Topics: Animals; Antineoplastic Agents; Cell Cycle; Cell Division; Drug Screening Assays, Antitumor; Enzyme Inhibitors; ErbB Receptors; Female; Mice; Mice, Nude; Models, Molecular; Neoplasm Transplantation; Neoplasms, Experimental; Phosphorylation; Quinazolines; Tumor Cells, Cultured | 1999 |
Anticancer efficacy of the irreversible EGFr tyrosine kinase inhibitor PD 0169414 against human tumor xenografts.
Topics: 3T3 Cells; Animals; Antineoplastic Agents; Area Under Curve; Drug Administration Routes; Drug Administration Schedule; Enzyme Inhibitors; ErbB Receptors; Humans; Infusion Pumps, Implantable; Liver; Mice; Mice, Inbred ICR; Mice, Nude; Mice, SCID; Neoplasm Transplantation; Neoplasms, Experimental; Phosphorylation; Quinazolines; Receptor Protein-Tyrosine Kinases; Transplantation, Heterologous; Treatment Outcome; Tumor Cells, Cultured | 2000 |
Antitumor effect and potentiation of cytotoxic drugs activity in human cancer cells by ZD-1839 (Iressa), an epidermal growth factor receptor-selective tyrosine kinase inhibitor.
Topics: Animals; Antineoplastic Agents; Apoptosis; Carboplatin; Cell Division; Cisplatin; Docetaxel; Dose-Response Relationship, Drug; Drug Synergism; ErbB Receptors; Female; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; Neoplasm Transplantation; Neoplasms, Experimental; Organoplatinum Compounds; Oxaliplatin; Paclitaxel; Quinazolines; Survival Rate; Taxoids; Thiophenes; Topotecan; Transplantation, Heterologous; Tumor Cells, Cultured | 2000 |
Inhibition of growth factor production and angiogenesis in human cancer cells by ZD1839 (Iressa), a selective epidermal growth factor receptor tyrosine kinase inhibitor.
Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Disease Models, Animal; Drug Synergism; Endothelial Growth Factors; ErbB Receptors; Female; Fibroblast Growth Factor 2; Gefitinib; Growth Substances; Humans; Immunohistochemistry; Inhibitory Concentration 50; Lymphokines; Mice; Mice, Inbred BALB C; Mice, Nude; Neoplasms, Experimental; Neovascularization, Pathologic; Protein-Tyrosine Kinases; Quinazolines; Transforming Growth Factor alpha; Tumor Cells, Cultured; Vascular Endothelial Growth Factor A; Vascular Endothelial Growth Factors; Xenograft Model Antitumor Assays | 2001 |
ZD1839 (Iressa), a novel epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, potently inhibits the growth of EGFR-positive cancer cell lines with or without erbB2 overexpression.
Topics: Cell Division; Epidermal Growth Factor; ErbB Receptors; Gefitinib; Genes, erbB-2; Humans; Mitogen-Activated Protein Kinases; Neoplasms, Experimental; Phosphorylation; Quinazolines; Tumor Cells, Cultured | 2001 |
Quinazoline analogues of folic acid as inhibitors of thymidylate synthetase from bacterial and mammalian sources.
Topics: Animals; Cell Division; Folic Acid; In Vitro Techniques; Lacticaseibacillus casei; Leukemia L1210; Methyltransferases; Mice; Neoplasms, Experimental; Quinazolines; Structure-Activity Relationship; Thymidylate Synthase | 1979 |
2,4-diamino-5-methyl-6-[(3,4,5-trimethoxyanilino)methyl]quinazoline (tmq), a potent non-classical folate antagonist inhibitor--I effect on dihydrofolate reductase and growth of rodent tumors in vitro and in vivo.
Topics: Animals; Antineoplastic Agents; Folic Acid Antagonists; Humans; In Vitro Techniques; Leukemia L1210; Mice; Neoplasms, Experimental; Quinazolines | 1979 |
Further evidence for a basis of selective activity and relative responsiveness during antifolate therapy of murine tumors.
Topics: Aminopterin; Animals; Aspartic Acid; Carcinoma, Ehrlich Tumor; Chick Embryo; DNA, Neoplasm; Folic Acid Antagonists; Intestine, Small; Leukemia L1210; Liver; Lymphoma; Methotrexate; Mice; Mice, Inbred C57BL; Neoplasms, Experimental; Quinazolines; Sarcoma 180; Tetrahydrofolate Dehydrogenase; Time Factors | 1975 |
ICI D1694, an inhibitor of thymidylate synthase for clinical study.
Topics: Animals; Breast Neoplasms; Cell Line; Cell Survival; Drug Screening Assays, Antitumor; Female; Folic Acid Antagonists; Humans; Leukemia L1210; Mice; Neoplasms, Experimental; Quinazolines; Thiophenes; Thymidylate Synthase; Tumor Cells, Cultured | 1991 |
Heterocyclic quinones. 17. A new in vivo active antineoplastic drug: 6,7-bis(1-aziridinyl)-4-[[3-(N,N-dimethylamino)propyl]amino]-5,8- quinazolinedione.
Topics: Animals; Antineoplastic Agents; Aziridines; Breast Neoplasms; Cell Division; Cell Line; Drug Screening Assays, Antitumor; Female; Humans; Leukemia L1210; Leukemia, Experimental; Melanoma, Experimental; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Molecular Structure; Neoplasms, Experimental; Quinazolines; Sarcoma, Experimental; Structure-Activity Relationship | 1991 |
Inhibitory effects of DN-9693 on platelet-enhanced tumor cell attachment to cultured endothelium.
Topics: 3',5'-Cyclic-AMP Phosphodiesterases; Animals; Blood Platelets; Calcium; Cells, Cultured; Endothelium, Vascular; Lung Neoplasms; Male; Melanoma, Experimental; Mice; Mice, Inbred C57BL; Microscopy, Electron, Scanning; Neoplasms, Experimental; Platelet Activation; Platelet Aggregation Inhibitors; Pulmonary Artery; Quinazolines; Tumor Cells, Cultured | 1990 |
Activity of batracylin (NSC-320846) against solid tumors of mice.
Topics: Adenocarcinoma; Animals; Antineoplastic Agents; Carcinoma, Intraductal, Noninfiltrating; Cell Survival; Cells, Cultured; Colonic Neoplasms; Drug Administration Schedule; Drug Screening Assays, Antitumor; Humans; Mammary Neoplasms, Experimental; Mice; Mice, Inbred Strains; Neoplasms, Experimental; Pancreatic Neoplasms; Quinazolines; Tumor Cells, Cultured | 1989 |
Cell cycle effects of trimetrexate (CI-898).
Topics: Animals; Antineoplastic Agents; Cell Cycle; Cell Survival; Cells, Cultured; Cricetinae; Demecolcine; Drug Evaluation, Preclinical; Female; Flow Cytometry; Injections, Intraperitoneal; Interphase; Leukemia L1210; Methotrexate; Mice; Neoplasms, Experimental; Ovary; Quinazolines; Trimetrexate | 1986 |
Histochemical comparison of the effects of a carcinogenic and a non-carcinogenic derivative of tricycloquinazoline.
Topics: Animals; Carcinogens; DNA; Electron Transport Complex IV; Glycerolphosphate Dehydrogenase; Histocytochemistry; Hyperplasia; L-Lactate Dehydrogenase; Mice; Neoplasms, Experimental; Phosphogluconate Dehydrogenase; Quinazolines; Skin; Skin Neoplasms; Succinate Dehydrogenase; Sulfhydryl Compounds | 1970 |
The apparent induction of thymidylate synthetase by amethopterin.
Topics: Animals; Aspartic Acid; Benzoates; Carcinoma, Hepatocellular; Enzyme Induction; Folic Acid; Hepatectomy; Liver; Liver Neoplasms; Liver Regeneration; Methotrexate; Methyltransferases; Neoplasms, Experimental; Quinazolines; Rats; Thymine Nucleotides; Uracil Nucleotides | 1971 |
Quinazoline antifolates as inhibitors of growth, dihydrofolate reductase, and thymidylate synthetase of mouse neuroblastoma cells in culture.
Topics: Animals; Cells, Cultured; Chromatography, Paper; Folic Acid Antagonists; Growth; Kinetics; Leucovorin; Methyltransferases; Mice; Neoplasms, Experimental; Neuroblastoma; Quinazolines; Thymidine; Thymidylate Synthase | 1974 |
Quinazolines. VI. Synthesis of 2,4-diaminoquinazolines from anthranilonitriles.
Topics: Animals; Chemical Phenomena; Chemistry; Culture Techniques; Folic Acid Antagonists; Lactobacillus; Mice; Neoplasms, Experimental; Nitriles; ortho-Aminobenzoates; Quinazolines; Streptococcus | 1970 |