chloroquine has been researched along with podophyllotoxin in 119 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (3.36) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 32 (26.89) | 29.6817 |
2010's | 75 (63.03) | 24.3611 |
2020's | 8 (6.72) | 2.80 |
Authors | Studies |
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Croft, SL; Gamenara, D; Grady, S; Heinzen, H; Kendrick, H; Moyna, G; Moyna, P; Ren, H; Yardley, V | 1 |
Chibale, K; Croft, SL; Fairlamb, AH; Haupt, H; Kendrick, H; Saravanamuthu, A; Yardley, V | 1 |
Croft, SL; del Rayo Camacho, M; Kirby, GC; Marley, D; Phillipson, JD; Warhurst, DC | 1 |
Brun, R; Cimanga, K; Dommisse, R; Hostyn, S; Kaiser, M; Lemière, G; Maes, BU; Mátyus, P; Pieters, L; Van Miert, S; Vlietinck, A | 1 |
Bauer, H; Davioud-Charvet, E; Krauth-Siegel, RL; Lee, B; Melchers, J; Rattray, L; Ruppert, T; Yardley, V | 1 |
Alvarez, A; Atherton, R; Coro, J; Little, S; Pérez, R; Rodríguez, H; Súarez, M; Wharton, H; Yardley, V | 1 |
Brun, R; Gilbert, IH; Gonzalez-Pacanowska, D; Johansson, NG; Kaiser, M; Kasinathan, G; Leal, I; Musso-Buendia, A; Nguyen, C; Ruda, GF; Ruiz-Pérez, LM; Sahlberg, BL; Schipani, A | 1 |
Croft, SL; Gilbert, IH; Gonzalez-Pacanowska, D; Gros, L; Jimenez, CJ; Little, S; Lorente, SO; Rattray, L; Ruiz-Perez, LM; Wharton, H; Yardley, V | 1 |
Ahua, KM; Brun, R; Diallo, D; Hay, AE; Hostettmann, K; Ioset, JR | 1 |
Bakunov, SA; Bakunova, SM; Bridges, AS; Brun, R; Hall, JE; Jones, SK; Kumar, EV; Lombardy, RJ; Patrick, DA; Tidwell, RR; Wenzler, T; Zhirnov, O | 1 |
Bringmann, G; Brun, R; Kaiser, M; Neumann, S | 1 |
Bongard, E; Brown, DM; Loakes, D; Too, K; Vivas, L; Yardley, V | 1 |
Brun, R; Gunzenhauser, S; Senn, M; Séquin, U | 1 |
Bakunov, SA; Bakunova, SM; Barszcz, T; Brun, R; Hall, JE; Tidwell, RR; Wenzler, T; Werbovetz, KA | 1 |
Brun, R; Kaiser, M; Kuettel, S; Perozzo, R; Scapozza, L; Zambon, A | 1 |
Bringmann, G; Bruhn, T; Brun, R; Faber, JH; Gampe, CM; Gelhaus, C; Leippe, M; Mikyna, M; Reichert, M; Reichert, Y | 1 |
Aldana, I; Bongard, E; Burguete, A; Charnaud, S; Lima, LM; Monge, A; Perez-Silanes, S; Solano, B; Vicente, E; Villar, R; Vivas, L | 1 |
Becker, K; Davioud-Charvet, E; Friebolin, W; Furrer, J; Jannack, B; Lanzer, M; Oeser, T; Sanchez, CP; Wenzel, N; Yardley, V | 1 |
Arai, C; Brun, R; Ge, JF; Ihara, M; Kaiser, M; Wittlin, S | 1 |
Brun, R; Faist, J; Kaiser, M; Saf, R; Schlapper, C; Seebacher, W; Weis, R | 1 |
Brun, R; Kehraus, S; König, GM; Krick, A; Pontius, A | 1 |
Bakunov, SA; Bakunova, SM; Barszcz, T; Brun, R; Tidwell, RR; Wenzler, T; Werbovetz, KA | 2 |
Alp, M; Brun, R; Göker, H; Yildiz, S | 1 |
Becker, K; Fritz-Wolf, K; Hu, Y; Rahlfs, S; Sturm, N; Wittlin, S; Zimmermann, H | 1 |
Brun, R; Connolly, JD; Efange, SM; Hoye, TR; Makolo, FL; Mbah, JA; McAkam, T; Nelson, DP; Nyongbela, KD; Wirmum, CK; Wittlin, S | 1 |
Bakunov, SA; Bakunova, SM; Barszcz, T; Bridges, AS; Brun, R; Jones, SK; Kumar, EV; Ohemeng, KA; Patrick, DA; Tidwell, RR; Wenzler, T; Werbovetz, KA | 1 |
Baell, JB; Brun, R; Charman, WN; Fairlamb, AH; Holloway, GA; Kaiser, M; Kostewicz, E; Novello, PM; Parisot, JP; Richardson, J; Street, IP; Watson, KG | 1 |
Bakunov, SA; Bakunova, SM; Barzcz, T; Brun, R; Chen, H; Jones, SK; Kumar, EV; Patrick, DA; Tidwell, RR; Wenzler, T; Werbovetz, KA | 1 |
Bolognesi, ML; Bongarzone, S; Brun, R; Cavalli, A; Lizzi, F; Luise Krauth-Siegel, R | 1 |
Austin, CP; Fidock, DA; Hayton, K; Huang, R; Inglese, J; Jiang, H; Johnson, RL; Su, XZ; Wellems, TE; Wichterman, J; Yuan, J | 1 |
Brun, R; Cos, P; Dhooghe, L; Dommisse, R; Hajós, G; Hostyn, S; Kaiser, M; Lemière, G; Maes, BU; Maes, L; Mátyus, P; Nagy, I; Pieters, L; Riedl, Z; Tapolcsányi, P; Van Baelen, G | 1 |
Bakunov, SA; Bakunova, SM; Brun, R; Ghebru, M; Tidwell, RR; Wenzler, T; Werbovetz, KA | 1 |
Brun, R; Lusvarghi, S; Mazzieri, MR; Pagliero, RJ; Pierini, AB | 1 |
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A | 1 |
Armstrong, T; Baell, JB; Holloway, GA; Novello, PM; Parisot, JP; Street, IP; Thompson, RC; Watson, KG | 1 |
Bauer, R; Brun, R; Gachet, MS; Kaiser, M; Kunert, O; Muñoz, RA; Schühly, W | 1 |
Amade, P; Cachet, N; Kaiser, M; Regalado, EL; Tasdemir, D; Thomas, OP | 1 |
Baumann, K; Bischof, SK; Bringmann, G; Brun, R; Dreher, J; Gulder, T; Kaiser, M; Moll, H; Müller, S; Stich, A; Winter, C | 1 |
Brun, R; Carballeira, NM; Herman, R; Kappe, SH; Lauinger, IL; Perozzo, R; Sanabria, D; Tarun, A; Tasdemir, D; Zloh, M | 1 |
Bourguet-Kondracki, ML; Copp, BR; Finlayson, R; Harper, JL; Kaiser, M; Page, MJ; Pearce, AN; Webb, VL | 1 |
Baragaña, B; Bosch-Navarrete, C; Brun, R; Gilbert, IH; González-Pacanowska, D; Johansson, NG; Kaiser, M; McCarthy, O; Roberts, SM; Sánchez, P; Whittingham, JL; Wilson, KS; Zhou, XX | 1 |
Bauer, R; Brun, R; Gachet, MS; Kaiser, M; Keller, W; Kunert, O; Muñoz, RA; Schuehly, W; Zehl, M | 1 |
Gerth, K; Jansen, R; Mohr, KI; Müller, R; Okanya, PW | 1 |
Charman, SA; Chibale, K; Fakorede, F; Gessner, RK; Gitari, PW; Hudson, A; Kaiser, M; Ndakala, AJ; October, N; Shackleford, DM; White, KL; Yeates, C | 1 |
Chibale, K; Feng, TS; Gut, J; Kumar, V; Mahajan, MP; Nasser, S; Raj, R; Rosenthal, PJ; Sachdeva, S; Singh, P; Vivas, L | 1 |
Chan, ST; Copp, BR; Kaiser, M; Page, MJ; Pearce, AN | 1 |
Brun, R; Ge, JF; Ihara, M; Kaiser, M; Liu, BQ; Shi, XL; Wittlin, S | 1 |
Anizon, F; Bouchikhi, F; Brun, R; Moreau, P | 1 |
Brun, R; Huang, TL; Kaiser, M; Mayence, A; Vanden Eynde, JJ; Yarlett, N | 1 |
Dürüst, Y; Kaiser, M; Karakuş, H; Tasdemir, D | 1 |
Boshoff, HI; Boyd, PD; Copp, BR; Kaiser, M; McCracken, ST | 1 |
Bettis, S; Brun, R; Fomovska, A; Huang, Q; Kaiser, M; Kozikowski, AP; McLeod, R; Mui, E; Pieroni, M; Stec, J; Witola, WH | 1 |
Agarwal, H; Bahar, M; Brun, R; Cason, E; Doskotch, RW; Drew, ME; Endeshaw, M; He, S; Kaiser, M; Kinghorn, AD; Li, C; Mahasenan, KV; Munde, M; Pandharkar, T; Werbovetz, KA; Wilson, WD; Zhu, X | 1 |
Copp, BR; Kaiser, M; Liew, LP | 1 |
Kaiser, M; McKeever, C; Rozas, I | 1 |
Barker, D; Rye, CE | 1 |
Andriamihaja, B; Bauer, JO; Lamshöft, M; Razakarivony, AA; Spiteller, M; Strohmann, C; Talontsi, FM | 1 |
El Sayed, I; Inokuchi, T; Kaiser, M; Lu, WJ; Maeda, T; Mei, ZW; Pang, CQ; Peng, W; Wang, L | 1 |
Campbell, M; Charman, SA; Gilbert, IH; Hudson, A; Kaiser, M; Katneni, K; Mital, A; Morizzi, J; Murugesan, D; Shackleford, DM; Yeates, C | 1 |
Egan, TJ; El Sayed, Iel T; Imai, K; Inokuchi, T; Kaiser, M; Lu, WJ; Mei, ZW; Wang, L; Wicht, KJ | 1 |
Arafa, RK; Boykin, DW; Brun, R; Ismail, MA; Jones, SK; Pandharkar, T; Patrick, DA; Tidwell, RR; Wenzler, T; Werbovetz, KA; Zhu, X | 1 |
Almohaywi, B; Avery, VM; Baell, JB; Campbell, M; Charman, SA; Ferrins, L; Hyland, C; Jones, AJ; Kaiser, M; Rahmani, R; Ryan, E; Smith, J; Sykes, ML; Teston, E; White, KL; Yin, J | 1 |
Bakunov, SA; Bakunova, SM; Barszcz, T; Boykin, DW; Brun, R; Jones, SK; Kumar, A; Patrick, DA; Tidwell, RR; Wenzler, T; Werbovetz, KA | 1 |
Bosch-Navarrete, C; Gilbert, IH; González-Pacanowska, D; Hampton, SE; Johansson, NG; Kahnberg, P; Kaiser, M; Recio, E; Schipani, A | 1 |
Brun, R; Harel, D; Prinz, H; Schepmann, D; Schmidt, TJ; Wünsch, B | 1 |
Belluti, F; Bisi, A; Bolognesi, ML; Brun, R; Cavalli, A; Colizzi, F; Gobbi, S; Kostrewa, D; Lauciello, L; Perozzo, R; Rampa, A; Recanatini, M; Scapozza, L | 1 |
Amewu, RK; Burrell-Saward, H; Chadwick, J; Hussain, A; Janneh, O; Miguel, C; O'Neill, PM; Panda, S; Rinki, R; Vivas, L; Ward, SA | 1 |
Bakunov, SA; Bakunova, SM; Brun, R; Patrick, DA; Tidwell, RR; Wenzler, T | 1 |
Batzer, A; Bode, HB; Chantratita, N; Grundmann, F; Kaiser, M; Kurz, M; Schiell, M; Thanwisai, A | 1 |
Anh Ngoc, T; Egan, TJ; Imai, K; Inokuchi, T; Kaiser, M; Kiguchi, R; Wang, MQ; Wang, N; Wicht, KJ | 1 |
Dardonville, C; Kaiser, M; Lagartera, L; Ríos Martínez, CH | 1 |
Chibale, K; Huang, J; Mahajan, A; Mekonnen, B; Meurillon, M; Naran, K; Sharma, RK; Tukulula, M; Warner, D | 1 |
Botta, B; Brun, R; Costi, R; De Vita, D; Di Santo, R; Friggeri, L; Kaiser, M; Moraca, F; Scipione, L; Tortorella, S; Zamperini, C | 1 |
Chibale, K; Gut, J; Njogu, PM; Rosenthal, PJ | 1 |
Andayi, WA; Chibale, K; Egan, TJ; Gut, J; Rosenthal, PJ | 1 |
Boykin, DW; Brun, R; Liu, ZY; Wenzler, T; Zhu, X | 1 |
Avery, VM; Baell, JB; Bergström, CA; Charman, SA; Ferrins, L; Gazdik, M; Jones, AJ; Kaiser, M; Rahmani, R; Ryan, E; Sykes, ML; Varghese, S; White, KL | 1 |
Bode, HB; Kaiser, M; Nollmann, FI; Reimer, D; Schultz, K | 1 |
Andricopulo, AD; Bwalya, AG; Carballeira, NM; Cordero-Maldonado, ML; Crawford, AD; Guido, RV; Itoe, MA; Kaiser, M; Mota, MM; Tasdemir, D | 1 |
Avery, VM; Barth, S; Duffy, S; Frank, W; Geffken, D; Held, J; Kamber, J; Kuna, K; Kurz, T; Leven, M; Mordmüller, B; Sax, S; Siethoff, C; Tschan, S; Wittlin, S | 1 |
Battistuzzi, G; Giannini, G | 1 |
Battistuzzi, G; Giannini, G; Vignola, D | 1 |
Dardonville, C; Kaiser, M; Montalvo-Quirós, S; Taladriz-Sender, A | 1 |
Bauer, JO; Happi, GM; Kouam, SF; Lamshöft, M; Spiteller, M; Strohmann, C; Talontsi, FM; Zühlke, S | 1 |
Gilbert, IH; Kaiser, M; Mital, A; Murugesan, D; Yeates, C | 1 |
Brun, R; Faist, J; Kaiser, M; Saf, R; Seebacher, W; Weis, R | 1 |
Brun, R; Göker, H; Kaiser, M; Karaaslan, C | 1 |
Faist, J; Hinteregger, C; Kaiser, M; Mäser, P; Saf, R; Seebacher, W; Weis, R | 1 |
Bringmann, G; Brun, R; Brünnert, D; Chatterjee, M; Efferth, T; Feineis, D; Kaiser, M; Li, J; Mudogo, V; Seo, EJ; Seupel, R | 1 |
Faist, J; Hochegger, P; Kaiser, M; Mäser, P; Saf, R; Seebacher, W; Weis, R | 2 |
Back, TG; Brun, R; Kaiser, M; Manivannan, S; Pastor, A; Snyder, FF; Tran, HA; Wen, X; Zheng, Z | 1 |
Barker, D; Bourguet-Kondracki, ML; Brunel, JM; Cadelis, MM; Copp, BR; Dubois, J; Kaiser, M | 1 |
Brun, R; Kaiser, M; Mazzieri, MR; Nieto, MJ; Pagliero, RJ | 1 |
Chianese, G; Erpenbeck, D; Kaiser, M; Luciano, P; Merten, C; Silber, J; Tasdemir, D; Topaloglu, B | 1 |
Copp, BR; Kaiser, M; Pearce, AN | 1 |
Awale, S; Bringmann, G; Bruhn, T; Brun, R; Feineis, D; Kaiser, M; Li, J; Mudogo, V; Seupel, R | 1 |
Alajlani, M; Bauer, R; Belaj, F; Brantner, A; Bucar, F; Faist, J; Hochegger, P; Kaiser, M; Kretschmer, N; Mäser, P; Mohsin, NU; Saf, R; Seebacher, W; Turek, I; Weis, R | 1 |
Bringmann, G; Brun, R; Efferth, T; Feineis, D; Kaiser, M; Mudogo, V; Seo, EJ; Tshitenge, DT | 1 |
Aliabadi, A; De Mieri, M; Ebrahimi, SN; Farimani, MM; Hamburger, M; Kaiser, M; Khodaei, B; Moradi, H | 1 |
Brun, R; Calvet, CM; Costi, R; De Leo, A; De Vita, D; Di Santo, R; Jennings, GK; Kaiser, M; Madia, VN; Mäser, P; Messore, A; Pescatori, L; Podust, LM; Saccoliti, F; Scipione, L; Tudino, V | 1 |
Bode, HB; Cai, X; Kaiser, M; Zhao, L | 1 |
Danton, O; Hamburger, M; Kaiser, M; Moridi Farimani, M; Nejad Ebrahimi, S; Neuburger, M; Potterat, O; Ramseyer, J; Salehi, P; Tabefam, M | 1 |
Battista, MR; Brun, R; Calvet, CM; Cirilli, R; Costi, R; De Leo, A; De Vita, D; Di Marco, A; Di Santo, R; Faggi, C; Jennings, GK; Kaiser, M; Madia, VN; Mäser, P; Messore, A; Pepe, G; Pescatori, L; Podust, LM; Saccoliti, F; Scipione, L; Summa, V; Tudino, V | 1 |
Awale, S; Bringmann, G; Bruhn, T; Brun, R; Feineis, D; Kaiser, M; Mudogo, V; Schmidt, D; Tshitenge, DT; Würthner, F | 1 |
Al-Harrasi, A; Babanezhad Harikandei, K; Bararjanian, M; Ebrahimi, SN; Kaiser, M; Salehi, P | 1 |
Awori, RM; Bode, HB; Groß, J; Kaiser, M; Opatz, T; Zhao, L | 1 |
Bucar, F; Kaiser, M; Kalt, MM; Ochensberger, S; Presser, A; Saf, R; Schuehly, W; Solnier, J | 1 |
Alajlani, M; Bauer, R; Belaj, F; Brantner, A; Dolensky, J; Hochegger, P; Kaiser, M; Kretschmer, N; Mäser, P; Mohsin, NU; Petritsch, M; Saf, R; Schühly, W; Seebacher, W; Weis, R | 1 |
Horiuchi, M; Ihara, M; Ikegami-Kawai, M; Itoh, I; Kaiser, M; Kojima, M; Miyagi, S; Mizukawa, Y; Nanga Chick, C; Sakanoue, S; Togashi, H; Tsubuki, M; Usuki, T | 1 |
Bringmann, G; Feineis, D; Kaiser, M; Lombe, BK; Mudogo, V | 1 |
Börgel, F; Jabor, VAP; Kaiser, M; Krauth-Siegel, RL; Lehmkuhl, K; Nonato, MC; Schepmann, D; Schmidt, TJ; Uth, JF; Wünsch, B | 1 |
Brun, R; Celik, I; Doganc, F; Eren, G; Goker, H; Kaiser, M | 1 |
Altucci, L; Benedetti, R; Brogi, S; Butini, S; Campiani, G; Carullo, G; Casagni, A; De Matteis, A; Díaz, JF; Federico, S; Galatello, P; Gemma, S; Ghanim, M; Ibrahim, O; Kelly, VP; Khan, T; Lamponi, S; Lucena-Agell, D; Magnano, S; McCabe, N; Nathwani, S; O'Sullivan, J; Papulino, C; Pozzetti, L; Ramunno, A; Relitti, N; Staiano, L; Turkington, R; Ulivieri, C; Valoti, M; Vanni, F; VanWemmel, R; Zisterer, D | 1 |
Beck, WT; Cirtain, MC; Danks, MK; Felsted, RL; Safa, AR; Suttle, DP; Trent, JM; Wolverton, JS | 1 |
Beck, WT; Pearce, HL; Zamora, JM | 1 |
Morgan, EH; Sorokin, LM; Yeoh, GC | 1 |
Arnold, AM; Whitehouse, JM | 1 |
1 review(s) available for chloroquine and podophyllotoxin
Article | Year |
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Quest for a potent antimalarial drug lead: Synthesis and evaluation of 6,7-dimethoxyquinazoline-2,4-diamines.
Topics: Animals; Antimalarials; Dose-Response Relationship, Drug; Drug Discovery; Female; Malaria, Falciparum; Mice; Mice, Inbred ICR; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Structure-Activity Relationship | 2021 |
118 other study(ies) available for chloroquine and podophyllotoxin
Article | Year |
---|---|
Design, synthesis, and biological evaluation of a series of simple and novel potential antimalarial compounds.
Topics: Animals; Antimalarials; Benzocycloheptenes; Drug Design; Nitrobenzenes; Oxazines; Plasmodium falciparum; Trypanosoma cruzi | 2001 |
Antiprotozoal and cytotoxicity evaluation of sulfonamide and urea analogues of quinacrine.
Topics: Animals; Antiprotozoal Agents; Leishmania; Parasitic Sensitivity Tests; Plasmodium; Quinacrine; Sulfonamides; Trypanosoma; Urea | 2001 |
Assessment of the antiprotozoal activity of Galphimia glauca and the isolation of new nor-secofriedelanes and nor-friedelanes.
Topics: Animals; Antiprotozoal Agents; Drug Screening Assays, Antitumor; Galphimia; Leishmania donovani; Plasmodium falciparum; Spectrum Analysis; Triterpenes; Trypanosoma brucei brucei; Tumor Cells, Cultured | 2002 |
Isoneocryptolepine, a synthetic indoloquinoline alkaloid, as an antiplasmodial lead compound.
Topics: Alkaloids; Animals; Antimalarials; Apocynaceae; Indole Alkaloids; Indoles; Molecular Structure; Plasmodium falciparum; Quinolines; Structure-Activity Relationship | 2005 |
Irreversible inactivation of trypanothione reductase by unsaturated Mannich bases: a divinyl ketone as key intermediate.
Topics: Animals; Antimalarials; Antiprotozoal Agents; Chromatography, High Pressure Liquid; Dimethyl Sulfoxide; Drug Storage; Glutathione; Glutathione Reductase; Humans; Ketones; Leishmania donovani; Magnetic Resonance Spectroscopy; Mannich Bases; NADH, NADPH Oxidoreductases; Plasmodium falciparum; Spectrometry, Mass, Electrospray Ionization; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Thioredoxin-Disulfide Reductase; Trypanocidal Agents; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2005 |
Alkyl-linked bis-THTT derivatives as potent in vitro trypanocidal agents.
Topics: Alkylation; Animals; Carboxylic Acids; Leishmania donovani; Molecular Structure; Plasmodium falciparum; Structure-Activity Relationship; Thiadiazines; Trypanocidal Agents; Trypanosoma brucei rhodesiense | 2006 |
Acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase.
Topics: Animals; Antimalarials; Erythrocytes; Humans; In Vitro Techniques; Models, Molecular; Nucleosides; Plasmodium falciparum; Pyrophosphatases; Stereoisomerism; Structure-Activity Relationship; Trityl Compounds; Uracil | 2006 |
Evaluation of azasterols as anti-parasitics.
Topics: Animals; Antimalarials; Azasteroids; Leishmania donovani; Methyltransferases; Plasmodium falciparum; Stereoisomerism; Sterols; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2006 |
Limonoid orthoacetates and antiprotozoal compounds from the roots of Pseudocedrela kotschyi.
Topics: Animals; Antiprotozoal Agents; Leishmania donovani; Limonins; Mali; Meliaceae; Molecular Structure; Plant Roots; Plants, Medicinal; Plasmodium falciparum; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2007 |
Synthesis and in vitro antiprotozoal activities of dicationic 3,5-diphenylisoxazoles.
Topics: Animals; Antimalarials; Benzamidines; Cations; Cell Line; Combinatorial Chemistry Techniques; Isoxazoles; Plasmodium falciparum; Rats; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei rhodesiense | 2007 |
Synthesis and antiprotozoal activities of simplified analogs of naphthylisoquinoline alkaloids.
Topics: Alkaloids; Animals; Antiprotozoal Agents; Eukaryota; Isoquinolines; Myoblasts, Skeletal | 2008 |
Anti-malarial activity of N6-modified purine analogues.
Topics: Animals; Antimalarials; Male; Mice; Molecular Structure; Plasmodium falciparum; Purines; Structure-Activity Relationship | 2007 |
Antiprotozoal polyacetylenes from the Tanzanian medicinal plant Cussonia zimmermannii.
Topics: Animals; Antiprotozoal Agents; Araliaceae; Leishmania donovani; Molecular Structure; Plants, Medicinal; Plasmodium falciparum; Polyynes; Tanzania; Trypanosoma brucei rhodesiense | 2007 |
Synthesis and in vitro antiprotozoal activity of bisbenzofuran cations.
Topics: Animals; Antimalarials; Benzofurans; Cations; Leishmania donovani; Plasmodium falciparum; Rats; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei rhodesiense | 2007 |
Synthesis and evaluation of antiparasitic activities of new 4-[5-(4-phenoxyphenyl)-2H-pyrazol-3-yl]morpholine derivatives.
Topics: Animals; Antimalarials; Leishmania donovani; Morpholines; Plasmodium falciparum; Pyrazoles; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma | 2007 |
Synthesis and pharmacological evaluation of fluorescent and photoactivatable analogues of antiplasmodial naphthylisoquinolines.
Topics: Alkaloids; Animals; Antimalarials; Fluorescent Dyes; Isoquinolines; Naphthalenes; Photoaffinity Labels; Plasmodium falciparum; Structure-Activity Relationship | 2007 |
Synthesis and structure-activity relationship of 3-phenylquinoxaline 1,4-di-N-oxide derivatives as antimalarial agents.
Topics: Animals; Antimalarials; Cattle; Cell Survival; Drug Design; Humans; KB Cells; Plasmodium falciparum; Quinoxalines; Structure-Activity Relationship | 2008 |
Antimalarial dual drugs based on potent inhibitors of glutathione reductase from Plasmodium falciparum.
Topics: Animals; Antimalarials; Biological Transport; Cell Line, Tumor; Chloroquine; Drug Resistance; Drug Therapy, Combination; Glutathione Reductase; Humans; In Vitro Techniques; Malaria; Mice; Mice, Inbred BALB C; Naphthalenes; Parasitic Sensitivity Tests; Plasmodium berghei; Plasmodium falciparum; Structure-Activity Relationship | 2008 |
Synthesis and in vitro antiprotozoal activities of water-soluble, inexpensive 3,7-bis(dialkylamino)phenoxazin-5-ium derivatives.
Topics: Animals; Antimalarials; Antiprotozoal Agents; Chloroquine; Drug Resistance; Leishmania donovani; Oxazines; Parasitic Sensitivity Tests; Plasmodium falciparum; Pyrimethamine; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2008 |
Antiplasmodial and antitrypanosomal activities of aminobicyclo[2.2.2]octyl omega-aminoalkanoates.
Topics: Animals; Antiprotozoal Agents; Bridged Bicyclo Compounds; Parasitic Sensitivity Tests; Plasmodium falciparum; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei rhodesiense | 2009 |
Antiprotozoal activities of heterocyclic-substituted xanthones from the marine-derived fungus Chaetomium sp.
Topics: Animals; Antiprotozoal Agents; Bacillus megaterium; Chaetomium; Chlorella; Drug Screening Assays, Antitumor; Escherichia coli; Leishmania donovani; Marine Biology; Microbial Sensitivity Tests; Models, Molecular; Parasitic Sensitivity Tests; Plasmodium falciparum; Rats; Trypanosoma cruzi; Xanthones | 2008 |
Synthesis and antiprotozoal activity of cationic 2-phenylbenzofurans.
Topics: Animals; Antiprotozoal Agents; Benzofurans; Cations; Disease Models, Animal; Leishmania; Mice; Molecular Structure; Structure-Activity Relationship; Trypanosoma; Trypanosomiasis | 2008 |
Synthesis and antiparasitic and antifungal evaluation of 2'-arylsubstituted-1H,1'H-[2,5']bisbenzimidazolyl-5-carboxamidines.
Topics: Amidines; Animals; Antifungal Agents; Antiparasitic Agents; Leishmania donovani; Microbial Sensitivity Tests; Parasitic Sensitivity Tests; Plasmodium falciparum; Structure-Activity Relationship; Trypanosoma brucei brucei; Trypanosoma cruzi | 2009 |
Compounds structurally related to ellagic acid show improved antiplasmodial activity.
Topics: Animals; Antimalarials; Cells, Cultured; Chloroquine; DNA, Complementary; Drug Resistance; Ellagic Acid; Glutathione Peroxidase; Glutathione Transferase; Heme; Humans; Kinetics; Plasmodium falciparum; Reverse Transcriptase Polymerase Chain Reaction | 2009 |
Okundoperoxide, a bicyclic cyclofarnesylsesquiterpene endoperoxide from Scleria striatinux with antiplasmodial activity.
Topics: Antimalarials; Chloroquine; Cyperaceae; Drug Resistance; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Plant Roots; Plants, Medicinal; Plasmodium falciparum; Sesquiterpenes; Stereoisomerism | 2009 |
Structure-activity study of pentamidine analogues as antiprotozoal agents.
Topics: Animals; Antimalarials; Cadaverine; Drug Resistance; Female; Imidazoles; Leishmania donovani; Mice; Myoblasts; Parasitic Sensitivity Tests; Pentamidine; Plasmodium falciparum; Rats; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei rhodesiense; Trypanosomiasis | 2009 |
Trypanothione reductase high-throughput screening campaign identifies novel classes of inhibitors with antiparasitic activity.
Topics: Animals; Antiparasitic Agents; Drug Evaluation, Preclinical; Humans; Microsomes, Liver; Molecular Structure; NADH, NADPH Oxidoreductases; Structure-Activity Relationship; Trypanosoma; Trypanosomiasis | 2009 |
Synthesis and antiprotozoal activities of dicationic bis(phenoxymethyl)benzenes, bis(phenoxymethyl)naphthalenes, and bis(benzyloxy)naphthalenes.
Topics: Animals; Antiprotozoal Agents; Benzene; Cell Survival; Leishmania donovani; Mice; Myoblasts; Naphthalenes; Parasitic Sensitivity Tests; Plasmodium falciparum; Rats; Structure-Activity Relationship; Trypanosoma brucei rhodesiense; Trypanosomiasis, African | 2009 |
Privileged structure-guided synthesis of quinazoline derivatives as inhibitors of trypanothione reductase.
Topics: Animals; Antiparasitic Agents; Cell Line; Computer Simulation; Drug Design; Enzyme Inhibitors; Glutathione Reductase; Humans; NADH, NADPH Oxidoreductases; Quinazolines; Rats; Structure-Activity Relationship; Trypanosoma cruzi | 2009 |
Synthesis and antiprotozoal activity of pyridyl analogues of pentamidine.
Topics: Animals; Antiprotozoal Agents; Female; Leishmania donovani; Mice; Pentamidine; Plasmodium falciparum; Pyridines; Rats; Structure-Activity Relationship | 2009 |
Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum.
Topics: Animals; Antimalarials; ATP Binding Cassette Transporter, Subfamily B, Member 1; Chromosome Mapping; Crosses, Genetic; Dihydroergotamine; Drug Design; Drug Resistance; Humans; Inhibitory Concentration 50; Mutation; Plasmodium falciparum; Quantitative Trait Loci; Transfection | 2009 |
Structure-activity relationship of antiparasitic and cytotoxic indoloquinoline alkaloids, and their tricyclic and bicyclic analogues.
Topics: Animals; Antimalarials; Antineoplastic Agents; Indole Alkaloids; Mice; Plasmodium berghei; Plasmodium falciparum; Structure-Activity Relationship | 2009 |
Synthesis and antiprotozoal activity of cationic 1,4-diphenyl-1H-1,2,3-triazoles.
Topics: Amidines; Animals; Antiprotozoal Agents; Cell Line; Cell Survival; Disease Models, Animal; Female; Leishmania donovani; Mice; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Rats; Stereoisomerism; Structure-Activity Relationship; Triazoles; Trypanosoma brucei rhodesiense | 2010 |
Synthesis, stereoelectronic characterization and antiparasitic activity of new 1-benzenesulfonyl-2-methyl-1,2,3,4-tetrahydroquinolines.
Topics: Animals; Antiprotozoal Agents; Cell Line; Humans; Leishmania donovani; Models, Molecular; Parasitic Sensitivity Tests; Plasmodium falciparum; Protozoan Infections; Quinolines; Structure-Activity Relationship; Trypanosoma; Trypanosoma cruzi | 2010 |
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship | 2010 |
Discovery of novel and potent benzhydryl-tropane trypanocides highly selective for Trypanosoma cruzi.
Topics: Animals; Cell Line; Drug Discovery; Rats; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma cruzi | 2010 |
Jacaranone-derived glucosidic esters from Jacaranda glabra and their activity against Plasmodium falciparum.
Topics: Animals; Antimalarials; Benzoquinones; Ecuador; Esters; Glucosides; Myoblasts; Nuclear Magnetic Resonance, Biomolecular; Parasitic Sensitivity Tests; Phenylacetates; Plasmodium falciparum; Rats | 2010 |
Antiprotozoal steroidal saponins from the marine sponge Pandaros acanthifolium.
Topics: Animals; Antiprotozoal Agents; Leishmania donovani; Marine Biology; Nuclear Magnetic Resonance, Biomolecular; Oceans and Seas; Plasmodium falciparum; Porifera; Saponins; Steroids; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2010 |
QSAR guided synthesis of simplified antiplasmodial analogs of naphthylisoquinoline alkaloids.
Topics: Alkaloids; Animals; Antimalarials; Isoquinolines; Magnetic Resonance Spectroscopy; Models, Molecular; Plasmodium falciparum; Quantitative Structure-Activity Relationship; Spectrometry, Mass, Electrospray Ionization; Spectroscopy, Fourier Transform Infrared | 2010 |
2-Hexadecynoic acid inhibits plasmodial FAS-II enzymes and arrests erythrocytic and liver stage Plasmodium infections.
Topics: Alkynes; Antimalarials; Binding Sites; Cell Line, Tumor; Computer Simulation; Erythrocytes; Fatty Acid Synthase, Type II; Fatty Acids, Unsaturated; Humans; Kinetics; Liver; Malaria, Falciparum; Plasmodium falciparum; Protozoan Proteins | 2010 |
Didemnidines A and B, indole spermidine alkaloids from the New Zealand ascidian Didemnum sp.
Topics: Animals; Antiprotozoal Agents; Indole Alkaloids; Leishmania donovani; Molecular Structure; New Zealand; Nuclear Magnetic Resonance, Biomolecular; Plasmodium falciparum; Spermidine; Structure-Activity Relationship; Trypanosoma; Urochordata | 2011 |
β-Branched acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase.
Topics: Antimalarials; Deoxyuridine; Enzyme Inhibitors; Humans; Models, Molecular; Plasmodium falciparum; Pyrophosphatases; Structure-Activity Relationship | 2011 |
Antiparasitic compounds from Cupania cinerea with activities against Plasmodium falciparum and Trypanosoma brucei rhodesiense.
Topics: Animals; Antiprotozoal Agents; Cells, Cultured; Crystallography, X-Ray; Diterpenes; Ecuador; Glycosides; Hexanes; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Polycyclic Sesquiterpenes; Rats; Sapindaceae; Sesquiterpenes; Triterpenes; Trypanosoma brucei rhodesiense | 2011 |
Marinoquinolines A-F, pyrroloquinolines from Ohtaekwangia kribbensis (Bacteroidetes).
Topics: Anti-Bacterial Agents; Antifungal Agents; Antimalarials; Antineoplastic Agents; Bacteroidetes; Drug Screening Assays, Antitumor; Female; Humans; India; Inhibitory Concentration 50; Microbial Sensitivity Tests; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Plasmodium falciparum; Pyrroles; Quinolines | 2011 |
Antimalarial pyrido[1,2-a]benzimidazoles.
Topics: Administration, Oral; Animals; Antimalarials; Benzimidazoles; Drug Resistance, Multiple; Humans; In Vitro Techniques; Injections, Intraperitoneal; L Cells; Malaria; Male; Mice; Microsomes, Liver; Plasmodium berghei; Plasmodium falciparum; Pyridines; Rats; Rats, Sprague-Dawley; Structure-Activity Relationship | 2011 |
Antiplasmodial and cytotoxicity evaluation of 3-functionalized 2-azetidinone derivatives.
Topics: Antimalarials; Azetidines; beta-Lactams; Cell Line, Tumor; Humans; Plasmodium falciparum; Triazoles | 2011 |
Antimalarial β-carbolines from the New Zealand ascidian Pseudodistoma opacum.
Topics: Animals; Antimalarials; Carbolines; Chloroquine; Drug Resistance; Molecular Structure; New Zealand; Nuclear Magnetic Resonance, Biomolecular; Plasmodium falciparum; Stereoisomerism; Urochordata | 2011 |
Synthesis and in vitro antiprotozoal activities of 5-phenyliminobenzo[a]phenoxazine derivatives.
Topics: Animals; Antimalarials; Antiprotozoal Agents; Drug Design; Inhibitory Concentration 50; Leishmania donovani; Malaria; Models, Chemical; Molecular Structure; Myoblasts; Oxazines; Parasitic Sensitivity Tests; Plasmodium falciparum; Pyridinium Compounds; Rats; Structure-Activity Relationship; Thiazoles; Trypanocidal Agents; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2011 |
Biological evaluation of glycosyl-isoindigo derivatives against the pathogenic agents of tropical diseases (malaria, Chagas disease, leishmaniasis and human African trypanosomiasis).
Topics: Animals; Antiprotozoal Agents; Drug Evaluation, Preclinical; Humans; Protozoan Infections | 2011 |
Bis(oxyphenylene)benzimidazoles: a novel class of anti-Plasmodium falciparum agents.
Topics: Animals; Antimalarials; Benzimidazoles; Cell Line; Humans; Inhibitory Concentration 50; Malaria, Falciparum; Parasitic Sensitivity Tests; Plasmodium falciparum; Rats | 2011 |
Synthesis and anti-protozoal activity of novel dihydropyrrolo[3,4-d][1,2,3]triazoles.
Topics: Animals; Antiprotozoal Agents; Cell Line; Eukaryota; Inhibitory Concentration 50; Magnetic Resonance Spectroscopy; Molecular Structure; Oxadiazoles; Protozoan Infections; Pyrroles; Rats; Spectrometry, Mass, Electrospray Ionization; Spectroscopy, Fourier Transform Infrared; Structure-Activity Relationship; Triazoles | 2012 |
Synthesis and antimalarial and antituberculosis activities of a series of natural and unnatural 4-methoxy-6-styryl-pyran-2-ones, dihydro analogues and photo-dimers.
Topics: Antimalarials; Antitubercular Agents; Coumarins; Dimerization; Fatty Acids, Monounsaturated; Inhibitory Concentration 50; Leishmania donovani; Light; Molecular Structure; Plasmodium falciparum; Pyrones | 2012 |
Synthesis, biological evaluation, and structure-activity relationships of N-benzoyl-2-hydroxybenzamides as agents active against P. falciparum (K1 strain), Trypanosomes, and Leishmania.
Topics: Antimalarials; Benzamides; Imides; Leishmania donovani; Parasitic Sensitivity Tests; Plasmodium falciparum; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2012 |
8,8-dialkyldihydroberberines with potent antiprotozoal activity.
Topics: Animals; Antimalarials; Antiprotozoal Agents; Berberine Alkaloids; Crystallography, X-Ray; Female; Inhibitory Concentration 50; Leishmania donovani; Mice; Mice, Inbred BALB C; Parasitic Sensitivity Tests; Plasmodium falciparum; Trypanosoma | 2013 |
Discovery and preliminary structure-activity relationship analysis of 1,14-sperminediphenylacetamides as potent and selective antimalarial lead compounds.
Topics: Acetamides; Animals; Antimalarials; Drug Discovery; Inhibitory Concentration 50; Malaria; Molecular Structure; Plasmodium falciparum; Spermine; Structure-Activity Relationship | 2013 |
Aminoalkyl derivatives of guanidine diaromatic minor groove binders with antiprotozoal activity.
Topics: Animals; Antiprotozoal Agents; Guanidine; Nucleic Acid Denaturation; Plasmodium falciparum; Trypanosoma brucei rhodesiense | 2013 |
Asymmetric synthesis and anti-protozoal activity of the 8,4'-oxyneolignans virolin, surinamensin and analogues.
Topics: Anisoles; Antiprotozoal Agents; Leishmania donovani; Lignans; Molecular Conformation; Parasitic Sensitivity Tests; Plasmodium falciparum | 2013 |
Antibacterial and antiplasmodial constituents of Beilschmiedia cryptocaryoides.
Topics: Acinetobacter calcoaceticus; Anti-Bacterial Agents; Antimalarials; Chloroquine; Drug Resistance; Escherichia coli; Lauraceae; Madagascar; Microbial Sensitivity Tests; Molecular Conformation; Plant Bark; Plasmodium falciparum; Pseudomonas stutzeri | 2013 |
Synthesis and in vitro antimalarial testing of neocryptolepines: SAR study for improved activity by introduction and modifications of side chains at C2 and C11 on indolo[2,3-b]quinolines.
Topics: Alkaloids; Animals; Antimalarials; Cell Line; Chloroquine; Drug Resistance; Indoles; Malaria; Mice; Parasitic Sensitivity Tests; Plasmodium berghei; Plasmodium falciparum; Quinolines; Rats; Structure-Activity Relationship | 2013 |
Discovery and structure-activity relationships of pyrrolone antimalarials.
Topics: Animals; Antimalarials; Cell Line; Drug Discovery; Magnetic Resonance Spectroscopy; Mass Spectrometry; Plasmodium falciparum; Pyrroles; Rats; Structure-Activity Relationship | 2013 |
Synthesis and antimalarial testing of neocryptolepine analogues: addition of ester function in SAR study of 2,11-disubstituted indolo[2,3-b]quinolines.
Topics: Alkaloids; Animals; Antimalarials; Cell Line; Cell Survival; Dose-Response Relationship, Drug; Indoles; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Quinolines; Rats; Structure-Activity Relationship | 2013 |
Synthesis and antiprotozoal activity of dicationic m-terphenyl and 1,3-dipyridylbenzene derivatives.
Topics: Animals; Antiprotozoal Agents; Benzene; Chagas Disease; Female; Leishmania donovani; Mice; Mice, Inbred Strains; Models, Chemical; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Pyridines; Structure-Activity Relationship; Terphenyl Compounds; Trypanosoma cruzi | 2013 |
3-(Oxazolo[4,5-b]pyridin-2-yl)anilides as a novel class of potent inhibitors for the kinetoplastid Trypanosoma brucei, the causative agent for human African trypanosomiasis.
Topics: Anilides; Animals; Humans; Mice; Myoblasts, Skeletal; Rats; Species Specificity; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei brucei; Trypanosomiasis, African | 2013 |
Synthesis and antiprotozoal activities of benzyl phenyl ether diamidine derivatives.
Topics: Animals; Antiprotozoal Agents; Dose-Response Relationship, Drug; Leishmania donovani; Mice; Molecular Structure; Myoblasts; Parasitic Sensitivity Tests; Pentamidine; Phenyl Ethers; Plasmodium falciparum; Rats; Structure-Activity Relationship; Trypanosoma brucei rhodesiense; Trypanosomiasis | 2013 |
Investigation of acyclic uridine amide and 5'-amido nucleoside analogues as potential inhibitors of the Plasmodium falciparum dUTPase.
Topics: Amides; Antimalarials; Enzyme Inhibitors; Kinetics; Nucleosides; Plasmodium falciparum; Protein Binding; Protozoan Proteins; Pyrophosphatases; Uridine | 2013 |
Natural product derived antiprotozoal agents: synthesis, biological evaluation, and structure-activity relationships of novel chromene and chromane derivatives.
Topics: Antiprotozoal Agents; Biological Products; Chemistry Techniques, Synthetic; Chromans; Inhibitory Concentration 50; Structure-Activity Relationship | 2013 |
Design, synthesis, and biological and crystallographic evaluation of novel inhibitors of Plasmodium falciparum enoyl-ACP-reductase (PfFabI).
Topics: Animals; Antimalarials; Cell Line; Coumarins; Crystallography, X-Ray; Drug Design; Drug Resistance, Multiple; Enoyl-(Acyl-Carrier-Protein) Reductase (NADH); Molecular Docking Simulation; Plasmodium falciparum; Protein Binding; Protein Conformation; Structure-Activity Relationship | 2013 |
Synthesis and evaluation of the antimalarial, anticancer, and caspase 3 activities of tetraoxane dimers.
Topics: Antimalarials; Antineoplastic Agents; Caspase 3; Cell Line, Tumor; Dimerization; Humans; Malaria, Falciparum; Neoplasms; Plasmodium falciparum; Tetraoxanes | 2013 |
Antiprotozoal activity of dicationic 3,5-diphenylisoxazoles, their prodrugs and aza-analogues.
Topics: Animals; Antiprotozoal Agents; Isoxazoles; Mice; Molecular Structure; Plasmodium falciparum; Prodrugs; Structure-Activity Relationship; Trypanosomiasis, African | 2014 |
Antiparasitic chaiyaphumines from entomopathogenic Xenorhabdus sp. PB61.4.
Topics: Animals; Antiparasitic Agents; Bacillus subtilis; Depsipeptides; Escherichia coli; Humans; Inhibitory Concentration 50; Micrococcus luteus; Molecular Structure; Nematoda; Nuclear Magnetic Resonance, Biomolecular; Parasitic Sensitivity Tests; Plasmodium falciparum; Saccharomyces cerevisiae; Thailand; Trypanosoma brucei rhodesiense; Trypanosoma cruzi; Xenorhabdus | 2014 |
Synthesis, β-haematin inhibition, and in vitro antimalarial testing of isocryptolepine analogues: SAR study of indolo[3,2-c]quinolines with various substituents at C2, C6, and N11.
Topics: Animals; Antimalarials; Cell Line; Cell Survival; Hemin; Humans; Indole Alkaloids; Indoles; Mice; Plasmodium falciparum; Quantitative Structure-Activity Relationship; Quinolines; Rats; Structure-Activity Relationship | 2014 |
Antiprotozoal activity and DNA binding of N-substituted N-phenylbenzamide and 1,3-diphenylurea bisguanidines.
Topics: Animals; Antiparasitic Agents; Benzamides; Binding Sites; Cell Line; Cell Survival; Disease Models, Animal; DNA; Dose-Response Relationship, Drug; Female; Guanidines; Mice; Mice, Inbred Strains; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Rats; Structure-Activity Relationship; Surface Plasmon Resonance; Trypanosoma brucei rhodesiense; Trypanosomiasis, African; Urea | 2014 |
Synthesis and antiplasmodial and antimycobacterial evaluation of new nitroimidazole and nitroimidazooxazine derivatives.
Topics: | 2013 |
New Promising Compounds with in Vitro Nanomolar Activity against Trypanosoma cruzi.
Topics: | 2013 |
Design, Synthesis, and Antiplasmodial Activity of Hybrid Compounds Based on (2R,3S)-N-Benzoyl-3-phenylisoserine.
Topics: | 2013 |
Synthesis, Antiplasmodial Activity, and β-Hematin Inhibition of Hydroxypyridone-Chloroquine Hybrids.
Topics: | 2013 |
Synthesis and antiparasitic activity of new bis-arylimidamides: DB766 analogs modified in the terminal groups.
Topics: Amides; Animals; Antiparasitic Agents; Cell Line; Chemistry Techniques, Synthetic; Leishmania; Plasmodium falciparum; Rats; Trypanosoma | 2014 |
Pyridyl benzamides as a novel class of potent inhibitors for the kinetoplastid Trypanosoma brucei.
Topics: Animals; Benzamides; Cell Line; HEK293 Cells; Humans; Microsomes, Liver; Myoblasts; Pyridines; Rats; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei brucei; Trypanosoma brucei rhodesiense | 2014 |
Xenortide Biosynthesis by Entomopathogenic Xenorhabdus nematophila.
Topics: Chromatography, High Pressure Liquid; Dipeptides; Leishmania; Molecular Structure; Multigene Family; Nuclear Magnetic Resonance, Biomolecular; Parasitic Sensitivity Tests; Plasmodium falciparum; Trypanosoma brucei brucei; Tryptamines; Xenorhabdus | 2014 |
2-Octadecynoic acid as a dual life stage inhibitor of Plasmodium infections and plasmodial FAS-II enzymes.
Topics: Animals; Antimalarials; Cell Line, Tumor; Dose-Response Relationship, Drug; Fatty Acid Synthase, Type II; Fatty Acids, Unsaturated; Humans; Malaria; Models, Molecular; Plasmodium berghei; Plasmodium falciparum; Structure-Activity Relationship; Zebrafish | 2014 |
Blood schizontocidal and gametocytocidal activity of 3-hydroxy-N'-arylidenepropanehydrazonamides: a new class of antiplasmodial compounds.
Topics: Animals; Antimalarials; Chloroquine; Malaria; Mice; Parasitemia; Parasitic Sensitivity Tests; Phenanthrenes; Plasmodium berghei; Plasmodium falciparum; Rats; Structure-Activity Relationship | 2014 |
Exploring in vitro and in vivo Hsp90 inhibitors activity against human protozoan parasites.
Topics: Animals; Antiprotozoal Agents; Cell Line, Tumor; Disease Models, Animal; HSP90 Heat-Shock Proteins; Humans; Mice; Parasitemia; Plasmodium falciparum; Protein Binding; Rats; Triazoles; Trypanosoma brucei rhodesiense | 2015 |
Hydroxamic acid based histone deacetylase inhibitors with confirmed activity against the malaria parasite.
Topics: Animals; Antimalarials; Cell Line, Tumor; Dipeptides; Disease Models, Animal; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Hydroxamic Acids; Malaria; Mice; Parasites; Plasmodium falciparum; Protein Isoforms | 2015 |
Antiprotozoal activity and DNA binding of dicationic acridones.
Topics: Acridines; Acridones; Antiprotozoal Agents; Binding Sites; Cations; DNA; Dose-Response Relationship, Drug; Leishmania donovani; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Structure-Activity Relationship; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2015 |
Antiplasmodial and Cytotoxic Triterpenoids from the Bark of the Cameroonian Medicinal Plant Entandrophragma congoënse.
Topics: Animals; Antimalarials; Cameroon; Chloroquine; Disease Resistance; Erythrocytes; Meliaceae; Molecular Structure; Muscle, Skeletal; Nuclear Magnetic Resonance, Biomolecular; Parasitic Sensitivity Tests; Plant Bark; Plant Stems; Plants, Medicinal; Plasmodium falciparum; Rats; Triterpenes | 2015 |
Discovery and optimisation studies of antimalarial phenotypic hits.
Topics: Animals; Antimalarials; Cell Line; Cell Survival; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Discovery; Humans; Malaria; Mice; Microsomes, Liver; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium berghei; Plasmodium falciparum; Rats; Solubility; Structure-Activity Relationship | 2015 |
Antiprotozoal activity of bicycles featuring a dimethylamino group at their bridgehead.
Topics: Animals; Antiprotozoal Agents; Bridged Bicyclo Compounds; Cells, Cultured; Plasmodium falciparum; Rats; Spectrum Analysis; Structure-Activity Relationship; Trypanosoma brucei rhodesiense | 2016 |
Synthesis and potent antiprotozoal activity of mono/di amidino 2-anilinobenzimidazoles versus Plasmodium falciparum and Trypanosoma brucei rhodesiense.
Topics: Aniline Compounds; Animals; Antiprotozoal Agents; Benzimidazoles; Cell Line; Humans; Malaria, Falciparum; Parasitic Sensitivity Tests; Plasmodium falciparum; Rats; Structure-Activity Relationship; Trypanosoma brucei rhodesiense; Trypanosomiasis, African | 2016 |
New derivatives of 7-chloroquinolin-4-amine with antiprotozoal activity.
Topics: Aminoquinolines; Animals; Antiprotozoal Agents; Cell Line; Cell Survival; Dose-Response Relationship, Drug; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Rats; Structure-Activity Relationship; Trypanosoma brucei rhodesiense | 2017 |
Dioncophyllines C
Topics: Alkaloids; Antimalarials; Antineoplastic Agents; Humans; Isoquinolines; Magnoliopsida; Molecular Structure; Multiple Myeloma; Nuclear Magnetic Resonance, Biomolecular; Plasmodium falciparum; Structure-Activity Relationship | 2017 |
New derivatives of quinoline-4-carboxylic acid with antiplasmodial activity.
Topics: Animals; Antimalarials; Parasitic Sensitivity Tests; Plasmodium falciparum; Quinolines; Spectrum Analysis; Structure-Activity Relationship | 2017 |
Synthesis and activity of nucleoside-based antiprotozoan compounds.
Topics: Animals; Antiprotozoal Agents; Carbon-13 Magnetic Resonance Spectroscopy; Inhibitory Concentration 50; Leishmania donovani; Plasmodium falciparum; Proton Magnetic Resonance Spectroscopy; Spectrophotometry, Infrared; Trypanosoma brucei brucei; Trypanosoma cruzi | 2017 |
Structure-activity relationship studies on thiaplidiaquinones A and B as novel inhibitors of Plasmodium falciparum and farnesyltransferase.
Topics: Animals; Anti-Bacterial Agents; Antimalarials; Cell Line; Cell Survival; Dose-Response Relationship, Drug; Farnesyltranstransferase; Microbial Sensitivity Tests; Molecular Structure; Plasmodium falciparum; Rats; Staphylococcus; Structure-Activity Relationship; Terpenes | 2017 |
Lead selection of antiparasitic compounds from a focused library of benzenesulfonyl derivatives of heterocycles.
Topics: Animals; Antiparasitic Agents; Benzyl Compounds; Dose-Response Relationship, Drug; Heterocyclic Compounds; Leishmania donovani; Molecular Structure; Myoblasts; Parasitic Sensitivity Tests; Plasmodium falciparum; Rats; Structure-Activity Relationship; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2017 |
Antiprotozoal Linear Furanosesterterpenoids from the Marine Sponge Ircinia oros.
Topics: Animals; Antiprotozoal Agents; Furans; Magnetic Resonance Spectroscopy; Molecular Structure; Porifera; Sesquiterpenes; Spectroscopy, Fourier Transform Infrared | 2017 |
Synthesis and antimalarial evaluation of artesunate-polyamine and trioxolane-polyamine conjugates.
Topics: Animals; Antimalarials; Artemisinins; Artesunate; Humans; Polyamines; Rats; Spectrum Analysis; Structure-Activity Relationship | 2017 |
Jozilebomines A and B, Naphthylisoquinoline Dimers from the Congolese Liana Ancistrocladus ileboensis, with Antiausterity Activities against the PANC-1 Human Pancreatic Cancer Cell Line.
Topics: Algorithms; Alkaloids; Animals; Antimalarials; Antineoplastic Agents, Phytogenic; Congo; Drug Screening Assays, Antitumor; HeLa Cells; Humans; Isoquinolines; Leishmania donovani; Magnoliopsida; Molecular Structure; Naphthalenes; Nuclear Magnetic Resonance, Biomolecular; Pancreatic Neoplasms; Plasmodium falciparum; Rats; Trypanosoma brucei rhodesiense; Trypanosoma cruzi; Tumor Cells, Cultured | 2017 |
Synthesis of new 1-benzyl tetrahydropyridinylidene ammonium salts and their antimicrobial and anticellular activities.
Topics: Animals; Anti-Bacterial Agents; Antifungal Agents; Antineoplastic Agents; Antiprotozoal Agents; Bacteria; Benzyl Compounds; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Humans; Mice; Microbial Sensitivity Tests; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Pyridines; Quaternary Ammonium Compounds; Rats; Saccharomyces cerevisiae; Salts; Structure-Activity Relationship; Trypanosoma brucei rhodesiense | 2018 |
Mbandakamine-Type Naphthylisoquinoline Dimers and Related Alkaloids from the Central African Liana Ancistrocladus ealaensis with Antiparasitic and Antileukemic Activities.
Topics: Africa, Central; Alkaloids; Antimalarials; Antineoplastic Agents, Phytogenic; Antiparasitic Agents; Caryophyllales; Cell Line, Tumor; Humans; Isoquinolines; Naphthalenes; Plasmodium falciparum; Quinolines | 2018 |
Phytochemical Study of Salvia leriifolia Roots: Rearranged Abietane Diterpenoids with Antiprotozoal Activity.
Topics: Abietanes; Antimalarials; Antiprotozoal Agents; Inhibitory Concentration 50; Leishmania donovani; Parasitic Sensitivity Tests; Phytochemicals; Plant Extracts; Plant Roots; Plasmodium falciparum; Salvia; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2018 |
Biological evaluation and structure-activity relationships of imidazole-based compounds as antiprotozoal agents.
Topics: Animals; Antiprotozoal Agents; Cell Line; Chagas Disease; Female; Humans; Imidazoles; Inhibitory Concentration 50; Leishmania donovani; Leishmaniasis, Visceral; Malaria, Falciparum; Mice; Mice, Inbred BALB C; Parasitic Sensitivity Tests; Plasmodium falciparum; Rats; Structure-Activity Relationship; Trypanosoma brucei rhodesiense; Trypanosoma cruzi; Trypanosomiasis, African | 2018 |
Methionine-Containing Rhabdopeptide/Xenortide-like Peptides from Heterologous Expression of the Biosynthetic Gene Cluster kj12ABC in Escherichia coli.
Topics: Amino Acids; Animals; Antineoplastic Agents; Antiparasitic Agents; Escherichia coli; Methionine; Multigene Family; Oligopeptides; Parasites; Rats; Xenorhabdus | 2018 |
Antiprotozoal Isoprenoids from Salvia hydrangea.
Topics: Animals; Antiprotozoal Agents; Cell Line; Leishmania donovani; Magnetic Resonance Spectroscopy; Molecular Structure; Plasmodium falciparum; Rats; Salvia; Spectrum Analysis; Terpenes; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2018 |
Design, Synthesis, and Biological Evaluation of New 1-(Aryl-1 H-pyrrolyl)(phenyl)methyl-1 H-imidazole Derivatives as Antiprotozoal Agents.
Topics: Animals; Antiprotozoal Agents; Cytochrome P-450 Enzyme Inhibitors; Drug Design; Drug Evaluation, Preclinical; Humans; Imidazoles; Parasitic Sensitivity Tests; Trypanosoma | 2019 |
Synthesis and structure-activity relationships for new 6-fluoroquinoline derivatives with antiplasmodial activity.
Topics: Animals; Antimalarials; Cell Line; Cell Survival; Disease Models, Animal; Drug Resistance; Malaria; Mice; Parasitic Sensitivity Tests; Plasmodium berghei; Plasmodium falciparum; Quinolines; Structure-Activity Relationship | 2019 |
Ealamines A-H, a Series of Naphthylisoquinolines with the Rare 7,8'-Coupling Site, from the Congolese Liana
Topics: Animals; Antineoplastic Agents, Phytogenic; Antiprotozoal Agents; Caryophyllales; Drug Screening Assays, Antitumor; Humans; Isoquinolines; Leishmania; Molecular Structure; Naphthalenes; Pancreatic Neoplasms; Plant Components, Aerial; Plant Leaves; Plasmodium; Rats; Trypanosoma | 2019 |
Synthesis, in-vitro antiprotozoal activity and molecular docking study of isothiocyanate derivatives.
Topics: Animals; Antiprotozoal Agents; Cell Line; Cell Survival; Dose-Response Relationship, Drug; Isothiocyanates; Leishmania donovani; Molecular Docking Simulation; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Rats; Structure-Activity Relationship; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2020 |
Structure, Biosynthesis, and Bioactivity of Photoditritide from
Topics: Anti-Bacterial Agents; Antiprotozoal Agents; Microbial Sensitivity Tests; Micrococcus luteus; Molecular Structure; Photorhabdus; Spectrum Analysis; Trypanosoma brucei rhodesiense | 2019 |
Palladium-catalysed synthesis of arylnaphthoquinones as antiprotozoal and antimycobacterial agents.
Topics: Anti-Bacterial Agents; Antiprotozoal Agents; Catalysis; Chemistry Techniques, Synthetic; Mycobacterium smegmatis; Palladium; Plasmodium falciparum; Quinones; Trypanosoma brucei rhodesiense | 2020 |
Preparation of new 1,3-dibenzyl tetrahydropyridinylidene ammonium salts and their antimicrobial and anticellular activities.
Topics: Animals; Anti-Bacterial Agents; Antifungal Agents; Antimalarials; Antineoplastic Agents; Candida albicans; Cell Line; Cell Proliferation; Cell Survival; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Epidermis; Escherichia coli; Female; Humans; Mice; Microbial Sensitivity Tests; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Pseudomonas aeruginosa; Quaternary Ammonium Compounds; Rats; Salts; Staphylococcus aureus; Structure-Activity Relationship | 2021 |
Spirombandakamine A
Topics: Alkaloids; Animals; Antiprotozoal Agents; Caryophyllales; Cell Line; Democratic Republic of the Congo; Isoquinolines; Molecular Structure; Phytochemicals; Plant Leaves; Plasmodium falciparum; Rats; Trypanosoma brucei rhodesiense | 2021 |
Synthesis and Biological Evaluation of Natural-Product-Inspired, Aminoalkyl-Substituted 1-Benzopyrans as Novel Antiplasmodial Agents.
Topics: Alkylation; Animals; Antimalarials; Benzopyrans; Biological Products; Biomimetic Materials; Chemistry Techniques, Synthetic; Erythrocytes; Kinetics; Mice; Plasmodium; Structure-Activity Relationship | 2021 |
Synthesis, in vitro antiprotozoal activity, molecular docking and molecular dynamics studies of some new monocationic guanidinobenzimidazoles.
Topics: Antiprotozoal Agents; Benzimidazoles; Cations; Dose-Response Relationship, Drug; Guanidine; Leishmania donovani; Models, Molecular; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Structure-Activity Relationship; Trypanosoma brucei rhodesiense; Trypanosoma cruzi | 2021 |
Design and synthesis of multifunctional microtubule targeting agents endowed with dual pro-apoptotic and anti-autophagic efficacy.
Topics: Antineoplastic Agents; Apoptosis; Autophagy; Carcinoma, Squamous Cell; Cell Line, Tumor; Humans; Microtubules; Mouth Neoplasms | 2022 |
Pharmacological, molecular, and cytogenetic analysis of "atypical" multidrug-resistant human leukemic cells.
Topics: ATP Binding Cassette Transporter, Subfamily B, Member 1; Chloroquine; Chromosome Banding; Chromosomes, Human, Pair 13; Colchicine; Dactinomycin; Drug Resistance; Drug Screening Assays, Antitumor; Humans; Leukemia; Membrane Glycoproteins; Molecular Weight; Podophyllotoxin; Teniposide; Tumor Cells, Cultured; Verapamil; Vinblastine; Vinca Alkaloids | 1987 |
Physical-chemical properties shared by compounds that modulate multidrug resistance in human leukemic cells.
Topics: Antibiotics, Antineoplastic; Antineoplastic Agents; Cell Line; Chemical Phenomena; Chemistry, Physical; Chloroquine; Computer Simulation; Doxorubicin; Drug Resistance; Humans; Leukemia; Naphthacenes; Podophyllotoxin; Quinacrine; Verapamil; Vinca Alkaloids | 1988 |
Transferrin endocytosis and iron uptake in developing myogenic cells in culture: effects of microtubular and metabolic inhibitors, sulphydryl reagents and lysosomotrophic agents.
Topics: 2,4-Dinitrophenol; Ammonium Chloride; Animals; Antimycin A; Azides; Cells, Cultured; Chick Embryo; Chloroquine; Colchicine; Dinitrophenols; Endocytosis; Iron; Methylamines; Muscles; Podophyllotoxin; Sodium Azide; Sulfhydryl Reagents; Transferrin; Vinblastine | 1988 |
Interaction of VP16-213 with the DNA repair antagonist chloroquine.
Topics: Animals; Chloroquine; DNA Repair; Drug Interactions; Etoposide; Female; Lymphoma; Mice; Mice, Inbred CBA; Neoplasms, Experimental; Podophyllotoxin; Vincristine | 1982 |