pyrroles has been researched along with marizomib in 114 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 54 (47.37) | 29.6817 |
2010's | 55 (48.25) | 24.3611 |
2020's | 5 (4.39) | 2.80 |
Authors | Studies |
---|---|
Buchanan, GO; Feling, RH; Fenical, W; Jensen, PR; Kauffman, CA; Mincer, TJ | 1 |
Corey, EJ; Reddy, LR; Saravanan, P | 1 |
Fenical, W; Jensen, PR; Mincer, TJ; Williams, PG | 1 |
Chao, TH; Deyanat-Yazdi, G; Fenical, WF; Jensen, PR; Lam, KS; Macherla, VR; Mai, B; Manam, RR; Mitchell, SS; Neuteboom, ST; Nicholson, B; Palladino, MA; Potts, BC; Reed, KA | 1 |
Danishefsky, SJ; Endo, A | 1 |
Corey, EJ; Fournier, JF; Reddy, BV; Reddy, LR | 1 |
Corey, EJ; Fournier, JF; Reddy, LR; Subba Reddy, BV | 1 |
Corey, EJ; Hogan, PC | 1 |
Anderson, KC; Berkers, C; Catley, L; Chao, TH; Chauhan, D; Hideshima, T; Letai, A; Li, G; Mitsiades, C; Mitsiades, N; Neuteboom, ST; Nicholson, B; Ovaa, H; Palladino, MA; Podar, K; Richardson, P; Velankar, M; Yasui, H | 1 |
Mulholland, NP; Pattenden, G; Walters, IA | 2 |
Chandra, J; Keating, M; Krupnik, Y; McConkey, D; Palladino, M; Ruiz, S | 1 |
Anderson, KC; Chauhan, D; Hideshima, T | 1 |
Bernasconi, P; Calatroni, S; Crosetto, N; Dikic, I | 1 |
Chao, TH; Cusack, JC; Liu, R; Neuteboom, ST; Niu, W; Palladino, MA; Palombella, VJ; Pien, C; Xia, L | 1 |
Blank, JL; Bruzzese, FJ; Cao, Y; Daniels, JS; Dick, LR; Labutti, J; Mazzola, AM; Patil, AD; Reimer, CL; Rolfe, M; Solomon, MS; Stirling, M; Tian, Y; Tsu, CA; Weatherhead, GS; Williamson, MJ; Zhang, JX | 1 |
Chao, TH; Deyanat-Yazdi, G; Lam, KS; Manam, RR; Mitchell, SS; Neuteboom, ST; Potts, BC; Reed, KA; Teisan, S; Xu, J | 1 |
Bacon, KB; Benet-Buchholz, J; Bitzer, J; Gantner, F; Mayer-Bartschmid, A; Müller, H; Reinemer, P; Stadler, M; Tichy, HV | 1 |
Beer, LL; Moore, BS | 1 |
Lam, KS; McArthur, KA; Potts, BC; Tsueng, G | 1 |
Ban, K; Chandra, J; Dujka, ME; McConkey, DJ; Miller, CP; Munsell, M; Palladino, M | 1 |
Lam, KS; McArthur, KA; Mitchell, SS; Potts, BC; Tsueng, G; Xu, J | 1 |
Fukuda, N; Kanai, M; Shibasaki, M | 1 |
Ma, G; Nguyen, H; Romo, D | 2 |
Ling, T; Macherla, VR; Manam, RR; McArthur, KA; Potts, BC | 1 |
Denora, N; Potts, BC; Stella, VJ | 1 |
Aggarwal, BB; Ahn, KS; Chao, TH; Chaturvedi, MM; Neuteboom, ST; Palladino, MA; Sethi, G; Younes, A | 1 |
Lam, KS; Tsueng, G | 3 |
Anderson, KC; Brahmandam, M; Chauhan, D; Hideshima, T; Munshi, N; Palladino, MA; Podar, K; Richardson, P; Singh, A | 1 |
Eustáquio, AS; Moore, BS; Noel, JP; Pojer, F | 1 |
Lam, KS; Teisan, S; Tsueng, G | 1 |
Anderson, KC; Azab, A; Azab, F; Burwick, N; Chauhan, D; Farag, M; Ghobrial, IM; Hideshima, T; Jia, X; Leleu, X; Melhem, M; Moreau, AS; Ngo, HT; Palladino, MA; Roccaro, AM; Runnels, J; Sacco, A; Treon, SP | 1 |
Eustáquio, AS; Moore, BS | 1 |
Baritaki, S; Berenson, J; Bonavida, B; Daniels, TR; Jazirehi, AR; Palladino, M; Penichet, ML; Spandidos, DA; Suzuki, E; Umezawa, K | 1 |
Asolkar, RN; Eustáquio, AS; Fenical, W; McGlinchey, RP; Moore, BS; Nett, M | 1 |
Bertani, S; Fenical, W; Jensen, P; Le Roch, K; McDaniel, E; Ponts, N; Prudhomme, J | 1 |
Hatakeyama, S; Ishihara, J; Kawano, K; Midori, M; Takahashi, K | 1 |
Cusack, JC; Houston, M; Liu, R; Ljungman, D; Palladino, MA; Sloss, CM; Wang, F; Xia, L | 1 |
Arima, S; Fukuda, T; Harigaya, Y; Nagamitsu, T; Omura, S; Sugiyama, K | 1 |
Fenical, W; Jensen, PR; Lam, KS; Lloyd, GK; Palladino, MA; Potts, BC | 1 |
Dring, CW; Lam, KS; Macherla, VR; Manam, RR; Neuteboom, ST; Potts, BC; Tsueng, G; Weiss, J | 1 |
Chandra, J; Keating, MJ; Miller, CP; Palladino, M; Rudra, S; Wierda, WG | 1 |
Sing Lam, K; Tsueng, G | 1 |
Chan, W; Heymach, J; McConkey, DJ; Wilkinson, M; Zhu, K | 1 |
Fuchs, O; Kuzelova, K; Marinov, I; Provaznikova, D; Spicka, I | 1 |
Tsukamoto, S; Yokosawa, H | 1 |
Alhamadsheh, MM; Beer, LL; Eustáquio, AS; Florova, G; Hazzard, C; Kale, AJ; Kobayashi, Y; Lechner, A; Liu, Y; McGlinchey, RP; Moore, BS; Reynolds, KA | 1 |
Baritaki, S; Bonavida, B; Chapman, A; Palladino, M; Spandidos, DA; Yeung, K | 1 |
Baerga-Ortiz, A | 1 |
Orlowski, RZ; Shah, JJ | 1 |
Gulder, TA; Hughes, CC; Kale, AJ; Moore, BS; Nett, M | 1 |
Baritaki, S; Berenson, J; Bonavida, B; Palladino, M; Yeung, K | 1 |
Dunner, K; McConkey, DJ; Zhu, K | 1 |
Anderson, KC; Chauhan, D; Ciccarelli, B; Palladino, MA; Richardson, PG; Singh, AV | 1 |
Anderson, KC; Chauhan, D; Lloyd, GK; Palladino, MA; Potts, BC; Singh, AV | 1 |
Ling, T; Macherla, VR; Potts, BC | 1 |
Lam, KS; Potts, BC | 1 |
Vollmar, AM; von Schwarzenberg, K | 1 |
Gulder, TA; Moore, BS | 1 |
Fremgen, T; Gladysheva, T; Ma, G; Nguyen, H; Romo, D | 1 |
Chida, N; Hasegawa, J; Kaiya, Y; Momose, T; Sato, T | 1 |
Albitar, MX; Anderson, KC; Baritaki, S; Berkers, C; Bonavida, B; Chandra, J; Chauhan, D; Cusack, JC; Fenical, W; Ghobrial, IM; Groll, M; Jensen, PR; Lam, KS; Lloyd, GK; McBride, W; McConkey, DJ; Miller, CP; Neuteboom, ST; Oki, Y; Ovaa, H; Pajonk, F; Palladino, MA; Potts, BC; Richardson, PG; Roccaro, AM; Sloss, CM; Spear, MA; Valashi, E; Younes, A | 1 |
Chao, TH; Enna, SJ; Hagenbuch, B; Lloyd, GK; Macherla, VR; Manam, RR; McArthur, K; Neuteboom, ST; Obaidat, A; Palladino, MA; Potts, BC; Wahlgren, B; Weiss, J | 1 |
Bitzer, J; Herrmann, J; Huo, L; Köpcke, B; Müller, R; Rachid, S; Stadler, M | 1 |
Goldschmidt, H; Moehler, T | 1 |
Fukuyama, T; Satoh, N; Yokoshima, S | 1 |
Kay, LE; Ruschak, AM; Schimmer, AD; Slassi, M | 1 |
Deska, J; Hähn, S; Kazmaier, U | 1 |
Liu, Z; Ma, Y; Qu, L; Yang, Z; Zhang, L | 1 |
Chandra, J; Debose, L; Hale, R; Macherla, VR; Manton, CA; Miller, CP; Palladino, MA; Potts, BC | 1 |
Kale, AJ; Lechner, A; McGlinchey, RP; Moore, BS | 1 |
Palladino, MA; Potts, BC; Steverding, D; Wang, X | 1 |
Drabkin, HA; Gemmill, RM; Lay, A; Lee, L; Lloyd, GK; Longenecker, A; McConkey, DJ; Millward, M; Neuteboom, ST; Palladino, MA; Price, T; Sharma, G; Spear, MA; Spencer, A; Sukumaran, S; Sweeney, C; Townsend, A | 1 |
Eustáquio, AS; Gulder, TA; Hafner, M; Lechner, A; Moore, BS | 1 |
Gallastegui, N; Groll, M | 1 |
Abe, M; Fujii, S | 1 |
Hu, Y; Wu, P; Zhang, J | 1 |
Mateos, MV; Ocio, EM; San Miguel, JF | 1 |
Blasdel, LK; Lee, D; Myers, AG; Sun, B | 1 |
Anderl, JL; Assaraf, YG; Cloos, J; Jansen, G; Kale, AJ; Kaspers, GJ; Moore, BS; Niewerth, D; Riethoff, LF; van Meerloo, J; Zweegman, S | 1 |
Burton, JW; Foster, RW; Garzya, V; Hallside, MS; Logan, AW; Marx, LB; Sprague, SJ; Thompson, AL | 1 |
Kuroda, J | 1 |
Diao, A; Ma, L | 1 |
Chandra, J; Corrales-Medina, FF; Manton, CA; Orlowski, RZ | 1 |
Anderson, KC; Chauhan, D; Das, DS; Ray, A; Richardson, P; Song, Y; Trikha, M | 1 |
Abraham, V; Bota, DA; Burrows, FJ; Desjardins, A; Di, K; Lloyd, GK; MacLaren, A; Trikha, M | 1 |
Bailey, CP; Bouchier-Hayes, L; Chandra, J; Johnson, B; Manton, CA; Singh, M | 1 |
Guo, L; Qu, G; Wu, C; Xie, Z; Yang, X; Zhang, S; Zhou, L | 1 |
Anderson, KC; Chanan-Khan, AA; Chauhan, D; Hofmeister, CC; Jakubowiak, AJ; Kaufman, JL; Laubach, JP; Reich, S; Richardson, PG; Talpaz, M; Trikha, M; Zimmerman, TM | 1 |
Cannell, PK; Harrison, SJ; Mainwaring, P; Millward, MJ; Padrik, P; Price, T; Reich, SD; Spencer, A; Trikha, M; Underhill, CR | 1 |
Anderson, KC; Burrows, FJ; Chauhan, D; Harrison, SJ; Levin, N; Reich, SD; Richardson, PG; Spencer, A; Trikha, M | 1 |
Kłoczko, J; Ołdziej, AE; Romaniuk, W; Zińczuk, J | 1 |
Moreau, P; Rajkumar, SV | 1 |
Fielding, E; Groenhagen, U; Leandrini De Oliveira, AL; Moore, BS; Schulz, S | 1 |
Bocchia, M; Brambilla, CZ; Candi, V; Gozzetti, A; Papini, G; Sirianni, S | 1 |
Dineshkumar, K; Hopper, W; Vasudevan, A | 1 |
Badros, A; Dhakal, B; Hari, P; Kwok, Y; MacLaren, A; Richardson, P; Singh, Z; Trikha, M | 1 |
Ma, H; Su, Z; Sun, F; Zhao, N | 1 |
Bullova, P; Cougnoux, A; Kopacek, J; Marzouca, G; Pacak, K | 1 |
Burton, JW; Marx, LB | 1 |
Grammatico, S; Petrucci, MT; Scalzulli, E; Vozella, F | 1 |
Groll, M; Nguyen, H; Romo, D; Vellalath, S | 1 |
Borhan, B; Favor, OK; Gholami, H; Kulshrestha, A; Staples, RJ | 1 |
Badodi, S; Benjamin-Ombo, VA; Frisira, E; Michod, D; Niklison-Chirou, MV; Rashid, F; Varma, SN | 1 |
Andreasson, KI; Ceribelli, M; Chen, L; Duveau, DY; Ferrer, M; Geraghty, AC; Ghanem, R; Gillespie, SM; Guha, R; Itkin, Z; Klumpp-Thomas, C; Kreimer, S; Lennon, J; Lin, GL; McKnight, C; Michael, S; Michalowski, AM; Minhas, P; Monje, M; Morris, PJ; Nagaraja, S; Ni, L; Qin, EY; Quezada, M; Raabe, EH; Shinn, P; Stanton, BZ; Thomas, CJ; Vitanza, NA; Warren, KE; Wilson, KM; Woo, PJ; Zhang, X | 1 |
Agarwal, P; Krishna, M; Lang, M; Liao, PJ; Linehan, WM; Matsumoto, S; Mitchell, JB; Neckers, L; Railkar, R; Ricketts, CJ; Sourbier, C; Trepel, JB; Wei, D; Wei, MH; Yang, Y | 1 |
Li, J; Sherman, DJ | 1 |
Datta, KK; Dong, LF; Dutt, M; Gowda, H; Hill, M; Kalimutho, M; Kalita-de Croft, P; Khanna, KK; Lee, A; Lu, X; Neuzil, J; Pouliot, N; Raninga, PV; Sinha, D | 1 |
Mason, WP; Richardson, PG; Roth, P; Weller, M | 1 |
Jeong, GS; Lee, HS | 1 |
Boccellato, C; Fullstone, G; Idbaih, A; Juric, V; Kolbe, E; Lamfers, MLM; Murphy, BM; Peters, N; Rehm, M; Verreault, M | 1 |
24 review(s) available for pyrroles and marizomib
Article | Year |
---|---|
Marine actinomycete diversity and natural product discovery.
Topics: Actinobacteria; Antibiotics, Antineoplastic; Biodiversity; Biological Factors; Geologic Sediments; Lactones; Pyrroles; Seawater | 2005 |
A novel proteasome inhibitor NPI-0052 as an anticancer therapy.
Topics: Animals; Antineoplastic Agents; Apoptosis; Humans; Lactones; Models, Biological; Molecular Structure; Multiple Myeloma; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles; Xenograft Model Antitumor Assays | 2006 |
Targeting ubiquitin in cancers.
Topics: Antineoplastic Agents; Boronic Acids; Bortezomib; Cell Communication; Cell Cycle; Genetic Therapy; Heat-Shock Proteins; Humans; Lactones; Neoplasms; Pyrazines; Pyrroles; Ubiquitin | 2006 |
Total synthesis of lactacystin and salinosporamide A.
Topics: Acetylcysteine; Enzyme Inhibitors; Lactones; Molecular Structure; Proteasome Inhibitors; Pyrroles; Stereoisomerism | 2007 |
Antiproliferative and proapoptotic effects of proteasome inhibitors and their combination with histone deacetylase inhibitors on leukemia cells.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Boronic Acids; Bortezomib; Cell Line, Tumor; Cell Proliferation; Drug Synergism; Enzyme Inhibitors; Histone Deacetylase Inhibitors; Humans; Lactones; Leukemia; Oligopeptides; Protease Inhibitors; Pyrazines; Pyrroles | 2009 |
Targeting the proteasome pathway.
Topics: Acetylcysteine; Animals; Antineoplastic Agents; Biological Products; Boronic Acids; Bortezomib; Drug Delivery Systems; Drug Discovery; Humans; Lactones; Neoplasms; Peptides; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Pyrroles; Structure-Activity Relationship; Ubiquitin; Ubiquitin-Activating Enzymes; Ubiquitins | 2009 |
Biotechnology and biochemistry of marine natural products.
Topics: Actinobacteria; Biochemistry; Biological Products; Biotechnology; Bryostatins; Fatty Acids, Omega-3; Lactones; Marine Biology; Pyrroles | 2009 |
Proteasome inhibitors in the treatment of multiple myeloma.
Topics: Antineoplastic Agents; Boronic Acids; Bortezomib; Humans; Lactones; Multiple Myeloma; Oligopeptides; Protease Inhibitors; Pyrazines; Pyrroles | 2009 |
Generating a generation of proteasome inhibitors: from microbial fermentation to total synthesis of salinosporamide a (marizomib) and other salinosporamides.
Topics: Animals; Drug Design; Enzyme Inhibitors; Fermentation; Humans; Lactones; Neoplasms; Proteasome Inhibitors; Pyrroles; Technology, Pharmaceutical | 2010 |
Targeting apoptosis pathways by natural compounds in cancer: marine compounds as lead structures and chemical tools for cancer therapy.
Topics: Alkaloids; Alkanes; Animals; Anti-Bacterial Agents; Antineoplastic Agents; Apoptosis; Aquatic Organisms; Biological Products; Bryostatins; Carbamates; Cell Proliferation; Depsipeptides; Dioxoles; Drug Screening Assays, Antitumor; Humans; Lactones; Macrolides; Microtubules; Models, Chemical; Neoplasms; Phenanthrolines; Phenazines; Proteasome Endopeptidase Complex; Pyrones; Pyrroles; Quinolines; Spiro Compounds; Steroids; Tetrahydroisoquinolines; Thiazoles; Trabectedin | 2013 |
Salinosporamide natural products: Potent 20 S proteasome inhibitors as promising cancer chemotherapeutics.
Topics: Antineoplastic Combined Chemotherapy Protocols; Biological Factors; Cysteine Proteinase Inhibitors; Humans; Lactones; Molecular Conformation; Neoplasms; Proteasome Inhibitors; Pyrroles | 2010 |
Marizomib, a proteasome inhibitor for all seasons: preclinical profile and a framework for clinical trials.
Topics: Animals; Antineoplastic Agents; Drug Evaluation, Preclinical; Humans; Lactones; Neoplasms; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles | 2011 |
Therapy of relapsed and refractory multiple myeloma.
Topics: Adrenal Cortex Hormones; Aged; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Boronic Acids; Bortezomib; Dexamethasone; Hematopoietic Stem Cell Transplantation; Humans; Lactones; Lenalidomide; Middle Aged; Multiple Myeloma; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Pyrroles; Secondary Prevention; Thalidomide | 2011 |
Novel proteasome inhibitors to overcome bortezomib resistance.
Topics: Allosteric Site; Animals; Antineoplastic Agents; Apoptosis; Boronic Acids; Bortezomib; Cell Line, Tumor; Chloroquine; Clioquinol; Drug Resistance, Neoplasm; Humans; Hydroxyquinolines; Lactones; Neoplasms; Oligopeptides; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Pyrroles; Threonine; Ubiquitinated Proteins; Ubiquitination | 2011 |
Synthesis of salinosporamide A and its analogs as 20S proteasome inhibitors and SAR summarization.
Topics: Lactones; Protease Inhibitors; Proteasome Inhibitors; Pyrroles; Structure-Activity Relationship | 2011 |
Clinical and marketed proteasome inhibitors for cancer treatment.
Topics: Boron Compounds; Boronic Acids; Bortezomib; Glycine; Humans; Lactones; Neoplasms; Oligopeptides; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Pyrroles; Structure-Activity Relationship; Threonine | 2013 |
Novel generation of agents with proven clinical activity in multiple myeloma.
Topics: Antineoplastic Combined Chemotherapy Protocols; Clinical Trials as Topic; Humans; Immunologic Factors; Lactones; Multiple Myeloma; Oligopeptides; Proteasome Inhibitors; Pyrroles; Recurrence; Thalidomide; Treatment Outcome | 2013 |
[Current status of clinical trials of novel agents for multiple myeloma].
Topics: Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic Combined Chemotherapy Protocols; Clinical Trials as Topic; Drug Approval; Drug Discovery; Histone Deacetylase Inhibitors; Humans; Hydroxamic Acids; Lactones; Molecular Targeted Therapy; Multiple Myeloma; Oligopeptides; Pyrroles; Thalidomide; Vorinostat | 2014 |
Marizomib, a potent second generation proteasome inhibitor from natural origin.
Topics: Actinobacteria; Antineoplastic Agents; Biological Products; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Humans; Lactones; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles; Structure-Activity Relationship | 2015 |
[Proteasome inhibitors in cancer therapy].
Topics: Antineoplastic Agents; Apoptosis; Boronic Acids; Bortezomib; Caspases; Dipeptides; Humans; Lactones; Multiple Myeloma; Neoplasms; Oligopeptides; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Proteolysis; Pyrroles; Thiazoles; Threonine | 2015 |
Second Generation Proteasome Inhibitors in Multiple Myeloma.
Topics: Animals; Boronic Acids; Bortezomib; Central Nervous System Neoplasms; Drug Discovery; Humans; Lactones; Multiple Myeloma; Neoplasm Recurrence, Local; Oligopeptides; Proteasome Inhibitors; Pyrroles; Threonine | 2017 |
Proteasome inhibitors for the treatment of multiple myeloma.
Topics: Antibodies, Monoclonal; Antineoplastic Agents; Boron Compounds; Bortezomib; Glycine; Hematologic Diseases; Humans; Lactones; Multiple Myeloma; Neoplasm Recurrence, Local; Oligopeptides; Proteasome Inhibitors; Pyrroles | 2018 |
Proteasome Inhibitors: Harnessing Proteostasis to Combat Disease.
Topics: Antineoplastic Agents; Boron Compounds; Bortezomib; Glycine; Humans; Lactones; Molecular Targeted Therapy; Multiple Myeloma; Oligopeptides; Proteasome Inhibitors; Proteostasis; Pyrroles | 2020 |
Proteasome inhibition for the treatment of glioblastoma.
Topics: Animals; Antineoplastic Agents; Bortezomib; Brain Neoplasms; Drug Development; Glioblastoma; Humans; Lactones; Proteasome Inhibitors; Pyrroles | 2020 |
4 trial(s) available for pyrroles and marizomib
Article | Year |
---|---|
Phase 1 clinical trial of the novel proteasome inhibitor marizomib with the histone deacetylase inhibitor vorinostat in patients with melanoma, pancreatic and lung cancer based on in vitro assessments of the combination.
Topics: Adult; Aged; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Carcinoma; Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Cell Proliferation; Drug Combinations; Female; Histone Deacetylase Inhibitors; Humans; Hydroxamic Acids; Lactones; Lung Neoplasms; Male; Melanoma; Middle Aged; Pancreatic Neoplasms; Proteasome Inhibitors; Pyrroles; Vorinostat | 2012 |
Phase 1 study of marizomib in relapsed or relapsed and refractory multiple myeloma: NPI-0052-101 Part 1.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Dexamethasone; Female; Humans; Lactones; Male; Maximum Tolerated Dose; Middle Aged; Multiple Myeloma; Pyrroles; Recurrence; Thalidomide | 2016 |
Phase I Clinical Trial of Marizomib (NPI-0052) in Patients with Advanced Malignancies Including Multiple Myeloma: Study NPI-0052-102 Final Results.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Drug Administration Schedule; Female; Humans; Lactones; Male; Middle Aged; Multiple Myeloma; Neoplasm Staging; Neoplasms; Proteasome Inhibitors; Pyrroles; Recurrence; Retreatment; Treatment Outcome; Young Adult | 2016 |
Marizomib irreversibly inhibits proteasome to overcome compensatory hyperactivation in multiple myeloma and solid tumour patients.
Topics: Caspases; Chymotrypsin; Enzyme Activation; Glioma; Humans; Lactones; Multiple Myeloma; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles; Trypsin | 2016 |
86 other study(ies) available for pyrroles and marizomib
Article | Year |
---|---|
Salinosporamide A: a highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus salinospora.
Topics: Actinomycetales; Adenocarcinoma; Colonic Neoplasms; Crystallography, X-Ray; Cysteine Endopeptidases; Humans; Inhibitory Concentration 50; Lactones; Magnetic Resonance Spectroscopy; Models, Molecular; Molecular Structure; Multienzyme Complexes; Protease Inhibitors; Proteasome Endopeptidase Complex; Pyrroles; Tumor Cells, Cultured | 2003 |
A simple stereocontrolled synthesis of salinosporamide A.
Topics: Antineoplastic Agents; Indicators and Reagents; Lactones; Magnetic Resonance Spectroscopy; Optical Rotation; Pyrroles; Spectrophotometry, Infrared; Stereoisomerism | 2004 |
Structure-activity relationship studies of salinosporamide A (NPI-0052), a novel marine derived proteasome inhibitor.
Topics: Actinobacteria; Animals; Antineoplastic Agents; Cell Line; Cell Line, Tumor; Humans; Lactones; Marine Biology; NF-kappa B; Proteasome Inhibitors; Pyrroles; Rabbits; Stereoisomerism; Structure-Activity Relationship | 2005 |
Total synthesis of salinosporamide A.
Topics: Actinomycetales; Lactones; Protease Inhibitors; Pyrroles; Selenium; Stereoisomerism | 2005 |
New synthetic route for the enantioselective total synthesis of salinosporamide A and biologically active analogues.
Topics: Catalysis; Cyclization; Lactones; Molecular Structure; Pyrroles; Stereoisomerism | 2005 |
An efficient, stereocontrolled synthesis of a potent omuralide-salinosporin hybrid for selective proteasome inhibition.
Topics: Enzyme Inhibitors; Lactones; Molecular Conformation; Proteasome Inhibitors; Pyrroles; Stereoisomerism | 2005 |
Proteasome inhibition by a totally synthetic beta-lactam related to salinosporamide A and omuralide.
Topics: beta-Lactams; Drug Stability; Half-Life; Kinetics; Lactones; Proteasome Inhibitors; Pyrroles | 2005 |
A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib.
Topics: Administration, Oral; Animals; Antineoplastic Agents; Apoptosis; Boronic Acids; Bortezomib; Caspases; Cell Movement; Cell Proliferation; Drug Synergism; Genes, bcl-2; Humans; Lactones; Lymphocytes; Mice; Mitochondria; Multiple Myeloma; NF-kappa B; Plasmacytoma; Protease Inhibitors; Proteasome Endopeptidase Complex; Pyrazines; Pyrroles; Tumor Cells, Cultured | 2005 |
A concise total synthesis of salinosporamide A.
Topics: Cyclization; Lactones; Protease Inhibitors; Proteasome Inhibitors; Pyrroles | 2006 |
The proteasome inhibitor NPI-0052 is a more effective inducer of apoptosis than bortezomib in lymphocytes from patients with chronic lymphocytic leukemia.
Topics: Antineoplastic Agents; Apoptosis; Boronic Acids; Bortezomib; Humans; Lactones; Leukemia, Lymphocytic, Chronic, B-Cell; Lymphocytes; Protease Inhibitors; Proteasome Inhibitors; Pyrazines; Pyrroles | 2006 |
NPI-0052 enhances tumoricidal response to conventional cancer therapy in a colon cancer model.
Topics: Adenocarcinoma; Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Boronic Acids; Bortezomib; Cell Cycle; Colonic Neoplasms; Drug Administration Routes; Drug Synergism; Female; Humans; Lactones; Mice; Mice, Nude; NF-kappa B; Proteasome Endopeptidase Complex; Pyrazines; Pyrroles; Tumor Cells, Cultured; Tumor Necrosis Factor-alpha; Xenograft Model Antitumor Assays | 2006 |
Comparison of biochemical and biological effects of ML858 (salinosporamide A) and bortezomib.
Topics: Animals; Antineoplastic Agents; Binding, Competitive; Boronic Acids; Bortezomib; Drug Stability; Female; HeLa Cells; HT29 Cells; Humans; Lactones; Mice; Mice, Nude; Mice, SCID; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Pyrroles; Xenograft Model Antitumor Assays | 2006 |
Salinosporamides D-J from the marine actinomycete Salinispora tropica, bromosalinosporamide, and thioester derivatives are potent inhibitors of the 20S proteasome.
Topics: Actinobacteria; Bahamas; Crystallography, X-Ray; Inhibitory Concentration 50; Lactones; Marine Biology; Molecular Conformation; Molecular Structure; Proteasome Inhibitors; Pyrroles | 2007 |
Cinnabaramides A-G: analogues of lactacystin and salinosporamide from a terrestrial streptomycete.
Topics: Acetylcysteine; Crystallography, X-Ray; Humans; Lactones; Molecular Conformation; Molecular Structure; Proteasome Inhibitors; Pyrroles; Streptomyces | 2007 |
Biosynthetic convergence of salinosporamides A and B in the marine actinomycete Salinispora tropica.
Topics: Amino Acids; Lactams; Lactones; Magnetic Resonance Spectroscopy; Micromonosporaceae; Molecular Structure; Oceans and Seas; Peptides; Pyrroles | 2007 |
Unique butyric acid incorporation patterns for salinosporamides A and B reveal distinct biosynthetic origins.
Topics: Butyric Acid; Lactams; Lactones; Magnetic Resonance Spectroscopy; Micromonosporaceae; Pyrroles | 2007 |
NPI-0052, a novel proteasome inhibitor, induces caspase-8 and ROS-dependent apoptosis alone and in combination with HDAC inhibitors in leukemia cells.
Topics: Animals; Apoptosis; Caspase 8; Cell Line, Tumor; Histone Deacetylase Inhibitors; Humans; Lactones; Leukemia; Mice; Oxidative Stress; Protease Inhibitors; Proteasome Inhibitors; Pyrroles; Reactive Oxygen Species; Tumor Burden; Tumor Cells, Cultured | 2007 |
Effects of halogens on the production of salinosporamides by the obligate marine actinomycete Salinispora tropica.
Topics: Actinomycetales; Bromides; Chromatography, High Pressure Liquid; Culture Media; Lactones; Molecular Structure; Pyrroles; Sodium Compounds; Sodium Fluoride; Sodium Iodide | 2007 |
Concise total synthesis of (+/-)-salinosporamide A, (+/-)-cinnabaramide A, and derivatives via a bis-cyclization process: implications for a biosynthetic pathway?
Topics: Color; Lactones; Molecular Structure; Pyrroles | 2007 |
Enantioselective total synthesis of (-)-Salinosporamide A (NPI-0052).
Topics: Crystallography, X-Ray; Lactones; Models, Molecular; Molecular Conformation; Pyrroles; Stereoisomerism | 2007 |
A mechanistic and kinetic study of the beta-lactone hydrolysis of Salinosporamide A (NPI-0052), a novel proteasome inhibitor.
Topics: beta-Cyclodextrins; Buffers; Chromatography, High Pressure Liquid; Deuterium Oxide; Drug Stability; Enzyme Inhibitors; Hydrogen-Ion Concentration; Hydrolysis; Kinetics; Lactones; Mass Spectrometry; Molecular Structure; Osmolar Concentration; Proteasome Inhibitors; Pyrroles; Solubility; Solutions; Temperature; Water | 2007 |
Salinosporamide A (NPI-0052) potentiates apoptosis, suppresses osteoclastogenesis, and inhibits invasion through down-modulation of NF-kappaB regulated gene products.
Topics: Active Transport, Cell Nucleus; Animals; Apoptosis; Cell Differentiation; Cell Line; Down-Regulation; Enzyme Activation; Gene Expression Regulation; Genes, Reporter; Humans; I-kappa B Proteins; Lactones; Mice; Mice, Knockout; Neoplasm Invasiveness; NF-kappa B; Osteoclasts; Phosphorylation; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles; RANK Ligand; Time Factors; Tumor Necrosis Factors | 2007 |
Stabilization effect of resin on the production of potent proteasome inhibitor NPI-0052 during submerged fermentation of Salinispora tropica.
Topics: Acrylic Resins; Anion Exchange Resins; Apoptosis; Fermentation; Humans; Lactones; Micromonosporaceae; Polystyrenes; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles | 2007 |
Combination of proteasome inhibitors bortezomib and NPI-0052 trigger in vivo synergistic cytotoxicity in multiple myeloma.
Topics: Animals; Boronic Acids; Bortezomib; Cell Line, Tumor; Cell Movement; Cell Survival; Endoplasmic Reticulum; Heat-Shock Proteins; Humans; Lactones; Mice; Multiple Myeloma; Neovascularization, Pathologic; NF-kappa B; Protease Inhibitors; Proteasome Endopeptidase Complex; Pyrazines; Pyrroles; Xenograft Model Antitumor Assays | 2008 |
Discovery and characterization of a marine bacterial SAM-dependent chlorinase.
Topics: Bacterial Proteins; Crystallography, X-Ray; Genes, Bacterial; Hydrocarbons, Chlorinated; Lactones; Micromonosporaceae; Protein Conformation; Pyrroles; S-Adenosylmethionine; Substrate Specificity | 2008 |
Defined salt formulations for the growth of Salinispora tropica strain NPS21184 and the production of salinosporamide A (NPI-0052) and related analogs.
Topics: Culture Media; Geologic Sediments; Industrial Microbiology; Lactones; Mass Spectrometry; Micromonosporaceae; Pyrroles; Sodium Chloride | 2008 |
A low-sodium-salt formulation for the fermentation of salinosporamides by Salinispora tropica strain NPS21184.
Topics: Culture Media; Fermentation; Industrial Microbiology; Lactams; Lactones; Micromonosporaceae; Pyrroles; Seawater; Sodium Compounds | 2008 |
Dual targeting of the proteasome regulates survival and homing in Waldenstrom macroglobulinemia.
Topics: Boronic Acids; Bortezomib; Cell Adhesion; Cell Death; Cell Movement; Cells, Cultured; Drug Delivery Systems; Drug Synergism; Humans; Lactones; Proteasome Inhibitors; Pyrazines; Pyrroles; Waldenstrom Macroglobulinemia | 2008 |
Mutasynthesis of fluorosalinosporamide, a potent and reversible inhibitor of the proteasome.
Topics: Binding Sites; Biological Factors; Cell Line, Tumor; Cell Proliferation; Drug Screening Assays, Antitumor; Genetic Engineering; Humans; Hydrocarbons, Fluorinated; Lactams; Lactones; Proteasome Inhibitors; Pyrroles; Saccharomyces cerevisiae; Structure-Activity Relationship | 2008 |
Inhibition of Yin Yang 1-dependent repressor activity of DR5 transcription and expression by the novel proteasome inhibitor NPI-0052 contributes to its TRAIL-enhanced apoptosis in cancer cells.
Topics: Apoptosis; Boronic Acids; Bortezomib; Cell Line, Tumor; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Hematopoietic Stem Cells; Humans; Lactones; Neoplasms; NF-kappa B; Protease Inhibitors; Pyrazines; Pyrroles; Receptors, TNF-Related Apoptosis-Inducing Ligand; RNA, Messenger; RNA, Small Interfering; TNF-Related Apoptosis-Inducing Ligand; Transcription, Genetic; Up-Regulation; YY1 Transcription Factor | 2008 |
Engineered biosynthesis of antiprotealide and other unnatural salinosporamide proteasome inhibitors.
Topics: Lactams; Lactones; Micromonosporaceae; Molecular Structure; Protease Inhibitors; Proteasome Endopeptidase Complex; Protein Engineering; Pyrroles | 2008 |
Marine actinomycetes: a new source of compounds against the human malaria parasite.
Topics: Actinobacteria; Animals; Antimalarials; Lactones; Marine Biology; Plasmodium falciparum; Pyrroles | 2008 |
Entry to heterocycles based on indium-catalyzed conia-ene reactions: asymmetric synthesis of (-)-salinosporamide A.
Topics: Catalysis; Cysteine Proteinase Inhibitors; Indium; Lactones; Proteasome Inhibitors; Pyrroles | 2008 |
A concise and straightforward total synthesis of (+/-)-salinosporamide A, based on a biosynthesis model.
Topics: Aldehydes; Lactones; Malonates; Models, Biological; Molecular Structure; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles; Pyrrolidinones; Stereoisomerism | 2008 |
Growth of Salinispora tropica strains CNB440, CNB476, and NPS21184 in nonsaline, low-sodium media.
Topics: Culture Media; Lactones; Micromonosporaceae; Pyrroles; Seawater; Sodium Chloride | 2008 |
Proteasome inhibition activates epidermal growth factor receptor (EGFR) and EGFR-independent mitogenic kinase signaling pathways in pancreatic cancer cells.
Topics: Adenocarcinoma; Animals; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Bevacizumab; Blotting, Western; Boronic Acids; Bortezomib; Cell Line, Tumor; Cetuximab; Deoxycytidine; ErbB Receptors; Erlotinib Hydrochloride; Female; Gemcitabine; Humans; Lactones; Mice; Mice, Nude; Pancreatic Neoplasms; Phosphatidylinositol 3-Kinases; Protease Inhibitors; Proteasome Inhibitors; Pyrazines; Pyrroles; Quinazolines; Signal Transduction; Xenograft Model Antitumor Assays | 2008 |
Total synthesis of salinosporamide A.
Topics: Cyclohexenes; Lactones; Pyrroles; Stereoisomerism; Substrate Specificity | 2008 |
Discovery and development of the anticancer agent salinosporamide A (NPI-0052).
Topics: Antineoplastic Agents; Drug Discovery; Drugs, Investigational; Lactones; Molecular Structure; Pyrroles | 2009 |
Antiprotealide is a natural product.
Topics: Actinobacteria; Animals; Biological Products; Drug Screening Assays, Antitumor; Humans; Inhibitory Concentration 50; Lactams; Lactones; Marine Biology; Molecular Structure; Proteasome Endopeptidase Complex; Pyrroles; Rabbits | 2009 |
Caspase-8 dependent histone acetylation by a novel proteasome inhibitor, NPI-0052: a mechanism for synergy in leukemia cells.
Topics: Acetylation; Antioxidants; Apoptosis; Boronic Acids; Bortezomib; Caspase 8; Drug Synergism; Drug Therapy, Combination; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Hydroxamic Acids; Immunoblotting; Immunoprecipitation; Lactones; Leukemia, Lymphocytic, Chronic, B-Cell; Leukemia, Myeloid, Acute; Oxidative Stress; Protease Inhibitors; Proteasome Inhibitors; Protein Processing, Post-Translational; Pyrazines; Pyrroles; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Superoxides; Tumor Cells, Cultured; Vorinostat | 2009 |
Effect of cobalt and vitamin B12 on the production of salinosporamides by Salinispora tropica.
Topics: Actinomycetales; Chromatography, High Pressure Liquid; Cobalt; Culture Media; Fermentation; Lactams; Lactones; Molecular Conformation; Pyrroles; Vitamin B 12 | 2009 |
Control of HIF-1alpha expression by eIF2 alpha phosphorylation-mediated translational repression.
Topics: Basic Helix-Loop-Helix Transcription Factors; Boronic Acids; Bortezomib; Cell Line, Tumor; Down-Regulation; Eukaryotic Initiation Factor-2; Gene Expression Regulation; Humans; Hypoxia-Inducible Factor 1, alpha Subunit; Lactones; Phosphorylation; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Protein Biosynthesis; Pyrazines; Pyrroles; RNA, Messenger; Vascular Endothelial Growth Factor A | 2009 |
Biosynthesis of the salinosporamide A polyketide synthase substrate chloroethylmalonyl-coenzyme A from S-adenosyl-L-methionine.
Topics: Bacterial Proteins; Chromatography, High Pressure Liquid; Cladribine; Cloning, Molecular; Gene Order; Genome, Bacterial; Kinetics; Lactones; Malonyl Coenzyme A; Micromonosporaceae; Models, Chemical; Molecular Sequence Data; Molecular Structure; Multigene Family; Mutation; Phylogeny; Polyketide Synthases; Pyrroles; S-Adenosylmethionine; Sequence Analysis, DNA; Substrate Specificity | 2009 |
Inhibition of epithelial to mesenchymal transition in metastatic prostate cancer cells by the novel proteasome inhibitor, NPI-0052: pivotal roles of Snail repression and RKIP induction.
Topics: Cell Differentiation; Cell Line, Tumor; Cell Movement; Epithelial Cells; Gene Expression Regulation, Neoplastic; Humans; Lactones; Male; Mesoderm; Neoplasm Invasiveness; Neoplasm Metastasis; NF-kappa B; Phosphatidylethanolamine Binding Protein; Prostatic Neoplasms; Protease Inhibitors; Proteasome Inhibitors; Pyrroles; Snail Family Transcription Factors; Transcription Factors | 2009 |
Function-oriented biosynthesis of beta-lactone proteasome inhibitors in Salinispora tropica.
Topics: Actinobacteria; Inhibitory Concentration 50; Lactones; Protease Inhibitors; Proteasome Inhibitors; Protein Engineering; Pyrroles; Structure-Activity Relationship | 2009 |
Pivotal roles of snail inhibition and RKIP induction by the proteasome inhibitor NPI-0052 in tumor cell chemoimmunosensitization.
Topics: Adenocarcinoma; Antineoplastic Agents; Apoptosis; Blotting, Western; Boronic Acids; Bortezomib; Cisplatin; Humans; Lactones; Leupeptins; Male; Melanoma; Membrane Potential, Mitochondrial; NF-kappa B; Phosphatidylethanolamine Binding Protein; Prostatic Neoplasms; Proteasome Inhibitors; Proto-Oncogene Proteins c-raf; Pyrazines; Pyrroles; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; RNA, Small Interfering; Snail Family Transcription Factors; TNF-Related Apoptosis-Inducing Ligand; Transcription Factors; Transfection; Tumor Cells, Cultured | 2009 |
Proteasome inhibitors activate autophagy as a cytoprotective response in human prostate cancer cells.
Topics: Animals; Autophagy; Autophagy-Related Protein 5; Autophagy-Related Protein 7; Boronic Acids; Bortezomib; Cell Line; Cell Line, Tumor; Cell Survival; Humans; Immunoblotting; Lactones; Lysosomes; Male; Microscopy, Electron, Transmission; Microtubule-Associated Proteins; Phagosomes; Prostatic Neoplasms; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Pyrroles; Reverse Transcriptase Polymerase Chain Reaction; RNA Interference; Ubiquitin-Activating Enzymes | 2010 |
Combination of novel proteasome inhibitor NPI-0052 and lenalidomide trigger in vitro and in vivo synergistic cytotoxicity in multiple myeloma.
Topics: Animals; Antineoplastic Agents; Apoptosis; Cell Division; Cell Line, Tumor; Cell Survival; Disease Models, Animal; Drug Resistance, Neoplasm; Drug Synergism; Humans; In Vitro Techniques; Lactones; Lenalidomide; Mice; Mice, SCID; Multiple Myeloma; Proteasome Inhibitors; Pyrroles; Thalidomide; Xenograft Model Antitumor Assays | 2010 |
Pharmacodynamic and efficacy studies of the novel proteasome inhibitor NPI-0052 (marizomib) in a human plasmacytoma xenograft murine model.
Topics: Animals; Antineoplastic Agents; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Humans; Kidney; Lactones; Male; Mice; Plasmacytoma; Proteasome Inhibitors; Pyrroles; Rats; Rats, Sprague-Dawley; Tumor Cells, Cultured; Xenograft Model Antitumor Assays | 2010 |
Concise formal synthesis of (-)-salinosporamide A (marizomib) using a regio- and stereoselective epoxidation and reductive oxirane ring-opening strategy.
Topics: Epoxy Compounds; Ethylene Oxide; Lactones; Proteasome Inhibitors; Pyrroles; Pyrrolidinones; Stereoisomerism | 2010 |
A(1,3)-strain enabled retention of chirality during bis-cyclization of beta-ketoamides: total synthesis of (-)-salinosporamide A and (-)-homosalinosporamide A.
Topics: Amides; Antineoplastic Agents; Crystallography, X-Ray; Cyclization; Lactones; Molecular Conformation; Pyrroles; Stereoisomerism | 2010 |
Bioinspired total synthesis and human proteasome inhibitory activity of (-)-salinosporamide A, (-)-homosalinosporamide A, and derivatives obtained via organonucleophile promoted bis-cyclizations.
Topics: Antineoplastic Agents; Catalysis; Crystallography, X-Ray; Cyclization; Humans; Lactones; Magnetic Resonance Spectroscopy; Molecular Conformation; Molecular Structure; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles; Stereoisomerism | 2011 |
Total synthesis of (-)-salinosporamide A.
Topics: Lactones; Molecular Structure; Pyrroles | 2011 |
Proteasome regulator marizomib (NPI-0052) exhibits prolonged inhibition, attenuated efflux, and greater cytotoxicity than its reversible analogs.
Topics: Antineoplastic Agents; ATP Binding Cassette Transporter, Subfamily B; ATP-Binding Cassette Transporters; Cell Adhesion; Cell Line, Tumor; Cell Survival; Humans; Lactams; Lactones; Proteasome Endopeptidase Complex; Pyrroles | 2011 |
Mining the cinnabaramide biosynthetic pathway to generate novel proteasome inhibitors.
Topics: Biosynthetic Pathways; Cell Line, Tumor; Humans; Lactones; Multigene Family; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles; Streptomyces | 2011 |
Total synthesis of (-)-salinosporamide A.
Topics: Antineoplastic Agents; Lactones; Molecular Structure; Proteasome Inhibitors; Pyrroles; Stereoisomerism | 2011 |
Stereoselective synthesis of deuterated β-cyclohexenylserine, a biosynthetic intermediate of the salinosporamides.
Topics: Cyclohexenes; Deuterium; Lactones; Molecular Structure; Pyrroles; Serine; Stereoisomerism | 2011 |
Specific and prolonged proteasome inhibition dictates apoptosis induction by marizomib and its analogs.
Topics: Apoptosis; Caspase 8; Humans; Lactones; Leukemia; Oxidative Stress; Protease Inhibitors; Pyrroles; Reactive Oxygen Species; Tumor Cells, Cultured | 2011 |
Bacterial self-resistance to the natural proteasome inhibitor salinosporamide A.
Topics: Actinobacteria; Biological Products; Boronic Acids; Bortezomib; Drug Resistance, Bacterial; Humans; Lactones; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Protein Subunits; Pyrazines; Pyrroles; Substrate Specificity | 2011 |
Trypanocidal activity of β-lactone-γ-lactam proteasome inhibitors.
Topics: Biological Products; Enzyme Inhibitors; Lactams; Lactones; Proteasome Inhibitors; Pyrroles; Trypanocidal Agents; Trypanosoma brucei brucei | 2012 |
Selective overproduction of the proteasome inhibitor salinosporamide A via precursor pathway regulation.
Topics: Amino Acid Sequence; Bacterial Proteins; Enzyme Inhibitors; Lactones; Micromonosporaceae; Molecular Sequence Data; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Protein Binding; Pyrroles; Recombinant Proteins | 2011 |
Analysing properties of proteasome inhibitors using kinetic and X-ray crystallographic studies.
Topics: Antineoplastic Agents; Boronic Acids; Bortezomib; Crystallography, X-Ray; Drug Design; Enzyme Inhibitors; Lactones; Multiple Myeloma; Oligopeptides; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Pyrroles; Saccharomyces cerevisiae; Threonine | 2012 |
[Molecular targeting agents for multiple myeloma].
Topics: Antibodies, Monoclonal, Humanized; Antineoplastic Agents; Boron Compounds; Boronic Acids; Bortezomib; Glycine; Histone Deacetylases; Humans; Immunologic Factors; Lactones; Lenalidomide; Molecular Targeted Therapy; Multiple Myeloma; Oligopeptides; Proteasome Inhibitors; Pyrazines; Pyrroles; Thalidomide | 2012 |
(S)-4-Trimethylsilyl-3-butyn-2-ol as an auxiliary for stereocontrolled synthesis of salinosporamide analogs with modifications at positions C2 and C5.
Topics: Aldehydes; Alkylation; Butanols; Crystallography, X-Ray; Esters; Humans; Lactones; Molecular Conformation; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles; Stereoisomerism; Trimethylsilyl Compounds | 2013 |
Antileukemic activity and mechanism of drug resistance to the marine Salinispora tropica proteasome inhibitor salinosporamide A (Marizomib).
Topics: Actinobacteria; Boronic Acids; Bortezomib; Catalysis; Cell Line, Tumor; Drug Resistance, Neoplasm; Humans; Lactones; Leukemia; Mutation; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Pyrroles; Up-Regulation | 2014 |
Diastereoselective synthesis of fused lactone-pyrrolidinones; application to a formal synthesis of (-)-salinosporamide A.
Topics: Cyclization; Lactones; Molecular Structure; Oxidation-Reduction; Pyrroles; Pyrrolidinones; Stereoisomerism | 2014 |
Efficacy of panobinostat and marizomib in acute myeloid leukemia and bortezomib-resistant models.
Topics: Antineoplastic Agents; Apoptosis; Blotting, Western; Boronic Acids; Bortezomib; Caspases; Cell Proliferation; Drug Combinations; Drug Resistance, Neoplasm; Flow Cytometry; Humans; Hydroxamic Acids; Indoles; Lactones; Leukemia, Myeloid, Acute; Panobinostat; Proteasome Inhibitors; Pyrazines; Pyrroles; Tumor Cells, Cultured | 2015 |
Synergistic anti-myeloma activity of the proteasome inhibitor marizomib and the IMiD immunomodulatory drug pomalidomide.
Topics: Adaptor Proteins, Signal Transducing; Angiogenesis Inhibitors; Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Caspases; Cell Line, Tumor; Down-Regulation; Drug Resistance, Neoplasm; Drug Synergism; Humans; Lactones; Mice, SCID; Multiple Myeloma; Peptide Hydrolases; Poly(ADP-ribose) Polymerases; Proteasome Inhibitors; Pyrroles; RNA, Small Interfering; Thalidomide; Transplantation, Heterologous; Ubiquitin-Protein Ligases | 2015 |
Marizomib activity as a single agent in malignant gliomas: ability to cross the blood-brain barrier.
Topics: Animals; Apoptosis; Blood-Brain Barrier; Cell Line, Tumor; Disease Models, Animal; Glioma; Lactones; Mice, Inbred BALB C; Mice, Nude; Proteasome Inhibitors; Pyrroles | 2016 |
Induction of cell death by the novel proteasome inhibitor marizomib in glioblastoma in vitro and in vivo.
Topics: Animals; Apoptosis; Biomarkers, Tumor; Bortezomib; Caspases; Cell Line, Tumor; Gene Expression Regulation, Neoplastic; Glioblastoma; Humans; Lactones; Mice; Proliferating Cell Nuclear Antigen; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles | 2016 |
Grisemycin, a Bridged Angucyclinone with a Methylsulfinyl Moiety from a Marine-Derived Streptomyces sp.
Topics: Anthraquinones; Crystallography, X-Ray; Hep G2 Cells; HL-60 Cells; Humans; Lactones; Marine Biology; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Pyrroles; Streptomyces; Streptomyces griseus | 2016 |
Multiple myeloma--translation of trial results into reality.
Topics: Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic Agents; Boron Compounds; Bortezomib; Bridged Bicyclo Compounds, Heterocyclic; Clinical Trials as Topic; Cyclic N-Oxides; Drug Approval; Drug Discovery; Glycine; Humans; Indolizines; Lactones; Lenalidomide; Multiple Myeloma; Oligopeptides; Practice Guidelines as Topic; Pyridinium Compounds; Pyrroles; Thalidomide | 2016 |
Coupled Biosynthesis of Volatiles and Salinosporamide A in Salinispora tropica.
Topics: Actinobacteria; Lactones; Molecular Structure; Pyrroles; Volatile Organic Compounds | 2016 |
Ligand Based-Pharmacophore Modeling and Extended Bi oactivity Prediction for Salinosporamide A, B and C from Marine Actino mycetes Salinispora tropica.
Topics: Actinobacteria; Aminopeptidases; Drug Discovery; Humans; Lactams; Lactones; Ligands; Metalloendopeptidases; Molecular Docking Simulation; Protein Binding; Pyrroles; Receptors, Glucocorticoid | 2017 |
Marizomib for central nervous system-multiple myeloma.
Topics: Adult; Central Nervous System Neoplasms; Humans; Lactones; Male; Middle Aged; Multiple Myeloma; Pyrroles | 2017 |
The activity and safety of novel proteasome inhibitors strategies (single, doublet and triplet) for relapsed/refractory multiple myeloma.
Topics: Antineoplastic Combined Chemotherapy Protocols; Boron Compounds; Glycine; Humans; Lactones; Multiple Myeloma; Neoplasm Recurrence, Local; Oligopeptides; Proteasome Inhibitors; Pyrroles; Retrospective Studies | 2018 |
Bortezomib Alone and in Combination With Salinosporamid A Induces Apoptosis and Promotes Pheochromocytoma Cell Death In Vitro and in Female Nude Mice.
Topics: Adrenal Gland Neoplasms; Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Bortezomib; Cell Line, Tumor; Cell Movement; Cell Proliferation; Cell Survival; Female; Lactones; Mice; Mice, Nude; Neoplasm Invasiveness; Neovascularization, Pathologic; Pheochromocytoma; Proteasome Inhibitors; Pyrroles | 2017 |
A Total Synthesis of Salinosporamide A.
Topics: Biological Products; Cyclization; Free Radicals; Lactones; Oxidation-Reduction; Proteasome Inhibitors; Pyrroles | 2018 |
(-)-Homosalinosporamide A and Its Mode of Proteasome Inhibition: An X-ray Crystallographic Study.
Topics: Catalytic Domain; Crystallography, X-Ray; Lactones; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles; X-Rays; Yeasts | 2018 |
Total Synthesis of (-)-Salinosporamide A via a Late Stage C-H Insertion.
Topics: Lactones; Molecular Structure; Proteasome Inhibitors; Pyrroles | 2019 |
NPI-0052 and γ-radiation induce a synergistic apoptotic effect in medulloblastoma.
Topics: Apoptosis; Cell Line, Tumor; Cerebellar Neoplasms; Chemoradiotherapy; Gamma Rays; Humans; Lactones; Medulloblastoma; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles | 2019 |
Therapeutic strategies for diffuse midline glioma from high-throughput combination drug screening.
Topics: Animals; Brain Neoplasms; Brain Stem Neoplasms; Cell Death; Cell Line, Tumor; Drug Evaluation, Preclinical; Drug Synergism; Female; Glioma; High-Throughput Screening Assays; Humans; Lactones; Male; Metabolomics; Mice; Panobinostat; Pyrroles; Reproducibility of Results; Sequence Analysis, RNA; Transcription, Genetic; Xenograft Model Antitumor Assays | 2019 |
Proteasome inhibition disrupts the metabolism of fumarate hydratase- deficient tumors by downregulating p62 and c-Myc.
Topics: Animals; Carcinoma, Renal Cell; Cell Line, Tumor; Female; Fumarate Hydratase; Gene Expression Regulation, Neoplastic; Germ-Line Mutation; Glutaminase; Glycolysis; Humans; Kidney Neoplasms; Lactate Dehydrogenase 5; Lactones; Leiomyomatosis; Mice; Mice, Nude; Neoplastic Syndromes, Hereditary; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Proto-Oncogene Proteins c-myc; Pyrroles; Sequestosome-1 Protein; Signal Transduction; Skin Neoplasms; Uterine Neoplasms; Xenograft Model Antitumor Assays | 2019 |
Marizomib suppresses triple-negative breast cancer via proteasome and oxidative phosphorylation inhibition.
Topics: Animals; Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Cell Proliferation; Epithelial-Mesenchymal Transition; Female; Humans; Lactones; Mice; Oxidative Phosphorylation; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrroles; Triple Negative Breast Neoplasms; Xenograft Model Antitumor Assays | 2020 |
Salinosporamide A, a Marine-Derived Proteasome Inhibitor, Inhibits T Cell Activation through Regulating Proliferation and the Cell Cycle.
Topics: Animals; Aquatic Organisms; CD4-Positive T-Lymphocytes; Cell Proliferation; Humans; Jurkat Cells; Lactones; Lymphocyte Activation; MAP Kinase Signaling System; Mice; Micromonosporaceae; Proteasome Inhibitors; Pyrroles | 2020 |
Marizomib sensitizes primary glioma cells to apoptosis induced by a latest-generation TRAIL receptor agonist.
Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Brain Neoplasms; CASP8 and FADD-Like Apoptosis Regulating Protein; Caspase 8; Cell Line, Tumor; Drug Resistance, Neoplasm; Glioma; Humans; Lactones; Myeloid Cell Leukemia Sequence 1 Protein; Proteasome Inhibitors; Pyrimidines; Pyrroles; Receptors, TNF-Related Apoptosis-Inducing Ligand; Signal Transduction; Spheroids, Cellular; Thiophenes; Time Factors | 2021 |