ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CANCER CELL CULTURE;
DRUG DESIGN;
DRUG STRUCTURE;
DRUG SYNTHESIS;
FEMALE;
HUMAN;
HUMAN CELL;
IC 50;
MALE;
POLYMERIZATION;
PRIORITY JOURNAL;
Design synthesis and anticancer evaluation of novel tetrahydroquinoline derivatives containing sulfonamide moiety
Ghorab, M. M.; Ragab, F. A.; Hamed, M. M. Design, synthesis and anticancer evaluation of novel tetrahydroquinoline derivatives containing sulfonamide moiety. Eur. J. Med. Chem., 2009, 44, 4211-17.
Inhibition of carbonic anhydrases with glycosyltriazole benzene sulfonamides
DOI 10.1021/jm701426t
Wilkinson, B. L.; Innocenti, A.; Vullo, D.; Supuran, C. T.; Poulsen, S. A. Inhibition of carbonic anhydrases with glycosyltriazole benzene sulfonamides. J. Med. Chem., 2008, 51, 1945-53. (Pubitemid 351438875)
Identification of 3,4-dihydroisoquinoline-2(1H)-sulfonamides as potent carbonic anhydrase inhibitors: Syn thesis, biological evaluation, and enzymeligand X-ray studies
Gitto, R.; Agnello, S.; Ferro, S.; DeLuca, L.; Vullo, D.; Brynda,J.; Mader, P.; Supuran, C. Y.; Chimi, A. Identification of 3,4-dihydroisoquinoline- 2(1H)-sulfonamides as potent carbonic anhydrase inhibitors: Synthesis, biological evaluation, and enzymeligand X-ray studies. J. Med. Chem., 2010, 53, 2401-08.
Pyridine analogues of nimesulide: Design, syn thesis, and in Vitro and in Vivo pharmacological evaluation as promising cyclooxygenase 1 and 2 inhibitors
Renard, J. F.; Arslan, D.; Garbacki, N.; Pirotte, B.; de Leval, X. Pyridine analogues of nimesulide: Design, synthesis, and in Vitro and in Vivo pharmacological evaluation as promising cyclooxygenase 1 and 2 inhibitors. J. Med. Chem., 2009, 52, 5864-71.
G2 arrest and apoptosis by 2-amino-N-quinoline-8 yl benzenesulfonamide (QBS), a novel cytotoxic compound
Kim, Y. H.; Shin, K. J.; Lee, T. G.; Kim, E.; Lee, M. S.; Ryu, S. H.; Suh, P. G. G2 arrest and apoptosis by 2-amino-N-quinoline-8 yl benzenesulfonamide (QBS), a novel cytotoxic compound. Biochemical Pharmacology, 2005, 69, 1333-41.
I and pharmacokinetic study of E7070, a chloroindolyl-sulfonamide anticancer agent, administered on a weekly schedule to patients with solid tumors
Dittrich, C.; Dumez, H.; Calvert, H.; Hanauske, A.; Faber, M.; Wanders, J.; Yule, M.; Ravic, M.; Fumoleau, P. Phase I and pharmacokinetic study of E7070, a chloroindolyl-sulfonamide anticancer agent, administered on a weekly schedule to patients with solid tumors. Clinical Cancer Research, 2003, 9, 5195-04.
Novel agents effective against solid tumors: The diarylsulfonylureas. Syn thesis, activities, and analysis of quantitative structure-activity relationships
Howbert, J. J.; Grossmann, C. S.; Crowell, T. A.; Rieder, B. J.; Harper, R. W.; Kramer, K. E.; Tao, E. V.; Aikins, J.; Poore, G. A.; Riezel, S. M.; Grindey, G. B.; Shaw, W. W.; Todd, G. C. Novel agents effective against solid tumors: the diarylsulfonylureas. Synthesis, activities, and analysis of quantitative structure-activity relationships. J. Med. Chem., 1990, 33, 2393-07.
N-(5-indanylsulfonyl)-N'-(4-chlorophenyl)urea, a novel agent equally cytotoxic to nonproliferating human colon adenocarcinoma cells
Houghton, P. J.; Bailey, F. C.; Germain, G. S.; Grindey, G. B.; Witt, B. C.; Houghton J. A. N-(5-Indanyl sulfonyl)-N'-(4- chlorophenyl)urea, a novel agent equally cytotoxic to nonproliferating human colon adenocarcinoma cells. Cancer Res, 1990, 50, 318-22. (Pubitemid 20041234)
Phase I clinical study of N-[(4-chlorophenyl)amino]carbonyl-2,3-dihydro- 1H-indene-5-sulfonamide (LY186641)
Hainsworth, J. D.; Hande, K. R.; Satterlee, W. G.; Kuttesch, J.; Johnson, D. H.; Grindey, G.; Jackson, L. E.; Greco, F. A phase I clinical study of N-[(4-Chlorophenyl)amino]carbonyl-2,3-dihydro- 1H-indene-5-sulfonamide (LY186641). Cancer Res, 1989, 49, 5217-20. (Pubitemid 19239372)
Phase II study of sulofenur, a novel sulfonylurea, in recurrent epithelial ovarian cancer
Brien, M. E.; Hardy, J.; Tan, S.; Walling, J.; Peters, B.; Hatty, S.; Wiltshaw, E. A. phase II study of sulofenur, a novel sulfonylurea, in recurrent epithelial ovarian cancer. Cancer Chemother. Pharmacol., 1992, 30, 245-48.
1,2,4 benzothiadiazine 1,1-dioxide. v Synthesis of built-in hydroxuguanidine tricycles as potential anticancer agents
Chern, J. W.; Rong, J. G. 1,2,4 benzothiadiazine 1,1-dioxide. V Synthesis of built-in hydroxuguanidine tricycles as potential anticancer agents. Tetrahedron Lett., 1991, 32, 2935-38.
Studies on 1,2,4-benzothiadiazine 1,1- dioxides VII and quinazolinones IV: Synthesis of novel built-In hydroxyguanidine tricycles as potential anticancer agents
Chern, J. W.; Liaw, Y. C.; Chen, C. S.; Rong, J. G.; Huang, C .L.; Chan, C H.; Wang, A. A. H. Studies on 1,2,4-benzothiadiazine 1,1- dioxides VII and quinazolinones IV: Synthesis of novel built-In hydroxyguanidine tricycles as potential anticancer agents. Heterocycles, 1993, 36, 1091-03.
The p16 status of tumor cell lines identifies small molecule inhibitors specific for cyclin-dependent kinase 4
Kubo, A.; Nakagawa, K.; Varma, R. K.; Conrad, N. K.; Cheng, J. Q.; Lee, W. C.; Testa, J. R.; Johnson, B. E.; Kaye, F. J.; Kelley, M. J. The p16 status of tumor cell lines identifies small molecule inhibitors specific for cyclin-dependent kinase 4. Clin. Cancer Res., 1999, 5, 4279-86. (Pubitemid 30013816)
Synthesis and biological evaluation of 2-styrylquinazolin-4(3H)-ones, a new class of antimitotic anticancer agents which inhibit tubulin polymerization
DOI 10.1021/jm00168a029
Jiang, B.; Hesson, D. P.; Dusak, B. A.; Dexter, D. L.; Kang, G. J.; Hamel, E. Synthesis and biological evaluation of 2- styrylquinazolin-4(3H)-ones, a new class of antimitotic anticancer agents which inhibit tubulin polymerization. J. Med. Chem., 1990, 33, 1721-28. (Pubitemid 20180634)
Synthesis and biological activity of new 2-amino-8-chloro-5,5-dioxo[1,2, 4]triazolo[2,3- b][1,4,2]benzodithiazines
Pomarnacka, E.; Bednarski, P. J.; Reszka, P.; Dziemidowicz-Borys, E.; Bienczak, A.; Werel, W.; Halasa, R. Synthesis and biological activity of new 2-amino-8-chloro-5,5-dioxo[1,2,4]triazolo[2,3- b][1,4,2]benzodithiazines. Eur. J. Med. Chem., 2006, 41, 633-39.
Syn thesis, structural characterization and biological evaluation of novel [1,2,4]triazolo[1,5-b][1,2,4]benzothiadiazinebenzothiazole conjugates as potential anticancer agents
Kamal, A.; Khan, M. N. A.; Reddy, K. S.; Srikanth, Y. V. V.; Sridhar, B. Synthesis, structural characterization and biological evaluation of novel [1,2,4]triazolo[1,5-b][1,2,4]benzothiadiazinebenzothiazole conjugates as potential anticancer agents. Chem. Biol. Drug. Des., 2008, 71, 78-86.
Synthesis and biological evaluation of mercapto triazolobenzothiadiazine linked aminobenzothiazoles as potential anticancer agents
Kamal, A.; Khan, M. N. A.; Srikanth, Y. V. V.; Rajesh, S. V. C. R. N. C. Synthesis and biological evaluation of mercapto triazolobenzothiadiazine linked aminobenzothiazoles as potential anticancer agents. Chem. Biol. Drug. Des., 2009, 73, 687-93.
Syn thesis, DNA-binding ability and evaluation of antitumour activity of triazolo[1,2,4] benzothiadiazine linked pyrrolo[2,1-c] [1,4]benzodiazepine conjugates
Kamal, A.; Khan, M. N. A.; Srikanth, Y. V. V.; Reddy, K. S.; Juvekar, A.; Sen, S.; Kurian, N.; Zingde, S. Synthesis, DNA-binding ability and evaluation of antitumour activity of triazolo[1,2,4] benzothiadiazine linked pyrrolo[2,1-c] [1,4]benzodiazepine conjugates. Bioorg. Med. Chem., 2008, 16, 7804-10.
Synthesis and biological evaluation of triazol-4-ylphenyl-bearing histone deacetylase inhibitors as anticancer agents
He, R.; Chen, Y.; Ougolkov, A. V.; Zhang, J. S.; Savoy, D. N.; Billadeau, D. D.; Kozikowski, A. P. Synthesis and biological evaluation of triazol-4-ylphenyl-bearing histone deacetylase inhibitors as anticancer agents. J. Med. Chem., 2010, 53, 1347-1356.
1-Acyl-1H-[1,2,4]triazole-3,5-diamine analogues as novel and potent anticancer cyclin-dependent kinase inhibitors: Synthesis and evaluation of biological activities
DOI 10.1021/jm050267e
Lin, R.; Connolly, P. J.; Huang, S.; Wetter, S. K.; Lu, Y.; Murray, W. V.; Emanuel, S. L.; Gruninger, R. H. Fiemtes-Pesquera, A. R.; Rugg, C. A.; Middleton, S. A.; Jolliffe, L. K. Acyl-1H-[1,2,4] triazole- 3,5-diamine analogues as novel and potent anticancer cyclindependent kinase inhibitors: Synthesis and evaluation of biological activities. J. Med. Chem., 2005, 48, 4208-11. (Pubitemid 40884921)
Syn thesis, DNA-binding ability and anticancer activity of benzothiazole/benzoxazole-pyrrolo[2,1-c][1,4]benzodiazepine conjugates
Kamal, A.; Reddy, K. S.; Khan, M. N. A.; Rajesh, V. C. R. N. C. S.; Ramaiah, M. J.; Pushpavalli, S. N. C. V. L.; Srinivas, C.; Bhadra, M. P.; Chourasia, M.; Sastry, G. N.; Juvekar, A.; Zingde, S.; Barkume, M. Synthesis, DNA-binding ability and anticancer activity of benzothiazole/benzoxazole- pyrrolo[2,1-c][1,4]benzodiazepine conjugates. Bioorg. Med. Chem., 2010, 18, 4747-61.
Synthesis and potential cytotoxic activity of new phenanthrylphenol- pyrrolobenzodiazepines
Kamal, A.; Sreekanth, K.; Kumar, P. P.; Shankaraiah, N.; Balakishan, G.; Ramaiah, M. J.; Pushpavalli, S. N.; Ray, P.; Bhadra, M. P. Synthesis and potential cytotoxic activity of new phenanthrylphenol-pyrrolobenzodiazepines. Eur. J. Med. Chem., 2010, 45, 2173-81.
Quinazolinone linked pyrrolo[2,1-c][1,4]benzodiazepine (PBD) conjugates: Design, synthesis and biological evaluation as potential anticancer agents
Kamal, A.; Bharathi, E. V.; Ramaiah, M. J.; Dastagiri, D.; Reddy, J. S.; Viswanath, A.; Sultana, F.; Pushpavalli, S. N.; Srivastava, H. K.; Sastry, G. N.; Bhadra, M. P.; Juvekar, A.; Sen, S.; Zingde, S. Quinazolinone linked pyrrolo[2,1-c][1,4]benzodiazepine (PBD) conjugates: Design, synthesis and biological evaluation as potential anticancer agents. Bioorg. Med. Chem., 2010, 18, 526-42.
Synthesis, structure analysis, and antibacterial activity of some novel 10-substituted 2-(4-piperidyl/phenyl)-5,5-dioxo[1,2,4]triazolo[1,5-b][1,2,4] benzothiadiazine derivatives
DOI 10.1016/j.bmcl.2007.07.043, PII S0960894X07008530
Kamal, A.; Khan, M. N. A.; Reddy, K. S.; Rohini, K.; Sastri, G. N.; Sateesh, B.; Sridhar, B. Synthesis, structure analysis, and antibacterial activity of some novel 10-substituted 2-(4-piperidyl/phenyl)- 5,5-dioxo[1,2,4]triazolo[1,5-b][1,2,4]benzothiadiazine derivatives. Bioorg. Med. Chem. Lett., 2007, 47, 5400-05. (Pubitemid 47391276)