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Volumn 342, Issue 7, 2009, Pages 420-427

Discovery and potency optimization of 2-amino-5-arylmethyl-1,3-thiazole derivatives as potential therapeutic agents for prostate cancer

Author keywords

Antiproliferative activity; Cytotoxicity; Drug likeness; Prostate cancer; Small molecules

Indexed keywords

3 (2 FURYL) N [5 (4 METHOXYBENZYL) 1,3 THIAZOL 2 YL]ACRYLAMIDE; 4 (4 BROMOPHENOXY) N [5 (4 FLUOROBENZYL) 1,3 THIAZOL 2 YL]BUTANAMIDE; 4 (4 CHLOROPHENOXY) N [5 (4 FLUOROBENZYL) 1,3 THIAZOL 2 YL]BUTANAMIDE; 5 (4 ISOPROPYLBENZYL) 1,3 THIAZOL 2 AMINE; 5 [2 CHLORO 5 (TRIFLUOROMETHYL)BENZYL] 1,3 THIAZOL 2 AMINE; 5 [4 CHLORO 3 (TRIFLUOROMETHYL)BENZYL] 1,3 THIAZOL 2 AMINE; ANTINEOPLASTIC AGENT; DIGITONIN; N (5 BENZYL 1,3 THIAZOL 2 YL)CHROMANE 3 CARBOXAMIDE; N [5 (4 CHLOROBENZYL) 1,3 THIAZOL 2 YL]CHROMANE 3 CARBOXAMIDE; N [5 (4 ETHYLBENZYL) 1,3 THIAZOL 2 YL]CHROMANE 3 CARBOXAMIDE; N [5 (4 FLUOROBENZYL) 1,3 THIAZOL 2 YL] 3 (2 FURYL)ACRYLAMIDE; N [5 (4 FLUOROBENZYL) 1,3 THIAZOL 2 YL] 3 (3 METHYLPHENYL)ACRYLAMIDE; N [5 (4 FLUOROBENZYL) 1,3 THIAZOL 2 YL] 3 (5 METHYL 2 FURYL)ACRYLAMIDE; N [5 (4 FLUOROBENZYL) 1,3 THIAZOL 2 YL] 3 [5 [TRANS 2 METHYLCYCLOPROPYL] 2 FURYL]PROPANAMIDE; N [5 (4 FLUOROBENZYL) 1,3 THIAZOL 2 YL] 3,4 DIMETHOXYBENZAMIDE; N [5 (4 FLUOROBENZYL) 1,3 THIAZOL 2 YL] 4,5,6,7 TETRAHYDRO 1 BENZOTHIOPHENE 3 CARBOXAMIDE; N [5 (4 FLUOROBENZYL) 1,3 THIAZOL 2 YL]CHROMANE 3 CARBOXAMIDE; N [5 (4 ISOPROPYLBENZYL) 1,3 THIAZOL 2 YL]CHROMANE 3 CARBOXAMIDE; N [5 (4 METHOXYBENZYL) 1,3 THIAZOL 2 YL]CHROMANE 3 CARBOXAMIDE; N [5 (4 METHYLBENZYL) 1,3 THIAZOL 2 YL]CHROMANE CARBOXAMIDE; N [5 [2 CHLORO 5 (TRIFLUOROMETHYL)BENZYL] 1,3 THIAZOL 2 YL]CHROMANE 3 CARBOXAMIDE; N [5 [4 CHLORO 3 (TRIFLUOROMETHYL)BENZYL] 1,3 THIAZOL 2 YL]CHROMANE 3 CARBOXAMIDE; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 67650046130     PISSN: 03656233     EISSN: 15214184     Source Type: Journal    
DOI: 10.1002/ardp.200800201     Document Type: Article
Times cited : (20)

References (11)
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    • For cytotoxicity experiments, higher seeding densities (10000 or 20000 cells per well) were used (see Experimental, section 4.2.2) to more accurately observe potentially diminishing number of cells. This is in contrast with the measurement of antiproliferative activity where initial seeding density (4000 cells per well) was chosen to allow more room for cell proliferation
    • For cytotoxicity experiments, higher seeding densities (10000 or 20000 cells per well) were used (see Experimental, section 4.2.2) to more accurately observe potentially diminishing number of cells. This is in contrast with the measurement of antiproliferative activity where initial seeding density (4000 cells per well) was chosen to allow more room for cell proliferation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.