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Volumn 56, Issue 6, 2013, Pages 2429-2446

Development of potent and selective indomethacin analogues for the inhibition of AKR1C3 (type 5 17β-hydroxysteroid dehydrogenase/prostaglandin F synthase) in castrate-resistant prostate cancer

Author keywords

[No Author keywords available]

Indexed keywords

2 [1 (4 CHLOROBENZOYL) 5 METHOXY 1H INDOL 3 YL)N[(TRIFLUOROMETHYL)SULFONYL]ACETAMIDE; 2 [1 (4 CHLOROBENZOYL) 5 METHOXY 1H INDOL 3 YL]ACETIC ACID; 2 [1 (4 CHLOROBENZOYL) 5 METHOXY 1H INDOL 3 YL]ACETYL CHLORIDE; 2 [1 (4 CHLOROBENZOYL) 5 METHOXY 1H INDOL 3 YL]N(NAPHTHALEN 2 YLSULFONYL)ACETAMIDE; 2 [1 (4 CHLOROBENZOYL) 5 METHOXY 1H INDOL 3 YL]N[[4 (TRIFLUOROMETHOXY)PHENYL]SULFONYL]ACETAMIDE; 2 [1 (4 CHLOROBENZOYL) 5 METHOXY 2 METHYL 1H INDOL 3 YL] N (METHYLSULFONYL)ACETAMIDE; 3 [1 (4 CHLOROBENZOYL) 3 ETHYL 5 METHOXY 1H INDOL 2 YL]PROPANOIC ACID; 3 [1 (4 CHLOROBENZOYL) 5 METHOXY 2 METHYL 1H INDOL 3 YL] PROPANOIC ACID; 3 [1 (4 CHLOROBENZOYL) 5 METHOXY 3 METHYL 1H INDOL 2 YL] 2 METHYLPROPANOIC ACID; 3 [1 (4 CHLOROBENZOYL) 5 METHOXY 3 METHYL 1H INDOL 2 YL] 2,2 DIMETHYLPROPANOIC ACID; 3 [1 (4 CHLOROBENZOYL) 5 METHOXY 3 METHYL 1H INDOL 2 YL]N (METHYLSULFONYL)PROPANAMIDE; 3 [1 (4 CHLOROBENZOYL) 5 METHOXY 3 METHYL 1H INDOL 2 YL]N TOSYLPROPANAMIDE; 3 [1 (4 CHLOROBENZOYL) 5 METHOXY 3 METHYL 1H INDOL 2 YL]N[(5 CHLOROTHIOPHEN 2 YL)SULFONYL]PROPANAMIDE; 3 [1 (4 CHLOROBENZOYL) 5 METHOXY 3 METHYL 1H INDOL 2 YL]PROPANOIC ACID; 9 (4 CHLOROBENZOYL) 6 METHOXY 2,3,4,9 TETRAHYDRO 1H CARBAZOLE 2 CARBOXYLIC ACID; 9 (4 CHLOROBENZOYL) 6 METHOXY 2,3,4,9 TETRAHYDRO 1H CARBAZOLE 3 CARBOXYLIC ACID; 9 (4 CHLOROBENZOYL) 6 METHOXY N (METHYLSULFONYL) 2,3,4,9 TETRAHYDRO 1H CARBAZOLE 3 CARBOXAMIDE; ALDO KETO REDUCTASE 1C3; INDOMETACIN DERIVATIVE; NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; PROSTAGLANDIN SYNTHASE; TESTOSTERONE 17BETA DEHYDROGENASE; UNCLASSIFIED DRUG;

EID: 84875751054     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm3017656     Document Type: Article
Times cited : (82)

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