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Volumn 22, Issue 1, 2014, Pages 292-302

Synthesis, modification and docking studies of 5-sulfonyl isatin derivatives as SARS-CoV 3C-like protease inhibitors

Author keywords

Docking studies; Inhibitor; Isatin; SARS

Indexed keywords

1 BENZYL 5 [(4 METHYLPIPERAZIN 1 YL)SULFONYL] 1H INDOLE 2,3 DIONE; 1 BENZYL 5 [(4 PHENYLPIPERAZIN 1 YL)SULFONYL] 1H INDOLE 2,3 DIONE; 1 BENZYL 5 [[4 (3 CHLOROBENZYL)PIPERAZIN 1 YL]SULFONYL] 1H INDOLE 2,3 DIONE; 1 BENZYL 5 [[4 (4 FLUOROPHENYL)PIPERAZIN 1 YL]SULFONYL] 1H INDOLE 2,3 DIONE; 1 METHYL 5 [(4 METHYLPIPERAZIN 1 YL)SULFONYL] 1H INDOLE 2,3 DIONE; 1 METHYL 5 [(4 PHENYLPIPERAZIN 1 YL)SULFONYL] 1H INDOLE 2,3 DIONE; 1,5,6,7 TETRAHYDRO CYCLOPENT[F]INDOLE 2,3 DIONE; 2,3 DIOXO INDOLINE 5 SULFONIC ACID; 3,3 DICHLORO 2 OXO INDOLINE 5 SULFONIC ACID; 5 (MORPHOLINOSULFONYL) 1H INDOLE 2,3 DIONE; 5 [(2 METHYLPIPERIDIN 1 YL)SULFONYL] 1H INDOLE 2,3 DIONE; 5 [(3,5 DIMETHYLPIPERIDIN 1 YL)SULFONYL] 1H INDOLE 2,3 DIONE; 5 [(4 METHYLPIPERAZIN 1 YL)SULFONYL] 1 BETA NAPHTHALENEMETHYL 1H INDOLE 2,3 DIONE; 5 [(4 METHYLPIPERAZIN 1 YL)SULFONYL] 1H INDOLE 2,3 DIONE; 5 [(4 METHYLPIPERIDIN 1 YL)SULFONYL] 1H INDOLE 2,3 DIONE; 5 [(4 PHENYLETHYLPIPERAZIN 1 YL)SULFONYL] 1H INDOLE 2,3 DIONE; 5 [(PIPERIDIN 1 YL)SULFONYL] 1H INDOLE 2,3 DIONE; 5 [4 (2 FUROYL)PIPERAZIN 1 YL SULFONYL] 1H INDOLE 2,3 DIONE; 5 [[4 (3 CHLOROBENZYL)PIPERAZIN 1 YL]SULFONYL] 1 BETA NAPHTHALENEMETHYL 1H INDOLE 2,3 DIONE; 5 [[4 (3 CHLOROBENZYL)PIPERAZINYL 1 YL]SULFONYL] 1H INDOLE 2,3 DIONE; 5 [[4 (3 TRIFLUOROMETHYLPHENYL)PIPERAZINYL 1 YL]SULFONYL] 1H INDOLE 2,3 DIONE; 5 [[4 (3,4,5 TRIMETHOXYBENZYL)PIPERAZINYL 1 YL]SULFONYL] 1H INDOLE 2,3 DIONE; 5 [[4 (4 FLUOROPHENYL)PIPERAZIN 1 YL]SULFONYL] 1 BETA NAPHTHALENEMETHYL 1H INDOLE 2,3 DIONE; 5 [[4 (4 FLUOROPHENYL)PIPERAZINYL 1 YL]SULFONYL] 1H INDOLE 2,3 DIONE; 5 [[4 (PYRIDIN 2 YL)PIPERAZIN 1 YL]SULFONYL] 1H INDOLE 2,3 DIONE; 5 CARBOXY 1H INDOLE 2,3 DIONE; 5 SULFONYL ISATIN DERIVATIVE; ISATIN DERIVATIVE; PROTEINASE INHIBITOR; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 84891482162     PISSN: 09680896     EISSN: 14643391     Source Type: Journal    
DOI: 10.1016/j.bmc.2013.11.028     Document Type: Article
Times cited : (87)

References (41)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.