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Volumn 11, Issue 2, 2014, Pages 457-467

Antitumor activity of FL118, a survivin, Mcl-1, XIAP, and cIAP2 selective inhibitor, is highly dependent on its primary structure and steric configuration

Author keywords

camptothecin analogue; cancer cells; FL118; human tumor animal models; IAP inhibitor; SAR analysis

Indexed keywords

10,11 METHYLENEDIOXYCAMPTOTHECIN 20 O(3 BROMOBENZOATE); 10,11 METHYLENEDIOXYCAMPTOTHECIN 20 O(3 IODOBENZOATE); 10,11 METHYLENEDIOXYCAMPTOTHECIN 20 O(3,4 DIMETHOXYBENZOATE); 10,11 METHYLENEDIOXYCAMPTOTHECIN 20 O(4 CHLOROBENZOATE); 10,11 METHYLENEDIOXYCAMPTOTHECIN 20 O(4 IODOBENZOATE); 10,11 METHYLENEDIOXYCAMPTOTHECIN 20 O(4 NITROBENZOATE); 10,11 METHYLENEDIOXYCAMPTOTHECIN 20 O(4BROMOBENZOATE); ANTINEOPLASTIC AGENT; CELL DNA; FL 118; HYDROXYL GROUP; INHIBITOR OF APOPTOSIS PROTEIN 2; IPRIFLAVONE; IRINOTECAN; LACTONE; PROTEIN MCL 1; SURVIVIN; UNCLASSIFIED DRUG; X LINKED INHIBITOR OF APOPTOSIS; 1,3 BENZODIOXOLE DERIVATIVE; 7-ETHYL-7-HYDROXY-10H-1,3-DIOXOLO(4,5-G)PYRANO(3',4':6,7)INDOLIZINO(1,2-B)QUINOLINE-8,11(7H,12H)-DIONE; INDOLIZINE DERIVATIVE; INHIBITOR OF APOPTOSIS PROTEIN; MICROTUBULE ASSOCIATED PROTEIN; PROTEIN BINDING;

EID: 84893267704     PISSN: 15438384     EISSN: 15438392     Source Type: Journal    
DOI: 10.1021/mp4004282     Document Type: Article
Times cited : (36)

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