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Volumn 18, Issue 2, 2010, Pages 543-556

Towards the synthesis of bisubstrate inhibitors of protein farnesyltransferase: Synthesis and biological evaluation of new farnesylpyrophosphate analogues

Author keywords

Farnesyltransferase inhibitors; FPP analogues; Imidazole; Malaria; Trypanosoma

Indexed keywords

2 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYL)MALONIC ACID; 2 (5,9,13 TRIMETHYLTETRADECA 2,4,8,12 TETRAENOYLAMINO)MALONIC ACID; 3 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYLIDENE)MALONIC ACID; 3 OXO 3 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYLOXY)PROPANOIC ACID; 4 OXO 4 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYLOXY)BUTANOIC ACID; 5,9,13 TRIMETHYL N (PHENYLSULFONYL)TETRADECA 4,8,12 TRIENAMIDE; 5,9,13 TRIMETHYLTETRADECA 2,4,8,12 TETRAENAMIDE; 5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENAMIDE; 5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENOYLSULFAMIC ACID; 8,12,16 TRIMETHYL 4 OXOHEPTADECA 7,11,15 TRIENOIC ACID; 9,13,17 TRIMETHYL 5 OXO OCTADECA 8,12,16 TRIENOIC ACID; DIETHYL 2 (3 (4,4,5,5 TETRAMETHYL 1,3,2 DIOXABOROLAN2 YL)MALONATE; DIETHYL 2 (5,9,13 TRIMETHYLTETRADECA 2,4,8,12 TETRAENOYLAMINO)MALONATE; DIETHYL 2 (5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENOYL)PENTANEDIOATE; DIETHYL 2 (5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENOYL)SUCCINATE; DIETHYL 2 (5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENOYLAMINO)MALONATE; DIETHYL 2 [3 (5 FORMYL 1 METHYL 1H IMIDAZOL 2 YL)ALLYL]MALONATE; DIETHYL 2 [3 (5 FORMYL 1 METHYL 1H IMIDAZOL 2 YL)PROPYL)MALONATE; DIETHYL 2 [3 [5 ((TERT BUTYLDIMETHYLSILYLOXY)METHYL) 1 METHYL 1H IMIDAZOL 2 YL)MALONATE; DIETHYL 2 [3 [5 ((TERT BUTYLDIMETHYLSILYLOXY)METHYL) 1 METHYL 1H IMIDAZOL 2 YL]PROPYL]MALONATE; DIMETHYL 2 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYL)MALONATE; DIMETHYL 3 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYLIDENE)MALONATE; DOCETAXEL; ETHYL 7,11,15 TRIMETHYL 3 OXOHEXADECA 6,10,14 TRIENOATE; FARNESYL DIPHOSPHATE; IMIDAZOLE; MALONIC ACID; N HYDROXY 5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENAMIDE; PROTEIN FARNESYLTRANSFERASE INHIBITOR; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 76449101336     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2009.12.017     Document Type: Article
Times cited : (14)

References (55)
  • 1
    • 76449109427 scopus 로고    scopus 로고
    • www.who.int/tdr/.
  • 2
    • 76449112024 scopus 로고    scopus 로고
    • www.mmv.org, 2007.
    • (2007)
  • 45
    • 76449097152 scopus 로고    scopus 로고
    • Replacement of the succinyl moiety by a malonyl group does not change the activity (unpublished results).
    • Replacement of the succinyl moiety by a malonyl group does not change the activity (unpublished results).
  • 50
    • 76449103613 scopus 로고    scopus 로고
    • ′ is the inhibitor dissociation constant of the enzyme-substrate-inhibitor complex.
    • ′ is the inhibitor dissociation constant of the enzyme-substrate-inhibitor complex.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.