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Volumn 41, Issue 41, 2000, Pages 7837-7841

Design and synthesis of histone deacetylase inhibitors: The development of apicidin transition state analogs

Author keywords

Apicidin; Histone deacetylase; Side chain; Transition state inhibitors

Indexed keywords

APICIDIN; APICIDIN DERIVATIVE; ENZYME INHIBITOR; HISTONE DEACETYLASE; UNCLASSIFIED DRUG;

EID: 0034619133     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)01366-6     Document Type: Article
Times cited : (19)

References (19)
  • 8
    • 85021441499 scopus 로고    scopus 로고
    • The semi-synthesis of apicidin was chosen in lieu of total synthesis due to both the ready availability of the natural product and the poor yields associated with the macrocyclization of linear tetrapeptides
  • 11
    • 85021449856 scopus 로고    scopus 로고
    • 4-MeOH), brominated (NBS) and formylated (N-formylbenzotriazole), all at room temperature
  • 12
    • 85021441340 scopus 로고    scopus 로고
    • Note
  • 19
    • 85021414184 scopus 로고    scopus 로고
    • Complete biological data will be published in a full report elsewhere


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.