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Volumn 7, Issue 2, 1999, Pages 241-250

Novel limonene phosphonate and farnesyl diphosphate analogues: Design, synthesis, and evaluation as potential protein-farnesyl transferase inhibitors

Author keywords

Antineoplastics; Antitumor compounds; Enzyme inhibitors; Phosphonic acids and derivatives; Terpenes and terpenoids

Indexed keywords

LIMONENE; PROTEIN FARNESYLTRANSFERASE; PROTEIN FARNESYLTRANSFERASE INHIBITOR; TERPENOID;

EID: 0033015439     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(98)00202-8     Document Type: Article
Times cited : (32)

References (38)
  • 38
    • 0031933368 scopus 로고    scopus 로고
    • 10 derivative of FMP, is a much poorer inhibitor of FTase than FMP. This is in accord with our proposal that hydrophobic bulk plays a key role in the binding of farnesyl-based inhibitors to FTase
    • 10 derivative of FMP, is a much poorer inhibitor of FTase than FMP. This is in accord with our proposal that hydrophobic bulk plays a key role in the binding of farnesyl-based inhibitors to FTase: Hohl, R. J.; Lewis, K. A.; Cermak, D. M.; Wiemer, D. F. Lipids 1998, 33, 39.
    • (1998) Lipids , vol.33 , pp. 39
    • Hohl, R.J.1    Lewis, K.A.2    Cermak, D.M.3    Wiemer, D.F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.