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Volumn 17, Issue 18, 2009, Pages 6707-6714

A new structural class of S-adenosylhomocysteine hydrolase inhibitors

Author keywords

Ilimaquinone; Inhibitor; Pharmacophore modeling; S Adenosylhomocysteine hydrolase

Indexed keywords

ADENOSYLHOMOCYSTEINASE; ADENOSYLHOMOCYSTEINASE INHIBITOR; ILIMAQUINONE; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 69249106092     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2009.07.061     Document Type: Article
Times cited : (19)

References (60)
  • 2
    • 0018800321 scopus 로고
    • For initial mechanistic insight into AdoHcy, see:
    • For initial mechanistic insight into AdoHcy, see:. Palmer J.L., and Abeles R.H. J. Biol. Chem. 254 (1979) 1217
    • (1979) J. Biol. Chem. , vol.254 , pp. 1217
    • Palmer, J.L.1    Abeles, R.H.2
  • 42
    • 0026471537 scopus 로고
    • Total syntheses of the diterpenoids (-)-kolavenol and (-)-agelasine B:
    • Total syntheses of the diterpenoids (-)-kolavenol and (-)-agelasine B:. Piers E., and Roberge J.Y. Tetrahedron Lett. 33 (1992) 6923
    • (1992) Tetrahedron Lett. , vol.33 , pp. 6923
    • Piers, E.1    Roberge, J.Y.2
  • 43
    • 69249158057 scopus 로고    scopus 로고
    • note
    • A sample was generously provided by Professor Sidney M. Hecht, University of Virginia.
  • 47
    • 12944320845 scopus 로고    scopus 로고
    • For recent AdoHcy hydrolase inhibitors, see:
    • For recent AdoHcy hydrolase inhibitors, see:. Yin X.Q., and Schneller S.W. Tetrahedron 61 (2005) 1839
    • (2005) Tetrahedron , vol.61 , pp. 1839
    • Yin, X.Q.1    Schneller, S.W.2
  • 56
    • 69249115690 scopus 로고    scopus 로고
    • note
    • This binding model implies that these compounds should function as competitive inhibitors of AdoHcy, however, we have not yet experimentally confirmed this prediction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.