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Volumn 18, Issue 14, 2008, Pages 3878-3881

Cyclobranol: A substrate for C25-methyl sterol side chains and potent mechanism-based inactivator of plant sterol methyltransferase

Author keywords

Cycloartenol; Cyclobranol; Mechanism based inhibitor; Phytosterol; Sterol C methylation; Sterol C24 methyltransferase

Indexed keywords

CYCLOBRANOL; METHYLTRANSFERASE INHIBITOR; PHYTOSTEROL;

EID: 47149100858     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.06.044     Document Type: Article
Times cited : (8)

References (23)
  • 10
    • 0004147511 scopus 로고    scopus 로고
    • Blackie Academic & Professional, London pp. 197-234
    • Goad L.J., and Akihisa T. Analysis of Sterols (1997), Blackie Academic & Professional, London pp. 197-234
    • (1997) Analysis of Sterols
    • Goad, L.J.1    Akihisa, T.2
  • 19
    • 0025021898 scopus 로고
    • 1H NMR signals for this compound in agreement with that shown in
    • 1H NMR signals for this compound in agreement with that shown in
    • (1990) Biochim. Biophys. Acta , vol.1042 , pp. 119
    • Nes, W.D.1    Le, P.H.2
  • 20
    • 0028948226 scopus 로고
    • In reviewing the results of the cyclobranol tested previously with the soybean SMT, we reported that it fails as a substrate (Ref. 2). Reexamination of the sample tested by GC-MS indicated that it was not in the free form, it was the C3-acetate (to protect the C3-group) which explains its inactivity
    • Guo D., Venkatramesh M., and Nes W.D. Lipids 30 (1995) 203 In reviewing the results of the cyclobranol tested previously with the soybean SMT, we reported that it fails as a substrate (Ref. 2). Reexamination of the sample tested by GC-MS indicated that it was not in the free form, it was the C3-acetate (to protect the C3-group) which explains its inactivity
    • (1995) Lipids , vol.30 , pp. 203
    • Guo, D.1    Venkatramesh, M.2    Nes, W.D.3
  • 21
    • 47149094268 scopus 로고    scopus 로고
    • note
    • The standard assays for generating kinetic constants and for product determination were as described in Ref. 2.
  • 22
    • 47149093913 scopus 로고    scopus 로고
    • note
    • 1H NMR analysis.
  • 23
    • 47149095057 scopus 로고    scopus 로고
    • 13C NMR spectra with assignment) of the product set of 24-ethyl(idene) sterols 5A, 6A, and 7A generated from 24(28)-methylene cycloartenol assayed with the soybean SMT1
    • 13C NMR spectra with assignment) of the product set of 24-ethyl(idene) sterols 5A, 6A, and 7A generated from 24(28)-methylene cycloartenol assayed with the soybean SMT1
    • (2002) Tetrahedron Lett. , pp. 437017
    • Dennis, A.1    Nes, W.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.