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Volumn 5, Issue 5, 1997, Pages 921-939

Synthesis and biological evaluation of potent glycosidase inhibitors: N-phenyl cyclic isourea derivatives of 5-amino- and 5-amino-C-(hydroxymethyl)-1,2,3,4-cyclopentanetetraols

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOSIDASE; GLYCOSIDASE INHIBITOR;

EID: 0030912242     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(97)00030-8     Document Type: Article
Times cited : (36)

References (21)
  • 2
    • 0001286750 scopus 로고
    • Ogawa, S.; Uchida, C. Chem. Lett. 1993, 173; Uchida, C; Yamagishi, T.; Ogawa, S. J. Chem. Soc., Perkin Trans, 1 1994, 589.
    • (1993) Chem. Lett. , pp. 173
    • Ogawa, S.1    Uchida, C.2
  • 8
    • 0000354881 scopus 로고
    • In this paper, nomenclature of cyclitols follows IUPAC-IUB 1973 recommendations for cyclitols (IUPAC Commission on the Nomenclature of Organic Chemistry (CNOC) and IUPAC-IUB Commission on Biochemical Nomenclature (CBN), Pure Appl. Chem., 1974, 37, 285).
    • (1974) Pure Appl. Chem. , vol.37 , pp. 285
  • 9
    • 0342347808 scopus 로고    scopus 로고
    • note
    • 1H NMR data.
  • 11
    • 0343217393 scopus 로고    scopus 로고
    • note
    • The D,L-notation of the compound numbers refers only to that of the absolute configuration of cyclitol or cyclitol moiety.
  • 14
    • 0342347807 scopus 로고    scopus 로고
    • note
    • The R,S-notation of the compound numbers refers to the absolute configuration of C-1 of N-phenyl cyclic isourea derivatives.
  • 16
    • 0342782869 scopus 로고    scopus 로고
    • note
    • i 4.2 μM (yeast). The latter results are almost compatible with those of N-n-butyl deoxynojirimycin. The bioassay was carried out by Professor Monica M. Palcic (University of Alberta) to whom our thanks are due. Synthesis and biological evaluation of the N-alkyl cyclic isourea derivatives will be reported elsewhere.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.