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Volumn 12, Issue 5, 2004, Pages 995-1002

Convenient synthesis and evaluation of glycosidase inhibitory activity of α- And β-galactose-type valienamines, and some N-alkyl derivatives

Author keywords

[No Author keywords available]

Indexed keywords

4 (HYDROXYMETHYL) 6 OCTYLAMINOCYCLOHEX 4 ENE 1,2,3 TRIOL(N OCTYL 5A CARBA ALPHA LEVO ARABINOHEX 5(5A) ENOPYRANOSYLAMINE); 6 AMINO 4 (HYDROXYMETHYL)CYCLOHEX 4 ENE 1,2,3 TRIOL(5A CARBA ALPHA DEXTRO LEVO ARABINOHEX 5(5A) ENOPYRANOSYLAMINE); 6 DECYLAMINO 4 (HYDROXYMETHYL)CYCLOHEX 4 ENE 1,2,3 TRIOL(N DECYL 5A CARBA ALPHA LEVO ARABINOHEX 5(5A) ENOPYRANOSYLAMINE); 6 DODECYLAMINO 4 (HYDROXYMETHYL)CYCLOHEX 4 ENE 1,2,3 TRIOL(N DODECYL 5A CARBA ALPHA LEVO ARABINOHEX 5(5A) ENOPYRANOSYLAMINE); 6 HEXYLAMINO 4 (HYDROXYMETHYL)CYCLOHEX 4 ENE 1,2,3 TRIOL(N HEXYL 5A CARBA BETA LEVO ARABINOHEX 5(5A) ENOPYRANOSYLAMINE); ALKYL GROUP; ALPHA GALACTOSIDASE; ALPHA GLUCOSIDASE; ALPHA MANNOSIDASE; AMINE; BETA GLUCOSIDASE; GLYCOSIDASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 1342343125     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2003.12.016     Document Type: Article
Times cited : (37)

References (18)
  • 9
    • 85030877144 scopus 로고    scopus 로고
    • note
    • When the mixture of 6α,β, isolated is treated similarly with excess sodium azide, the proportion of the β-azide 7β, formed is likely to increase about 1.5 to 2.0 fold.
  • 11
    • 0023194831 scopus 로고
    • 3), was prepared from (1S,2R,3S,4S,6R)-1,2- diacetoxy-3,4-dibromo-6-(bromomethyl)cyclohexane:
    • 3), was prepared from (1S,2R,3S,4S,6R)-1,2- diacetoxy-3,4-dibromo-6-(bromomethyl)cyclohexane: Ogawa S., Uematsu Y., Yoshida S., Sasaki N., Suami T. J. Carbohydr. Chem. 6:1987;471.
    • (1987) J. Carbohydr. Chem. , vol.6 , pp. 471
    • Ogawa, S.1    Uematsu, Y.2    Yoshida, S.3    Sasaki, N.4    Suami, T.5
  • 12
    • 85030880483 scopus 로고    scopus 로고
    • note
    • The protected N-alkylamines were here demonstrated to be easily isolated and purified, allowing us to subject them to further chemical modification. Practically, one-pot processing of treatment of 13α,β with alkyl amines, followed by hydrolysis, can improve isolated yields of the corresponding free amines. The reaction conditions have not yet been optimized.
  • 13
    • 85030885875 scopus 로고    scopus 로고
    • note
    • All biological assays were carried out in a standard manner by Dr. Akihiro Tomoda (Hokko Chemical Industry, Co. Ltd.).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.