메뉴 건너뛰기




Volumn 12, Issue 24, 2004, Pages 6569-6579

Synthesis and glycosidase inhibitory activity of some N-substituted 5a-carba-β-fuco- and β-galactopyranosylamines, and selected derivatives

Author keywords

Galactopyranosylamine; Glycosidase inhibitor

Indexed keywords

ALPHA GALACTOSIDASE; BETA GALACTOSIDASE; BETA GLUCOSIDASE; GLYCOSIDASE INHIBITOR; N (2 PHENYLETHYL) 5A CARBA BETA DEXTRO,LEVO FUCOPYRANOSYLAMINE; N (4 PHENYLBUTYL) 5A CARBA BETA LEVO FUCOPYRANOSYLAMINE; N BUTYL 5A CARBA BETA DEXTRO GALACTOPYRANOSYLAMINE; N DECYL 5A CARBA BETA DEXTRO GALACTOPYRANOSYLAMINE; N DECYL 5A CARBA BETA LEVO FUCOPYRANOSYLAMINE; N DODECYL 5A CARBA BETA DEXTRO GALACTOPYRANOSYLAMINE; N DODECYL 5A CARBA BETA LEVO FUCOPYRANOSYLAMINE; N HEXYL 5A CARBA BETA DEXTRO,LEVO FUCOPYRANOSYLAMINE; N OCTYL 5A CARBA BETA LEVO FUCOPYRANOSYLAMINE; N OCTYL 5A CARBA BETA LEVO GALACTOPYRANOSYLAMINE; UNCLASSIFIED DRUG;

EID: 20844444311     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2004.09.023     Document Type: Article
Times cited : (8)

References (21)
  • 8
    • 8844251701 scopus 로고    scopus 로고
    • note
    • Other than compound l-12, the tri-O-benzyl and 1,2-O-isopropylidene derivatives were subjected to conventional conditions for epoxidation. Exclusive selectivity was obtained for l-12
  • 9
    • 8844252485 scopus 로고    scopus 로고
    • note
    • Unless otherwise noted, when both racemic and optically active compounds were subjected to reaction, the processing for the latter were reported
  • 15
    • 8844250282 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.