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Volumn 2, Issue 12, 2000, Pages 1733-1736

Stereoselective inhibition of α-L-fucosidases by N-benzyl aminocyclopentitols

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA LEVO FUCOSIDASE; AMINOALCOHOL; BENZYLAMINE DERIVATIVE; ENZYME INHIBITOR; GLYCOSIDASE; GLYCOSIDE;

EID: 0034658825     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol005895z     Document Type: Article
Times cited : (24)

References (23)
  • 8
    • 0040601367 scopus 로고    scopus 로고
    • note
    • In glycosidases, cleavage of the glycosidic C(1)-O(1) bond begins before protonation of the leaving group oxygen atom O(1) by the catalyzing acid; therefore the protonated glycoside only appears with a strongly elongated C(1)-O(1) bond (see ref 1c).
  • 14
    • 0040008058 scopus 로고    scopus 로고
    • note
    • + - HCl), 220, 208, 202, 190, 162, 106.
  • 16
    • 0040008056 scopus 로고    scopus 로고
    • note
    • 3 calcd 237.1365).
  • 17
    • 84984529975 scopus 로고
    • Other acyclic amino-alcohol glycosidase inhibitors are known, such as tris(hydroxymethyl) aminomethane: (a) Larner, J.; Gillespie, R. E. J Biol. Chem. 1956, 233, 709.
    • (1956) J Biol. Chem. , vol.233 , pp. 709
    • Larner, J.1    Gillespie, R.E.2
  • 20
    • 0041195350 scopus 로고    scopus 로고
    • note
    • There was no observable inhibition by 1, 8, or 9 for the following glycosidases (1 mM nitrophenyl glycoside, 0.1 mM inhibitor in 0.1 M HEPES pH 6.8, 25 °C): green coffee beans α-galactosidase, Escherichia coli β-galactosidase, yeast β-glucosidase, almond β-glucosidase, jack beans α-mannosidase, snail acetone powder β-mannosidase. 2 was not tested with these enzymes.
  • 22
    • 0032814101 scopus 로고    scopus 로고
    • and references cited therein
    • (b) Peer, A.; Vasella, A. Helv. Chim. Acta 1999, 82, 1044 and references cited therein.
    • (1999) Helv. Chim. Acta , vol.82 , pp. 1044
    • Peer, A.1    Vasella, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.