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Volumn 2, Issue 2, 2000, Pages 151-154

Synthesis and evaluation of aminocyclopentitol inhibitors of β-glucosidases

Author keywords

[No Author keywords available]

Indexed keywords

AMINOALCOHOL; BETA GLUCOSIDASE; CYCLOPENTANE DERIVATIVE; ENZYME INHIBITOR;

EID: 0034719245     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol991252b     Document Type: Article
Times cited : (40)

References (27)
  • 7
    • 11944256494 scopus 로고
    • The C(1)-O(1) bond cleavage precedes the protonation step in the enzymatic hydrolysis with phenolic leaving groups. Protonation does not occur with acidic leaving groups such as pyridine or fluoride. Review on mechanisms: Sinnott, M. L. Chem. Rev. 1990, 90, 1171-1202.
    • (1990) Chem. Rev. , vol.90 , pp. 1171-1202
    • Sinnott, M.L.1
  • 24
    • 0001885593 scopus 로고
    • i(β-D-gluco-pyrannosylamine) = 24 μM for β-glucosidase from Trichoderma reesei: Kolarova, N.; Trgina, R.; Linek, K.; Farkas, V. Carbohydr. Res. 1995, 273, 109.
    • (1983) Carbohydr. Res. , vol.116 , pp. 95
    • Legler, G.1    Herrchen, M.2
  • 26
    • 0029155704 scopus 로고
    • i(β-D-gluco-pyrannosylamine) = 24 μM for β-glucosidase from Trichoderma reesei: Kolarova, N.; Trgina, R.; Linek, K.; Farkas, V. Carbohydr. Res. 1995, 273, 109.
    • (1995) Carbohydr. Res. , vol.272 , pp. 17
    • Legler, G.1    Stütz, A.E.2    Immich, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.