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Volumn 13, Issue 19, 2003, Pages 3161-3166

Reversed hydroxamate-bearing thermolysin inhibitors mimic a high-energy intermediate along the enzyme-catalyzed proteolytic reaction pathway

Author keywords

[No Author keywords available]

Indexed keywords

ENZYME; ENZYME INHIBITOR; HYDROXAMIC ACID; THERMOLYSIN INHIBITOR; UNCLASSIFIED DRUG;

EID: 0042833023     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(03)00720-0     Document Type: Article
Times cited : (10)

References (27)
  • 2
    • 0003931970 scopus 로고    scopus 로고
    • Barrett, A. J., Rawlings, N. D., Woessner, J. F. Eds: Academic: New York
    • Beynon, R. J.; Beaumont, A. In Handbook of Proteolytic Enzymes; Barrett, A. J., Rawlings, N. D., Woessner, J. F. Eds: Academic: New York, 1998; p 1037.
    • (1998) Handbook of Proteolytic Enzymes , pp. 1037
    • Beynon, R.J.1    Beaumont, A.2
  • 5
    • 0000049891 scopus 로고
    • In Protease Inhibitors; Barrett, A. J., Salvesan, G., Eds.; Elsevier Science: Amsterdam
    • Powers, J. C.; Harper, J. W. Inhibitors of Metalloproteases. In Protease Inhibitors; Barrett, A. J., Salvesan, G., Eds.; Elsevier Science: Amsterdam, 1986; p 219.
    • (1986) Inhibitors of Metalloproteases , pp. 219
    • Powers, J.C.1    Harper, J.W.2
  • 6
    • 0024298964 scopus 로고
    • (a) Kraut J. Science. 242:1988;533
    • (1988) Science , vol.242 , pp. 533
    • Kraut, J.1
  • 10
    • 0001883029 scopus 로고
    • Transition state affinity and the design of enzyme inhibitors
    • Page, M. I., Williams, A., Eds.; Royal Chemical Society: London
    • (c) Wolfenden, R. Transition State Affinity and the Design of Enzyme Inhibitors. In Enzyme Mechansims; Page, M. I., Williams, A., Eds.; Royal Chemical Society: London, 1987; p 97.
    • (1987) Enzyme Mechansims , pp. 97
    • Wolfenden, R.1
  • 15
    • 85031082550 scopus 로고    scopus 로고
    • note
    • 6, 300 MHz) δ 22.6, 23.5, 26.2, 40.0, 51.2, 52.5, 75.6, 129.4, 129.7, 129.8, 135.1, 174.9.
  • 25
    • 0000914658 scopus 로고
    • (a) The deprotonation may most likely be resulted as a consequence of the high Lewis acidity of the zinc ion: Izquierdo-Martin M., Stein R.L. J. Am. Chem. Soc. 114:1992;325 (b) Cross J.B., Duca J.S., Kaminski J.J., Madison V.S. J. Am. Chem. Soc. 124:2002;11004.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 325
    • Izquierdo-Martin, M.1    Stein, R.L.2
  • 26
    • 0037130658 scopus 로고    scopus 로고
    • The deprotonation may most likely be resulted as a consequence of the high Lewis acidity of the zinc ion
    • (a) The deprotonation may most likely be resulted as a consequence of the high Lewis acidity of the zinc ion: Izquierdo-Martin M., Stein R.L. J. Am. Chem. Soc. 114:1992;325 (b) Cross J.B., Duca J.S., Kaminski J.J., Madison V.S. J. Am. Chem. Soc. 124:2002;11004.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11004
    • Cross, J.B.1    Duca, J.S.2    Kaminski, J.J.3    Madison, V.S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.