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Volumn 119, Issue 1, 1997, Pages 38-41

Stereochemistry in inactivation of carboxypeptidase A. Structural analysis of the inactivated carboxypeptidase A by an enantiomeric pair of 2-benzyl-3,4-epoxybutanoic acids

Author keywords

[No Author keywords available]

Indexed keywords

2 BENZYL 3,4 EPOXYBUTYRIC ACID; CARBOXYPEPTIDASE A; ENZYME INHIBITOR; UNCLASSIFIED DRUG;

EID: 0031042263     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9622463     Document Type: Article
Times cited : (32)

References (41)
  • 3
    • 1842322721 scopus 로고
    • Barrett, A. J., Salvesen, G., Eds.; Elsevier: Amsterdam, Chapter 6
    • (a) Powers, J. C.; Harper, J. W. In Proteinase Inhibitors; Barrett, A. J., Salvesen, G., Eds.; Elsevier: Amsterdam, 1986; Chapter 6.
    • (1986) Proteinase Inhibitors
    • Powers, J.C.1    Harper, J.W.2
  • 27
    • 0004294576 scopus 로고
    • Wainer, I. W., Drayer, D. E., Eds.; Marcel Dekker: New York
    • (c) Drug Stereochemistry; Wainer, I. W., Drayer, D. E., Eds.; Marcel Dekker: New York, 1988.
    • (1988) Drug Stereochemistry
  • 31
    • 79955830423 scopus 로고
    • Lwowski, W., Ed.; Pergamon Press: Oxford
    • N1 which is thought to be the preferred process for the Lewis acid catalyzed ring cleavage: Lewars, E. G. In Comprehensive Heterocyclic Chemistry; Lwowski, W., Ed.; Pergamon Press: Oxford, 1984; Vol. 7, pp 108-109.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.7 , pp. 108-109
    • Lewars, E.G.1
  • 32


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.