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Volumn , Issue SPEC. ISS., 1999, Pages 1500-1504

A new synthesis of peptidyl epoxysuccinates for probing cysteine protease-inhibitor P3/S3 binding interactions

Author keywords

Cysteine protease inhibitors; E 64 analogs; Peptide synthesis; Peptidyl epoxysuccinates

Indexed keywords

(2ALPHA,3BETA) 3 [[(3 PHENYL 1 [[(5 HYDROXYPENTYL)AMINO]CARBONYL]PROPYL)AMINO]CARBONYL]OXIRANE CARBOXYLIC ACID; ALOXISTATIN; CATHEPSIN B; CATHESTATIN C; CIRCINAMIDE; CRUZIPAIN; CYSTEINE PROTEINASE; CYSTEINE PROTEINASE INHIBITOR; EPOXIDE; ESTER DERIVATIVE; FALCIPAIN; N [N (3 CARBOXYOXIRANE 2 CARBONYL)LEUCYL]AGMATINE; PEPTIDYL EPOXYSUCCINATE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0032776064     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-3648     Document Type: Article
Times cited : (8)

References (49)
  • 5
    • 34249771657 scopus 로고
    • P. S. Anderson, G. L. Kenyon and G. R. Marshall, Eds.; ESCOM Science Publishers: Leiden
    • McKerrow, J. H. In Perspec. Drug Discov. Design; P. S. Anderson, G. L. Kenyon and G. R. Marshall, Eds.; ESCOM Science Publishers: Leiden, 1994; Vol. 2; pp 437.
    • (1994) Perspec. Drug Discov. Design , vol.2 , pp. 437
    • McKerrow, J.H.1
  • 15
    • 0000125456 scopus 로고
    • P. G. Sammes, Ed.; Pergamon: Oxford
    • Rich, D. H. In Comprehensive Medicinal Chemistry; P. G. Sammes, Ed.; Pergamon: Oxford, 1990; Vol. 2; pp 391.
    • (1990) Comprehensive Medicinal Chemistry , vol.2 , pp. 391
    • Rich, D.H.1
  • 40
    • 0003130388 scopus 로고
    • Diethyl epoxysuccinate was prepared from D-(-)-tartrate using Mori's procedure (Mori, K.; Iwasawa, H. Tetrahedron 1980, 36, 87). The diester was converted to the monoacid using KOH in EtOH, and then to the p-nitrophenyl ester 9 using DCC and p-nitrophenol according to the known procedure.
    • (1980) Tetrahedron , vol.36 , pp. 87
    • Mori, K.1    Iwasawa, H.2
  • 46
    • 0345556907 scopus 로고    scopus 로고
    • That the minor set of epoxide signals corresponds to the diastereomers of 14 was confirmed in several cases by performing coupling of acid 13 with the D-amino acid enantiomer of 12
    • That the minor set of epoxide signals corresponds to the diastereomers of 14 was confirmed in several cases by performing coupling of acid 13 with the D-amino acid enantiomer of 12.
  • 48
    • 0345556908 scopus 로고    scopus 로고
    • All enzyme kinetic assays are performed at UCSF as described in refs. 14-16
    • All enzyme kinetic assays are performed at UCSF as described in refs. 14-16.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.