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Volumn 9, Issue 3, 1999, Pages 497-500

Leucine-phenylalanine dipeptide-based N-mesyloxysuccinimides: Synthesis of all four stereoisomers and their assay against serine proteases

Author keywords

[No Author keywords available]

Indexed keywords

3 (N ACETYLLEUCYLAMINO) 3 BENZYL 1 [(METHYLSULFONYL)OXY]SUCCINIMIDE; CHYMOTRYPSIN A; LEUKOCYTE ELASTASE; SERINE PROTEINASE; UNCLASSIFIED DRUG;

EID: 0033535070     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(99)00017-7     Document Type: Article
Times cited : (20)

References (22)
  • 12
    • 0013564122 scopus 로고    scopus 로고
    • note
    • 5b,7
  • 13
    • 0013564183 scopus 로고    scopus 로고
    • note
    • 1H NMR spectra of 8-13 were dependent on the concentration of the sample used in the analysis.
  • 17
    • 0013588535 scopus 로고    scopus 로고
    • note
    • 14
  • 18
    • 0000110272 scopus 로고
    • On this basis, at least, it might be expected that compounds of the type 10 and 13 would be less susceptible than 1 to the ring-opening step required to give enzyme inactivation
    • It is also well documented that the greater the substitution on a cyclic compound (e.g. as in a succinimide) the less prone it is to ring-opening (see Allinger, N. L.; Zalkow, V. J. Org. Chem. 1960, 25, 701). On this basis, at least, it might be expected that compounds of the type 10 and 13 would be less susceptible than 1 to the ring-opening step required to give enzyme inactivation.
    • (1960) J. Org. Chem. , vol.25 , pp. 701
    • Allinger, N.L.1    Zalkow, V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.