메뉴 건너뛰기




Volumn 7, Issue 5, 1999, Pages 821-830

Non-thiazolidinedione antihyperglycaemic agents. Part 3: The effects of stereochemistry on the potency of α-methoxy-β-phenylpropanoic acids

Author keywords

Antihyperglycaemic; Enzymes and enzyme reactions; Resolution; X ray crystal structures

Indexed keywords

ANTIDIABETIC AGENT; PROPIONIC ACID DERIVATIVE;

EID: 0033136064     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(99)00034-6     Document Type: Article
Times cited : (36)

References (45)
  • 14
    • 0001981607 scopus 로고    scopus 로고
    • The thiazolidinedione moiety has been replaced by a variety of other heterocyclic systems, although few of these modifications have given compounds with high anti-hyperglycaemic potency. See for example
    • The thiazolidinedione moiety has been replaced by a variety of other heterocyclic systems, although few of these modifications have given compounds with high anti-hyperglycaemic potency. See for example: Hulin, B.; McCarthy, P. A.; Gibbs, E. M. Curr. Pharmaceut. Design 1996, 2, 85.
    • (1996) Curr. Pharmaceut. Design , vol.2 , pp. 85
    • Hulin, B.1    McCarthy, P.A.2    Gibbs, E.M.3
  • 32
    • 85068949570 scopus 로고    scopus 로고
    • The failure to demonstrate significant base-induced deuterium exchange of the α-hydrogen atom under NMR conditions has been used to confirm the stability of this stereo center in the racemate 1; Haigh, D. Unpublished results. Unpublished results
    • The failure to demonstrate significant base-induced deuterium exchange of the α-hydrogen atom under NMR conditions has been used to confirm the stability of this stereo center in the racemate 1;
    • Haigh, D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.