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Volumn 23, Issue 20, 2013, Pages 5641-5645

N-glucosides as human sodium-dependent glucose cotransporter 2 (hSGLT2) inhibitors

Author keywords

Diabetes; Glucoside; N glucoside; SGLT2; Sodium dependent glucose cotransporter

Indexed keywords

GLUCOSE; GLUCOSIDE;

EID: 84884290137     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2013.08.042     Document Type: Article
Times cited : (25)

References (24)
  • 17
    • 84884291430 scopus 로고    scopus 로고
    • Eur. Pat. Appl. EP1348710, 2003
    • Reactions without any additives in refluxing MeOH were sluggish and finally led to a complex mixture. There is a patent literature, in which ammonium sulfate is used as an additive; see Tam, T. F.; Karimian, K.; Leung-Toung, R. C. S. H.; Zhao, Y.; Wodzinska, J. M.; Li, W.; Lowrie, J. N. Eur. Pat. Appl. EP1348710, 2003; Chem. Abstr. 2003, 139, 276904.
    • (2003) Chem. Abstr. , vol.139 , pp. 276904
    • Tam, T.F.1    Karimian, K.2    Leung-Toung, R.C.S.H.3    Zhao, Y.4    Wodzinska, J.M.5    Li, W.6    Lowrie, J.N.7
  • 18
    • 84884280880 scopus 로고
    • Pigman et al. reported that glucosylaniline underwent hydrolysis or isomerization in aqueous solutions; see, Although 8a was hydrolyzed under acidic aqueous condition, it remained stable under the assay condition of hSGLT inhibitory activities (pH 7.4; see Ref. 15a)
    • Pigman et al. reported that glucosylaniline underwent hydrolysis or isomerization in aqueous solutions; see W. Pigman, E.A. Cleveland, D.H. Couch, and J.H. Cleveland J. Am. Chem. Soc. 1951 1976 73 Although 8a was hydrolyzed under acidic aqueous condition, it remained stable under the assay condition of hSGLT inhibitory activities (pH 7.4; see Ref. 15a)
    • (1976) J. Am. Chem. Soc. , vol.1951 , pp. 73
    • Pigman, W.1    Cleveland, E.A.2    Couch, D.H.3    Cleveland, J.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.