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Volumn 21, Issue 16, 2011, Pages 4888-4890

Bioactive sulfoximines: Syntheses and properties of Vioxx® analogs

Author keywords

COX 2 selective inhibitor (COXIB); hERG activity; Sulfoximine; Vioxx (Rofecoxib)

Indexed keywords

CYCLOOXYGENASE 2; IMINE; POTASSIUM CHANNEL HERG; ROFECOXIB; SULFOXIMINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79960903495     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2011.06.029     Document Type: Article
Times cited : (67)

References (45)
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    • For a recent example, where buthionine sulfoximine (BSO) was applied as inhibitor for the glutathione biosynthesis, see
    • For a recent example, where buthionine sulfoximine (BSO) was applied as inhibitor for the glutathione biosynthesis, see: K. Takahashi, R. Tatsunami, T. Oba, and Y. Tampo Biol. Pharm. Bull. 33 2010 556
    • (2010) Biol. Pharm. Bull. , vol.33 , pp. 556
    • Takahashi, K.1    Tatsunami, R.2    Oba, T.3    Tampo, Y.4
  • 21
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    • For the initial demonstration, that BSO blocks the GSH synthesis by inhibiting the γ-glutamylcysteine synthetase, see
    • For the initial demonstration, that BSO blocks the GSH synthesis by inhibiting the γ-glutamylcysteine synthetase, see: A. Meister Science 220 1983 472
    • (1983) Science , vol.220 , pp. 472
    • Meister, A.1
  • 23
    • 79960918257 scopus 로고    scopus 로고
    • For a recent example of the patent literature related to medicinal chemistry, see WO 115548 A1 (Bayer Schering Pharma AG)
    • For a recent example of the patent literature related to medicinal chemistry, see: von Nussbaum, F.; Karthaus, D.; Anlauf, S.; Delbeck, M.; Li, V. M.-J.; Meibom, D.; Lustig, K.; Schneider, D. WO 115548 A1, 2010 (Bayer Schering Pharma AG).
    • (2010)
    • Von Nussbaum, F.1    Karthaus, D.2    Anlauf, S.3    Delbeck, M.4    Li, V.M.-J.5    Meibom, D.6    Lustig, K.7    Schneider, D.8
  • 42
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    • The biochemical assays for the determinations of the hERG blocking potencies were performed by Cytocentrics, Rostock, Germany. Quinidine served as reference compound. Details are given in the Supplementary data. The following references were relevant for those experiments
    • The biochemical assays for the determinations of the hERG blocking potencies were performed by Cytocentrics, Rostock, Germany. Quinidine served as reference compound. Details are given in the Supplementary data. The following references were relevant for those experiments: M.C. Sanguinetti, C. Jiang, M.E. Curran, and M.T. Keating Cell 81 1995 299
    • (1995) Cell , vol.81 , pp. 299
    • Sanguinetti, M.C.1    Jiang, C.2    Curran, M.E.3    Keating, M.T.4
  • 45
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    • Here, only racemic sulfoximines have been investigated. Optically active products should be accessible via the corresponding known sulfoxides. For their preparation, see
    • Here, only racemic sulfoximines have been investigated. Optically active products should be accessible via the corresponding known sulfoxides. For their preparation, see: F. Caturla, M. Amat, R.F. Reinoso, M. Córdoba, and G. Warrellow Bioorg. Med. Chem. Lett. 16 2006 3209
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 3209
    • Caturla, F.1    Amat, M.2    Reinoso, R.F.3    Córdoba, M.4    Warrellow, G.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.