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Volumn 17, Issue 17, 2007, Pages 4866-4872

Carbonic anhydrase inhibitors. Interaction of the antiepileptic drug sulthiame with twelve mammalian isoforms: Kinetic and X-ray crystallographic studies

Author keywords

Antiepileptic; Carbonic anhydrase; Sulfamate; Sulfonamide; Sultam; Sulthiame; X ray crystallography

Indexed keywords

ACETAZOLAMIDE; AMINO ACID; ANTICONVULSIVE AGENT; BRINZOLAMIDE; CARBONATE DEHYDRATASE INHIBITOR; DICLOFENAMIDE; DORZOLAMIDE; ETHOXZOLAMIDE; METHAZOLAMIDE; SULFONAMIDE; SULTIAME; TOPIRAMATE;

EID: 34547585390     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2007.06.044     Document Type: Article
Times cited : (34)

References (48)
  • 23
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    • Nishimori I. Acatalytic CAs: carbonic anhydrase-related proteins. In: Supuran C.T., Scozzafava A., and Conway J. (Eds). Carbonic anhydrase: Its inhibitors and Activators (2004), CRC Press, Boca Raton 25
    • (2004) Carbonic anhydrase: Its inhibitors and Activators , pp. 25
    • Nishimori, I.1
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    • Alterio, V.; De Simone, G.; Monti, S.M.; Scozzafava, A.; Supuran, C.T. Bioorg. Med. Chem. Lett. 2007, 17, in press. (doi 10.1016/j.bmcl.2007.05.045).
  • 38
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    • 2 solutions in water at 20 °C were used as substrate. Stock solutions of inhibitors were prepared at a concentration of 10 mM (in DMSO-water 1:1, v/v) and dilutions up to 0.1 nM done with the assay buffer mentioned above. Inhibitor and enzyme solutions were preincubated together for 10 min at room temperature prior to assay, in order to allow for the formation of the E-I complex.
    • 2 solutions in water at 20 °C were used as substrate. Stock solutions of inhibitors were prepared at a concentration of 10 mM (in DMSO-water 1:1, v/v) and dilutions up to 0.1 nM done with the assay buffer mentioned above. Inhibitor and enzyme solutions were preincubated together for 10 min at room temperature prior to assay, in order to allow for the formation of the E-I complex.
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    • Khalifah, R.G.1
  • 39
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    • note
    • 23 Coordinates and structure factors have been deposited with the Protein Data Bank (PDB accession code 2Q1Q). The crystallographic parameters and refinement statistics are summarized in Table 2.
  • 41
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    • Oxford Diffraction. CrysAlis RED. 2006, Version 1.171.32.2. Oxford Diffraction Ltd.
  • 47
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    • Multiple binding modes observed in X-ray structures of carbonic anhydrase inhibitor complexes and other systems: consequences for structure-based drug design
    • Supuran C.T., Scozzafava A., and Conway J. (Eds), CRC Press, Boca Raton
    • Antel J., Weber A., Sotriffer C.A., and Klebe G. Multiple binding modes observed in X-ray structures of carbonic anhydrase inhibitor complexes and other systems: consequences for structure-based drug design. In: Supuran C.T., Scozzafava A., and Conway J. (Eds). Carbonic anhydrase-Its inhibitors and activators (2004), CRC Press, Boca Raton 45
    • (2004) Carbonic anhydrase-Its inhibitors and activators , pp. 45
    • Antel, J.1    Weber, A.2    Sotriffer, C.A.3    Klebe, G.4
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    • Development of sulfonamide carbonic anhydrase inhibitors
    • Supuran C.T., Scozzafava A., and Conway J. (Eds), CRC Press, Boca Raton
    • Supuran C.T., Scozzafava A., and Casini A. Development of sulfonamide carbonic anhydrase inhibitors. In: Supuran C.T., Scozzafava A., and Conway J. (Eds). Carbonic anhydrase-Its inhibitors and activators (2004), CRC Press, Boca Raton 67
    • (2004) Carbonic anhydrase-Its inhibitors and activators , pp. 67
    • Supuran, C.T.1    Scozzafava, A.2    Casini, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.