From Wikipedia, the free encyclopedia
Zenarestat
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Names
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Preferred IUPAC name
{3-[(4-Bromo-2-fluorophenyl)methyl]-7-chloro-2,4-dioxo-3,4-dihydroquinazolin-1(2H)-yl}acetic acid
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Identifiers
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ChemSpider
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KEGG
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UNII
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InChI=1S/C17H11BrClFN2O4/c18-10-2-1-9(13(20)5-10)7-22-16(25)12-4-3-11(19)6-14(12)21(17(22)26)8-15(23)24/h1-6H,7-8H2,(H,23,24) Key: SXONDGSPUVNZLO-UHFFFAOYSA-N InChI=1/C17H11BrClFN2O4/c18-10-2-1-9(13(20)5-10)7-22-16(25)12-4-3-11(19)6-14(12)21(17(22)26)8-15(23)24/h1-6H,7-8H2,(H,23,24) Key: SXONDGSPUVNZLO-UHFFFAOYAB
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C1=CC2=C(C=C1Cl)N(C(=O)N(C2=O)CC3=C(C=C(C=C3)Br)F)CC(=O)O
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Properties
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C17H11BrClFN2O4
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Molar mass
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441.64 g/mol
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Melting point
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223 to 224 °C (433 to 435 °F; 496 to 497 K)
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Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Zenarestat (FK-366; FR-74366) is an
aldose reductase inhibitor. It was investigated as a treatment of
diabetic neuropathy and
cataract, but its development was terminated.
[1]
References
- M. Hashimoto et al., EP 218999; eidem, US 4734419 (1987, 1988 both to Fujisawa)
- Inhibition kinetics and effect on sorbitol accumulation: S. Ao et al., Metabolism 40, 77 (1991)
- Pharmacokinetics and metabolism in diabetic rats: Y. Tanaka et al., Drug Metab. Dispos. 21, 677 (1993)
- M. Kanamaru et al., J. Clin. Pharmacol. 33, 1122 (1993).
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fast-acting | |
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short-acting | |
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long-acting | |
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ultra-long-acting | |
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inhalable | |
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