1sqt

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Revision as of 17:10, 12 November 2007

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spinqualitylabelsall models 1sqt, resolution 1.90Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image

Substituted 2-Naphthamidine Inhibitors of Urokinase

Contents 1 Overview 2 Disease 3 About this Structure 4 Reference

Overview

Several 8-substituted 2-naphthamidine-based inhibitors of the serine, protease urokinase plasminogen activator (uPA) are described. Direct, attachment of five-membered saturated or unsaturated rings improved, inhibitor performance; substitution with sulfones further improved binding, profiles. Combination of these substituents or of previously described, NH-linked heteroaromatic rings with 6-phenyl amide substituents provided, further enhancements to potency and selectivity.

Disease

Known disease associated with this structure: Alzheimer disease, late-onset, susceptibility to OMIM:[191840]

About this Structure

1SQT is a Single protein structure of sequence from Homo sapiens with UI3 as ligand. Active as U-plasminogen activator, with EC number 3.4.21.73 Full crystallographic information is available from OCA.

Reference

Interaction with the S1 beta-pocket of urokinase: 8-heterocycle substituted and 6,8-disubstituted 2-naphthamidine urokinase inhibitors., Wendt MD, Geyer A, McClellan WJ, Rockway TW, Weitzberg M, Zhao X, Mantei R, Stewart K, Nienaber V, Klinghofer V, Giranda VL, Bioorg Med Chem Lett. 2004 Jun 21;14(12):3063-8. PMID:15149645

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