1uk1

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==Overview==
==Overview==
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A novel class of quinazolinone derivatives as potent, poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors has been discovered. Key, to success was application of a rational discovery strategy involving, structure-based design, combinatorial chemistry, and classical SAR for, improvement of potency and bioavailability. The new inhibitors were shown, to bind to the nicotinamide-ribose binding site (NI site) and the, adenosine-ribose binding site (AD site) of NAD+.
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A novel class of quinazolinone derivatives as potent poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors has been discovered. Key to success was application of a rational discovery strategy involving structure-based design, combinatorial chemistry, and classical SAR for improvement of potency and bioavailability. The new inhibitors were shown to bind to the nicotinamide-ribose binding site (NI site) and the adenosine-ribose binding site (AD site) of NAD+.
==Disease==
==Disease==
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[[Category: protein-inhibitor complex]]
[[Category: protein-inhibitor complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 17:02:49 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:25:20 2008''

Revision as of 13:25, 21 February 2008


1uk1, resolution 3.Å

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Crystal structure of human poly(ADP-ribose) polymerase complexed with a potent inhibitor

Contents

Overview

A novel class of quinazolinone derivatives as potent poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors has been discovered. Key to success was application of a rational discovery strategy involving structure-based design, combinatorial chemistry, and classical SAR for improvement of potency and bioavailability. The new inhibitors were shown to bind to the nicotinamide-ribose binding site (NI site) and the adenosine-ribose binding site (AD site) of NAD+.

Disease

Known diseases associated with this structure: Xeroderma pigmentosum (1) OMIM:[173870]

About this Structure

1UK1 is a Single protein structure of sequence from Homo sapiens with as ligand. Active as NAD(+) ADP-ribosyltransferase, with EC number 2.4.2.30 Full crystallographic information is available from OCA.

Reference

Rational approaches to discovery of orally active and brain-penetrable quinazolinone inhibitors of poly(ADP-ribose)polymerase., Hattori K, Kido Y, Yamamoto H, Ishida J, Kamijo K, Murano K, Ohkubo M, Kinoshita T, Iwashita A, Mihara K, Yamazaki S, Matsuoka N, Teramura Y, Miyake H, J Med Chem. 2004 Aug 12;47(17):4151-4. PMID:15293985

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