2i3z

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{{STRUCTURE_2i3z| PDB=2i3z | SCENE= }}
{{STRUCTURE_2i3z| PDB=2i3z | SCENE= }}
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'''rat DPP-IV with xanthine mimetic inhibitor #7'''
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===rat DPP-IV with xanthine mimetic inhibitor #7===
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==Overview==
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A series of xanthine mimetics containing 5,5 and 5,6 heterocycle fused imidazoles were synthesized as dipeptidyl peptidase IV inhibitors. Compound 7 is potent (h-DPPIV K(i)=2nM) and exhibits excellent selectivity and no species specificity against rat and human enzymes. The X-ray structure confirms that the binding mode of 7 to rat DPPIV is similar to the parent xanthines.
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{{ABSTRACT_PUBMED_17010607}}
==About this Structure==
==About this Structure==
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[[Category: Inhibitor]]
[[Category: Inhibitor]]
[[Category: Peptidase]]
[[Category: Peptidase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 07:02:24 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 07:52:54 2008''

Revision as of 04:52, 28 July 2008

Image:2i3z.png

Template:STRUCTURE 2i3z

rat DPP-IV with xanthine mimetic inhibitor #7

Template:ABSTRACT PUBMED 17010607

About this Structure

2I3Z is a Single protein structure of sequence from Rattus norvegicus. Full crystallographic information is available from OCA.

Reference

Xanthine mimetics as potent dipeptidyl peptidase IV inhibitors., Kurukulasuriya R, Rohde JJ, Szczepankiewicz BG, Basha F, Lai C, Jae HS, Winn M, Stewart KD, Longenecker KL, Lubben TW, Ballaron SJ, Sham HL, von Geldern TW, Bioorg Med Chem Lett. 2006 Dec 15;16(24):6226-30. Epub 2006 Sep 28. PMID:17010607

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