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2iit

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(New page: 200px<br /> <applet load="2iit" size="450" color="white" frame="true" align="right" spinBox="true" caption="2iit, resolution 2.35&Aring;" /> '''Human dipeptidyl pe...)
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[[Image:2iit.gif|left|200px]]<br />
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[[Image:2iit.gif|left|200px]]<br /><applet load="2iit" size="350" color="white" frame="true" align="right" spinBox="true"
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<applet load="2iit" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="2iit, resolution 2.35&Aring;" />
caption="2iit, resolution 2.35&Aring;" />
'''Human dipeptidyl peptidase 4 in complex with a diazepan-2-one inhibitor'''<br />
'''Human dipeptidyl peptidase 4 in complex with a diazepan-2-one inhibitor'''<br />
==Overview==
==Overview==
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Replacement of the triazolopiperazine ring of sitagliptin (DPP-4, IC(50)=18nM) with 3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one gave, dipeptidyl peptidase IV (DPP-4) inhibitor 1 which is potent (DPP-4, IC(50)=2.6nM), selective, and efficacious in an oral glucose tolerance, test in mice. It was selected for extensive preclinical development as a, potential back-up candidate to sitagliptin.
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Replacement of the triazolopiperazine ring of sitagliptin (DPP-4 IC(50)=18nM) with 3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one gave dipeptidyl peptidase IV (DPP-4) inhibitor 1 which is potent (DPP-4 IC(50)=2.6nM), selective, and efficacious in an oral glucose tolerance test in mice. It was selected for extensive preclinical development as a potential back-up candidate to sitagliptin.
==About this Structure==
==About this Structure==
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2IIT is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with NAG, NA and 872 as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Dipeptidyl-peptidase_IV Dipeptidyl-peptidase IV], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.14.5 3.4.14.5] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2IIT OCA].
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2IIT is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=NAG:'>NAG</scene>, <scene name='pdbligand=NA:'>NA</scene> and <scene name='pdbligand=872:'>872</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Dipeptidyl-peptidase_IV Dipeptidyl-peptidase IV], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.14.5 3.4.14.5] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2IIT OCA].
==Reference==
==Reference==
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[[Category: Biftu, T.]]
[[Category: Biftu, T.]]
[[Category: Scapin, G.]]
[[Category: Scapin, G.]]
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[[Category: Weber, A.E.]]
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[[Category: Weber, A E.]]
[[Category: 872]]
[[Category: 872]]
[[Category: NA]]
[[Category: NA]]
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[[Category: hydrolase; alpha/beta; beta-propeller; dimer]]
[[Category: hydrolase; alpha/beta; beta-propeller; dimer]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 22:44:54 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:53:08 2008''

Revision as of 15:53, 21 February 2008


2iit, resolution 2.35Å

Drag the structure with the mouse to rotate

Human dipeptidyl peptidase 4 in complex with a diazepan-2-one inhibitor

Overview

Replacement of the triazolopiperazine ring of sitagliptin (DPP-4 IC(50)=18nM) with 3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one gave dipeptidyl peptidase IV (DPP-4) inhibitor 1 which is potent (DPP-4 IC(50)=2.6nM), selective, and efficacious in an oral glucose tolerance test in mice. It was selected for extensive preclinical development as a potential back-up candidate to sitagliptin.

About this Structure

2IIT is a Single protein structure of sequence from Homo sapiens with , and as ligands. Active as Dipeptidyl-peptidase IV, with EC number 3.4.14.5 Full crystallographic information is available from OCA.

Reference

(3R)-4-[(3R)-3-Amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(2,2,2-trifluoro ethyl)-1,4-diazepan-2-one, a selective dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes., Biftu T, Feng D, Qian X, Liang GB, Kieczykowski G, Eiermann G, He H, Leiting B, Lyons K, Petrov A, Sinha-Roy R, Zhang B, Scapin G, Patel S, Gao YD, Singh S, Wu J, Zhang X, Thornberry NA, Weber AE, Bioorg Med Chem Lett. 2007 Jan 1;17(1):49-52. Epub 2006 Oct 5. PMID:17055272

Page seeded by OCA on Thu Feb 21 17:53:08 2008

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