2p95

Revision as of 00:15, 13 November 2007 by OCA (talk | contribs) (New page: left|200px<br /> <applet load="2p95" size="450" color="white" frame="true" align="right" spinBox="true" caption="2p95, resolution 2.20Å" /> '''Factor xa in comple...)
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Factor xa in complex with the inhibitor 5-chloro-N-((1R,2S)-2-(4-(2-oxopyridin-1(2H)-YL)benzamido) cyclopentyl)thiophene-2-carboxamide

File:2p95.gif


2p95, resolution 2.20Å

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OverviewOverview

In the search of Factor Xa (FXa) inhibitors structurally different from, the pyrazole-based series, we identified a viable series of enantiopure, cis-(1R,2S)-cycloalkyldiamine derivatives as potent and selective, inhibitors of FXa. Among them, cyclohexyldiamide 7 and cyclopentyldiamide, 9 were the most potent neutral compounds, and had good anticoagulant, activity comparable to the pyrazole-based analogs. Crystal structures of, 7-FXa and 9-FXa illustrate binding similarities and differences between, the five- and the six-membered core systems, and provide rationales for, the observed SAR of P1 and linker moieties.

DiseaseDisease

Known disease associated with this structure: Factor X deficiency OMIM:[227600]

About this StructureAbout this Structure

2P95 is a Protein complex structure of sequences from Homo sapiens with ME5 as ligand. Active as Coagulation factor Xa, with EC number 3.4.21.6 Full crystallographic information is available from OCA.

ReferenceReference

SAR and X-ray structures of enantiopure 1,2-cis-(1R,2S)-cyclopentyldiamine and cyclohexyldiamine derivatives as inhibitors of coagulation Factor Xa., Qiao JX, Chang CH, Cheney DL, Morin PE, Wang GZ, King SR, Wang TC, Rendina AR, Luettgen JM, Knabb RM, Wexler RR, Lam PY, Bioorg Med Chem Lett. 2007 Aug 15;17(16):4419-27. Epub 2007 Jun 10. PMID:17588746

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