2pr3

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Revision as of 00:20, 13 November 2007 by OCA (talk | contribs) (New page: left|200px<br /> <applet load="2pr3" size="450" color="white" frame="true" align="right" spinBox="true" caption="2pr3, resolution 1.5Å" /> '''Factor XA inhibitor'...)
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File:2pr3.gif


2pr3, resolution 1.5Å

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Factor XA inhibitor

OverviewOverview

A novel series of pyrrolidine-1,2-dicarboxamides was discovered as factor, Xa inhibitors using structure-based drug design. This series consisted of, a neutral 4-chlorophenylurea P1, a biphenylsulfonamide P4 and a D-proline, scaffold (1, IC(50) = 18 nM). Optimization of the initial hit resulted in, an orally bioavailable, subnanomolar inhibitor of factor Xa (13, IC(50) =, 0.38 nM), which was shown to be efficacious in a canine electrolytic model, of thrombosis with minimal bleeding.

DiseaseDisease

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

About this StructureAbout this Structure

2PR3 is a Protein complex structure of sequences from Homo sapiens with CA and 237 as ligands. Active as Coagulation factor Xa, with EC number 3.4.21.6 Full crystallographic information is available from OCA.

ReferenceReference

Structure-based drug design of pyrrolidine-1, 2-dicarboxamides as a novel series of orally bioavailable factor Xa inhibitors., Van Huis CA, Bigge CF, Casimiro-Garcia A, Cody WL, Dudley DA, Filipski KJ, Heemstra RJ, Kohrt JT, Narasimhan LS, Schaum RP, Zhang E, Bryant JW, Haarer S, Janiczek N, Leadley RJ Jr, McClanahan T, Thomas Peterson J, Welch KM, Edmunds JJ, Chem Biol Drug Des. 2007 Jun;69(6):444-50. PMID:17581239

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