2o5d
From Proteopedia
(Difference between revisions)
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| - | [[Image:2o5d. | + | {{Seed}} |
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{{STRUCTURE_2o5d| PDB=2o5d | SCENE= }} | {{STRUCTURE_2o5d| PDB=2o5d | SCENE= }} | ||
| - | + | ===Thiazolone-acylsulfonamides as novel HCV NS5B polymerase allosteric inhibitors: Convergence of structure-based drug design and X-ray crystallographic study=== | |
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| - | + | The line below this paragraph, {{ABSTRACT_PUBMED_17276060}}, adds the Publication Abstract to the page | |
| + | (as it appears on PubMed at http://www.pubmed.gov), where 17276060 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_17276060}} | ||
==About this Structure== | ==About this Structure== | ||
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[[Category: Structure-based drug design]] | [[Category: Structure-based drug design]] | ||
[[Category: Viral rna-directed rna polymerase]] | [[Category: Viral rna-directed rna polymerase]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | |
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 20:41:59 2008'' | ||
Revision as of 17:42, 28 July 2008
Thiazolone-acylsulfonamides as novel HCV NS5B polymerase allosteric inhibitors: Convergence of structure-based drug design and X-ray crystallographic study
Template:ABSTRACT PUBMED 17276060
About this Structure
Full crystallographic information is available from OCA.
Reference
Thiazolone-acylsulfonamides as novel HCV NS5B polymerase allosteric inhibitors: convergence of structure-based drug design and X-ray crystallographic study., Yan S, Appleby T, Larson G, Wu JZ, Hamatake RK, Hong Z, Yao N, Bioorg Med Chem Lett. 2007 Apr 1;17(7):1991-5. Epub 2007 Jan 19. PMID:17276060
Page seeded by OCA on Mon Jul 28 20:41:59 2008
