3hdz
From Proteopedia
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+ | [[Image:3hdz.jpg|left|200px]] | ||
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3hdz", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
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+ | {{STRUCTURE_3hdz| PDB=3hdz | SCENE= }} | ||
- | + | ===Identification, Synthesis, and SAR of Amino Substituted Pyrido[3,2b]pryaziones as Potent and Selective PDE5 Inhibitors=== | |
- | Description: Identification, Synthesis, and SAR of Amino Substituted Pyrido[3,2b]pryaziones as Potent and Selective PDE5 Inhibitors | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
+ | The line below this paragraph, {{ABSTRACT_PUBMED_19540112}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 19540112 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_19540112}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | 3HDZ is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3HDZ OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:19540112</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Brown, D G.]] | ||
+ | [[Category: Cubbage, J W.]] | ||
+ | [[Category: Hughes, R O.]] | ||
+ | [[Category: Jacobsen, E J.]] | ||
+ | [[Category: Walker, J K.]] | ||
+ | [[Category: Alternative splicing]] | ||
+ | [[Category: Camp]] | ||
+ | [[Category: Cgmp]] | ||
+ | [[Category: Cgmp-binding]] | ||
+ | [[Category: Hydrolase]] | ||
+ | [[Category: Inhibition]] | ||
+ | [[Category: Magnesium]] | ||
+ | [[Category: Metal-binding]] | ||
+ | [[Category: Nucleotide-binding]] | ||
+ | [[Category: Pde-5]] | ||
+ | [[Category: Pde5]] | ||
+ | [[Category: Phosphoprotein]] | ||
+ | [[Category: Polymorphism allosteric enzyme]] | ||
+ | [[Category: Zinc]] | ||
+ | |||
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 8 09:28:05 2009'' |
Revision as of 06:28, 8 July 2009
Identification, Synthesis, and SAR of Amino Substituted Pyrido[3,2b]pryaziones as Potent and Selective PDE5 Inhibitors
Template:ABSTRACT PUBMED 19540112
About this Structure
3HDZ is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Owen DR, Walker JK, Jon Jacobsen E, Freskos JN, Hughes RO, Brown DL, Bell AS, Brown DG, Phillips C, Mischke BV, Molyneaux JM, Fobian YM, Heasley SE, Moon JB, Stallings WC, Joseph Rogier D, Fox DN, Palmer MJ, Ringer T, Rodriquez-Lens M, Cubbage JW, Blevis-Bal RM, Benson AG, Acker BA, Maddux TM, Tollefson MB, Bond BR, Macinnes A, Yu Y. Identification, synthesis and SAR of amino substituted pyrido[3,2b]pyrazinones as potent and selective PDE5 inhibitors. Bioorg Med Chem Lett. 2009 Aug 1;19(15):4088-91. Epub 2009 Jun 6. PMID:19540112 doi:10.1016/j.bmcl.2009.06.012
Page seeded by OCA on Wed Jul 8 09:28:05 2009