3ivh: Difference between revisions
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===Design and Synthesis of Potent BACE-1 Inhibitors with Cellular Activity: Structure-Activity Relationship of P1 Substituents=== | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | <!-- | ||
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{{ABSTRACT_PUBMED_19811916}} | |||
==About this Structure== | |||
3IVH 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=3IVH OCA]. | |||
==Reference== | |||
<ref group="xtra">PMID:19811916</ref><references group="xtra"/> | |||
[[Category: Homo sapiens]] | |||
[[Category: Memapsin 2]] | |||
[[Category: Pan, H.]] | |||
[[Category: Alternative splicing]] | |||
[[Category: Alzheimer's disease]] | |||
[[Category: Aspartyl protease]] | |||
[[Category: Bace-1 inhibitor]] | |||
[[Category: Disulfide bond]] | |||
[[Category: Glycoprotein]] | |||
[[Category: Hydrolase]] | |||
[[Category: Membrane]] | |||
[[Category: Polymorphism]] | |||
[[Category: Protease]] | |||
[[Category: Structure-based drug design]] | |||
[[Category: Transmembrane]] | |||
[[Category: Zymogen]] | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 6 09:29:00 2010'' |
Revision as of 10:29, 6 January 2010
Design and Synthesis of Potent BACE-1 Inhibitors with Cellular Activity: Structure-Activity Relationship of P1 SubstituentsDesign and Synthesis of Potent BACE-1 Inhibitors with Cellular Activity: Structure-Activity Relationship of P1 Substituents
Template:ABSTRACT PUBMED 19811916
About this StructureAbout this Structure
3IVH is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
- ↑ Sealy JM, Truong AP, Tso L, Probst GD, Aquino J, Hom RK, Jagodzinska BM, Dressen D, Wone DW, Brogley L, John V, Tung JS, Pleiss MA, Tucker JA, Konradi AW, Dappen MS, Toth G, Pan H, Ruslim L, Miller J, Bova MP, Sinha S, Quinn KP, Sauer JM. Design and synthesis of cell potent BACE-1 inhibitors: structure-activity relationship of P1' substituents. Bioorg Med Chem Lett. 2009 Nov 15;19(22):6386-91. Epub 2009 Sep 19. PMID:19811916 doi:10.1016/j.bmcl.2009.09.061
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