3czr
From Proteopedia
(New page: '''Unreleased structure''' The entry 3czr is ON HOLD Authors: Wang, Z., Sudom, A., Walker, N.P. Description: Crystal Structure of 11beta-HSD1 in Complex with Arylsulfonylpiperazine Inh...) |
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+ | {{STRUCTURE_3czr| PDB=3czr | SCENE= }} | ||
- | + | '''Crystal Structure of Human 11-beta-Hydroxysteroid Dehydrogenase (HSD1) in Complex with Arylsulfonylpiperazine Inhibitor''' | |
- | Description: Crystal Structure of 11beta-HSD1 in Complex with Arylsulfonylpiperazine Inhibitor | ||
+ | ==Overview== | ||
+ | High-throughput screening of a small-molecule compound library resulted in the identification of a series of arylsulfonylpiperazines that are potent and selective inhibitors of human 11beta-Hydroxysteroid Dehydrogenase Type 1 (11beta-HSD1). Optimization of the initial lead resulted in the discovery of compound (R)-45 (11beta-HSD1 IC(50)=3nM). | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun | + | ==About this Structure== |
+ | 3CZR is a [[Single protein]] 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=3CZR OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | Discovery and initial SAR of arylsulfonylpiperazine inhibitors of 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1)., Sun D, Wang Z, Di Y, Jaen JC, Labelle M, Ma J, Miao S, Sudom A, Tang L, Tomooka CS, Tu H, Ursu S, Walker N, Yan X, Ye Q, Powers JP, Bioorg Med Chem Lett. 2008 Jun 15;18(12):3513-6. Epub 2008 May 10. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18511278 18511278] | ||
+ | [[Category: 11-beta-hydroxysteroid dehydrogenase]] | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Single protein]] | ||
+ | [[Category: Sudom, A.]] | ||
+ | [[Category: Walker, N P.]] | ||
+ | [[Category: Wang, Z.]] | ||
+ | [[Category: 11beta]] | ||
+ | [[Category: Dehydrogenase]] | ||
+ | [[Category: Endoplasmic reticulum]] | ||
+ | [[Category: Glycoprotein]] | ||
+ | [[Category: Hydroxysteroid]] | ||
+ | [[Category: Lipid metabolism]] | ||
+ | [[Category: Membrane]] | ||
+ | [[Category: Microsome]] | ||
+ | [[Category: Nadp]] | ||
+ | [[Category: Oxidoreductase]] | ||
+ | [[Category: Polymorphism]] | ||
+ | [[Category: Signal-anchor]] | ||
+ | [[Category: Steroid metabolism]] | ||
+ | [[Category: Transmembrane]] | ||
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun 18 12:12:09 2008'' |
Revision as of 09:12, 18 June 2008
Crystal Structure of Human 11-beta-Hydroxysteroid Dehydrogenase (HSD1) in Complex with Arylsulfonylpiperazine Inhibitor
Overview
High-throughput screening of a small-molecule compound library resulted in the identification of a series of arylsulfonylpiperazines that are potent and selective inhibitors of human 11beta-Hydroxysteroid Dehydrogenase Type 1 (11beta-HSD1). Optimization of the initial lead resulted in the discovery of compound (R)-45 (11beta-HSD1 IC(50)=3nM).
About this Structure
3CZR is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Discovery and initial SAR of arylsulfonylpiperazine inhibitors of 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1)., Sun D, Wang Z, Di Y, Jaen JC, Labelle M, Ma J, Miao S, Sudom A, Tang L, Tomooka CS, Tu H, Ursu S, Walker N, Yan X, Ye Q, Powers JP, Bioorg Med Chem Lett. 2008 Jun 15;18(12):3513-6. Epub 2008 May 10. PMID:18511278 Page seeded by OCA on Wed Jun 18 12:12:09 2008
Categories: 11-beta-hydroxysteroid dehydrogenase | Homo sapiens | Single protein | Sudom, A. | Walker, N P. | Wang, Z. | 11beta | Dehydrogenase | Endoplasmic reticulum | Glycoprotein | Hydroxysteroid | Lipid metabolism | Membrane | Microsome | Nadp | Oxidoreductase | Polymorphism | Signal-anchor | Steroid metabolism | Transmembrane