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6f2u

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m (Protected "6f2u" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6f2u is ON HOLD until Paper Publication
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==Potent and selective Aldo-Keto Reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a Bioisosteric Scaffold Hopping Approach to Flufenamic acid==
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<StructureSection load='6f2u' size='340' side='right' caption='[[6f2u]], [[Resolution|resolution]] 1.88&Aring;' scene=''>
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Authors: Goyal, P., Wahlgren, W.Y., Friemann, R.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6f2u]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6F2U OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6F2U FirstGlance]. <br>
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Description: Potent and selective Aldo-Keto Reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a Bioisosteric Scaffold Hopping Approach to Flufenamic acid
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CJ2:3-[(4-methoxyphenyl)methyl]-5-oxidanyl-~{N}-[3-(trifluoromethyl)phenyl]-1,2,3-triazole-4-carboxamide'>CJ2</scene>, <scene name='pdbligand=NAP:NADP+NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NAP</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6f2u FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6f2u OCA], [http://pdbe.org/6f2u PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6f2u RCSB], [http://www.ebi.ac.uk/pdbsum/6f2u PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6f2u ProSAT]</span></td></tr>
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[[Category: Wahlgren, W.Y]]
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/AK1C3_HUMAN AK1C3_HUMAN]] Catalyzes the conversion of aldehydes and ketones to alcohols. Catalyzes the reduction of prostaglandin (PG) D2, PGH2 and phenanthrenequinone (PQ) and the oxidation of 9-alpha,11-beta-PGF2 to PGD2. Functions as a bi-directional 3-alpha-, 17-beta- and 20-alpha HSD. Can interconvert active androgens, estrogens and progestins with their cognate inactive metabolites. Preferentially transforms androstenedione (4-dione) to testosterone.
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__TOC__
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</StructureSection>
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[[Category: Friemann, R]]
[[Category: Goyal, P]]
[[Category: Goyal, P]]
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[[Category: Friemann, R]]
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[[Category: Wahlgren, W Y]]
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[[Category: 17b-hsd5]]
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[[Category: Akr1c3]]
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[[Category: Aldo-keto reductase 1c3]]
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[[Category: Bioisosterism]]
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[[Category: Crpc]]
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[[Category: Inhibitor]]
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[[Category: Oxidoreductase]]
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[[Category: Scaffold hopping]]
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[[Category: X-ray crystallography]]

Revision as of 06:01, 4 April 2018

Potent and selective Aldo-Keto Reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a Bioisosteric Scaffold Hopping Approach to Flufenamic acid

6f2u, resolution 1.88Å

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