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2J14

3,4,5-Trisubstituted Isoxazoles as Novel PPARdelta Agonists: Part2

Summary for 2J14
Entry DOI10.2210/pdb2j14/pdb
Related1GWX 1Y0S 2AWH 2B50 2BAW 2GWX 3GWX
DescriptorPEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR DELTA, (3-{4-[2-(2,4-DICHLORO-PHENOXY)-ETHYLCARBAMOYL]-5-PHENYL-ISOXAZOL-3-YL}-PHENYL)-ACETIC ACID (3 entities in total)
Functional Keywordstranscription, nuclear receptor fold, transcription regulation, ppar, zinc, receptor, activator, fatty acids, nuclear protein, alternative splicing, zinc-finger, dna-binding, metal-binding
Biological sourceHOMO SAPIENS (HUMAN)
Cellular locationNucleus: Q03181
Total number of polymer chains2
Total formula weight66384.38
Authors
Primary citationEpple, R.,Azimioara, M.,Russo, R.,Xie, Y.,Wang, X.,Cow, C.,Wityak, J.,Karanewsky, D.,Bursulaya, B.,Kreusch, A.,Tuntland, T.,Gerken, A.,Iskandar, M.,Saez, E.,Seidel, H.M.,Tian, S.S.
3,4,5-Trisubstituted Isoxazoles as Novel Ppardelta Agonists. Part 2
Bioorg.Med.Chem.Lett., 16:5488-, 2006
Cited by
PubMed: 16931011
DOI: 10.1016/J.BMCL.2006.08.052
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.8 Å)
Structure validation

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