Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C34H30N2O5 |
Molecular Weight | 546.6124 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(CCOC2=CC=C(C[C@H](NC3=CC=CC=C3C(=O)C4=CC=CC=C4)C(O)=O)C=C2)N=C(O1)C5=CC=CC=C5
InChI
InChIKey=ZZCHHVUQYRMYLW-HKBQPEDESA-N
InChI=1S/C34H30N2O5/c1-23-29(36-33(41-23)26-12-6-3-7-13-26)20-21-40-27-18-16-24(17-19-27)22-31(34(38)39)35-30-15-9-8-14-28(30)32(37)25-10-4-2-5-11-25/h2-19,31,35H,20-22H2,1H3,(H,38,39)/t31-/m0/s1
Molecular Formula | C34H30N2O5 |
Molecular Weight | 546.6124 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 1. Discovery of a novel series of potent antihyperglycemic and antihyperlipidemic agents. | 1998 Dec 3 |
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The PPARs: from orphan receptors to drug discovery. | 2000 Feb 24 |
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Asymmetry in the PPARgamma/RXRalpha crystal structure reveals the molecular basis of heterodimerization among nuclear receptors. | 2000 Mar |
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Synthesis of a high-affinity fluorescent PPARgamma ligand for high-throughput fluorescence polarization assays. | 2003 Oct 1 |
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Binding analyses between Human PPARgamma-LBD and ligands. | 2004 Jan |
|
GI262570, a peroxisome proliferator-activated receptor {gamma} agonist, changes electrolytes and water reabsorption from the distal nephron in rats. | 2005 Feb |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:02:43 GMT 2023
by
admin
on
Sat Dec 16 16:02:43 GMT 2023
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Record UNII |
3433GY7132
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C98233
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3433GY7132
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C422415
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274687-78-4
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170364
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C81693
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FARGLITAZAR
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DTXSID1047310
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8064
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CHEMBL107367
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100000177891
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LL-82
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196808-45-4
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Related Record | Type | Details | ||
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