Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H12O2 |
| Molecular Weight | 212.2439 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=PYHXGXCGESYPCW-UHFFFAOYSA-N
InChI=1S/C14H12O2/c15-14(16)13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13H,(H,15,16)
| Molecular Formula | C14H12O2 |
| Molecular Weight | 212.2439 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis, molecular modeling, and structure-activity relationship of benzophenone-based CAAX-peptidomimetic farnesyltransferase inhibitors. | 2001 Aug 30 |
|
| Hydrolytically active tetranuclear nickel complexes with structural resemblance to the active site of urease. | 2002 Oct 7 |
|
| Gastrointestinally distributed UDP-glucuronosyltransferase 1A10, which metabolizes estrogens and nonsteroidal anti-inflammatory drugs, depends upon phosphorylation. | 2004 Jul 2 |
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| Synthesis and characterization of high nuclearity iron(III) phosphonate molecular clusters. | 2008 Jul 7 |
|
| cyclo-Hexa-μ(2)-diphenyl-acetato-κO:O'-hexa-μ(3)-oxido-hexa-kis[phenyl-tin(IV)]. | 2008 Nov 26 |
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| Condensed bridgehead nitrogen heterocyclic system: synthesis and pharmacological activities of 1,2,4-triazolo-[3,4-b]-1,3,4-thiadiazole derivatives of ibuprofen and biphenyl-4-yloxy acetic acid. | 2008 Oct |
|
| catena-Poly[[diaqua-bis(diphenyl-acetato)-zinc(II)]-μ-4,4'-bipyridine]. | 2009 Feb 18 |
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| The guinea pig ileum lacks the direct, high-potency, M(2)-muscarinic, contractile mechanism characteristic of the mouse ileum. | 2009 Oct |
|
| Separation of carboxylates by hydrophilic interaction liquid chromatography on titania. | 2010 Jan 1 |
|
| Pd(II)-catalyzed enantioselective C-H olefination of diphenylacetic acids. | 2010 Jan 20 |
|
| Kinetic resolution of the racemic 2-hydroxyalkanoates using the enantioselective mixed-anhydride method with pivalic anhydride and a chiral acyl-transfer catalyst. | 2010 Jan 4 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 03:22:20 GMT 2023
by
admin
on
Sat Dec 16 03:22:20 GMT 2023
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| Record UNII |
658NCZ0NKO
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| Record Status |
Validated (UNII)
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