Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C18H18O2 |
| Molecular Weight | 266.3343 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C\C=C\CC(C(O)=O)C1=CC=C(C=C1)C2=CC=CC=C2
InChI
InChIKey=ZVRCODPBROUJIT-NSCUHMNNSA-N
InChI=1S/C18H18O2/c1-2-3-9-17(18(19)20)16-12-10-15(11-13-16)14-7-5-4-6-8-14/h2-8,10-13,17H,9H2,1H3,(H,19,20)/b3-2+
| Molecular Formula | C18H18O2 |
| Molecular Weight | 266.3343 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Optical Activity | ( + / - ) |
DescriptionSources: https://pubs.acs.org/doi/abs/10.1021/ja01519a066
Sources: https://pubs.acs.org/doi/abs/10.1021/ja01519a066
Xenyhexenic acid is a biphenyl organic compound, discovered in 1958. When fed to rats, xenyhexenic acid inhibited hypercholesterolemia and hyperlipemia that been induced by the administration of Triton.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:06:09 GMT 2025
by
admin
on
Mon Mar 31 18:06:09 GMT 2025
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| Record UNII |
4293LHY68W
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| Record Status |
Validated (UNII)
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29703
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admin on Mon Mar 31 18:06:09 GMT 2025 , Edited by admin on Mon Mar 31 18:06:09 GMT 2025
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| Code System | Code | Type | Description | ||
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C66667
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964-82-9
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SUPERSEDED | |||
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95040-85-0
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NON-SPECIFIC STEREOCHEMISTRY | |||
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SUB00107MIG
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PRIMARY | |||
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100000079375
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PRIMARY | |||
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1018
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PRIMARY | |||
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4293LHY68W
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PRIMARY | |||
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447465-23-8
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PRIMARY | |||
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CHEMBL2104483
Created by
admin on Mon Mar 31 18:06:09 GMT 2025 , Edited by admin on Mon Mar 31 18:06:09 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |