Details
Stereochemistry | RACEMIC |
Molecular Formula | C10H9ClO3 |
Molecular Weight | 212.63 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(\C=C\C(O)=O)C1=CC=C(Cl)C=C1
InChI
InChIKey=FPLZDFIDWYDARU-AATRIKPKSA-N
InChI=1S/C10H9ClO3/c11-8-3-1-7(2-4-8)9(12)5-6-10(13)14/h1-6,9,12H,(H,13,14)/b6-5+
Molecular Formula | C10H9ClO3 |
Molecular Weight | 212.63 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 1 |
Optical Activity | ( + / - ) |
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: Q9HAB3 Gene ID: 79581.0 Gene Symbol: SLC52A2 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/10571257 |
PubMed
Title | Date | PubMed |
---|---|---|
Gamma-hydroxybutyrate receptor function studied by the modulation of nitric oxide synthase activity in rat frontal cortex punches. | 1999 Dec 1 |
|
Gamma-butyrolactone (GBL) disruption of passive avoidance learning in the day-old chick appears to be due to its effect on GABAB not gamma-hydroxybutyric [corrected] acid (GHB) receptors. | 2009 Feb 11 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:44:51 GMT 2023
by
admin
on
Sat Dec 16 08:44:51 GMT 2023
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Record UNII |
535Z468F1A
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Record Status |
Validated (UNII)
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Record Version |
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535Z468F1A
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admin on Sat Dec 16 08:44:51 GMT 2023 , Edited by admin on Sat Dec 16 08:44:51 GMT 2023
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SALT/SOLVATE -> PARENT |