Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H8ClO3.Na |
| Molecular Weight | 234.611 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].OC(\C=C\C([O-])=O)C1=CC=C(Cl)C=C1
InChI
InChIKey=FOMSNJCIQOFNOT-IPZCTEOASA-M
InChI=1S/C10H9ClO3.Na/c11-8-3-1-7(2-4-8)9(12)5-6-10(13)14;/h1-6,9,12H,(H,13,14);/q;+1/p-1/b6-5+;
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-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. | 2009-02-11 |
|
| Gamma-hydroxybutyrate receptor function studied by the modulation of nitric oxide synthase activity in rat frontal cortex punches. | 1999-12-01 |
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430440-66-7
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DTXSID10109992
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M69F856TOG
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admin on Tue Apr 01 16:29:21 GMT 2025 , Edited by admin on Tue Apr 01 16:29:21 GMT 2025
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23681234
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admin on Tue Apr 01 16:29:21 GMT 2025 , Edited by admin on Tue Apr 01 16:29:21 GMT 2025
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ACTIVE MOIETY
SUBSTANCE RECORD