Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C9H12ClNO4S |
| Molecular Weight | 265.714 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NCC(O)(CS(O)(=O)=O)C1=CC=C(Cl)C=C1
InChI
InChIKey=WBSMZVIMANOCNX-UHFFFAOYSA-N
InChI=1S/C9H12ClNO4S/c10-8-3-1-7(2-4-8)9(12,5-11)6-16(13,14)15/h1-4,12H,5-6,11H2,(H,13,14,15)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Activaton of GABAB receptor inhibits the excitability of rat small diameter trigeminal root ganglion neurons. | 2004 |
|
| Expression cloning of GABA(B) receptors uncovers similarity to metabotropic glutamate receptors. | 1997-03-20 |
|
| Hypotensive and hypertensive effects of catecholamines intrathecally injected in anesthetized rats. | 1996-06-10 |
|
| Involvement of cholinergic systems in the deficit of place learning in Morris water maze task induced by baclofen in rats. | 1995-06-19 |
|
| 2-Hydroxy-saclofen: an improved antagonist at central and peripheral GABAB receptors. | 1988-09-23 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID30922408
Created by
admin on Mon Mar 31 22:10:24 GMT 2025 , Edited by admin on Mon Mar 31 22:10:24 GMT 2025
|
PRIMARY | |||
|
1564
Created by
admin on Mon Mar 31 22:10:24 GMT 2025 , Edited by admin on Mon Mar 31 22:10:24 GMT 2025
|
PRIMARY | |||
|
117354-64-0
Created by
admin on Mon Mar 31 22:10:24 GMT 2025 , Edited by admin on Mon Mar 31 22:10:24 GMT 2025
|
PRIMARY | |||
|
X5IFR0UF10
Created by
admin on Mon Mar 31 22:10:24 GMT 2025 , Edited by admin on Mon Mar 31 22:10:24 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
