Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C8H14O4S |
| Molecular Weight | 206.259 |
| Optical Activity | ( + ) |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CC[C@H](CCCS)C(O)=O
InChI
InChIKey=FNLNSQHJKVQCBP-LURJTMIESA-N
InChI=1S/C8H14O4S/c9-7(10)4-3-6(8(11)12)2-1-5-13/h6,13H,1-5H2,(H,9,10)(H,11,12)/t6-/m0/s1
| Molecular Formula | C8H14O4S |
| Molecular Weight | 206.259 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 16:29:27 GMT 2025
by
admin
on
Tue Apr 01 16:29:27 GMT 2025
|
| Record UNII |
KR47E7VT2X
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
KR47E7VT2X
Created by
admin on Tue Apr 01 16:29:27 GMT 2025 , Edited by admin on Tue Apr 01 16:29:27 GMT 2025
|
PRIMARY | |||
|
848952-62-5
Created by
admin on Tue Apr 01 16:29:27 GMT 2025 , Edited by admin on Tue Apr 01 16:29:27 GMT 2025
|
PRIMARY | |||
|
11310264
Created by
admin on Tue Apr 01 16:29:27 GMT 2025 , Edited by admin on Tue Apr 01 16:29:27 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
RACEMATE -> ENANTIOMER |
Pretreatment with the same doses (15, 30, 60 mg/kg, p.o.) of GPI-16476 or GPI-16477, two enantiomers of GPI-5693, also inhibited cocaine-induced reinstatement similar to GPI-5693.
|