Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H7NOS |
| Molecular Weight | 117.169 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CSCCN1
InChI
InChIKey=HBDDRESWUAFAHY-UHFFFAOYSA-N
InChI=1S/C4H7NOS/c6-4-3-7-2-1-5-4/h1-3H2,(H,5,6)
| Molecular Formula | C4H7NOS |
| Molecular Weight | 117.169 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Bafilomycins produced in culture by Streptomyces spp. isolated from marine habitats are potent inhibitors of autophagy. | 2010-03-26 |
|
| Discovery and pharmacological characterization of aryl piperazine and piperidine ethers as dual acting norepinephrine reuptake inhibitors and 5-HT1A partial agonists. | 2009-12-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:54:08 GMT 2025
by
admin
on
Mon Mar 31 20:54:08 GMT 2025
|
| Record UNII |
SK56OUS8CH
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
243-581-8
Created by
admin on Mon Mar 31 20:54:08 GMT 2025 , Edited by admin on Mon Mar 31 20:54:08 GMT 2025
|
PRIMARY | |||
|
88402
Created by
admin on Mon Mar 31 20:54:08 GMT 2025 , Edited by admin on Mon Mar 31 20:54:08 GMT 2025
|
PRIMARY | |||
|
27540
Created by
admin on Mon Mar 31 20:54:08 GMT 2025 , Edited by admin on Mon Mar 31 20:54:08 GMT 2025
|
PRIMARY | |||
|
20196-21-8
Created by
admin on Mon Mar 31 20:54:08 GMT 2025 , Edited by admin on Mon Mar 31 20:54:08 GMT 2025
|
PRIMARY | |||
|
DTXSID00174033
Created by
admin on Mon Mar 31 20:54:08 GMT 2025 , Edited by admin on Mon Mar 31 20:54:08 GMT 2025
|
PRIMARY | |||
|
SK56OUS8CH
Created by
admin on Mon Mar 31 20:54:08 GMT 2025 , Edited by admin on Mon Mar 31 20:54:08 GMT 2025
|
PRIMARY |