Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H16N6OS |
| Molecular Weight | 268.339 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(NCC[S+]([O-])CC1=C(C)NC=N1)=NC#N
InChI
InChIKey=HOJLJLYVNQFCRE-UHFFFAOYSA-N
InChI=1S/C10H16N6OS/c1-8-9(16-7-15-8)5-18(17)4-3-13-10(12-2)14-6-11/h7H,3-5H2,1-2H3,(H,15,16)(H2,12,13,14)
| Molecular Formula | C10H16N6OS |
| Molecular Weight | 268.339 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:14:11 GMT 2025
by
admin
on
Mon Mar 31 19:14:11 GMT 2025
|
| Record UNII |
H6V3T9UG74
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
H6V3T9UG74
Created by
admin on Mon Mar 31 19:14:11 GMT 2025 , Edited by admin on Mon Mar 31 19:14:11 GMT 2025
|
PRIMARY | |||
|
DTXSID50969219
Created by
admin on Mon Mar 31 19:14:11 GMT 2025 , Edited by admin on Mon Mar 31 19:14:11 GMT 2025
|
PRIMARY | |||
|
62949
Created by
admin on Mon Mar 31 19:14:11 GMT 2025 , Edited by admin on Mon Mar 31 19:14:11 GMT 2025
|
PRIMARY | |||
|
54237-72-8
Created by
admin on Mon Mar 31 19:14:11 GMT 2025 , Edited by admin on Mon Mar 31 19:14:11 GMT 2025
|
PRIMARY | |||
|
30731
Created by
admin on Mon Mar 31 19:14:11 GMT 2025 , Edited by admin on Mon Mar 31 19:14:11 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ENANTIOMER -> RACEMATE | |||
|
ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> METABOLITE |
MAJOR
URINE
|
