Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H3N5O |
| Molecular Weight | 137.0995 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)C1=NC=NC1=[N+]=[N-]
InChI
InChIKey=IKZLMSPFYNDYIL-UHFFFAOYSA-N
InChI=1S/C4H3N5O/c5-3(10)2-4(9-6)8-1-7-2/h1H,(H2,5,10)
| Molecular Formula | C4H3N5O |
| Molecular Weight | 137.0995 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Antitumor imidazotetrazines. 40. Radiosyntheses of [4-11C-carbonyl]- and [3-N-11C-methyl]-8-carbamoyl-3-methylimidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one (temozolomide) for positron emission tomography (PET) studies. | 2002-12-05 |
|
| Causative agent of vascular pain among photodegradation products of dacarbazine. | 2002-08 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:03:30 GMT 2025
by
admin
on
Mon Mar 31 22:03:30 GMT 2025
|
| Record UNII |
XLJ646260P
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
230-284-3
Created by
admin on Mon Mar 31 22:03:30 GMT 2025 , Edited by admin on Mon Mar 31 22:03:30 GMT 2025
|
PRIMARY | |||
|
7008-85-7
Created by
admin on Mon Mar 31 22:03:30 GMT 2025 , Edited by admin on Mon Mar 31 22:03:30 GMT 2025
|
PRIMARY | |||
|
22420
Created by
admin on Mon Mar 31 22:03:30 GMT 2025 , Edited by admin on Mon Mar 31 22:03:30 GMT 2025
|
PRIMARY | |||
|
53426585
Created by
admin on Mon Mar 31 22:03:30 GMT 2025 , Edited by admin on Mon Mar 31 22:03:30 GMT 2025
|
PRIMARY | |||
|
DTXSID10939135
Created by
admin on Mon Mar 31 22:03:30 GMT 2025 , Edited by admin on Mon Mar 31 22:03:30 GMT 2025
|
PRIMARY | |||
|
XLJ646260P
Created by
admin on Mon Mar 31 22:03:30 GMT 2025 , Edited by admin on Mon Mar 31 22:03:30 GMT 2025
|
PRIMARY | |||
|
1643554
Created by
admin on Mon Mar 31 22:03:30 GMT 2025 , Edited by admin on Mon Mar 31 22:03:30 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|