Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H5N5 |
| Molecular Weight | 99.0946 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC(N)=NN1
InChI
InChIKey=PKWIYNIDEDLDCJ-UHFFFAOYSA-N
InChI=1S/C2H5N5/c3-1-5-2(4)7-6-1/h(H5,3,4,5,6,7)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of nickel(II) triazolenaphthalocyanine and related macrocycles. | 2001 Jan 12 |
|
| Convenient synthesis of fused heterocyclic 1,3,5-triazines from some N-acyl imidates and heterocyclic amines as anticancer and antioxidant agents. | 2005 Aug |
|
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005 Jun |
|
| Hexaaqua-hexa-kis(μ(2)-3,5-diamino-4H-1,2,4-triazole)trinickel(II) tris-(hexa-fluoridosilicate) icosa-hydrate. | 2008 May 10 |
|
| Differentiation between [1,2,4]triazolo[1,5-a] pyrimidine and [1,2,4]triazolo[4,3-a]-pyrimidine regioisomers by 1H-15N HMBC experiments. | 2010 Aug |
|
| Diamino-1,2,4-triazole derivatives are selective inhibitors of TYK2 and JAK1 over JAK2 and JAK3. | 2010 Dec 15 |
|
| Metal based biologically active compounds: design, synthesis, and antibacterial/antifungal/cytotoxic properties of triazole-derived Schiff bases and their oxovanadium(IV) complexes. | 2010 Jul |
|
| 3,5-Diamino-1-phenyl-1,2,4-triazolium bromide. | 2010 Jun 16 |
|
| Bis[bis-(3,5-diamino-1H-1,2,4-triazol-4-ium)copper(I)] tris-(hexa-fluoridosilicate). | 2010 Oct 23 |
|
| A carbon-supported copper complex of 3,5-diamino-1,2,4-triazole as a cathode catalyst for alkaline fuel cell applications. | 2010 Sep 8 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C272
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID0025367
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
166592
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
167392
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
I01TWM5267
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
215-937-2
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
167391
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
C531
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
15078
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
1895
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
75425
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
D006144
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY | |||
|
1455-77-2
Created by
admin on Sat Dec 16 20:08:49 UTC 2023 , Edited by admin on Sat Dec 16 20:08:49 UTC 2023
|
PRIMARY |
ACTIVE MOIETY
