Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C8H15N4O14P3 |
| Molecular Weight | 484.1444 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)C1=NN(C=N1)[C@@H]2O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]2O
InChI
InChIKey=MMJOCKKLRMRSEQ-AFCXAGJDSA-N
InChI=1S/C8H15N4O14P3/c9-6(15)7-10-2-12(11-7)8-5(14)4(13)3(24-8)1-23-28(19,20)26-29(21,22)25-27(16,17)18/h2-5,8,13-14H,1H2,(H2,9,15)(H,19,20)(H,21,22)(H2,16,17,18)/t3-,4-,5-,8-/m1/s1
| Molecular Formula | C8H15N4O14P3 |
| Molecular Weight | 484.1444 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:48:17 GMT 2025
by
admin
on
Mon Mar 31 22:48:17 GMT 2025
|
| Record UNII |
XA6L2VRY2M
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
63142-71-2
Created by
admin on Mon Mar 31 22:48:17 GMT 2025 , Edited by admin on Mon Mar 31 22:48:17 GMT 2025
|
PRIMARY | |||
|
45578
Created by
admin on Mon Mar 31 22:48:17 GMT 2025 , Edited by admin on Mon Mar 31 22:48:17 GMT 2025
|
PRIMARY | |||
|
122108
Created by
admin on Mon Mar 31 22:48:17 GMT 2025 , Edited by admin on Mon Mar 31 22:48:17 GMT 2025
|
PRIMARY | |||
|
XA6L2VRY2M
Created by
admin on Mon Mar 31 22:48:17 GMT 2025 , Edited by admin on Mon Mar 31 22:48:17 GMT 2025
|
PRIMARY | |||
|
DTXSID10212490
Created by
admin on Mon Mar 31 22:48:17 GMT 2025 , Edited by admin on Mon Mar 31 22:48:17 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
METABOLITE -> PARENT |
a degradative pathway involving deribosylation and amide hydrolysis to yield a triazole carboxylic acid metabolite; excreted renally.
|
||
|
PARENT -> METABOLITE |