Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H14N6O5 |
| Molecular Weight | 298.2554 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC2=C(N=C(N)NC2=O)N1[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O
InChI
InChIKey=FNXPTCITVCRFRK-UMMCILCDSA-N
InChI=1S/C10H14N6O5/c11-9-14-6-3(7(20)15-9)13-10(12)16(6)8-5(19)4(18)2(1-17)21-8/h2,4-5,8,17-19H,1H2,(H2,12,13)(H3,11,14,15,20)/t2-,4-,5-,8-/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 8-Aminoguanosine Exerts Diuretic, Natriuretic, and Glucosuric Activity via Conversion to 8-Aminoguanine, Yet Has Direct Antikaliuretic Effects. | 2017-12 |
|
| 8-Aminoguanosine and 8-Aminoguanine Exert Diuretic, Natriuretic, Glucosuric, and Antihypertensive Activity. | 2016-12 |
|
| Inhibitors of human purine nucleoside phosphorylase. Synthesis of pyrrolo[3,2-d]pyrimidines, a new class of purine nucleoside phosphorylase inhibitors as potentially T-cell selective immunosuppressive agents. Description of 2,6-diamino-3,5-dihydro-7-(3-thienylmethyl)-4H-pyrrolo[3,2-d] pyrimidin-4-one. | 1992-05-01 |
|
| Synthesis of 8-amino-3-deazaguanine via imidazole precursors. Antitumor activity and inhibition of purine nucleoside phosphorylase. | 1986-10 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
90390
Created by
admin on Mon Mar 31 19:08:42 GMT 2025 , Edited by admin on Mon Mar 31 19:08:42 GMT 2025
|
PRIMARY | |||
|
SHO2CA1BRO
Created by
admin on Mon Mar 31 19:08:42 GMT 2025 , Edited by admin on Mon Mar 31 19:08:42 GMT 2025
|
PRIMARY | |||
|
DTXSID10959515
Created by
admin on Mon Mar 31 19:08:42 GMT 2025 , Edited by admin on Mon Mar 31 19:08:42 GMT 2025
|
PRIMARY | |||
|
135518164
Created by
admin on Mon Mar 31 19:08:42 GMT 2025 , Edited by admin on Mon Mar 31 19:08:42 GMT 2025
|
PRIMARY | |||
|
3868-32-4
Created by
admin on Mon Mar 31 19:08:42 GMT 2025 , Edited by admin on Mon Mar 31 19:08:42 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
