Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H4N6 |
| Molecular Weight | 136.1148 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC=NC2=C1NN=N2
InChI
InChIKey=HRYKDUPGBWLLHO-UHFFFAOYSA-N
InChI=1S/C4H4N6/c5-3-2-4(7-1-6-3)9-10-8-2/h1H,(H3,5,6,7,8,9,10)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Structure-activity relationships for the binding of ligands to xanthine or guanine phosphoribosyl-transferase from Toxoplasma gondii. | 1995 Nov 9 |
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| New 2-(2'-phenyl-9'-benzyl-8'-azapurin-6'-ylamino)-carboxylic acid methylesters as ligands for A1 adenosine receptors. | 2001 Dec |
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| Novel carbocyclic nucleosides containing a cyclobutyl ring: adenosine analogues. | 2001 Sep |
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| Erythro- and threo-2-hydroxynonyl substituted 2-phenyladenines and 2-phenyl-8-azaadenines: ligands for A1 adenosine receptors and adenosine deaminase. | 2002 Mar |
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| The yeast ISN1 (YOR155c) gene encodes a new type of IMP-specific 5'-nucleotidase. | 2003 May 7 |
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| N6-cycloalkyl-2-phenyl-3-deaza-8-azaadenines: a new class of A1 adenosine receptor ligands. A comparison with the corresponding adenines and 8-azaadenines. | 2003 Nov-Dec |
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| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005 Jun |
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| Arabidopsis eIF2alpha kinase GCN2 is essential for growth in stress conditions and is activated by wounding. | 2008 Dec 24 |
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| QSAR study on a novel series of 8-azaadenine analogues proposed as A1 adenosine receptor antagonists. | 2008 Jan |
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| A QSAR study for modeling of 8-azaadenine analogues proposed as A1 adenosine receptor antagonists using genetic algorithm coupling adaptive neuro-fuzzy inference system (ANFIS). | 2010 |
Patents
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| Code System | Code | Type | Description | ||
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70746
Created by
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77751
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DTXSID0061537
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WPP3R9U93J
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214-375-5
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32797
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1123-54-2
Created by
admin on Fri Dec 15 16:41:35 GMT 2023 , Edited by admin on Fri Dec 15 16:41:35 GMT 2023
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SUBSTANCE RECORD
