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| Formula | C5H6N6 |
| Net Charge | 0 |
| Average Mass | 150.145 |
| Monoisotopic Mass | 150.06539 |
| SMILES | Nc1nc(N)c2ncnc2n1 |
| InChI | InChI=1S/C5H6N6/c6-3-2-4(9-1-8-2)11-5(7)10-3/h1H,(H5,6,7,8,9,10,11) |
| InChIKey | MSSXOMSJDRHRMC-UHFFFAOYSA-N |
| Wikipedia |
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| Roles Classification |
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| Chemical Role: | Bronsted base A molecular entity capable of accepting a hydron from a donor (Brønsted acid). |
| Application: | antineoplastic agent A substance that inhibits or prevents the proliferation of neoplasms. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| 9H-purine-2,6-diamine (CHEBI:40235) has functional parent adenine (CHEBI:16708) |
| 9H-purine-2,6-diamine (CHEBI:40235) has role antineoplastic agent (CHEBI:35610) |
| 9H-purine-2,6-diamine (CHEBI:40235) is a 2,6-diaminopurines (CHEBI:38001) |
| 9H-purine-2,6-diamine (CHEBI:40235) is a primary amino compound (CHEBI:50994) |
| Incoming Relation(s) |
| reversine (CHEBI:70723) has functional parent 9H-purine-2,6-diamine (CHEBI:40235) |
| Synonyms | Source |
|---|---|
| 9H-PURINE-2,6-DIAMINE | PDBeChem |
| 9H-purine-2,6-diamine | PDBeChem |
| 2,6-DIAMINOPURINE | PDBeChem |
| 2,6-diaminopurine | ChEBI |
| 2-aminoadenine | ChemIDplus |
| UniProt Name | Source |
|---|---|
| 2,6-diaminopurine | UniProt |
| Manual Xrefs | Databases |
|---|---|
| 6AP | PDBeChem |
| 2,6-Diaminopurine | Wikipedia |
| CPD0-2060 | MetaCyc |
| Registry Numbers | Sources |
|---|---|
| Reaxys:745238 | Reaxys |
| CAS:1904-98-9 | ChemIDplus |
| Citations |
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