EMBL-EBI | Chemical Biology | ChEBI
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| Formula | CH5N3O |
| Net Charge | 0 |
| Average Mass | 75.071 |
| Monoisotopic Mass | 75.04326 |
| SMILES | N=C(N)NO |
| InChI | InChI=1S/CH5N3O/c2-1(3)4-5/h5H,(H4,2,3,4) |
| InChIKey | WFBHRSAKANVBKH-UHFFFAOYSA-N |
| Roles Classification |
|---|
| Biological Role: | antiviral agent A substance that destroys or inhibits replication of viruses. |
| Application: | antineoplastic agent A substance that inhibits or prevents the proliferation of neoplasms. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| N-hydroxyguanidine (CHEBI:43089) has functional parent carbamimidoylazanium (CHEBI:616459) |
| N-hydroxyguanidine (CHEBI:43089) has functional parent guanidine (CHEBI:42820) |
| N-hydroxyguanidine (CHEBI:43089) has role antineoplastic agent (CHEBI:35610) |
| N-hydroxyguanidine (CHEBI:43089) has role antiviral agent (CHEBI:22587) |
| N-hydroxyguanidine (CHEBI:43089) is a guanidines (CHEBI:24436) |
| N-hydroxyguanidine (CHEBI:43089) is a one-carbon compound (CHEBI:64708) |
| N-hydroxyguanidine (CHEBI:43089) is conjugate base of N-hydroxyguanidinium (CHEBI:194307) |
| Incoming Relation(s) |
| N-hydroxyguanidinium (CHEBI:194307) is conjugate acid of N-hydroxyguanidine (CHEBI:43089) |
| IUPAC Name |
|---|
| 1-hydroxyguanidine |
| Synonyms | Source |
|---|---|
| N-hydroxy-guanidine | ChEBI |
| hydroxyguanidine | ChemIDplus |
| N''-hydroxyguanidine | ChEBI |
| Registry Numbers | Sources |
|---|---|
| Reaxys:1741719 | Reaxys |
| CAS:13115-21-4 | ChemIDplus |
| Citations |
|---|