CHEBI:81724 - diminazene

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ChEBI Name diminazene
ChEBI ID CHEBI:81724
Definition A triazene derivative that is triazene in which each of the terminal nitrogens is substituted by a 4-carbamimidoylphenyl group.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C14H15N7
Net Charge 0
Average Mass 281.31580
Monoisotopic Mass 281.13889
InChI InChI=1S/C14H15N7/c15-13(16)9-1-5-11(6-2-9)19-21-20-12-7-3-10(4-8-12)14(17)18/h1-8H,(H3,15,16)(H3,17,18)(H,19,20)
InChIKey XNYZHCFCZNMTFY-UHFFFAOYSA-N
SMILES NC(=N)c1ccc(NN=Nc2ccc(cc2)C(N)=N)cc1
Roles Classification
Biological Role(s): trypanocidal drug
A drug used to treat or prevent infections caused by protozoal organisms belonging to the suborder Trypanosomatida.
Application(s): antiparasitic agent
A substance used to treat or prevent parasitic infections.
trypanocidal drug
A drug used to treat or prevent infections caused by protozoal organisms belonging to the suborder Trypanosomatida.
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ChEBI Ontology
Outgoing diminazene (CHEBI:81724) has role antiparasitic agent (CHEBI:35442)
diminazene (CHEBI:81724) has role trypanocidal drug (CHEBI:36335)
diminazene (CHEBI:81724) is a carboxamidine (CHEBI:35359)
diminazene (CHEBI:81724) is a triazene derivative (CHEBI:72573)
diminazene (CHEBI:81724) is conjugate base of diminazene(2+) (CHEBI:82614)
Incoming diminazene(2+) (CHEBI:82614) is conjugate acid of diminazene (CHEBI:81724)
IUPAC Name
4,4'-triaz-1-ene-1,3-diyldibenzenecarboximidamide
INNs Sources
diminazène WHO MedNet
diminazene ChemIDplus
diminazeno ChemIDplus
diminazenum ChemIDplus
Synonym Source
4,4'-(1-triazene-1,3-diyl)bis-benzenecarboximidamide ChemIDplus
Manual Xrefs Databases
BRN PDBeChem
C18388 KEGG COMPOUND
DB03608 DrugBank
Diminazen Wikipedia
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Registry Numbers Types Sources
3153756 Reaxys Registry Number Reaxys
536-71-0 CAS Registry Number KEGG COMPOUND
536-71-0 CAS Registry Number ChemIDplus
5757660 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
24533295 PubMed citation Europe PMC
7902657 PubMed citation Europe PMC
Last Modified
05 August 2014