CHEBI:82615 - diminazene diaceturate

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ChEBI Name diminazene diaceturate
ChEBI ID CHEBI:82615
Definition An N-acetylglycinate salt resulting from the reaction of diminazene with 2 mol eq. of N-acetylglycine.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C22H29N9O6
Net Charge 0
Average Mass 515.52240
Monoisotopic Mass 515.22408
InChI InChI=1S/C14H15N7.2C4H7NO3/c15-13(16)9-1-5-11(6-2-9)19-21-20-12-7-3-10(4-8-12)14(17)18;2*1-3(6)5-2-4(7)8/h1-8H,(H3,15,16)(H3,17,18)(H,19,20);2*2H2,1H3,(H,5,6)(H,7,8)
InChIKey OKQSSSVVBOUMNZ-UHFFFAOYSA-N
SMILES CC(=O)NCC(O)=O.CC(=O)NCC(O)=O.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 diaceturate (CHEBI:82615) has part diminazene(2+) (CHEBI:82614)
diminazene diaceturate (CHEBI:82615) has role antiparasitic agent (CHEBI:35442)
diminazene diaceturate (CHEBI:82615) has role trypanocidal drug (CHEBI:36335)
diminazene diaceturate (CHEBI:82615) is a N-acetylglycinate salt (CHEBI:82616)
Synonyms Sources
(triaz-1-ene-1,3-diyldi-4,1-phenylene)bis(iminomethanaminium) bis(acetamidoacetate) IUPAC
1,3-bis(4-guanylphenyl)triazene diaceturate ChemIDplus
1,3-bis(p-amidinophenyl)triazene bis(N-acetylglycinate) ChemIDplus
4,4'-(diazoamino)dibenzamidine diaceturate ChemIDplus
4,4'-diamidinodiazoaminobenzene diaceturate ChemIDplus
di-(4-amidinophenyl)-triazine-(N-1,3)-diaceturate ChemIDplus
diminazene aceturate ChemIDplus
diminazene bis(N-acetylglycinate) ChEBI
Brand Names Sources
Berenil ChemIDplus
Beronal ChemIDplus
Bevenil ChemIDplus
Ganasag ChemIDplus
Ganaseg ChemIDplus
Manual Xrefs Databases
BRN PDBeChem
DB03608 DrugBank
US2838485 Patent
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Registry Numbers Types Sources
3841323 Reaxys Registry Number Reaxys
908-54-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
23665493 PubMed citation Europe PMC
23959549 PubMed citation Europe PMC
24476993 PubMed citation Europe PMC
24893117 PubMed citation Europe PMC
7902657 PubMed citation Europe PMC
8086477 PubMed citation Europe PMC
Last Modified
05 August 2014