CHEBI:75425 - guanazole

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ChEBI Name guanazole
ChEBI ID CHEBI:75425
Definition An aromatic amine that is 1,2,4-triazole substituted at positions 3 and 5 by amino groups.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C2H5N5
Net Charge 0
Average Mass 99.09460
Monoisotopic Mass 99.05450
InChI InChI=1S/C2H5N5/c3-1-5-2(4)7-6-1/h(H5,3,4,5,6,7)
InChIKey PKWIYNIDEDLDCJ-UHFFFAOYSA-N
SMILES Nc1n[nH]c(N)n1
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): EC 1.17.4.1 (ribonucleoside-diphosphate reductase) inhibitor
An EC 1.17.* (oxidoreductase acting on CH or CH2) inhibitor that inhibits the action of ribonucleoside-diphosphate reductase (EC 1.17.4.1).
DNA synthesis inhibitor
Any substance that inhibits the synthesis of DNA.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing guanazole (CHEBI:75425) has role antineoplastic agent (CHEBI:35610)
guanazole (CHEBI:75425) has role DNA synthesis inhibitor (CHEBI:59517)
guanazole (CHEBI:75425) has role EC 1.17.4.1 (ribonucleoside-diphosphate reductase) inhibitor (CHEBI:74213)
guanazole (CHEBI:75425) is a aromatic amine (CHEBI:33860)
guanazole (CHEBI:75425) is a triazoles (CHEBI:35727)
IUPAC Name
1H-1,2,4-triazole-3,5-diamine
Synonyms Sources
3,5-Diamino-1,2,4-triazole ChemIDplus
3,5-Diamino-1H-1,2,4-triazole NIST Chemistry WebBook
3,5-Diamino-s-triazole ChemIDplus
Registry Numbers Types Sources
112467 Reaxys Registry Number Reaxys
1455-77-2 CAS Registry Number NIST Chemistry WebBook
1455-77-2 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
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Last Modified
02 September 2013