CHEBI:77751 - 8-azaadenine

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ChEBI Name 8-azaadenine
ChEBI ID CHEBI:77751
Definition A triazolopyrimidine that is [1,2,3]triazolo[4,5-d]pyrimidine bearing an amino substituent at position 7.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C4H4N6
Net Charge 0
Average Mass 136.11480
Monoisotopic Mass 136.04974
InChI InChI=1S/C4H4N6/c5-3-2-4(7-1-6-3)9-10-8-2/h1H,(H3,5,6,7,8,9,10)
InChIKey HRYKDUPGBWLLHO-UHFFFAOYSA-N
SMILES Nc1ncnc2[nH]nnc12
Metabolite of Species Details
Mycoplasma genitalium (NCBI:txid2097) See: PubMed
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): Mycoplasma genitalium metabolite
Any bacterial metabolite produced during a metabolic reaction in Mycoplasma genitalium.
EC 1.17.3.2 (xanthine oxidase) inhibitor
An EC 1.17.3.* (oxidoreductase acting on CH or CH2 with oxygen as acceptor) inhibitor that interferes with the action of xanthine oxidase (EC 1.17.3.2).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 8-azaadenine (CHEBI:77751) has role Mycoplasma genitalium metabolite (CHEBI:131604)
8-azaadenine (CHEBI:77751) has role EC 1.17.3.2 (xanthine oxidase) inhibitor (CHEBI:35634)
8-azaadenine (CHEBI:77751) is a aromatic amine (CHEBI:33860)
8-azaadenine (CHEBI:77751) is a nucleobase analogue (CHEBI:67142)
8-azaadenine (CHEBI:77751) is a triazolopyrimidines (CHEBI:48435)
Incoming 8-aza-2'-deoxyadenosine 5'-monophosphate (CHEBI:102466) has functional parent 8-azaadenine (CHEBI:77751)
IUPAC Name
1H-[1,2,3]triazolo[4,5-d]pyrimidin-7-amine
Synonyms Sources
1H-1,2,3-Triazolo[4,5-d]pyrimidin-7-amine NIST Chemistry WebBook
1H-v-Triazolo(4,5-d)pyrimidin-7-amine NIST Chemistry WebBook
3H-N-Triazolo(4,5-d)pyrimidin-7-amine ChemIDplus
6-Amino-8-azapurine ChemIDplus
7-Amino-1-v-triazolo(d)pyrimidine ChemIDplus
7-Amino-1H-v-triazolo(4,5-d)pyrimidine ChemIDplus
7-Amino-v-triazolo(d)pyrimidine ChemIDplus
Registry Numbers Types Sources
1123-54-2 CAS Registry Number ChemIDplus
1123-54-2 CAS Registry Number NIST Chemistry WebBook
609432 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
17361728 PubMed citation Europe PMC
22817898 PubMed citation Europe PMC
23148644 PubMed citation Europe PMC
23623927 PubMed citation Europe PMC
24557725 PubMed citation Europe PMC
Last Modified
04 April 2016