ChEBI Name 3-methyladenine
ChEBI ID CHEBI:38635
Definition A methyladenine that is adenine substituted with a methyl group at position N-3.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:40596, CHEBI:1590, CHEBI:21828
Supplier Information
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Formula C6H7N5
Net Charge 0
Average Mass 149.15348
Monoisotopic Mass 149.07015
InChI InChI=1S/C6H7N5/c1-11-3-10-5(7)4-6(11)9-2-8-4/h2-3H,7H2,1H3
InChIKey FSASIHFSFGAIJM-UHFFFAOYSA-N
SMILES Cn1cnc(N)c2ncnc12
Roles Classification
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
autophagy inhibitor
Any compound that inhibits the process of autophagy (the self-digestion of one or more components of a cell through the action of enzymes originating within the same cell).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 3-methyladenine (CHEBI:38635) has role autophagy inhibitor (CHEBI:88230)
3-methyladenine (CHEBI:38635) has role human metabolite (CHEBI:77746)
3-methyladenine (CHEBI:38635) is a methyladenine (CHEBI:25272)
IUPAC Names
3-methyl-3H-purin-6-amine
3-methyladenine
Synonyms Sources
3-methyl-3H-adenine ChemIDplus
3-METHYL-3H-PURIN-6-YLAMINE PDBeChem
3-Methyladenine KEGG COMPOUND
6-amino-3-methylpurine NIST Chemistry WebBook
Manual Xrefs Databases
3-Methyl-Adenines MetaCyc
ADK PDBeChem
C00913 KEGG COMPOUND
DB04104 DrugBank
HMDB0011600 HMDB
LSM-4733 LINCS
View more database links
Registry Numbers Types Sources
146087 Reaxys Registry Number Reaxys
146087 Beilstein Registry Number Beilstein
279109 Gmelin Registry Number Gmelin
5142-23-4 CAS Registry Number ChemIDplus
5142-23-4 CAS Registry Number ChemIDplus
5142-23-4 CAS Registry Number NIST Chemistry WebBook
6503822 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
16139832 PubMed citation Europe PMC
22770225 PubMed citation Europe PMC
23819759 PubMed citation Europe PMC
24297644 PubMed citation Europe PMC
24830781 PubMed citation Europe PMC
25708950 PubMed citation Europe PMC
Last Modified
25 February 2016
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