Record Information
Version1.0
Creation Date2016-09-30 22:32:28 UTC
Update Date2020-04-22 15:04:05 UTC
BMDB IDBMDB0000542
Secondary Accession Numbers
  • BMDB00542
Metabolite Identification
Common Name8-Hydroxyadenine
Description8-Hydroxyadenine, also known as 8-oxoa or 6-amino-purin-8-ol, belongs to the class of organic compounds known as purinones. These are purines in which the purine moiety bears a C=O group. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring. Based on a literature review a significant number of articles have been published on 8-Hydroxyadenine.
Structure
Thumb
Synonyms
ValueSource
7,8-Dihydro-8-oxoadenineChEBI
8-oxo-7,8-DihydroadenineChEBI
8-OxoAChEBI
OxyadenineChEBI
6-Amino-1,7-dihydro-8H-purin-8-oneHMDB
6-Amino-8-hydroxypurineHMDB
6-Amino-purin-8(9H)-oneHMDB
6-Amino-purin-8-olHMDB
8-Hydroxy-1H-purin-6-amineHMDB
8-OxoadenineHMDB
OksadenHMDB
OxadenHMDB
7,8-DHOAHMDB
Chemical FormulaC5H5N5O
Average Molecular Weight151.1261
Monoisotopic Molecular Weight151.049409807
IUPAC Name6-amino-7H-purin-8-ol
Traditional Name6-amino-8-hydroxypurine
CAS Registry Number21149-26-8
SMILES
NC1=NC=NC2=C1NC(O)=N2
InChI Identifier
InChI=1S/C5H5N5O/c6-3-2-4(8-1-7-3)10-5(11)9-2/h1H,(H4,6,7,8,9,10,11)
InChI KeyRGKBRPAAQSHTED-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as purinones. These are purines in which the purine moiety bears a C=O group. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassImidazopyrimidines
Sub ClassPurines and purine derivatives
Direct ParentPurinones
Alternative Parents
Substituents
  • 6-aminopurine
  • Purinone
  • Aminopyrimidine
  • Pyrimidine
  • Imidolactam
  • Azole
  • Imidazole
  • Heteroaromatic compound
  • Urea
  • Azacycle
  • Organic oxide
  • Organopnictogen compound
  • Primary amine
  • Organooxygen compound
  • Organonitrogen compound
  • Amine
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Organic oxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cytoplasm
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-0.82ALOGPS
logP-0.19ChemAxon
logS-1.4ALOGPS
pKa (Strongest Acidic)8.89ChemAxon
pKa (Strongest Basic)5.11ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area100.71 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity39.67 m³·mol⁻¹ChemAxon
Polarizability13.45 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular Locations
  • Cytoplasm
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0000542
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB022105
KNApSAcK IDC00043227
Chemspider ID4511108
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN ID5527
PubChem Compound95215
PDB IDNot Available
ChEBI ID134104
References
Synthesis ReferenceMakarieva, Tatyana N.; Guzii, Alla G.; Dmitrenok, Andrei S.; Dmitrenok, Pavel S.; Krasokhin, Vladimir B.; Stonik, Valentin A. 8-Oxoadenine, 9-methyl-8-oxoadenine, and trihydroxylated sterols from a Far Eastern thorectidae sponge. Natural Product Communications (2006), 1(9), 711-714.
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available