CHEBI:10432 - 2-naphthol

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ChEBI Name 2-naphthol
ChEBI ID CHEBI:10432
Definition A naphthol carrying a hydroxy group at position 2.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C10H8O
Net Charge 0
Average Mass 144.173
Monoisotopic Mass 144.05751
InChI InChI=1S/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H
InChIKey JWAZRIHNYRIHIV-UHFFFAOYSA-N
SMILES OC1=CC2=CC=CC=C2C=C1
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Homo sapiens (NCBI:txid9606) Found in urine (BTO:0001419). See: PubMed
Roles Classification
Chemical Role(s): radical scavenger
A role played by a substance that can react readily with, and thereby eliminate, radicals.
Biological Role(s): genotoxin
A role played by a chemical compound to induce direct or indirect DNA damage. Such damage can potentially lead to the formation of a malignant tumour, but DNA damage does not lead inevitably to the creation of cancerous cells.
human xenobiotic metabolite
Any human metabolite produced by metabolism of a xenobiotic compound in humans.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
human urinary metabolite
Any metabolite (endogenous or exogenous) found in human urine samples.
Application(s): antinematodal drug
A substance used in the treatment or control of nematode infestations.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-naphthol (CHEBI:10432) has role antinematodal drug (CHEBI:35444)
2-naphthol (CHEBI:10432) has role genotoxin (CHEBI:50902)
2-naphthol (CHEBI:10432) has role human urinary metabolite (CHEBI:84087)
2-naphthol (CHEBI:10432) has role human xenobiotic metabolite (CHEBI:76967)
2-naphthol (CHEBI:10432) has role mouse metabolite (CHEBI:75771)
2-naphthol (CHEBI:10432) has role radical scavenger (CHEBI:48578)
2-naphthol (CHEBI:10432) is a naphthol (CHEBI:35682)
Incoming β-naphthyl N-acetylphenylalaninate (CHEBI:7219) has functional parent 2-naphthol (CHEBI:10432)
2-naphthyl α-D-glucoside (CHEBI:90256) has functional parent 2-naphthol (CHEBI:10432)
2-naphthyl α-L-fucoside (CHEBI:90252) has functional parent 2-naphthol (CHEBI:10432)
2-naphthyl β-D-galactoside (CHEBI:90140) has functional parent 2-naphthol (CHEBI:10432)
2-naphthyl β-D-glucoside (CHEBI:90258) has functional parent 2-naphthol (CHEBI:10432)
2-naphthyl β-L-fucoside (CHEBI:90254) has functional parent 2-naphthol (CHEBI:10432)
2-naphthyl butyrate (CHEBI:90150) has functional parent 2-naphthol (CHEBI:10432)
2-naphthyl dihydrogen phosphate (CHEBI:91043) has functional parent 2-naphthol (CHEBI:10432)
2-naphthyl octanoate (CHEBI:90250) has functional parent 2-naphthol (CHEBI:10432)
2-naphthyl sulfate (CHEBI:167215) has functional parent 2-naphthol (CHEBI:10432)
2-naphthyl tetradecanoate (CHEBI:90249) has functional parent 2-naphthol (CHEBI:10432)
4-amino-3-hydroxynaphthalene-1-sulfonic acid (CHEBI:19024) has functional parent 2-naphthol (CHEBI:10432)
6-bromo-2-naphthol (CHEBI:34466) has functional parent 2-naphthol (CHEBI:10432)
Oil red O (CHEBI:88213) has functional parent 2-naphthol (CHEBI:10432)
Sudan I (CHEBI:30958) has functional parent 2-naphthol (CHEBI:10432)
Sudan III (CHEBI:82535) has functional parent 2-naphthol (CHEBI:10432)
Sudan IV (CHEBI:88014) has functional parent 2-naphthol (CHEBI:10432)
tolnaftate (CHEBI:9620) has functional parent 2-naphthol (CHEBI:10432)
IUPAC Name
naphthalen-2-ol
Synonyms Sources
2-hydroxynaphthalene HMDB
2-Naftol ChemIDplus
2-naftolo ChemIDplus
2-naphthalenol NIST Chemistry WebBook
2-Naphthol KEGG COMPOUND
2-naphthol UniProt
2-naphtol ChemIDplus
beta-hydroxynaphthalene ChemIDplus
β-hydroxynaphthalene NIST Chemistry WebBook
β-Naftol ChemIDplus
β-naftolo ChemIDplus
beta-Naphthol KEGG COMPOUND
beta-Naphthol KEGG COMPOUND
β-naphthol NIST Chemistry WebBook
β-naphthyl alcohol ChemIDplus
β-naphthyl hydroxide ChemIDplus
β-Naphtol ChemIDplus
Isonaphthol ChemIDplus
Brand Names Sources
Antioxygene BN HMDB
Azogen Developer A HMDB
C.I. Azoic Coupling Component 1 ChemIDplus
C.I. Developer 5 ChemIDplus
Developer A ChemIDplus
Developer AMS ChemIDplus
Developer BN ChemIDplus
Manual Xrefs Databases
03V PDBeChem
2-Naphthol Wikipedia
3370 DrugCentral
C11713 KEGG COMPOUND
CPD-8131 MetaCyc
FDB000877 FooDB
HMDB0012322 HMDB
View more database links
Registry Numbers Types Sources
135-19-3 CAS Registry Number KEGG COMPOUND
135-19-3 CAS Registry Number NIST Chemistry WebBook
135-19-3 CAS Registry Number ChemIDplus
27395 Gmelin Registry Number Gmelin
742134 Reaxys Registry Number Reaxys
742134 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
13386410 PubMed citation Europe PMC
14751800 PubMed citation Europe PMC
18515997 PubMed citation Europe PMC
18856458 PubMed citation Europe PMC
20260560 PubMed citation Europe PMC
22069470 PubMed citation Europe PMC
22740618 PubMed citation Europe PMC
23344974 PubMed citation Europe PMC
29987264 PubMed citation Europe PMC
30572877 PubMed citation Europe PMC
30828382 PubMed citation Europe PMC
32206945 PubMed citation Europe PMC
33862438 PubMed citation Europe PMC
34033865 PubMed citation Europe PMC
Last Modified
08 June 2021