CHEBI:421840 - O-methylsalicylic acid

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ChEBI Name O-methylsalicylic acid
ChEBI ASCII Name O-methylsalicylic acid
Definition A methoxybenzoic acid that is the methyl ether of salicylic acid.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C8H8O3
Net Charge 0
Average Mass 152.14730
Monoisotopic Mass 152.04734
InChI InChI=1S/C8H8O3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3,(H,9,10)
SMILES COc1ccccc1C(O)=O
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): flavouring agent
A food additive that is used to added improve the taste or odour of a food.
Application(s): flavouring agent
A food additive that is used to added improve the taste or odour of a food.
non-steroidal anti-inflammatory drug
An anti-inflammatory drug that is not a steroid. In addition to anti-inflammatory actions, non-steroidal anti-inflammatory drugs have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins.
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ChEBI Ontology
Outgoing O-methylsalicylic acid (CHEBI:421840) has role flavouring agent (CHEBI:35617)
O-methylsalicylic acid (CHEBI:421840) has role non-steroidal anti-inflammatory drug (CHEBI:35475)
O-methylsalicylic acid (CHEBI:421840) is a methoxybenzoic acid (CHEBI:25238)
O-methylsalicylic acid (CHEBI:421840) is conjugate acid of O-methylsalicylate (CHEBI:59128)
Incoming cyprosulfamide (CHEBI:132270) has functional parent O-methylsalicylic acid (CHEBI:421840)
O-methylsalicylate (CHEBI:59128) is conjugate base of O-methylsalicylic acid (CHEBI:421840)
2-methoxybenzoic acid
Synonyms Sources
2-Anisic acid ChemIDplus
2-Methoxy-benzoic acid ChEMBL
o-anisic acid ChEBI
o-Methoxybenzoic acid ChemIDplus
ortho-methoxybenzoic acid ChEBI
Salicylic acid methyl ether ChemIDplus
Manual Xrefs Databases
2-Methoxybenzoic_acid Wikipedia
HMDB0032604 HMDB
O-Methoxybenzoic_acid Wikipedia
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Registry Numbers Types Sources
509929 Beilstein Registry Number Beilstein
509929 Reaxys Registry Number Reaxys
579-75-9 CAS Registry Number NIST Chemistry WebBook
579-75-9 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
1650428 PubMed citation Europe PMC
19812218 PubMed citation Europe PMC
3425858 PubMed citation Europe PMC
9252874 PubMed citation Europe PMC
Last Modified
22 June 2016