CHEBI:30794 - malonic acid

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ChEBI Name malonic acid ChEBI ID CHEBI:30794 Definition An α,ω-dicarboxylic acid in which the two carboxy groups are separated by a single methylene group. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:44060, CHEBI:6660, CHEBI:25132 Supplier Information ChemicalBook:CB5323625, eMolecules:530468, ZINC000169743014 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Malonic acid is a dicarboxylic acid with structure CH2(COOH)2. The ionized form of malonic acid, as well as its esters and salts, are known as malonates. For example, diethyl malonate is malonic acid's diethyl ester. The name originates from the Greek word μᾶλον (malon) meaning 'apple'. Read full article at Wikipedia Formula C3H4O4 Net Charge 0 Average Mass 104.06146 Monoisotopic Mass 104.01096 InChI InChI=1S/C3H4O4/c4-2(5)1-3(6)7/h1H2,(H,4,5)(H,6,7) InChIKey OFOBLEOULBTSOW-UHFFFAOYSA-N SMILES OC(=O)CC(O)=O Metabolite of Species Details Homo sapiens (NCBI:txid9606) See: DOI 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): human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing malonic acid (CHEBI:30794) has role human metabolite (CHEBI:77746) malonic acid (CHEBI:30794) is a α,ω-dicarboxylic acid (CHEBI:28383) malonic acid (CHEBI:30794) is conjugate acid of malonate(1−) (CHEBI:30795) Incoming 3-(benzyloxy)-3-oxopropanoic acid (CHEBI:84093) has functional parent malonic acid (CHEBI:30794) 3-oxo-3-ureidopropanoic acid (CHEBI:49049) has functional parent malonic acid (CHEBI:30794) N-malonyltryptophan (CHEBI:142268) has functional parent malonic acid (CHEBI:30794) O-malonyl-D-carnitine (CHEBI:86047) has functional parent malonic acid (CHEBI:30794) O-malonyl-L-carnitine (CHEBI:85470) has functional parent malonic acid (CHEBI:30794) O-malonylcarnitine (CHEBI:73028) has functional parent malonic acid (CHEBI:30794) S-malonyl-4'-phosphopantetheine (CHEBI:132976) has functional parent malonic acid (CHEBI:30794) aminomalonic acid (CHEBI:17475) has functional parent malonic acid (CHEBI:30794) bumadizone (CHEBI:76119) has functional parent malonic acid (CHEBI:30794) elesclomol (CHEBI:79369) has functional parent malonic acid (CHEBI:30794) ethylmalonic acid (CHEBI:741548) has functional parent malonic acid (CHEBI:30794) heptylmalonic acid (CHEBI:70747) has functional parent malonic acid (CHEBI:30794) hydroxymalonic acid (CHEBI:16513) has functional parent malonic acid (CHEBI:30794) isoprothiolane (CHEBI:6047) has functional parent malonic acid (CHEBI:30794) malonamide (CHEBI:48537) has functional parent malonic acid (CHEBI:30794) malonate ester (CHEBI:38083) has functional parent malonic acid (CHEBI:30794) malonyl-CoA methyl ester (CHEBI:71244) has functional parent malonic acid (CHEBI:30794) methylmalonic acid (CHEBI:30860) has functional parent malonic acid (CHEBI:30794) oxomalonic acid (CHEBI:30842) has functional parent malonic acid (CHEBI:30794) malonate(1−) (CHEBI:30795) is conjugate base of malonic acid (CHEBI:30794) carboxyacetyl group (CHEBI:50650) is substituent group from malonic acid (CHEBI:30794) malonyl group (CHEBI:25134) is substituent group from malonic acid (CHEBI:30794) IUPAC Name propanedioic acid Synonyms Sources H2malo IUPAC HOOC‒CH2‒COOH IUPAC Malonic acid KEGG COMPOUND MALONIC ACID PDBeChem Propanedioic acid KEGG COMPOUND Manual Xrefs Databases C00001193 KNApSAcK C00383 KEGG COMPOUND DB02175 DrugBank HMDB0000691 HMDB LMFA01170041 LIPID MAPS MALONATE MetaCyc Malonic_acid Wikipedia MLA PDBeChem View more database links Registry Numbers Types Sources 141-82-2 CAS Registry Number KEGG COMPOUND 141-82-2 CAS Registry Number ChemIDplus 141-82-2 CAS Registry Number NIST Chemistry WebBook 1751370 Reaxys Registry Number Reaxys 2550 Gmelin Registry Number Gmelin Citation Last Modified 18 April 2024