CHEBI:16244 - 4-(trimethylammonio)butanoate

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ChEBI Name 4-(trimethylammonio)butanoate ChEBI ID CHEBI:16244 Definition An amino-acid betaine γ-aminobutyric acid zwitterion in which all of the hydrogens attached to the nitrogen are replaced by methyl groups. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:20484, CHEBI:12047 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C7H15NO2 Net Charge 0 Average Mass 145.19954 Monoisotopic Mass 145.11028 InChI InChI=1S/C7H15NO2/c1-8(2,3)6-4-5-7(9)10/h4-6H2,1-3H3 InChIKey JHPNVNIEXXLNTR-UHFFFAOYSA-N SMILES C[N+](C)(C)CCCC([O-])=O Metabolite of Species Details Escherichia coli (NCBI:txid562) See: PubMed Homo sapiens (NCBI:txid9606) See: DOI Roles Classification Biological Role(s): human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). Escherichia coli metabolite Any bacterial metabolite produced during a metabolic reaction in Escherichia coli. View more via ChEBI Ontology ChEBI Ontology Outgoing 4-(trimethylammonio)butanoate (CHEBI:16244) has functional parent γ-aminobutyrate (CHEBI:30566) 4-(trimethylammonio)butanoate (CHEBI:16244) has functional parent γ-aminobutyric acid zwitterion (CHEBI:59888) 4-(trimethylammonio)butanoate (CHEBI:16244) has role Escherichia coli metabolite (CHEBI:76971) 4-(trimethylammonio)butanoate (CHEBI:16244) has role human metabolite (CHEBI:77746) 4-(trimethylammonio)butanoate (CHEBI:16244) is a amino-acid betaine (CHEBI:22860) 4-(trimethylammonio)butanoate (CHEBI:16244) is conjugate base of 4-(trimethylammonio)butanoic acid (CHEBI:1941) Incoming 4-(trimethylammonio)butanoic acid (CHEBI:1941) is conjugate acid of 4-(trimethylammonio)butanoate (CHEBI:16244) IUPAC Name 4-(trimethylammonio)butanoate Synonyms Sources 3-Dehydroxycarnitine HMDB 4-(N-trimethylamino)butyrate ChemIDplus 4-(trimethylamino)butanoate UniProt 4-butyrobetaine ChemIDplus Actinine ChemIDplus butyrobetaine ChemIDplus deoxycarnitine ChemIDplus γ-Butyrobetain ChemIDplus γ-butyrobetaine ChemIDplus Manual Xrefs Databases ECMDB21336 ECMDB GAMMA-BUTYROBETAINE MetaCyc HMDB0006831 HMDB View more database links Registry Numbers Types Sources 3538300 Reaxys Registry Number Reaxys 3538300 Beilstein Registry Number Beilstein 407-64-7 CAS Registry Number ChemIDplus Citations Types Sources 3148329 PubMed citation Europe PMC 398096 PubMed citation Europe PMC Last Modified 22 December 2016