CHEBI:35619 - L-α-aminobutyric acid

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ChEBI Name L-α-aminobutyric acid ChEBI ID CHEBI:35619 ChEBI ASCII Name L-alpha-aminobutyric acid Definition An optically active form of α-aminobutyric acid having L-configuration. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:35723, CHEBI:376, CHEBI:46346, CHEBI:18734 Supplier Information ChemicalBook:CB3741533, eMolecules:476611, ZINC000000901351 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C4H9NO2 Net Charge 0 Average Mass 103.11980 Monoisotopic Mass 103.06333 InChI InChI=1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1 InChIKey QWCKQJZIFLGMSD-VKHMYHEASA-N SMILES CC[C@H](N)C(O)=O Metabolite of Species Details Homo sapiens (NCBI:txid9606) See: DOI Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) 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). (via alpha-aminobutyric acid ) View more via ChEBI Ontology ChEBI Ontology Outgoing L-α-aminobutyric acid (CHEBI:35619) has role human metabolite (CHEBI:77746) L-α-aminobutyric acid (CHEBI:35619) is a α-aminobutyric acid (CHEBI:35621) L-α-aminobutyric acid (CHEBI:35619) is a non-proteinogenic L-α-amino acid (CHEBI:83822) L-α-aminobutyric acid (CHEBI:35619) is conjugate acid of L-2-aminobutyrate (CHEBI:28340) L-α-aminobutyric acid (CHEBI:35619) is enantiomer of D-α-aminobutyric acid (CHEBI:28797) L-α-aminobutyric acid (CHEBI:35619) is tautomer of L-α-aminobutyrate zwitterion (CHEBI:74359) Incoming N-[(2S)-2-aminobutanoyl]glycine (CHEBI:144728) has functional parent L-α-aminobutyric acid (CHEBI:35619) L-2-amino-4-methoxy-cis-but-3-enoic acid (CHEBI:40719) has functional parent L-α-aminobutyric acid (CHEBI:35619) L-2-amino-4-methoxy-trans-but-3-enoic acid (CHEBI:156361) has functional parent L-α-aminobutyric acid (CHEBI:35619) brivaracetam (CHEBI:133013) has functional parent L-α-aminobutyric acid (CHEBI:35619) L-2-aminobutyrate (CHEBI:28340) is conjugate base of L-α-aminobutyric acid (CHEBI:35619) D-α-aminobutyric acid (CHEBI:28797) is enantiomer of L-α-aminobutyric acid (CHEBI:35619) L-α-aminobutyric acid residue (CHEBI:40545) is substituent group from L-α-aminobutyric acid (CHEBI:35619) L-α-aminobutyrate zwitterion (CHEBI:74359) is tautomer of L-α-aminobutyric acid (CHEBI:35619) IUPAC Name (2S)-2-aminobutanoic acid Synonyms Sources (−)-2-aminobutyric acid ChemIDplus (2S)-2-aminobutyric acid ChEBI (S)-2-Aminobutanoate KEGG COMPOUND (S)-2-Aminobutanoic acid KEGG COMPOUND (S)-2-Aminobutyric acid KEGG COMPOUND L-(+)-2-aminobutyric acid ChEBI L-2-Aminobuttersäure ChEBI L-2-aminobutyric acid ChemIDplus L-α-amino-n-butyric acid NIST Chemistry WebBook L-α-aminobutyric acid NIST Chemistry WebBook L-butyrine ChemIDplus S-Butyrine HMDB Manual Xrefs Databases AA0409 RESID ABA PDBeChem C02356 KEGG COMPOUND CPD0-1942 MetaCyc HMDB0000452 HMDB LMFA01100034 LIPID MAPS YMDB01570 YMDB View more database links Registry Numbers Types Sources 1492-24-6 CAS Registry Number ChemIDplus 1492-24-6 CAS Registry Number NIST Chemistry WebBook 1720935 Reaxys Registry Number Reaxys 278145 Gmelin Registry Number Gmelin Citations Types Sources 16098526 PubMed citation Europe PMC 1700029 PubMed citation Europe PMC 4572987 PubMed citation Europe PMC 575311 PubMed citation Europe PMC Last Modified 03 September 2019