CHEBI:75145 - 2-aminooctanoic acid

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ChEBI Name 2-aminooctanoic acid ChEBI ID CHEBI:75145 Definition An α-amino fatty acid that is caprylic acid which is substituted at position 2 by an amino group. Stars This entity has been manually annotated by the ChEBI Team. 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 C8H17NO2 Net Charge 0 Average Mass 159.22610 Monoisotopic Mass 159.12593 InChI InChI=1S/C8H17NO2/c1-2-3-4-5-6-7(9)8(10)11/h7H,2-6,9H2,1H3,(H,10,11) InChIKey AKVBCGQVQXPRLD-UHFFFAOYSA-N SMILES CCCCCCC(N)C(O)=O Metabolite of Species Details Homo sapiens (NCBI:txid9606) Found in human blood serum. See: MetaboLights Study 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). View more via ChEBI Ontology ChEBI Ontology Outgoing 2-aminooctanoic acid (CHEBI:75145) has role human metabolite (CHEBI:77746) 2-aminooctanoic acid (CHEBI:75145) is a α-amino fatty acid (CHEBI:59755) 2-aminooctanoic acid (CHEBI:75145) is conjugate acid of 2-aminooctanoate (CHEBI:142420) 2-aminooctanoic acid (CHEBI:75145) is conjugate base of 1-carboxyheptan-1-aminium (CHEBI:142421) 2-aminooctanoic acid (CHEBI:75145) is tautomer of 2-aminooctanoic acid zwitterion (CHEBI:133660) Incoming 1-carboxyheptan-1-aminium (CHEBI:142421) is conjugate acid of 2-aminooctanoic acid (CHEBI:75145) 2-aminooctanoate (CHEBI:142420) is conjugate base of 2-aminooctanoic acid (CHEBI:75145) 2-aminooctanoic acid zwitterion (CHEBI:133660) is tautomer of 2-aminooctanoic acid (CHEBI:75145) Synonyms Sources (±)-2-aminooctanoic acid ChemIDplus (+/-)-2-aminooctanoic acid ChemIDplus 2-amino-DL-caprylic acid ChemIDplus 2-aminocaprylic acid ChEBI α-aminocaprylic acid ChEBI α-aminooctanoic acid ChEBI D,L-2-aminooctanoic acid ChEBI dl-2-aminocaprylic acid NIST Chemistry WebBook DL-2-aminooctanoic acid ChEBI dl-α-amino-n-caprylic acid NIST Chemistry WebBook DL-α-aminocaprylic acid ChemIDplus NSC 20147 NIST Chemistry WebBook Manual Xrefs Databases CPD-3687 MetaCyc HMDB0000991 HMDB LMFA01100056 LIPID MAPS View more database links Registry Numbers Types Sources 1722614 Reaxys Registry Number Reaxys 644-90-6 CAS Registry Number NIST Chemistry WebBook 644-90-6 CAS Registry Number ChemIDplus Citations Types Sources 14030438 PubMed citation Europe PMC 965460 PubMed citation Europe PMC Last Modified 16 October 2018