CHEBI:16296 - D-tryptophan

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ChEBI Name D-tryptophan ChEBI ID CHEBI:16296 ChEBI ASCII Name D-tryptophan Definition The D-enantiomer of tryptophan. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:21110, CHEBI:42297, CHEBI:42206, CHEBI:42235, CHEBI:42157, CHEBI:4257, CHEBI:13028 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 C11H12N2O2 Net Charge 0 Average Mass 204.22526 Monoisotopic Mass 204.08988 InChI InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m1/s1 InChIKey QIVBCDIJIAJPQS-SECBINFHSA-N SMILES N[C@H](Cc1c[nH]c2ccccc12)C(O)=O 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): bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. Daphnia magna metabolite A Daphnia metabolite produced by the species Daphnia magna. (via tryptophan ) View more via ChEBI Ontology ChEBI Ontology Outgoing D-tryptophan (CHEBI:16296) has role bacterial metabolite (CHEBI:76969) D-tryptophan (CHEBI:16296) is a D-α-amino acid (CHEBI:16733) D-tryptophan (CHEBI:16296) is a tryptophan (CHEBI:27897) D-tryptophan (CHEBI:16296) is conjugate acid of D-tryptophanate (CHEBI:32716) D-tryptophan (CHEBI:16296) is conjugate base of D-tryptophanium (CHEBI:32717) D-tryptophan (CHEBI:16296) is enantiomer of L-tryptophan (CHEBI:16828) D-tryptophan (CHEBI:16296) is tautomer of D-tryptophan zwitterion (CHEBI:57719) Incoming D-tryptophan derivative (CHEBI:47997) has functional parent D-tryptophan (CHEBI:16296) D-tryptophanyl radical (CHEBI:32723) has functional parent D-tryptophan (CHEBI:16296) D-tryptophanyl radical cation (CHEBI:32724) has functional parent D-tryptophan (CHEBI:16296) D-tryptophanium (CHEBI:32717) is conjugate acid of D-tryptophan (CHEBI:16296) D-tryptophanate (CHEBI:32716) is conjugate base of D-tryptophan (CHEBI:16296) L-tryptophan (CHEBI:16828) is enantiomer of D-tryptophan (CHEBI:16296) 1-D-tryptophano group (CHEBI:32720) is substituent group from D-tryptophan (CHEBI:16296) D-tryptophan residue (CHEBI:29955) is substituent group from D-tryptophan (CHEBI:16296) D-tryptophano group (CHEBI:32719) is substituent group from D-tryptophan (CHEBI:16296) D-tryptophyl group (CHEBI:32718) is substituent group from D-tryptophan (CHEBI:16296) D-tryptophan zwitterion (CHEBI:57719) is tautomer of D-tryptophan (CHEBI:16296) IUPAC Name D-tryptophan Synonyms Sources (2R)-2-amino-3-(1H-indol-3-yl)propanoic acid IUPAC (R)-tryptophan ChemIDplus D-Tryptophan KEGG COMPOUND D-TRYPTOPHAN PDBeChem DTR PDBeChem Manual Xrefs Databases C00525 KEGG COMPOUND D-TRYPTOPHAN MetaCyc DB03225 DrugBank DTR PDBeChem HMDB0013609 HMDB YMDB00998 YMDB View more database links Registry Numbers Types Sources 153-94-6 CAS Registry Number KEGG COMPOUND 153-94-6 CAS Registry Number ChemIDplus 83743 Gmelin Registry Number Gmelin 86198 Reaxys Registry Number Reaxys 86198 Beilstein Registry Number Beilstein Citations Types Sources 21560237 PubMed citation Europe PMC 22156410 PubMed citation Europe PMC 22336999 PubMed citation Europe PMC 24097941 PubMed citation Europe PMC Last Modified 14 September 2015