CHEBI:28225 - D-leucine

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ChEBI Name D-leucine ChEBI ID CHEBI:28225 ChEBI ASCII Name D-leucine Definition The D-enantiomer of leucine. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:41908, CHEBI:4202, CHEBI:21045 Supplier Information ChemicalBook:CB6677228, eMolecules:514646, ZINC000000388396 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C6H13NO2 Net Charge 0 Average Mass 131.17296 Monoisotopic Mass 131.09463 InChI InChI=1S/C6H13NO2/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t5-/m1/s1 InChIKey ROHFNLRQFUQHCH-RXMQYKEDSA-N SMILES CC(C)C[C@@H](N)C(O)=O Metabolite of Species Details Saccharomyces cerevisiae (NCBI:txid4932) See: PubMed 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. Saccharomyces cerevisiae metabolite Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ). Daphnia magna metabolite A Daphnia metabolite produced by the species Daphnia magna. (via leucine ) View more via ChEBI Ontology ChEBI Ontology Outgoing D-leucine (CHEBI:28225) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) D-leucine (CHEBI:28225) has role bacterial metabolite (CHEBI:76969) D-leucine (CHEBI:28225) is a D-α-amino acid (CHEBI:16733) D-leucine (CHEBI:28225) is a leucine (CHEBI:25017) D-leucine (CHEBI:28225) is conjugate acid of D-leucinate (CHEBI:32623) D-leucine (CHEBI:28225) is conjugate base of D-leucinium (CHEBI:32624) D-leucine (CHEBI:28225) is enantiomer of L-leucine (CHEBI:15603) D-leucine (CHEBI:28225) is tautomer of D-leucine zwitterion (CHEBI:143079) Incoming D-leucine derivative (CHEBI:84114) has functional parent D-leucine (CHEBI:28225) D-leucinium (CHEBI:32624) is conjugate acid of D-leucine (CHEBI:28225) D-leucinate (CHEBI:32623) is conjugate base of D-leucine (CHEBI:28225) L-leucine (CHEBI:15603) is enantiomer of D-leucine (CHEBI:28225) D-leucine residue (CHEBI:30005) is substituent group from D-leucine (CHEBI:28225) D-leucino group (CHEBI:32626) is substituent group from D-leucine (CHEBI:28225) D-leucyl group (CHEBI:32625) is substituent group from D-leucine (CHEBI:28225) D-leucine zwitterion (CHEBI:143079) is tautomer of D-leucine (CHEBI:28225) IUPAC Name D-leucine Synonyms Sources (2R)-2-amino-4-methylpentanoic acid IUPAC (R)-(−)-leucine NIST Chemistry WebBook (R)-leucine ChemIDplus D-2-Amino-4-methylvaleric acid KEGG COMPOUND D-Leucin ChEBI D-Leucine KEGG COMPOUND D-LEUCINE PDBeChem D-Leuzin ChEBI DLE PDBeChem Manual Xrefs Databases C01570 KEGG COMPOUND DB01746 DrugBank DLE PDBeChem HMDB0013773 HMDB YMDB00997 YMDB View more database links Registry Numbers Types Sources 1721721 Reaxys Registry Number Reaxys 328-38-1 CAS Registry Number KEGG COMPOUND 328-38-1 CAS Registry Number ChemIDplus 328-38-1 CAS Registry Number NIST Chemistry WebBook 82675 Gmelin Registry Number Gmelin Citations Last Modified 14 September 2015