CHEBI:84355 - 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate

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ChEBI Name 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate ChEBI ID CHEBI:84355 ChEBI ASCII Name 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate Definition 3-(4-hydroxycyclohex-2-en-1-ylidene)pyruvate obtained by deprotonation of the carboxy group of 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid; major species at pH 7.3. Stars This entity has been manually annotated by the ChEBI Team. Submitter Kristian Axelsen 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 C9H9O4 Net Charge -1 Average Mass 181.16590 Monoisotopic Mass 181.05063 InChI InChI=1S/C9H10O4/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1,3,5,7,10H,2,4H2,(H,12,13)/p-1/b6-5-/t7-/m0/s1 InChIKey MPMDLNLJFJLITQ-RBSILHGTSA-M SMILES O[C@@H]1CC\C(=C/C(=O)C([O-])=O)C=C1 Metabolite of Species Details Bacillus subtilis (NCBI:txid1423) See: PubMed Roles Classification Biological Role(s): bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. View more via ChEBI Ontology ChEBI Ontology Outgoing 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate (CHEBI:84355) has role bacterial metabolite (CHEBI:76969) 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate (CHEBI:84355) is a 3-(4-hydroxycyclohex-2-en-1-ylidene)pyruvate (CHEBI:64789) 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate (CHEBI:84355) is conjugate base of 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid (CHEBI:85357) Incoming 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid (CHEBI:85357) is conjugate acid of 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate (CHEBI:84355) IUPAC Name (3E)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoate Synonym Source 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate UniProt Manual Xref Database CPD-17511 MetaCyc View more database links Citations Types Sources 22483065 PubMed citation SUBMITTER 23317005 PubMed citation SUBMITTER Last Modified 06 April 2015