CHEBI:137658 - 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid

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ChEBI Name 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid ChEBI ID CHEBI:137658 ChEBI ASCII Name 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid Definition A 3-(4-hydroxycyclohex-2-en-1-ylidene)pyruvic acid having 1Z,4R stereochemistry. 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 C9H10O4 Net Charge 0 Average Mass 182.174 Monoisotopic Mass 182.05791 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)/b6-5+/t7-/m0/s1 InChIKey MPMDLNLJFJLITQ-XPPMVYLVSA-N SMILES [C@@H]1(C=C/C(/CC1)=C\C(=O)C(=O)O)O Metabolite of Species Details Bacillus subtilis (NCBI:txid1423) See: PubMed Roles Classification Chemical Role(s): 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. View more via ChEBI Ontology ChEBI Ontology Outgoing 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid (CHEBI:137658) has role bacterial metabolite (CHEBI:76969) 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid (CHEBI:137658) is a 3-(4-hydroxycyclohex-2-en-1-ylidene)pyruvic acid (CHEBI:64942) 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid (CHEBI:137658) is conjugate acid of 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate (CHEBI:136782) Incoming 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate (CHEBI:136782) is conjugate base of 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid (CHEBI:137658) IUPAC Name (3Z)-3-[(4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoic acid Synonyms Sources (3Z)-Δ3,Δ5-exocyclic-H2HPP ChEBI 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]-2-oxopropanoic acid ChEBI 3Z-ex-H2HPP ChEBI Registry Number Type Source 22690132 Reaxys Registry Number Reaxys Citation Type Source 22765234 PubMed citation Europe PMC Last Modified 05 July 2017