| 词条 | 3-Fumarylpyruvic acid |
| 释义 |
| ImageFile = 3-Fumarylpyruvic acid.svg | ImageSize = 200px | ImageAlt = | IUPACName = (E)-4,6-Dioxohept-2-enedioic acid | OtherNames = | Section1 = {{Chembox Identifiers | CASNo = 75164-74-8 | PubChem = 5280525 | PubChem1 = 6857354 | PubChem1_Comment = (dianion) | ChEBI = 1506 | KEGG = C02514 | ChemSpiderID = 4444156 | SMILES = OC(=O)\\C=C\\C(=O)CC(=O)C(O)=O | InChI=1S/C7H6O6/c8-4(1-2-6(10)11)3-5(9)7(12)13/h1-2H,3H2,(H,10,11)(H,12,13)/b2-1+ | InChIKey =AZCFLHZUFANAOR-OWOJBTEDSA-N }} | Section2 = {{Chembox Properties | C=7|H=6|O=6 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}3-Fumarylpyruvic acid, or 3-fumarylpyruvate, is a dicarboxylic acid formed from the isomerisation of 3-maleylpyruvate by maleylpyruvate isomerase.[1] It is converted into fumarate and pyruvate by 3-fumarylpyruvate hydrolase.[2] References1. ^{{cite journal | author = Lack L | date = 1961 | title = Enzymic cis-trans isomerization of maleylpyruvic acid | journal = J. Biol. Chem. | volume = 236 | pages = 2835–2840 | pmid=14461395}} {{DEFAULTSORT:Fumarylpyruvic acid, 3-}}{{organic-compound-stub}}2. ^{{cite journal | title = Molecular and biochemical characterization of the 5-nitroanthranilic acid degradation pathway in Bradyrhizobium sp. strain JS329 |author = Qu, Y. |author2 = Spain, J.C. |last-author-amp = yes |journal = J. Bacteriol. |year = 2011 |volume = 193 |pages = 3057–3063 |pmid = 21498645 |doi=10.1128/JB.01188-10 |pmc=3133195}} 1 : Dicarboxylic acids |
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