| 词条 | Ustalic acid |
| 释义 |
| ImageFile = Ustalic acid.svg | ImageSize = 200px | ImageAlt = | SystematicName = (2,2’-(1,3-Dioxolane-4,5-diylidene)bis(phenylacetic acid) |Section1={{Chembox Identifiers | CASNo = 470699-70-8 | PubChem = 21680754 | ChemSpiderID = 10298265 | SMILES = O=C(O)C(=C2OCOC2=C(c1ccccc1)C(O)=O)c3ccccc3 | InChI = 1/C19H14O6/c20-18(21)14(12-7-3-1-4-8-12)16-17(25-11-24-16)15(19(22)23)13-9-5-2-6-10-13/h1-10H,11H2,(H,20,21)(H,22,23)/b16-14+,17-15+ | InChIKey = KEGGPAWMZOAQMC-YXLFCKQPBQ | StdInChI = 1S/C19H14O6/c20-18(21)14(12-7-3-1-4-8-12)16-17(25-11-24-16)15(19(22)23)13-9-5-2-6-10-13/h1-10H,11H2,(H,20,21)(H,22,23)/b16-14+,17-15+ | StdInChIKey = KEGGPAWMZOAQMC-YXLFCKQPSA-N }} |Section2={{Chembox Properties | C=19 | H=14 | O=6 | Appearance = White solid | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }} Ustalic acid is a naturally occurring chemical compound found in the poisonous mushroom Tricholoma ustale. OccurrenceThe compound was first reported by Japanese researcher Hirokazu Kawagishi and colleagues in 2002, who isolated about 190 milligrams of the chemical from {{convert|30.3|kg|abbr=on}} of fresh mushrooms and determined its complete structure.[1] ToxicityUstalic acid is an inhibitor of the sodium-potassium pump (Na+/K+-ATPase), found in the plasma membrane of all animal cells. Physiologically, inhibition of the sodium-potassium pump generally causes diarrhea, as it prevents water reabsorption from the intestines. When force-fed to mice, ustalic acid causes them to sit still in a crouched position, hesitant to move, and induces tremors and abdominal contractions. High enough concentrations of the toxin (10 milligrams per mouse) cause death.[1] Biosynthetically, ustalic acid is thought to originate from oxidative cleavage of the red pigment phlebiarubron.[3] SynthesisA low-yield total synthesis of the dimethyl ester of ustalic acid was reported in 2006, starting with phlebiarubrone. The oxidation was achieved with lead tetraacetate.[3] Hayakawa and colleagues reported a more efficient synthesis in 2008, using sesamol as a starting point. This procedure requires eight steps, and uses Suzuki–Miyaura coupling and oxidation of methylene acetal. References1. ^1 2 {{cite journal |author1=Sano, Y |author2=Sayama, K |author3=Arimoto, Y |author4=Inakuma, T |author5=Kobayashi, K |author6=Koshino, H |author7=Kawagishi, H |title=Ustalic acid as a toxin and related compounds from the mushroom Tricholoma ustale |journal=Chemical Communications |year=2002 |issue=13 |pages=1384–5 |pmid=12125567 |doi=10.1039/B202607D}} [1][2]2. ^1 2 {{cite journal |author1=Sawayama,Y |author2=Tsujimoto, T |author3=Sugino, K |author4=Nishikawa, T |author5=Isobe, M |author6=Kawagishi, H |title=Syntheses of naturally occurring terphenyls and related compounds |year=2006 |journal=Bioscience, Biotechnology, and Biochemistry |volume=70 |issue=12 |pages=2998–3003 |pmid=17151478 |doi=10.1271/bbb.60389}} {{open access}} }} 3 : Mycotoxins found in Basidiomycota|Dicarboxylic acids|Dioxolanes |
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