Names | |
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Preferred IUPAC name
3-Decanoyl-4-hydroxy-5-methylidenefuran-2(5H)-one | |
Other names
3-[(Z)-1-hydroxydecylidene]-5-methylenetetrahydrofuran-2,4-dione
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Identifiers | |
CAS Number
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3D model (JSmol)
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ChEMBL |
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ChemSpider |
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PubChem CID
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CompTox Dashboard (EPA)
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InChI
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SMILES
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Properties | |
Chemical formula
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C15H22O4 |
Molar mass | 266.34 g/mol |
Appearance | Colorless crystalline powders (Na salt) |
Melting point | 113-115 (A), 85-88 (B), 125-128 (C), 103-106 (D) |
Solubility in water
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Insoluble (Na salt) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Agglomerins are bacterial natural products, identified as metabolites of Pantoea agglomerans which was isolated in 1989 from river water in Kobe, Japan.[1] They belong to the class of tetronate antibiotics, which include tetronomycin, tetronasin, and abyssomicin C. The members of the agglomerins differ only in the composition of the acyl chain attached to the tetronate ring. They possess antibiotic activity against anaerobic bacteria and weak activity against aerobic bacteria in vitro. The structures were solved in 1990.[2] Agglomerin A is the major component (38%), followed by agglomerin B (30%), agglomerin C (24%), and agglomerin D (8%).[3]