| 词条 | 4-Fluoro-L-threonine |
| 释义 |
| Name = 4-Fluoro-L-threonine | ImageFile = 4-Fluorothreonine.svg | ImageSize = | ImageAlt = | IUPACName = (2S,3S)-2-Amino-4-fluoro-3-hydroxybutanoic acid | OtherNames = 4-Fluorothreonine | Section1 = {{Chembox Identifiers | CASNo = 102130-93-8 | PubChem = 128057 | SMILES = C([C@H]([C@@H](C(=O)O)N)O)F | ChemSpiderID = 113553 | InChI = 1/C4H8FNO3/c5-1-2(7)3(6)4(8)9/h2-3,7H,1,6H2,(H,8,9)/t2-,3+/m1/s1 | InChIKey = GTFWIYJIEXNAOL-GBXIJSLDBB | StdInChI = 1S/C4H8FNO3/c5-1-2(7)3(6)4(8)9/h2-3,7H,1,6H2,(H,8,9)/t2-,3+/m1/s1 | StdInChIKey = GTFWIYJIEXNAOL-GBXIJSLDSA-N }} | Section2 = {{Chembox Properties | C=4|H=8|F=1|N=1|O=3 | MolarMass = | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}4-Fluoro-L-threonine is an antibacterial made by Streptomyces cattleya. It is formed by the fluorothreonine transaldolase catalysed transfer of fluoroacetaldehyde onto threonine.[1] References1. ^{{cite journal | vauthors = Murphy CD, O'Hagan D, Schaffrath C | date = 2001 | title = Identification of a PLP-Dependent Threonine Transaldolase: A Novel Enzyme Involved in 4-Fluorothreonine Biosynthesis in Streptomyces cattleya This work was supported by the Biotechnological and Biological Sciences Research Council and the University of St Andrews | journal = Angew. Chem. Int. Ed. Engl. | volume = 40 | pages = 4479–4481 | pmid = 12404452 | doi = 10.1002/1521-3773(20011203)40:23<4479::AID-ANIE4479>3.0.CO;2-1 | issue = 23}} {{DEFAULTSORT:Fluoro-L-threonine, 4-}}{{organic-compound-stub}} 5 : Organofluorides|Amino acid derivatives|Halohydrins|Halogen-containing natural products|Fluorine-containing natural products |
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