| 词条 | Fuculose |
| 释义 |
| verifiedrevid = 447363246 | Name = L-Fuculose | ImageFile = L-Fuculose_furanose_chemical_structure.png | ImageSize = 120px | ImageFile2 = L-Fuculose_chemical_structure.png | ImageSize2 = 140px | IUPACName = (3R,4S,5S)-2-(Hydroxymethyl)-5-methyltetrahydrofuran-2,3,4-triol | OtherNames = 6-Deoxy-L-tagatose | Section1 = {{Chembox Identifiers | CASNo_Ref = {{cascite|correct|??}} | CASNo = 13074-08-3 | PubChem = 6857362 | SMILES = O[C@H]1[C@@H](O)C(O)(CO)O[C@H]1C }} | Section2 = {{Chembox Properties | Formula = C6H12O5 | MolarMass = 164.16 g/mol }} }}Fuculose or 6-deoxy-tagatose is a ketohexose deoxy sugar.[1][2] Fuculose is involved in the process of sugar metabolism.[3] It is both a human and Escherichia coli metabolite and catalyzes the production of dihydroxyacetone phosphate(DHAP).[4] See also
References1. ^{{cite book |title=Essentials of Carbohydrate Chemistry and Biochemistry | first = Thisbe K. | last = Lindhorst | name-list-format = vanc |publisher=Wiley-VCH |edition=1 |year=2007 |isbn=3-527-31528-4}} {{Carbohydrates}}{{biochem-stub}}2. ^{{cite book |title=Essentials of Carbohydrate Chemistry |publisher=Springer | first =John F. | last = Robyt | name-list-format = vanc | edition = 1st |year=1997 |isbn=0-387-94951-8}} 3. ^{{cite journal | vauthors = Wen L, Zang L, Huang K, Li S, Wang R, Wang PG | title = Efficient enzymatic synthesis of L-rhamnulose and L-fuculose | journal = Bioorganic & Medicinal Chemistry Letters | volume = 26 | issue = 3 | pages = 969–972 | date = February 2016 | pmid = 26778148 | pmc = 5984655 | doi = 10.1016/j.bmcl.2015.12.051 }} 4. ^{{cite journal | vauthors = Joerger AC, Gosse C, Fessner WD, Schulz GE | title = Catalytic action of fuculose 1-phosphate aldolase (class II) as derived from structure-directed mutagenesis | journal = Biochemistry | volume = 39 | issue = 20 | pages = 6033–41 | date = May 2000 | pmid = 10821675 | doi = 10.1021/bi9927686 }} 2 : Deoxy sugars|Ketohexoses |
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