Chemical Component Summary | |
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Name | 5-FLUOROURIDINE |
Identifiers | 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-fluoro-pyrimidine-2,4-dione |
Formula | C9 H11 F N2 O6 |
Molecular Weight | 262.192 |
Type | NON-POLYMER |
Isomeric SMILES | C1=C(C(=O)NC(=O)N1[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O)F |
InChI | InChI=1S/C9H11FN2O6/c10-3-1-12(9(17)11-7(3)16)8-6(15)5(14)4(2-13)18-8/h1,4-6,8,13-15H,2H2,(H,11,16,17)/t4-,5-,6-,8-/m1/s1 |
InChIKey | FHIDNBAQOFJWCA-UAKXSSHOSA-N |
Chemical Details | |
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Formal Charge | 0 |
Atom Count | 29 |
Chiral Atom Count | 4 |
Bond Count | 30 |
Aromatic Bond Count | 0 |
Drug Info: DrugBank
DrugBank ID | DB01629? |
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Name | 5-fluorouridine |
Groups | experimental |
Description | 5-fluorouridine is also known as FUrd, 5-Fluorouracil 1-beta-D-ribofuranoside, 5-Fur, or 5-Fluoro-uridine. 5-fluorouridine is a solid. This compound belongs to the pyrimidine nucleosides and analogues. These are compounds comprising a pyrimidine base attached to a sugar. 5-fluorouridine is known to target uridine phosphorylase. FUrd is often used in chemical and biochemical comparison studies with fluorouracil and thymine analogs. |
Synonyms |
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Categories |
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CAS number | 316-46-1 |
Drug Targets
Name | Target Sequence | Pharmacological Action | Actions |
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Superoxide dismutase [Cu-Zn] | MATKAVCVLKGDGPVQGIINFEQKESNGPVKVWGSIKGLTEGLHGFHVHE... | unknown | |
Uridine phosphorylase | MSKSDVFHLGLTKNDLQGATLAIVPGDPDRVEKIAALMDKPVKLAShref... | unknown | |
Thyroxine-binding globulin | MSPFLYLVLLVLGLHATIHCASPEGKVTACHSSQPNATLYKMSSINADFA... | unknown | inducer |
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison
T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS.
Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682
Related Resource References
Resource Name | Reference |
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PubChem | 9427 |
ChEMBL | CHEMBL54918 |
ChEBI | CHEBI:40154 |
CCDC/CSD | DAXGEP |