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Clevudine

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Category Hepatitis B Virus (HBV)
CAS 163252-36-6
Description Clevudine is an inhibitor of hepatitis B virus (HBV). It is metabolized in cells by the cellular thymidine kinase as well as deoxycytidine kinase to its monophosphate, and subsequently to the di- and triphosphate, which are biologically active.
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Product Information

Synonyms 1-(2'-Deoxy-2'-fluoro-β-L-arabinofuranosyl)-5-methyluracil; L-FMAU; 1-(2-Deoxy-2-fluoro-β-L-arabinofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione; L FMAU; LFMAU; Levovir; 2'-Fluoro-5-methyl-b-L-arabinofuranosyluracil
IUPAC Name 1-[(2S,3R,4S,5S)-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione
Molecular Weight 260.22
Molecular Formula C10H13FN2O5
Canonical SMILES CC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)F
InChI InChI=1S/C10H13FN2O5/c1-4-2-13(10(17)12-8(4)16)9-6(11)7(15)5(3-14)18-9/h2,5-7,9,14-15H,3H2,1H3,(H,12,16,17)/t5-,6+,7-,9-/m0/s1
InChIKey GBBJCSTXCAQSSJ-XQXXSGGOSA-N
Melting Point 184-185 °C
Purity ≥98% by HPLC
Density 1.55±0.1 g/cm3
Solubility Soluble in DMSO (Slightly), Methanol (Slightly)
Appearance White Solid
Application Antiviral Agents
Storage Store at -20°C
Complexity 413
Exact Mass 260.08084968
Index Of Refraction 1.592
In Vitro Clevudine (L-FMAU) shows some activity against Epstein-Barr virus.
PSA 104.55000
Target HBV; DNA/RNA Synthesis; Orthopoxvirus
XLogP3-AA -0.9

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