Elvucitabine

CAS : 181785-84-2

Ref. 3D-FE22660

Informations sur le produit

• Nom: Elvucitabine
• Synonymes: 4-Amino-1-[(2S,5R)-2,5-dihydro-5-(hydroxymethyl)-2-furanyl]-5-fluoro-2(1H)-pyrimidinoneACH 126443L-Fd 4C, 2(1H)-Pyrimidinone, 4-amino-1-[(2S,5R)-2,5-dihydro-5-(hydroxymethyl)-2-furanyl]-5-fluoro-, 2(1H)-Pyrimidinone, 4-amino-1-[2,5-dihydro-5-(hydroxymethyl)-2-furanyl]-5-fluoro-, (2S-cis)-, 4-Amino-1-[(2S,5R)-2,5-dihydro-5-(hydroxymethyl)-2-furanyl]-5-fluoro-2(1H)-pyrimidinone, 4-amino-5-fluoro-1-[(2S,5R)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrimidin-2(1H)-one, <span class="text-smallcaps">L</span>-Fd 4C, Ach 126443, Beta-<span class="text-smallcaps">L</span>-Fd4C, L-Fd 4C

Description

Elvucitabine is a nucleoside analog that inhibits the replication of HIV-1. It is active against HIV-1 isolates resistant to other antiviral drugs, such as zidovudine. Elvucitabine is a prodrug that is metabolized by liver enzymes to its active form, cytidine monophosphate (CMP). This drug has shown antiviral potency in vitro and in vivo against HIV-1. The pharmacokinetic properties of elvucitabine are similar to those of other nucleoside analogs, with an elimination rate of about 70%. This drug also has potential for use in treatment of hepatitis B and C. Elvucitabine has been shown to have biochemical research applications in cancer treatment and the study of growth factors.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 227.19 g/mol
• Formule: C₉H₁₀FN₃O₃
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C9H10FN3O3/c10-6-3-13(9(15)12-8(6)11)7-2-1-5(4-14)16-7/h1-3,5,7,14H,4H2,(H2,11,12,15)/t5-,7+/m1/s1
• Code InChI: InChIKey=HSBKFSPNDWWPSL-VDTYLAMSSA-N
• SMILES: Nc1nc(=O)n([C@@H]2C=C[C@H](CO)O2)cc1F