Tenofovir Disoproxil Fumarate

CAS No. 202138-50-9

Tenofovir Disoproxil Fumarate( Bis(POC)-PMPA )

Catalog No. M13146 CAS No. 202138-50-9

Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 41 In Stock
25MG 61 In Stock
50MG 83 In Stock
100MG 113 In Stock
200MG 154 In Stock
500MG 227 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Tenofovir Disoproxil Fumarate
  • Note
    Research use only, not for human use.
  • Brief Description
    Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B.
  • Description
    Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B.(In Vitro):Tenofovir shows cytotoxic effects on cell viability in HK-2 cells, with IC50 values of 9.21 and 2.77 μM at 48 and 72 h in MTT assay, respectively. Tenofovir diminishes ATP levels in HK-2 cells. Tenofovir (3.0 to 28.8 μM) increases oxidative stress and protein carbonylation in HK-2 cells. Furthermore, Tenofovir induces apoptosis in HK-2 cells, and that apoptosis is induced via mitochondrial damage. Tenofovir and M48U1 formulated in 0.25% HEC each inhibits the replication of both R5-tropic HIV-1BaL and X4-tropic HIV-1IIIb in activated PBMCs, and inhibits several laboratory strains and patient-derived HIV-1 isolates. The combined formulation of M48U1 and tenofovir in 0.25% HEC exhibits synergistic antiretroviral activity against infection with R5-tropic HIV-1BaL, and is not toxic to PBMCs.
  • In Vitro
    Tenofovir shows cytotoxic effects on cell viability in HK-2 cells, with IC50 values of 9.21 and 2.77 μM at 48 and 72 h in MTT assay, respectively. Tenofovir diminishes ATP levels in HK-2 cells. Tenofovir (3.0 to 28.8 μM) increases oxidative stress and protein carbonylation in HK-2 cells. Furthermore, Tenofovir induces apoptosis in HK-2 cells, and that apoptosis is induced via mitochondrial damage. Tenofovir and M48U1 formulated in 0.25% HEC each inhibits the replication of both R5-tropic HIV-1BaL and X4-tropic HIV-1IIIb in activated PBMCs, and inhibits several laboratory strains and patient-derived HIV-1 isolates. The combined formulation of M48U1 and tenofovir in 0.25% HEC exhibits synergistic antiretroviral activity against infection with R5-tropic HIV-1BaL, and is not toxic to PBMCs.
  • In Vivo
    Tenofovir Disoproxil fumarate (20, 50, 140, or 300mg/kg) administered to BLT mice, shows dose dependent activity during vaginal HIV challenge in BLT humanized mice. Tenofovir Disoproxil fumarate (50, 140, 300?mg/kg) significantly reduces HIV transmission in BLT mice. Tenofovir Disoproxil fumarate (0.5, 1.5, or 5.0 mg/kg/day, p.o.) induces a dose-dependent decline in serum viremia in woodchucks chronically infected with WHV. Tenofovir Disoproxil fumarate administration is safe and effective in the woodchuck model of chronic HBV infection.
  • Synonyms
    Bis(POC)-PMPA
  • Pathway
    Microbiology/Virology
  • Target
    HIV
  • Recptor
    HIV reverse transcriptase
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    202138-50-9
  • Formula Weight
    635.51
  • Molecular Formula
    C19H30N5O10P·C4H4O4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:128 mg/mL (201.41 mM)
  • SMILES
    C(\C=C\C(=O)O)(=O)O.C(OCOP(=O)(CO[C@@H](CN1C2=NC=NC(=C2N=C1)N)C)OCOC(OC(C)C)=O)(OC(C)C)=O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Murphy RA,etal.Establishment of HK-2 Cells as a Relevant Model to Study Tenofovir-Induced Cytotoxicity.Int J Mol Sci. 2017 Mar 1;18(3).
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