Tenofovir Alafenamide Hemifumarate

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Reagent Code: #57898
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CAS Number 1392275-56-7

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Weight 1069 g/mol
Formula C₄₆H₆₂N₁₂O₁₄P₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Tenofovir Alafenamide Hemifumarate is the hemifumarate salt of tenofovir alafenamide, a lipophilic prodrug of the antiviral nucleotide analog tenofovir. It serves as a key active pharmaceutical ingredient (API) in formulations for treating HIV-1 infection, chronic hepatitis B, and as pre-exposure prophylaxis (PrEP). Compared to tenofovir disoproxil fumarate (TDF), it provides targeted intracellular delivery, lower systemic exposure, and reduced renal and bone toxicity risks. It acts by inhibiting viral reverse transcriptase, preventing DNA chain elongation.

This high-purity (≥94.5%) solid is intended for pharmaceutical research, development, synthesis of combination therapies, and manufacturing of antiviral drugs. CAS: 1392275-56-2. Molecular formula: C23H30N5O9P · 0.5 C4H4O4. Molecular weight: 717.48 g/mol.

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Test Parameter Specification
Appearance Solid
Purity 94.5

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,380.00
inventory 50mg
10-20 days ฿1,220.00
inventory 1g
10-20 days ฿8,080.00

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Tenofovir Alafenamide Hemifumarate
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Tenofovir Alafenamide Hemifumarate is the hemifumarate salt of tenofovir alafenamide, a lipophilic prodrug of the antiviral nucleotide analog tenofovir. It serves as a key active pharmaceutical ingredient (API) in formulations for treating HIV-1 infection, chronic hepatitis B, and as pre-exposure prophylaxis (PrEP). Compared to tenofovir disoproxil fumarate (TDF), it provides targeted intracellular delivery, lower systemic exposure, and reduced renal and bone toxicity risks. It acts by inhibiting viral r

Tenofovir Alafenamide Hemifumarate is the hemifumarate salt of tenofovir alafenamide, a lipophilic prodrug of the antiviral nucleotide analog tenofovir. It serves as a key active pharmaceutical ingredient (API) in formulations for treating HIV-1 infection, chronic hepatitis B, and as pre-exposure prophylaxis (PrEP). Compared to tenofovir disoproxil fumarate (TDF), it provides targeted intracellular delivery, lower systemic exposure, and reduced renal and bone toxicity risks. It acts by inhibiting viral reverse transcriptase, preventing DNA chain elongation.

This high-purity (≥94.5%) solid is intended for pharmaceutical research, development, synthesis of combination therapies, and manufacturing of antiviral drugs. CAS: 1392275-56-2. Molecular formula: C23H30N5O9P · 0.5 C4H4O4. Molecular weight: 717.48 g/mol.

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