Adefovir
Description References- Product Name
- Adefovir
- CAS No.
- 106941-25-7
- Chemical Name
- Adefovir
- Synonyms
- PMEA;GS-393;gs0393;Adefovi;ADEFOVIR;A Duff Vee;Adefovir98%;Adefovir API;adefovir ,97%;Adefovir(PMEA)
- CBNumber
- CB2698137
- Molecular Formula
- C8H12N5O4P
- Formula Weight
- 273.19
- MOL File
- 106941-25-7.mol
Adefovir Property
- Melting point:
- >260°C
- Boiling point:
- 632.5±65.0 °C(Predicted)
- Density
- 1.88
- storage temp.
- -20°C
- solubility
- 0.1 M NaOH: ≥5mg/mL
- form
- powder
- pka
- pKa1 2.0, pKa2 6.8(at 25℃)
- color
- white to beige
- InChIKey
- SUPKOOSCJHTBAH-UHFFFAOYSA-N
- CAS DataBase Reference
- 106941-25-7(CAS DataBase Reference)
Safety
- Hazard Codes
- T
- Risk Statements
- 25
- Safety Statements
- 45
- RIDADR
- 2811
- WGK Germany
- 3
- RTECS
- SZ6563500
- HazardClass
- 6.1
- PackingGroup
- Ⅲ
- HS Code
- 29339900
- Hazardous Substances Data
- 106941-25-7(Hazardous Substances Data)
N-Bromosuccinimide Price
- Product number
- SML0240
- Product name
- Adefovir
- Purity
- ≥98% (HPLC)
- Packaging
- 10mg
- Price
- $110
- Updated
- 2024/03/01
- Product number
- SML0240
- Product name
- Adefovir
- Purity
- ≥98% (HPLC)
- Packaging
- 50mg
- Price
- $441
- Updated
- 2024/03/01
- Product number
- 18650
- Product name
- Adefovir
- Purity
- ≥95%
- Packaging
- 10mg
- Price
- $32
- Updated
- 2024/03/01
- Product number
- 18650
- Product name
- Adefovir
- Purity
- ≥95%
- Packaging
- 50mg
- Price
- $139
- Updated
- 2024/03/01
- Product number
- 18650
- Product name
- Adefovir
- Purity
- ≥95%
- Packaging
- 100mg
- Price
- $243
- Updated
- 2024/03/01
Adefovir Chemical Properties,Usage,Production
Description
Adefovir (Trade name: Preveon, Hepsera) is a prescription drug used for the treatment of chronic infections of hepatitis B virus. It can be formulated as the pivoxil prodrug adefovir dipivoxil. However, it shows no effect against HIV-1. As a orally administrated acyclic nucleotide analog reverse transcriptase inhibitor, it blocking the reproduction of HBV through inhibiting the reverse transcriptase in the body. One of its advantages over another anti-HBV drug, lamivudine is that it is much harder for the virus to develop resistance to it.
References
https://www.drugbank.ca/drugs/DB00718
http://en.wikipedia.org/wiki/Adefovir
Chemical Properties
Pale Brown Solid
Uses
Used as an antiviral
Uses
Adefovir has been used to study its anti-retro viral effect on porcine endogenous retrovirus (PERV) activity.
Definition
ChEBI: Adefovir is a member of the class of phosphonic acids that is methylphosphonic acid in which one of the methyl hydrogens has been replaced by a 2-(6-amino-9H-purin-9-yl)ethoxy group. An inhibitor of HIV-1 reverse transcriptase, the bis(t-butoxycarbonyloxymethyl) ester (dipivoxil ester) prodrug is used to treat chronic hepatitis B viral infection. It has a role as a HIV-1 reverse transcriptase inhibitor, a drug metabolite, an antiviral drug, a nephrotoxic agent and a DNA synthesis inhibitor. It is a member of 6-aminopurines, an ether and a member of phosphonic acids. It is functionally related to an adenine. It is a conjugate acid of an adefovir(1-).
Acquired resistance
It has a lower propensity to induce drug resistance than lamivudine. Clinical trials of patients receiving 48 weeks of therapy did not identify any cases of resistance. Longer courses yield resistant strains of HBV with mutations in the DNA polymerase gene; other rare variants of resistant strains have been identified. Lamivudine-resistant strains of HBV retain susceptibility to adefovir.
Pharmaceutical Applications
A nucleotide analog of adenosine monophosphate, administered orally as its prodrug, adefovir dipivoxil.
Biochem/physiol Actions
Adefovir is an antiviral drug that after intracellular conversion to adefovir diphosphate inhibits hepatitis B virus (HBV) DNA polymerase (reverse transcriptase).
Pharmacokinetics
Oral absorption： c. 60%
Cmax 10 mg/kg oral： 18.4 ng/mL
Plasma half-life： c. 7.5 h.
Volume of distribution： 392 mL/kg
Plasma protein binding： Not known
The prodrug is metabolized to adefovir, which is excreted by the kidneys and therefore requires dose adjustment in patients with impaired renal function. It does not induce cytochrome P450 at standard doses and does not influence the metabolism or plasma concentrations of the other licensed medications used in the treatment of hepatitis B.
Clinical Use
Treatment of chronic hepatitis B virus infection in patients >12 years of age
Side effects
It is generally well tolerated, with headache, pharyngitis, abdominal pain and peripheral neuropathy being the most common side effects. Nephrotoxicity has been observed in some patients, with those receiving higher doses and longer courses of therapy at greater risk. Exacerbation of hepatitis has been reported in patients immediately following discontinuation of treatment. Most exacerbations occur within 12 weeks of stopping therapy, and elevations of alanine aminotransferase (ALT) up to 10 times the upper limit of normal can be observed in over 25% of patients. Lactic acidosis has been reported in a few patients and is an indication for immediate discontinuation.
Adefovir Preparation Products And Raw materials
Raw materials
Preparation Products
Adefovir Suppliers
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- 86-10-82849933
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- China
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- 400-0066400 13621662912
- Fax
- 021-55660885
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View Lastest Price from Adefovir manufacturers
- Product
- Adefovir 106941-25-7
- Price
- US $0.00-0.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 20TONS
- Release date
- 2024-09-29
- Product
- Adefovir 106941-25-7
- Price
- US $0.00-0.00/Kg/Drum
- Min. Order
- 1KG
- Purity
- 99%min HPLC
- Supply Ability
- 500kgs
- Release date
- 2021-09-16
- Product
- Adefovir 106941-25-7
- Price
- US $0.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 500000kg
- Release date
- 2024-10-28