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Adefovir dipivoxil

Adefovir dipivoxil Structure
CAS No.
142340-99-6
Chemical Name:
Adefovir dipivoxil
Synonyms
ADEFOVIR;Hepsera;Preveon;GS 0840;Ade Vove;adefuweizhi;BIS POM PMEA;ADEFOVIR PIVOXIL;Adefovir Dipivoxl;Adefovir Dipivoxi
CBNumber:
CB6237644
Molecular Formula:
C20H32N5O8P
Molecular Weight:
501.47
MOL File:
142340-99-6.mol
MSDS File:
SDS
Modify Date:
2023/6/8 17:06:35

Adefovir dipivoxil Properties

Melting point 98-102°C
Boiling point 641.0±65.0 °C(Predicted)
Density 1.35±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility ethanol: soluble50mg/mL
pka 4.16±0.10(Predicted)
form solid
color White to Off-White
Merck 14,151
InChIKey WOZSCQDILHKSGG-UHFFFAOYSA-N
CAS DataBase Reference 142340-99-6(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302+H312+H332
Precautionary statements  P261-P264-P280-P301+P312-P302+P352+P312-P304+P340+P312
Hazard Codes  Xn
Risk Statements  20/21/22
Safety Statements  36/37
WGK Germany  3
RTECS  UA2459362
HS Code  2933.99.8290
NFPA 704
0
3 0

Adefovir dipivoxil price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) A9730 Adefovir dipivoxil 142340-99-6 50MG ₹12416.28 2022-06-14 Buy
Sigma-Aldrich(India) A9730 Adefovir dipivoxil 142340-99-6 100MG ₹25287.2 2022-06-14 Buy
TCI Chemicals (India) A2414 Adefovir Dipivoxil 142340-99-6 100MG ₹6600 2022-05-26 Buy
TCI Chemicals (India) A2414 Adefovir Dipivoxil 142340-99-6 1G ₹15700 2022-05-26 Buy
Product number Packaging Price Buy
A9730 50MG ₹12416.28 Buy
A9730 100MG ₹25287.2 Buy
A2414 100MG ₹6600 Buy
A2414 1G ₹15700 Buy

Adefovir dipivoxil Chemical Properties,Uses,Production

Description

Adefovir dipivoxil is the first nucleotide analog to be launched in the US as an oral treatment for hepatitis B virus (HBV) infections. It can be easily prepared in 4 steps from adenine. Adefovir dipivoxil acts as a bioavailable ester prodrug which is rapidly hydrolyzed to free adefovir and further anabolized to its active form, adefovir diphosphate, by two intracellular phosphotylation steps. The diphosphate competitively inhibits reverse transcriptase and/or causes chain termination when incorporated into growing DNA. Adefovir dipivoxil has a broad antiviral spectrum against retro-, herpes- and hepadnaviruses. The drug inhibits HBV replication, decreases HBV DNA levels and improves liver histology of patients infected with HBV wild type and resistant to other antivirals such as lamivudine. It also demonstrated activity in hepatitis B”e” antigennegative, or precore mutant, patients and in patients co-infected with HIV. To date, no adefovir dipivoxil-associated resistance mutations have been identified in patients up to 136 weeks with the drug. The oral bioavailability of adefovir after oral administration of its dipivoxil prodrug is approximately 30%. It is mainly excreted unchanged in the urine and its plasma elimination half-life is 4.2 h. However, a long intracellular half-life (17 h) of the active bisphosphorylated metabolite enables once-daily dosing. The most prominent adverse effect of adefovir dipivoxil is nephrotoxicity (which has prevented the drug from being marketed for HIV infections where the drug required administration at higher doses).

Chemical Properties

White Solid

Uses

Adefovir Dipivoxil(Preveon, Hepsera) works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body. It is approved for the treatment of chronic hepatitis B in adults with evidence of active vir

General Description

Adefovir is an orally active prodrug that is indicated for thetreatment of the chronic form of hepatitis B. The dipivoxil moieties are hydrolyzed by ubiquitous esterases to yieldadefovir, which is phosphorylated by adenylate kinase toyield adefovir diphosphate. This compound is inhibitory atHBV DNA polymerase. In addition, adefovir undergoes incorporationinto viral DNA and causes chain termination.Adefovir is poorly absorbed by the oral route, but the dipivoxilester groups cause the bioavailability to increase toapproximately 60%.

Mechanism of action

Adefovir dipivoxil is an orally active prodrug indicated for the treatment of chronic hepatitis B. The drug is hydrolyzed by extracellular esterases to produce adefovir, which in turn is phosphorylated by adenylate kinase to adefovir diphosphate, which inhibits HBV DNA polymerase. Incorporation of adefovir into viral DNA also leads to DNA chain termination. As shown in Figure 43.9, adefovir dipivoxyl is activated in two steps involving an esterase that exposes a free phosphate group (adefovir), followed by addition of a second phosphate by adenylate kinase to form adefovir diphosphate, the active form of the drug.

Clinical Use

Adefovir dipivoxil joins interferon and lamivudine in the treatment of chronic HBV. It can be used singly or in combination with lamivudine. Early clinical studies indicate benefit of the use of adefovir dipivoxil to treat lamivudine-resistant HBV with a low level of resistant virus developing to monotherapy with adefovir dipivoxil.

Metabolism

Adefovir is poorly absorbed orally, but the bioavailability of adefovir dipivoxil reaches approximately 59%. The drug is absorbed to an equal extent with or without the presence of food. Adefovir is excreted renally unchanged.

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Adefovir dipivoxil Spectrum

BIS POM PMEA BIS(PIVALOYLOXYMETHYL)-9-[2-(PHOSPHONOMETHOXY)ETHYL]ADENINE 9-[2-[bis[(pivaloyloxy)methoxy]phosphinyl]methoxy]ethyl]adenine ADEFOVIR DIPIVOXIL ADEFOVIR PIVOXIL Adefovir dipivoxil,9-(2[bis(Pivaloyloxymethoxy)phosphorylmethoxy]ethyl)adenine Bis(Pivaloyloxymethyl)-9-[(R)-2-(Phosphonomethoxy)Ethyl]Adenine Adefovir Dipivoxyl AdefovirDipivoxl98.5%Min Adefovir Dipivoxl ADEFOVIR DIPIVOLIX Adefovir Dipivoxi ADEFOVIR DIPVOXIL 9-(2[bis(Pivaloyloxymethoxy)phosphorylmethoxy]ethyl)adenine Adefovir dipivoxil ADV 2,2-DiMethyl-propanoic Acid 1,1'-[[[[2-(6-AMino-9H-purin-9-yl)ethoxy]Methyl]phosphinylidene]bis(oxyMethylene)] Ester Preveon Adefovir Dipivoxil API Ade Vove 1,1'-[[[[2-(6-amino-9H-purin-9-yl)ethoxy]methyl]phosphinylidene]bis(oxymethylene)]-2,2-dimethyl-propanoic acid ester Adefovir dipivoxil, >=99.5% ((((2-(6-Amino-9H-purin-9-yl)ethoxy)methyl)phosphoryl)-bis(oxy))bis(methylene) bis(2,2-dimethy Di(pivaloyloxymethyl) ester Adefovir Dipivoxil Tablets adefuweizhi BIS-POM PMEA; PREVEON; HEPSERA 3-{[2-(6-amino-9H-purin-9-yl)ethoxy]methyl}-8,8-dimethyl-3-oxido-7-oxo-2,4,6-trioxa-3-phosphanon-1-yl pivalate (non-preferred Adefovir Impurity 3 Adefovir Dipivoxil(Preveon, Hepsera) Adefovir Dipivoxil > GS 0840 Propanoic acid, 2,2-dimethyl-, 1,1'-[[[[2-(6-amino-9H-purin-9-yl)ethoxy]methyl]phosphinylidene]bis(oxymethylene)] ester ((((2-(6-amino-9H-purin-9-yl)ethoxy)methyl)phosphoryl)bis(oxy))bis(methylene) bis(2,2-dimethylpropanoate) Adefovir dipivoxil USP/EP/BP Adefovir Dipivoxil (GS 0840) Adefovir DipivoxilQ: What is Adefovir Dipivoxil Q: What is the CAS Number of Adefovir Dipivoxil Q: What is the storage condition of Adefovir Dipivoxil Q: What are the applications of Adefovir Dipivoxil Hepsera ADEFOVIR Hepsera|||GS 0840|||Preveon 142340-99-6 142341-99-6 C20H32N5O8P Pharmaceutical raw material API Bis-POM PMEA, Preveon, Hepsera Nucleotides Pharmaceuticals Adefovir APIs Active Pharmaceutical Ingredients Other Products Bases & Related Reagents Inhibitors Intermediates & Fine Chemicals 142340-99-6