Top Suppliers:I want be here


142340-99-6

142340-99-6 structure
142340-99-6 structure
  • Name: Adefovir Dipivoxil
  • Chemical Name: Adefovir dipivoxil
  • CAS Number: 142340-99-6
  • Molecular Formula: C20H32N5O8P
  • Molecular Weight: 501.470
  • Catalog: API Synthetic anti-infective drugs Antiviral drugs
  • Create Date: 2018-02-07 08:00:00
  • Modify Date: 2026-06-30 10:43:04
  • Adefovir Dipivoxil works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body.Target: NRTIs; HBVAdefovir Dipivoxil works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body. Adefovir Dipivoxil is used for treatment of hepatitis B and herpes simplex virus infection [1-3]. Adefovir Dipivoxil is approved for the treatment of chronic hepatitis B in adults with evidence of active viral replication and either evidence of persistent elevations in serum aminotransferases (primarily ALT) or histologically active disease. Adefovir Dipivoxil is a failed treatment for HIV[3, 4].

Name Adefovir dipivoxil
Synonyms Adefovir Impurity 3
9-[2-[Bis(pivaloyloxymethoxy)phosphorylmethoxy]ethyl]adenine
ADEFOVIR
Ade Vove
Adefovir dipivoxil 100 μg/mL in Acetonitrile
ADEFOVIR PIVOXIL
AdefovirDipivoxlMin
Adefovir dipivoxil ADV
9-(2[bis(Pivaloyloxymethoxy)phosphorylmethoxy]ethyl)adenine
Adefovir dipivoxil, >=
Bis(Pivaloyloxymethyl)-9-[(R)-2-(Phosphonomethoxy)Ethyl]Adenine
Hepsera
Adefovir Dipivoxil (bis-POM PMEA), nucleotide analog reverse transcriptase inhibitor
ADEFOVIR DIPVOXIL
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 e the applications of Adefovir Dipivoxil
Preveon
MFCD00869897
ADEFOVIR DIPIVOXIL
((((2-(6-Amino-9H-purin-9-yl)ethoxy)methyl)phosphoryl)-bis(oxy))bis(methylene) bis(2,2-dimethy
ADEFOVIR DIPIVOLIX
Adefovir dipivoxil //BP
Adefovir Dipivoxyl
BIS(PIVALOYLOXYMETHYL)-9-[2-(PHOSPHONOMETHOXY)ETHYL]ADENINE
Di(pivaloyloxymethyl) ester
Adefovir Dipivoxil >
Adefovir Dipivoxi
Hsera|||GS 0840|||Preveon
Adefovir Dipivoxl
1,1'-[[[[2-(6-amino-9H-purin-9-yl)ethoxy]methyl]phosphinylidene]bis(oxymethylene)]-2,2-dimethyl-propanoic acid ester
Hsera
BIS POM PMEA
Adefovir dipivoxil,9-(2[bis(Pivaloyloxymethoxy)phosphorylmethoxy]ethyl)adenine
2,2-DiMethyl-propanoic Acid 1,1'-[[[[2-(6-Amino-9H-purin-9-yl)ethoxy]Methyl]phosphinylidene]bis(oxyMethylene)] Ester
adefuweizhi
GS 0840
Adefovir Dipivoxil API
EINECS 200-001-8
Adefovir dipivoxil - Bio-X
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, 10 mM in DMSO
BIS-POM PMEA; PREVEON; HSERA
9-[2-[bis[(pivaloyloxy)methoxy]phosphinyl]methoxy]ethyl]adenine
Adefovir Dipivoxil Tablets
Adefovir Dipivoxil(Preveon, Hsera)
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
Description Adefovir Dipivoxil works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body.Target: NRTIs; HBVAdefovir Dipivoxil works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body. Adefovir Dipivoxil is used for treatment of hepatitis B and herpes simplex virus infection [1-3]. Adefovir Dipivoxil is approved for the treatment of chronic hepatitis B in adults with evidence of active viral replication and either evidence of persistent elevations in serum aminotransferases (primarily ALT) or histologically active disease. Adefovir Dipivoxil is a failed treatment for HIV[3, 4].
Related Catalog
References

[1]. Marcellin, P., et al., Adefovir dipivoxil for the treatment of hepatitis B e antigen-positive chronic hepatitis B. N Engl J Med, 2003. 348(9): p. 808-16.

[2]. Manolakopoulos, S., et al., Long-term therapy with adefovir dipivoxil in hepatitis B e antigen-negative patients developing resistance to lamivudine. Aliment Pharmacol Ther, 2008. 27(3): p. 266-73.

[3]. Committee, A.I.S., A randomized placebo-controlled trial of adefovir dipivoxil in advanced HIV infection: the ADHOC trial. HIV Med, 2002. 3(4): p. 229-38.

[4]. Fisher, E.J., et al., The safety and efficacy of adefovir dipivoxil in patients with advanced HIV disease: a randomized, placebo-controlled trial. AIDS, 2001. 15(13): p. 1695-700.

Density 1.4±0.1 g/cm3
Boiling Point 641.0±65.0 °C at 760 mmHg
Melting Point 98-102ºC
Molecular Formula C20H32N5O8P
Molecular Weight 501.470
Flash Point 341.5±34.3 °C
Exact Mass 501.198853
PSA 176.79000
LogP 2.45
Vapour Pressure 0.0±1.9 mmHg at 25°C
Index of Refraction 1.569
Storage condition −20°C
Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302-H312-H332
Precautionary Statements P280
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi
Risk Phrases R20/21/22
Safety Phrases 36/37
RIDADR NONH for all modes of transport

~75%

142340-99-6 structure

142340-99-6

Literature: WO2010/110506 A1, ; Page/Page column 7 ;

~%

142340-99-6 structure

142340-99-6

Literature: WO2007/13085 A1, ; Page/Page column 10-11 ;

~%

142340-99-6 structure

142340-99-6

Literature: European Journal of Medicinal Chemistry, , vol. 63, p. 869 - 881

~%

142340-99-6 structure

142340-99-6

Literature: EP2330107 A2, ; Page/Page column 6 ;

~%

142340-99-6 structure

142340-99-6

Literature: Journal of Medicinal Chemistry, , vol. 39, # 25 p. 4958 - 4965

~%

142340-99-6 structure

142340-99-6

Literature: Journal of Medicinal Chemistry, , vol. 39, # 25 p. 4958 - 4965

~%

142340-99-6 structure

142340-99-6

Literature: US2012/238753 A1, ;

~%

142340-99-6 structure

142340-99-6

Literature: US2012/238753 A1, ;

~%

142340-99-6 structure

142340-99-6

Literature: European Journal of Medicinal Chemistry, , vol. 63, p. 869 - 881
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.