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ChemicalBook--->CAS DataBase List--->911208-73-6

911208-73-6

911208-73-6 Structure

911208-73-6 Structure
IdentificationBack Directory
[Name]

3-(Hexadecyloxy)propyl hydrogen ((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonat
[CAS]

911208-73-6
[Synonyms]

CMX-157
HDP-Tenofovir
Tenofovir exalidex
TENOFOVIR EXALIDEX; HDP-TENOFOVIR; TENOFOVIR; CMX-157; CMX157; CMX 157
3-(Hexadecyloxy)propyl hydrogen ((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phospho
3-(Hexadecyloxy)propyl hydrogen ((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonat
3-(Hexadecyloxy)propyl hydrogen ((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonate
Phosphonic acid, P-[[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl]-, mono[3-(hexadecyloxy)propyl] ester
[Molecular Formula]

C28H52N5O5P
[MDL Number]

MFCD23843795
[MOL File]

911208-73-6.mol
[Molecular Weight]

569.72
Chemical PropertiesBack Directory
[Melting point ]

172 - 174°C
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly, Sonicated), DMSO (Slightly, Heated, Sonicated), Ethanol
[form ]

Solid
[color ]

White to Off-White
Hazard InformationBack Directory
[Uses]

Tenofovir Exalidex is a prodrug of nucleoside analog used in the treatment of hepatitis B virus.
[in vivo]

Tenofovir exalidex (Sprague-Dawley rats) is orally available and has no apparent toxicity when given orally to rats for 7 days at doses of 10, 30, or 100 mg/kg/day[2]. Tenofovir exalidex (5-10 mg/kg; oral gavage; daily for a period of 16 days) decreases liver HBV DNA levels dose-dependently[3].

Animal Model:Female transgenic mice HBV transgenic Tg05 mice (C57BL/6)[1]
Dosage:5 mg/kg, 10 mg/kg
Administration:Oral gavage; daily for a period of 16 days
Result:The reductions in HBV DNA were 55% and 97% for low-dose (5 mg/kg/day) and high-dose (10 mg/kg/day), respectively.
[IC 50]

HIV-1; HIV-2
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