(1R)-Tenofovir amibufenamide

Modify Date: 2025-11-09 23:14:41

(1R)-Tenofovir amibufenamide Structure
(1R)-Tenofovir amibufenamide structure
Common Name (1R)-Tenofovir amibufenamide
CAS Number 1571076-15-7 Molecular Weight 490.49
Density N/A Boiling Point N/A
Molecular Formula C22H31N6O5P Melting Point N/A
MSDS N/A Flash Point N/A

 Use of (1R)-Tenofovir amibufenamide


(1R)-Tenofovir amibufenamide ((1R)-HS-10234) is the isomer of Tenofovir amibufenamide, is an orally active antiviral agent. (1R)-Tenofovir amibufenamide ((1R)-HS-10234) is a HIV infection inhibitor and HBV infection inhibitor. (1R)-Tenofovir amibufenamide ((1R)-HS-10234) can be used for HIV infections, hepatitis B research[1].

 Names

Name (1R)-Tenofovir amibufenamide

 (1R)-Tenofovir amibufenamide Biological Activity

Description (1R)-Tenofovir amibufenamide ((1R)-HS-10234) is the isomer of Tenofovir amibufenamide, is an orally active antiviral agent. (1R)-Tenofovir amibufenamide ((1R)-HS-10234) is a HIV infection inhibitor and HBV infection inhibitor. (1R)-Tenofovir amibufenamide ((1R)-HS-10234) can be used for HIV infections, hepatitis B research[1].
Related Catalog
References

[1]. Shahar N, et, al. Tenofovir prodrug and pharmaceutical uses thereof. WO2014032481.

 Chemical & Physical Properties

Molecular Formula C22H31N6O5P
Molecular Weight 490.49
InChIKey ORHSFGJQGPUCRR-LXAPUOBYSA-N
SMILES CC(C)OC(=O)C(C)(C)NP(=O)(COC(C)Cn1cnc2c(N)ncnc21)Oc1ccccc1
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.
Top Suppliers:I want be here


Get all suppliers and price by the below link:

(1R)-Tenofovir amibufenamide suppliers

(1R)-Tenofovir amibufenamide price

Related Compounds: More...
(R,1R)-Tenofovir amibufenamide
1571076-37-3
Tenofovir amibufenamide
1571076-26-0
[[(1R)-2-(6-aMino-9H-purin-9-yl)-1-Methylethoxy]Methyl]-, Monophenylester
379270-35-6
[(1R,9aR)-5-methyl-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-5-ium-1-yl] propanoate,bromide
17934-72-4
(1R,8R,8aS)-8-(triisopropylsilyloxy)-octahydroindolizin-1-ol
914616-18-5
(1R,5S)-ethyl 5-(N-(tert-butoxycarbonyl)-4-nitrophenylsulfonamido)cyclohex-3-enecarboxylate
1287204-66-3
(1R,3S,5S,6S)-ethyl 5-(tert-butoxycarbonylamino)-7-oxabicyclo[4.1.0]heptane-3-carboxylate
1287204-68-5
(1R-<1α,7(Z),7aβ>)-(1-hydroxy-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl)methyl 2-methylbut-2-enoate
6922-62-9
(1R,2R,4R,SS)-N-[(1E)-benzylidene]-2-(2-trimethylsilyloxy-4-methylcyclohexyl)propane-2-sulfinamide
622840-45-3
Methyl 2-(4-chlorophenyl)pyrimidine-4-carboxylate
2436338-70-2
1-{2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylbutanamido]ethyl}-1H-imidazole-4-carboxylic acid
2171687-37-7
1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]-1,2,3,4-tetrahydroquinoline-3-carboxylic acid
2171910-41-9
1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanoyl]-2-propylpyrrolidine-2-carboxylic acid
2172067-76-2
2-{4-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylbutanoyl]morpholin-3-yl}acetic acid
2171438-82-5
2-({2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)ethyl]phenyl}formamido)-2-methylpropanoic acid
2171850-88-5
(2R)-1-[4-chloro-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)benzoyl]pyrrolidine-2-carboxylic acid
2171151-02-1
3-({1-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]cyclobutyl}formamido)-3-methylbutanoic acid
2172306-27-1
2-[({1-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]cyclopropyl}formamido)methyl]-3-methylbutanoic acid
2171912-32-4
3-[2-cyclopropyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]-2,2-dimethylpropanoic acid
2172383-92-3