Basic information Safety Supplier Related

9-[(R)-2-(Phosphonomethoxy)propyl]adenine monohydrate

Basic information Safety Supplier Related

9-[(R)-2-(Phosphonomethoxy)propyl]adenine monohydrate Basic information

Product Name:
9-[(R)-2-(Phosphonomethoxy)propyl]adenine monohydrate
Synonyms:
  • 9-[(R)-2-(Phosphonomethoxy)propyl]adenine monohydrate
  • Unii-99yxe507il
  • Tenofovir Monohydrate
  • Tenofovir (15 mg)
  • Tenofovir (hydrate)
  • [[(1R)-2-(6-Amino-9H-purin-9-yl)-1-methylethoxy]methyl]phosphonic acid monohydrate
  • PMPA Monohydrate
  • (R)-(((1-(6-Amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonic acid hydrate
CAS:
206184-49-8
MF:
C9H16N5O5P
MW:
305.23
EINECS:
808-956-8
Product Categories:
  • ALIMTA
Mol File:
206184-49-8.mol
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9-[(R)-2-(Phosphonomethoxy)propyl]adenine monohydrate Chemical Properties

Melting point:
270-274oC
storage temp. 
2-8°C
solubility 
Aqueous Acid (Slightly), DMSO (Slightly)
form 
Solid
color 
White to Off-White
Stability:
Hygroscopic
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Safety Information

HS Code 
2933599550
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9-[(R)-2-(Phosphonomethoxy)propyl]adenine monohydrate Usage And Synthesis

Chemical Properties

WHITE POWDER SOLID

Uses

Tenofovir Monohydrate is an HIV-1 RT inhibitor and antiretroviral drug.

Uses

antineoplastic, thymidylate synthase inhibitor

Definition

ChEBI: A hydrate that is the monohydrate form of anhydrous tenovir.

General Description

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Tenofovir is a nucleotide analog reverse transcriptase inhibitor, and is widely used as an antiretroviral agent, for the treatment of HIV infection.

Biological Activity

tenofovir hydrate is an inhibitor of reverse transcriptase used for the treatment of the human immunodeficiency virus 1(hiv-1) and hepatitis b [1].tenofovir hydrate is an antiviral pro-drug and the class of nucleoside reverse transcriptase inhibitor. in addition, tenofovir hydrate has been reported to have a dependent relation between intracellular the drug concentrations and prevent function of hiv-1infection with ec50 values of 29 fmol/106, 40 fmol/106 , 77 fmol/106 and 411 fmol/106 cells for inoculum size 1, 5, 20 and 100 respectively. and the ec90 values of tenofovir hydrate are 267 fmol/106, 348 fmol/106, 640 fmol/106 and 2866 fmol/106 cells for virus inoculums size 1, 5, 20 and 100, respectively [1].

References

[1] duwal s1, schütte c, von kleist m.pharmacokinetics and pharmacodynamics of the reverse transcriptase inhibitor tenofovir and prophylactic efficacy against hiv-1 infection. plos one. 2012;7(7):e40382. doi: 10.1371/journal.pone.0040382. epub 2012 jul 11.

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