Date published: 2025-10-5

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Tenofovir Monohydrate (CAS 206184-49-8)

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Alternate Names:
[(2R)-1-(6-aminopurin-9-yl)propan-2-yl]oxymethylphosphonic acid hydrate
Application:
Tenofovir Monohydrate is an HIV-1 RT inhibitor and antiretroviral drug
CAS Number:
206184-49-8
Molecular Weight:
305.23
Molecular Formula:
C9H16N5O5P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tenofovir Monohydrate is a crystalline form of tenofovir, incorporating a single molecule of water (monohydrate). This form is utilized in scientific research to understand the interactions and stability of nucleotide analogs within biological systems. Tenofovir itself is structurally related to adenosine and includes a phosphonic acid group, which is crucial for its interaction with biological enzymes, particularly those involved in the synthesis of nucleic acids. In biochemical research, Tenofovir Monohydrate is primarily used to study how nucleotide analogs inhibit enzymes like reverse transcriptase (RT). These enzymes are key to the replication process of some viruses, synthesizing DNA strands from RNA templates. Tenofovir Monohydrate competes with natural nucleotides, incorporating into the growing DNA chain and preventing further elongation due to its lack of a 3′ hydroxyl group, which is essential for the formation of phosphodiester bonds with subsequent nucleotides. Additionally, Tenofovir Monohydrate is important in research focused on understanding viral resistance mechanisms. Studies involving this compound help identify how viral mutations can reduce sensitivity to nucleotide analogs, providing insights into viral adaptation and the development of resistance. Tenofovir Monohydrate is also employed in studies aimed at optimizing the delivery and stability of nucleotide analogs. Researchers examine how the monohydrate form influences the solubility and stability of the compound in various environments, aiding in the development of formulations that maximize its effectiveness in scientific applications.


Tenofovir Monohydrate (CAS 206184-49-8) References

  1. Liquid chromatographic assay for the antiviral nucleotide analogue tenofovir in plasma using derivatization with chloroacetaldehyde.  |  Sparidans, RW., et al. 2003. J Chromatogr B Analyt Technol Biomed Life Sci. 791: 227-33. PMID: 12798182
  2. Simultaneous quantification of emtricitabine and tenofovir in human plasma using high-performance liquid chromatography after solid phase extraction.  |  Rezk, NL., et al. 2005. J Chromatogr B Analyt Technol Biomed Life Sci. 822: 201-8. PMID: 16005269
  3. Segmented polyurethane intravaginal rings for the sustained combined delivery of antiretroviral agents dapivirine and tenofovir.  |  Johnson, TJ., et al. 2010. Eur J Pharm Sci. 39: 203-12. PMID: 19958831
  4. Selective Lewis acid catalyzed assembly of phosphonomethyl ethers: three-step synthesis of tenofovir.  |  Ocampo, CE., et al. 2015. Org Lett. 17: 820-3. PMID: 25664399
  5. Development and validation of an LC-MS/MS assay for tenofovir and tenofovir alafenamide in human plasma and cerebrospinal fluid.  |  Ocque, AJ., et al. 2018. J Pharm Biomed Anal. 156: 163-169. PMID: 29709783
  6. Monoclonal antibodies with subnanomolar affinity to tenofovir for monitoring adherence to antiretroviral therapies: from hapten synthesis to prototype development.  |  Cavalera, S., et al. 2020. J Mater Chem B. 8: 10439-10449. PMID: 33124633
  7. A simple liquid chromatographic method for the determination of tenofovir in rat plasma and its application to pharmacokinetic studies[J].  |  Ravi P R, Joseph S, Avula U S R. 2015,. Acta Chromatographica,. 27(4):: 597-612.
  8. Development and validation of a LC–MS/MS assay for tenofovir and tenofovir alafenamide in human plasma: Application in a bioequivalence study[J].  |  Chuong N N, Nguyen N H N, Tran H V,. 2023,. MedPharmRes,. 7(3):: 32-41.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tenofovir Monohydrate, 100 mg

sc-394169
100 mg
$121.00