Date published: 2025-10-19

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Desthiazolylmethyloxycarbonyl Ritonavir (CAS 176655-55-3)

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Application:
Desthiazolylmethyloxycarbonyl Ritonavir is a metabolite of the selective HIV-1 protease inhibitor Ritonavir
CAS Number:
176655-55-3
Molecular Weight:
579.80
Molecular Formula:
C32H45N5O3S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Desthiazolylmethyloxycarbonyl Ritonavir (D-ritonavir) is a derivative of ritonavir, specifically designed for research use to study the biochemical properties of the parent compound. This derivative is particularly useful in the analysis of protease inhibition mechanisms and the metabolic stability of ritonavir. The primary mechanism of action of D-ritonavir involves the inhibition of the HIV-1 protease enzyme, similar to ritonavir. This enzyme plays a critical role in the viral life cycle by cleaving the polyprotein precursors into mature protein components necessary for assembling new virus particles. D-ritonavir binds to the active site of the HIV-1 protease, preventing it from processing the viral polyproteins, thereby leading to the production of immature, non-infectious viral particles. This action allows researchers to dissect how protease inhibitors affect the viral assembly and maturation process. In the context of research, D-ritonavir is used extensively to study the interaction between the protease inhibitor and the protease enzyme in a detailed manner. It helps in understanding the structural basis of enzyme inhibition and the design of more effective protease inhibitors based on the modifications and interactions observed with D-ritonavir. Additionally, D-ritonavir serves as a valuable tool in metabolic studies. Its modified structure makes it a suitable analog for examining how structural changes influence the absorption, distribution, metabolism, and excretion (ADME) properties of ritonavir. Researchers use D-ritonavir to investigate how the introduction of the desthiazolylmethyloxycarbonyl group affects the metabolic stability and enzymatic interactions compared to the parent compound.


Desthiazolylmethyloxycarbonyl Ritonavir (CAS 176655-55-3) References

  1. Interaction of human cytochrome P4503A4 with ritonavir analogs.  |  Sevrioukova, IF. and Poulos, TL. 2012. Arch Biochem Biophys. 520: 108-16. PMID: 22410611
  2. Understanding the mechanism of cytochrome P450 3A4: recent advances and remaining problems.  |  Sevrioukova, IF. and Poulos, TL. 2013. Dalton Trans. 42: 3116-26. PMID: 23018626
  3. Pyridine-substituted desoxyritonavir is a more potent inhibitor of cytochrome P450 3A4 than ritonavir.  |  Sevrioukova, IF. and Poulos, TL. 2013. J Med Chem. 56: 3733-41. PMID: 23586711
  4. Ritonavir analogues as a probe for deciphering the cytochrome P450 3A4 inhibitory mechanism.  |  Sevrioukova, IF. and Poulos, TL. 2014. Curr Top Med Chem. 14: 1348-55. PMID: 24805065
  5. Characterization of ritonavir-mediated inactivation of cytochrome P450 3A4.  |  Rock, BM., et al. 2014. Mol Pharmacol. 86: 665-74. PMID: 25274602
  6. Current Approaches for Investigating and Predicting Cytochrome P450 3A4-Ligand Interactions.  |  Sevrioukova, IF. and Poulos, TL. 2015. Adv Exp Med Biol. 851: 83-105. PMID: 26002732
  7. Integrated structural and evolutionary analysis reveals common mechanisms underlying adaptive evolution in mammals.  |  Slodkowicz, G. and Goldman, N. 2020. Proc Natl Acad Sci U S A. 117: 5977-5986. PMID: 32123117
  8. Evaluating the 'wrong-way-round' electrospray ionization of antiretroviral drugs for improved detection sensitivity.  |  Venter, P. and van Onselen, R. 2023. Anal Bioanal Chem. 415: 1187-1193. PMID: 36637494

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Desthiazolylmethyloxycarbonyl Ritonavir, 5 mg

sc-207550
5 mg
$393.00