Date published: 2025-10-16

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Ritonavir-d6 (CAS 155213-67-5 (unlabeled))

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Application:
Ritonavir-d6 is a deuterated selective HIV-1 protease inhibitor
CAS Number:
155213-67-5 (unlabeled)
Molecular Weight:
726.98
Molecular Formula:
C37H42D6N6O5S2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ritonavir-d6 is a deuterated form of ritonavir, where six hydrogen atoms are replaced by deuterium. This subtle modification significantly impacts the molecule′s mass and vibrational modes without altering the chemical structure or the mechanism of action, making it a valuable tool in scientific research, particularly in mass spectrometry and NMR spectroscopy studies. Ritonavir-d6 retains the primary mechanism of action of ritonavir, which is the inhibition of the HIV-1 protease enzyme. This enzyme is essential for the viral replication process, as it cleaves the viral polyprotein precursors into mature protein components that are necessary for assembling new virus particles. By inhibiting this protease, ritonavir-d6 prevents the maturation of the virus, effectively stopping the production of infectious viral particles. In research settings, ritonavir-d6 is primarily used as an internal standard in analytical methods. The introduction of deuterium atoms increases the molecular weight slightly, which helps in distinguishing the compound from ritonavir in mass spectrometric analyses. This is particularly useful in pharmacokinetic studies where precise measurement of ritonavir levels in biological samples is needed to understand its metabolism and distribution. Moreover, ritonavir-d6 is utilized in metabolic studies to trace the pathways and byproducts of ritonavir metabolism. The deuterium labeling allows researchers to track the compound through various metabolic processes, helping to identify metabolites and understand the enzyme kinetics involved in the metabolism of ritonavir without the interference from endogenous compounds.


Ritonavir-d6 (CAS 155213-67-5 (unlabeled)) References

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  2. Hair and plasma data show that lopinavir, ritonavir, and efavirenz all transfer from mother to infant in utero, but only efavirenz transfers via breastfeeding.  |  Gandhi, M., et al. 2013. J Acquir Immune Defic Syndr. 63: 578-84. PMID: 24135775
  3. Validation of simultaneous quantitative method of HIV protease inhibitors atazanavir, darunavir and ritonavir in human plasma by UPLC-MS/MS.  |  Mishra, T. and Shrivastav, PS. 2014. ScientificWorldJournal. 2014: 482693. PMID: 24587725
  4. Impact of Tesamorelin, a Growth Hormone-Releasing Factor (GRF) Analogue, on the Pharmacokinetics of Simvastatin and Ritonavir in Healthy Volunteers.  |  Teng, S., et al. 2013. Clin Pharmacol Drug Dev. 2: 237-45. PMID: 27121785
  5. Pharmacokinetics of adjusted-dose 8-hourly lopinavir/ritonavir in HIV-infected children co-treated with rifampicin.  |  Rabie, H., et al. 2019. J Antimicrob Chemother. 74: 2347-2351. PMID: 31081020
  6. Simultaneous Determination of 6 Antiretroviral Drugs in Human Hair Using an LC-ESI+-MS/MS Method: Application to Adherence Assessment.  |  Wu, Y., et al. 2021. Ther Drug Monit. 43: 756-765. PMID: 33587427
  7. A Pharmacokinetic Dose-Optimization Study of Cabotegravir and Bictegravir in a Mouse Pregnancy Model.  |  Mohan, H., et al. 2022. Pharmaceutics. 14: PMID: 36145509
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ritonavir-d6, 10 mg

sc-355967
10 mg
$3125.00