Date published: 2026-1-30

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Ziagen (CAS 136470-78-5)

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Alternate Names:
Abacavir
Application:
Ziagen is a carbocyclic nucleoside analogue with inhibitory activity against HIV-1
CAS Number:
136470-78-5
Purity:
≥98%
Molecular Weight:
286.33
Molecular Formula:
C14H18N6O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ziagen, chemically known as abacavir sulfate, is a nucleoside reverse transcriptase inhibitor (NRTI) widely studied in scientific research for its role in combating HIV/AIDS. Its mechanism of action involves interference with the activity of HIV reverse transcriptase, an enzyme crucial for viral replication. Abacavir is phosphorylated intracellularly to its active form, abacavir triphosphate, which competes with natural nucleotides for incorporation into viral DNA, leading to chain termination and inhibition of viral replication. Research on abacavir has extended beyond its antiretroviral properties, delving into its impact on immune function, drug resistance mechanisms, and potential synergies with other antiretroviral agents. Studies have investigated the pharmacokinetics and pharmacodynamics of abacavir to optimize dosing strategies and enhance its effectiveness in suppressing viral load and preventing the emergence of drug-resistant HIV strains. Additionally, research has explored the safety profile of abacavir, including its potential for adverse drug reactions such as hypersensitivity reactions, highlighting the importance of pharmacovigilance in clinical practice. Furthermore, investigations into novel drug delivery systems and formulations aim to improve the bioavailability and patient adherence to abacavir-based antiretroviral therapy. Understanding the mechanisms of action and the research applications of abacavir provides valuable insights into its role in HIV/AIDS management and the ongoing efforts to combat this global public health challenge.


Ziagen (CAS 136470-78-5) References

  1. Abacavir-lamivudine-zidovudine vs indinavir-lamivudine-zidovudine in antiretroviral-naive HIV-infected adults: A randomized equivalence trial.  |  Staszewski, S., et al. 2001. JAMA. 285: 1155-63. PMID: 11231744
  2. Prospective screening for human leukocyte antigen-B*5701 avoids abacavir hypersensitivity reaction in the ethnically mixed French HIV population.  |  Zucman, D., et al. 2007. J Acquir Immune Defic Syndr. 45: 1-3. PMID: 17356469
  3. Absence of mitochondrial toxicity in hearts of transgenic mice treated with abacavir.  |  Kohler, JJ., et al. 2010. Cardiovasc Toxicol. 10: 146-51. PMID: 20379802
  4. Nucleoside Reverse Transcriptase Inhibitors Suppress Laser-Induced Choroidal Neovascularization in Mice.  |  Mizutani, T., et al. 2015. Invest Ophthalmol Vis Sci. 56: 7122-9. PMID: 26529046
  5. Abacavir Induces Arterial Thrombosis in a Murine Model.  |  Collado-Diaz, V., et al. 2018. J Infect Dis. 218: 228-233. PMID: 29346575
  6. The PD1 inhibitory pathway and mature dendritic cells contribute to abacavir hypersensitivity in human leukocyte antigen transgenic PD1 knockout mice.  |  Song, B., et al. 2021. Toxicology. 463: 152971. PMID: 34606953
  7. CRISPR editing of CCR5 and HIV-1 facilitates viral elimination in antiretroviral drug-suppressed virus-infected humanized mice.  |  Dash, PK., et al. 2023. Proc Natl Acad Sci U S A. 120: e2217887120. PMID: 37126704
  8. Nuclear lamina erosion-induced resurrection of endogenous retroviruses underlies neuronal aging.  |  Zhang, H., et al. 2023. Cell Rep. 42: 112593. PMID: 37261950
  9. 1592U89, a novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity.  |  Daluge, SM., et al. 1997. Antimicrob Agents Chemother. 41: 1082-93. PMID: 9145874
  10. Abacavir.  |  Foster, RH. and Faulds, D. 1998. Drugs. 55: 729-36; discussion 737-8. PMID: 9585869

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ziagen, 1 g

sc-338739
1 g
$130.00

Ziagen, 5 g

sc-338739A
5 g
$400.00