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Amantadine-d15 Hydrochloride (CAS 665-66-7 (unlabeled))

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Application:
Amantadine-d15 Hydrochloride is an antagonist of the NMDA receptor
CAS Number:
665-66-7 (unlabeled)
Purity:
98%
Molecular Weight:
202.80
Molecular Formula:
C10H3D15ClN
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Amantadine-d15 Hydrochloride, chemically distinguished by the substitution of fifteen hydrogen atoms with deuterium (D), is an isotopically labeled variant of amantadine hydrochloride. This modification significantly alters its physical properties, notably its vibrational modes, due to the increased mass of deuterium compared to hydrogen, which can be particularly advantageous in spectroscopic studies for elucidating the compound′s interaction mechanisms at the molecular level. In research, Amantadine-d15 Hydrochloride serves as a pivotal tool in the study of viral replication processes, especially in the context of the influenza A virus. It is employed to investigate the mechanisms by which viral particles penetrate host cellular membranes, offering a unique window into the dynamics of viral entry and uncoating. The isotopic labeling enhances the resolution of nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry analyses, making it an indispensable compound for tracing the distribution and metabolic pathways of amantadine in complex biological systems without the interference of background signals from naturally occurring isotopes. This refined understanding aids in the development of antiviral strategies and the exploration of viral resistance mechanisms, providing a foundational platform for the synthesis of novel antiviral agents.


Amantadine-d15 Hydrochloride (CAS 665-66-7 (unlabeled)) References

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  2. Functional studies indicate amantadine binds to the pore of the influenza A virus M2 proton-selective ion channel.  |  Jing, X., et al. 2008. Proc Natl Acad Sci U S A. 105: 10967-72. PMID: 18669647
  3. Simultaneous determination of amantadine, rimantadine and memantine in chicken muscle using multi-walled carbon nanotubes as a reversed-dispersive solid phase extraction sorbent.  |  Wu, YL., et al. 2014. J Chromatogr B Analyt Technol Biomed Life Sci. 965: 197-205. PMID: 25043282
  4. On-line multi-residue analysis of fluoroquinolones and amantadine based on an integrated microfluidic chip coupled to triple quadrupole mass spectrometry.  |  Tang, M., et al. 2020. Anal Methods. 12: 5322-5331. PMID: 33135716
  5. Application of multi-parameter population model based on endogenous population biomarkers and flow volume in wastewater epidemiology.  |  Hou, C., et al. 2021. Sci Total Environ. 759: 143480. PMID: 33213920
  6. Simultaneous determination of five antiviral drug residues and stability studies in honey using a two-step fraction capture coupled to liquid chromatography tandem mass spectrometry.  |  Wang, Z., et al. 2021. J Chromatogr A. 1638: 461890. PMID: 33465584
  7. Fully Automatic Multi-Class Multi-Residue Analysis of Veterinary Drugs Simultaneously in an Integrated Chip-MS Platform.  |  Tang, M., et al. 2021. J Agric Food Chem. 69: 14320-14329. PMID: 34779203
  8. Comparison of LC-MS3 and LC-MRM Methods for Quantifying Amantadine and Its Application in Therapeutic Amantadine Monitoring in Human Plasma.  |  Sun, Q., et al. 2022. Molecules. 27: PMID: 36364446
  9. Ion channel activity of influenza A virus M2 protein: characterization of the amantadine block.  |  Wang, C., et al. 1993. J Virol. 67: 5585-94. PMID: 7688826
  10. Simultaneous determination of amantadine, rimantadine and chlorpheniramine in animal-derived food by liquid chromatography-tandem mass spectrometry after fast sample preparation  |  Zhao, S., Li, D., Qiu, J., Wang, M., Yang, S., & Chen, D. 2014. Analytical methods. 6(17): 7062-7067.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Amantadine-d15 Hydrochloride, 1 mg

sc-217620
1 mg
$454.00