Date published: 2025-10-19

1-800-457-3801

SCBT Portrait Logo
Seach Input

S-(+)-Clopidogrel Hydrogen Sulfate (CAS 120202-66-6)

5.0(2)
Write a reviewAsk a question

See product citations (1)

Alternate Names:
Clopidogrel Bisulphate; Clopidogrel sulfate; Iscover
Application:
S-(+)-Clopidogrel Hydrogen Sulfate is an irreversible inhibitor of P2Y12
CAS Number:
120202-66-6
Molecular Weight:
419.90
Molecular Formula:
C16H16ClNO2S•H2SO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

S-(+)-Clopidogrel hydrogen sulfate, an enantiomer of clopidogrel, is a potent and selective inhibitor of adenosine diphosphate (ADP) receptor on platelet cell membranes. This compound functions by irreversibly modifying the P2Y12 component of ADP receptors, thus inhibiting platelet aggregation. Its unique mechanism involves the hepatic cytochrome P450 system, where it is metabolized to an active thiol metabolite that binds covalently to the P2Y12 receptor, leading to a sustained inhibition of platelet activation and aggregation. This attribute makes it a focal point in research studies investigating the pathways of platelet aggregation and the development of antiplatelet agents. Specifically, its role in the elucidation of the ADP receptor signaling mechanism and the interplay between genetic polymorphisms in the cytochrome P450 system with drug efficacy has been a subject of extensive study. Moreover, S-(+)-clopidogrel hydrogen sulfate′s enantiomeric specificity highlights the significance of stereochemistry in the pharmacodynamic properties of drugs, guiding research towards the development of more selective and efficient therapeutic agents in areas beyond its traditional applications, strictly focusing on its biochemical and molecular interactions.


S-(+)-Clopidogrel Hydrogen Sulfate (CAS 120202-66-6) References

  1. Formation of the thiol conjugates and active metabolite of clopidogrel by human liver microsomes.  |  Zhang, H., et al. 2012. Mol Pharmacol. 82: 302-9. PMID: 22584220
  2. Activation of platelet protein kinase C by ultraviolet light B mediates platelet transfusion-related acute lung injury in a two-event animal model.  |  Zhi, L., et al. 2013. Transfusion. 53: 722-31. PMID: 22853798
  3. Clopidogrel variability: role of plasma protein binding alterations.  |  Ganesan, S., et al. 2013. Br J Clin Pharmacol. 75: 1468-77. PMID: 23116430
  4. Validation of a method for quantitation of the clopidogrel active metabolite, clopidogrel, clopidogrel carboxylic acid, and 2-oxo-clopidogrel in feline plasma.  |  Lyngby, JG., et al. 2017. J Vet Cardiol. 19: 384-395. PMID: 28602635
  5. Clopidogrel Carboxylic Acid Glucuronidation is Mediated Mainly by UGT2B7, UGT2B4, and UGT2B17: Implications for Pharmacogenetics and Drug-Drug Interactions .  |  Kahma, H., et al. 2018. Drug Metab Dispos. 46: 141-150. PMID: 29138287
  6. An automated cocktail method for in vitro assessment of direct and time-dependent inhibition of nine major cytochrome P450 enzymes - application to establishing CYP2C8 inhibitor selectivity.  |  Kahma, H., et al. 2021. Eur J Pharm Sci. 162: 105810. PMID: 33753217

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

S-(+)-Clopidogrel Hydrogen Sulfate, 100 mg

sc-220001
100 mg
$82.00

S-(+)-Clopidogrel Hydrogen Sulfate, 1 g

sc-220001A
1 g
$165.00

S-(+)-Clopidogrel Hydrogen Sulfate, 5 g

sc-220001B
5 g
$560.00