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Postion:Product Catalog >API>Blood System Drugs>Anticoagulant and Antiplatelet Drugs>Ticagrelor
Ticagrelor
  • Ticagrelor

Ticagrelor NEW

Price $40 $60 $74
Package 10mg 25mg 50mg
Min. Order:
Supply Ability: 10g
Update Time: 2025-04-30

Product Details

Product Name: Ticagrelor CAS No.: 274693-27-5
Purity: 99.77% Supply Ability: 10g
Release date: 2025/04/30

Product Introduction

Bioactivity

NameTicagrelor
DescriptionTicagrelor (AR-C 126532XX), produced by AstraZeneca, is an inhibitor of platelet aggregation. Unlike clopidogrel, ticagrelor is not a prodrug required metabolic activation. The drug was approved for use in the European Union by the European Commission on December 3, 2010, and by the US FDA on July 20, 2011. Its trade names are Brilinta (US), Brilique(EU) and Possia(EU).
In vitroTicagrelor has a half-life (t1/2) of approximately 7-8.5 hours and exhibits a dose-related inhibition of platelet aggregation; a 100-400 mg dose achieves complete inhibition within 2 hours. It is well-tolerated, with no serious adverse events or significant changes in laboratory values observed. Ticagrelor is rapidly absorbed, reaching peak levels in 1.3-2 hours. Within the studied dosage range, both the peak concentration of Ticagrelor and the area under the curve (from time zero to infinity) increase in a dose-proportional manner, indicating linear pharmacokinetics.
In vivoIn binding studies on CHO-K1 cells transfected with rh-P2Y12 receptors, Ticagrelor exhibited efficient and reversible binding, with a kon (association rate constant) of 0.00011/(nM·s), a Kd (equilibrium dissociation constant) of 10.5 nM, and a koff (dissociation rate constant) of 0.00087/s. The half-lives for association and dissociation were 4 and 14 minutes, respectively, suggesting that the concentration of the drug that binds to platelets determines the extent of platelet inhibition. Ticagrelor is an active drug that does not require metabolic activation. It does not directly compete with ADP at the ADP binding site but rather occupies a nearby site, causing a change in the conformation of the binding site that leads to a reversible conformational change in the receptor. The binding of Ticagrelor to the receptor is reversible with quick onset/off rates.
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility InformationDMSO : 50 mg/mL (95.68 mM), Sonication is recommended.
5% DMSO+40 % PEG300+5 % Tween 80+50 % Saline : 5 mg/mL (9.57 mM), In vivo: Please add co-solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately.
KeywordsTicagrelor | P2YReceptor | P2Y12 | P2Y Receptor | P2Y | Inhibitor | inhibit | CYP2C9 | AZD-6140 | AZD 6140
Inhibitors RelatedTebuconazole | 1-Ethynylnaphthalene | Diflubenzuron | Apigenin | Gemfibrozil | Fenofibrate | 1-Aminobenzotriazole | Methoxsalen | Uridine-5'-diphosphate disodium salt | Naringin | Naringenin | Tauroursodeoxycholate
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Company Profile Introduction

TargetMol Chemicals Inc. is headquartered in Boston, MA, and specializes in products and services that serve the research needs of chemical and biological scientists worldwide. With a client base in 40+ countries, TargetMol has evolved into one of the biggest global research suppliers for compound libraries and small molecule compounds. 170+ Compound Libraries, 10000+ Noval Small Molecucles,16000+ Nature Compounds TargetMol diligently updates and offers over 170 types of compound libraries and a wide range of high-quality research chemicals, including inhibitors, activators, natural products, peptides, antibodies , and novel life-science kits for laboratory and scientific use. In addition, our lab allows us to conduct CADD (computer-aided drug design) and chemical synthesis to meet the customization needs of our clients.

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