Selatogrel
A novel antiplatelet drug
{{Drugbox
| verifiedfields = changed
| verifiedrevid = 477002123
| IUPAC_name = (2S)-2-[[4-[[3-(2-chlorophenyl)-1,2,4-oxadiazol-5-yl]methyl]piperazin-1-yl]methyl]-4-methyl-1,3-thiazole-5-carboxylic acid
| image = Selatogrel.svg
| image_size = 200px
| image_alt = Chemical structure of Selatogrel
}}
Selatogrel is a novel antiplatelet drug that acts as a P2Y12 receptor antagonist. It is being developed for the treatment of acute coronary syndrome (ACS) and other conditions where inhibition of platelet aggregation is desired.
Mechanism of Action[edit | edit source]
Selatogrel works by selectively inhibiting the P2Y12 receptor, a key receptor involved in the activation of platelets. By blocking this receptor, selatogrel prevents the binding of adenosine diphosphate (ADP), a potent platelet activator, thereby reducing platelet aggregation and thrombus formation.
Pharmacokinetics[edit | edit source]
Selatogrel is administered via subcutaneous injection, which allows for rapid absorption and onset of action. The drug is designed to provide quick and effective platelet inhibition, which is crucial in the acute management of thrombotic events.
Clinical Development[edit | edit source]
Selatogrel is currently undergoing clinical trials to evaluate its efficacy and safety in patients with acute coronary syndrome. Preliminary studies have shown promising results, with rapid onset of action and significant inhibition of platelet aggregation.
Potential Benefits[edit | edit source]
The rapid action of selatogrel makes it a potentially valuable option in emergency settings where quick platelet inhibition is necessary. Its subcutaneous route of administration offers a convenient alternative to oral antiplatelet agents, especially in patients who are unable to take oral medications.
Side Effects[edit | edit source]
As with other antiplatelet agents, the primary side effect of selatogrel is an increased risk of bleeding. Other potential side effects include bruising, nausea, and headache.
Related pages[edit | edit source]
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