Atiprosin
Atiprosin[edit | edit source]
Atiprosin (also known by its developmental code name AY-28,228) is a compound primarily studied for its potential as an antihypertensive agent. Although it was never commercially introduced or marketed, its pharmacological profile indicates that it acts primarily as a selective α1-adrenergic receptor antagonist.
Mechanism of Action[edit | edit source]
Atiprosin's primary mechanism of action is attributed to its role as a selective antagonist for the α1-adrenergic receptor. By targeting these receptors, it is believed that Atiprosin could mitigate the effects of certain types of hypertension, or high blood pressure.
Secondary Effects[edit | edit source]
In addition to its antihypertensive properties, Atiprosin has been found to possess some antihistamine activity. However, its efficacy in this role is considerably weaker. When compared to its primary function as an alpha blocker, its antihistamine activity is approximately 15 times weaker. This secondary property might have implications for potential side effects or drug interactions, though extensive studies in this area were never completed due to its non-commercial status.
Developmental History[edit | edit source]
While the potential therapeutic benefits of Atiprosin were identified during the research phase, the compound was never advanced to the stage of commercial production or marketing. The reasons for this decision remain speculative, but could range from challenges in production, unforeseen side effects, or economic considerations that made its introduction to the market unfeasible.
Synthesis[edit | edit source]
See Also[edit | edit source]
References[edit | edit source]
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Contributors: Prab R. Tumpati, MD
