Drug intelligence / Profile preview

aspirin + pterostilbene

Development stage
Unknown
Modality
Small Molecules
Administration
Oral
01

Overview

Aspirin + pterostilbene is an experimental oral combination of the nonsteroidal anti-inflammatory drug aspirin with the polyphenolic stilbenoid pterostilbene, intended to exploit complementary antiplatelet, anti-inflammatory, and chemopreventive properties. Aspirin irreversibly acetylates and inhibits cyclooxygenase-1 and cyclooxygenase-2, suppressing thromboxane A2 and prostaglandin synthesis, while pterostilbene, a dimethoxy analog of resveratrol, exhibits antioxidant, anti-inflammatory, metabolic, and anticancer activities via modulation of oxidative stress pathways, apoptotic and autophagic signaling, and nuclear receptors. Preclinical work has examined both covalent aspirin–stilbene conjugates and simple co-administration of aspirin with pterostilbene for enhanced inhibition of cancer cell growth, but there is no established approved medicinal product under this exact combination name.

02

Targets

GPIIb/IIIa (Integrin alpha-IIb/beta-3)Sucrase-IsomaltaseUGT1A9 (UDP-glucuronosyltransferase 1A9)UGT1A6 (UDP-glucuronosyltransferase 1A6)ALOX12 (Arachidonate 12-lipoxygenase, 12S type)AR (Adrenergic receptors)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)PGHS-1 (Prostaglandin G/H Synthase 1)

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