PAFAH1B3 inhibitors belong to a distinctive chemical class that targets the PAFAH1B3 gene product, also known as platelet-activating factor acetylhydrolase 1b, subunit 3. This enzyme plays a crucial role in cellular processes by catalyzing the hydrolysis of platelet-activating factor (PAF), a lipid signaling molecule involved in various physiological functions, including inflammation, immune response, and neurotransmission. PAFAH1B3, a subunit of the PAFAH1B complex, is specifically implicated in the deacetylation of PAF, leading to the modulation of PAF-mediated cellular responses. Inhibitors designed to target PAFAH1B3 act by disrupting its enzymatic activity, thereby influencing the levels of PAF and potentially impacting downstream signaling pathways.
PAFAH1B3 inhibitors is carefully designed to interact with the catalytic site of the enzyme, inhibiting its normal function. These inhibitors often exhibit specificity for PAFAH1B3, distinguishing them from inhibitors that may affect other related enzymes. Researchers employ various molecular design strategies to optimize the affinity and selectivity of these inhibitors, aiming to enhance their efficacy in laboratory settings. Understanding the structural intricacies of both the enzyme and the inhibitors is critical for the development of potent compounds that can selectively modulate PAFAH1B3 activity.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ginkgolide B | 15291-77-7 | sc-201037B sc-201037 sc-201037C sc-201037A | 5 mg 10 mg 25 mg 50 mg | $46.00 $64.00 $114.00 $201.00 | 8 | |
Ginkgolide B, a terpenoid extracted from Ginkgo biloba, can inhibit PAFAH1B3 by binding to the catalytic site and preventing the hydrolysis of platelet-activating factor (PAF). | ||||||
Miltefosine | 58066-85-6 | sc-203135 | 50 mg | $81.00 | 8 | |
This alkylphosphocholine can insert into cell membranes and potentially disrupt the interaction of PAFAH1B3 with its substrates. | ||||||
ET-18-OCH3 | 77286-66-9 | sc-201021 sc-201021A sc-201021B sc-201021C sc-201021F | 5 mg 25 mg 50 mg 100 mg 1 g | $111.00 $436.00 $843.00 $1576.00 $3756.00 | 6 | |
As an ether lipid, edelfosine can inhibit PAFAH1B3 by integrating into membranes and altering lipid environment, which is crucial for PAFAH1B3's activity. | ||||||
Lyso-PAF (C18) | 74430-89-0 | sc-203123 sc-203123A | 1 mg 25 mg | $56.00 $342.00 | ||
Lyso-PAF can inhibit PAFAH1B3 by acting as a substrate analog, preventing the enzyme from interacting with actual PAF molecules. | ||||||
rac-Modipafant | 122956-68-7 | sc-505389 | 10 mg | $8500.00 | ||
Modipafant, as a PAF receptor antagonist, can indirectly inhibit PAFAH1B3 by preventing PAF signaling and reducing its substrate availability. | ||||||