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Irsogladine maleate is a selective PDE4 inhibitor that facilitates gap junction intercellular communication through muscarinic acetylcholine receptor binding. It is a potent inhibitor of angiogenesis in wild-type and plasminogen activator-deficient mice. Inhibition of PDE4 prevents the hydrolysis of cAMP, an important secondary messenger molecule that is heavily involved in signal transduction. It enhances gap junction intercellular communication (GJIC) by promoting the transfer of Lucifer yellow CH between isolated rabbit gastric epithelial cells. These protective effects can be reversed by the nitric oxide synthase inhibitor L-NAME. Irsogladine maleate functions as an inhibitor of COX-1/2 and PDE.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Irsogladine maleate, 50 mg | sc-201190 | 50 mg | $64.00 | |||
Irsogladine maleate, 250 mg | sc-201190A | 250 mg | $153.00 |