Description
An inhibitor of PLA2 ( IC50 = 39 μM); inhibits release of arachidonic acid from rat polymorphonuclear leukocytes (IC50 = 24 μM); inhibits radioligand binding to L-type calcium channels in porcine heart membranes (IC50 = 0.39 μM)
Formal name: 3,8-dihydroxy-4,9-dimethyl-1,6-bis[(1Z)-1-methyl-1-propen-1-yl]-11H-dibenzo[b,e][1,4]dioxepin-11-one
Synonyms:
Molecular weight: 380.4
CAS: 139959-71-0
Purity: ≥95%
Formulation: A solid
Product Type|Biochemicals|Ion Channel Modulation|Blockers||Product Type|Biochemicals|Natural Products|Microbial Metabolites||Product Type|Biochemicals|Small Molecule Inhibitors|Phospholipases||Research Area|Immunology & Inflammation|Innate Immunity||Research Area|Lipid Biochemistry|Glycerophospholipids|Phospholipases