Isosafrole Size:Contact [email protected] for quotation InChi: InChI=1S/C26H32O11/c1-32-18-7-12(3-5-16(18)28)24-14-10-35-25(15(14)11-34-24)13-4-6-17(19(8-13)33-2)36-26-23(31)22(30)21(29)20(9-27)37-26/h3-8

InChi: InChI=1S/C26H32O11/c1-32-18-7-12(3-5-16(18)28)24-14-10-35-25(15(14)11-34-24)13-4-6-17(19(8-13)33-2)36-26-23(31)22(30)21(29)20(9-27)37-26/h3-8

InChiKey: WGLMBRZXZDAQHP-UHFFFAOYSA-N

Smiles: COC1=CC=C(C=C1OCCCN1CCC(CC1)C(=O)C1=CC=C(F)C=C1)C1CNC(=O)C1

as indicated by the enhanced colocalization with PSD-95

Formula: C17H22F2N4O3S2

Isosafrole Size:Contact [email protected] for quotation InChi: InChI=1S/C26H32O11/c1-32-18-7-12(3-5-16(18)28)24-14-10-35-25(15(14)11-34-24)13-4-6-17(19(8-13)33-2)36-26-23(31)22(30)21(29)20(9-27)37-26/h3-8Isosafrole, a stiripentol analog, is a potent LDH inhibitor. Stiripentol is a new generation antiepileptic drug, and its chemical structure is unrelated to other antiepileptic drugs. Seizures and epileptiform activity are reduced by inhibition of the metabolic pathway via lactate dehydrogenase (LDH), which is a component of the astrocyte neuron lactate shuttle. Isosafrole is a substructure of stiripentol that lacks the hydroxyl group and tertiary