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Description

A cell-permeable, thiadiazole-pyridazine compound that acts as an inhibitor of Stearoyl-CoA Desaturase 1 (SCD1) with an IC50 of 2.3 nM. In vivo, it exhibits an ED50 of 1-3 mg/kg, p.o., in mouse liver PD assays.

Structure formula

SAF-569406-10MG

Miscellaneous

Certificate of Analysis (specimen)

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Product data sheet

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