Name | XEN723 |
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Description | XEN723 is a novel and potent thiazolylimidazolidinone inhibitor of Stearoyl-CoA Desaturase (SCD1) with IC50s of 45 and 524 nM in mouse and HepG2 cell, respectively. |
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Related Catalog | |
Target |
IC50: 45 nM (SCD1 in Mouse), 524 nM (SCD1 in HepG2 cell)[1] |
In Vitro | XEN723 is a novel and potent thiazolylimidazolidinone inhibitor of Stearoyl-CoA Desaturase (SCD1) with IC50s of 45 and 524 nM in mouse and HepG2 cell, respectively. XEN723 demonstrates an improvement in SCD1 in vitro potency of more than 560-fold compare to the original high throughput screen (HTS) hit[1]. |
References |
Molecular Formula | C21H20FN5O2S |
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Molecular Weight | 425.48 |
Storage condition | 2-8℃ |