| Bioactivity | Eliglustat is an specific, potent and orally active glucocerebroside synthase inhibitor with an IC50 of 24 nM. | ||||||||||||
| Target | IC50: 24 nM (glucocerebroside synthase) | ||||||||||||
| Invitro | Eliglustat tartrate shows good potency with an IC50 of 24 nM and specificity against the target enzyme[1].Incubating K562 or B16/F10 cells for 72 h with increasing amounts of Genz-112638 (0.6-1000 nM) results in a dose-dependent reduction of cell surface levels of both GM1 and GM3. The mean IC50 value for inhibiting the cell surface presentation of GM1 in K562 cells was 24 nM (range 14-34 nM) and that for GM3 in B16/F10 cells was 29 nM (range 12-48 nM)[1]. | ||||||||||||
| In Vivo | Mice that received drug prior to significant accumulation of substrate (10 weeks of age) showed reduced levels of glucosylceramide and number of Gaucher cells in the spleen, lung and liver when compared to age-matched control animals[1]. | ||||||||||||
| Name | Eliglustat | ||||||||||||
| CAS | 491833-29-5 | ||||||||||||
| Formula | C23H36N2O4 | ||||||||||||
| Molar Mass | 404.54 | ||||||||||||
| Appearance | Solid | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
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| Reference | [1]. McEachern KA, et al. A specific and potent inhibitor of glucosylceramide synthase for substrate inhibition therapy ofGaucher disease. Mol Genet Metab. 2007 Jul;91(3):259-68. |