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Eliglustat hemitartrate (Synonyms: Genz-112638; Eliglustat tartrate)

Cat. No.: HY-14885A Purity: 99.83%
Data Sheet SDS Handling Instructions

Eliglustat hemitartrate is an specific, potent and orally active glucocerebroside synthase inhibitor with an IC50 of 24 nM.

For research use only. We do not sell to patients.
Eliglustat hemitartrate Chemical Structure

Eliglustat hemitartrate Chemical Structure

CAS No. : 928659-70-5

Size Price Stock Quantity
10 mM * 1 mL in DMSO $317 In-stock
1 mg $90 In-stock
5 mg $150 In-stock
10 mg $300 In-stock
50 mg $750 In-stock
100 mg $1050 In-stock
200 mg   Get quote  
500 mg   Get quote  

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Other Forms of Eliglustat hemitartrate:

  • Biological Activity

  • Protocol

  • Technical Information

  • Purity & Documentation

  • References

Description

Eliglustat hemitartrate is an specific, potent and orally active glucocerebroside synthase inhibitor with an IC50 of 24 nM.

IC50 & Target

IC50: 24 nM (glucocerebroside synthase)[1]

In Vitro

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].

Clinical Trial
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References
Preparing Stock Solutions
Concentration Volume Mass 1 mg 5 mg 10 mg
1 mM 1.0426 mL 5.2128 mL 10.4257 mL
5 mM 0.2085 mL 1.0426 mL 2.0851 mL
10 mM 0.1043 mL 0.5213 mL 1.0426 mL
Please refer to the solubility information to select the appropriate solvent.
Cell Assay
[1]

The inhibitory activity of Genz-112638 is determined indirectly by measuring its effect on the cell surface levels of the gangliosides GM1 and GM3 on either K562 or B16/F10 cells. GM1 levels on the K562 cells are determined by incubating the cells with increasing amounts of Genz-112638 (0.6-1000 nM) for 72 h after which the cells are harvested and stained using 10 μg of recombinant cholera toxin-FITC in 100 μL phosphate buffered saline (PBS) containing 0.5% bovine serum albumin (BSA) for 30 min on ice. Cells are ished, resuspended in PBS containing 0.5% BSA and the fluorescence quantitated[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Administration
[1]

Mouse: Genz-112638 is dissolved in water for injection and administered in a dose escalation from 75 mg/kg/day to 150 mg/kg/day over the course of nine days, with three days at each dose and increments of 25 mg/kg/day. Mice are weighed three times per week to monitor the potential impact of the drug on their overall health. Animals are killed by carbon dioxide inhalation[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

References
Molecular Weight

959.17

Formula

C₅₀H₇₈N₄O₁₄

CAS No.

928659-70-5

Storage
Powder -20°C 3 years
  4°C 2 years
In solvent -80°C 6 months
  -20°C 1 month
Shipping

Room temperature in continental US; may vary elsewhere

Solvent & Solubility

10 mM in DMSO

* "<1 mg/mL" means slightly soluble or insoluble. "≥" means soluble, but saturation unknown.

Purity: 99.83%

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Eliglustat hemitartrate
Cat. No.:
HY-14885A
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