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GSK-LSD1 dihydrochloride

Catalog No. T2315Cas No. 2102933-95-7
Alias GSK-LSD1 2HCl, GSK-LSD1 (hydrochloride)

GSK-LSD1 dihydrochloride (GSK-LSD1 2HCl) is a specificity irreversible LSD1 inhibitor (IC50: 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B).

GSK-LSD1 dihydrochloride

GSK-LSD1 dihydrochloride

Purity: 100%
Catalog No. T2315Alias GSK-LSD1 2HCl, GSK-LSD1 (hydrochloride)Cas No. 2102933-95-7
GSK-LSD1 dihydrochloride (GSK-LSD1 2HCl) is a specificity irreversible LSD1 inhibitor (IC50: 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B).
Pack SizePriceAvailabilityQuantity
1 mg$34In Stock
2 mg$48In Stock
5 mg$65In Stock
10 mg$105In Stock
25 mg$221In Stock
50 mg$335In Stock
100 mg$549In Stock
500 mg$1,170In Stock
1 mL x 10 mM (in DMSO)$65In Stock
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Purity:100%
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Product Introduction

Bioactivity
Description
GSK-LSD1 dihydrochloride (GSK-LSD1 2HCl) is a specificity irreversible LSD1 inhibitor (IC50: 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B).
Targets&IC50
LSD1:16 nM
In vitro
GSK-LSD1 induces gene expression changes in cancer cell lines with average EC50 of < 5 nM and inhibits cancer cell line growth with average EC50 of < 5 nM. [1]
AliasGSK-LSD1 2HCl, GSK-LSD1 (hydrochloride)
Chemical Properties
Molecular Weight289.24
FormulaC14H22Cl2N2
Cas No.2102933-95-7
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 4.23 mg/mL (14.63 mM), Sonication is recommended.
H2O: 10 mg/mL (34.57 mM)
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM3.4573 mL17.2867 mL34.5734 mL172.8668 mL
5 mM0.6915 mL3.4573 mL6.9147 mL34.5734 mL
10 mM0.3457 mL1.7287 mL3.4573 mL17.2867 mL
H2O
1mg5mg10mg50mg
20 mM0.1729 mL0.8643 mL1.7287 mL8.6433 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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