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GSK-LSD1 dihydrochloride

GSK-LSD1 dihydrochloride
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).
Catalog No. T2315Cas No. 2102933-95-7
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Purity:100%
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GSK-LSD1 dihydrochloride

Purity: 99.22%
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).
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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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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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In Vivo Formulation Calculator (Clear solution)

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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