GSK-LSD1 Dihydrochloride

GSK-LSD1 Dihydrochloride Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:GSK-LSD1 dihydrochloride;GSK-LSD1 2HCl
CAS:2102933-95-7
Package:1 mL * 10mM (in DMSO);10 mg;100 mg;2 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: LEAP CHEM CO., LTD.
Tel: +86-852-30606658
Email: market18@leapchem.com
Products Intro: Product Name:GSK-LSD1 Dihydrochloride
CAS:2102933-95-7
Package:1g; 5g; 25g; 1kg; 5kg; 25kg
Company Name: Aladdin Scientific
Tel: +1-+1(833)-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:GSK-LSD1 Dihydrochloride
CAS:2102933-95-7
Purity:>=98% Package:$59.9/5mg;$99.9/10mg;Bulk package Remarks:98%
Company Name: MedChemexpress LLC  
Tel: 021-58955995
Email: sales@medchemexpress.cn
Products Intro: Product Name:GSK-LSD1 Dihydrochloride
CAS:2102933-95-7
Purity:80RMB/5mg Package:>98%
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Products Intro: Product Name:GSK-LSD1 Dihydrochloride
CAS:2102933-95-7
Purity:99% Package:1mg;5mg;10mg
GSK-LSD1 Dihydrochloride Basic information
Product Name:GSK-LSD1 Dihydrochloride
Synonyms:GSK LSD1 dihydrochloride,Monoamine Oxidase,GSK-LSD-1 dihydrochloride,Inhibitor,inhibit,GSK-LSD1,MAO,GSKLSD1 dihydrochloride,Histone Demethylase
CAS:2102933-95-7
MF:C14H21ClN2
MW:252.79
EINECS:
Product Categories:
Mol File:2102933-95-7.mol
GSK-LSD1 Dihydrochloride Structure
GSK-LSD1 Dihydrochloride Chemical Properties
storage temp. Store at -20°C
solubility DMF: 1 mg/ml; DMSO: 25 mg/ml; Ethanol: 0.1 mg/ml; PBS (pH 7.2): 10 mg/ml
form A crystalline solid
Safety Information
MSDS Information
GSK-LSD1 Dihydrochloride Usage And Synthesis
DescriptionLysine-specific demethylase 1 (LSD1) belongs to the family of flavin adenine dinucleotide (FAD)-dependent amine oxidases that include monoamine oxidases (MAOs) and polyamine oxidase (PAO).1 LSD1 specifically demethylates mono- and dimethylated histone H3 lysine 4, resulting in transcriptional repression.2 It also controls the tumor suppressor activity of p53 by demethylating a specific p53 lysine residue (LYS370).3 GSK-LSD1 is an irreversible, mechanism-based inhibitor of LSD1 (IC50 = 16 nM) that is >1,000-fold selective over the closely related FAD-utilizing enzymes LSD2, MAO-A, and MAO-B.4 GSK-LSD1 induces gene expression changes in various cancer cell lines, inhibiting their proliferation (EC50s <5 nM).4 See the Structural Genomics Consortium (SGC) website for more information.
storageStore at +4°C
References1. Shi, Y., Lan, F., Matson, C., et al. Histone demethylation mediated by the nuclear amine oxidase homolog LSD1 Cell 119(7),941-953(2004).
2. Forneris, F., Binda, C., Vanoni, M.A., et al. Human histone demethylase LSD1 reads the histone code J. Biol. Chem. 280(50),41360-41365(2005).
3. Huang, J., Sengupta, R., Espejo, A.B., et al. p53 is regulated by the lysine demethylase LSD1 Nature 449,105-108(2007).
4. Epigenetics probes collection ,(2014).
GSK-LSD1 Dihydrochloride Preparation Products And Raw materials
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