489476-M
LSD1 Inhibitor
The LSD1 Inhibitor, also referenced under CAS 927019-63-4, controls the biological activity of LSD1. This small molecule/inhibitor is primarily used for Cell Signaling applications.
Synonym(s):
LSD1 Inhibitor, LSD Inhibitor I, BHC110 Inhibitor I, Histone Lysine Demethylase Inhibitor III, KDM1 Inhibitor I
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About This Item
Empirical Formula (Hill Notation):
C15H40Cl4N8
CAS Number:
Molecular Weight:
474.34
UNSPSC Code:
12352200
assay
≥95% (HPLC)
form
solid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze, protect from light
color
pale yellow to yellow
solubility
water: 50 mg/mL
storage temp.
−20°C
General description
A bisguanidine polyamine analogue that exhibits noncompetitive and specific LSD1 inhibition, with 14.1% remaining LSD1 activity at 10 µM in vitro, and is shown to significantly increase methylation at the histone 3 lysine 4 chromatin mark (H3K4me1 and H3K4me2) dose-dependently from 0.25 µM to 10 µM, without affecting global H3K9me2 (which is not a LSD1 substrate) levels in HCT116 human colon carcinoma cells. This compound induces reexpression of several epigenetically silenced genes including SFRP1, SFRP4, SFRP5, and GATA5 more effectively when compared with siRNA treatment, particularly in the case of SFRP4 and SFRP5.
Preparation Note
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Other Notes
Sharma, SK., et al. 2010 J. Med. Chem.53, 5197.
Huang, Y., et al. 2007. Proc. Natl. Acad. Sci.104, 8023.
Bi, X., et al. 2006. Bioorg. Med. Chem. Lett.16, 3229.
Huang, Y., et al. 2007. Proc. Natl. Acad. Sci.104, 8023.
Bi, X., et al. 2006. Bioorg. Med. Chem. Lett.16, 3229.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Toxicity: Standard Handling (A)
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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