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.
別名:
LSD1 Inhibitor, LSD Inhibitor I, BHC110 Inhibitor I, Histone Lysine Demethylase Inhibitor III, KDM1 Inhibitor I
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About This Item
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アッセイ
≥95% (HPLC)
形状
solid
メーカー/製品名
Calbiochem®
保管条件
OK to freeze
protect from light
色
pale yellow to yellow
溶解性
water: 50 mg/mL
保管温度
−20°C
詳細
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.
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.
警告
Toxicity: Standard Handling (A)
再構成
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
その他情報
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.
法的情報
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(℃)
Not applicable
試験成績書(COA)
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