S 2101

目录号: GC33339纯度: >98%
S2101是一个赖氨酸特异性去甲基化酶1(LSD1)抑制剂,其IC50值为0.99μM,Ki值为0.61μM,Kinact/Ki值为4560M/s。

S 2101
Cas No.: 1239262-36-2
规格价格库存数量操作
5mg¥1,980.00现货
1
10mg¥3,150.00现货
1
25mg¥6,300.00现货
1

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产品描述 Description

S 2101 is a lysine-specific demethylase 1 (LSD1) inhibitor with an IC50 of 0.99 μM, Ki of 0.61 μM and Kinact/Ki of 4560 M/s.

S 2101 is a lysine-specific demethylase 1 (LSD1) inhibitor with an IC50 of 0.99 μM, Ki of 0.61 μM and Kinact/Ki of 4560 M/s. S 2101 also displays much lower inhibition activity toward MAO-B (Ki=17 µM, Kinact/Ki=18 M/s) and MAO-A (Ki=110 µM, Kinact/Ki=60 M/s). The treatment of HEK293T cells with S 2101 results in a dose-dependent increase in the level of H3K4me2, which must have accumulated by the inactivation of LSD1. During the course of S 2101 treatment, the amounts of histone H3 and LSD1 in the nuclear extracts remain essentially unaffected. Because the treatment with 1 μM S 2101 generates a level of H3K4me2 similar to that elicited by 50 μM 2-PCPA, S 2101 is assumed to have approximately 50-fold stronger LSD1 inhibition activity than 2-PCPA in human cells[1].

[1]. Mimasu S, et al. Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSD1/KDM1 . Biochemistry. 2010 Aug 3;49(30):6494-503.

实验参考方法 Experimental Reference Method

Kinase experiment:

HEK293T cells are grown in 100 mm dishes in Dulbecco’s modified Eagle’s medium containing 10% FBS and a 100 units/mL penicillin, 100 μg/mL streptomycin antibiotic solution under a 5% CO2 atmosphere at 37°C. Cells at approximately 70% confluency are treated with S 2101 for 24 h, detached, and rinsed several times with ice-cold PBS. Nuclear extracts are prepared using a extraction kit, according to the manufacturer’s instructions. Each nuclear extract is electrophoresed on a 10 to 20% SDS-polyacrylamide gel and then transferred to a nitrocellulose membrane. The proteins on the membranes are probed with primary antibodies and then with a secondary antibody and are detected with a chemiluminescent system. The band intensities are visualized with an image analyzer[1].

References:

[1]. Mimasu S, et al. Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSD1/KDM1 . Biochemistry. 2010 Aug 3;49(30):6494-503.

产品文档 Product Documents

化学性质Chemical Properties

CAS 号
1239262-36-2
SMILES
FC1=CC(F)=CC([C@H]2[C@H](N)C2)=C1OCC3=CC=CC=C3.Cl
分子式
C16H16ClF2NO
分子量
311.75 g/mol
溶解性
Soluble in DMSO
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol