跳转至内容
Merck
CN

SML1072

GSK-LSD1

≥98% (HPLC), lysine specific demethylase 1 (LSD1) inhibitor, powder

别名:

GSK-LSD1(反式外消旋) 二盐酸盐, rel-N-[(1R,2S)-2-苯基环丙基] -4-哌啶胺盐酸盐(1:2)

登录 查看公司和协议定价

选择尺寸


关于此项目

经验公式(希尔记法):
C14H20N2 · 2HCl
化学文摘社编号:
分子量:
289.24
UNSPSC代码:
51111800
PubChem化学物质编号:
NACRES:
NA.77
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

GSK-LSD1, ≥98% (HPLC)

质量水平

方案

≥98% (HPLC)

表单

powder

颜色

white to beige

溶解性

H2O: 20 mg/mL, clear

储存温度

2-8°C

SMILES字符串

C1(N[C@@H]2C[C@H]2C3=CC=CC=C3)CCNCC1

InChI

1S/C14H20N2/c1-2-4-11(5-3-1)13-10-14(13)16-12-6-8-15-9-7-12/h1-5,12-16H,6-10H2/t13-,14+/m0/s1

InChI key

BASFYRLYJAZPPL-UONOGXRCSA-N

应用

GSK-LSD1已用作小鼠中的赖氨酸特异性脱甲基酶 1(LSD1)抑制剂,用于研究败血症诱导的死亡率。它还被用作抑制剂,用于研究苯乙肼激活人类免疫缺陷病毒(HIV)潜伏期是否由 LSD1 引起。

生化/生理作用

GSK-LSD1 是赖氨酸特异性脱甲基酶 1 的有效选择性抑制剂。
GSK-LSD1 是赖氨酸特异性脱甲基酶 1(LSD1)的有效选择性抑制剂。GSK-LSD1 通过改变基因表达模式有效抑制不同癌细胞系的增殖。有关完整特征描述的详细信息,请访问 Structural Genomics Consortium(SGC)网站上的 GSK-LSD1 探针目录

要了解用于表观遗传目标的其他 SGC 化学探针,请访问 sigma.com/sgc

特点和优势

GSK-LSD1 是一种表观遗传化学探针,是与 Structural Genomics Consortium (SGC) 合作研发的。想要了解更多信息并查看其他SGC表观遗传探针,请访问sigma.com/SGC
这种化合物是基因调控研究的特色产品。点击此处发现更多特色基因调控产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Bastian Ramms et al.
Diabetes, 71(12), 2513-2529 (2022-09-27)
The transition from lean to obese states involves systemic metabolic remodeling that impacts insulin sensitivity, lipid partitioning, inflammation, and glycemic control. Here, we have taken a pharmacological approach to test the role of a nutrient-regulated chromatin modifier, lysine-specific demethylase (LSD1)
HIV-1 infection of microglial cells in a reconstituted humanized mouse model and identification of compounds that selectively reverse HIV latency
Llewellyn GN, et al.
Journal of Neurovirology, 1-12 (2017)
PKCα-LSD1-NF-κB-Signaling Cascade Is Crucial for Epigenetic Control of the Inflammatory Response
Kim D, et al.
Molecular Cell, 69(3), 398-411 (2018)
Cavan P Bailey et al.
Frontiers in immunology, 11, 2196-2196 (2020-10-13)
Cell therapies such as chimeric-antigen receptor (CAR) T-cells and NK cells are cutting-edge methods for treating cancer and other diseases. There is high interest in optimizing drug treatment regimens to best work together with emerging cell therapies, such as targeting
Carl M Gay et al.
Cancer cell, 39(3), 346-360 (2021-01-23)
Despite molecular and clinical heterogeneity, small cell lung cancer (SCLC) is treated as a single entity with predictably poor results. Using tumor expression data and non-negative matrix factorization, we identify four SCLC subtypes defined largely by differential expression of transcription

商品

We offer a variety of small molecule research tools, such as transcription factor modulators, inhibitors of chromatin modifying enzymes, and agonists/antagonists for target identification and validation in gene regulation research; a selection of these research tools is shown below.

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持