首页工具

登录

搜索结果

Search Results for " lsd "

31

抑制剂 & 化合物

6

重组蛋白

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T81913	LSD
	LSD为光免疫研究中使用的酞菁偶联物。
T31361	Deethyl-LSD LAE 32,Lysergic acid ethylamide,LAE-32,N-Ethyllysergamide,LAE32
	Deethyl-LSD is reported to have some LSD-like effects but is weaker and shorter-lasting, with an active dose reported to be between 0.5 and 1.5 milligrams.
T2315	GSK-LSD1 dihydrochloride GSK-LSD1 (hydrochloride),GSK-LSD1 2HCl	Histone Demethylase	Chromatin/Epigenetic
	GSK-LSD1 dihydrochloride (GSK-LSD1 2HCl) 是一种特异性不可逆的 LSD1 抑制剂(IC50: 16 nM)。GSK-LSD1 dihydrochloride 对 LSD1 的选择性是其他密切相关的 FAD 利用酶（即 MAO-A、LSD2、MAO-B）的 1000 倍以上。
T67871	LSD1-IN-24	Histone Demethylase; PD-1/PD-L1	Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Immunology/Inflammation
	LSD1-IN-24 是一种具有选择性和有效性的 LSD1 抑制剂，IC50 值为 0.247 μM。LSD1-IN-24 可诱导 PD-L1 的表达，加强 T 细胞杀伤反应，可用于癌症相关疾病。
T83966	LSD1-IN-30	Histone Demethylase	Chromatin/Epigenetic
	LSD1-IN-30 是赖氨酸特异性脱甲基酶 1 (LSD1) 抑制剂，具有抗癌活性，可用于研究小细胞肺癌和急性髓细胞白血病。
T63140	LSD1-IN-20	Histone Demethylase	Chromatin/Epigenetic
	LSD1-IN-20 是一种有效的 LSD1/G9a 双重抑制剂，其 Ki 值分别为 0.44 和 0.68 μM。LSD1-IN-20 在体外实验中对 THP-1 白血病细胞和 MDA-MB-231 乳腺癌细胞显示出抗增殖活性，72 h 时 IC50 分别为 0.51 和 1.60 μM。
T77635	LSD1-IN-27	Histone Demethylase; PD-1/PD-L1	Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Immunology/Inflammation
	LSD1-IN-27 是一种高效的 LSD1 抑制剂，IC50 值为 13 nM。LSD1-IN-27 对胃癌细胞的干细胞性和迁移有抑制作用。LSD1-IN-27 对 BGC-823 和 MFC 细胞中 PD-L1 的表达有抑制作用。LSD1-IN-27 可增强对胃癌的 T 细胞免疫反应。
T36625	LSD1/HDAC6-IN-1 LSD1/HDAC6-IN-1
	LSD1/HDAC6-IN-1 is an orally active compound that functions as a dual inhibitor, targeting lysine specific demethylase 1 (LSD1) and histone deacetylase 6 (HDAC6). This compound demonstrates promising anti-tumor activity and is particularly valuable for research focused on multiple myeloma (MM) [1].
T11882	Pulrodemstat benzenesulfonate LSD1-IN-7 benzenesulfonate,CC-90011 benzenesulfonate	Histone Demethylase	Chromatin/Epigenetic
	Pulrodemstat benzenesulfonate (CC-90011 benzenesulfonate) 是一种有效的口服活性赖氨酸特异性去甲基化酶 1 (LSD1) 抑制剂，IC50为 0.25 nM，具有抗癌活性。它诱导急性髓细胞性白血病和小细胞肺癌细胞分化，对 LSD2、MOA-A 和 MAO-B 的酶抑制作用较小。
T11881	LSD1-IN-6	Histone Demethylase	Chromatin/Epigenetic
	LSD1-IN-6 increases dimethylated Lys4 of histone H3, shows no effect on expression of LSD1. LSD1-IN-6 is a potent and reversible inhibitor of lysine-specific demethylase 1 (LSD1), with an IC50 of 123 nM.
T11880	LSD1-IN-5	Histone Demethylase	Chromatin/Epigenetic
	LSD1-IN-5 increases dimethylated Lys4 of histone H3, shows no effect on expression of LSD1. LSD1-IN-5 is a potent and reversible inhibitor of lysine-specific demethylase 1 (LSD1), with an IC50 of 121 nM.
T60362	LSD1-IN-22
	LSD1-IN-22 是一种有效的赖氨酸特异性去甲基化酶 1 (LSD1) 抑制剂(Ki= 98 nM)。LSD1-IN-22 对某些癌细胞具有抗增殖活性。
T60381	LSD1-IN-12
	LSD1-IN-12 (compound 2) 是有效的 LSD1抑制剂，Ki 值分别为 1.1 μM (LSD1), 61 μM (LSD2), 2.3 μM (MAO-A), 和 3.5 μM (MAO-B)。
T62674	LSD1-IN-21
	LSD1-IN-21 是一种有效的、具有血脑屏障通透性的 LSD1 (赖氨酸特异性去甲基化酶-1) 抑制剂 (IC50: 0.956 μM)。LSD1-IN-21 能够明显减少促炎细胞因子 TNF-α，表现出良好的抗癌和抗炎效果。
T62099	LSD1-IN-13
	LSD1-IN-13 (compound 7e) 是一种口服具有活力的 LSD1 抑制剂 (IC50: 24.43 nM)，也能够激活 CD86 表达 (EC50: 470 nM)。LSD1-IN-13 可以诱导 AML (急性髓系白血病) 细胞系分化。
T63716	LSD1-IN-18
	LSD1-IN-18 是有效的、非共价的、选择性的 LSD1 抑制剂 (Ki:0.156 μM; KD: 0.075 μM)。LSD1-IN-18 在 THP-1 白血病细胞和 MDA-MB-231 乳腺癌细胞中表现出抗增殖效果，其IC50(72 h) 分别为 0.16 和 0.21 μM。
T74855	LSD1-IN-25	Histone Demethylase	Chromatin/Epigenetic
	LSD1-IN-25（Compound 9j）是一种高效、选择性及口服活性的LSD1抑制剂，具有46 nM的IC50（Ki值为30.3 nM），并能够诱导癌细胞的凋亡（apoptosis）。
T61405	LSD1-IN-14
	LSD1-IN-14, a powerful and specific inhibitor of LSD1 (with an IC50 value of 0.89 μM), effectively suppresses the growth of A549 and THP-1 cells and promotes the apoptosis of tumor cells [1].
T82254	GSK-LSD1	Histone Demethylase	Chromatin/Epigenetic
	GSK-LSD1是一种LSD1抑制剂，能够降低肥胖小鼠模型的摄食量和体重，同时提升胰岛素敏感性与血糖控制。此外，GSK-LSD1对NAFLD也有改善作用，并能抑制COVID-19患者PBMC中SARS-CoV-2诱导的细胞因子释放。GSK-LSD1对抑制癌症的生长与转移也显示出潜在效果。
T61021	LSD1-IN-16
	LSD1-IN-16 (compound 4b) 是 LSD1的有效抑制剂，可抑制 LSD1-CoREST、MAO-A 和 MAO-B，IC50值分别为 0.015、0.024 和 0.366 μM。LSD1-IN-16 在前列腺癌 LNCaP 细胞中表现出细胞生长阻滞，IC50值为 15.2 μM。
T63920	LSD1-IN-19
	LSD1-IN-19 (compound 29) 是一种选择性的、有效的、非共价的 LSD1 抑制剂 (Ki: 0.108 μM, KD: 0.068 μM)。LSD1-IN-19 在 THP-1 白血病细胞和 MDA-MB-231 乳腺癌细胞中具有抗增殖效果，其72h 的IC50值分别为 0.17 和 0.40 μM。
T74858	LSD1-IN-26
	LSD1-IN-26（compound 12u）是一种对LSD1具有高效抑制作用的化合物，表现出25.3 nM的IC50值。该化合物对MAO-A和MAO-B亦有一定抑制效果，其IC50值分别为1234.57 nM和3819.27 nM。此外，LSD1-IN-26能够显著促进MGC-803细胞的凋亡，适用于胃癌的研究领域。
T61022	LSD1-IN-17
	LSD1-IN-17 (compound 5b) 是 LSD1的有效抑制剂，可抑制LSD1-CoREST、MAO-A 和MAO-B，IC50值分别为 0.005、0.028 和 0.820 μM。LSD1-IN-17 在前列腺癌 LNCaP 细胞中表现出细胞生长阻滞，IC50值为 17.2 μM。
T60941	LSD1-IN-15
	LSD1-IN-15 (compound 1b) 是一种有效的 LSD1抑制剂，可抑制 LSD1-CoREST、MAO-A 和 MAO-B，IC50值分别为 0.149、0.028 和 0.327 μM。LSD1-IN-15 显示前列腺癌 LNCaP 细胞中的细胞生长停滞，IC50值为 9.9 μM。
T62679	LSD1-IN-13 hydrochloride
	LSD1-IN-13 hydrochloride (compound 7e) 是一种口服具有活力的 LSD1 抑制剂 (IC50: 24.43 nM)。LSD1-IN-13 hydrochloride 能够激活 CD86 表达 (EC50: 470 nM)。LSD1-IN-13 hydrochloride 可以诱导 AML (急性髓系白血病) 细胞系分化。
T78888	LSD1-UM-109	Histone Demethylase	Chromatin/Epigenetic
	LSD1-UM-109为一强效可逆LSD1抑制剂，其IC50为3.1 nM。在MV4;11急性白血病细胞系中，该化合物抑制细胞生长，IC50值达0.6 nM，在H1417小细胞肺癌细胞系中，IC50值为1.1 nM。
T60361	LSD1/2-IN-4
	LSD1/2-IN-4 是一种 PCPA 衍生物，是 LSD1 和 LSD2 的抑制剂。LSD1/2-IN-4 对 LSD1 和 LSD2 具有抑制作用，其Ki 值分别为 0.11 μM 和 130 μM。LSD1/2-IN-4 可用于多种癌症的研究，如 T 细胞急性淋巴细胞白血病 (TALL) 。
T60360	LSD1/2-IN-3
	LSD1/2-IN-3 是赖氨酸特异性去甲基化酶 1 (LSD1) 的选择性抑制剂，Ki 值是 11 nM，而对LSD2的 Ki 值为 7 μM。LSD1在肿瘤干细胞中异常表达，LSD1/2-IN-3 能够抑制LSD1活性和癌细胞增殖。
T62818	LSD1/ER-IN-1
	LSD1/ER-IN-1 (compound 11g) 是一种有效的 ER 和 LSD1 抑制剂，能够作用于 LSD1 (IC50: 1.55 μM)。LSD1/ER-IN-1 能够高亲和力的选择 Erα 蛋白，α/β 比为 7.11。LSD1/ER-IN-1 对 MCF-7 乳腺癌细胞表现出良好的抗增殖效果 (IC50: 8.79 μM)。
T32906	LSZ
	LSZ is an analog of LSD.
T36627	Lysine-specific Demethylase Inhibitor (1C) (hydrochloride)
	Lysine-specific demethylase inhibitor (1C) (LSD inhibitor (1C)) is an inhibitor of LSD1, a repressive demethylase selective for histone H3 lysine 4 (H3K4).1,2LSD inhibitor (1C) inhibits LSD1 activity by 85.9% when used at a concentration of 10 μM.1It increases the level of H3K4 methylation, including H3K4me1 and H3K4me2 but not H3K9me2 levels, in HCT116 human colon carcinoma cells.2LSD inhibitor (1C) also induces re-expression of the Wnt signaling pathway proteins secreted frizzle-related protei...

化合物

Cat.No: T81913

Cat.No: T31361

Synonym: LAE 32,Lysergic acid ethylamide,LAE-32,N-Ethyllysergamide,LAE32

GSK-LSD1 dihydrochloride

Cat.No: T2315

Synonym: GSK-LSD1 (hydrochloride),GSK-LSD1 2HCl

Target: Histone Demethylase

Cat.No: T67871

Target: Histone Demethylase, PD-1/PD-L1

Cat.No: T83966

Target: Histone Demethylase

Cat.No: T63140

Target: Histone Demethylase

Cat.No: T77635

Target: Histone Demethylase, PD-1/PD-L1

LSD1/HDAC6-IN-1

Cat.No: T36625

Synonym: LSD1/HDAC6-IN-1

Pulrodemstat benzenesulfonate

Cat.No: T11882

Synonym: LSD1-IN-7 benzenesulfonate,CC-90011 benzenesulfonate

Target: Histone Demethylase

Cat.No: T11881

Target: Histone Demethylase

Cat.No: T11880

Target: Histone Demethylase

Cat.No: T60362

Cat.No: T60381

Cat.No: T62674

Cat.No: T62099

Cat.No: T63716

Cat.No: T74855

Target: Histone Demethylase

Cat.No: T61405

Cat.No: T82254

Target: Histone Demethylase

Cat.No: T61021

Cat.No: T63920

Cat.No: T74858

Cat.No: T61022

Cat.No: T60941

LSD1-IN-13 hydrochloride

Cat.No: T62679

Cat.No: T78888

Target: Histone Demethylase

Cat.No: T60361

Cat.No: T60360

Cat.No: T62818

Cat.No: T32906

Lysine-specific Demethylase Inhibitor (1C) (hydrochloride)

Cat.No: T36627

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPY-03056	LSD1 Protein, Human, Recombinant (His & GST) BHC110,LSD1,KDM1,AOF2,lysine (K)-specific demethyla...	Human	Baculovirus Insect Cells
	LSD1 belongs to the flavin monoamine oxidase family. It contains 1 SWIRM domain and is a component of an RCOR/GFI/LSD1/HDAC complex. LSD1 interacts directly with GFI1 and GFI1B. LSD1 specifically removes histone H3K4me2 to H3K4me1 or H3K4me0 through a FAD-dependent oxidative reaction. When forming a complex with an androgen receptor (and possibly other nuclear hormone receptors), LSD1 changes its substrates to H3K9me2. Thus LSD1 is considered to act as a coactivator or a corepressor. It may play...
TMPH-01213	DNASE1L3 Protein, Human, Recombinant (His) DNase I homolog protein DHP2,DNAS1L3,DNase I-like 3,Deoxyrib...	Human	Baculovirus Insect Cells
	Has DNA hydrolytic activity. Is capable of both single- and double-stranded DNA cleavage, producing DNA fragments with 3'-OH ends. Can cleave chromatin to nucleosomal units and cleaves nucleosomal and liposome-coated DNA. Acts in internucleosomal DNA fragmentation (INDF) during apoptosis and necrosis. The role in apoptosis includes myogenic and neuronal differentiation, and BCR-mediated clonal deletion of self-reactive B cells. Is active on chromatin in apoptotic cell-derived membrane-coated mic...
TMPH-01212	DNASE1L3 Protein, Human, Recombinant (His & Myc) LSD,Liver and spleen DNase,Deoxyribonuclease I-like...	Human	E. coli
	Has DNA hydrolytic activity. Is capable of both single- and double-stranded DNA cleavage, producing DNA fragments with 3'-OH ends. Can cleave chromatin to nucleosomal units and cleaves nucleosomal and liposome-coated DNA. Acts in internucleosomal DNA fragmentation (INDF) during apoptosis and necrosis. The role in apoptosis includes myogenic and neuronal differentiation, and BCR-mediated clonal deletion of self-reactive B cells. Is active on chromatin in apoptotic cell-derived membrane-coated mic...
TMPH-01214	DNASE1L3 Protein, Human, Recombinant DHP2,Deoxyribonuclease I-like 3,Deoxyribonuclease gamma,DNas...	Human	E. coli
	Has DNA hydrolytic activity. Is capable of both single- and double-stranded DNA cleavage, producing DNA fragments with 3'-OH ends. Can cleave chromatin to nucleosomal units and cleaves nucleosomal and liposome-coated DNA. Acts in internucleosomal DNA fragmentation (INDF) during apoptosis and necrosis. The role in apoptosis includes myogenic and neuronal differentiation, and BCR-mediated clonal deletion of self-reactive B cells. Is active on chromatin in apoptotic cell-derived membrane-coated mic...
TMPH-03560	lsdA Protein, S. aureus, Recombinant (His & Myc)	Staphylococcus aureus	E. coli
	lsdA Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 35.1 kDa and the accession number is Q6GA85.
TMPH-03561	lsdB Protein, S. aureus, Recombinant (His & SUMO)	Staphylococcus aureus	E. coli
	Cell wall-anchored surface receptor that extracts heme from oxidized metHb to enable growth on hemoglobin as a sole iron source. Rapidly extracts heme from hemoglobin and transfers it to IsdA or IsdC, which then relays it to the membrane transporter/IsdEF for internalization. Promotes also resistance to hydrogen peroxide and killing by neutrophils. lsdB Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is ...

重组蛋白

LSD1 Protein, Human, Recombinant (His & GST)

Cat.No: TMPY-03056

Species: Human

Expression System: Baculovirus Insect Cells

DNASE1L3 Protein, Human, Recombinant (His)

Cat.No: TMPH-01213

Species: Human

Expression System: Baculovirus Insect Cells

DNASE1L3 Protein, Human, Recombinant (His & Myc)

Cat.No: TMPH-01212

Species: Human

Expression System: E. coli

DNASE1L3 Protein, Human, Recombinant

Cat.No: TMPH-01214

Species: Human

Expression System: E. coli

lsdA Protein, S. aureus, Recombinant (His & Myc)

Cat.No: TMPH-03560

Species: Staphylococcus aureus

Expression System: E. coli

lsdB Protein, S. aureus, Recombinant (His & SUMO)

Cat.No: TMPH-03561

Species: Staphylococcus aureus

Expression System: E. coli

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼