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Search Results for " hdac in 6 "

Targets Recommended: Virus Protease HDAC

50

抑制剂 & 化合物

13

重组蛋白

1

同位素标记化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T6327	Tubacin	Virus Protease; HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology
	Tubacin 是一种高效、选择性、可逆、可渗透细胞的 HDAC6 抑制剂，IC50 为 4 nM，选择性是 HDAC1 的约 350 倍。
T71587	Fluoxetine succinate ester	Others	Others
	Fluoxetine succinate ester is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class. It is used for the treatment of major depressive disorder, obsessive–compulsive disorder, bulimia nervosa, panic disorder, and premenstrual dysphoric disorder.
T69753	HDAC6 degrader 9c	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6 degrader 9c 是一种小分子组蛋白脱乙酰酶 6 （HDAC6）降解剂，可用于研究癌症或其他疾病。
T72012	HDAC-IN-6	Others	Others
	HDAC-IN-6 is an HDAC inhibitor, targeting HDAC2, HDAC3, HDAC4, HDAC5, HDAC7, HDAC8, and HDAC9.
T60954	HDAC6-IN-6	Others	Others
	HDAC6-IN-6 (化合物 6a) 是 HDAC6的有效抑制剂，可以穿透血脑屏障，IC50值为0.025 μM。HDAC6-IN-6 对 AChE 和 Aβ1-42自聚集具有有效的抑制活性，IC50值分别为 0.72 和 3.0 μM。HDAC6-IN-6 可促进神经突起生长而没有显著的神经毒性。
T82226	HDAC6-IN-21	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6-IN-21（化合物13）为一种靶向组蛋白去乙酰化酶6（histone deacetylase 6（HDAC6））的不可逆抑制剂。
T79769	HDAC6-IN-23	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6-IN-23（化合物9）是一种口服活性HDAC6抑制剂。
T60856	HDAC6-IN-9	Others	Others
	HDAC6-IN-9 (compound 12c) 是 HDAC6的强效选择性抑制剂，具有抗增殖活性。HDAC6-IN-9 对 HDAC6、HDAC1、HDAC3、HDAC8 和 HDAC10 的 IC50值分别为 4.2, 11.8, 15.2, 139.6, 21.3 nM。
T73043	HDAC6-IN-15	Others	Others
	HDAC6-IN-15 是一种选择性组蛋白脱乙酰酶 6(HDAC6)抑制剂。HDAC6-IN-15 对 HDAC6具有有效的抑制活性，IC50值为 38.2 nM。HDAC6-IN-15 可用于癌症和神经退行性疾病的研究。
T74617	HDAC6-IN-8	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	Compound 12c has been synthesized with modifications to the Cap group and exhibits broad-spectrum enzyme inhibitory activity as evidenced by enzyme inhibition assays. Compounds 9m and 9q show a preference for inhibiting HDAC6, demonstrating selective inhibitory activity among representative subtypes.
T79771	HDAC6-IN-22	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6-IN-22（化合物30）是一种针对HDAC6的抑制剂，其IC50值为4.63 nM。该化合物在体外及体内均展现出对多发性骨髓瘤细胞的抗增殖能力。HDAC6-IN-22 可诱导G2期的细胞周期阻滞，并通过线粒体路径促进细胞凋亡。
T78768	HDAC6-IN-16	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6-IN-16（compound 5c）是基于Quinazolin-4(3H)-One的一种HDAC6抑制剂，具备抑制肿瘤细胞集落形成的抗癌活性。该化合物能够引发G2期细胞周期阻滞并诱导细胞凋亡(apoptosis)。
T36625	LSD1/HDAC6-IN-1 LSD1/HDAC6-IN-1	Others	Others
	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].
T82225	HDAC6-IN-24	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6-IN-24（化合物N1）是一种HDAC6抑制剂。
T63472	HDAC6-IN-4	Others	Others
	HDAC6-IN-4 (C10) 是一种口服具有活力的、高度选择性的、有效的、无明显毒性的 HDAC6 抑制剂 (IC50: 23 nM)。HDAC6-IN-4 能够诱导肿瘤细胞凋亡 (apoptosis)，表现出高效的抗肿瘤效果。
T63247	HDAC6-IN-12	Others	Others
	HDAC6-IN-12 是 HDAC6 的有效抑制剂，能够结合 DNA 链中，导致 DNA 损伤，表现出抗癌作用，能够用于研究癌症。
T79523	HDAC6-IN-18	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6-IN-18（化合物4）是首个针对HDAC6亚型的不可逆选择性抑制剂，显示出有效的抗多发性骨髓瘤活性。该抑制剂在RPMI8266、U266以及MM.1S细胞系中表现出对HDAC6的抑制效力，其IC50值分别为0.17、0.7和0.42 μM[1]。
T73031	HDAC6-IN-14	Others	Others
	HDAC6-IN-14 是一种高选择性 HDAC6(HDAC) 抑制剂，IC50为 42 nM。HDAC6-IN-14 的选择性是 HDAC1/HDAC2/HDAC3/HDAC4 的 100 倍以上。
T61139	HDAC6-IN-3	Others	Others
	HDAC6-IN-3 (Compound 14) is a potent anti-prostate cancer agent that acts as an orally active inhibitor of HDAC6. It has IC50 values ranging from 0.02-1.54 μM for HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, and HDAC10. Additionally, HDAC6-IN-3 also demonstrates effective inhibition of MAO-A (IC50 = 0.79 μM) and LSD1 [1].
T61044	HDAC6-IN-11	Others	Others
	HDAC6-IN-11 (Compound 9) 对癌细胞具有抗增殖活性。HDAC6-IN-11 是 HDAC6 的选择性抑制剂，IC50值为 20.7 nM。HDAC6-IN-11 的选择性是其他 HDAC 异构体的 300 多倍。
T61792	HDAC6-IN-10	Others	Others
	HDAC6-IN-10 is a potent and specific HDAC6 inhibitor, exhibiting an IC50 value of 0.73 nM. It demonstrates remarkable selectivity towards HDAC6, with a selectivity range of 144 to 10,941-fold over other HDAC isoforms. Furthermore, HDAC6-IN-10 exhibits notable anti-proliferative effects on multiple myeloma cells [1].
T82224	HDAC6-IN-25	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6-IN-25(化合物8)作为高选择性HDAC6抑制剂，其IC50值达0.6 nM。
T78769	HDAC6-IN-17	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6-IN-17（化合物5b）是一种选择性HDAC6抑制剂，其IC50值针对HDAC6为150 nM，相比于HDAC8（1400 nM）和HDAC4（2300 nM）显示出较高的抑制活性。此化合物对人类癌细胞系展现出显著的细胞毒性，常用于癌症的研究领域。
T78839	HDAC6-IN-19	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC6-IN-19（Compound 14g）是一种选择性HDAC6抑制剂，具有2.68 nM的IC50值。同时，该化合物对HDAC1、HDAC2和HDAC3也表现出一定的抑制作用，其IC50值分别为61.6 nM、98.7 nM和103 nM。此外，HDAC6-IN-19在抑制包括白血病、结肠癌、黑色素瘤和乳腺癌等多种癌细胞系的增殖方面显示出有效性。
T62046	HDAC6-IN-5	Others	Others
	HDAC6-IN-5 (化合物 11b) 是有效的、血脑屏障通透性的 HDAC6抑制剂(IC50= 0.025 μM)。HDAC6-IN-5 抑制 AChE 活性和 Aβ1-42自聚集和，IC50分别为 0.88 和 1.1 μM。HDAC6-IN-5 能够促进神经突起生长，且无明显神经毒性。
T61474	HDAC6-IN-13	Others	Others
	HDAC6-IN-13 (Compound 35m) is a potent and highly selective orally active inhibitor of HDAC6, with an IC50 of 0.019 μM. It also demonstrates inhibitory activity against HDAC1, HDAC2, and HDAC3, with IC50 values of 1.53 μM, 2.06 μM, and 1.03 μM, respectively. HDAC6-IN-13 exhibits substantial blood-brain barrier permeability and displays anti-inflammatory properties [1].
T61888	mTOR/HDAC6-IN-1	Others	Others
	mTOR/HDAC6-IN-1 是一种有效的组蛋白去乙酰酶 (HDAC6)和哺乳动物雷帕霉素 (mTOR) 的双重抑制剂，对于HDAC6 和 mTOR 的IC50值分别为56 nM 和133.7 nM。mTOR/HDAC6-IN-1 对细胞自噬 (autophagy)、细胞凋亡 (apoptosis)具有明显的诱导作用，对迁移具有抑制作用。mTOR/HDAC6-IN-1 在三阴性乳腺癌 (TNBC) 的研究中具有潜力
T77658	BChE/HDAC6-IN-2	Others	Others

T78799	BChE/HDAC6-IN-1	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	BChE/HDAC6-IN-1为高效的BChE及HDAC6选择性双重抑制剂，具有分别为4 nM与8.9 nM的IC50值。在aβ1-42诱导的小鼠模型中，BChE/HDAC6-IN-1能够改善认知功能障碍，显示出在阿尔茨海默病(AD)研究中的应用潜力。
T77922	HDAC6 degrader-1	PROTACs	PROTAC
	HDAC6Degrader-1是一种PROTAC，融合了作为HDAC6结合剂的Nexturastat A（Nex A）选择性抑制剂，连接肽及E3泛素连接酶配体。该化合物显著促进HDAC6降解，具备对其他HDAC亚型的高选择性，并有效抑制细胞增殖。
T64187	HDAC1/6-IN-1	Others	Others
	HDAC1/6-IN-1 是一种有效的 GLP (IC50: 1.3 nM)、HDAC6 (IC50: 13 nM) 和 HDAC1 (IC50: 89 nM)的多靶点抑制剂。HDAC1/6-IN-1 能在蛋白水平上抑制 H3K9 的甲基化和去乙酰化。HDAC1/6-IN-1 能够将癌细胞的细胞周期阻滞在 G0/G1 期，能够诱导癌细胞凋亡，可阻止癌细胞迁移和入侵。
T74003	HDAC3/6-IN-2	Others	Others
	HDAC3/6-IN-2 (化合物 15) 是一种高效的HDAC6和HDAC3抑制剂，IC50值分别为0.368 μM和0.635 μM。此化合物不仅具备抗肿瘤活性，能够诱导癌细胞凋亡，同时通过降低HDAC6和HDAC3水平，与H3乙酰化和α-微管蛋白的上调有关。
T75018	HDAC6 degrader-3	PROTACs	PROTAC
	HDAC6degrader-3 是一种有效的选择性 HDAC6降解剂，通过三元复合物形成和泛素-蛋白酶体途径，IC50值为 19.4 nM。HDAC6degrader-3 对 HDAC6和 HDAC1的 IC50值分别为 4.54 nM 和 0.647 μM。HDAC6degrader-3 引起 α-微管蛋白的强烈高度乙酰化。
T75017	PROTAC HDAC6 degrader 1	Others	Others
	PROTACHDAC6 degrader (Compound A6) 为有效且选择性的PROTACHDAC6降解剂，具有3.5 nM的DC50。在髓系白血病细胞系中，通过诱导凋亡（apoptosis）表现出抗增殖活性。
T61315	HDAC6/HSP90-IN-2	Others	Others
	HDAC6/HSP90-IN-2 (compound 6e) 是HDAC6和Hsp90的双抑制剂其IC50s 分别为106 nM 和61 nM。HDAC6/HSP90-IN-2 (compound 6e) 可用于癌症的研究。
T63531	HDAC6/HSP90-IN-1	Others	Others
	HDAC6/HSP90-IN-1 是有效的、选择性的 HDAC6 (IC50: 4.3 nM) 和 HSP90 (IC50: 46.8 nM) 的双重抑制剂。HDAC6/HSP90-IN-1 能够下调 INF-γ 处理的 H1975 肺癌细胞中 PD-L1 的表达。HDAC6/HSP90-IN-1 在 H1975 异种移植小鼠中表现出肿瘤生长的抑制作用。
T79710	PI3Kα/HDAC6-IN-1	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	PI3Kα/HDAC6-IN-1（化合物21j）是一种针对PI3Kα/HDAC6的双重抑制剂，其IC50值分别为2.9 nM和26 nM。该化合物还能抑制AKT(Ser473)的磷酸化，诱导α-微管蛋白的积累，并促进其乙酰化，但对乙酰化组蛋白H3和H4无显著影响。在L-363细胞系中，PI3Kα/HDAC6-IN-1显示了高效的抑制活性（IC50=0.17 μM），表现出良好的抗癌潜力。
T61727	HDAC6/8/BRPF1-IN-1	Others	Others
	HDAC6/8/BRPF1-IN-1 is a dual inhibitor that targets HDAC6, HDAC8, and the bromodomain and PHD finger containing protein 1 (BRPF1). It exhibits inhibitory activity against HDAC1, HDAC6, and HDAC8 with IC50 values of 797 nM, 344 nM, and 908 nM, respectively. In addition, it inhibits BRPF1 with a Kd value of 175.2 nM. This compound is utilized in cancer research [1].
T2294	BG45	Apoptosis; HDAC	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair
	BG45是一个 HDAC I 型抑制剂，选择性抑制 HDAC3，IC50为289 nM。它抑制 HDAC1/2/6的效力大大降低，IC50分别为2、2.2和>20μM。
T77664	KH16	Apoptosis; HDAC	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair
	KH16 是一种高效的 HDAC 抑制剂，特异性靶向I类HDACs（HDAC1, HDAC2及HDAC3），IC50值介于6至34 nM之间。KH16 能够激发细胞凋亡，并能够抑制多种肿瘤细胞中的基因表达模式。
T6865	Quisinostat dihydrochloride Quisinostat 2HCl,Quisinostat (JNJ-26481585) 2HCl,JNJ26854165(Quisinostat) 2HCl,JNJ-26481585 2HCl	Apoptosis; HDAC; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair
	Quisinostat dihydrochloride (JNJ26854165(Quisinostat) 2HCl) 是一种有口服活性，高效的 pan-HDAC 抑制剂，具有广泛的抗肿瘤活性。它对 HDAC1、HDAC2、HDAC4、HDAC10和HDAC11 的IC50值分别为 0.11 nM、0.33 nM、0.64 nM、0.46 nM 和 0.37 nM。
T62545	HDAC-IN-43	Others	Others
	HDAC-IN-43 是一种强效的 HDAC 1/3/6 抑制剂，对 HDAC 1、HDAC 3 和 HDAC 6 的 IC50 值分别为 82 nM、45 nM 和 24 nM。HDAC-IN-43 是一种弱的 PI3K/mTOR 抑制剂，对 PI3K 和 mTOR 的 IC50 值分别为 3.6 μM 和 3.7 μM。HDAC-IN-43 具有广谱的抗增殖效果。
T62920	HDAC-IN-38	Others	Others
	HDAC-IN-38 是一种 HDAC 的有效抑制剂。HDAC-IN-38 对 HDAC1、2、3、5、6 和 8 具有类似的微摩尔抑制作用，也可以提高组蛋白乙酰化水平 (H3K14 或 H4K5)。HDAC-IN-38 能够提高脑血流量 (CBF)，减轻认知障碍，改善海马萎缩。
T61510	PIM-1/HDAC-IN-1	Others	Others
	PIM-1/HDAC-IN-1 (compound 4d) is a potent inhibitor of PIM-1, with an IC 50 of 343.87 nM. It also exhibits strong inhibitory activity and selectivity against HDAC 1 and HDAC 6, with IC 50 values of 63.65 and 62.39 nM, respectively. Furthermore, PIM-1/HDAC-IN-1 demonstrates apoptosis-inducing potential in MCF-7 cell lines, specifically inducing pre-G1 apoptosis and causing cell cycle arrest at the G2/M phase [1].
T61583	CDK/HDAC-IN-1	Others	Others
	CDK/HDAC-IN-1 exhibits potent inhibitory activity towards CDK2/4/6 and HDAC6, with IC50 values of 60.9 ± 2.9 nM, 276 ± 22.3 nM, 27.2 ± 4.2 nM, and 128.6 ± 0.4 nM, respectively.
T78708	JAK/HDAC-IN-2	JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	JAK/HDAC-IN-2 是一款高效的 JAK/HDAC 双靶点抑制剂，能在纳摩尔浓度范围内有效抑制 HDAC3/6 与 JAK1/2。此化合物不仅促进细胞凋亡，还能抑制组蛋白去乙酰化和 STAT3 磷酸化，对血液肿瘤和实体肿瘤细胞展现出了显著的抗增殖效果。
T79674	HDAC-IN-64	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC-IN-64 (Compound 13) 为HDAC抑制剂，对HDAC4/6的IC50值为24 nM及85 nM。其对前列腺癌（PCA）细胞表现出抗增殖与抗迁移效果，并能抑制LNCaP和RWPE-1细胞的生长，GI50值分别达到0.32 μM与1.1 μM。
T74783	HDAC-IN-53	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HDAC-IN-53是一种口服活性的选择性HDAC1-3抑制剂，其IC50分别为47 nM、125 nM和450 nM。该化合物不针对II类HDAC(HDAC4、5、6、7、9；IC50>10 μM)展现抑制作用。HDAC-IN-53能够诱导caspase依赖的细胞凋亡并在裸鼠中显著抑制人肿瘤异种移植物生长，同时抑制携带MC38结肠癌的免疫活性小鼠的肿瘤发展。
T83947	HDAC4 CHDI Degrader 11	Others	Others
	HDAC4 CHDI Degrader 11是一种高效且选择性的HDAC4降解剂（PROTAC），其在Jurkat E6-1细胞和Jurkat细胞中的DC50值分别为4 nM和6 nM。该化合物由类IIa HDAC抑制剂三氟甲基噁二唑通过连接体与Von Hippel-Lindau (VHL) 蛋白的配体连接而成。在亨廷顿病小鼠细胞模型中，HDAC4 CHDI Degrader 11能强效地降解HDAC4（DC50= 1nM）。在神经母细胞瘤细胞系中，可与P-糖蛋白抑制剂Elacridar联用以实现更有效的降解。
T36629	Givinostat	Others	Others
	Givinostat (ITF-2357) is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively. Givinostat (ITF2357) suppresses total LPS-induced IL-1β production robustly compared with the reduction by ITF3056. At 25, 50, and 100 nM, Givinostat reduced IL-1β secretion more than 70%. Givinostat (ITF-2357) suppresses the production of IL-6 in PBMCs stimulated with TLR agonists as well as the combination of IL-12 plus IL-18. IL-6 secretion decreases to 50% at 50 nM Givinostat, but at 1...

化合物

Cat.No: T6327

Target: Virus Protease, HDAC

Fluoxetine succinate ester

Cat.No: T71587

Target: Others

HDAC6 degrader 9c

Cat.No: T69753

Target: HDAC

Cat.No: T72012

Target: Others

Cat.No: T60954

Target: Others

Cat.No: T82226

Target: HDAC

Cat.No: T79769

Target: HDAC

Cat.No: T60856

Target: Others

Cat.No: T73043

Target: Others

Cat.No: T74617

Target: HDAC

Cat.No: T79771

Target: HDAC

Cat.No: T78768

Target: HDAC

LSD1/HDAC6-IN-1

Cat.No: T36625

Synonym: LSD1/HDAC6-IN-1

Target: Others

Cat.No: T82225

Target: HDAC

Cat.No: T63472

Target: Others

Cat.No: T63247

Target: Others

Cat.No: T79523

Target: HDAC

Cat.No: T73031

Target: Others

Cat.No: T61139

Target: Others

Cat.No: T61044

Target: Others

Cat.No: T61792

Target: Others

Cat.No: T82224

Target: HDAC

Cat.No: T78769

Target: HDAC

Cat.No: T78839

Target: HDAC

Cat.No: T62046

Target: Others

Cat.No: T61474

Target: Others

mTOR/HDAC6-IN-1

Cat.No: T61888

Target: Others

BChE/HDAC6-IN-2

Cat.No: T77658

Target: Others

BChE/HDAC6-IN-1

Cat.No: T78799

Target: HDAC

HDAC6 degrader-1

Cat.No: T77922

Target: PROTACs

Cat.No: T64187

Target: Others

Cat.No: T74003

Target: Others

HDAC6 degrader-3

Cat.No: T75018

Target: PROTACs

PROTAC HDAC6 degrader 1

Cat.No: T75017

Target: Others

HDAC6/HSP90-IN-2

Cat.No: T61315

Target: Others

HDAC6/HSP90-IN-1

Cat.No: T63531

Target: Others

PI3Kα/HDAC6-IN-1

Cat.No: T79710

Target: HDAC

HDAC6/8/BRPF1-IN-1

Cat.No: T61727

Target: Others

Cat.No: T2294

Target: Apoptosis, HDAC

Cat.No: T77664

Target: Apoptosis, HDAC

Quisinostat dihydrochloride

Cat.No: T6865

Synonym: Quisinostat 2HCl,Quisinostat (JNJ-26481585) 2HCl,JNJ26854165(Quisinostat) 2HCl,JNJ-26481585 2HCl

Target: Apoptosis, HDAC, Autophagy

Cat.No: T62545

Target: Others

Cat.No: T62920

Target: Others

PIM-1/HDAC-IN-1

Cat.No: T61510

Target: Others

CDK/HDAC-IN-1

Cat.No: T61583

Target: Others

JAK/HDAC-IN-2

Cat.No: T78708

Target: JAK

Cat.No: T79674

Target: HDAC

Cat.No: T74783

Target: HDAC

HDAC4 CHDI Degrader 11

Cat.No: T83947

Target: Others

Cat.No: T36629

Target: Others

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPH-01474	HDAC6 Protein, Human, Recombinant (His) Protein deacetylase HDAC6,Histone...	Human	E. coli
	HDAC6 Protein, Human, Recombinant (His) is expressed in E. coli.
TMPJ-00567	NCR1 Protein, Human, Recombinant (hFc) hNKp46,Natural cytotoxicity triggering rec...	Human	HEK293 Cells
	Natural cytotoxicity triggering receptor 1(NCR1) is a single-pass type I membrane protein .It contains 2 Ig-like (immunoglobulin-like) domains and belongs to the natural cytotoxicity receptor (NCR) family. The protein is a natural killer (NK) lymphocyte-activating receptor. It is involved in major aspects of NK immune function and shows a high degree of lineage specificity in blood and bone marrow.
TMPY-03128	LAIR1 Protein, Mouse, Recombinant (hFc) leukocyte-associated immunoglobulin-like receptor 1...	Mouse	HEK293 Cells
	LAIR1 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 39.6 kDa and the accession number is Q8BG84-6.
TMPJ-00827	Tau-D Protein, Human, Recombinant (His) PHF-Tau,MAPTL,MAPT,Paired Helical Filament-Tau,Microtubule-A...	Human	E. coli
	Microtubule-Associated Protein TAU is abundantly expressed in neurons of the central nervous system and less commonly expressed elsewhere, but is also expressed at very low levels in CNS astrocytes and oligodendrocytes. Tau interacts with tubulin to stabilize microtubules and promotes tubulin assembly into microtubules. The C-terminus of TAU binds axonal microtubules while the N-terminus binds neural plasma membrane components, suggesting that tau acts as a linker protein. When tau is defective,...
TMPY-05798	VEGF145 Protein, Human, Recombinant 血管内皮生长因子,vascular endothelial growth factor A,VPF,MVCD1,VEGF...	Human	HEK293 Cells
	VEGF145 Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 16.92 kDa and the accession number is P15692-6.
TMPY-04277	CD45 Protein, Mouse, Recombinant (hFc) Cd45,protein tyrosine phosphatase, recepto...	Mouse	HEK293 Cells
	CD45 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 71.7 kDa and the accession number is P06800-6.
TMPY-02600	NRG1 beta 1 Protein, Human, Recombinant (EGF Domain, hFc) neuregulin 1,HRGA,NRG1 β1,HGL,MST131,MSTP131,HRG,AR...	Human	HEK293 Cells
	NRG1 beta 1 Protein, Human, Recombinant (EGF Domain, hFc) is expressed in HEK293 mammalian cells with Fc tag. The predicted molecular weight is 36.7 kDa and the accession number is Q02297-6.
TMPY-02705	NRG1 beta 1 Protein, Human, Recombinant (hFc) MSTP131,HRG1,NRG1-IT2,ARIA,HGL,SMDF,GGF,HRG,NDF,MST131,neure...	Human	HEK293 Cells
	NRG1 beta 1 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with Fc tag. The predicted molecular weight is 55.2 kDa and the accession number is Q02297-6.
TMPY-03010	NRG1 beta 1 Protein, Human, Recombinant NDF,GGF,MSTP131,Neuregulin 1,MST131,ARIA,NRG1-IT2,S...	Human	HEK293 Cells
	NRG1 beta 1 Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 26.8 kDa and the accession number is Q02297-6.
TMPK-00614	NKp46/NCR1 Protein, Human, Recombinant (His) NKp46,MAR-1,Ly94,NCR1,NKP46FLJ99094,CD335	Human	HEK293 Cells
	NKp46, along with NKp30 and NKp44, are activating receptors that have been collectively termed the natural cytotoxicity receptors (NCR).These receptors lack significant sequence homology to one another. They are expressed almost exclusively by NK cells and play a major role in triggering some of the key lytic activities of NK cells. NKp46/NCR1 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with N-His tag. The predicted molecular weight is 27.5 kDa and the accession numb...
TMPK-00615	NKp46/NCR1 Protein (Primary Amine Labeling), Human, Recombinant (His), Biotinylated CD335,NCR1,NKp46,NKP46FLJ99094,Ly94,MAR-1	Human	HEK293 Cells
	NKp46, along with NKp30 and NKp44, are activating receptors that have been collectively termed the natural cytotoxicity receptors (NCR).These receptors lack significant sequence homology to one another. They are expressed almost exclusively by NK cells and play a major role in triggering some of the key lytic activities of NK cells. NKp46/NCR1 Protein (Primary Amine Labeling), Human, Recombinant (His), Biotinylated is expressed in HEK293 mammalian cells with N-His tag. The predicted molecular we...
TMPK-01364	SIRP alpha V6 Protein, Human, Recombinant (His & Avi), Biotinylated SIRP α,MFR,SHPS1,SIRPA,BIT,SHPS-1,MYD-1,SIRP alpha,P84,CD172...	Human	HEK293 Cells
	Signal regulatory protein α (SIRPα) is a regulatory membrane glycoprotein from SIRP family expressed mainly by myeloid cells and also by stem cells or neurons.SIRPα acts as inhibitory receptor and interacts with a broadly expressed transmembrane protein CD47 also called the "don´t eat me" signal.Cancer cells highly expressed CD47 that activate SIRP α and inhibit macrophage-mediated destruction. SIRP alpha V6 Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian c...
TMPK-01358	SIRP alpha V6 Protein, Human, Recombinant (His & Avi) P84,SIRPA,SIRP alpha,SHPS-1,MFR,BIT,MYD1,SIRP α V6,...	Human	HEK293 Cells
	Signal regulatory protein α (SIRPα) is a regulatory membrane glycoprotein from SIRP family expressed mainly by myeloid cells and also by stem cells or neurons.SIRPα acts as inhibitory receptor and interacts with a broadly expressed transmembrane protein CD47 also called the "don´t eat me" signal.Cancer cells highly expressed CD47 that activate SIRP α and inhibit macrophage-mediated destruction. SIRP alpha V6 Protein, Human, Recombinant (His & Avi) is expressed in HEK293 mammalian cells with C-Hi...

重组蛋白

HDAC6 Protein, Human, Recombinant (His)

Cat.No: TMPH-01474

Species: Human

Expression System: E. coli

NCR1 Protein, Human, Recombinant (hFc)

Cat.No: TMPJ-00567

Species: Human

Expression System: HEK293 Cells

LAIR1 Protein, Mouse, Recombinant (hFc)

Cat.No: TMPY-03128

Species: Mouse

Expression System: HEK293 Cells

Tau-D Protein, Human, Recombinant (His)

Cat.No: TMPJ-00827

Species: Human

Expression System: E. coli

VEGF145 Protein, Human, Recombinant

Cat.No: TMPY-05798

Species: Human

Expression System: HEK293 Cells

CD45 Protein, Mouse, Recombinant (hFc)

Cat.No: TMPY-04277

Species: Mouse

Expression System: HEK293 Cells

NRG1 beta 1 Protein, Human, Recombinant (EGF Domain, hFc)

Cat.No: TMPY-02600

Species: Human

Expression System: HEK293 Cells

NRG1 beta 1 Protein, Human, Recombinant (hFc)

Cat.No: TMPY-02705

Species: Human

Expression System: HEK293 Cells

NRG1 beta 1 Protein, Human, Recombinant

Cat.No: TMPY-03010

Species: Human

Expression System: HEK293 Cells

NKp46/NCR1 Protein, Human, Recombinant (His)

Cat.No: TMPK-00614

Species: Human

Expression System: HEK293 Cells

NKp46/NCR1 Protein (Primary Amine Labeling), Human, Recombinant (His), Biotinylated

Cat.No: TMPK-00615

Species: Human

Expression System: HEK293 Cells

SIRP alpha V6 Protein, Human, Recombinant (His & Avi), Biotinylated

Cat.No: TMPK-01364

Species: Human

Expression System: HEK293 Cells

SIRP alpha V6 Protein, Human, Recombinant (His & Avi)

Cat.No: TMPK-01358

Species: Human

Expression System: HEK293 Cells

Cat. No.	Product Name	Target	Signaling Pathways
TMIJ-0050	Butyricacid-d7
	Butyricacid-d7 是 Butyricacid 的氘代化合物。Butyricacid 的 CAS 号为 107-92-6。Butyric acid 是一种从许多乳制品中分离出来的脂肪酸，具有抗癌活性。它抑制组蛋白去乙酰化酶 (HDAC) 并诱导胶质瘤细胞凋亡和 G1 期细胞周期停滞。此外，它在低剂量时刺激上皮细胞增殖，在高剂量时抑制增殖。

同位素标记化合物

Cat.No: TMIJ-0050

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