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Cat. No. | Product Name | ||
---|---|---|---|
L8000 | 干细胞分化化合物库 | 1197 compounds | |
1197 种干细胞分化信号通路相关的生物活性小分子化合物的特有集合,可用于高通量、高内涵筛选; |
Cat. No. | Product Name | Form | Specificity Of Inhibition |
---|---|---|---|
C0048 |
Deacetylase Inhibitor Cocktail (100× in 70% DMSO)
去乙酰化酶抑制剂 Cocktail(100× in 70% DMSO) |
Solution (100× in 70% DMSO) | Class I/II/III HDAC |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2157 |
M344
MS 344,Histone Deacetylase Inhibitor III |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
M344 (Histone Deacetylase Inhibitor III) 是一种组蛋白去乙酰化酶抑制剂,IC50为 100 nM。 | |||
T3206 |
NKL 22
Histone Deacetylase Inhibitor IV,PAOA |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
NKL 22 (Histone Deacetylase Inhibitor IV) 是一种有效的选择性组蛋白脱乙酰基酶(HDAC) 抑制剂,对 HDAC2/4/5/7/8 具有选择性,抑制HDAC1和HDAC3的IC50值分别为 199 和 69 nM。它可改善亨廷顿氏病转基因小鼠的疾病表型和转录异常。 | |||
T3193 |
Pimelic diphenylamide 106
Histone Deacetylase Inhibitor VII,TC-H 106,RGFA-8 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Pimelic diphenylamide 106 (RGFA-8) 是一种缓慢和紧密结合的I 类HDAC 抑制剂,对HDAC1、 2和3的IC50值分别150、760和370 nM。 | |||
T39233 |
SIRT7 inhibitor 97491
|
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
SIRT7 inhibitor 97491 是SIRT7的有效抑制剂,IC50为 325 nM。SIRT7 inhibitor 97491以剂量依赖性的方式降低 SIRT7 去乙酰化酶活性。它通过在 K373/382 处进行乙酰化来提高 p53 的稳定性,从而防止肿瘤进展。它通过 caspase 途径促进凋亡。 | |||
T6055 |
Quisinostat
奎诺司他,JNJ-26481585 |
Apoptosis; HDAC; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Quisinostat (JNJ-26481585) 是一种高效的,具有口服活性的 pan-HDAC 抑制剂,对 HDAC1、HDAC2、HDAC4、HDAC10、HDAC11 作用的 IC50值范围为 0.11-0.64 nM。它在成神经细胞瘤中能诱导自噬,具有广泛的抗肿瘤活性。 | |||
T4328 |
OSS_128167
SIRT6-IN-1 |
HBV; Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology |
OSS_128167 (SIRT6-IN-1) 是一种选择性沉默调节蛋白 6 (SIRT6) 抑制剂,对 SIRT6,SIRT1 和 SIRT2 的 IC50分别为 89 μM,1578 μM 和 751 μM。它具有抗 HBV、抗癌、抗炎和抗病毒活性,可抑制 HBV 的转录和复制。 | |||
T6481 |
Droxinostat
NS 41080,4-(4-氯-2-甲基苯氧基)-N-羟基丁酰胺 |
Apoptosis; HDAC | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Droxinostat (NS 41080) 是HDAC3、HDAC6和HDAC8抑制剂,IC50分别为16.9、2.47和1.46 μM。 | |||
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。 | |||
T8508 |
HDAC-IN-3
GSK3117391A |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-3 (GSK3117391A)是组蛋白脱乙酰酶抑制剂,可治疗慢性炎症性疾病。 | |||
T7691 |
NSC 3852
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
NSC 3852 是一种有效的组蛋白脱乙酰酶抑制剂。 | |||
T38318L |
Acetyl Pentapeptide-1 acetate
|
Histone Demethylase | Chromatin/Epigenetic |
Acetyl Pentapeptide-1 acetate 是一种组蛋白脱乙酰酶抑制剂。 | |||
T8517 |
Belinostat
PX105684,PXD101,贝利司他,PXD-101 |
HDAC; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Belinostat (PXD101) 是一种异羟肟酸型组蛋白脱乙酰酶抑制剂,具有抗肿瘤活性,在 HeLa 细胞提取物中的IC50为 27 nM。 | |||
T2489 |
Ricolinostat
ACY-1215,Rocilinostat |
Apoptosis; HDAC | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Ricolinostat (Rocilinostat) 是一种选择性HDAC6抑制剂,IC50为 5 nM。它还抑制HDAC1,HDAC2和HDAC3,IC50分别为 58,48 和 51 nM。 | |||
T3983 |
TMP195
TFMO 2,TMP 195 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
TMP195 (TFMO 2) 是一种选择性 IIa 类组蛋白脱乙酰酶 (HDAC) 抑制剂。对 HDAC4、HDAC5、HDAC7,HDAC9的 Ki 值分别为59、60、26,5 nM。 | |||
T4019 |
Cambinol
SIRT1/2 Inhibitor IV,NSC 112546 |
Apoptosis; Phospholipase; Sirtuin | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
Cambinol (SIRT1/2 Inhibitor IV) 是一种SIRT1和SIRT2的抑制剂,IC50值分别为 56 μM 和 59 μM。它是中性鞘磷脂酶的外泌体抑制剂。 | |||
T3358 |
ITSA-1
ITSA1 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
ITSA-1 是一种具有膜渗透性的HDAC 激活剂,抵消曲古抑菌素 A (TSA) 诱导的细胞周期停滞,组蛋白乙酰化和转录水平。 | |||
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。 | |||
T6678 |
Splitomicin
1-Naphthalenepropanoic Acid,斯普利特麻一辛 |
Sirtuin; HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Splitomicin (1-Naphthalenepropanoic Acid) 是 NAD(+) 依赖性组蛋白去乙酰化酶 Sir2p 的特异性抑制剂,可抑制酵母提取物中 HDAC,IC50为 60 μM。 | |||
T14947 |
CHDI-390576
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
CHDI-390576 是一种具有中枢神经系统渗透性、选择性和高效性的二苯甲酰异羟肟酸 IIa 类组蛋白脱乙酰酶(HDAC) 抑制剂,抑制 IIa 类 HDAC 4、HDAC 5、HDAC 7、HDAC 9 ,可用于研究癌症。 | |||
T37427 |
(2R/S)-6-PNG
6-Prenylnaringenin,(±)-6-Prenylnaringenin |
Calcium Channel; HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism |
(2R/S)-6-PNG (6-Prenylnaringenin) 是新型天然组蛋白脱乙酰酶抑制剂,具有抗癌抗肿瘤活性,可阻断T型钙通道可减轻小鼠的神经性和内脏疼痛。 | |||
T79903 |
Sirtuin-1 inhibitor 1
|
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Sirtuin-1 inhibitor 1 是一种针对去乙酰化酶-1(Sirtuin-1)的抑制剂,可用于研究机体的衰老和细胞的死亡。 | |||
T16729 |
Remetinostat
SHP-141 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Remetinostat (SHP-141) 是一种基于异羟肟酸的组蛋白脱乙酰酶抑制剂,可用于治疗皮肤 T 细胞淋巴瘤的研究。 | |||
T73515 |
MC2590
|
Apoptosis; HDAC | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair |
MC2590 是一种具有有效性和选择性的组蛋白脱乙酰酶 (HDAC) 抑制剂 ,抑制 HDAC1-3、-6、-8 和 -10 的活性,诱导细胞周期停滞,促进细胞凋亡。 | |||
T6111 |
Selisistat
EX-527,司来司他,SEN0014196 |
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Selisistat (EX-527) 是一种去乙酰化酶 SIRT1 的抑制剂 (IC50=38 nM),具有有效性和特异性。Selisistat 可以用于神经系统疾病如亨廷顿舞蹈病的研究。 | |||
T30579 |
BRD4097
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
BRD4097是HDAC1/2/3/8检测中的阴性对照品,是一种选择性组蛋白去乙酰化酶(HDAC3)抑制剂,可用于保护b 细胞和改善胰岛素抵抗,有助于促进认知功能和增强学习和记忆的形成。 | |||
T17028 |
Tefinostat
CHR-2845 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Tefinostat (CHR-2845) 是一种有效的单核细胞/巨噬细胞靶向组蛋白脱乙酰酶 (HDAC) 抑制剂。 Tefinostat 可被胞内酯酶人羧酸酯酶-1 (hCE-1) 裂解成活性酸 CHR-2847。Tefinostat 具有抗肿瘤活性,可用于研究白血病和晚期血液系统恶性肿瘤。 | |||
T24131 |
HDAC3-IN-T247
HDAC3 inhibitor T247,HDAC3 inhibitor-T247,HDAC3 IN T247,T247 |
Histone Demethylase; Antiviral | Chromatin/Epigenetic; Immunology/Inflammation |
HDAC3-IN-T247 (HDAC3 inhibitor T247) 是一种具有选择性和有效性的组蛋白去乙酰化酶 3(HDAC3) 抑制剂,具有抗癌和抗病毒活性。HDAC3-IN-T247 以剂量依赖的方式诱导人结肠癌 HCT116 细胞中 NF-κB 乙酰化。HDAC3-IN-T247 抑制癌细胞增殖。 | |||
T21505 |
Suberoyl bis-hydroxamic acid
SBHA,软木肟酸,Suberohydroxamic acid |
Apoptosis; HDAC | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Suberoyl bis-hydroxamic acid (SBHA) 是一种竞争性且可透过细胞的HDAC1和HDAC3抑制剂,ID50值分别为 0.25 μM 和 0.30 μM。它使肿瘤细胞易于凋亡并促进线粒体凋亡途径,可研究甲状腺髓样癌。 | |||
T1583 |
Vorinostat
MK0683,伏立诺他,suberoylanilide hydroxamic acid,SAHA |
Apoptosis; Mitophagy; Virus Protease; HDAC; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology |
Vorinostat (SAHA) 是一种泛的组蛋白脱乙酰酶 (HDAC) 抑制剂 (IC50=10 nM),对 HDAC1/2/3/6/7/11 均有抑制活性。 Vorinostat 具有抗肿瘤活性,可以诱导细胞分化,阻滞细胞周期,诱导细胞凋亡。 | |||
T16962 |
SW-100
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
SW-100 是一种选择性组蛋白去乙酰化酶 6 抑制剂,IC50为2.3 nM。它有提高的穿过血脑屏障的能力,相对于其他 HDAC 同工酶,还显示出对 HDAC6 的至少高 1000 倍的选择性。 | |||
T2078 |
Fimepinostat
CUDC-907,PI3K/HDAC Inhibitor,CUDC 907 |
Apoptosis; PI3K; HDAC | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
Fimepinostat (CUDC 907) 是一种 I 型PI3K 及 I 和 II 型HDAC 酶抑制剂,作用于 PI3Kα/PI3Kβ/PI3Kδ 和 HDAC1/HDAC2/HDAC3/HDAC10 ,IC50分别为 19/54/39 nM 和 1.7/5.0/1.8/2.8 nM。 | |||
T38521 |
Patamostat mesylate
E 3123 mesylate,E-3123 mesylate,E3123 mesylate |
Apoptosis; HDAC | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Patamostat (E-3123) mesylate 是一种组蛋白去乙酰化酶(HDAC)抑制剂。Patamostat mesylate 增加乙酰化的组蛋白和微管蛋白在肿瘤细胞中积累,促使细胞周期终止和细胞凋亡。Patamostat mesylate具有抗肿瘤活性,可用于研究多发性骨髓瘤。 | |||
T77334 |
HDAC-IN-57
|
Apoptosis; HDAC | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-57 是一种具有口服活性的组蛋白脱乙酰酶 (HDAC) 泛抑制剂,对 HDAC1, HDAC2, HDAC6, HDAC8 具有抑制作用, IC50 值分别为 2.07 nM, 4.71 nM, 2.4 nM 和 107 nM。HDAC-IN-57 对 LSD1具有抑制作用, IC50 值为 1.34 μΜ。HDAC-IN-57 具有抗肿瘤活性,可诱导凋亡 (apoptosis)。 | |||
T41275 |
PF-04753299
|
Others | Others |
PF-04753299 是一种有效的、选择性的LpxC 抑制剂。PF-04753299 对淋球菌分离株具有杀菌作用,对大肠杆菌、铜绿假单胞菌和肺炎菌株的抑制的MIC90值分别为 2 μg/ml、4 μg/ml 和 16 μg/ml。PF-04753299 用于革兰氏阴性菌感染的研究。 | |||
T3661 |
Citarinostat
ACY241,HDAC-IN-2 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Citarinostat (ACY241) 是一种强效、选择性和口服组蛋白脱乙酰酶 (HDAC) 抑制剂,具有抗肿瘤活性,对 HDAC1、HDAC2、HDAC3、HDAC6 和 HDAC8 的 IC50分别为 35、45、46、2.6 和 137 nM。 | |||
T64529 |
MDL-800
MDL 800,MDL800 |
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
SIRT6, responsible for deacetylation of histone H3 Nε-acetyl-lysines 9 (H3K9ac) and 56 (H3K56ac), is a tumor suppressor which has frequently been found to have low expression in various cancers. MDL-800 is a selective SIRT6 activator. It increased the deacetylase activity of SIRT6 by up to 22-fold and led to a global decrease in H3K9ac and H3K56ac levels in human hepatocellular carcinoma (HCC) cells. Also, it inhibited the proliferation of HCC cells via SIRT6-driven cell-cycle arrest and was eff... | |||
T1852 |
Rac-Belinostat
NSC726630,PXD101,PX-105684 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Rac-Belinostat (PX-105684) 是一种具有抗肿瘤活性的新型异羟肟酸型组蛋白脱乙酰酶 (HDAC) 抑制剂。 Belinostat 靶向 HDAC 酶,从而抑制肿瘤细胞增殖、诱导细胞凋亡、促进细胞分化和抑制血管生成。这种药物可以使耐药肿瘤细胞对其他抗肿瘤药物敏感,可能是通过一种涉及胸苷酸合酶下调的机制。 | |||
T0005 |
Aspirin
阿司匹林,Acetylsalicylate,Acetylsalicylic Acid,邻乙酰水杨酸,ASA |
Mitophagy; Virus Protease; COX; Autophagy | Autophagy; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Aspirin (Acetylsalicylic Acid) 是一种选择性 COX 抑制剂,具有多种药理活性。它是组蛋白去乙酰化酶抑制剂,可上调细胞周期阻滞蛋白 p21,抑制携带 COX-1 的卵巢 Y 细胞。 它还抑制 HUVEC 和新生大鼠心室心肌细胞中 COX-2 的表达,分别减少 PG 的产生和 ERK 和 NF-KB 的下调。 | |||
T27083 |
Crebinostat
|
Epigenetic Reader Domain; Histone Acetyltransferase; HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Crebinostat 是一种有效的组蛋白去乙酰化酶 (HDAC) 抑制剂,对 HDAC1、HDAC2、HDAC3 和 HDAC6 有抑制作用, IC50 分别为 0.7 nM、1.0 nM、2.0 nM 和 9.3 nM。Crebinostat 可增加在体外神经元的突触蛋白 1 斑点沿树突 (synapsin-1 punctae along dendrites) 的密度。Crebinostat 可调节染色质介导的神经可塑性,增强小鼠的记忆。Crebinostat 可诱导组蛋白 H3 和组蛋白 H4 乙酰化,并增强 cAMP 反应元件结合蛋白 (CREB) 靶基因 Egr1 的表达。 | |||
T25629 |
LAQ 824
LAQ824,LAQ-824 |
Others | Others |
LAQ 824 is an inhibitor of histone deacetylase. | |||
T27648 |
J1075
J 1075,J-1075 |
Others | Others |
J1075 is an histone deacetylase 8 (HDAC8) inhibitor. | |||
T27553 |
HPB
|
Others | Others |
HPB is a selective HDAC6 deacetylase inhibitor | |||
T69884 |
M122
|
Others | Others |
M122 is a selective histone deacetylase HDAC1 and HDAC2 inhibitor and potent antitumor agent. | |||
T27004 |
CHIC35
CHIC-35,CHIC 35 |
Others | Others |
CHIC-35 is a selective deacetylase SIRT1 inhibitor. | |||
T84649 |
CAY10398
MD 85 |
Others | Others |
CAY10398 is a compound that serves as an isoform-selective inhibitor of histone deacetylase (HDAC1). | |||
T25566 |
KBH-A42
KBH-A-42,KBHA42,KBH-A 42,KBH A 42 |
Others | Others |
KBH-A42 is an inhibitor of histone deacetylase. | |||
T27644 |
J1037
J 1037,J-1037 |
Others | Others |
J1037 is a novel Histone Deacetylase 8 (HDAC8) inhibitor . | |||
T11543 |
HDAC-IN-5
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-5 is a histone deacetylase (HDAC) inhibitor. | |||
T27645 |
J1038
J-1038,J 1038 |
Others | Others |
J1038 is a novel Histone Deacetylase 8 (HDAC8) Inhibitor . | |||
T24834 |
ß-Hydroxymethyl chalcone
Beta-Hydroxymethyl chalcone,Betahydroxymethyl chalcone,Beta Hydroxymethyl chalcone |
Others | Others |
-Hydroxymethyl chalcone is the first selective Histone Deacetylase 2 inhibitor. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T14305 |
Apicidin
OSI 2040 |
Apoptosis; HDAC; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Apicidin (OSI 2040) 是组蛋白去乙酰化酶(HDAC)抑制剂,具有抗寄生虫活性和抗增殖活性。Apicidin 通过减少 APP/PS1 小鼠中的 Abeta 负荷来减轻记忆缺陷,抑制细胞生长增殖,诱导细胞凋亡和自噬,可用于研究白血病。 | |||
T6270 |
Trichostatin A
曲古柳菌素A,曲古抑菌素A,TSA |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Trichostatin A (TSA) 属于二烯异羟肟酸类的天然衍生物。Trichostatin A 是一种组蛋白去乙酰化酶抑制剂 (IC50=1.8 nM),具有可逆性和特异性。Trichostatin A 导致核心组蛋白过度乙酰化,从而调节染色质结构。 | |||
T37067 |
9-hydroxy Stearic Acid
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
9-hydroxy Stearic Acid 是一种羟基脂肪酸,是9-PAHSA 的活性代谢物。9-hydroxy Stearic Acid 是由9-PAHSA 通过肝脏和胰腺的羧基酯脂肪酶形成的。9-hydroxy Stearic Acid (5 μM)抑制HT-29结肠癌细胞裂解物中组蛋白去乙酰化酶1 (HDAC1)的表达。3 .当浓度为100 μM.1时,可抑制HT-29细胞的增殖,并诱导细胞周期阻滞于G0/ g1期。 | |||
T70778 |
Depudecin
|
Others | Others |
Depudecin is a polyketide obtained from the fungus Alternaria brassicicola and having a highly unusual structure of an 11-carbon chain containing two epoxides and six stereogenic centres. It is an inhibitor of histone deacetylase (HDAC) both in vivo and in vitro and also exhibits anti-angiogenic activity. | |||
T74368 |
OKI-006
|
Others | Others |
OKI-006 是一种有效的、具有口服活性的组蛋白脱乙酰酶 (HDAC) 抑制剂。OKI-006 是天然产物HDAC 抑制剂 largazole 的独特同系物。组蛋白去乙酰化酶 (HDAC) 在表观基因组调控中起关键作用,并且组蛋白乙酰化在许多人类癌症中失调。OKI-006 具有研究癌症疾病的潜力。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-00051 |
Chitin deacetylase Protein, Amylomyces rouxii, Recombinant (His)
Chitin deacetylase,MrCDA,CDA |
Amylomyces rouxii | E. coli |
Hydrolyzes the N-acetamido groups of N-acetyl-D-glucosamine residues in chitin to form chitosan and acetate. Chitin deacetylase Protein, Amylomyces rouxii, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 49.9 kDa and the accession number is P50325. | |||
TMPY-03431 |
HDAC4 Protein, Human, Recombinant (aa 612-1084)
histone deacetylase 4,HA6116,HDAC-4,HD4,BDMR,HDAC-A... |
Human | Baculovirus Insect Cells |
HDAC4 (histone deacetylase 4), belongs to class II of the histone deacetylase/AcuC/APhA family. Histone Deacetylases (HDACs) are a group of enzymes closely related to sirtuins. They catalyze the removal of acetyl groups from lysine residues in histones and non-histone proteins, resulting in transcriptional repression. In general, they do not act autonomously but as components of large multiprotein complexes, such as pRb-E2F and mSin3A, that mediate important transcription regulatory pathways. Th... | |||
TMPY-01333 |
HDAC8 Protein, Human, Recombinant (GST)
histone deacetylase 8,CDA07,MRXS6,RPD3,CDLS5,WTS,HD... |
Human | Baculovirus Insect Cells |
HDAC8 Protein, Human, Recombinant (GST) is expressed in Baculovirus insect cells with GST tag. The predicted molecular weight is 68 kDa and the accession number is Q9BY41-1. | |||
TMPH-01474 |
HDAC6 Protein, Human, Recombinant (His)
Protein deacetylase HDAC6,Histone deacetylase |
Human | E. coli |
HDAC6 Protein, Human, Recombinant (His) is expressed in E. coli. | |||
TMPY-02317 |
HDAC8 Protein, Mouse, Recombinant (His)
histone deacetylase 8,2610007D20Rik |
Mouse | Baculovirus Insect Cells |
HDAC8 Protein, Mouse, Recombinant (His) is expressed in Baculovirus insect cells with His tag. The predicted molecular weight is 43.1 kDa and the accession number is Q8VH37-1. | |||
TMPH-00095 |
HDT2 Protein, Arabidopsis thaliana, Recombinant (His)
Histone deacetylase HDT2,Histone deacetylase |
Arabidopsis thaliana | P. pastoris (Yeast) |
Probably mediates the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. HDT2 Protein, Arabidopsis thaliana, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 34.3 kDa and the accession number is Q56WH4. | |||
TMPH-01472 |
HDAC11 Protein, Human, Recombinant (GST)
HDAC11,Histone deacetylase 11 |
Human | E. coli |
Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. HDAC11 Protein, Human, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 66.... | |||
TMPH-01476 |
HDAC9 Protein, Human, Recombinant (His)
HDAC9,Histone deacetylase-related protein,MEF2-inte... |
Human | E. coli |
HDAC9 Protein, Human, Recombinant (His) is expressed in E. coli. | |||
TMPH-01473 |
HDAC3 Protein, Human, Recombinant (His & SUMO)
Protein deacylase HDAC3,RPD3-2,Protein deacetylase ... |
Human | E. coli |
HDAC3 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 64.8 kDa and the accession number is O15379. | |||
TMPH-01471 |
HDAC1 Protein, Human, Recombinant (His & SUMO)
Histone deacetylase 1,Protein deacetylase ... |
Human | E. coli |
HDAC1 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 71.1 kDa and the accession number is Q13547. | |||
TMPH-03437 |
CDA2 Protein, S. cerevisiae, Recombinant (His)
CDA2,Chitin deacetylase 2 |
Saccharomyces cerevisiae | P. pastoris (Yeast) |
Hydrolyzes the N-acetamido groups of N-acetyl-D-glucosamine residues in chitin to form chitosan and acetate. Chitosan is a component of the spore wall. CDA2 Protein, S. cerevisiae, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 34.9 kDa and the accession number is Q06703. | |||
TMPH-00024 |
LpxC Protein, Acinetobacter baumannii, Recombinant (His)
UDP-3-O-acyl-N-acetylglucosamine deacetylase,UDP-3-... |
Acinetobacter baumannii | E. coli |
Catalyzes the hydrolysis of UDP-3-O-myristoyl-N-acetylglucosamine to form UDP-3-O-myristoylglucosamine and acetate, the committed step in lipid A biosynthesis. LpxC Protein, Acinetobacter baumannii, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 37.1 kDa and the accession number is B2I1I9. | |||
TMPH-00959 |
AADAC Protein, Human, Recombinant (His & Myc & SUMO)
EC:3.1.1.3,DAC,AADAC,Arylacetamide deacetylase |
Human | E. coli |
AADAC Protein, Human, Recombinant (His & Myc & SUMO) is expressed in E. coli. | |||
TMPH-03180 |
LpxC Protein, Pseudomonas aeruginosa, Recombinant (His & SUMO)
UDP-3-O-acyl-N-acetylglucosamine deacetylase,lpxC,U... |
Pseudomonas aeruginosa | E. coli |
Catalyzes the hydrolysis of UDP-3-O-myristoyl-N-acetylglucosamine to form UDP-3-O-myristoylglucosamine and acetate, the committed step in lipid A biosynthesis. LpxC Protein, Pseudomonas aeruginosa, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 49.4 kDa and the accession number is P47205. | |||
TMPH-00555 |
LpxC Protein, E. coli, Recombinant (His)
lpxC,UDP-3-O-acyl-N-acetylglucosamine deacetylase,U... |
E. coli | E. coli |
Catalyzes the hydrolysis of UDP-3-O-myristoyl-N-acetylglucosamine to form UDP-3-O-myristoylglucosamine and acetate, the committed step in lipid A biosynthesis. | |||
TMPH-03179 |
LpxC Protein, Pseudomonas aeruginosa, Recombinant (His & Myc & SUMO)
UDP-3-O-[R-3-hydroxymyristoyl]-N-acetylglucosamine deace... |
Pseudomonas aeruginosa | E. coli |
Catalyzes the hydrolysis of UDP-3-O-myristoyl-N-acetylglucosamine to form UDP-3-O-myristoylglucosamine and acetate, the committed step in lipid A biosynthesis. LpxC Protein, Pseudomonas aeruginosa, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Myc tag. The predicted molecular weight is 53.4 kDa and the accession number is A6VB79. | |||
TMPH-02378 |
LpxC Protein, Klebsiella pneumoniae, Recombinant (His & Myc)
UDP-3-O-acyl-N-acetylglucosamine deacetylase,UDP-3-... |
Klebsiella pneumoniae | E. coli |
Catalyzes the hydrolysis of UDP-3-O-myristoyl-N-acetylglucosamine to form UDP-3-O-myristoylglucosamine and acetate, the committed step in lipid A biosynthesis. | |||
TMPH-03569 |
IcaB Protein, S. aureus, Recombinant (His & Myc)
Intercellular adhesion protein B,Poly-beta-1,6-N-acetyl-D-gl... |
Staphylococcus aureus | E. coli |
Catalyzes the N-deacetylation of poly-beta-1,6-N-acetyl-D-glucosamine (PNAG, also referred to as PIA), a biofilm adhesin polysaccharide. N-deacetylation is crucial for attachment of the polysaccharide to the bacterial cell surface; it leads to the introduction of positive charges in the otherwise neutral PIA polymer, allowing electrostatic interactions. IcaB Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular ... | |||
TMPJ-00459 |
Esterase D Protein, Human, Recombinant (His)
FGH,Methylumbelliferyl-Acetate Deacetylase,ESD,S-Fo... |
Human | E. coli |
Human Esterase D is a cytoplasmic serine hydrolase that belongs to the esterase D family. Esterase D is involved in the detoxification of formaldehyde. Esterase D plays a part in a variety of substrates, including O-acetylated sialic acids, which may involves in the recycling of sialic acids. Esterase D is used as a genetic marker for retinoblastoma and Wilson’s disease. | |||
TMPH-00712 |
PGAB Protein, E. coli, Recombinant (His & Myc)
Poly-beta-1,6-N-acetyl-D-glucosamine N-deacetylase,... |
E. coli | E. coli |
Catalyzes the N-deacetylation of poly-beta-1,6-N-acetyl-D-glucosamine (PGA), a biofilm adhesin polysaccharide. N-deacetylation promotes PGA export through the PgaA porin. PGAB Protein, E. coli, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 82.6 kDa and the accession number is P75906. | |||
TMPH-01007 |
NDST1 Protein, Human, Recombinant (His & SUMO)
Glucosaminyl N-deacetylase/N-sulfotransferase 1,[He... |
Human | E. coli |
NDST1 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 73.5 kDa and the accession number is P52848. | |||
TMPH-02798 |
SIRT3 Protein, Mouse, Recombinant (His & Myc)
Regulatory protein SIR2 homolog 3,Sirt3,NAD-dependent protei... |
Mouse | E. coli |
SIRT3 Protein, Mouse, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 36.3 kDa and the accession number is Q8R104. | |||
TMPH-02709 |
SAP130 Protein, Mouse, Recombinant (His)
Sap130,130 kDa Sin3-associated polypeptide,Sin3-associated p... |
Mouse | E. coli |
Acts as a transcriptional repressor. May function in the assembly and/or enzymatic activity of the mSin3A corepressor complex or in mediating interactions between the complex and other regulatory complexes. SAP130 Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 28.8 kDa and the accession number is Q8BIH0. | |||
TMPH-01804 |
OARD1 Protein, Human, Recombinant (His & Myc)
OARD1,ADP-ribose glycohydrolase OARD1,Terminal ADP-ribose pr... |
Human | E. coli |
OARD1 Protein, Human, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 24.3 kDa and the accession number is Q9Y530. | |||
TMPH-01742 |
SIRT6 Protein, Human, Recombinant (GST)
Protein mono-ADP-ribosyltransferase sirtuin-6,NAD-dependent ... |
Human | E. coli |
SIRT6 Protein, Human, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 66.0 kDa and the accession number is Q8N6T7. | |||
TMPH-00907 |
MACROD1 Protein, Human, Recombinant (His)
MACROD1,Protein LRP16,O-acetyl-ADP-ribose deacetylase |
Human | E. coli |
MACROD1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 41.5 kDa and the accession number is Q9BQ69. | |||
TMPH-00908 |
MACROD1 Protein, Human, Recombinant (His & Myc)
ADP-ribose glycohydrolase MACROD1,MACROD1,[Protein ADP-ribos... |
Human | Baculovirus Insect Cells |
MACROD1 Protein, Human, Recombinant (His & Myc) is expressed in Baculovirus. | |||
TMPJ-01121 |
MORF4L2 Protein, Human, Recombinant (His)
MORF4L2,Transcription Factor-Like Protein MRGX,Protein MSL3-... |
Human | E. coli |
Mortality Factor 4-Like Protein 2 (MORF4L2) is a member of the mortality factor (MORF) family. MORF4L2 localizes in the nucleus, possessing a protein kinase C phosphorylation site and a tyrosine phosphorylation site. MORF4L2 interacts with the Rb tumor suppressor and it has histone deacetylase activity which can either repress or promote the activity of the B-Myb promoter depending on the tissue. In addition, MORF4L2 is involved in cell growth, regulation, and senescence. | |||
TMPY-03283 |
HBP1 Protein, Human, Recombinant (GST)
HMG-box transcription factor 1 |
Human | E. coli |
HBP1 is a sequence-specific DNA-binding transcription factor. It is involved in many biological processes. It was reported that HBP1 binds to p16(INK4A) promoter and activates p16(INK4A) expression. We found that trichostatin A (TSA), an inhibitor of HDAC (histone deacetylase), induces p16(INK4A) expression in an HBP1-dependent manner. HBP1 activates or represses the expression of some specific genes during cell growth and differentiation. HBP1 was acetylated by p3/CBP in two regions: repression... | |||
TMPY-01869 |
SIRT1 Protein, Human, Recombinant (His)
SIR2L1,sirtuin 1 |
Human | E. coli |
SIRT1 belongs to the sirtuin family. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. SIRT1 is included in class I of the sirtuin family. It is a NAD-dependent protein deacetylase, which regulates processes such as apoptosis and muscle differentiation by deacetylating key proteins. It deacetylates 'Lys-382' of p53/TP53 and impairs its ability to induce proapoptotic program and modulate cell senescence. SIRT1 also deacetylates TAF1B and there... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TMIJ-0163 |
Valproic Acid-d4
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Valproic Acid-d4 是 Valproic Acid 的氘代化合物。Valproic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 | |||
TMIJ-0431 |
2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid
|
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2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid 是 2-pentanoic Acid 的氘代化合物。2-pentanoic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 | |||
TMID-0120 |
Valproic Acid-d15
|
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Valproic Acid-d15 是 Valproic Acid 的氘代化合物。Valproic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 |