331
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Cat. No. | Product Name | ||
---|---|---|---|
L3400 | 临床期小分子药物库 | 3404 compounds | |
3404 个临床期化合物集合,可用于高通量筛选和高内涵筛选; |
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 <em>HDAC</em> |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T63399L |
mTOR/HDAC-IN-1 HCl
mTOR/HDAC-IN-1 HCl(2815286-02-1 Free base) |
HDAC; mTOR | Chromatin/Epigenetic; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
mTOR/HDAC-IN-1 HCl 是一种有效的 mTOR 和 HDAC 双重抑制剂,具有潜在的抗炎、抗增殖、自噬和诱导凋亡作用,可用于研究癌症。mTOR/HDAC-IN-1 HCl 是一种有效的 mTOR 和 HDAC 双重抑制剂,具有潜在的抗炎、抗增殖、自噬和凋亡诱导作用,可用于研究癌症。 | |||
T60082 |
HDAC-IN-40
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-40 是一种有效的基于烷氧基酰胺的 HDAC 抑制剂,对 HDAC2 和 HDAC6 的 Ki 分别为 60 nM 和 30 nM。HDAC-IN-40 具有抗肿瘤作用。 | |||
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。 | |||
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)。 | |||
T2025 |
HDAC-IN-7
HBI-8000,西达本胺杂质,CS055,Chidamide impurity |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-7 (HBI-8000) 是 Chidamide 的一种杂质。Chidamide 是一种可口服的 HDAC 酶 I 类 HDAC1/2/3 和 IIb 类 HDAC10 抑制剂。 | |||
T10245 |
ACY-957
HDAC Inhibitor C001 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
ACY-957 (HDAC Inhibitor C001) 是一种具有口服活性,选择性的 HDAC1 和 HDAC2 抑制剂,对 HDAC1/2/3 的 IC50 值分别为 7 nM,18 nM 和 1300 nM,对 HDAC4/5/6/7/8/9 无作用。 | |||
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。 | |||
T25489 |
HDAC-IN-20
HDACIN20,HDAC-inhibitor-20,HDAC inhibitor 20 |
Others | Others |
HDAC-IN-20 is used as an HDAC inhibitor that acts by preventing HDAC-mediated diseases. | |||
T73181 |
HDAC-IN-51
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-51 是一种 HDAC 抑制剂。 | |||
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。 | |||
T67878 |
HDAC-IN-52
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-52 是一种含吡啶的 HDAC 抑制剂,对HDAC1,HDAC2,HDAC3 和 HDAC10具有抑制作用, IC50 分别为 0.189,0.227,0.440 和 0.446 μM。HDAC-IN-52 可用于研究癌症。 | |||
T63260 |
Snail/HDAC-IN-1
|
Apoptosis; Antifungal | Apoptosis; Microbiology/Virology |
Snail/HDAC-IN-1是一种Snail/HDAC 抑制剂剂,具有抗菌抗癌活性, 可降低Snail蛋白的表达,诱导细胞凋亡,可用于研究实体肿瘤。 | |||
T7082 |
HDAC8-IN-1
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC8-IN-1 是一种 HDAC8 抑制剂,在癌细胞系中的 IC50 为 27.2 nM,有抗增殖作用。 | |||
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。 | |||
T39990 |
HDAC-IN-26
|
Others | Others |
HDAC-IN-26 is a highly selective class I HDAC inhibitor with an EC 50 value of 4.7 nM. | |||
T61962 |
PARP-1/HDAC-IN-1
|
Others | Others |
PARP-1/HDAC-IN-1 是有效的 PARP-1/HDAC6双重抑制剂,IC50分别为 68.90 nM 和 510 nM。PARP-1/HDAC-IN-1 具有抗癌、抗迁移和抗血管生成活性。 | |||
T11543 |
HDAC-IN-5
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-5 is a histone deacetylase (HDAC) inhibitor. | |||
T6392 |
AR42
OSU-HDAC42,AR-42,(S)-(+)-N-羟基-4-(3-甲基-2-苯基丁酰氨基)苯甲酰胺,AR 42,HDAC-42 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
AR42 (OSU-HDAC42) 是一种 HDAC 抑制剂(IC50: 30 nM)。 | |||
T11542 |
HDAC-IN-4
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-4 is a selective HDAC6 and HDAC10 inhibitor (pIC50s: 7.2 and 6.8 in BRET assay) with antitumoral activity. | |||
T12455 | PI3K/HDAC-IN-1 | PI3K | PI3K/Akt/mTOR signaling |
PI3K/HDAC-IN-1 is a potent PI3K and HDAC dual inhibitor(IC50s of 8.1 nM and 1.4 nM, respectively). | |||
T24133 |
HDAC8-IN-20a
HDAC8 IN 20a,HDAC8IN20a,HDAC8 inhibitor-20a,HDAC8 inhibitor 20a |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC8-IN-20a (HDAC8 inhibitor-20a) 是一种有效的、具有选择性的HDAC8抑制剂,IC50为27 nM。HDAC8-IN-20a 可阻断生长受体存活信号的激活。 | |||
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。 | |||
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。 | |||
T63416 |
HDAC-IN-39
|
Others | Others |
HDAC-IN-39 是 HDAC 的有效抑制剂,能够作用于HDAC1、HDAC2、HDAC3,他们的IC50值分别为 1.07 μM、1.47 μM 和 2.27 μM。HDAC-IN-39 能够诱导细胞周期阻滞在 G2/M 期,同时也能够明显抑制微管聚合。HDAC-IN-39 对耐药癌细胞表现出良好的抗癌作用。 | |||
T61248 |
HDAC-IN-32
|
Others | Others |
HDAC-IN-32 is a highly effective HDAC inhibitor presenting IC50 values of 5.2, 11, and 28 nM for HDAC1, HDAC2, and HDAC6, respectively. This compound demonstrates notable anti-proliferative properties against tumor cells, as well as significant in vivo antitumor efficacy, which can elicit antitumor immunity [1]. | |||
T78818 |
HDAC-IN-63
|
Others | Others |
HDAC-IN-63(化合物63)是一种针对FLT3和HDAC的双重抑制剂,其中,对FLT3的IC50为0.844 nM,对HDAC1的IC50为30.0 nM。该化合物能有效抑制MV4-11细胞的增殖(IC50为92 nM),在MV4-11细胞中诱导apoptosis并造成细胞周期阻滞。HDAC-IN-63可以应用于急性髓系白血病(AML)的相关研究。 | |||
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。 | |||
T63803 |
HDAC-IN-44
|
Others | Others |
HDAC-IN-44 是 HDAC 抑制剂 (IC50: 61.2 nM),具有强抗癌效果。 | |||
T72012 |
HDAC-IN-6
|
Others | Others |
HDAC-IN-6 is an HDAC inhibitor, targeting HDAC2, HDAC3, HDAC4, HDAC5, HDAC7, HDAC8, and HDAC9. | |||
T63696 |
HDAC-IN-9
|
Others | Others |
HDAC-IN-9 是有效的、选择性的 tubulin 和 HDAC 双重抑制剂。HDAC-IN-9 对 A549 细胞的侵袭和迁移表现出抑制作用。HDAC-IN-9 在体外和体内均表现出有效的抗肿瘤和抗血管生成活性。 | |||
T79541 |
HDAC-IN-61
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-61(compound 12k)为口服生效的HDAC抑制剂,表现出针对Bel-7402细胞线的明显抗癌活性,其IC50值仅为30 nM,适用于癌症研究领域。 | |||
T79371 |
HDAC-IN-62
|
Autophagy | Autophagy |
HDAC-IN-62(Compound 5),是一款针对HDAC6/8/11的HDAC抑制剂,IC50分别为0.78、1.0、1.2μM。该化合物通过诱导自噬(Autophagy)来抑制微胶质细胞的激活,进而抑制一氧化氮产生,显示出抗炎和抗抑郁的效果。此外,HDAC-IN-62还能抑制实验小鼠大脑中的微胶质细胞活化。 | |||
T62072 |
HDAC-IN-47
|
Others | Others |
HDAC-IN-47 是一种口服具有活力的组蛋白去乙酰化酶 (HDAC) 的抑制剂,对 HDAC1、HDAC2、HDAC3、HDAC6、HDAC8 的 IC50 值分别为 19.75 nM、57.8 nM、40.27 nM、5.63 nM、302.73 nM。HDAC-IN-47 可以将细胞周期阻滞在 G2/M 期,抑制细胞自噬,能够利用 Bax/Bcl-2 和 caspase-3 通路诱导凋亡,在体内具有抗癌活性。 | |||
T73179 |
HDAC-IN-50
|
Others | Others |
HDAC-IN-50是一种口服活性的有效FGFR和HDAC双重抑制剂,其IC50值针对FGFR1、FGFR2、FGFR3、FGFR4、HDAC1、HDAC2、HDAC6、HDAC8分别为0.18、1.2、0.46、1.4、1.3、1.6、2.6、13 nM。该化合物能诱导(Apoptosis)及使细胞周期在G0/G1期停滞,降低pFGFR1、pERK、pSTAT3的表达,展现出抗肿瘤活性。 | |||
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。 | |||
T62799 |
HDAC-IN-28
|
Others | Others |
HDAC-IN-28 是一种 HDAC 的新型抑制剂,能够显著抑制肿瘤生长和转移。 | |||
T62649 |
HDAC-IN-34
|
Others | Others |
HDAC-IN-34 (compound 27) 是一种 HDAC 的有效抑制剂,能够作用于 HDAC1 (IC50: 0.022 μM) 和 HDAC6 (IC50: 0.45 μM)。HDAC-IN-34 可以与 DNA 结合,造成 DNA 损伤。HDAC-IN-34 利用 p53 信号通路引起细胞凋亡。HDAC-IN-34 对 HCT-116 细胞表现出明显的抗增殖作用 (IC50: 1.41 μM)。 | |||
T62514 |
HDAC-IN-46
|
Others | Others |
HDAC-IN-46 (compound 12c) 是一种 HDAC 的有效抑制剂,能够作用于 HDAC1 (IC50: 0.21 μM) 和 HDAC6 (IC50: 0.021 μM)的。HDAC-IN-46 在 MDA-MB-231 细胞中可以上调 p-p38,下调 Bcl-xL 和 cyclin D1。HDAC-IN-46 能够将细胞周期阻滞在 G2 期,并诱导细胞凋亡 (apoptosis)。HDAC-IN-46 能够用于三阴性乳腺癌 (TNBC) 的研究。 | |||
T78767 |
HDAC-IN-60
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-60 (化合物21a) 作为一种高效HDAC抑制剂,能增强细胞内ROS生成,导致DNA损伤,阻碍G2/M期细胞周期,且触发线粒体相关凋亡途径促进细胞死亡。 | |||
T78920 |
HDAC-IN-58
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-58为HDAC抑制剂,特异性针对HDAC6,其IC50值达2.06 nM。适用于慢性疾病,如神经退行性和精神疾病的研究。 | |||
T61954 |
HDAC-IN-29
|
Others | Others |
HDAC-IN-29 (化合物 13b) 是有效的泛 HDAC 抑制剂,具有抗肿瘤活性。 | |||
T62708 |
HDAC-IN-37
|
Others | Others |
HDAC-IN-37 是一种 HDAC 的有效抑制剂,作用于 HDAC1 (IC50: 0.0551 μM)、HDAC3 (IC50: 1.24 μM)、HDAC8 (IC50: 0.948 μM) 和 HDAC6 (IC50: 34.2 μM)。HDAC-IN-37 能够缓慢诱导组蛋白乙酰化。HDAC-IN-37 阻碍细胞由 G1 期向 S 期转变,诱导早期细胞凋亡。 | |||
T63422 |
HDAC-IN-45
|
Others | Others |
HDAC-IN -45 是小分子 HDAC 抑制剂,能够与 Y303 残基形成氢键,表现出抗癌作用。HDAC-IN-45 能够明显抑制 HDAC1、HDAC2 和 HDAC3 亚型,他们的 IC50值分别为 0.108、0.585 和 0.563 μM。 | |||
T61630 |
HDAC-IN-42
|
Others | Others |
HDAC-IN-42 (compound 14f) is a highly potent and selective inhibitor of histone deacetylase (HDAC) enzymes, with IC50 values of 0.19 μM for HDAC1 and 4.98 μM for HDAC6. It exhibits remarkable anticancer properties and inhibits cell proliferation. Additionally, HDAC-IN-42 induces apoptosis and causes cell cycle arrest specifically at the G2/M phase [1]. | |||
T61429 |
HDAC-IN-33
|
Others | Others |
HDAC-IN-33 is a highly potent HDAC inhibitor, effectively inhibiting HDAC1, HDAC2, and HDAC6 with IC50 values of 24, 46, and 47 nM, respectively. This compound demonstrates significant antiproliferation activity against tumor cells and exhibits remarkable in vivo antitumor efficacy. Additionally, HDAC-IN-33 initiates the activation of antitumor immunity [1]. | |||
T78766 |
HDAC-IN-59
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-59(compound 13a)为一种高效HDAC抑制剂。该化合物能增强细胞内ROS生成,导致DNA损伤,阻止G2/M期细胞周期进程,并激活线粒体途径引发细胞凋亡。 | |||
T78532 |
HDAC-IN-55
|
Others | Others |
HDAC-IN-55(8j)是一种小分子化合物,能够上调E-钙粘蛋白的表达并抑制癌细胞的增殖。 | |||
T9963 |
MPT0B390
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
MPT0B390 是 HDAC 抑制剂和 TIMP3 诱导剂,可抑制肿瘤生长、转移和血管生成。 | |||
T36575 |
HDAC3 Inhibitor
|
Others | Others |
HDAC3 inhibitor is an allosteric inhibitor of histone deacetylase 3 (HDAC3; Ki = 0.16 nM). It is selective for HDAC3 over HDAC1 and HDAC2 (IC50s = 0.95, 11.81, and 95.45 nM, respectively, using recombinant HDACs). In addition, it is selective for acute myeloid, monocytic, and lymphoblastic leukemia cell lines (EC50s = 36.37, 76.64, and 151.7 nM, respectively) over chronic myeloid, acute promyelocytic, and acute lymphoblastic cells (EC50s = 2,160, >10,000, and >10,000 nM, respectively). | |||
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. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TQ0207 |
Sulforaphane
萝卜硫素 |
Apoptosis; Nrf2; HDAC | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation |
Sulforaphane 是存在于多种蔬菜中的一种天然异硫氰酸酯。它可以激活Nrf2,并通过 AMPK 依赖性信号传导抑制高糖诱导的胰腺癌。它增加肿瘤抑制蛋白的转录并抑制组蛋白脱乙酰酶的活性,具有抗癌和抗炎活性。 | |||
T2266 |
SantacruzaMate A
CAY-10683 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
SantacruzaMate A (CAY-10683) 是一种高效选择性的HDAC2抑制剂,IC50为 119 pM。 | |||
T7052 |
Gnetol
|
Tyrosinase; COX; HDAC; AChR | Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Neuroscience; Proteases/Proteasome |
Gnetol 是从买麻藤的根中分离出来的一种酚类。它是酪氨酸酶抑制剂,对鼠酪氨酸酶的 IC50为 4.5 μM,可抑制黑色素的生物合成。它有效抑制 COX-1和 HDAC,具有抗氧化、抗增殖、抗癌和保肝活性,还具有浓度依赖性的 α-淀粉酶、α-葡萄糖苷酶和脂肪形成活性。 | |||
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。 | |||
TN1911 |
Marein
马里苷,马里甙 |
transporter; Akt; HDAC; AMPK | Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Metabolism; PI3K/Akt/mTOR signaling |
Marein 能通过CaMKK/AMPK/GLUT1促进葡萄糖摄取,IRS/Akt/GSK-3β增加糖原合成,并通过Akt/FoxO1减少糖异生,从而改善 HepG2 细胞中高葡萄糖诱导的胰岛素抵抗。它对甲基乙二醛诱导的 PC12 细胞损伤具有神经保护作用,还有抗氧化、降压、降血脂和抗糖尿病作用。 | |||
T3753 |
Sinapinic Acid
Sinapic acid,芥子酸,Synapoic acid |
Apoptosis; RAAS; Reactive Oxygen Species; HDAC | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Endocrinology/Hormones; Immunology/Inflammation; Metabolism; NF-κB |
Sinapinic Acid (Synapoic acid) 是从 Hydnophytum formicarumJack. 根中分离到的酚类,是HDAC 抑制剂,对ACE-I 的活性也有抑制作用。它有抗肿瘤活性,诱导肿瘤细胞凋亡,具有抗氧化、抗糖尿病的作用。 | |||
T6S0033 |
Crotonoside
巴豆苷;异鸟苷,巴豆苷,Isoguanosine,2-HYDROXYADENOSINE |
Others; FLT; HDAC | Angiogenesis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Others; Tyrosine Kinase/Adaptors |
Crotonoside (Isoguanosine) 是从中草药巴豆中分离出来的一种天然产物。 它抑制 FLT3 和 HDAC3/6,有治疗急性髓性白血病 (AML)的研究潜力。 | |||
T7064 |
Valproic Acid
Sodium valproate,2-Propylpentanoic Acid,丙戊酸,VPA,Depakine,2-Propylvaleric Acid |
Mitophagy; Gamma-secretase; HIV Protease; GABA Receptor; Sodium Channel; HDAC; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Proteases/Proteasome; Stem Cells |
Valproic Acid (2-Propylpentanoic Acid) 是一种 HDAC 抑制剂,可抑制 HDAC1 活性,诱导 HDAC2 降解,具有口服活性。Valproic Acid 可以用于癫痫和躁郁症的研究。 | |||
T19687 |
Phenylethyl isothiocyanate
JC 5411,2-苯基乙基异硫代氰酸酯,JC5411,JC-5411 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Phenylethyl isothiocyanate (JC5411) 是一种 HDAC 抑制剂。它有可能用于治疗良性前列腺肥大。 | |||
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。 | |||
T2140 |
Parthenolide
(-)-Parthenolide,小白菊内酯 |
Apoptosis; Mitophagy; NF-κB; HDAC; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; NF-κB |
Parthenolide ((-)-Parthenolide) 是一种从药草短舌匹菊中发现的倍半萜内酯。 它抑制NF-κB 活化,有抗炎活性。它还可抑制HDAC1蛋白,但不影响其他I/II 类HDAC。 | |||
TN4220 |
Homobutein
3-O-Methylbutein,2',4,4'-Trihydroxy-3-methoxychalcone |
Antioxidant; NF-κB; HDAC; Parasite; Immunology/Inflammation related | Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology; NF-κB; oxidation-reduction |
Homobutein (3-O-Methylbutein) 是 HDAC 和 NF-κB 的双重抑制剂,IC50 分别为 190 和 38 μM。 Homobutein 是一种铁螯合剂,具有抗癌、抗炎、抗寄生虫和抗氧化活性。 | |||
T36797 |
1-Alaninechlamydocin
|
Others | Others |
1-Alaninechalmydocin is a fungal metabolite originally isolated from a Great Lakes-derived Tolypocladium sp. and an inhibitor of histone deacetylases (HDACs). It reduces total HDAC activity in HeLa cell lysates in a concentration-dependent manner. 1-Alaninechlamydocin reduces proliferation of MIA PaCa-2, PANC-1, and hTERT-HPNE cells (GI50s = 5.3, 14, and 2.0 nM, respectively). | |||
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。 | |||
T36303 |
Psammaplin A
|
Others | Others |
Psammaplin A, a marine metabolite, functions as a robust inhibitor of HDAC and DNA methyltransferases, displaying notable potency and selectivity as a DAC1 inhibitor, with an IC50 value of 0.9 nM. It exhibits antimicrobial effects against Gram-positive bacteria and inhibits both DNA synthesis and DNA gyrase activity, also demonstrating antitumor activity[1][2]. | |||
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. | |||
TN2095 |
Pomiferin
|
NOS; NF-κB; PDE | Immunology/Inflammation; Metabolism; NF-κB |
Pomiferin is a natural product inhibitor of carbonic anhydrase I and II isoenzymes. It has anticancer, antibacterial and antidiabetic properties. Pomiferin has anti-inflammatory and neuroprotective activities. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-03431 |
HDAC4 Protein, Human, Recombinant (aa 612-1084)
histone deacetylase 4,HA6116,HDAC-4,HD4,BDMR,HD... |
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,HD8,HDA... |
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-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. | |||
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-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-01474 |
HDAC6 Protein, Human, Recombinant (His)
Protein deacetylase HDAC6,Histone deacetylase 6, |
Human | E. coli |
HDAC6 Protein, Human, Recombinant (His) is expressed in E. coli. | |||
TMPH-01475 |
HDAC7 Protein, Human, Recombinant (His)
|
Human | E. coli |
N/A. HDAC7 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 26 kDa and the accession number is Q8WUI4 (BC064840). | |||
TMPH-01471 |
HDAC1 Protein, Human, Recombinant (His & SUMO)
Histone deacetylase 1,Protein deacetylase HDAC1, |
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-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. | |||
TMPY-03056 |
LSD1 Protein, Human, Recombinant (His & GST)
BHC110,LSD1,KDM1,AOF2,lysine (K)-specific demethylase 1A |
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... | |||
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... | |||
TMPH-02217 |
SMARCA4 Protein, Human, Recombinant (His)
Transcription activator BRG1,Protein brahma homolog 1,SWI/SN... |
Human | P. pastoris (Yeast) |
Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Component of SWI/SNF chromatin remodeling complexes that carry out key enzymatic activities, changing chromatin structure by altering DNA-histone contacts within a nucleosome in an ATP-dependent manner. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating the calcium-dependent release of a repressor compl... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIH-0260 |
HDAC-IN-4-d4
|
||
HDAC-IN-4-d4 是 HDAC-IN-4 的氘代化合物。 | |||
TMID-0120 |
Valproic Acid-d15
|
||
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。 | |||
TMIJ-0431 |
2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid
|
||
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。 | |||
TMIJ-0163 |
Valproic Acid-d4
|
||
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-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。 |