HDAC(组蛋白去乙酰化酶)
Histone deacetylases (HDACs), known for their ability to target histones as well as more than 50 non-histone proteins, are classified into three major classes according to their homology to yeast proteins, including class I (HDAC1, HDAC2, HDAC3 and HDAC8), class II (HDAC4, HDAC5, HDAC7 and HDAC9) and class IV (HDAC11). HDAC inhibitors, a large group of compounds that is able to induce the accumulation of acetylated histones as well as non-histone proteins, are divided into several structural classes including hydroxamates, cyclic peptides, aliphatic acids and benzamides. HDAC inhibitors have been investigated for their efficacy as anticancer agents in the treatment of a wild range of cancers.
Products for HDAC
- Cat.No. 产品名称 Information
- GC13926 BMS-345541(free base) BMS-345541(free base) 是 IKK 催化亚基的选择性抑制剂 (IKK-2 IC50=0.3 μM, IKK-1 IC50=4 μM)。 BMS-345541(游离碱)结合在 IKK 的变构位点。
-
GC12667
4SC-202
4SC-202(盐的形式),4SC-202
An HDAC1-3 and KDM1A inhibitor - GC13764 Nexturastat A A potent, cell-permeable HDAC6 inhibitor
-
GC15857
Sodium butyrate
丁酸钠
A short-chain fatty acid and HDAC inhibitor -
GC15410
Bufexamac
丁苯羟酸; Bufexamic acid
An NSAID and a class IIb HDAC inhibitor -
GC11424
Valproic acid
丙戊酸; VPA; 2-Propylpentanoic Acid
A class I HDAC inhibitor -
GC16143
Varenicline Hydrochloride
6,7,8,9-四氢-6,10-甲桥-6H-吡嗪并[2,3-H][3]苯并氮杂卓盐酸盐,CP 526555 hydrochloride
Varenicline Hydrochloride (CP 526555 hydrochloride) 是一种高亲和力、选择性的 α4β2 尼古丁乙酰胆碱受体 (nAChR) 部分激动剂和完整的 α7 nAChR 激动剂。 -
GC17703
TMP269
TMP 269;TMP-269
A selective class IIa HDAC inhibitor -
GC14285
RGFP966
RGFP 966;RGFP-966
RGFP966是一种N-(o-aminophenyl)carboxamide HDAC抑制剂,对HDAC3的IC50为0.08 μM,是一类针对HDAC3的慢开/慢关竞争性紧密结合抑制剂。 -
GC10322
Tubastatin A HCl
TubastatinA盐酸盐,TSA HCl;Tubastatin A hydrochloride
A potent HDAC6 inhibitor - GC12019 TCS HDAC6 20b An HDAC6 inhibitor
-
GC13237
LMK 235
N-[[6-(羟基氨基)-6-氧代己基]氧基]-3,5-二甲基-苯甲酰胺
A selective inhibitor of HDAC4 and HDAC5 -
GC16386
Tubacin
HDAC6抑制剂
Tubacin (tubulin acetylation inducer)是一种选择性抑制组蛋白去乙酰化酶6 (HDAC6),诱导α-微管蛋白乙酰化的小分子,IC50为0.004µM。 -
GC13591
TC-H 106
RGFA-8; TC-H 106; Histone Deacetylase Inhibitor VII
A tight-binding inhibitor of class I HDACs -
GC11095
Pyroxamide
N-羟基-N'-3-吡啶基辛二酰胺
A HDAC inhibitor -
GC15040
NSC 3852
8-羟基-5-硝基喹啉
A tumor cell differentiating agent -
GC15536
NCH 51
NCH-51
An HDAC inhibitor - GC13435 KD 5170 An inhibitor of class I and II HDACs
-
GC14340
Tasquinimod
他喹莫德; ABR-215050
An orally-active anti-cancer compound -
GC10423
RG2833
RG 2833;RG-2833;RGFP-109;RGFP109;RGFP 109
An HDAC inhibitor -
GC14243
Resminostat hydrochloride
RAS2410 hydrochloride;4SC-201 hydrochloride;RAS 2410 hydrochloride;RAS-2410 hydrochloride
An orally bioavailable HDAC inhibitor -
GC15830
Daminozide
丁酰肼
Selective inhibitor of KDM2/7 histone demethylases -
GC11975
CHAPS
3-[3-(胆酰胺丙基)二甲氨基]丙磺酸内盐
CHAPS 是胆酸的衍生物,是一种用于溶解膜蛋白的两性离子去污剂。 -
GC16456
M344
4-(二甲氨基)-N-[7-(羟基氨基)-7-氧庚]苯甲酰胺,Histone Deacetylase Inhibitor III,MS344
HDAC inhibitor -
GC14590
AR-42 (OSU-HDAC42)
HDAC inhibitor,novel and potent
-
GC15114
LAQ824 (NVP-LAQ824,Dacinostat)
达诺司他,LAQ-824, NVP-LAQ 824
A hydroxamate-based HDAC inhibitor -
GC13408
CI994 (Tacedinaline)
4-乙酰氨基-N-(2'-氨基苯基)-苯甲酰胺,N-acetyldinaline; CI-994; Goe-5549
An inhibitor of HDAC1, -2, and -3 - GC10839 Tubastatin A Tubastatin A 是一种有效的选择性 HDAC6 抑制剂,IC50 值为 15 nM。并且Tubastatin A也是一种新型GPX4抑制剂,Tubastatin A 直接与 GPX4 结合,诱导乳腺癌细胞铁死亡。
-
GC13706
Droxinostat
4-(4-氯-2-甲基苯氧基)-N-羟基丁酰胺,NS 41080
An inhibitor of HDAC3, HDAC6, and HDAC8 -
GC15794
Valproic acid sodium salt (Sodium valproate)
丙戊酸钠; Sodium Valproate sodium
Valproic acid sodium salt (Sodium valproate)(VPA)是一种具有口服活性的组蛋白脱乙酰酶 (HDAC)抑制剂,IC50 值为1.5mM,抑制HDAC1的IC50值为400μM,同时可诱导HDAC2的降解。 -
GC14682
PCI-24781 (CRA-024781)
阿贝司他; 艾贝司他; CRA 024781; PCI-24781
An HDAC inhibitor -
GC12115
CUDC-907
CUDC-907
CUDC 是一种口服生物可利用的小分子 PI3K 和 HDAC 双重抑制剂,作用于 PI3K α 和 HDAC1 / 2 / 3 / 10,IC50 分别为 19 nm 和 1.7 nm / 5 nm / 1.8 nm / 2.8 nm .在 WSU DLCL2 细胞中评估了双功能 HDAC 和 PI3K 抑制剂 CUDC-907 的抗肿瘤活性。 -
GC15962
Belinostat (PXD101)
贝利司他(PXD101),PXD-101, PXD 101, PX105684, PX-105684
Belinostat (PXD101) 是 HeLa 细胞提取物中组蛋白脱乙酰酶 (HDAC) 活性的新型异羟肟酸型抑制剂,IC50 为 27 nM 。 -
GC16734
Pracinostat (SB939)
(2E)-3-[2-丁基-1-[2-(二乙基氨基)乙基]-1H-苯并咪唑-5-基]-N-羟基丙烯酰胺,SB-939, SB 939
A pan-HDAC inhibitor
-
GC15965
MC1568
MC 1568, MC-1568
A selective class IIa HDAC inhibitor -
GC15879
Resminostat (RAS2410)
RAS2410; 4SC-201
Resminostat (RAS2410) (RAS2410; 4SC-201) 是一种有效的 HDAC1、HDAC3 和 HDAC6 抑制剂,平均 IC50 值分别为 42.5、50.1、71.8 nM,对 HDAC8 的活性较低,IC50 为 877 nM . -
GC15002
Sodium Phenylbutyrate
苯丁酸钠; 4-PBA sodium; 4-Phenylbutyric acid sodium; Benzenebutyric acid sodium
A chemical chaperone -
GC15315
Scriptaid
Scriptide; GCK1026
HDAC inhibitor -
GC17836
ITF2357 (Givinostat)
N-[4-[(羟基氨基)羰基]苯基]氨基甲酸[6-[(二乙基氨基)甲基]-2-萘基]甲酯盐酸盐水合物,ITF-2357, Givinostat (hydrochloride monohydrate)
HDAC inhibitor with anti-inflammatory and antineoplastic activities
-
GC16008
CUDC-101
7-[[4-(3-乙炔基苯基氨基)-7-甲氧基喹唑啉-6-基]氧基]-N-羟基庚酰胺,CUDC101, CUDC 101
A multi-target inhibitor of HDACs, EGFR, and HER2 -
GC18008
PCI-34051
N-羟基-1-(4-甲氧基苄基)-1H-吲哚-6-甲酰胺,PCI34051, PCI 34051
A potent, selective HDAC8 inhibitor -
GC15476
JNJ-26481585
JNJ26481585
A pan-HDAC inhibitor -
GC13055
Mocetinostat (MGCD0103, MG0103)
N-(2-氨基苯基)-4-([[4-(吡啶-3-基)嘧啶-2-基]氨基]甲基)苯甲酰胺,MGCD-0103
An orally available HDAC inhibitor -
GC17390
Vorinostat (SAHA, MK0683)
伏立诺他; SAHA; Suberoylanilide hydroxamic acid
An HDAC inhibitor
-
GC14998
Rocilinostat (ACY-1215)
Ricolinostat
A selective inhibitor of HDAC6 -
GN10357
Parthenolide
小白菊内酯; (-)-Parthenolide
A natural inhibitor of NOD2 and NF-κB signaling -
GC12961
Apicidin
OSI 2040
A cell-permeable HDAC inhibitor
-
GC11334
Romidepsin (FK228, depsipeptide)
罗米地辛; FK 228; FR 901228; NSC 630176
A class I HDAC inhibitor -
GC15526
Trichostatin A (TSA)
曲古抑菌素A; TSA
Trichostatin A (TSA) 是一种有效的组蛋白脱乙酰酶 (HDAC) 抑制剂和抗真菌抗生素,对 HDAC 的 IC50 值为 1.8 nM,具有抑制细胞生长和诱导细胞分化。 -
GC12257
Panobinostat (LBH589)
帕比司他; LBH589; NVP-LBH589
A pan-HDAC inhibitor