HDAC
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.
HDAC 相关产品(175)
- GC14016SulforaphaneCAS: 4478-93-7纯度: >98.00% / >99.00% / >97.00%
萝卜硫素 (SFN) 称为 [1-isothiocyanato-4-(methylsulfinyl)butane]。
- GC14439Santacruzamate A (CAY10683)CAS: 1477949-42-0纯度: >99.00%
Santacruzamate A (CAY10683)是一种天然氨基甲酸酯衍生物,可抑制HDAC2和HDAC6活性,IC 50 值分别为0.119nM和434nM。
- GC14597ITSA-1 (ITSA1)CAS: 200626-61-5纯度: >98.00%
ITSA-1 (ITSA1)是一种组蛋白去乙酰化酶(HDAC)激活剂,可以防止动脉层流剪切力诱导的内皮细胞脱落,并降低血管内皮细胞(vECs)中VCAM-1的表达。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC10417 | ACY-241 | 1316215-12-9 | >98.50% | |
An HDAC6 inhibitor | ||||
| GC11360 | ORY-1001 | 1431326-61-2 | - | |
An LSD1 inhibitor | ||||
| GC11574 | HPOB | 1429651-50-2 | - | |
A potent and selective inhibitor of HDAC6 | ||||
| GC11949 | MI-192 | 1415340-63-4 | - | |
A selective HDAC2/3 Inhibitor | ||||
| GC12074 | BG45 | 926259-99-6 | >99.50% | |
A selective HDAC3 inhibitor | ||||
| GC12334 | HNHA | 926908-04-5 | - | |
HDAC inhibitor | ||||
| GC12484 | BRD73954 | 1440209-96-0 | >98.00% | |
A dual inhibitor of HDAC6 and HDAC8 | ||||
| GC12667 | 4SC-202 | 1186222-89-8 | >99.50% | |
An HDAC1-3 and KDM1A inhibitor | ||||
| GC12822 | BML-210(CAY10433) | 537034-17-6 | - | |
A potent, synthetic HDAC inhibitor | ||||
| GC12971 | CAY10603 | 1045792-66-2 | >99.50% | |
An exceptionally potent inhibitor of HDAC6 | ||||
| GC13764 | Nexturastat A | 1403783-31-2 | >98.00% | |
A potent, cell-permeable HDAC6 inhibitor | ||||
| GC13925 | Nullscript | 300816-11-9 | >98.00% | |
A negative control for scriptaid | ||||
| GC14016 | Sulforaphane | 4478-93-7 | >98.00% / >99.00% / >97.00% | |
萝卜硫素 (SFN) 称为 [1-isothiocyanato-4-(methylsulfinyl)butane]。 | ||||
| GC14058 | CBHA | 174664-65-4 | >98.00% | |
Inhibitor of histone deacetylases | ||||
| GC14367 | UF 010 | 537672-41-6 | >99.50% | |
A class I HDAC inhibitor | ||||
| GC14439 | Santacruzamate A (CAY10683) | 1477949-42-0 | >99.00% | |
Santacruzamate A (CAY10683)是一种天然氨基甲酸酯衍生物,可抑制HDAC2和HDAC6活性,IC 50 值分别为0.119nM和434nM。 | ||||
| GC14597 | ITSA-1 (ITSA1) | 200626-61-5 | >98.00% | |
ITSA-1 (ITSA1)是一种组蛋白去乙酰化酶(HDAC)激活剂,可以防止动脉层流剪切力诱导的内皮细胞脱落,并降低血管内皮细胞(vECs)中VCAM-1的表达。 | ||||
| GC15410 | Bufexamac | 2438-72-4 | >98.00% | |
An NSAID and a class IIb HDAC inhibitor | ||||
| GC15857 | Sodium butyrate | 156-54-7 | >99.00% | |
A short-chain fatty acid and HDAC inhibitor | ||||
| GC17472 | Oxamflatin | 151720-43-3 | >98.00% | |
Inhibitor of histone deacetylases | ||||
| GC18206 | WT161 | 1206731-57-8 | >98.50% | |
A potent inhibitor of HDAC6 | ||||
| GC18402 | GSK3117391 | 1018673-42-1 | >98.50% | |
An HDAC inhibitor | ||||
| GC19020 | ACY-738 | 1375465-91-0 | >98.50% | |
ACY-738是一种具有口服活性的选择性组蛋白去乙酰化酶6(HDAC6;IC 50 =1.7nM)抑制剂。 | ||||
| GC19129 | EDO-S101 | 1236199-60-2 | >98.00% | |
An HDAC inhibitor and DNA alkylating agent | ||||
