CHD7 inhibitors are a class of chemical compounds designed to specifically target and inhibit the activity of the chromodomain helicase DNA binding protein 7 (CHD7). CHD7 is a member of the CHD family of proteins, which are characterized by the presence of chromodomains, helicase domains, and DNA-binding domains. These proteins are involved in chromatin remodeling, a critical process for regulating gene expression by altering the structure of chromatin to either promote or inhibit access to genetic information. CHD7, in particular, plays a pivotal role in the regulation of gene expression during development, influencing processes such as cellular differentiation, proliferation, and the establishment of cell identity.
Structurally, CHD7 inhibitors can vary widely and may include small molecules, peptides, or larger biomolecules engineered to bind to specific domains of the CHD7 protein. These inhibitors typically interact with the ATPase/helicase domain of CHD7, which is essential for its chromatin remodeling activity. By inhibiting this domain, these compounds prevent CHD7 from utilizing ATP to alter chromatin structure, thereby impeding its ability to modulate gene expression. The study of CHD7 inhibitors is crucial for understanding the functional mechanisms by which CHD7 influences chromatin dynamics and gene regulation. By examining how these inhibitors affect CHD7 activity, researchers can gain insights into the broader implications of chromatin remodeling on cellular functions such as transcriptional regulation, DNA repair, and replication. Research into CHD7 inhibitors also sheds light on the intricate balance of chromatin states that dictate cellular behavior and development, providing a deeper understanding of the role of CHD7 in maintaining the epigenetic landscape of cells.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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Romidepsin | 128517-07-7 | sc-364603 sc-364603A | 1 mg 5 mg | ¥2414.00 ¥7017.00 | 1 | |
罗米地辛是一种组蛋白去乙酰化酶抑制剂,可影响组蛋白的乙酰化状态,从而影响染色质结构和CHD(染色质结构域螺旋酶DNA结合)功能。 | ||||||
Mocetinostat | 726169-73-9 | sc-364539 sc-364539B sc-364539A | 5 mg 10 mg 50 mg | ¥2369.00 ¥2730.00 ¥16178.00 | 2 | |
莫西他诺是一种组蛋白去乙酰化酶抑制剂,可改变组蛋白的乙酰化状态,影响染色质结构和CHD(染色质结构域螺旋酶DNA结合)活性。 | ||||||
BIX01294 hydrochloride | 1392399-03-9 | sc-293525 sc-293525A sc-293525B | 1 mg 5 mg 25 mg | ¥406.00 ¥1241.00 ¥4513.00 | ||
BIX-01294是一种G9a和GLP组蛋白甲基转移酶抑制剂,可影响组蛋白甲基化,从而影响CHD(染色质结构域螺旋酶DNA结合)的染色质重塑活性。 | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | ¥632.00 ¥2933.00 ¥11056.00 | 163 | |
蛋白酶体抑制剂通过阻止蛋白质降解来影响CHD(染色质结构域螺旋酶DNA结合),导致CHD(染色质结构域螺旋酶DNA结合)水平升高和细胞功能改变。 | ||||||
Nutlin-3 | 548472-68-0 | sc-45061 sc-45061A sc-45061B | 1 mg 5 mg 25 mg | ¥632.00 ¥2392.00 ¥8619.00 | 24 | |
MDM2抑制剂,通过稳定p53并影响与CHD(染色质域螺旋酶DNA结合)活性相关的下游通路,间接影响CHD(染色质域螺旋酶DNA结合)。 | ||||||
C646 | 328968-36-1 | sc-364452 sc-364452A | 10 mg 50 mg | ¥2933.00 ¥10436.00 | 5 | |
p300/CBP组蛋白乙酰转移酶抑制剂,通过调节乙酰化水平和染色质结构,间接影响CHD(染色质域螺旋酶DNA结合)。 | ||||||
EPZ6438 | 1403254-99-8 | sc-507456 | 1 mg | ¥745.00 | ||
EZH2特异性抑制剂,通过靶向Polycomb Repressive Complex 2(PRC2)并改变染色质结构,间接影响CHD(染色质域螺旋酶DNA结合)。 | ||||||
GSK-J4 | 1373423-53-0 | sc-507551 | 100 mg | ¥14385.00 | ||
赖氨酸特异性脱甲基酶1(LSD1)和组蛋白去乙酰化酶的双重抑制剂,通过调节组蛋白修饰间接影响CHD(染色质域螺旋酶DNA结合)。 | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | ¥643.00 ¥2053.00 ¥1038.00 | 21 | |
拓扑异构酶I抑制剂,通过诱导DNA损伤和影响染色质结构间接调节CHD(染色质结构域螺旋酶DNA结合),从而影响CHD(染色质结构域螺旋酶DNA结合)的结合和活性。 |