histone acetyltransferases

TTK21 是 CBP/p300 组蛋白乙酰转移酶活性的激活剂，与葡萄糖基碳纳米球结合时，可通过血脑屏障，对成人大脑神经发生和长期记忆功能有益。

Curcumin-D6 is deuterium-labeled curcumin (Turmeric yellow). Curcumin (T1516) (Turmeric yellow) is a natural phenolic compound with various pharmacological effects,including anti-inflammatory,antioxidant,anti-proliferative and anti-angiogenic activities. Curcumin (T1516) is an inhibitor of p300 histone acetyltransferases (HATs),and also shows inhibitory effects on NF-κB and MAPKs.

Garcinol 是一种从印度藤黄提取的聚异戊二烯基二苯甲酮，对乙酰胆碱酯酶和丁酰胆碱酯酶具有抗胆碱酯酶的特性，IC50分别为 0.66 µM 和 7.39 µM。它还抑制组蛋白乙酰转移酶和 p300/CPB 相关因子，具有抗炎和抗癌活性。

C646 是一种组蛋白乙酰转移酶 p300 的抑制剂 (Ki=400 nM)，具有竞争性和选择性，对其他乙酰转移酶作用较小。C646 具有细胞凋亡诱导剂和放射增敏剂的作用。

Selective p300 histone acetyltransferase (HAT) inhibitor (IC50 = 50-500 nM). Exhibits approximately 100-fold selectivity for p300 over PCAF (IC50 = 200 μM). Inhibits p300-dependent transcription. Active in vivo. Lau et al (2000) HATs off: selective synthetic inhibitors of the histone acetyltransferases p300 and PCAF. Mol.Cell. 5 589 PMID:10882143 |Liu et al (2008) The structural basis of protein acetylation by the p300/CBP transcriptional coactivator. Nature. 451 846 PMID:18273021 |Burns et al (2005) Iso-coenzyme A. J.Biol.Chem. 280 16550 PMID:15708855 |Cebrat et al (2003) Synthesis and analysis of potential prodrugs of coenzyme A analogues for the inhibition of the histone acetyltransferase p300. Bioorg.Med.Chem. 11 3307 PMID:12837541

WM-8014 (MOZ-IN-3) 是一种 MOZ，属于组蛋白乙酰转移酶的抑制剂，IC50值为 55 nM。

KAT6-IN-1(compound E)是一种选择性和可口服的组蛋白乙酰转移酶KAT6A和KAT6B抑制剂，具有抗肿瘤活性，可用于研究癌症。