| Cat. No. | Product Name | Information | 
            
                
            	| PC-72239 | CCT077791 PCAF/p300 inhibitor | CCT077791 (CCT077791) is a small molecule inhibitor of PCAF and p300 histone acetyltransferase with IC50 of 2.2 uM and IC95 of 35 uM, respectively. | 
            
                
            	| PC-72238 | NU9056 Tip60 (KAT5) inhibitor | NU9056 (NU 9056) is a specific Tip60 (KAT5) histone acetyltransferase inhibitor with IC50 of <2 uM. | 
            
                
            	| PC-72165 | CPI-1612 EP300/CBP inhibitor | CPI-1612 (CPI 1612) is a highly potent, selective, orally bioavailable EP300/CBP histone acetyltransferase inhibitor with IC50 of 8.1 nM (EP300 HAT SPA). | 
            
                
            	| PC-38289 | WM-3835 KAT7 inhibitor | WM-3835 (WM 3835) is a potent, high-specific, cell-permeable inhibitor of MYST acetyltransferase HBO1 (KAT7 or MYST2). | 
            
                
            	| PC-38126 | CCS1477 p300/CBP inhibitor | CCS1477 (Inobrodib) is an orally bioavailable, potent, and selective inhibitor of the p300/CBP bromodomain, binds to p300 and CBP with Kds of 1.3 and 1.7 nM respectively. | 
            
                
            	| PC-36166 | TTK21 CBP/p300 inhibitor | TTK21 (CBP-p300 activator TTK21) is a small molecule activator of CBP/p300 histone acetyltransferase activity with a maximal effect at a concentration of 275 uM. | 
            
                
            	| PC-35580 | WM-1119 KAT6A inhibitor | WM-1119 (WM1119) is a highly potent, selective inhibitor of lysine acetyltransferase KAT6A with Kd of 2 nM, shows greate bioavailability and specificity for KAT6A than WM-8014. | 
            
                
            	| PC-35579 | WM-8014 KAT6A inhibitor | WM-8014 (WM8014) is a highly potent, selective inhibitor of lysine acetyltransferase KAT6A with Kd of 5 nM and IC50 of 8 nM. | 
            
                
            	| PC-35322 | CPTH2 GCN5 inhibitor | CPTH2 is a specific histone acetyltransferase inhibitor modulating Gcn5 network in vitro and in vivo, inhibits H3 acetylation and induces cell-cycle perturbation and apoptosis in U-937 cells. | 
            
                
            	| PC-35321 | CPTH6 hydrobromide GCN5/PCAF inhibitor | CPTH6 hydrobromide is a thiazole derivative that can reduce histone acetylation and histone acetyltransferase (HAT) activity in human leukemia cells, CPTH6 is a specific Gcn5/pCAF inhibitor. | 
            
                
            	| PC-35320 | CPTH6 GCN5/PCAF inhibitor | CPTH6 is a thiazole derivative that can reduce histone acetylation and histone acetyltransferase (HAT) activity in human leukemia cells, CPTH6 is a specific Gcn5/pCAF inhibitor. | 
            
                
            	| PC-35191 | MC2884 HAT/EZH2 inhibitor | MC2884 is a novel hybrid, dual HAT/EZH2 inhibitor with IC50 of 3.27, 8.35 and 4.56 uM for CBP, KAT5 and p300, respectively. |