| Cat. No. | Product Name | Information | 
            
                
            	| PC-45052 | Remodelin hydrobromide NAT10 inhibitor | Remodelin hydrobromide is a potent inhibitor of the acetyl-transferase protein NAT10 that acetylates both histones and microtubules. | 
            
                
            	| PC-45051 | Remodelin NAT10 inhibitor | Remodelin is a potent inhibitor of the acetyl-transferase protein NAT10 that acetylates both histones and microtubules. | 
            
                
            	| PC-25583 | Anacardic acid HAT inhibitor | Anacardic acid is a small molecule inhibitor of histone acetyltransferase (HAT) with IC50 of 8.5 and 5.0 uM for p300 and PCAF respectively. | 
            
                
            	| PC-25107 | KI-TOX-A3 TOX-KAT7 inhibitor | KI-TOX-A3 is a specific TOX protein (thymocyte selection-associated high mobility group box) binder (KD=0.92 uM) and potent TOX-KAT7 PPI inhibitor with IC50 of 0.51 uM. | 
            
                
            	| PC-24370 | Curcumin p300 inhibitor | Curcumin (Diferuloylmethane) is a specific p300/CREB-binding protein acetyltransferase, inhibits acetylation of histone/nonhistone proteins and histone acetyltransferase-dependent chromatin transcription. | 
            
                
            	| PC-24309 | LFW273 Snail inhibitor | LFW273 is a specific, orally bioavailable small molecule inhibitor of zinc-finger transcription factor Snail with binding Kd of 1.7 uM, inhibits CREB-binding protein (CBP)-Snail interaction with Kd of 7.3 uM in MST assays. | 
            
                
            	| PC-24033 | EPS496 p300 inhibitor | EPS496 is a small molecule inhibitor of histone acetyltransferase p300, binds effectively to p300 and inhibits p300 kinase activation. | 
            
                
            	| PC-23724 | CHI-KAT8i5 KAT8 inhibitor | CHI-KAT8i5 is a specific small molecule inhibitor of KAT8 (lysine acetyltransferase 8), directly binds to KAT8 with SPR KD of 19.72 uM, suppresses esophageal squamous cell carcinoma (ESCC) growth through targeting KAT8/c-Myc signaling pathway. | 
            
                
            	| PC-21986 | EPIC-0628 HOTAIR-EZH2 inhibitor | EPIC-0628 (EPIC0628) is a selective and potent inhibitor that selectively disrupts the HOTAIR-EZH2 interaction and promotes ATF3 expression, enhances the temozolomide efficacy in glioblastoma. | 
            
                
            	| PC-21843 | SGF29 inhibitor DC60 SGF29 inhibitor | SGF29 inhibitor DC60 is a small molecule inhibitor of Spt-Ada-Gcn5 acetyltransferase (SAGA)-associated factor 29 (SGF29, CCDC101) with IC50 of 6.4 uM, binds to SGF29 second Tudor domain (SGF29 Tudor 2) and blocks SGF29 chromatin binding domain. | 
            
                
            	| PC-20867 | MG149 Tip60 (KAT5) inhibitor | MG149 is a selective histone acetyltransferase Tip60 (KAT5) inhibitor with IC50 of 74 uM, with no activity against PCAF and p300. |