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Chemical Structure Cat. No. Product Name CAS No.
TX-1918 Chemical Structure
 BCP16358 TX-1918 503473-32-3
TX-1918 is a cell-permeable tyrphostin derivative that inhibits eukaryotic elongation factor-2 kinase (eEF-2K; IC50 = 440 nM).
NI-57 Chemical Structure
 BCP17964 NI-57 1883548-89-7
NI-57 is a potent inhibitor of the bromodomains of BRPF proteins that binds to BRPF1B, BRPF2, and BRPF3 with Kd values of 31, 108, and 408 nM, respectively.
GSK8573 Chemical Structure
 BCP16859 GSK8573 1693766-04-9
GSK-8573 is the inactive control of GSK-2801.
Apicidin Chemical Structure
 BCP13245 Apicidin 183506-66-3
Apicidin, a natural fugal metabolite, is a selective inhibitor of HDAC.
GNE-272 Chemical Structure
 BCP19967 GNE-272 1936428-93-1
GNE-272 is a potent and selective in vivo probe for the bromodomains of CBP/EP300 with IC50 values of 0.02, 0.03 and 13 μM for CBP, EP300 and BRD4, respectively.
MOZ-IN-2 Chemical Structure
 BCP29432 MOZ-IN-2 2055397-88-9
MOZ-IN-2 is an inhibitor of protein MOZ, a member of histone acetyltransferases, with an IC50 of 125 μM.
Remodelin Chemical Structure
 BCP11087 Remodelin 949912-58-7
Remodelin is a novel potent and selective inhibitor of the acetyl-transferase protein NAT10.
Remodelin hydrobromide Chemical Structure
 BCP19055 Remodelin hydrobromide 1622921-15-6
Remodelin HBr salt is a novel potent and selective inhibitor of the acetyl-transferase protein NAT10.
MOZ-IN-3 Chemical Structure
 BCP29114 MOZ-IN-3 2055397-18-5
MOZ-IN-3 is an inhibitor of MOZ, a member of histone acetyltransferases, with an IC50 of 55 nM.
PF-CBP1 hydrochloride Chemical Structure
 BCP24255 PF-CBP1 hydrochloride 2070014-93-4
PF-CBP1 hydrochloride is a highly selective inhibitor of the CREB binding protein bromodomain.
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