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Histone Acetyltransferase

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Histone Acetyltransferase

Chemical Structure Cat. No. Product Name CAS No.
GSK4027 Chemical Structure
BCP25140 GSK4027 2079896-25-4
GSK 4027 is a chemical probe for the PCAF/GCN5 bromodomain with an pIC50 of 7.4±0.11 for PCAF in a time-resolved fluorescence resonance energy transfer (TR-FRET) assay.
WM-1119 Chemical Structure
BCP29433 WM-1119 2055397-28-7
WM-1119 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.
YF-2 Chemical Structure
BCP30850 YF-2 1311423-89-8
YF2 is a First-in-Class Histone Acetyltransferase (HAT) Activators for Precision Targeting of Epigenetic Derangements in Lymphoma.
NSC228155 Chemical Structure
BCP30383 NSC228155 113104-25-9
NSC228155 is an inhibitor of KIX-KID interaction that acts by enhancing tyrosine phosphorylation of EGFR.
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.
Anacardic acid Chemical Structure
BCP27645 Anacardic acid 16611-84-0
Anacardic Acid, extracted from cashew nut shell liquid, is a histone acetyltransferase inhibitor, inhibits HAT activity of p300 and PCAF, with IC50s of ∼8.5 μM and ∼5 μM, respectively.
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