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Chemical Structure Cat. No. Product Name CAS No.
A-893 Chemical Structure
BCP31184 A-893 1868232-32-9
A-893 is a cell-active inhibitor of Methyltransferase SMYD2, with an IC50 of 2.8 nM.
SIS-17 Chemical Structure
BCP31156 SIS-17 2374313-54-7
SIS17 is a mammalian histone deacetylase 11 (HDAC 11) inhibitor with an IC50 value of 0.83 μM, inhibits the demyristoylation HDAC11 substrate, serine hydroxymethyl transferase 2, without inhibiting other HDACs.
3-Deazaneplanocin A hydrochloride Chemical Structure
BCP21084 3-Deazaneplanocin A hydrochloride 120964-45-6
3-Deazaneplanocin A hydrochloride is a potent histone methyltransferase EZH2 inhibitor.
Cl-amidine hydrochloride Chemical Structure
BCP31104 Cl-amidine hydrochloride 1373232-26-8
Cl-amidine hydrochloride is a peptidylarginine deminase (PAD) inhibitor, with an IC50 5.9 μM for PAD4.
GeA-69 Chemical Structure
BCP31007 GeA-69 2143475-98-1
GeA-69 is a novel selective allosteric inhibitor targeting macrodomain 2 of poly-adenosine-diphosphate-ribose polymerase 14.
BSI-401 Chemical Structure
BCP27642 BSI-401 142404-10-2
BSI-401 is a novel PARP-1 inhibitor with both oral bioavailability and strong antitumor potency.
WHI-P 97 Chemical Structure
BCP29062 WHI-P 97 211555-05-4
WHI-P97 is a rationally designed potent inhibitor of JAK-3.
Bisindoylmaleimide X Chemical Structure
BCP25395 Bisindoylmaleimide X 1241725-89-2
Bisindolylmaleimide X is a cell-permeable, reversible, ATP-competitive protein kinase C (PKC) inhibitor (IC50 = 15 nM, rat brain PKC).
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.
Sinefungin Chemical Structure
BCP28648 Sinefungin 58944-73-3
Sinefungin is a potent inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2'-)-methyltransferase, and viral multiplication. Sinefungin, a SET7/9 inhibitor, ameliorates renal fibrosis by inhibiting H3K4 methylation .
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