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Chemical Structure Cat. No. Product Name CAS No.
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 .
Gamma-Oryzanol Chemical Structure
 BCP13528 Gamma-Oryzanol 11042-64-1
Gamma-Oryzanol is a triterpenoid.
Lomeguatrib Chemical Structure
 BCP07818 Lomeguatrib 192441-08-0
Inhibitor of O6-methylguanine-DNA methyltransferase (MGMT); (IC50 = 0.009 μM in cell-free extracts from HeLa S3 cells); attenuates MGMT activity in vitro and in vivo.
Zebularine Chemical Structure
 BCP12209 Zebularine 3690-10-6
Zebularine(NSC309132; 4-Deoxyuridine) is a DNA methylation inhibitor that forms a covalent complex with DNA methyltransferases, also inhibits cytidinedeaminase with Ki of 2 μM.
RG108 Chemical Structure
 BCP06930 RG108 48208-26-0
RG108 is a non-nucleoside DNA methyltransferase (DNMT) inhibitor.
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