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Chemical Structure Cat. No. Product Name CAS No.
Valemetostat Chemical Structure
 BCP31915 Valemetostat 1809336-39-7
Valemetostat, also known as DS-3201, is an antineoplastic drug candidate.
KDOAM-25 Chemical Structure
 BCP31703 KDOAM-25 2230731-99-2
KDOAM-25 is a potent and highly selective KDM5 sub-family of histone lysine demethylases inhibitor with IC50s of 71 nM, 19 nM, 69 nM, 69 nM for KDM5A, KDM5B, KDM5C, KDM5D, respectively. KDOAM-25 increases global H3K4 methylation at transcriptional start sites and impairs proliferation in multiple myeloma MM1S cells.
Gusacitinib HCl Chemical Structure
 BCP31676 Gusacitinib HCl GusacitinibHCl
Gusacitinib (ASN-002) is a potent dual inhibitor of spleen tyrosine kinase (SYK) and janus kinase (JAK) with IC50 values of 5-46 nM.
Gusacitinib Chemical Structure
 BCP31675 Gusacitinib 1425381-60-7
Gusacitinib (ASN-002) is a potent dual inhibitor of spleen tyrosine kinase (SYK) and janus kinase (JAK) with IC50 values of 5-46 nM.
OXFBD04 Chemical Structure
 BCP31554 OXFBD04 OXFBD04
OXFBD04 shows improved BRD4(1) affinity (IC50 = 166 nM), optimised physicochemical properties (LE = 0.43; LLE = 5.74; SFI = 5.96), and greater metabolic stability (t½ = 388 min).
CBP-IN-1 Chemical Structure
 BCP31464 CBP-IN-1 2222941-37-7
CBP-IN-1 is a potent p300/CBP bromodomain inhibitor.
MZ 1 Chemical Structure
 BCP31482 MZ 1 1797406-69-9
MZ1 is a potent inducer of reversible, long-lasting and selective removal of BRD4 over BRD2 and BRD3.
DMNQ Chemical Structure
 BCP31298 DMNQ 6956-96-3
DMNQ is a superoxide generating agent. DMNQ mimicks high glucose-suppressed SIRT2 and SIRT6 expression.
Pterosin B Chemical Structure
 BCP09994 Pterosin B 34175-96-7
Pterosin B is isolated and purified from the aerial parts of Pteris semipinnata.
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.
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