Home   >  

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

Epigenetics

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.
123下一页末页共 493 条记录 1 / 50 页 
0086-15971444841