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Chemical Structure Cat. No. Product Name CAS No.
123C4 Chemical Structure
BCP44969 123C4 2034159-30-1
123C4 is a novel, potent, and selective agonist of the tyrosine kinase EphA4 receptor.
MLT-943 Chemical Structure
BCP44966 MLT-943 1832576-04-1
MLT-943 is a novel potent and selective MALT1 protease inhibitor.
PF-04802367 Chemical Structure
BCP44964 PF-04802367 1962178-27-3
PF-04802367 is a highly selective GSK-3 inhibitor with an IC50 of 2.1 nM based on a recombinant human GSK-3β enzyme assay and 1.1 nM based on ADP-Glo assay.
TDI-10229 Chemical Structure
BCP44963 TDI-10229 TDI-10229
TDI-10229 is a potent and orally bioavailable inhibitor of soluble adenylyl cyclase (sAC, ADCY10).
Antibacterial agent 26 Chemical Structure
BCP44962 Antibacterial agent 26 75369-40-3
Antibacterial agent 27 Chemical Structure
BCP44961 Antibacterial agent 27 65795-51-9
BAY-598 R-isomer Chemical Structure
BCP44956 BAY-598 R-isomer 1906920-28-2
BAY-598 R-isomer is the R-isomer of BAY589.
TAK-418 Chemical Structure
BCP44939 TAK-418 1818252-53-7
TAK-418 is a novel inhibitor of the epigenetic modulator lysine-specific demethylase 1A (LSD1).
KDM2A/7A-IN-1 Chemical Structure
BCP44938 KDM2A/7A-IN-1 2169272-46-0
KDM2A/7A-IN-1 is a first-in-class, selective and cell-permeable inhibitor of histone lysine demethylases KDM2A/7A, with an IC50 of 0.16 μM for KDM2A, exhibits 75 fold selevtivity over other JmjC lysine demethylases, and is inactive on methyl transferases, and histone acetyl transferases.
BMS-P5 hydrochloride Chemical Structure
BCP44953 BMS-P5 hydrochloride 1549811-36-0
BMS-P5 is a Novel Peptidylarginine Deiminase 4 (PAD4) Inhibitor with pIC50 values in the range of 5-​7.5.
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