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Chemical Structure Cat. No. Product Name CAS No.
AMZ30 Chemical Structure
BCP30812 AMZ30 1313613-09-0
AMZ30 is a selective, covalent inhibitors of protein phosphatase methylesterase-1(PME-1; IC50=600 nM); selectively inactivates PME-1 and reduces the demethylated form of PP2A in living cells.
Pleconaril Chemical Structure
BCP20819 Pleconaril 153168-05-9
Pleconaril is a capsid inhibitor used previously to treat enterovirus infections. Pleconaril is effective in inhibiting replication with an IC50 of 50 nM.
PKR Inhibitor Chemical Structure
BCP30785 PKR Inhibitor 608512-97-6
PKR Inhibitor is an inhibitor of RNA-activated protein kinase (PKR) (IC50 = 210 nM). It is an imidazolo-oxindole derivative that binds to ATP-binding site of PKR and rescues PKR-dependent translation block in vitro. C16 has neuroprotective activity against cell damage in human neuroblastoma cells and neuroinflammation in acute excitotoxic rat model
BAM15 Chemical Structure
BCP30750 BAM15 210302-17-3
BAM 15 is a novel mitochondrial protonophore uncoupler.
ATFB-SE Chemical Structure
BCP30744 ATFB-SE 126695-58-7
ATFB-SE is a useful protective group in antibody drug conjugates.
V-9302 Chemical Structure
BCP30741 V-9302 1855871-76-9
V-9302 is a competitive antagonist of transmembrane glutamine flux, selectively and potently targeting the amino acid transporter ASCT2.
APS-5 Chemical Structure
BCP30735 APS-5 193884-53-6
Tiazofurine Chemical Structure
BCP30734 Tiazofurine 60084-10-8
Tiazofurin is a synthetic nucleoside analogue with antineoplastic activity. Tiazofurin (TR) is anabolized intracellularly to an analogue of NAD, tiazole-4-carboxamide adenine dinucleotide (TAD), a potent inhibitor of IMP dehydrogenase (IMPDH); IMPDH is the rate-limiting enzyme for de novo purine synthesis. Inhibition of IMPDH results in reduced levels of guanylates, resulting in the inhibition tumor cell growth in vitro and in vivo.
DLin-KC2-DMA Chemical Structure
BCP30733 DLin-KC2-DMA 1190197-97-7
DLin-KC2-DMA is a cationic/ionizable lipid for siRNA delivery.
GSK8612 Chemical Structure
BCP30728 GSK8612 GSK8612
GSK8612 is a highly selective and potent Tank-binding Kinase-1 (TBK1) inhibitor, with a pIC50 of 6.8 for recombinant TBK1.
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