Home   >  
Others Pathway
  >  
Others

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

Others

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.
123下一页末页共 823 条记录 1 / 83 页 
0086-15971444841