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 About 7 results found for searched term "66-81-9" (0.099 seconds)

Cat.No.  Name Target
M2165 WAY-362450 (Turofexorate isopropyl) Farnesoid X Receptor
XL335; FXR-450
WAY-362450 (Turofexorate isopropyl; XL335) is a potent, selective, and orally bioavailable FXR agonist with EC50 of 4 nM.
M7295 SID 26681509 Others
SID 26681509 is a cathepsin L inhibitor.
M14308 SID 26681509 quarterhydrate Cathepsin
SID 26681509 quarterhydrate is a potent, reversible, competitive, and selective inhibitor of human cathepsin L with an IC50 of 56 nM.
M24577 Namilumab CSF-1R (c-Fms)
AMG-203; Anti-Human CSF2 Recombinant Antibody
Namilumab (AMG203) is a human IgG1 monoclonal antibody that binds with high affinity to the GM-CSF ligand, potently neutralizing GM-CSF. Namilumab can be used for the research of rheumatoid arthritis.
M49733 AChE/BACE1/GSK3β-IN-1 Gamma-secretase/Beta-secretase
AChE/BACE1/GSK3β-IN-1 is an orally active triple inhibitor of AChE/BACE1/GSK3β.
M52813 EGF-R (661-681) T669 Peptide p38 MAPK
EGF-R (661-681) T669 Peptide is a MAPK substrate that can used to measure MAPK catalytic activity.
M4879 Cycloheximide DNA/RNA Synthesis
Naramycin A; Actidione; CHX; FT 3422-2; NM-MCD 80
Cycloheximide (Naramycin A) is an inhibitor of protein biosynthesis in eukaryotic organisms, with IC50 of 532.5 nM. Cycloheximide binds to the E-site of the 60S subunit of the ribosome during the protein synthesis process in eukaryotic cells, blocking the ribosome translocation process mediated by eEF2 and preventing the synthesis of new proteins. Cycloheximide suppresses ferroptosis and inhibits autophagy.



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