668467-91-2 | LDN-57444 (Catalog# : 110606)LDN-57444 is a Uch-L1 inhibitor with Ki= 0.4 M. Ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) is an intracellular protein abundantly expressed in neurons, and a mutation in UC
64232-83-3 | L189 (Catalog# : 91001)L189 inhibits base excision repair (BER) and non-homologous end joining (NHEJ), which specifically sensitizes cancer cells to DNA damage and increases the cytotoxicity of DNA-dam
603139-19-1 | MK-0822 (Catalog# : 101915)MK-0822 is an inhibitor of cathepsin K with potential anti-osteoporotic activity. It selectively binds to and inhibits the activity of cathepsin K, which may result in a reductio
667463-62-9 | MLS-2052 (Catalog# : 52582)6-BIO(6-Bromoindirubin-3'-oxime) is a potent and selective inhibitor of GSK-3 and CDK1CcyclinB complex with IC50 of 5 nM /320 nM/83 nM for GSK-3/CDK1/CDK5 respectively.
65472-88-0 | Naftifine (Catalog# : 16122834)Naftifine is an allylamine antifungal drug for the topical treatment of tinea pedis, tinea cruris, and tinea corporis (fungal infections). Its precise mechanism of action is unkn
6384-92-5 | NMDA (Catalog# : 52811)NMDA(N-Methyl-D-aspartic acid) is an amino acid derivative that acts as a specific agonist at the NMDA receptor mimicking the action of glutamate, the neurotransmitter which norm