Cat. No. |
Product Name |
Information |
PC-38114 |
T-690
|
T-690 is a potent, selective, oral inhibitor of glucosylceramide synthase (GCS) with IC50 of 15 nM. |
PC-38105 |
RA 5557
UGT8 inhibitor
|
RA 5557 is a brain-penetrant, selective, oral UGT8 inhibitor, inhibits galactosylceramide biosynthesis. |
PC-38098 |
PXS-5129A
LOXL2 inhibitor
|
PXS-5129A is the pro-drug form of PXS-5120A, a potent, selective, irreversible inhibitor of Lysyl oxidase-like 2 (LOXL2). |
PC-38097 |
PXS-5120A
LOXL2 inhibitor
|
PXS-5120A is a potent, selective, irreversible inhibitor of Lysyl oxidase-like 2 (LOXL2) with IC50 of 5 and 6 nM (hLOXL2 and mLOXL2). |
PC-38092 |
MSDC-0602K
|
MSDC-0602K (Azemiglitazone) is a PPARγ-sparing thiazolidinedione insulin sensitizer, targets mitochondrial pyruvate carrier protein (MPC) Mpc1 and Mpc2. |
PC-38061 |
DFO-5
|
DFO-5 (Oseltamivir Epoxy Impurity) is an oseltamivir impurity. |
PC-38055 |
DiI
|
Dil (DiIC18(3)) is a fluorescent neuronal tracer that labels cell bodies, axons, dendrites, and dendritic spines. |
PC-38046 |
Lipid L319
|
L-319 (O-8670) is an ionizable (pKa = 6.38) and biodegradable lipid that has been used in the formation of lipid nanoparticles. |
PC-38021 |
FTO inhibitor Dac51
FTO inhibitor
|
FTO inhibitor Dac51 (Dac51, UUN44923) is a potent, small-molecule compound that can inhibit the activity of m6A demethylase FTO, inhibits FTO-mediated demethylation of m6A with IC50 of 0.4 uM. |
PC-38017 |
LY3475070
CD73 inhibitor
|
LY3475070 (LY-3475070) is a potent, selective and orally bioavailable inhibitor of the ectoenzyme CD73 with IC50 of 28 nM, targeting the adenosine pathway against the tumor microenvironment. |
PC-38009 |
Cofilin inhibitor SZ-3
Cofilin inhibitor
|
Cofilin inhibitor SZ-3 (SZ-3) is a first-in-class small-molecule inhibitor of cofilin, shows potent anti-inflammatory activities. |
PC-36161 |
BAY 2402234
DHODH inhibitor
|
BAY 2402234 (BAY2402234) is a novel potent, selective, orally bioavailable DHODH inhibitor with IC50 of 1.2 nM (human full-length DHODH). |