| Cat. No. |
Product Name |
Information |
| 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). |
| PC-36152 |
ZZW-115
NUPR1 inhibitor
|
ZZW-115 (ZZW115, ZZW 115) is a potent inhibitor of NUPR1 (Kd=2.1 uM), an intrinsically disordered protein (IDP) with an entirely disordered conformation. |
| PC-36150 |
BMS-466442
|
BMS-466442 (BMS466442) is small molecule inhibitor of the Alanine-Serine-Cysteine-1 Transporter (ASC-1, SLC7A10), selectively inhibits asc-1 mediated D-serine uptake in human asc-1 expressing cells and primary cultures with IC50 of 36.8 and 19.7 nM, respectively. |
