| Cat. No. |
Product Name |
Information |
| PC-38407 |
RJW100
LRH-1 (NR5A2) agonist
|
RJW100 (RJW 100) is a phospholipid mimetic as liver receptor homolog-1 (LRH-1, NR5A2) agonist with pEC50 of 6.6 and 7.5 for (LRH-1) and steroidogenic factor-1 (SF-1, NR5A1), respectively. |
| PC-38400 |
Inaxaplin
APOL1 inhibitor
|
Inaxaplin (VX-147, VX147) is a potent small molecule inhibitor of apolipoprotein L1 (APOL1) channel with IC50 values of 2.3 nM for APOL1 G0, 1.3 nM for APOL1 G1, and 1.1 nM for APOL1 G2, inhibits APOL1-mediated flux and cell death. |
| PC-38392 |
Farudodstat
DHODH inhibitor
|
Farudodstat (ASLAN003) is a highly potent, selective dihydroorotate dehydrogenase (DHODH) inhibitor with IC50 of 35 nM (human DHODH), significantly inhibits protein synthesis via activation AP-1 transcription, induces cell differentiation of AML cell lines. |
| PC-38369 |
Pirepemat
cognition-promoting agent
|
Pirepemat (IRL752) is a new phenyl-pyrrolidine derivative and cognition-promoting agent with regioselective central nervous system transmission-enhancing properties, enhances norepinephrine, dopamine, and acetylcholine neurotransmission in the cerebral cortex. |
| PC-73459 |
Abimtrelvir
Antiviral
|
Abimtrelvir is a novel antiviral agent. |
| PC-73455 |
Vutiglabridin
Insulin sensitizer
|
Vutiglabridin (HSG4112) is a synthetic structural analog of glabridin and insulin sensitizer, novel anti-obesity agent. |
| PC-73418 |
Feniralstat
Kallikrein inhibitor
|
Feniralstat (KVD-824) is a potent, selective kallikrein inhibitor with IC50 of 6.7 nM for human plasma kallikrein (pKal), dispays no inhibition against human KLKl, FXIa and Factor Xlla (IC50>40 uM). |
| PC-73396 |
CB253
r(G4C2)exp inhibitor
|
CB253 is a small molecule that selectively binds the hairpin form of r(G4C2)exp, inhibiting mechanisms that drive c9ALS/FTD pathobiology. |
| PC-73386 |
PRG-A01
SOD1 aggregation inhibitor
|
PRG-A01 (PRG-A-01, Chem-036) is a chemical inhibitor against SOD1 misfolding and aggregation, inhibits the neuronal cell death caused by mutant-SOD1 overexpression. |
| PC-73365 |
SpiD7
UPR activator
|
SpiD7 is a spirocyclic dimer compound that activates the unfolded protein response (UPR), selectively inhibits growth and induce apoptosis of cancer cells. |
| PC-73362 |
4BPPNit
Glycosylation modulator
|
4BPPNit is a small molecule significantly augmented glycosylation of α-dystroglycan, in part through upregulation of LARGE1 glycosyltransferase gene expression. |
| PC-73358 |
Mito-C
NEET protein inhibitor
|
Mito-C is a specific chemical compound targeting NEETs proteins, induces mitochondrial network fragmentation and represses dengue viral replication. |
