| Cat. No. |
Product Name |
Information |
| PC-38841 |
UK5099
MPC blocker
|
UK5099 (PF-1005023) is a potent inhibitor of the mitochondrial pyruvate carrier (MPC), inhibits pyruvate-dependent oxygen consumption by rat heart mitochondria with IC50 of 50 nM. |
| PC-38837 |
Silibinin A
|
Silibinin is a flavonolignan isolated from milk thistle, Silybum marianum, that has been shown to exhibit antioxidant and antineoplastic activities. |
| PC-38797 |
ERX-41
LIPA inhibitor
|
ERX-41 is a small molecule that binds to lysosomal acid lipase A (LIPA), and induces endoplasmic reticulum (ER) stress resulting in cell death, blocks proliferation of ER-α⁺ BC cells and TNBC cells in vitro. |
| PC-38788 |
Sarcomere inhibitor W7
Sarcomere inhibitor
|
Sarcomere inhibitor W7 is a small-molecule sarcomere Ca2+ desensitizer, decreases intact cardiac myocyte contractility in a Ca2+ transient amplitude-independent manner. |
| PC-38785 |
EVT-701
Mitochondrial complex 1 inhibitor
|
EVT-701 is a highly potent, selective, and safe mitochondrial complex 1 (MC1) inhibitor, reduces NADH abundance with IC50 of 300 nM. |
| PC-38779 |
LCL521
Acid ceramidase inhibitor
|
LCL521 is a small molecular inhibitor of acid ceramidase (ACDase), a lysosomotropic inhibitor with anticancer activity. |
| PC-38777 |
STK793590
DJ-1/PARK7 inhibitor
|
STK793590 (DJ-1/PARK7 inhibitor 15) is a potent inhibitor of the Parkinson's disease associated protein DJ-1/PARK7 with Kd/IC50 of 0.1/0.28 uM, respectively. |
| PC-38774 |
PXS-5505
pan-LOX inhibitor
|
PXS-5505 is an orally available, small-molecule, irreversible inhibitor of all lysyl oxidases (pan-LOX) family members, with potential antifibrotic activity. |
| PC-38773 |
LSALT peptide
DPEP-1 inhibitor
|
Metablok (LSALT peptide) is a specific DPEP1-binding peptide and nonenzymatic dipeptidase-1 (DPEP-1) inhibitor. |
| PC-38767 |
S202
Ceramide galactosyltransferase inhibitor
|
S202 is a potent, selective and brain-penetrant small molecule inhibitor of ceramide galactosyltransferase (CGT) with IC50 of 15 nM in the cell-lysate assays and 3.6 nM in intact-cell assays. |
| PC-38755 |
CT-179
OLIG2 inhibitor
|
CT-179 is a small molecule inhibitor of protein transcription factor OLIG2 (Oligodendrocyte transcription factor 2), CT-179 is a putative disruptor of OLIG2 homodimerization. |
| PC-38753 |
PAT1inh-B01
SLC26A6 (PAT1) inhibitor
|
PAT1inh-B01 is a small-molecule, selective SLC26A6 (putative anion transporter 1, PAT1) inhibitor, could fully inhibit PAT1-mediated anion exchange with IC50 of 350 nM. |
