| Cat. No. |
Product Name |
Information |
| PC-25886 |
Them1 inhibitor Compound U11
Them1 inhibitor
|
Them1 inhibitor Compound U11 is a small molecule inhibitor of thioesterase superfamily member 1 (Them1) with IC50 of 3.63 uM, selectively inhibits Them1 by binding the START domain (Kd=0.67 uM). |
| PC-25885 |
Them1 inhibitor Compound U1
Them1 inhibitor
|
Them1 inhibitor Compound U1 is a small molecule inhibitor of thioesterase superfamily member 1 (Them1) with IC50 of 8.64 uM, selectively inhibits Them1 by binding the START domain (Kd=5.97 uM). |
| PC-25882 |
PPTD free base
ZIP14 inhibitor
|
PPTD free base is the first selective small-molecule inhibitor of membrane-bound metal transporter ZIP14/SLC39A14, efficiently blocks ZIP14-mediated uptake of zinc, iron, manganese and cadmium, while sparing the closely related transporter ZIP8/SLC39A8. |
| PC-25881 |
ZIP14 inhibitor PPTD
ZIP14 inhibitor
|
ZIP14 inhibitor PPTD is the first selective small-molecule inhibitor of membrane-bound metal transporter ZIP14/SLC39A14, efficiently blocks ZIP14-mediated uptake of zinc, iron, manganese and cadmium, while sparing the closely related transporter ZIP8/SLC39A8. |
| PC-25841 |
3-Nitrooxypropanol
MCR inhibitor
|
3-Nitrooxypropanol (Abrucomstat, 3-NOP) is a small molecule inhibitor of methane formation in the rumen, specifically inhibits methyl-coenzyme M reductase (MCR), inhibit methanogenesis, in vitro and in vivo. |
| PC-25820 |
TP-5801
TNK1 inhibitor
|
TP-5801 is a potent, specific inhibitor of Thirty-eight-negative kinase-1 (TNK1) with IC50 of 1.4 nM, inhibits TNK1-transformed cells. |
| PC-25798 |
YL0441
ΔFOSB inhibitor
|
YL0441 is a highly effective inhibitor of AP1 transcription factor ΔFOSB with IC50 of 13.7 uM and 12.3 uM, disrupts ΔFOSB/JUND and ΔFOSB/ΔFOSB binding to DNA, inhibits AP1-transcription factor-mediated expression of the luciferase reporter gene with IC50 of 0.1 uM. |
| PC-25795 |
ASX-173
Asparagine synthetase inhibitor
|
ASX-173 is a selective, cell-penetrable small molecule inhibitor of human asparagine synthetase (ASNS), inhibits L-asparagine production with IC50 of 0.5 uM,, induces the integrated stress response (ISR), and reduces cell growth in HEK-293A cells. |
| PC-25784 |
ML345
IDE inhibitor, NLRP3 inhibitor
|
ML345 is a potent, selective Insulin-degrading enzyme (IDE, Insulysin) with IC50 of 188 nM, targets a specific cysteine residue (Cys819) in IDE, also is a highly potent and selective NLRP3 inhibitor, directly targets tyrosine 381 (Y381) and disrupts its essential interaction with NIMA-related kinase 7 (NEK7). |
| PC-25765 |
TRF1-TIN2 interaction inhibitor 1
TRF1 inhibitor
|
TRF1-TIN2 interaction inhibitor 1 (Compound 40) is a first-in-class inhibitor of the TRF1:TIN2 interaction with IC50 of 67 uM, binds to TRFH domain of TRF1 (TRF1 TRFH) with KD of 29 uM, disrupts shelterin complex assembly. |
| PC-25748 |
PKSI-527
Plasma kallikrein inhibitor, PLK inhibitor
|
PKSI-527 is a highly selective plasma kallikrein inhibitor, suppresses collagen-induced arthritis (CIA) by modifying the kallikrein-kinin system, also is a selective PLK inhibitor. |
| PC-25741 |
SB-633825
TIE2 inhibitor, STK10 inhibitor
|
SB-633825 is a potent and ATP-competitive inhibitor of TIE2, LOK (STK10) and BRK with IC50s of 3.5 nM, 66 nM, 150 nM, respectively, inhibits cancer cell growth and angiogenesis. |
