| Cat. No. |
Product Name |
Information |
| 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 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-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. |
| PC-73312 |
FQI2
LSF inhibitor
|
Factor quinolinone inhibitor 2 (FQI2) is a small molecule inhibitor of transcription factor LSF, inhibits LSF DNA-binding activity both in vitro and in cells (IC50=0.71 uM). |
| PC-73311 |
FQI1
LSF inhibitor
|
Factor quinolinone inhibitor 1 (FQI1) is a small molecule inhibitor of transcription factor LSF, inhibits LSF DNA-binding activity both in vitro and in cells (IC50=2.1 uM). |
| PC-73280 |
Quinabactin
ABA agonist
|
Quinabactin is a small molecule abscisic acid (ABA) receptor agonist that preferentially activates dimeric ABA receptors and possesses ABA-like potency in vivo. |
| PC-73279 |
Opabactin
ABA agonist
|
Opabactin is an abscisic acid (ABA) mimic and agonist Arabidopsis subfamily III/II ABA receptors with nanomolar potency (7 nM). |
| PC-73278 |
Antabactin
ABA antagonist
|
Antabactin (ANT) is a highly potent pan-abscisic acid (ABA) receptor antagonist with EC50 of 760 nM and picomolar dissociation constant, disrupts signaling by preventing receptor-PP2C interactions. |
| PC-73272 |
Heparanase-IN-2
Heparanase inhibitor
|
Heparanase-IN-2 is a potent, small molecule Heparanase (Hpse) inhibitor with IC50 of 0.12 uM. |
