| Cat. No. |
Product Name |
Information |
| 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-73311 |
FQI1
LSF inhibitor
|
Factor quinolinone inhibitor 1 (FQI1) is a small molecule inhibitor of transcription factor Late SV40 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 ABA receptor 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. |
| PC-73271 |
Heparanase-IN-1
Heparanase inhibitor
|
Heparanase-IN-1 is a small molecule Heparanase (Hpse) inhibitor with IC50 of 0.56 uM. |
| PC-73270 |
SST0872AA1
Heparanase inhibitor
|
SST0872AA1 is a potent, small molecule Heparanase (Hpse) inhibitor with IC50 of 0.08 uM. |
| PC-73269 |
SST0871AA1
Heparanase inhibitor
|
SST0871AA1 is a small molecule Heparanase (Hpse) inhibitor with IC50 of 0.64 uM. |
| PC-73217 |
Ceapin-A7
ATF6 inhibitor
|
Ceapin-A7 is a selective inhibitor of ATF6α with IC50 of 0.59 uM, selective over ATF6β, PERK and other branches of the unfolded protein response (UPR). |
| PC-73185 |
Hi 76-0079
HSL inhibitor
|
Hi 76-0079 (NNC0076-0079) is a specfic, small molecule inhibitor of hormone-sensitive lipase (HSL) with IC50 of 0.11 uM. |
| PC-73175 |
SGN-2FF
Fucosylation inhibitor
|
SGN-2FF is a potent and orally active inhibitor of glycoprotein fucosylation, directly inhibits fucosyltransferase activity. |
