Cat. No. |
Product Name |
Information |
PC-47039 |
GQ352
Gαq/11 inhibitor
|
GQ352 is a small molecule Gαq/11 inhibitor, directly binds to the Gαq and inhibits the dissociation of Gαβγ heterotrimers with IC50 value of 8.9 uM. |
PC-38655 |
ELOVL1-IN-27
ELOVL1 inhibitor
|
ELOVL1-IN-27 is a highly potent, selective, CNS-penetrant inhibitor of elongation of very long chain fatty acid 1 enzyme (ELOVL1) with IC50 of 13 nM (C26:0 VLCFA inhibition in HEK cell). |
PC-38598 |
Azo-resveratrol
Tyrosinase inhibitor
|
Azo-resveratrol is a potent mushroom tyrosinase inhibitor with IC50 of 36.28 uM. |
PC-38531 |
ML266
GCase chaperone
|
ML266 (CID 46943215) is a non-inhibitory chaperone of glucocerebrosidase (GCase) enzyme, does not inhibit the enzyme’s action, but can facilitate its translocation to the lysosome. |
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-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-73217 |
Ceapin A7
ATF6α 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-73176 |
PPA904
Photosensitizer
|
PPA-904 is a specific phenothiazine photosensitizer in photodynamic therapy (PDT) research, especially topical application for cutaneous leishmaniasis in vivo. |
PC-73160 |
ALC-0315
Vaccine adjuvant
|
ALC-0315 is a synthetic ionizable amino lipid that has been used in combination with other lipids in the formation of lipid nanoparticles, has attracted attention as a component of the SARS-CoV-2 vaccine. |
PC-73159 |
JHU37160
DREADD agonist
|
JHU37160 a high affinity, highly potent, BBB penetrant activator (agonist) of hM3Dq and hM4Di DREADDs with Ki 1.9 nM and 3.6 nM for hM3Dq and hM4Di in vitro. |