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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.

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