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首页-小分子抑制剂&激动剂-Others-Other Targets

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Cat. No. Product Name Information
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.
PC-73159

JHU37160

DREADD agonist

JHU37160 is 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.
PC-73151

Eptifibatide

Glycoprotein IIb/IIIa inhibitor

Eptifibatide (Integrilin) is a synthetic homodetic cyclic peptide, inhibits platelet aggregation by selectively blocking the platelet glycoprotein IIb/IIIa receptor.

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