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Cat. No. Product Name Information
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-73252

BIRT-377

LFA-1 inhibitor

BIRT-377 (BIRT377) is a potent, orally active negative allosteric modulator of LFA-1 (lymphocyte function-associated antigen-1) with Kd of 26 nM.
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-73184

NG-497

ATGL inhibitor

NG-497 is a potent, highly selective, nontoxic inhibitor of human adipose triglyceride lipase (ATGL, PNPLA2) with IC50 of 1 uM.
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-73175

SGN-2FF

Fucosylation inhibitor

SGN-2FF is a potent and orally active inhibitor of glycoprotein fucosylation, directly inhibits fucosyltransferase activity.
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.
PC-73158

JHU37152

DREADD agonist

JHU37152 is a high affinity and highly potent activator (agonist) of hM3Dq and hM4Di DREADDs with Ki 1.8 nM and 8.7 nM for hM3Dq and hM4Di in vitro.
PC-73151

Eptifibatide

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

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