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Cat. No. Product Name Information
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.
PC-73150

Eptifibatide acetate

Glycoprotein IIb/IIIa inhibitor

Eptifibatide acetate is a synthetic homodetic cyclic peptide, inhibits platelet aggregation by selectively blocking the platelet glycoprotein IIb/IIIa receptor.
PC-73149

DLin-MC3-DMA

DLin-MC3-DMA is an ionizable amino lipid (apparent pKa = 6.44) that has been used in combination with other lipids in the formation of lipid nanoparticles.
PC-73143

MCU-i11

MICU1 inhibitor

MCU-i11 is a specific MICU1 targeting compound that negative modulate mitochondrial Ca2+ uptake.
PC-73142

MCU-i4

MICU1 inhibitor

MCU-i4 is a specific MICU1 targeting compound that negative modulate mitochondrial Ca2+ uptake.
PC-73139

ASN90

O-GlcNAcase inhibitor

ASN90 is a potent, selective, substrate-competitive O-GlcNAcase (OGA) inhibitor with IC50 of 10.2 nM.
PC-73138

KVD900

Plasma kallikrein inhibitor

Sebetralstat (KVD900) is a potent, selective, competitive and reversible inhibitor of human plasma kallikrein (PKa) enzyme with Ki of 3.02 nM.
PC-73136

Naphthyridine-azaquinolone

Slipped-CAG DNA binder

Naphthyridine-azaquinolone (NA) is a specific small molecule that specifically binds slipped-CAG DNA intermediates of expansion mutations.
PC-73135

PGAM1 inhibitor KH3

PGAM1 inhibitor

PGAM1 inhibitor KH3 is a potent, allosteric small molecule inhibitor of phosphoglycerate mutase 1 (PGAM1) with IC50 of 105 nM.

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