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Cat. No. Product Name Information
PC-73090

IPA

SNARE inhibitor

IPA (Inhibitor of Priming Activity) is a small-molecule compound that binds Sec18 (Kd=3.84 uM) and blocks SNARE activation, inhibits vacuole fusion at the SNARE priming stage with IC50 of 50 uM.
PC-73087

BRD4780

TMED9 inhibitor

BRD4780 is a small molecule that releases MUC1-fs from TMED9-enriched compartments and promotes its anterograde trafficking to the lysosome, directly binds to TMED9.
PC-73086

TMPRSS6 inhibitor Cpd-B

TMPRSS6 inhibitor

TMPRSS6 inhibitor Cpd-B (TMPRSS6-IN-Cpd-B) is a highly potent (IC50=7.6 nM), specific small molecule inhibitor of TMPRSS6 (matriptase-2).
PC-73085

TMPRSS6 inhibitor 8

TMPRSS6 inhibitor

TMPRSS6 inhibitor 8 (TMPRSS6-IN-8) is a highly potent (IC50=8.1 nM), peptidomimetic inhibitor of TMPRSS6 (matriptase-2).
PC-73083

SPI-21

Spt5-Pol II inhibitor

SPI-21 (Spt5-Pol II inhibitor 21) is a small-molecule inhibitor of Spt5-Pol II with IC50 of 25.2 uM.
PC-73082

Endosidin17

VPS35 inhibitor

Endosidin17 (ES17) is a small molecule targets retromer component VPS35, binds to VPS35 Impairs interaction with RABG3f, causes dose-dependent stabilization of VPS35 with EC50 of 0.9 uM.
PC-73077

PCC0208017

pan-MARK inhibitor

PCC0208017 is a potent, selective dual small-molecule inhibitor of MARK3 and MARK4 with IC50 of 1.8 and 2.01 nM, respectively.
PC-73073

Perforin inhibitor 16

Perforin inhibitor

Perforin inhibitor 16 (Perforin-IN-16) is a small molecule Perforin inhibitor with IC50 of 1.13 uM in KHYG1 assay.
PC-73066

SCO-792

Enteropeptidase inhibitor

SCO-792 (SCO792) is a potent, selective, reversible enteropeptidase inhibitor with IC50 of 4.6 and 5.4 nM for rat and human enteropeptidase, respectively.
PC-73065

ASB17061

Chymase inhibitor

ASB17061 (ASB-17061) is an orally active, selective chymase inhibitor with IC50 of 0.03 uM and 0.02 uM for mMCP-4 and human chymase, respecitvely.
PC-73058

SWE101

sEH-P inhibitor

SWE101 (SWE-101, SWE 101) is a potent, selective, in vivo active inhibitor of soluble epoxide hydrolase (sEH) phosphatase domain (sEH-P) with IC50 of 58 nM.
PC-73057

AZ67

PFKFB3 inhibitor

AZ67 is a selective small molecule PFKFB3 inhibitor with IC50 of 18 nM, reduces cellular levels of F2,6BP with IC50 of 0.51 uM.

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