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Cat. No. Product Name Information
PC-25149

LIBX-A403

ACSL4 inhibitor

LIBX-A403 is a potent, selective Acyl-coenzyme A synthetase long-chain family member 4 (ACSL4) inhibitor with IC50 of 49 nM and MST KD of 0.29 uM, with no activity against ACSL3.
PC-25143

MMTC/57E

SNAT2 inhibitor

MMTC/57E (Compound 57E) is a selective small molecule inhibitor of sodium-coupled neutral amino acid transporter 2 (SNAT2, SLC38A2) with IC50 of 0.8 uM.
PC-25137

GI-Y1

GSDMD inhibitor

GSDMD inhibitor Y1 (GI-Y1) is a selective gasdermin D (GSDMD) inhibitor, binds to GSDMD with SPR KD of 7.69 uM, shows cardioprotective effects.
PC-25120

UNC7437

IPMK inhibitor

UNC7437 is a potent selective inhibitor of inositol phosphate multikinase (IPMK) with IC50 of 26.2 nM, decreased cellular proliferation and tritiated inositol phosphate levels in human U251-MG glioblastoma cells.
PC-25115

M6766

ERO1α inhibitor

M6766 is a potent, selective inhibitor of endoplasmic reticulum oxidoreductase 1α (ERO1α) with IC50 of 1.4 uM and KD of 1.1 uM.
PC-25093

Simepdekinra

IL-17A modulator

Simepdekinra is a potent, selective modulator of interleukin 17A (IL-17A).
PC-25050

NNZ-2591

Neuroprotective agent

Ercanetide (NNZ-2591, NNZ 2591) is an analogue of endogenous diketopiperazine cyclo-glycyl-proline (cyclic GP), shows neuroprotective effect.
PC-25037

Crovozalpon

Z α1-antitrypsin inhibitor

Crovozalpon is a small molecule inhibitor of Z-α1-antitrypsin polymerization.
PC-25025

Rivasterat

Endothelial dysfunction blocker

Rivasterat (CU06-1004, Sac-1004) is a small molecule vascular leakage blocker and endothelial dysfunction blocker, inhibits endothelial hyperpermeability induced by VEGF, histamine and thrombin via stabilization of cortical actin ring and AJ proteins at the cell-cell junction.
PC-25014

MG-257

Galectin-3/TREM2 inhibitor

MG-257 is a small molecule ligand of galectin-3, impedes interaction between TREM2 and galectin-3 with IC50 of 91 nM in TR-FRET assays, attenuates TREM2 signaling.
PC-25011

YT-II-100

CPSF3 inhibitor

YT-II-100 is a novel small molecule inhibitor of Cleavage and Polyadenylation Specific Factor 3 (CPSF3), increases the global abundance of R-loops.
PC-25008

Veonetinib

Tyrosine kinase inhibitor

Veonetinib (Example 3) is an effective inhibitor of tyrosine kinase, exhibits IC50 values of 0.1 μM and 0.4 μM in A549 cells and LOVO cells, respectively.

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