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Cat. No. Product Name Information
PC-45088

SP-420

Iron chelating agent

Petadeferitrin (SP-420) is a desferrithiocin analogue and iron chelating agent that has iron-clearing efficiency with ICE value of 26.7, SP-420 is more potent than desferrithiocin.
PC-42072

BAPTA

Mg2+ chelator

BAPTA is a cell-permeant, calcium-specific chelator with high selectivity over Mg2+.
PC-45623

GW4869

nSMase inhibitor

GW-4869 (GW4869, GW 4869) is a cell-permeable, potent, specific, non-competitive inhibitor of neutral sphingomyelinase (nSMase) with IC50 of 1 uM.
PC-42082

TPEN

LIN28 inhibitor

TPEN (TPEDA) is a potent, cell-permeable inhibitor of LIN28 that abolishes LIN28-mediated oligouridylation with IC50 of 2.5 uM, also is a specific cell-permeable heavy metal chelator.
PC-42281

GGTI298

GGTase I inhibitor

GGTI298 (GGTI-298) is a CAAZ peptidomimetic geranylgeranyltransferase I (GGTase I) inhibitor that inhibits the processing of geranylgeranylated Rap1A with little effect on processing of farnesylated Ha-Ras (IC50s are 3 and >10 uM respectively).
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-25013

TREM2 agonist C1

TREM2 agonist

TREM2 agonist C1 is a structural analog of VG-3927 and small molecule agonist of triggering receptor expressed on myeloid cells 2 (TREM2) with KD of 71.36 uM in MST assays.
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.

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