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Cat. No. Product Name Information
PC-26467

GALK1-IN-1

GALK1 inhibitor

GALK1-IN-1 is an effective ATP-competitive galactokinase 1 (GALK1) inhibitor with IC50 of 1 uM in luminescence GALK-ATP-depletion assay.
PC-26445

PON2 inhibitor 2

PON2 inhibitor

PON2 inhibitor 2 is a potent, specific small molecule inhibitor of paraxonase 2 (PON2) with IC50 of 56 nM, inhibits the lactonase activity of PON2.
PC-26416

NFYi5

NF-Y inhibitor

NFYi5 is a specific small molecule inhibitor of Nuclear Transcription Factor-Y (NF-Y), inhibits NF-Y-dependent transcriptional activity, dose dependently inhibits activity of the NF-Y reporter in both human and rat cardiac fibroblasts with IC50 of 19.95 and 12.73 uM respectively.
PC-26386

IVMT-Rx-4

MDA-9/Syntenin inhibitor

IVMT-Rx-4 is a small molecule inhibitor of MDA-9/Syntenin, specifically interrupt MDA-9/Syntenin signaling, leading to an inhibition in progression of PC cells to bone metastasis.
PC-26377

NBDHEX

GST inhibitor

NBDHEX is a potent glutathione S-transferase (GST) inhibitor, inhibits human glutathione S-transferases GSTA1-1, GSTP1-1 and GSTM2-2 with IC50 of 25 uM, 0.8 uM and <0.01 uM, is cytotoxic toward P-glycoprotein-overexpressing tumor cell lines.
PC-26353

Rexaceract

GCase PAM, GCase activator

Rexaceract (GT-02287) is a potent, selective positive allosteric modulator (PAM) of beta-glucocerebrosidase (β-glucocerebrosidase, β-glucosidase, or GCase) with KD of 17-24 uM at pH 7.4, enhances the function of lysosomal GCase.
PC-26307

JX24120

MAT2B inhibitor

JX24120 is a specific inhibitor for methionine adenosyltransferase MAT2B, directly binds to MAT2B with SPR KD of 4.72 uM, inhibits S-adenosylmethionine (SAMe) synthesis.
PC-26291

UNC11676A

MDA5 inhibitor

UNC11676A is a specific small molecule inhibitor of RNA helicase MDA5 with IC50 of 6 uM, >18-fold selective inhibition over LGP2 and DDX1.
PC-26266

CVN14

CD38 inhibitor

CVN14 is a potent, selective, uncompetitive and brain-penetrant CD38 inhibitor with IC50 of 19 nM and 2 nM for human and mouse CD38 respectively.
PC-26242

E8431

DCSTAMP antagonist

E8431 (Z2371498431) is a specific small molecule antagonist of fusogenic protein DCSTAMP, disrupts DCSTAMP-RAP1B interaction and inhibits RAP1-RAC1 signaling-mediated cytoskeletal reorganization required for osteoclast maturation and fusion, demonstrats significant osteoclastogenesis inhibition (IC50=0.7758 μM) without cytotoxic effects on mBMMs.
PC-26237

HF13141-H5

GGCX inhibitor

HF13141-H5 is a potent, selective inhibitor of γ-Glutamyl carboxylase (GGCX) with IC50 of 240 nM-1 uM in cell-based assays, inhibits γ-carboxylation of vitamin K-dependent clotting factors (VKDCFs) and shows anticoagulant effect.
PC-26220

Thiostrepton

FOXM1 inhibitor, PRX3 inhibitor

Thiostrepton is a thiazole antibiotic that selectively inhibits FOXM1, also significantly inhibits ETV4 K97-Khib, thereby promoting ferroptosis and suppressing ICC cell migration, invasion, and lung metastasis, covalently inhibits Peroxiredoxin 3 (PRX3), disrupting redox balance and selectively induces tumor cell death.

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