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Cat. No. Product Name Information
PC-23451

PF-07328948

BDK inhibitor

PF-07328948 is the first potent, selective branched-chain ketoacid dehydrogenase kinase (BDK or BCKDK) with in vitro IC50 of 15 nM, and cellular IC50 of 46 nM in human skeletal muscle BDK activity assay.
PC-23450

UNC10142

CHD1 inhibitor

UNC10142 is a first-in-class, specific, cell-active small molecule antagonist of the tandem chromodomains of CHD1 (Chromodomain-Helicase DNA-Binding Protein 1) with binding IC50 of 1.7 uM in TR-FRET assays.
PC-23443

164A10

Pin1 degrader

164A10 is a potent Pin1 destabilizer and degrader with IC50 of 4.1 nM in DELFIA displacement assay, destabilizes Pin1 in vitro and also results more effective in causing Pin1 degradation in cells.
PC-23442

158H9

Pin1 degrader

158H9 is a potent Pin1 destabilizer and degrader with IC50 of 21.5 nM in DELFIA displacement assay, destabilizes Pin1 in vitro and also results more effective in causing Pin1 degradation in cells.
PC-23441

BJP-07-017-3

Pin1 inhibitor

BJP-07-017-3 is a potent, selective, covalent, cell-permeable peptide Pin1 inhibitor (Ki=15 nM), IC50 of 9 nM in DELFIA assays, covalently targets Cys113, a highly conserved cysteine located in the Pin1 active site.
PC-23439

KB-151

Phagocytosis inhibitor

KB-151 is a small molecule phagocytosis inhibitor with IC50 of 2.7 uM in human PBMCs, shows no significant toxicity.
PC-23438

KB-208

Phagocytosis inhibitor

KB-208 is a small molecule phagocytosis inhibitor with IC50 of 4.2 uM in human PBMCs, shows no significant toxicity.
PC-23404

NAC1 inhibitor NIC3

NAC1 inhibitor

NAC1 inhibitor NIC3 is a specific small molecule inhibitor of oncogenic nucleus accumbens-associated protein-1 (NAC1), inhibits NAC1 homodimerization, leading to proteasomal NAC1 degradation.
PC-23394

OGT 2115

Heparanase inhibitor

OGT 2115 is a potent, specific, cell-permeable and orally active heparanase inhibitor with IC50 of 0.4 uM, inhibits the expression and activity of heparanase.
PC-23379

BIM-46174

Heterotrimeric Gα/Gβγ inhibitor

BIM-46174 is a selective inhibitor of heterotrimeric G-protein complex Gα/Gβγ subunits, abrogates cancer cell invasion controlled by several GPCR agonists.
PC-23378

GQ262

Gαq/11 inhibitor

GQ262 is a small molecule Gαq/11 protein inhibitor with IC50 of <10 uM, inhibits MP41 cell proliferation with IC50 of 5.1 uM.
PC-23377

GQ127

Gαq/11 inhibitor

GQ127 is a potent, selective Gαq/11 signaling pathway inhibitor with IC50 of 22.4 uM. GQ127 shows good efficacy and safety in inositol monophosphate (IP1) assay by directly inhibiting Gαq/11 proteins.

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