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Cat. No. Product Name Information
PC-27423

Enterobactin

Iron chelator

Enterobactin is an iron transport compound and iron chelator from Salmonella typhimurium, not only help bacteria uptake iron but also reduce the antibacterial activity of macrophages during the process of Salmonella typhimurium infecting macrophages, is also involved in the oxidative stress response of Escherichia coli.
PC-27422

3,4,3-LI(1,2-HOPO)

Chelating agent

3,4,3-LI(1,2-HOPO) (Enfipaxetan) is a metal chelating agent, exhibits extremely high affinity for lanthanide metal ions, sensitizes the emission of Sm(III), Eu(III), and Tb(III) in the Visible range and the emission of Pr(III), Nd(III), Sm(III), and Yb(III).
PC-27405

APOL1-IN-1

APOL1 inhibitor

APOL1-IN-1 (Compound 87) is a small molecule inhibitor of apolipoprotein L1 (APOL1).
PC-27404

Alcedaplin

APOL1 inhibitor

Alcedaplin is a small molecule inhibitor of apolipoprotein L1 (APOL1) function.
PC-27395

BCT2029

BLVRB inhibitor

BCT2029 is a potent Biliverdin IXb reductase (BLVRB, biliverdin reductase IXβ) inhibitor, inhibits BLVRB reductive activity using both FMN (flavin mononucleotide, IC50=194 nM) and DCPIP (2,6-dichlorophenolindophenol; IC50=28 nM) as substrates.
PC-27394

BCT2102

BLVRB ligand

BCT2102 is a cell-permeable acceptor ligand of Biliverdin IXb reductase (BLVRB), demonstrates specific energy transfer and inform equilibrium binding affinities, target engagement, and residence time analyses in vitro and cellular nanoBRET assays.
PC-27393

BCT2101

BLVRB ligand

BCT2101 is a cell-permeable acceptor ligand of Biliverdin IXb reductase (BLVRB), demonstrates specific energy transfer and inform equilibrium binding affinities, target engagement, and residence time analyses in vitro and cellular nanoBRET assays.
PC-27391

[18F]FB-HTL

PET ligand

[18F]FB-HTL is a BBB-penetrable fluorine-18-labelled small-molecule HaloTag ligand and PET reporter ligand for quantitative imaging of gene expression in the brain.
PC-27390

Spermidine

CAS 124-20-9

Spermidine is a polyamine essential for various biological processes, has long been recognized as a signaling molecule, promotes cell growth, regeneration, and autophagy, targets GGA-rich small RNAs for virulence regulation.
PC-27388

ALOX15-IN-1

ALOX15 inhibitor

ALOX15-IN-1 (Compound 8b) is a potent, substrate-selective and allosteric inhibitor of mammalian Arachidonic acid 15-lipoxygenase (ALOX15) orthologs, inhibits linoleate oxygenase activity of rabbit and human ALOX15 with IC50 of 0.04 uM, without affecting arachidonic acid oxygenation.
PC-27382

SKF-91488

HNMT inhibitor

SKF-91488 (Homodimaprit, SKF 91488) is a potent, noncompetitive histamine N-methyltransferase (HNMT) inhibitor with Ki of 0.9 uM, blocks histamine metabolism and increases histamine concentrations, can increase blood pressure and enhance bronchoconstriction.
PC-27381

CC-156

HSD17B1 inhibitor

CC-156 is a potent, selective 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1, HSD17B1) with IC50 of 44 nM.

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