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Cat. No. Product Name Information
PC-62653

Ionomycin calcium salt

Ionomycin is an ionophore produced by the bacterium Streptomyces conglobatus, used in research to raise the intracellular level of calcium (Ca2+) and as a research tool to understand Ca2+ transport across biological membranes.
PC-62651

MS37452

CBX7 inhibitor

MS-37452 is a small-molecule modulator of methyl-lysine binding for CBX7 chromodomain.
PC-62649

E260

FER kinase inhibitor

E260 is a novel inhibitor of the Fer/FerT kinase with Kd of 0.85 uM, selectively evokes metabolic stress and necrotic death in cancer cells.
PC-62638

MS2734

NNMT inhibitor

MS2734 is a bisubstrate Nicotinamide N-methyltransferase (NNMT) with IC50 of 14 uM, Kd of 2.7 uM.
PC-62601

KH 176

ROS-redox modulator

KH176 (Sonlicromanol) is a chemical entity derivative of Trolox and small molecule ROS-redox modulator, shows potential treatment for mitochondrial disorders.
PC-62590

YPC-21661

ZNF143 inhibitor

YPC-21661 is a novel small molecule inhibitor of the transcription factor Zinc-finger protein 143 (ZNF143).
PC-62589

YPC-22026

ZNF143 inhibitor

YPC-22026, a metabolically stable derivative of YPC-21661, is a novel small molecule inhibitor of the transcription factor Zinc-finger protein 143 (ZNF143), inhibits the binding of ZNF143 to DNA.
PC-62585

TRAF-STOP 6860766

TRAF-STOP 6860766 (SMI-6860766, SMI6860766) is a small molecule inhibitor that blocks the interaction between CD40 and TRAF6 (TRAF-STOP), while leaving CD40-TRAF2/3/5 interactions intact, thereby preserving CD40-mediated immunity.
PC-62579

N-acetyl lysyltyrosylcysteine amide

MPO inhibitor

N-acetyl lysyltyrosylcysteine amide (KYC) is a potent, tripeptide inhibitor of myeloperoxidase (MPO), inhibits MPO-mediated hypochlorous acid (HOCl) formation (IC50=7 uM) and nitration/oxidation of LDL.
PC-62577

Visomitin

Visomitin (SKQ1 bromide, PDTP) is a mitochondria-targeted antioxidant that decreases transmembrane potential and production of reactive oxygen species (ROS).
PC-62535

SPL-707

SPPL2a inhibitor

SPL-707 (SPL707) is the first selective, orally active signal peptide peptidase-like 2a (SPPL2a) inhibitor with IC50 of 77 nM, shows 25-fold selectivity over γ-secretase and SPP.
PC-62489

GAPDS

GAPDH inhibitor, GAPDH segregator

GAPDS is a small molecule that targets the glycolytic enzyme glyceraldehyde 3-phosphate dehydrogenase (GAPDH).

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