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首页-小分子抑制剂&激动剂-Others-Other Targets

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Cat. No. Product Name Information
PC-26454

SMEI inhibitor 20e

SMEI inhibitor

SMEI inhibitor 20e is a small molecule inhibitor targeting SCN1A-associated severe myoclonic epilepsy of infancy (SMEI), shows potent antiseizure efficacy in zebrafish behavioral assays and significantly reduces locomotion-related seizure parameters, elevates 5-HT levels via TPH2 upregulation.
PC-26450

ACSS2-IN-1

ACSS2 inhibitor

ACSS2-IN-1 is a higly potent acetyl-CoA synthetase 2 (ACSS2) inhibitor with biochemical IC50 of 0.01 nM to <1 nM.
PC-26444

TQ416

PON2 inhibitor

TQ416 is a small molecule paraoxonase 2 (PON2) inhibitor, restores NF-κB transcriptional activity suppressed by N-(3-oxododecanoyl)-L-homoserine lactone (3OC12HSL, C12) with IC50 of 400 nM, rescues 3OC12HSL-induced cell death.
PC-26435

IDE activator Ia2

IDE activator

IDE activator Ia2 (IDE activator 2) is a potent, selective activator of insulin degrading enzyme (IDE), the hydrolysis of SP1 and FRET1 by IDE, significantly stimulates IDE proteolytic activity.
PC-26434

IDE activator Ia1

IDE activator

IDE activator Ia1 (IDE activator 1) is a potent, selective activator of insulin degrading enzyme (IDE), activates the hydrolysis of SP1 and FRET1 by IDE to ∼200% and ∼500%, activates the degradation of Aβ by ∼700%.
PC-26433

IDE inhibitor Ii1

IDE inhibitor

IDE inhibitor Ii1 (IDE inhibitor 1) is a potent, selective inhibitor of insulin degrading enzyme (IDE) with Ki of 1.7 nM.
PC-26432

BDM35899

IDE activator

BDM35899 is a small activator of insulin degrading enzyme (IDE) with pEC50 of 5.3, binds to polyanion-binding site of IDE, activates both Aβ and insulin hydrolysis by IDE, decreases glucose-stimulating insulin secretion in β-pancreatic cells.
PC-26431

BDM43124

IDE inhibitor

BDM43124 is the methyl ester precursor of BDM43079, which is a selective inhibitor of insulin degrading enzyme (IDE) with IC50 of 0.1 uM, inhibits the hydrolysis of amyloid-β1-40 by IDE in in SH-SY5Y cells.
PC-26430

BDM43079

IDE inhibitor

BDM43079 is a selective small molecule inhibitor of insulin degrading enzyme (IDE) with IC50 of 0.1 uM, selective of hIDE versus a panel of metalloproteases including hNEP.
PC-26428

BDM71230

IDE activator

BDM71230 is a potent, small molecule Insulin-Degrading Enzyme (IDE) activator with EC50 of 1.9 uM in glucose stimulated insulin secretion (GSIS) by pancreatic β-cells assay, 4.1-fold activation at 100 uM.
PC-26427

PKR1 agonist IS39

PKR1 agonist

PKR1 agonist IS39 is a selective, metabolically stable, non-peptide Prokineticin receptor-1 (PKR1, PROKR1) agonist, protects cardiomyocytes from doxorubicin-induced cytotoxicity.
PC-26426

APE1 inhibitor C10

APE1 inhibitor

APE1 inhibitor C10 (Refi-10) is a specific small molecule inhibitor of redox activity of APE1 with binding affinity (SPR Kd) of 189 nM, inhibits the redox function, but not the DNA repair function of APE1.

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