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Cat. No. Product Name Information
PC-45694

NK-252

Nrf2 activator

NK-252 (NK252) is a small molecule Nrf2 activator, exhibits a greater Nrf2-activating potential than oltipraz (OPZ).
PC-45182

Dimethyl fumarate

Nrf2 activator

Dimethyl fumarate (DMF, BG-12) exerts anti-inflammatory and pro-metabolic effects in a variety of cell types, activates the Nrf2 pathway.
PC-43044

14-3-3 inhibitor WS3

14-3-3 inhibitor, NRF2 inhibitor

14-3-3 inhibitor WS3 is a potent, allosteric inhibitor of 14-3-3 proteins, potently inhibits the NRF2-ARE signal with IC50 of 135 nM in A549 cells, selectively inhibits NRF2 activity in tumor cells.
PC-42917

CDDO-EA

Nrf2 activator

CDDO-EA (DDO ethyl amide, RTA405) is a potent Nrf2 activator that upregulates Nrf2 expression and resulted in translocation of Nrf2 into the nucleus.
PC-42916

RTA-408

Nrf2 activator

RTA-408 (Omaveloxolone, RTA408) is a potent Nrf2 activator that increases expression of Nrf2 target genes and decreases expression of inflammatory mediators.
PC-44663

CDDO-Im

PPAR agonist, Nrf2 activator

CDDO-Im (RTA-403) is a potent Nrf2 activator that elevates protein levels of Nrf2 and induces Nrf2/ARE signaling, also activates PPAR with Ki values of 232 and 344 nM for PPARα and PPARγ.
PC-45198

Ezetimibe

Nrf2 activator, NPC1L1 inhibitor

Ezetimibe is a potent Niemann-Pick C1-Like 1 (NPC1L1) cholesterol absorption receptor inhibitor that inhibits sterol absorption without affecting the absorption of other molecules.
PC-42172

TBHQ

Nrf2 activator

TBHQ (tert-Butylhydroquinone) is a phenolic antioxidant and a selective inducer and activator of Nrf2 that ameliorates doxorubicin-induced cardiotoxicity in vivo.
PC-42187

ML385

NRF2 inhibitor

ML385 (ML-385) is a first-in-class small molecule inhibitor of NRF2 that binds to Neh1 DNA binding domain of NRF2 (IC50=1.9 uM) and inhibits the downstream target gene expression.
PC-27017

Keap1-p-p62-IN-2

Nrf2 inhibitor, Keap1-p-p62 inhibitor

Keap1-p-p62-IN-2 is a selective and effective Nrf2 inhibitor that inhibits Kelch-like ECH-associated protein 1-phosphorylated p62 (Keap1-p-p62) interaction with IC50 of 0.096 uM, >6-fold selectivity over inhibition of Keap1-Nrf2 interaction.
PC-27016

Keap1-p-p62 inhibitor 13

Nrf2 inhibitor, Keap1-p-p62 inhibitor

Keap1-p-p62 inhibitor 13 (Keap1-p-p62-IN-1) is a selective and effective Nrf2 inhibitor that inhibits Kelch-like ECH-associated protein 1-phosphorylated p62 (Keap1-p-p62) interaction with IC50 of 0.11 uM, high selectivity over inhibition of Keap1-Nrf2 interaction.
PC-26889

SLOS-1811-06 tR1

Nrf2 activator

SLOS-1811-06 tR1 is a potent, small molecule activator of NRF2 with EC50 of 0.98 nM in ARE-luciferase reporter assays, shows inhibitory activity of NRF2-KEAP1 with IC50 of 0.17 nM in BRET assays, protects hiPSC-derived RGCs from hypoxia/reoxygenation injury.

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