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Cat. No. Product Name Information
PC-27500

Sipasterol

Neuroprotective steroid

Sipasterol (5α-Androstane-3β,5,6β-triol, 5α-androst-3β,5,6β-triol, Triol) is a synthetic steroid with neuroprotective effect against hypoxia/reoxygenation induced neuronal injuries, through inhibition of AMPK signaling.
PC-25727

ARUK2010489

NUAK1 inhibitor

ARUK2010489 is a potent, selective and highly brain penetrant NUAK1 inhibitor with pIC50 of 8.7, displays no CDK2 activity.
PC-23514

UCB9386

NUAK1 inhibitor

UCB9386 is a potent, selective and brain-penetrant inhibitor of NUAK1 (NUAK family SnF1-like kinase-1) with biochemical pIC50 of 10.1.
PC-22623

KHKI-01215

NUAK2 inhibitor

KHKI-01215 is a highly potent NUAK family kinase 2 (NUAK2) inhibitor with IC50 of 52 nM.
PC-22622

KHKI-01128

NUAK2 inhibitor

KHKI-01128 is a highly potent NUAK family kinase 2 (NUAK2) inhibitor with IC50 of 24 nM.
PC-21279

WZ4003

NUAK inhibitor

WZ4003 is a potent, highly specific protein kinase inhibitor of NUAK kinase with IC50 of 20 nM and 100 nM for NUAK1 and NUAK2, respectively.
PC-20481

Metformin

AMPK activator

Metformin (1,1-Dimethylbiguanide) is a traditional anti-diabetic drug, functions by inhibiting complex I in the mitochondrial respiratory chain, activates AMPK and enhances insulin sensitivity.
PC-20473

RX-375

AMPK activator

RX-375 (RX375) is an indirect small-molecule activator of AMPK by directly binds to Prohibitins (PHB1 and PHB2), induces dissociation of AMPK-PHBs complex.
PC-20056

BI-9774

AMPK activator

BI-9774 (BI 9774) is a potent pan-AMPK activator with EC50 of 64 nM in an ADP-Glo kinase assay with human AMPK (α1β1γ1) and EC50 of 8 nM in a cellular GLUT4 translocation assay.
PC-47031

KI-301670

NUAK1 inhibitor

KI-301670 is a novel potent, specific NUAK1 inhibitor, disturbs NUAK1 signaling by targeting its ATP binding site, effectively inhibits the PI3K/AKT pathway in pancreatic cancer cells.
PC-47025

PXL770 monohydrate potassium salt

AMPK activator

PXL770 is a novel orally bioavailable, small-molecule direct AMPK activator with EC50 of 16.2, 42.1 and 64 nM for α1β1γ1, α1β1γ2 and α1β1γ3, directly increases AMPK activity by both allosteric activation and protection from dephosphorylation.
PC-47024

PXL770

AMPK activator

PXL770 is a novel orally bioavailable, small-molecule direct AMPK activator with EC50 of 16.2, 42.1 and 64 nM for α1β1γ1, α1β1γ2 and α1β1γ3, directly increases AMPK activity by both allosteric activation and protection from dephosphorylation.

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