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AMPK activator 11

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Catalog No. T79226Cas No. 2948304-00-3

AMPK Activator 11 is a nanomolar potent inhibitor of cell proliferation in various colorectal carcinomas (CRCs), acting through the selective activation of AMP-activated protein kinase (AMPK) and enhancement of oxidative phosphorylation (OXPHOS) (mitochondrial metabolism). This compound demonstrates particular efficacy in inhibiting RKO xenograft growth, rendering it useful for anti-tumor and metabolic disease research [1].

AMPK activator 11

AMPK activator 11

😃Good
Catalog No. T79226Cas No. 2948304-00-3
AMPK Activator 11 is a nanomolar potent inhibitor of cell proliferation in various colorectal carcinomas (CRCs), acting through the selective activation of AMP-activated protein kinase (AMPK) and enhancement of oxidative phosphorylation (OXPHOS) (mitochondrial metabolism). This compound demonstrates particular efficacy in inhibiting RKO xenograft growth, rendering it useful for anti-tumor and metabolic disease research [1].
Pack SizePriceAvailabilityQuantity
25 mg$1,5206-8 weeks
50 mg$1,9806-8 weeks
100 mg$2,5006-8 weeks
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Product Introduction

Bioactivity
Description
AMPK Activator 11 is a nanomolar potent inhibitor of cell proliferation in various colorectal carcinomas (CRCs), acting through the selective activation of AMP-activated protein kinase (AMPK) and enhancement of oxidative phosphorylation (OXPHOS) (mitochondrial metabolism). This compound demonstrates particular efficacy in inhibiting RKO xenograft growth, rendering it useful for anti-tumor and metabolic disease research [1].
In vitro
AMPK activator 11 (Compound 18a) inhibits the growth and migration of CRC cells with an IC50 below 1 μM at 0-30 μM for 0-7 days [1]. At 0-0.1 μM for 24 hours, it significantly increases the oxygen consumption rate (OCR) in RKO cells with minimal changes in extracellular acidification rate (ECAR), upregulating p-AMPK and mitochondrial complexes III and V, indicating selective activation of OXPHOS in CRC [1].
In vivo
AMPK activator 11 (Compound 18a) was administered intraperitoneally at doses of 2.5 or 10 mg/kg for 25 days, selectively inhibiting tumor growth in an RKO cell xenograft model in vitro without toxicity [1].
Chemical Properties
Molecular Weight408.45
FormulaC25H20N4O2
Cas No.2948304-00-3
Storage & Solubility Information
StorageShipping with blue ice.

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