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GSK621

Catalog No.
B6020
AMPK agonist
Grouped product items
SizePriceStock Qty
1mg
$73.00
Ship with 5-10 days
5mg
$250.00
Ship with 5-10 days
10mg
$460.00
Ship with 5-10 days

Tel: +1-832-696-8203

Email: [email protected]

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Background

GSK621 is a specific and potent agonist of AMP-activated protein kinase (AMPK) with IC50 values ranging from 13 to 30 µM for cell lines [1].

AMPK is a heterotrimeric serine/threonine kinase. It is a sensor of cellular energy. It regulates multiple cellular metabolic pathways. Activation of AMPK inactivates the phosphorylation of acetyl-Coa carboxylase (ACC), and hence inhibits the biosynthesis of fatty acid. Activation of AMPK also inhibits protein synthesis that is dependent on mammalian target of rapamycin complex 1. AMPK also promotes autophagy, fatty acid oxidation, glucose uptake and glycolysis [1].

In cells, at the opposite, GSK621 showed more potency to activate AMPK than A-769662, based on the ACC phosphorylation level. In MOLM-14 cells, 200 µM A-769662 is just as potent as 30 µM GSK621 to induce the phosphorylation of ULK1 (S555) and ACC (S79), two direct AMPK substrates. In AML cell lines (OCI-AML3, HL-60 and MOLM-14) and primary AML samples, the phosphorylation at AMPKα T172, a marker of AMPK activation, was markedly increased, and the phosphorylation of ULK1 (S555) and ACC (S79) was stimulated by GSK621 [1].

In animals with xenograft MOLM-14 cells, intraperitoneal injection of GSK621 at 30 mg/kg twice daily reduced leukemia growth and markedly extended survival compared to treatment with 10 mg/kg GSK621 twice daily or vehicle. These results correlated to increased AMPK activity indicated by the induction of apoptosis and increased ACC S79 phosphorylation [1].

Reference:
[1].  Sujobert P, Poulain L, Paubelle E, et al. Co-activation of AMPK and mTORC1 induces cytotoxicity in acute myeloid leukemia. Cell reports, 2015, 11(9): 1446-1457.

Product Citation

Chemical Properties

Physical AppearanceA crystalline solid
StorageStore at 2-8°C
M.Wt489.91
Cas No.1346607-05-3
FormulaC26H20ClN3O5
SolubilitySoluble in DMSO
Chemical Name6-chloro-5-(2'-hydroxy-3'-methoxy-[1,1'-biphenyl]-4-yl)-3-(3-methoxyphenyl)-1H-pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione
SDFDownload SDF
Canonical SMILESCOC1=CC=CC(C2=CC=C(N3C(Cl)=CC(NC(N4C5=CC=CC(OC)=C5)=O)=C3C4=O)C=C2)=C1O
Shipping ConditionEvaluation sample solution : ship with blue ice.All other available size: ship with RT , or blue ice upon request
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.

Protocol

Cell experiment [1]:

Cell lines

MV4-11, OCI-AML3, OCI-AML2, HL-60, Kasumi, HEL, UT7, NB4, TF-1, KG1A, Nomo p28, SKM-1, U937, YHP1, MOLM-14, Mo7e, K562, MOLM-13, EOL-1 and SET-2 cell lines

Preparation method

This compound is soluble in DMSO. General tips for obtaining a higher concentration: Please warm the tube at 37 °C for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below - 20 °C for several months.

Reacting condition

30 μM; 4 days

Applications

In a set of 20 cell lines, GSK621 inhibited the proliferation of all 20 lines, with the IC50 values ranged from 13 to 30 μM, and promoted apoptosis in 17 cell lines.

Animal experiment [1]:

Animal models

Mice bearing MOLM-14 cell xenografts

Dosage form

10 or 30 mg/kg; i.p.; b.i.d.

Applications

In mice bearing MOLM-14 cell xenografts, GSK621 (30 mg/kg; i.p.; b.i.d.) reduced leukemia growth, and substantially extended survival.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1]. Sujobert P, Poulain L, Paubelle E, et al. Co-activation of AMPK and mTORC1 induces cytotoxicity in acute myeloid leukemia. Cell reports, 2015, 11(9): 1446-1457.

Quality Control

Quality Control & MSDS

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Chemical structure

GSK621

Related Biological Data

GSK621