GSK-690693 [937174-76-0]

Cat# HY-10249-10mg

Size : 10mg

Brand : MedChemExpress

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Description

GSK-690693 is an ATP-competitive pan-Akt inhibitor with IC50s of 2 nM, 13 nM, 9 nM for Akt1, Akt2 and Akt3, respectively. GSK-690693 is also an AMPK inhibitor, affects Unc-51-like autophagy activating kinase 1 (ULK1) activity and robustly inhibits STING-dependent IRF3 activation[1][2][3].

IC50 & Target[1]

Akt1

2 nM (IC50)

Akt3

9 nM (IC50)

Akt2

13 nM (IC50)

PKCη

2 nM (IC50)

PKCθ

2 nM (IC50)

PrkX

5 nM (IC50)

PAK6

6 nM (IC50)

PAK4

10 nM (IC50)

PKCδ

14 nM (IC50)

PKCβ1

19 nM (IC50)

PKCε

21 nM (IC50)

PKA

24 nM (IC50)

PKG1β

33 nM (IC50)

AMPK

50 nM (IC50)

PAK5

52 nM (IC50)

DAPK3

81 nM (IC50)

Autophagy

 

Cellular Effect
Cell Line Type Value Description References
A549 IC50
105.33 μM
Compound: GSK690693
Cytotoxicity against human A549 cells assessed as decrease in cell viability after 24 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as decrease in cell viability after 24 hrs by MTT assay
[PMID: 29966916]
A549 IC50
11.83 μM
Compound: GSK690693
Cytotoxicity against human A549 cells incubated for 24 hrs by MTT assay
Cytotoxicity against human A549 cells incubated for 24 hrs by MTT assay
[PMID: 39047611]
BT-474 IC50
0.05 μM
Compound: 3g, GSK-690693
Antiproliferative activity against human BT474 cells
Antiproliferative activity against human BT474 cells
[PMID: 18800763]
BT-474 IC50
0.14 μM
Compound: 3g, GSK-690693
Inhibition of AKT-mediated GSK3-beta phosphorylation in human BT474 cells
Inhibition of AKT-mediated GSK3-beta phosphorylation in human BT474 cells
[PMID: 18800763]
BT-474 IC50
138 nM
Compound: GSK-690693
Inhibition of GSK3-beta phosphorylation in human BT474 cells
Inhibition of GSK3-beta phosphorylation in human BT474 cells
[PMID: 19179070]
BT-474 IC50
69 nM
Compound: GSK-690693
Antiproliferative activity against human BT474 cells
Antiproliferative activity against human BT474 cells
[PMID: 19179070]
C6 IC50
14.5 μM
Compound: GSK690693
Cytotoxicity against rat C6 cells assessed as decrease in cell viability after 24 hrs by MTT assay
Cytotoxicity against rat C6 cells assessed as decrease in cell viability after 24 hrs by MTT assay
[PMID: 29966916]
HCT-116 IC50
8.2 μM
Compound: GSK690693
Growth inhibition of human HCT116 cells after 72 hrs by coulter counter method
Growth inhibition of human HCT116 cells after 72 hrs by coulter counter method
[PMID: 24900862]
HFF IC50
>23000 nM
Compound: GSK-690693
Antiproliferative activity against human HFF cells
Antiproliferative activity against human HFF cells
[PMID: 19179070]
HFF IC50
>23 μM
Compound: GSK-690693
Antiproliferative activity against human HFF cells
Antiproliferative activity against human HFF cells
[PMID: 19179070]
HFF IC50
16.3 μM
Compound: 3g, GSK-690693
Cytotoxicity against HFF cells
Cytotoxicity against HFF cells
[PMID: 18800763]
JeKo-1 IC50
3 μM
Compound: GSK690693
Antiproliferative activity against human JeKo1 cells after 72 hrs by CellTiter Glo assay
Antiproliferative activity against human JeKo1 cells after 72 hrs by CellTiter Glo assay
[PMID: 28704757]
JVM-2 IC50
1.6 μM
Compound: GSK690693
Antiproliferative activity against human JVM2 cells after 72 hrs by CellTiter Glo assay
Antiproliferative activity against human JVM2 cells after 72 hrs by CellTiter Glo assay
[PMID: 28704757]
LNCaP IC50
0.02 μM
Compound: 3g, GSK-690693
Antiproliferative activity against human LNCaP cells
Antiproliferative activity against human LNCaP cells
[PMID: 18800763]
LNCaP IC50
21 nM
Compound: GSK-690693
Antiproliferative activity against human LNCAP cells
Antiproliferative activity against human LNCAP cells
[PMID: 19179070]
Maver1 IC50
5.1 μM
Compound: GSK690693
Antiproliferative activity against human Maver1 cells after 72 hrs by CellTiter Glo assay
Antiproliferative activity against human Maver1 cells after 72 hrs by CellTiter Glo assay
[PMID: 28704757]
NCI-H460 IC50
5.4 μM
Compound: GSK690693
Growth inhibition of human NCI-H460 cells after 72 hrs by coulter counter method
Growth inhibition of human NCI-H460 cells after 72 hrs by coulter counter method
[PMID: 24900862]
PC-3 IC50
14.1 μM
Compound: GSK690693
Antiproliferative activity against human PC3 cells after 72 hrs by MTT assay
Antiproliferative activity against human PC3 cells after 72 hrs by MTT assay
[PMID: 30151089]
PC-3 IC50
15.5 μM
Compound: GSK690693
Antiproliferative activity against human PC3 cells after 72 hrs by MTT assay
Antiproliferative activity against human PC3 cells after 72 hrs by MTT assay
[PMID: 24308997]
Sf9 IC50
0.89 μM
Compound: 3g, GSK-690693
Inhibition of human recombinant ROCK1 expressed in Sf9 cells
Inhibition of human recombinant ROCK1 expressed in Sf9 cells
[PMID: 18800763]
Z-138 IC50
3.1 μM
Compound: GSK690693
Antiproliferative activity against human Z138 cells after 72 hrs by CellTiter Glo assay
Antiproliferative activity against human Z138 cells after 72 hrs by CellTiter Glo assay
[PMID: 28704757]
In Vitro

GSK690693 is very selective for the Akt isoforms versus the majority of kinases in other families. However, GSK690693 is less selective for members of the AGC kinase family including PKA, PrkX, and PKC isozymes with IC50 of 24 nM, 5 nM, and 2-21 nM, respectively. GSK690693 also potently inhibits AMPK and DAPK3 from the CAMK family with IC50 of 50 nM and 81 nM, respectively, and PAK4, 5, and 6 from the STE family with IC50 of 10 nM, 52 nM, and 6 nM, respectively. GSK690693 inhibits the phosphorylation of GSK3β in tumor cells with IC50 ranging from 43 nM to 150 nM. GSK690693 treatment leads to a dose-dependent increase in the nuclear accumulation of the transcription factor FOXO3A. GSK690693 potently inhibits the proliferation of T47D, ZR-75-1, BT474, HCC1954, MDA-MB-453, and LNCaP cells with IC50 of 72 nM, 79 nM, 86 nM, 119 nM, 975 nM, and 147 nM, respectively. GSK690693 treatment induces apoptosis at concentrations > 100 nM in both LNCaP and BT474 cells[1]. Consistent with the role of AKT in cell survival, GSK690693 induces apoptosis in sensitive ALL cell lines[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Solvent & Solubility
In Vitro: 

DMSO : 20 mg/mL (47.01 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.3503 mL 11.7513 mL 23.5026 mL
5 mM 0.4701 mL 2.3503 mL 4.7005 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

Select the appropriate dissolution method based on your experimental animal and administration route.

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  10% DMSO    90% Corn Oil

    Solubility: ≥ 2.5 mg/mL (5.88 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.

  • Protocol 2

    Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: 2 mg/mL (4.70 mM); Clear solution; Need ultrasonic

    This protocol yields a clear solution of 2 mg/mL.

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

    Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.

For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  20% HP-β-CD/10 mM Citrate pH 2.0

    Solubility: 10 mg/mL (23.50 mM); Clear solution; Need ultrasonic

Purity & Documentation
References

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