GSK3-IN-3

SKU:BHB21901715
Research Validated
Overview
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GSK3-IN-3 (CAS 331963-27-0) is an inhibitor supplied as a solid. Relevant to PI3K/Akt/mTOR and Stem Cell/Wnt research. Molecular formula C24H35N3O4, molecular weight 429.55 g/mol.
Purity 99.22%
CAS Number 331963-27-0
Molecular Weight 429.55 g/mol
Form Solid
Storage Powder -20°C; in solvent -80°C
Options selector
Catalog no. Size
HY-153089-5MG 5 mg
HY-153089-10MG 10 mg
HY-153089-25MG 25 mg
HY-153089-50MG 50 mg
HY-153089-100MG 100 mg
HY-153089-200MG 200 mg
HY-153089-500MG 500 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg, 500 mg
  • Lead time: varies by selected option.
  • Storage: Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: transfer to -20°C as soon as possible.
Field Specification
CAS no. 331963-27-0
Applications
  • Functional Assay (In Vitro)
Molecular weight 429.55
Molecular formula C24H35N3O4
Purity 99.22%
SMILES O=C(C1=C(N(CC)C2=C(C1=O)C=CC=C2)O)NNC(CCCCCCCCCCC)=O
Form Solid
Storage Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-153089
Main SKU BHB21901715
Inhibitors

Compound Overview

GSK3-IN-3 is a mitophagy inducer that promotes Parkin-dependent mitophagy and also acts as a GSK-3 inhibitor, with an IC50 value of 3.01 μM. It is neither ATP- nor substrate-competitive and shows neuroprotective activity against 6-OHDA[1][2][3]. It is supplied as an off-white to light yellow solid (C24H35N3O4, MW 429.55) at 99.22% purity.

Physical & Chemical Properties

CAS Number 331963-27-0
Molecular Formula C24H35N3O4
Molecular Weight 429.55 g/mol
Purity 99.22%
Appearance Solid
Color Off-white to light yellow
SMILES O=C(C1=C(N(CC)C2=C(C1=O)C=CC=C2)O)NNC(CCCCCCCCCCC)=O
Signaling Pathway PI3K/Akt/mTOR; Stem Cell/Wnt; Autophagy
Solubility In Vitro: DMSO: 4.17 mg/mL (9.71 mM; Requires sonication and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Storage Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.

Biological Activity

IC50 & Target

IC50: 3.01 μM (GSK-3)[3]

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Maestro I, et al. Phenotypic Assay Leads to Discovery of Mitophagy Inducers with Therapeutic Potential for Parkinson's Disease. ACS Chem Neurosci. 2021 Dec 15;12(24):4512-4523.

[2]. Morales-García JA, et al. Glycogen synthase kinase-3 inhibitors as potent therapeutic agents for the treatment of Parkinson disease. ACS Chem Neurosci. 2013 Feb 20;4(2):350-60.

[3]. Palomo V, et al. Exploring the binding sites of glycogen synthase kinase 3. Identification and characterization of allosteric modulation cavities. J Med Chem. 2011 Dec 22;54(24):8461-70.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.

In Vitro

SolventSolubilityNotes
DMSO4.17 mg/mL (9.71 mM)requires sonication and warming and heat to 60°C; use freshly opened DMSO (absorbed moisture lowers solubility)

Aliquot the stock solution and store it at -80°C (up to 6 months) or -20°C (up to 1 month); avoid repeated freeze-thaw cycles.

Data provided by the manufacturer.

In Vitro

In Parkin-expressing U2OS-iMLS cells, GSK3-IN-3 (VP07) (25 μM; 24 h) induces mitophagy, though with restricted potency[1]. Mitochondrial fission accompanied by a change in mitochondrial morphology results from GSK3-IN-3 (1.56-25 μM; 24 h) in U2OS-iMLS-Parkin cells[1]. GSK3-IN-3 (VP0.7) (5 μM, 10 μM;) offers neuroprotection against 6-OHDA in SH-SY5Y cells, albeit within an in vitro cellular model of Parkinson's disease[2].

Immunofluorescence[1]

Cell LineParkin-expressing U2OS-iMLS cells
Concentration1.56 μM, 3.12 μM, 6.25 μM, 12.5 μM, and 25 μM;
Incubation Time24 hours
ResultInduced a mitochondrial morphology change from a filament-shaped network to a more round-shaped network.

Cell Viability Assay[2]

Cell LineSH-SY5Y cells
Concentration0.5 μM, 1 μM, 3 μM, 5 μM, and 10 μM
Incubation Time16 hours; with 35 μM 6-OHDA
ResultInhibited cell growth with an IC50 value of 2.57 μM.

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price on some sizes?
A.Availability and lead time for those sizes are confirmed on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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Mitochondrial dysfunction-mediated metabolic remodeling of TCA cycle promotes Parkinson's disease through inhibition of H3K4me3 demethylation. Cell Death Discov 2025 Jul 29;11(1):351. PMID: 40730642

Isoquercitrin from Apocynum venetum L. Exerts Antiaging Effects on Yeasts via Stress Resistance Improvement and Mitophagy Induction through the Sch9/Rim15/Msn Signaling Pathway. Antioxidants (Basel) 2023 Oct 31;12(11):1939. PMID: 38001792

iScience. 2025 Dec 8.

Activation of Nemo-like Kinase in Diamond Blackfan Anemia suppresses early erythropoiesis by preventing mitochondrial biogenesis. J Biol Chem 2024 Aug;300(8):107542. PMID: 38992436

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