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Miransertib

Catalog No. T3467   CAS 1313881-70-7
Synonyms: ARQ-092, AKT inhibitor 2

Miransertib (ARQ-092) is an orally bioavailable, selective, and potent allosteric Akt inhibitor.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.
Miransertib Chemical Structure
Miransertib, CAS 1313881-70-7
Pack Size Availability Price/USD Quantity
1 mg In stock $ 44.00
5 mg In stock $ 98.00
10 mg In stock $ 172.00
25 mg In stock $ 363.00
50 mg In stock $ 597.00
100 mg In stock $ 955.00
500 mg In stock $ 1,890.00
1 mL * 10 mM (in DMSO) In stock $ 116.00
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Purity: 99.93%
Purity: 98.83%
Purity: 98%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Miransertib (ARQ-092) is an orally bioavailable, selective, and potent allosteric Akt inhibitor.
Targets&IC50 Akt3:8.1 nM, Akt2:14 nM, Akt1:2.7 nM
In vitro ARQ 092 blocks membrane translocation of inactive AKT and even dephosphorylates the membrane-associated active form, thereby perturbing AKT activity. Treatment with 50-500 nM ARQ 092 significantly blocks αMβ2 integrin function in neutrophils and reduces P-selectin exposure and glycoprotein Ib/IX/V-mediated agglutination in platelets[2]. In a large panel of diverse cancer cell lines, ARQ 092 inhibits proliferation across multiple tumor types but are most potent in leukemia, breast, endometrial, and colorectal cancer cell lines. Moreover, inhibition by ARQ 092 is more prevalent in cancer cell lines containing PIK3CA/PIK3R1 mutations compared to those with wt-PIK3CA/PIK3R1 or PTEN mutations[1]. ARQ 092 targets the PI3K/AKT pathway and AKT specifically and reduces phosphorylation of GSK3α and GSK3β in mutation-positive cells[3].
Cell Research Cells (MDA-MB-453: 1.5×106; NCI-H1650: 1×106; KU-19-19: 0.7×106) are plated into 6 well plates, left overnight, and then treated with full media containing different concentrations (0, 0.012, 0.037, 0.11, 0.33, and 1 μM) of AKT inhibitors (ARQ 092, ARQ 751, MK-2206, GDC-0068) for 2 hours. Cells are treated under designated conditions and lysates are extracted. Proteins are resolved from extracts using SDS-PAGE followed by immunoblotting. (Only for Reference)
Synonyms ARQ-092, AKT inhibitor 2
Molecular Weight 432.52
Formula C27H24N6
CAS No. 1313881-70-7

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 50 mg/mL (115.6 mM)

TargetMolReferences and Literature

1. Yu Y, et al. PLoS One. 2015, 10(10):e20140479. 2. Kim K, et al. Haematologica. 2017, 102(2):246-259. 3. Lindhurst MJ, et al. Sci Rep. 2015, 5:17162. 4. Han P, Hou Y, Zhao Y, et al. Low-dose decitabine modulates T cell homeostasisand restores immune tolerance in immune thrombocytopenia[J]. Blood. 2021

TargetMolCitations

1. Han P, Hou Y, Zhao Y, et al. Low-dose decitabine modulates T cell homeostasisand restores immune tolerance in immune thrombocytopenia. Blood. 2021

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Clinical Compound Library Anti-Cancer Drug Library Inhibitor Library Drug Repurposing Compound Library Anti-Parasitic Compound Library Kinase Inhibitor Library Bioactive Compounds Library Max Reprogramming Compound Library Anti-Obesity Compound Library Anti-Infection Compound Library

Related Products

Related compounds with same targets
PF-AKT400 Triciribine phosphate AT13148 Haginin A Dehydroglyasperin D Lupalbigenin PI3K/Akt/mTOR-IN-2 MKC-1

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Keywords

Miransertib 1313881-70-7 Cytoskeletal Signaling Microbiology/Virology PI3K/Akt/mTOR signaling Parasite Akt anti-proliferative PKB Akt1 Protein kinase B Inhibitor ARQ092 Akt3 AKT1-E17K Akt2 inhibit ARQ-092 p-PRAS40 ARQ 092 anti-tumor p-Akt AKT inhibitor 2 inhibitor

 

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