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GJ103 sodium salt

Catalog No. T4251Cas No. 1459687-96-7

GJ103 sodium salt is an active analog of GJ072, a read-through compound. It has been shown to reduce the surface tension of aqueous solutions, which makes it easier for molecules to move through the solution. It has also been shown to reduce the viscosity of aqueous solutions, which makes it easier for molecules to move through the solution. Additionally, it has been shown to reduce the pH of aqueous solutions, which can have a variety of effects on the biochemical and physiological processes of living organisms.

GJ103 sodium salt

GJ103 sodium salt

Purity: 99.88%
Catalog No. T4251Cas No. 1459687-96-7
GJ103 sodium salt is an active analog of GJ072, a read-through compound. It has been shown to reduce the surface tension of aqueous solutions, which makes it easier for molecules to move through the solution. It has also been shown to reduce the viscosity of aqueous solutions, which makes it easier for molecules to move through the solution. Additionally, it has been shown to reduce the pH of aqueous solutions, which can have a variety of effects on the biochemical and physiological processes of living organisms.
Pack SizePriceAvailabilityQuantity
2 mg$42In Stock
5 mg$78In Stock
10 mg$126In Stock
25 mg$256In Stock
50 mg$442In Stock
100 mg$481In Stock
1 mL x 10 mM (in DMSO)$72In Stock
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Purity:99.88%
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Product Introduction

Bioactivity
Description
GJ103 sodium salt is an active analog of GJ072, a read-through compound. It has been shown to reduce the surface tension of aqueous solutions, which makes it easier for molecules to move through the solution. It has also been shown to reduce the viscosity of aqueous solutions, which makes it easier for molecules to move through the solution. Additionally, it has been shown to reduce the pH of aqueous solutions, which can have a variety of effects on the biochemical and physiological processes of living organisms.
In vitro
GJ072 induces ATM kinase on both TGA and TAG stop codons and restored ATMpSer1981 autophosphorylation and SMC1pSer966 transphosphorylation as measured by FACS. GJ072 is active in A-T cells with a homozygous TAA mutation. GJ072 is able to induce detectable full-length ATM protein in treated A-T cells. Early structure-activity relationship studies generates eight active analogs of GJ072. Some GJ072 analogs (e.g., GJ103, GJ106, GJ109, and GJ111) consistently demonstrates their activities in all three PTCs by both FCATMpSer1981 and IRIF assays. GJ071 and GJ072 and some of their analogs (such as GJ103) have similar read-through activity as RTC13 or RTC14, but are more tolerable than RTC13 and RTC14 to A-T cells. GJ103 does not show obvious cytotoxicity in A-T cells at concentration as high as 300 μM.
In vivo
GJ103 sodium salt is water soluble, which will enable us to evaluate its in vivo activity by systematic administration.
Cell Research
Cell proliferation assay is used to measure cytotoxicity. Cells are seeded into a flat-bottom 96-well plate, including control wells containing complete growth medium alone as blank absorbance readings. After RTC treatment (GJ103), activated-XTT Solution is added into each well, and the cells are returned to the cell culture incubator for 12-14 hours. The absorbance is measured at 480 nM with relevant 630 nM to assess nonspecific readings.
Chemical Properties
Molecular Weight364.36
FormulaC16H13N4NaO3S
Cas No.1459687-96-7
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: Soluble
DMSO: 50 mg/mL (137.23 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.7445 mL13.7227 mL27.4454 mL137.2269 mL
5 mM0.5489 mL2.7445 mL5.4891 mL27.4454 mL
10 mM0.2745 mL1.3723 mL2.7445 mL13.7227 mL
20 mM0.1372 mL0.6861 mL1.3723 mL6.8613 mL
50 mM0.0549 mL0.2745 mL0.5489 mL2.7445 mL
100 mM0.0274 mL0.1372 mL0.2745 mL1.3723 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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