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RI-1

🥰Excellent
Catalog No. T2276Cas No. 415713-60-9
Alias RI1, RAD51 inhibitor 1

RI-1 (RAD51 inhibitor 1) is a RAD51 inhibitor (IC50: 5-30 μM).

RI-1

RI-1

🥰Excellent
Purity: 99.62%
Catalog No. T2276Alias RI1, RAD51 inhibitor 1Cas No. 415713-60-9
RI-1 (RAD51 inhibitor 1) is a RAD51 inhibitor (IC50: 5-30 μM).
Pack SizePriceAvailabilityQuantity
2 mg$37In Stock
5 mg$59In Stock
10 mg$105In Stock
25 mg$162In Stock
50 mg$198In Stock
100 mg$369In Stock
1 mL x 10 mM (in DMSO)$66In Stock
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Purity:99.62%
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Product Introduction

Bioactivity
Description
RI-1 (RAD51 inhibitor 1) is a RAD51 inhibitor (IC50: 5-30 μM).
Targets&IC50
RAD51:<30 μM
In vivo
PluriSIns 1 showed single-agent toxicity (LD50: 20-40 μM) in three cancer cell lines: HeLa cells, MCF-7 and U2OS. Through direct and specific disruption of HsRAD51 and inhibition of RAD51, RI-1 inhibited the ability of RAD51 to form filaments on ssDNA, resulting in increased cellular susceptibility to DNA damage.RI-1 caused a decrease in γ-H2AX foci in G2-phase cells and an increase in the level of unrepaired DSBs 6 h after radiation.
Kinase Assay
DNA binding assays: All reactions are performed in black non-binding polystyrene 384-well plates with reaction volumes of 30–100 μL. Purified DNA strand exchange proteins and chemical compounds are pre-incubated at room temperature for 5 minutes; they are then further incubated at 37°C for 30 min with 100 nM of ssDNA substrate, consisting of a 45-mer poly-dT tagged with Alexa 488 at the 5' terminus (synthesized and purified by Integrated DNA Technologies). Reactions are performed in 20 mM HEPES pH 7.5, 10 mM MgCl2, 0.25 μM BSA, 2% glycerol, 30 mM NaCl, 4% DMSO and 2 mM ATP. Some conditions included DTT or TCEP (tris(2-carboxyethyl)phosphine) as indicated. DNA binding is measured as a function of fluorescence polarization (FP) with a Safire2 plate reader, using the following settings: excitation 470±5 nM, emission 530±5 nM, 10 reads/well, Z height and G factor auto-calibrated from control wells. Displayed error bars represent standard deviation. For experiments involving a titration of protein concentrations, data are fit to an equation that accounts for the cooperative nature by which recombinase proteins bind DNA. For experiments involving a titration of RI-1, protein concentrations are selected to give an ~80% saturation of the FP signal in the absence of RI-1.
Cell Research
Cytotoxicity is determined by loss of colony-forming ability. Experiments are performed in triplicate. Crystal violet stained colonies are imaged with a CCD camera and counted using NIH Image software. Error bars denote standard error.(Only for Reference)
AliasRI1, RAD51 inhibitor 1
Chemical Properties
Molecular Weight361.61
FormulaC14H11Cl3N2O3
Cas No.415713-60-9
SmilesClC1=C(N2CCOCC2)C(=O)N(C1=O)c1ccc(Cl)c(Cl)c1
Relative Density.1.61 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 36.2 mg/mL (100 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.7654 mL13.8271 mL27.6541 mL138.2705 mL
5 mM0.5531 mL2.7654 mL5.5308 mL27.6541 mL
10 mM0.2765 mL1.3827 mL2.7654 mL13.8271 mL
20 mM0.1383 mL0.6914 mL1.3827 mL6.9135 mL
50 mM0.0553 mL0.2765 mL0.5531 mL2.7654 mL
100 mM0.0277 mL0.1383 mL0.2765 mL1.3827 mL

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