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Darolutamide

Darolutamide
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Purity:99.62%
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Darolutamide

Catalog No. T6915Cas No. 1297538-32-9
Darolutamide (BAY-1841788) is an androgen receptor (AR) antagonist that blocks AR nuclear translocation (Ki: 11 nM).
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Pack SizePriceAvailabilityQuantity
1 mg$45In Stock
2 mg$64In Stock
5 mg$107In Stock
10 mg$169In Stock
25 mg$279In Stock
50 mg$397In Stock
100 mg$590In Stock
500 mg$1,280In Stock
1 mL x 10 mM (in DMSO)$108In Stock
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Product Introduction

Bioactivity
Description
Darolutamide (BAY-1841788) is an androgen receptor (AR) antagonist that blocks AR nuclear translocation (Ki: 11 nM).
In vitro
In AR-HEK293 cells stably expressing full-length hAR, ODM-201 inhibits human AR (hAR) with IC50 of 26 nM. ODM-201 inhibits VCaP cell proliferation with IC50 of 230 nM, while has no effect on the viability of AR-negative cell lines tested, DU-145 prostate cancer cells and H1581 lung cancer cells. [1]
In vivo
In mice bearing VCaP xenografts, ODM-201 (50?mg/kg, p.o.) significantly inhibits castration-resistant prostate tumor growth. [1]
Kinase Assay
AR binding affinity: AR binding affinities of test compounds are studied in cytosolic lysates obtained from ventral prostates of castrated rats by a competition binding assay. Fresh prostates are minced and homogenized with Buffer A containing protease inhibitors. The homogenates are centrifuged and the resultant supernatants are treated with a dextran-coated charcoal solution to remove endogenous steroids. The dissociation constant of the radio ligand [3H]mibolerone for isolated rat ARs is determined in a saturation binding experiment. For the determination of Ki values, prostate cytosol preparations and 1?nM [3H]mibolerone are incubated with increasing concentrations of test compounds overnight. After the incubation, bound and free steroids are separated by treatment with 100?μL of dextran-coated charcoal suspension. Bound radioactivity is determined by counting 100?μL of supernatant fraction in 200?μL of scintillation fluid using a microbeta counter. All procedures are carried out at 0–4?°C.
Cell Research
VCaP cells are treated with a submaximal concentration of mibolerone (0.1?nM) and increasing concentrations of test compounds in steroid-free assay medium supplemented with 4?mM GlutaMAX. After a 4-day incubation with the compounds, cell viability is measured using a WST-1 cell proliferation assay. To rule out non-AR –mediated toxicity, AR-negative PC cells (DU-145) and lung cancer cells (H1581) are treated with an increasing concentration of ODM-201, and cell viability is measured as described above.(Only for Reference)
AliasODM-201, BAY-1841788
Chemical Properties
Molecular Weight398.85
FormulaC19H19ClN6O2
Cas No.1297538-32-9
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 70 mg/mL (175.5 mM)
Ethanol: 36 mg/mL (90.3 mM)
H2O: < 1 mg/mL (insoluble or slightly soluble)
Solution Preparation Table
DMSO/Ethanol
1mg5mg10mg50mg
1 mM2.5072 mL12.5360 mL25.0721 mL125.3604 mL
5 mM0.5014 mL2.5072 mL5.0144 mL25.0721 mL
10 mM0.2507 mL1.2536 mL2.5072 mL12.5360 mL
20 mM0.1254 mL0.6268 mL1.2536 mL6.2680 mL
50 mM0.0501 mL0.2507 mL0.5014 mL2.5072 mL
DMSO
1mg5mg10mg50mg
100 mM0.0251 mL0.1254 mL0.2507 mL1.2536 mL

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