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BMS 195614

BMS 195614
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Purity:97.7%
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BMS 195614

Catalog No. T22192Cas No. 253310-42-8
BMS 195614 (BMS614) is a selective RARα antagonist. BMS 195614 can bind to the RARα subunit.
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Pack SizePriceAvailabilityQuantity
1 mg$181In Stock
5 mg$418In Stock
10 mg$619In Stock
25 mg$988In Stock
50 mg$1,330In Stock
100 mg$1,780In Stock
500 mg$3,580In Stock
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Product Introduction

Bioactivity
Description
BMS 195614 (BMS614) is a selective RARα antagonist. BMS 195614 can bind to the RARα subunit.
In vitro
BMS 195614 reversed the induction effect of selective RARα agonists, AM580, AM80 and BMS 194753 on differentiation of the acute promyelocytic leukemia cell lines, NB4 and HL60 [1]. Treatment with retinoic acid (RA) (1 uM) for 72 hrs significantly reduced T47D breast cancer cells migration. But RA in combination with BMS 195614 did not affect the cell movement [2]. In cells of a bovine stromal-vascular fraction from intramuscular fat, BMS 195614 significantly diminished the anti-adipogenic effect of ATRA [3].
In vivo
BMS 195614 displayed poor in vivo activity in mice when administered orally. Treatment with BMS 195614 at oral doses for 1 month showed no inhibition to spermatogenesis [4]. Oral administration of BMS 195614 did not suppress spermatogenesis in mice [5].
AliasBMS614
Chemical Properties
Molecular Weight448.51
FormulaC29H24N2O3
Cas No.253310-42-8
Storage & Solubility Information
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 10.1 mg/mL (22.5 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2296 mL11.1480 mL22.2960 mL111.4802 mL
5 mM0.4459 mL2.2296 mL4.4592 mL22.2960 mL
10 mM0.2230 mL1.1148 mL2.2296 mL11.1480 mL
20 mM0.1115 mL0.5574 mL1.1148 mL5.5740 mL

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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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