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BMS 182874 hydrochloride

Catalog No. T21790Cas No. 1215703-04-0

BMS 182874 hydrochloride is a nonpeptide endothelin (El) receptor antagonist.

BMS 182874 hydrochloride

BMS 182874 hydrochloride

Purity: 97.01%
Catalog No. T21790Cas No. 1215703-04-0
BMS 182874 hydrochloride is a nonpeptide endothelin (El) receptor antagonist.
Pack SizePriceAvailabilityQuantity
1 mg$74In Stock
2 mg$98In Stock
5 mg$151In Stock
10 mg$227In Stock
25 mg$381In Stock
50 mg$531In Stock
100 mg$738In Stock
200 mg$996In Stock
1 mL x 10 mM (in DMSO)$157In Stock
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Purity:97.01%
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Product Introduction

Bioactivity
Description
BMS 182874 hydrochloride is a nonpeptide endothelin (El) receptor antagonist.
In vitro
BMS-l 82874 inhibited ET-l -stimulated inositol phosphate accumulation (KB 75 nM) and calcium mobilization (Ki = 140 nM) without suppressing the maximal responses in VSM-A10 cells. BMS-182874 competitively inhibited the binding of [125I]ET-1 to ETA receptors in rat vascular smooth muscle A10 (VSM-A10) cell membranes (Ki = 61 nM) and in CHO cells stably expressing the human ETA receptor (Ki = 48 nM), but was a weak inhibitor at ETB receptors (Ki > 50 μM) and non-ET receptors.
In vivo
BMS-182874 blunted the pressor response to exogenous ET-l when administered either orally (ED50 = 30 μmol/kg) or intravenously (ED50 = 24 μmol/kg) to conscious, normotensive rats.
Chemical Properties
Molecular Weight381.88
FormulaC17H20ClN3O3S
Cas No.1215703-04-0
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 50 mg/mL (130.93 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6186 mL13.0931 mL26.1862 mL130.9312 mL
5 mM0.5237 mL2.6186 mL5.2372 mL26.1862 mL
10 mM0.2619 mL1.3093 mL2.6186 mL13.0931 mL
20 mM0.1309 mL0.6547 mL1.3093 mL6.5466 mL
50 mM0.0524 mL0.2619 mL0.5237 mL2.6186 mL
100 mM0.0262 mL0.1309 mL0.2619 mL1.3093 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
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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