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ET receptor antagonist 3

ET receptor antagonist 3
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ET receptor antagonist 3

Catalog No. T79575
"ET receptor antagonist 3 (compound 17d) is an orally active ET receptor antagonist with an IC50 of 0.26 nM, utilized for pulmonary arterial hypertension (PAH) research. This compound demonstrates efficacy in mitigating monocrotaline-induced PAH in a rat model [1]."
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Product Introduction

Bioactivity
Description
"ET receptor antagonist 3 (compound 17d) is an orally active ET receptor antagonist with an IC50 of 0.26 nM, utilized for pulmonary arterial hypertension (PAH) research. This compound demonstrates efficacy in mitigating monocrotaline-induced PAH in a rat model [1]."
In vivo
Administered orally at 150 mg/kg/day and 300 mg/kg/day starting 48 hours post-MCT treatment for 21 to 26 days, ET receptor antagonist 3 (compound 17d) significantly reduced mean pulmonary arterial pressure (mPAP) in MCT-exposed rats, decreased levels of HIF1α, ANP, and TNNI3, exhibited antioxidant activity, and inhibited lipid peroxidation [1].
Chemical Properties
Molecular Weight548.61
FormulaC27H28N6O5S
Cas No.
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year

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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。
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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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