1346598-70-6
Chemical Structure
Debutyldronedarone-d6 hydrochloride
Synonym(s): SR35021-dd6 hydrochloride
- CAS No.: 1346598-70-6
- Formula:C27H31D6ClN2O5S
- Molecular Weight:543.15
IUPAC Name: N-(2-butyl-3-(4-(3-(butylamino)propoxy-1,1,2,2,3,3-d6)benzoyl)benzofuran-5-yl)methanesulfonamide hydrochloride
InChIKey: ZDXBTJLIQYUYSZ-TWVPJIPGSA-N
SMILES: CS(=O)(NC1=CC=C(C2=C1)OC(CCCC)=C2C(C3=CC=C(C=C3)OC([2H])(C([2H])(C([2H])(NCCCC)[2H])[2H])[2H])=O)=O.Cl[H]
Biological Activity: Debutyldronedarone-d6 hydrochloride (SR35021-d6 hydrochloride) is the deuterated-labeled Debutyldronedarone (HY-12753). Debutyldronedarone (SR35021) is a Cytochrome P450 enzyme inhibitor and a Thyroid Hormone Receptor inhibitor, and it is a metabolite of Dronedarone (HY-A0016). Debutyldronedarone inhibits the binding of T3 to TRα1 and TRβ1. Debutyldronedarone reduces the incidence of reperfusion-induced ventricular fibrillation in anesthetized rats, while decreasing their heart rate and blood pressure. Debutyldronedarone can be used in studies related to ventricular fibrillation and atrial fibrillation[1][2].
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Debutyldronedarone-d6 hydrochloride | 99.27% | Debutyldronedarone-d6 hydrochloride (SR35021-d6 hydrochloride) is the deuterated-labeled Debutyldronedarone (HY-12753). Debutyldronedarone (SR35021) is a Cytochrome P450 enzyme inhibitor and a Thyroid Hormone Receptor inhibitor, and it is a metabolite of Dronedarone (HY-A0016). Debutyldronedarone inhibits the binding of T3 to TRα1 and TRβ1. Debutyldronedarone reduces the incidence of reperfusion-induced ventricular fibrillation in anesthetized rats, while decreasing their heart rate and blood pressure. Debutyldronedarone can be used in studies related to ventricular fibrillation and atrial fibrillation. | ||||||||||||||||||||
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Debutyldronedarone-d7 | Debutyldronedarone-d7 (SR35021-d7) is the deuterated-labeled Debutyldronedarone (HY-12753). Debutyldronedarone (SR35021) is a Cytochrome P450 enzyme inhibitor and a Thyroid Hormone Receptor inhibitor, and it is a metabolite of Dronedarone (HY-A0016). Debutyldronedarone inhibits the binding of T3 to TRα1 and TRβ1. Debutyldronedarone reduces the incidence of reperfusion-induced ventricular fibrillation in anesthetized rats, while decreasing their heart rate and blood pressure. Debutyldronedarone can be used in studies related to ventricular fibrillation and atrial fibrillation. | |||||||||||||||||||||
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Debutyldronedarone | Debutyldronedarone (SR35021) is a Cytochrome P450 enzyme inhibitor and a Thyroid Hormone Receptor inhibitor, and it is a metabolite of Dronedarone (HY-A0016). Debutyldronedarone inhibits the binding of T3 to TRα1 and TRβ1. Debutyldronedarone reduces the incidence of reperfusion-induced ventricular fibrillation in anesthetized rats, while decreasing their heart rate and blood pressure. Debutyldronedarone can be used in studies related to ventricular fibrillation and atrial fibrillation. | |||||||||||||||||||||
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- [1]. Therapeutic Goods Administration. Australian Public Assessment Report for Dronedarone Hydrochloride, submission PM-2008-3045-3, Australian Government Department of Health and Ageing, 2008.
- [2]. Van Beeren HC, et al. Dronerarone acts as a selective inhibitor of 3,5,3'-triiodothyronine binding to thyroid hormone receptor-alpha1: in vitro and in vivo evidence. Endocrinology. 2003 Feb;144(2):552-8. [Content Brief]
