
CAS 1103522-45-7
:Aprocitentan
- Act-132577
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Despropyl Macitentan
CAS:Compounds containing a pyrimidine ring, whether or not hydrogenated, or piperazine ring in the structure, nesoiFormula:C16H14Br2N6O4SColor and Shape:Off-White SolidMolecular weight:543.9164N-Despropyl Macitentan
CAS:Formula:C16H14Br2N6O4SPurity:98%Color and Shape:SolidMolecular weight:546.1932Ref: IN-DA008TD9
1gTo inquire250mgTo inquire1mg99.00€5mg196.00€10mg201.00€25mg239.00€50mg535.00€100mg556.00€N-Despropyl Macitentan (Aprocitentan)
CAS:Formula:C16H14Br2N6O4SColor and Shape:White To Off-White SolidMolecular weight:546.19Aprocitentan
CAS:Aprocitentan (ACT-132577) is ETA and ETB antagonist .Formula:C16H14Br2N6O4SPurity:97.35%Color and Shape:White SolidMolecular weight:546.19Ref: TM-T7817
1mg55.00€5mg110.00€1mL*10mM (DMSO)135.00€10mg166.00€25mg295.00€50mg416.00€100mg622.00€200mg840.00€Aprocitentan
CAS:N-(5-(4-Bromophenyl)-6-(2-((5-bromopyrimidin-2-yl)oxy)ethoxy)pyrimidin-4-yl)sulfamideFormula:C16H14Br2N6O4SPurity:99%Molecular weight:546.19N-Despropyl-macitentan
CAS:Controlled ProductApplications N-Despropyl-macitentan, is an active metabolite which is part of a family of endothelin receptor antagonist that allows for treatment of pulmonary arterial hypertension (PAH)
References Atsmon, J., et al.: Clin. Pharmacokinet., 525, 685 (2013); Sidharta, P.N., et al.: Clin. Drug Invest. (2014)Formula:C16H14Br2N6O4SColor and Shape:NeatMolecular weight:546.19Aprocitentan
CAS:Apcitentan is a vasoactive drug that belongs to the group of endothelin receptor antagonists. It is used in the treatment of erectile dysfunction and pulmonary hypertension. Apcitentan inhibits the angiotensin system, which includes angiotensin-converting enzyme (ACE), angiotensin II type 1 receptor (AT1R) and angiotensin II type 2 receptor (AT2R). This inhibition increases the levels of endothelin and dopamine β-hydroxylase, thereby decreasing blood pressure. Apcitentan has been shown to increase glomerular filtration rate and reduce proteinuria in patients with chronic kidney disease. In vivo studies have shown that apcitentan is rapidly absorbed from the gastrointestinal tract, reaching peak concentrations within one hour. The pharmacodynamics of apcitentan are characterized by an inhibitory effect on pde5. Pharmacokinetic studies have found that apcitentan is metabolized by CYP
Formula:C16H14Br2N6O4SPurity:Min. 95%Molecular weight:546.19 g/mol










