441798-33-0 Usage
Description
Macitentan, also known as ACT-064992, is an endothelin receptor antagonist that received US FDA approval in October 2013 for the treatment of pulmonary arterial hypertension (PAH) (WHO group I) to delay disease progression. It was discovered through structure-activity relationship (SAR) studies starting with the bosentan structure, with the main goals of increasing potency for both endothelin receptor A and B (ETA and ETB) subtypes, improving tissue distribution to reach the target receptors, and avoiding bile salt transport inhibition.
Uses
Used in Pharmaceutical Industry:
Macitentan is used as a therapeutic agent for the treatment of pulmonary arterial hypertension (PAH) to delay disease progression and reduce hospitalization for PAH. It was approved for PAH by the United States Food and Drug Administration (FDA) in 2013. Macitentan has been associated with a low rate of serum enzyme elevations during therapy, but has yet to be implicated in cases of clinically apparent acute liver injury.
Originator
Actelion
Pharmaceuticals Ltd. (Switzerland)
Clinical Use
Endothelin receptor antagonist:
Treatment of pulmonary arterial hypertension
Synthesis
The preparation of the drug began with reaction of commercial
4-bromophenylacetate (112) with dimethylcarbonate (113) under
basic conditions to yield the malonate ester 114. Treatment
of this diester with sodium methoxide and formamidine
hydrochloride 115 provided the desired intermediate 4,6-
dihydroxypyrimidine as a tautomeric mixture; from this system,
dichloride 116 was generated in 60–80% yield upon treatment with
warm phosphorus oxychloride in N,N-dimethylaniline. Reaction of
116 with excess sulfonyl urea potassium salt 117 provided
chloropyrimidine 118 in high yield (83–93%). This was reacted
with bromochloropyrimidine 119 in an SNAr reaction to provide
macitentan (XV) in 88% yield.
Synthesis of sulfamide potassium salt 117 was accomplished
via sequential reaction of chlorosulfonyl isocyanate (120) with t-
BuOH and propylamine/Et3N to provide ester sulfamide 121,followed by Boc removal and treatment with potassium t-butoxide
to yield 117. This material could be isolated by trituration with
diethyl ether.
Drug interactions
Potentially hazardous interactions with other drugs
Antibacterials: concentration reduced by rifampicin
- avoid.
Antidepressants: avoid with St John’s wort.
Antiepileptics: avoid with carbamazepine,
fosphenytoin and phenytoin.
Mode of action
Macitentan is an orally available dual endothelin receptor (ETR) antagonist with potential antihypertensive and antineoplastic activity. Upon administration, macitentan and its metabolites block the binding of endothelin isoform 1 (ET-1) to type-A and type-B ETR on both the tumor cells and the endothelial cells in the tumor vasculature. This prevents ET-1 mediated signaling transduction which may decrease tumor cell proliferation, progression, and angiogenesis in tumor tissue. ET-1, a potent vasoconstrictor that plays an important role in inflammation and tissue repair, is, together with its receptors, overexpressed varyingly in many tumor cell types.
references
[1]. marc iglarz, christoph binkert, keith morrison, et al. pharmacology of macitentan, an orally active tissue-targeting dual endothelin receptor antagonist. journal of pharmacology and experimental therapeutics, 2008, 327:736-745.
Check Digit Verification of cas no
The CAS Registry Mumber 441798-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,1,7,9 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 441798-33:
(8*4)+(7*4)+(6*1)+(5*7)+(4*9)+(3*8)+(2*3)+(1*3)=170
170 % 10 = 0
So 441798-33-0 is a valid CAS Registry Number.
