ChemicalBook--->CAS DataBase List--->414910-30-8

414910-30-8

414910-30-8 Structure

414910-30-8 Structure
IdentificationBack Directory
[Name]

Casopitant
[CAS]

414910-30-8
[Synonyms]

GW 679769B
Casopitant Mesylate
(2R,4S)-4-(4-Acetyl-1-piperazinyl)-N-[(1R)-1-[3,5-bis(trifluoroMethyl)phenyl]ethyl]-2-(4-fluoro-2-Methylphenyl)-N-Methyl-
[Molecular Formula]

C31H39F7N4O5S
[MDL Number]

MFCD18382224
[MOL File]

414910-30-8.mol
[Molecular Weight]

712.719
Chemical PropertiesBack Directory
[solubility ]

Acetonitrile: Slightly soluble: 0.1-1 mg/ml
Methanol: Slightly soluble: 0.1-1 mg/ml
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

It is a novel, orally active tachykinin NK1 receptor antagonist; efficacy of Casopitant mesilate in patients receiving emetogenic chemotherapy.
[in vivo]

In a ferret-model of Cisplatin- induced emesis, Casopitant (GW679769) inhibits retching and vomiting and reduced nausea-like behaviours in a dose-dependent manner. The pharmacokinetics and brain penetration of casopitant are studied in the ferret-model of cisplatin-induced emesis. Following a single intraperitoneal dose, radioactive labeled Casopitant ([14C]Casopitant) is rapidly absorbed, with plasma and brain concentrations being approximately equal at two hours post-dosing. [14C]Casopitant is found in the brain as the parent compound and two major oxidative metabolites (M1 and M2), accounting for approximately 76%, 19%, and 3% of the radioactivity, respectively; suggesting that the pharmacologic activity of Casopitant in the ferret is largely attributable to the parent compound. Casopitant possesses a high affinity for brain NK1 receptors in the ferret[2].

[IC 50]

NK1; CYP3A4
[References]

[1] ROMANO DI FABIO*. Discovery and Biological Characterization of (2R,4S)-1′-Acetyl-N-{(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethyl}-2-(4-fluoro-2-methylphenyl)-N-methyl-4,4′-bipiperidine-1-carboxamide as a New Potent and Selective Neurokinin 1 (NK1) Receptor Antagonist Clinical Candidate[J]. Journal of Medicinal Chemistry, 2011, 54 4: 1071-1079. DOI: 10.1021/jm1013264
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