US2022204468A1PendingUtilityA1

Dp antagonist

Assignee: ONO PHARMACEUTICAL COPriority: Sep 20, 2018Filed: Mar 15, 2022Published: Jun 30, 2022
Est. expirySep 20, 2038(~12.1 yrs left)· nominal 20-yr term from priority
C07C 2601/14C07C 235/78C07C 2601/02A61P 25/20C07D 309/06A61P 25/00C07C 235/56A61P 43/00A61K 31/351A61P 25/18C07C 327/48A61K 31/216C07C 235/64C07C 2602/08C07C 233/81A61K 31/196A61K 9/2054
73
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

An object of the present invention is to provide a DP receptor antagonist. A compound represented by general formula (I):(wherein all symbols are as shown in the specification) and a pharmaceutically acceptable salt thereof have DP receptor antagonistic activity and are also highly safe, and thus are useful as active ingredients of pharmaceuticals for DP receptor-mediated diseases. In addition, the compound represented by the general formula (I) and the pharmaceutically acceptable salt thereof also have good transferability to the central nervous system, and thus are particularly useful as a preventive and/or therapeutic agent for diseases associated with DP receptors present in the central nervous system among DP receptor-mediated diseases, that is, sleep-wake disorders.

Claims

exact text as granted — not AI-modified
1 . A method for treating a DP receptor-mediated disease, comprising administering an effective amount of a compound that is {4-Chloro-3-[(2,6-dimethyl-4-{2-[(2R)-oxan-2-yl]ethoxy}benzene-1-carbothioyl)amino]phenyl}acetic acid or a pharmaceutically acceptable salt thereof to a patient in need of prevention and/or treatment of the DP receptor-mediated disease. 
     
     
         2 . The method according to  claim 1 , wherein {4-Chloro-3-[(2,6-dimethyl-4-{2-[(2R)-oxan-2-yl]ethoxy}benzene-1-carbothioyl)amino]phenyl}acetic acid is administered. 
     
     
         3 . The method according to  claim 1 , wherein a pharmaceutically acceptable salt of {4-Chloro-3-[(2,6-dimethyl-4-{2-[(2R)-oxan-2-yl]ethoxy}benzene-1-carbothioyl)amino]phenyl}acetic acid is administered. 
     
     
         4 . The method according to  claim 1 , wherein the DP receptor-mediated disease is allergic disease, systemic mastocytosis, systemic mast cell activation disorder, anaphylactic shock, respiratory tract constriction, urticaria, eczema, acne, allergic bronchopulmonary aspergillosis, sinusitis, migraine, nasal polyps, hypersensitivity vasculitis, eosinophilia, contact dermatitis, a disease accompanied by itching, a disease caused secondarily as a result of behavior accompanied by itching, a disease accompanied by flushing, inflammation, chronic obstructive pulmonary disease, ischemia-reperfusion injury, cerebrovascular accident, autoimmune disease, cerebral trauma, liver disorder, graft rejection, rheumatoid arthritis, pleurisy, osteoarthritis, Crohn's disease, ulcerative colitis, irritable bowel syndrome, interstitial cystitis, muscular dystrophy, polymyositis, cancer, leukemia, viral infection, multiple sclerosis, sleep-wake disorder, or platelet aggregation. 
     
     
         5 . The method according to  claim 4 , wherein DP receptor-mediated disease is sleep-wake disorder, and the sleep-wake disorder is a disease comprises hypersomnia, insomnia, residual sleepiness of sleep apnea syndrome, circadian rhythm sleep-wake disorder, hypersomnia associated with neurodegenerative disease, hypersomnia associated with mental illness, or morbid sleep apnea during daytime.

Join the waitlist — get patent alerts

Track US2022204468A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.