IP Library › Granted Patent US 11,793,823
Granted Patent B2
US 11,793,823 · App. 17/699,784 · Granted Oct 24, 2023

Compounds and pharmaceutical uses thereof

Inventors: Guochuan Emil Tsai (Pasadena, CA); Yi-Wen Mao (New Taipei, TW); Lu-Ping Lu (New Taipei, TW); Wei-Hua Chang (New Taipei, TW); Han-Yi Hsieh (New Taipei, TW); Jhe Wei Hu (New Taipei, TW); Tsai-Miao Shih (New Taipei, TW); ChanHui Huang (New Taipei, TW)
Assignee: SyneuRx International (Taiwan) Corp.
A61K31/7048A23L33/10A23L33/40A61K31/235A61K31/36A61K31/40A61K31/415A61K31/7034A61P25/18C07C69/90C07D207/34C07D231/14C07D317/68C07H15/22C07H15/26A23V2002/00
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Quick Facts
Patent No.
US 11,793,823
App. No.
17/699,784
Granted
Oct 24, 2023
Kind
B2
Abstract

A compound of Formula (I): or a pharmaceutically acceptable salt thereof, in which Ring X is a 3 to 7 membered monocyclic ring, at least one of R 1 , R 2 , R 3 , and R 4 is OR 5 or CH 2 OR 5 and the other R 1 , R 2 , R 3 , and R 4 each independently are halogen, OH, OR 5 , CH 2 OR 5 , CO 2 H, OC═OR 6 , (C═O)R 6 , R 6 , C1-10 alkyl, C2-10 alkenyl, C2-10 alkynyl, H, or absent. Also provided herein are therapeutic uses of the compound of Formula (I).

Claims (20)

1. A compound of Formula (III), or a pharmaceutically acceptable salt thereof:

wherein the compound is of Formula (III)

 in which R 4 is of the formula

 and each of R 1 , R 2 , and R 3 , independently, is selected from the group consisting of:

each of n and o being, independently, 0 or 1; and each of m and p being, independently, 1, 2, 3, 4, or 5.

2. The compound of claim 1 , wherein each of R 1 , R 2 , R 3 , and R 4 , is, independently, unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents selected from the group consisting of C 1-3 alkyl, halogen, —CF 3 , —CN, —NO 2 , —SH, —OH, —S(C 1-3 alkyl), —NH 2 , NH(C 1-3 alkyl), N(C 1-3 alkyl) 2 , and —O(C 1-3 alkyl).

3. The compound of claim 1 , wherein the compound is of Formula (III) and wherein R 4 is selected from the group consisting of

and

wherein each of R 1 , R 2 , and R 3 , independently, is selected from the group consisting of

4. The compound of claim 3 , wherein the compound of Formula (III) is α-Rib-8G, α-Rib-12G, α-Rib-16G, α-Rib-20G, α-Rib-24G, β-Rib-8G, β-Rib-12G, β-Rib-16G, β-Rib-20G, or β-Rib-24G.

5. A composition, comprising one or more compounds of claim 1 and a carrier.

6. The composition of claim 5 , wherein the composition is a nutraceutical composition, a health food, or a medical food.

7. A method of inhibiting D-amino acid oxidase (DAAO) in a subject, comprising administering to a subject in need thereof an effective amount of the composition of claim 5 .

8. The method of claim 7 , wherein the subject is a human having, suspected of having, or at risk for a central nervous system (CNS) disorder or a metabolic disorder.

9. The method of claim 8 , wherein the CNS disorder is selected from the group consisting of schizophrenia, psychotic disorders, Alzheimer's disease, frontotemporal dementia, vascular dementia, dementia with Lewy bodies, senile dementia, mild cognitive impairment, benign forgetfulness, closed head injury, autistic spectrum disorder, Asperger's disorder, fragile X syndrome, attention deficit hyperactivity disorders, attention deficit disorder, obsessive compulsive disorder, tic disorders, childhood learning disorders, premenstrual syndrome, depression, major depressive disorder, anhedonia, suicidal ideation and/or behaviors, bipolar disorder, anxiety disorders, panic disorder, post-traumatic stress disorder, chronic mild and unpredictable stress, eating disorders, addiction disorders, personality disorders, Parkinson's disorder, Huntington's disorder, multiple sclerosis, amyotrophic lateral sclerosis, ataxia, Friedreich's ataxia, Tourette's syndrome, nocturnal enuresis, non-epileptic seizures, blepharospasm, Duchenne muscular dystrophy, and stroke.

10. The method of claim 8 , wherein the metabolic disorder is selected from the group consisting of obesity, hyperlipidemia, hypercholesterolemia, hyperglycemia, hyperinsulinemia, insulin resistance, and diabetes.

11. The method of claim 9 , wherein the human subject is further treated by one or more additional pharmaceutical agents for treating and/or reducing the risk for a CNS disorder.

12. The method of claim 8 , wherein the composition is administered to the subject by oral administration, by injection, by topical administration, or by inhalation.

13. The method of claim 8 , wherein the composition is placed in a medical device selected from the group consisting of an inhaler, a nebulizer, a nasal spray, and a vaporization aerosol device for administration to the subject.

14. The method of claim 8 , wherein the subject is administered the composition continuously or at a frequency of every five minutes to one time every three months.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2022
From: TSAI, GUOCHUAN EMIL; MAO, YI-WEN; LU, LU-PING; CHANG, WEI-HUA; HSIEH, HAN-YI; HU, JHE WEI; SHIH, TSAI-MIAO; HUANG, CHANHUI
To: SYNEURX INTERNATIONAL (TAIWAN) CORP.
Reel/Frame 059574/0449 →
Continuity (3)
Continuation PCTCN2021089301 · Apr 23, 2021
Provisional Application 63014448 · Apr 23, 2020
Related Publication 20220218730A1 · Jul 14, 2022