Binge behavior regulators
Methods and compositions utilizing 2-aminoindan derivatives collectively represented by Formula I as described and defined in the specification for regulating binge behavior, particularly binge drinking, are disclosed.
1. A method of regulating consumption of an alcoholic beverage, comprising administering to a subject in need thereof a pharmaceutically acceptable salt of a compound represented by Formula I, or a composition comprising the same:
wherein:
each of R 1 and R 2 is independently selected from the group consisting of H, (C 1 -C 8 )alkyl, (C 2 -C 4 )alkenyl, (C 2 -C 8 )alkynyl, (C 3 -C 8 )cycloalkyl, aryl, heteroaryl, heteroalicyclic, —O(C 1 -C 6 )alkyl, OH, —OS(═O) 2 —(C 1 -C 6 )alkyl, S(═O)R 5 , —CO 2 R 5 , —CONR 5 R 6 , —COR 5 , —CF 3 , CN, —SR 5 , —SO 2 NR 5 R 6 , —SO 2 R 5 , —OCO—(C 1 -C 6 )alkyl, —NCO—(C 1 -C 6 )alkyl, —CH 2 O—(C 1 -C 6 )alkyl, —(C 1 -C 6 )alkyl-OH, and halogen, or, alternatively, R 1 and R 2 together with two or more of the phenyl carbon atoms form a X 1 —(CR 5 R 6 )m—X 2 -ring, wherein each of X 1 and X 2 is independently selected from O, NH or S and m is 1, 2, 3, or 4;
each of R 3 and R 4 is independently selected from the group consisting of H, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, (C 3 -C 8 ) cycloalkyl, and —(CH 2 )p-thienyl, wherein p is 1, 2, 3, or 4, wherein at least one of R 3 and R 4 is H; and
each of R 5 and R 6 is independently selected from the group consisting of H, (C 1 -C8)alkyl, (C 2 -C 8 )alkenyl, (C 3 -C 8 )cycloalkyl and aryl,
thereby regulating the consumption of the alcoholic beverage.
2. The method of claim 1 , wherein the consumption of the alcoholic beverage is associated with binge drinking.
3. The method of claim 1 , wherein an amount of alcohol consumption during a drinking session is reduced.
4. The method of claim 1 , wherein the pharmaceutically acceptable salt of the compound is administered before, simultaneously with, or subsequent to, consumption of the alcoholic beverage.
5. The method of claim 1 , wherein the pharmaceutically acceptable salt of the compound is administered simultaneously with the alcoholic beverage.
6. The method of claim 5 , wherein the pharmaceutically acceptable salt of the compound is incorporated in the alcoholic beverage.
7. The method according to claim 6 , wherein the amount of the pharmaceutically acceptable salt of the compound is in a range selected from 0.15 mg/ml to 0.60 mg/ml, 0.15 mg/ml to 0.5 mg/ml, 0.15 mg/ml to 0.40 mg/ml, 0.18 to 0.50 mg/ml, 0.18 to 0.40 mg/ml, 0.20 to 0.40 mg/ml, 0.20 to 0.30 mg/ml, 0.20 to 0.25 mg/ml, or 0.20 to 0.23 mg/ml.
8. The method of claim 1 , wherein at least one of R 3 and R 4 is H.
9. The method of claim 1 , wherein the pharmaceutically acceptable salt of the compound of Formula I is the pharmaceutically acceptable salt of:
5-methoxy-2-aminoindan;
5,6-dimethoxy-2-aminoindan; or
5-methoxy-2-(N-propylamino) indan.
10. The method of claim 9 , wherein the pharmaceutically acceptable salt of the compound of Formula I is the pharmaceutically acceptable salt of: 5-methoxy-2-aminoindan.
11. The method of claim 9 , wherein the pharmaceutically acceptable salt of the compound is formulated as a free-flowing powder, a tablet, a capsule, a lozenge, a liquid, a liquid concentrate, or a syrup.
12. The method of claim 1 , wherein the composition is a unit dosage form composition.
13. The method of claim 12 , wherein an amount of the pharmaceutically acceptable salt of the compound in the unit dosage form ranges from 30 mg to 130 mg.
14. The method of claim 13 , wherein the amount of the pharmaceutically acceptable salt of the compound in the unit dosage form is 70 mg.
15. The method of claim 1 , wherein the pharmaceutically acceptable salt of the compound is administered to the subject orally.
16. The method of claim 1 , wherein the pharmaceutically acceptable salt is an acid addition salt.
17. The method of claim 16 , wherein the acid addition salt is a hydrochloric acid addition salt, a hydrobromic acid addition salt, ascorbic acid addition salt, a besylate addition salt, a camphorsulfonic acid addition salt, a citric acid addition salt, a malic addition salt, a methanesulfonic acid addition salt, a naphthalenesulfonic acid addition salt, an oxalic acid addition salt, a phosphoric acid addition salt, a p-toluenesulfonic acid addition salt, a p-succinic acid addition salt, a p-sulfuric acid addition salt, a p-tartaric acid addition salt, or a p-trifluoroacetic acid addition salt.
18. A method of regulating binge behavior, comprising administrating to a subject in need thereof a pharmaceutically acceptable salt of a compound represented by Formula I:
wherein:
each of R 1 and R 2 is independently selected from the group consisting of H, (C 1 -C 8 )alkyl, (C 2 -C 4 )alkenyl, (C 2 -C 8 )alkynyl, (C 3 -C 8 )cycloalkyl, aryl, heteroaryl, heteroalicyclic, —O(C 1 -C 6 )alkyl, OH, —OS(═O) 2 -(C 1 -C 6 )alkyl, —S(═O)R 5 , —CO 2 R 5 , —CONR 5 R 6 , —COR 5 , —CF 3 , CN, —SR 5 , —SO 2 NR 5 R 6 , —SO 2 R 5 , —OCO—(C 1 -C 6 )alkyl, —NCO—(C 1 -C 6 )alkyl, —CH 2 O—(C 1 -C 6 )alkyl, —(C 1 -C 6 )alkyl-OH, and halogen, or, alternatively, R 1 and R 2 together with two or more of the phenyl carbon atoms form a X 1 —(CR 5 R 6 ) m—X 2 -ring, wherein each of X 1 and X 2 is independently selected from O, NH or S and m is 1, 2, 3, or 4;
each of R 3 and R 4 is independently selected from the group consisting of H, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, (C 3 -C 8 )cycloalkyl, and —(CH 2 )p— thienyl, wherein p is 1, 2, 3, or 4, wherein at least one of R 3 and R 4 is H; and
each of R 5 and R 6 is independently selected from the group consisting of H, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 3 -C 8 )cycloalkyl and aryl,
thereby regulating the binge behavior.
19. The method of claim 18 , wherein the pharmaceutically acceptable salt is an acid addition salt.
20. The method of claim 19 , wherein the acid addition salt is a hydrochloric acid addition salt, a hydrobromic acid addition salt, ascorbic acid addition salt, a besylate addition salt, a camphorsulfonic acid addition salt, a citric acid addition salt, a malic addition salt, a methanesulfonic acid addition salt, a naphthalenesulfonic acid addition salt, an oxalic acid addition salt, a phosphoric acid addition salt, a p-toluenesulfonic acid addition salt, a p-succinic acid addition salt, a p-sulfuric acid addition salt, a p-tartaric acid addition salt, or a p-trifluoroacetic acid addition salt.