Claims
- 1. A terpene amino alcohol of the formula ##STR202## wherein X.sup.1 is a hydrogen atom or a hydroxyl group and Y.sup.1 is a hydrogen atom, or X.sup.1 and Y.sup.1 taken together represent a bond; X.sup.2 is a hydrogen atom or a hydroxyl group and Y.sup.2 is a hydrogen atom, or X.sup.2 and Y.sup.2 taken together represent a bond; Q.sup.1 and Q.sup.2 are such that either one is Y.sup.3 with the other being ##STR203## and X.sup.3 is a hydrogen atom or a hydroxyl group; Y.sup.3 is a hydroxyl group when X.sup.3 is a hydrogen atom, or Y.sup.3 is a hydrogen atom or a hydroxyl group when X.sup.3 is a hydroxyl group; R.sup.1 and R.sup.2 may be the same or different and each is a hydrogen atom, a lower alkyl group which may be substituted, an aryl group which may be substituted or a 4-piperidinyl group which may be substituted, provided that at least one of R.sup.1 and R.sup.2 is a 4-piperidinyl group which may be substituted, or R.sup.1 and R.sup.2 taken together with the adjacent nitrogen atom form a piperidino group; and n is an integer of 0 to 2; or a pharmacologically acceptable ester or salt thereof.
- 2. The compound according to claim 1, which is 3,7-dimethyl-1-piperidino-6-octene-2,3-diol.
- 3. The compound according to claim 1, which is 1-piperidino-3,7,11-trimethyl-2,3-dodecanediol.
- 4. The compound according to claim 1, which is 1-[(1-benzylpiperidin-4-yl)amino]-3,7,11-trimethyl-2,3-dodecanediol.
- 5. The compound according to claim 1, which is 3,7-dimethyl-2-piperidino-6-octene-1,3-diol.
- 6. The compound according to claim 1, which is 2-[(1-benzylpiperidin-4-yl)amino]-3,7,11-trimethyl-1,3-dodecanediol.
- 7. A pharmaceutical composition for the prevention or treatment of allergic diseases or disorders of cerebral function, which comprises an amount, effective for the prevention or treatment of said allergic diseases or disorders of cerebral function, of a terpene amino alcohol of the formula ##STR204## wherein X.sup.1 is a hydrogen atom or a hydroxyl group and Y.sup.1 is a hydrogen atom, or X.sup.1 and Y.sup.1 taken together represent a bond; X.sup.2 is a hydrogen atom or a hydroxyl group and Y.sup.2 is a hydrogen atom, or X.sup.2 and Y.sup.2 taken together represent a bond; Q.sup.1 and Q.sup.2 are such that either one is Y.sup.3 with the other being ##STR205## and X.sup.3 is a hydrogen atom or a hydroxyl group; Y.sup.3 is a hydroxyl group when X.sup.3 is a hydrogen atom, or Y.sup.3 is a hydrogen atom or a hydroxyl group when X.sup.3 is a hydroxyl group; R.sup.1 and R.sup.2 may be the same or different and each is a hydrogen atom, a lower alkyl group which may be substituted, an aryl group which may be substituted or a 4-piperidinyl group which may be substituted, provided that at least one of R.sup.1 and R.sup.2 is a 4-piperidinyl group which may be substituted, or R.sup.1 and R.sup.2 taken together with the adjacent nitrogen atom form a piperidino group; and n is an integer of 0 to 2; or a pharmacologically acceptable ester or salt thereof; and a pharmacologically acceptable carrier or diluent therefor.
- 8. The composition according to claim 7, wherein the terpene amino alcohol is 3,7-dimethyl-1-piperidino-6-octene-2,3-diol.
- 9. The composition according to claim 7, wherein the terpene amino alcohol is 1-piperidino-3,7,11-trimethyl-2,3-dodecanediol.
- 10. The composition according to claim 7, wherein the terpene amino alcohol is 1-[(1-benzylpiperidin-4-yl)amino]-3,7,11-trimethyl-2,3-dodecanediol.
- 11. The composition according to claim 7, wherein the terpene amino alcohol is 3,7-dimethyl-1-piperidino-6-octene-1,3-diol.
- 12. The composition according to claim 7, wherein the terpene amino alcohol is 2-[(1-benzylpiperidin-4-yl)amino]-3,7,11-trimethyl-2,3-dodecanediol.
- 13. A method for preventing or treating allergic diseases or disorders of cerebral function which comprises administering to an animal in need thereof an effective amount for the prevention or treatment of said allergic diseases or disorders of cerebral function of a terpene amino alcohol of the formula ##STR206## wherein X.sup.1 is a hydrogen atom or a hydroxyl group and Y.sup.1 is a hydrogen atom, or X.sup.1 and Y.sup.1 taken together represent a bond; X.sup.2 is a hydrogen atom or a hydroxyl group and Y.sup.2 is a hydrogen atom, or X.sup.2 and Y.sup.2 taken together represent a bond; Q.sup.1 and Q.sup.2 are such that either one is Y.sup.3 with the other being ##STR207## and X.sup.3 is a hydrogen atom or a hydroxyl group; Y.sup.3 is a hydroxyl group when X.sup.3 is a hydrogen atom, or Y.sup.3 is a hydrogen atom or a hydroxyl group when X.sup.3 is a hydroxyl group; R.sup.1 and R.sup.2 may be the same or different and each is a hydrogen atom, a lower alkyl group which may be substituted, an aryl group which may be substituted or a 4-piperidinyl group which may be substituted, provided that at least one of R.sup.1 and R.sup.2 is a 4-piperidinyl group which may be substituted, or R.sup.1 and R.sup.2 taken together with the adjacent nitrogen atom form a piperidino group; and n is an integer of 0 to 2; or a pharmacologically acceptable ester or salt thereof.
- 14. The method according to claim 13, wherein the terpene amino alcohol is 3,7-dimethyl-1-piperidino-6-octene-2,3-diol.
- 15. The method according to claim 13, wherein the terpene amino alcohol is 1-piperidino-3,7,11-trimethyl-2,3-dodecanediol.
- 16. The method according to claim 13, wherein the terpene amino alcohol is 1-[(1-benzylpiperidin-4-yl)amino]-3,7,11-trimethyl-2,3-dodecanediol.
- 17. The method according to claim 13, wherein the terpene amino alcohol is 3,7-dimethyl-1-piperidino-6-octene-1,3-diol.
- 18. The method according to claim 13, wherein the terpene amino alcohol is 2-[(1-benzylpiperidin-4-yl)amino]-3,7,11-trimethyl-2,3-dodecanediol.
Priority Claims (3)
Number |
Date |
Country |
Kind |
60-160782 |
Jul 1985 |
JPX |
|
61-50784 |
Mar 1986 |
JPX |
|
61-84822 |
Apr 1986 |
JPX |
|
Parent Case Info
This application is a divisional of application Ser. No. 07/887,431, filed Jul. 21, 1986, now U.S. Pat. No. 4,946,857.
Non-Patent Literature Citations (4)
Entry |
Susumu et al. Chem. Abstracts, vol. 97(15); 127837m (1982). |
Koichi et al. Chem. Abstrcts, vol. 106, 17; 131715s (1987). |
Susumu et al. Chem. Abstracts, vol. 97, 23; 198413f (1982). |
Takasago Perfumery Co., Chem. Abstracts, vol. 95, 3; 25331h (1981). |
Divisions (1)
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Number |
Date |
Country |
Parent |
887431 |
Jul 1986 |
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