Methods for inducing anti-anxiety and calming effects in animals and humans
Phenolic compounds with a phenolic molecule to which are covalently linked an oxygen-containing group, a nitrogen or another oxygen containing group, and a C 1 -C 4 alkoxy group, or their precursor compounds, obtainable from monocotyledonous plants, or by chemical synthesis, have been found to calm and/or reduce anxiety and related behaviors and states in humans and animals. Additional chemical compounds of the present invention may include benzoxazinoids-cyclic hydroxyamic acids, lactams, and corresponding glucosides, which may serve as precursors to phenolic compounds. The phenolic compounds and precursors of phenolic compounds of the present invention, at concentrations suitable for human and animal therapeutic use, may be obtained from monocotyledonous plants such as corn in their early growth states which are timely harvested for optimum yield.
1. A process for producing one or more chemical compounds defined as:
wherein “R” represents C 1 -C 4 alkoxy, with the provision the R is in the 4 or 5 ring position;
wherein “n” represents one of the integers 0, 1 or 2;
wherein “B” represents H and “A” represents —OH, —NH 2 or NHCR′, where R′ denotes C 1 -C 4 alkyl; and “B A” represents
or pharmaceutically acceptable salts thereof, the process comprising the steps of:
identifying at least one monocotyledonous plant that is a source of said one or more chemical compounds;
growing said at least one monocotyledonous plant to an immature state;
harvesting said at least one monocotyledonous plant while in the immature state;
drying said at least one monocotyledonous plant at a temperature in a range of about 40° C. to about 45° C. to convert precursor compounds present in the monocotyledonous plant to one or more of the chemical compounds and produce a dried harvested plant containing phenols in total amounts greater than 17.0 mg/gm and combined amounts of 4-hydroxycinnamic acid and 4-hydroxy-3-methoxycinnamic acid totaling no more than 1.5 mg/gm (dry weight); and
obtaining at least one chemical compound from said dried harvested plant.
2. A process as defined in claim 1 , further producing by said process one or more chemical compounds defined as:
wherein “R 1 ” is selected from the group consisting of H and OCH 3 ;
wherein “R 2 ” is selected from the group consisting of H and Glucose (as a glucoside)
wherein “R 3 ” is selected from the group consisting of H, OH, and OCH 3 ; or
pharmaceutically acceptable salts thereof.
3. A process as defined in claim 1 , wherein the source having one or more of the chemical compounds comprises a monocotyledonous plant selected from the group consisting of corn, wheat, barley, rye, oats, rice, sorghum, millet, bamboo, Job's Tears, barley-like grasses, and wild grasses.
4. A process as defined in claim 1 , wherein said monocotyledonous plant is immature corn, Zea mays.
5. A process as defined in claim 4 , wherein said immature corn has been grown to a height between about 45 centimeters and about 122 centimeters.
6. A process as defined in claim 4 , wherein said immature corn has been grown to a height that does not exceed between about 30 centimeters and about 45 centimeters.
7. A process as defined in claim 4 , wherein said immature corn has been grown for less than ten weeks after planting.
8. A process for producing one or more chemical compounds defined as:
wherein “R” represents C 1 -C 4 alkoxy, with stipulation that R is in the 4 or 5 ring position;
wherein “n” represents one of the integers 0, 1 or 2;
or pharmaceutically acceptable salts thereof, the process comprising the steps of:
identifying at least one monocotyledonous plant that is a source of said one or more chemical compounds;
growing said at least one monocotyledonous plant to an immature state;
harvesting said at least one monocotyledonous plant while in the immature state;
drying said at least one monocotyledonous plant at a temperature in a range of about 40° C. to about 45° C. to convert precursor compounds present in the monocotyledonous plant to one or more of the defined chemical compounds and produce a dried harvested plant containing phenols in total amounts greater than 17.0 mg/gm and combined amounts of 4-hydroxycinnamic acid and 4-hydroxy-3-methoxycinnamic acid totaling no more than 1.5 mg/gm (dry weight); and
obtaining at least one of the chemical compounds from the dried harvested plant.
9. A process as defined in claim 8 , wherein one of said chemical compounds comprise 6-methoxy-2,3-benzoxazolinone defined as:
or one or more pharmaceutically acceptable salts thereof.
10. A process as defined in claim 8 , wherein one of said chemical compounds comprise 5-methoxy-2,3-benzoxazolinone defined as:
or one or more pharmaceutically acceptable salts thereof.
11. A process as defined in claim 8 , wherein the source having one or more of the chemical compounds comprises a monocotyledonous plant selected from the group consisting of corn, wheat, barley, rye, oats, rice, sorghum, millet, bamboo, Job's Tears, barley-like grasses, and wild grasses.
12. A process as defined in claim 8 , wherein said monocotyledonous plant is immature corn, Zea mays.
13. A process as defined in claim 12 , wherein said immature corn has been grown to a height between about 45 centimeters and about 122 centimeters.
14. A process as defined in claim 12 , wherein said immature corn has been grown to a height that does not exceed between about 30 centimeters and about 45 centimeters.
15. A process as defined in claim 12 , wherein said immature corn has been grown for less than ten weeks after planting.
16. A process for producing one or more chemical compounds defined as:
wherein “R 1 ” is selected from the group consisting of H and OCH 3 ;
wherein “R 2 ” is selected from the group consisting of H and Glucose (as a glucoside)
wherein “R 3 ” is selected from the group consisting of H, OH, and OCH 3 ; or
pharmaceutically acceptable salts thereof, the process comprising the steps of:
identifying at least one monocotyledonous plant that is a source of said one or more chemical compounds;
growing said at least one monocotyledonous plant to an immature state;
harvesting said at least one monocotyledonous plant while in the immature state;
drying said at least one monocotyledonous plant in the immature state at a temperature in the range of between about 40° C. and about 45° C. so as to convert precursor compounds present in said at least one monocotyledonous plant to one or more of the chemical compounds and maximize conversion of precursors into active molecules; and
obtaining at least one of the chemical compounds from a dried harvested plant.
17. A process as defined in claim 16 , wherein the source having one or more of the chemical compounds comprises a monocotyledonous plant selected from the group consisting of corn, wheat, barley, rye, oats, rice, sorghum, millet, bamboo, Job's Tears, barley-like grasses, and wild grasses.
18. A process as defined in claim 16 , wherein said monocotyledonous plant is immature corn, Zea mays.
19. A process as defined in claim 18 , wherein said immature corn has been grown to a height between about 45 centimeters and about 122 centimeters.
20. A process as defined in claim 18 wherein said immature corn has been grown to a height that does not exceed between about 30 centimeters and about 45 centimeters.
21. A process as defined in claim 18 , wherein said immature corn has been grown for less than ten weeks after planting.
22. A process as defined in claim 16 , wherein said dried harvested plant contains phenols in total amounts greater than 17.0 mg/gm (dry weight).
23. A process as defined in claim 16 , wherein said dried harvested plant contains combined amounts of 4-hydroxycinnamic acid and 4-hydroxy-3-methoxycinnamic acid totaling no more than 1.5 mg/gm (dry weight).
24. A process for producing one or more chemical compounds defined as:
wherein “R” represents C 1 -C 4 alkoxy, with the provision the R is in the 4 or 5 ring position;
wherein “n” represents one of the integers 0, 1 or 2;
wherein “B” represents H and “A” represents —OH, —NH 2 or NHCR′, where R′ denotes C 1 -C 4 alkyl; and “B A” represents
or pharmaceutically acceptable salts thereof, the process comprising the steps of:
identifying a monocotyledonous plant that is a source of one or more of the chemical compounds;
growing the monocotyledonous plant for a period less than ten weeks after planting and to a height between about 45 centimeters and about 122 centimeters;
harvesting the monocotyledonous plant;
drying the monocotyledonous plant at a temperature in the range of between about 40° C. and about 45° C. to convert precursor compounds present in said at least one monocotyledonous plant to one or more of the chemical compounds and maximize conversion of precursors to active molecules; and
obtaining at least one of the chemical compounds from a dried harvested plant.