Claims Analysis
Total Claims: 19
Claim 1
Independent Claim
96 words
A potent selective excitatory amino acid neurotransmitter receptor antagonist having the general formula: ##STR4## wherein R 1 and R 2 are the same or different and are selected from the group consisting of hydrogen, lower alkyl (C 1 to C 6 ), alkyl (C 7 to C 12 ), fatty acid chain (C 13 to C 24 ), aryl, aralkyl, hydroxyl, the stereoisomers being in their resolved or racemic form; n and m=1, 2, or 3 and z=0, 1 or 2; the cycloalkyl ring being replaced with the cycloalkenyl ring; and the pharmaceutically acceptable salts thereof.
Claim 2
Dependent Claim
96 words
A potent selective excitatory amino acid neurotransmitter receptor antagonist having the general formula: ##STR4## wherein R 1 and R 2 are the same or different and are selected from the group consisting of hydrogen, lower alkyl (C 1 to C 6 ), alkyl (C 7 to C 12 ), fatty acid chain (C 13 to C 24 ), aryl, aralkyl, hydroxyl, the stereoisomers being in their resolved or racemic form; n and m=1, 2, or 3 and z=0, 1 or 2; the cycloalkyl ring being replaced with the cycloalkenyl ring; and the pharmaceutically acceptable salts thereof.
Claim 3
Dependent Claim
26 words
The potent selective excitatory amino acid neurotransmitter receptor antagonist of claim 1 where R 1 and R 2 are both hydrogen and n=1, m=2 and z=1.
Claim 4
Dependent Claim
10 words
The compound according to claim 1 that is 3-{2-phosphonoethylcyclohexyl}-2-aminopropanoic acid.
Claim 5
Dependent Claim
10 words
The compound according to claim 1 that is 4-[2-phosphonomethylcyclohexyl]-2-aminobutanoic acid.
Claim 6
Dependent Claim
28 words
A pharmaceutical composition for relieving pain which comprises a pain relieving effective amount of one or more compounds of claim 1 with a pharmaceutically acceptable carrier and/or diluent.
Claim 7
Dependent Claim
35 words
A process of relieving pain in an animal in need thereof which comprises administering said compound of claim 1 or 5 parenterally, nasally, orally, rectally or a combination thereof to said animal in need thereof.
Claim 8
Dependent Claim
29 words
A pharmaceutical composition for treatment of convulsions or epilepsy which comprises an effective amount of one or more compounds of claim 1 with a pharmaceutically acceptable carrier and/or diluent.
Claim 9
Dependent Claim
31 words
A process for treating convulsions or epilepsy which comprises administering said compound of claim 1 or 7 parenterally, orally, nasally, rectally or a combination thereof to said animal in need thereof.
Claim 10
Dependent Claim
27 words
A pharmaceutical composition of enhancing cognition which comprises a cognition enhancing amount of one or more compounds of claim 1 with a pharmaceutically acceptable carrier and/or diluent.
Claim 11
Dependent Claim
29 words
A process of enhancing cognition which comprises administering said compound of claim 1 or 9 parenterally, orally, nasally, rectally or a combination thereof to said animal in need thereof.
Claim 12
Dependent Claim
88 words
A potent, selective excitatory amino acid neurotransmitter receptor antagonist having the general formula: ##STR5## wherein R 1 and R 2 are the same or different and are selected from the group consisting of hydrogen, lower alkyl (C 1 to C 6 ), alkyl (C 7 to C 12 ), fatty acid chain (C 13 to C 24 ), aryl, aralkyl and hydroxyl; the stereoisomers being in their resolved or racemic form; n=1 and m=0, 1, 2 or 3; z=0, 1 or 2; and the pharmaceutically acceptable salts thereof.
Claim 13
Dependent Claim
88 words
A potent, selective excitatory amino acid neurotransmitter receptor antagonist having the general formula: ##STR5## wherein R 1 and R 2 are the same or different and are selected from the group consisting of hydrogen, lower alkyl (C 1 to C 6 ), alkyl (C 7 to C 12 ), fatty acid chain (C 13 to C 24 ), aryl, aralkyl and hydroxyl; the stereoisomers being in their resolved or racemic form; n=1 and m=0, 1, 2 or 3; z=0, 1 or 2; and the pharmaceutically acceptable salts thereof.
Claim 14
Dependent Claim
29 words
The potent, selective excitatory amino acid neurotransmitter receptor antagonist of claim 11 wherein m=1, 2 or 3 and the sum of n+m is a number from 2 to 5.
Claim 15
Dependent Claim
19 words
The potent, selective excitatory amino acid neurotransmitter receptor antagonist of claim 12 wherein the sum of n+m is 3.
Claim 16
Dependent Claim
89 words
A potent, selective excitatory amino acid neurotransmitter receptor antagonist having the general formula: ##STR6## wherein R 1 and R 2 are the same or different and are selected from the group consisting of hydrogen, lower alkyl (C 1 to C 6 ), alkyl (C 7 to C 12 ), fatty acid chain (C 13 to C 24 ), aryl, aralkyl, hydroxyl; the stereoisomers being in their resolved or racemic form; z=0, 1 or 2; the cycloalkyl ring being replaced with the cycloalkenyl ring; and the pharmaceutically acceptable salts thereof.
Claim 17
Dependent Claim
89 words
A potent, selective excitatory amino acid neurotransmitter receptor antagonist having the general formula: ##STR6## wherein R 1 and R 2 are the same or different and are selected from the group consisting of hydrogen, lower alkyl (C 1 to C 6 ), alkyl (C 7 to C 12 ), fatty acid chain (C 13 to C 24 ), aryl, aralkyl, hydroxyl; the stereoisomers being in their resolved or racemic form; z=0, 1 or 2; the cycloalkyl ring being replaced with the cycloalkenyl ring; and the pharmaceutically acceptable salts thereof.
Claim 18
Dependent Claim
98 words
A potent selective excitatory amino acid neurotransmitter receptor antagonist having the general formula: ##STR7## wherein R 1 and R 2 are the same or different and are selected from the group consisting of hydrogen, lower alkyl (C 1 to C 6 ), alkyl (C 7 to C 12 ), fatty acid chain (C 13 to C 24 ), aryl, aralkyl, hydroxyl, the stereoisomers being in their resolved or racemic form; n and m=1, 2, or 3 and z=0, 1 or 2; the cyclic ring is either a cycloalkanyl or a cycloalkenyl ring and the pharmaceutically acceptable salts thereof.
Claim 19
Dependent Claim
98 words
A potent selective excitatory amino acid neurotransmitter receptor antagonist having the general formula: ##STR7## wherein R 1 and R 2 are the same or different and are selected from the group consisting of hydrogen, lower alkyl (C 1 to C 6 ), alkyl (C 7 to C 12 ), fatty acid chain (C 13 to C 24 ), aryl, aralkyl, hydroxyl, the stereoisomers being in their resolved or racemic form; n and m=1, 2, or 3 and z=0, 1 or 2; the cyclic ring is either a cycloalkanyl or a cycloalkenyl ring and the pharmaceutically acceptable salts thereof.