Back to results
US 2002/0120149 A1Published application
Substituted hydrazine derivatives
OwnerSyed M. Ali, Kurt R. Brunden +4inventors
InventorsSyed M. Ali, Kurt R. Brunden, Dario Doller, Brian Herbert, Jack B. Jiang, Amy Jordan
Life of this patent
Estimating the term…
Abstract
A method for the inhibition of high affinity glycine transporters, compounds that inhibit these transporters; pharmaceutically active compositions comprising such compounds; and the use of such compounds either as above, or in formulations for the control or prevention of disease states in which glycine is involved are disclosed.
Claims12
A compound of the structure
- 38
- wherein R1 and R4 are each independently an aryl group;
- and
- R2 and R3 are each independently selected from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, alkoxy, alkenoxy, alkynoxy, aliphatic acyl, —C1-C3 alkylamino, alkenylamino, alkynylamino, di(C1-C3 alkyl)amino, —C(O)O—(C1-C3 alkyl), —C(O)NH—(C1-C3 alkyl), —CH═NOH, —C(O)N(C1-C3 alkyl)2, haloalkyl, alkoxycarbonyl, alkoxyalkoxy, carboxaldehyde, carboxamide, cycloalkyl, cycloalkenyl, cycloalkynyl, aryl, aroyl, aryloxy, arylamino, biaryl, thioaryl, heterocyclyl, heterocycloyl, alkylaryl, aralkenyl, aralkyl, alkylheterocyclyl, heterocyclylalkyl, —SO2—(C1-C3 alkyl), —SO3—(C1-C3 alkyl), sulfonamido, carbamate, aryloxyalkyl, carboxyl, —C(O)NH(benzyl) and —(CH2)tR5;
- wherein R5 is selected from the group consisting of hydrogen, amino, hydroxy, alkoxy, aliphatic acyl, —CN, carboxyl, carboxamide, alkoxycarbonyl, —C(O)NHOH, —C(O)NHNH2 and carboxaldehyde;
- and
- t is an integer of one to four;
- wherein R1, R2, R3, R4and R5 are unsubstituted or substituted with at least one electron donating or electron withdrawing group;
- and wherein R2 and R3 taken together may form a ring;
- and pharmaceutically acceptable salts thereof.
7 more elements
Dependencies are inferred from the claim text.