The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jan. 05, 1993

Filed:

Jul. 19, 1991
Applicant:
Inventors:

Roberto Pellicciari, Perugia, IT;

Benedetto Natalini, Perugia, IT;

Maura Marinozzi, Fermo, IT;

Alexis A Cordi, St. Louis, MO (US);

Joseph B Monahan, Black Jack, MO (US);

Thomas H Lanthorn, Ballwin, MO (US);

Assignee:

G. D. Searle & Co., Chicago, IL (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
A61K / ;
U.S. Cl.
CPC ...
514572 ; 514484 ; 514513 ; 514531 ; 514562 ; 514563 ; 514570 ; 514616 ; 558251 ; 558254 ; 558255 ; 560-1 ; 560 16 ; 560 38 ; 560 39 ; 560 41 ; 560105 ; 560106 ; 560115 ; 560118 ; 560122 ; 560123 ; 560124 ; 560250 ; 562426 ; 562443 ; 562444 ; 562450 ; 562500 ; 562506 ; 564153 ; 564154 ; 564155 ; 564157 ;
Abstract

Compounds, compositions and methods are described for treating a CNS disorder such as a cognitive disorder, epilepsy, depression, Parkinson's disease, Alzheimer's disease, a neurodegenerative disease or neurotoxic injury. Compound of interest are 2-amino-4,5-methyleneadipic acid compounds and derivatives defined by the formula I: ##STR1## wherein R.sup.1 is selected from hydrido, alkyl, cycloalkyl, aralkyl, aryloxyalkyl, arylthioalkyl, ##STR2## with each of R.sup.2, R.sup.3, R.sup.4 and R.sup.5 being independently selected from hydrido, alkyl, cycloalkyl, aryl and aralkyl; wherein each of X and Y is independently selected from hydroxyl, alkoxy, alkylthio, amino and ##STR3## with each of R.sup.6 and R.sup.7 being independently selected from hydrido, alkyl, cycloalkyl, aryl and aralkyl; wherein any of R.sup.1 through R.sup.7 groups having a substitutable position may be substituted with one or more substituents selected from hydroxyl, halo, alkyl, haloalkyl, cyano, alkoxy, alkylthio, sulfinyl, sulfonyl, sulfinylalkyl, sulfonylalkyl, amino, acyl, acyloxy, alkoxycarbonyl and aminocarbonyl; or a pharmaceutically-acceptable salt thereof.


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