Abstract: The present invention is directed to the use of esters of hexahydro-8-hydroxy-2,6-methano-2H-quinolizin-3(4H)-one and hexahydro-8-hydroxy-2,6-methano-2H-quinolizines in the manufacture of a medicament for producing an orexigenic effect.
Abstract: The present invention relates to piperidyl sulfonamides and sulfoxamides which are useful as inhibitors of cholesterol biosynthesis and as agents which lower total serum cholesterol in patients in need thereof.
Type:
Grant
Filed:
December 18, 1992
Date of Patent:
September 27, 1994
Assignee:
Merrell Dow Pharmaceuticals Inc.
Inventors:
Marion W. Wannamaker, William A. VanSickle, William R. Moore
Abstract: The present invention relates to certain novel piperidyl ethers and thioethers which are useful as inhibitors of cholesterol biosynthesis and as agents which lower total serum cholesterol in patients in need thereof.
Type:
Grant
Filed:
July 15, 1993
Date of Patent:
September 20, 1994
Assignee:
Merrell Dow Pharmaceuticals Inc.
Inventors:
Charlotte L. Barney, James R. McCarthy, Marion W. Wannamaker
Abstract: The present invention pertains to a process for producing a 2-imidazolone from a ureidoacetal. The ureidoacetal is subjected to an acid catalyzed condensation in order to produce the 2-imidazolone. The reaction is conducted in an alcoholic solvent in order to minimize the production of a polymeric by-product.
Abstract: This invention relates to the enhancement of memory and cognition and the treatment of Alzheimer's disease and Wernicke-Korsakoff syndrome by administration of 5-(R.sub.n -phenyl)-4-alkyl-3H-1,2,4-triazole-3-thiones of the formula ##STR1## wherein R is halogen, trifluoromethyl, C.sub.1-4 lower alkyl orC.sub.1-4 lower alkoxy,n is zero, 1 or 2, andR.sub.2 represents hydrogen or C.sub.1-3 lower alkyl; andR.sub.4 independently represents C.sub.1-3 lower alkyl.
Abstract: Adenosine analogues which act selectively at adenosine receptors and which act in general as adenosine antagonists are disclosed. From in vitro studies it is known that specific physiological effects can be distinguished as a result of this selectivity and that adenosine receptor activity in vitro correlates with adenosine receptor activity in vivo.Pharmaceutical preparations of the subject compounds can be prepared on the basis of the selective binding activity of the compounds disclosed herein which will enhance certain physiological effects while minimizing others, such as decreasing blood pressure without decreasing heart rate.
Abstract: The present invention is directed to gelatin treated polyhydric alcohol compositions, their preparation, and to pharmaceutical lozenges prepared therefrom. The pre-granulation of a polyhydric alcohol with an aqueous gelatin solution prior to compression, produces lozenges having a delayed rate of dissolution.
Abstract: Controlled release pharmaceutical beads are provided having a multi-layered core and a multi-layered periphery. The core contains at least (A) an inner portion having a suitable organic acid and (B) a sustainably-acid-releasing coating thereover. The periphery contains at least (A) an inner portion having a mixture of at least (i) a pharmaceutical compound and (ii) a surface-active agent, and (B) a sustainably-drug-releasing exterior coating.
Type:
Grant
Filed:
December 22, 1992
Date of Patent:
June 14, 1994
Assignee:
Merrell Dow Pharmaceuticals Inc.
Inventors:
Kazuo Noda, Yoshiyuki Hirakawa, Hiroyuki Yoshino, David D. MacLaren, Paul F. Skultety, John R. Lefler, Greg M. Beck
Abstract: The present invention relates to 4-amino-.DELTA..sup.4 -steroids which are inhibitors of 5.alpha.-reductase. The compounds are useful for treating DHT-mediated diseases.
Type:
Grant
Filed:
December 20, 1992
Date of Patent:
June 7, 1994
Assignee:
Merrell Dow Pharmaceuticals Inc.
Inventors:
Philip M. Weintraub, Joseph P. Burkhart, Thomas R. Blohm
Abstract: The present invention relates to a method of effecting immunosuppression in a patient in need thereof comprising administering to said patient an effective immunosuppressive amount of certain 5'-amine substituted adenosine analogs.
Abstract: The present invention relates to compounds of the formula ##STR1## wherein A is methylene, oxygen, sulfur or N-B wherein B is R.sub.1 or COR.sub.2 wherein R.sub.1 is hydrogen, a C.sub.1 -C.sub.4 alkyl or an Ar-Z-group wherein Ar is aryl and Z is a C.sub.0 -C.sub.4 alkyl and R.sub.2 is a --CF.sub.3, a C.sub.1 -C.sub.10 alkyl or an Ar-Z group;R is hydrogen or a C.sub.1 -C.sub.
Abstract: The present invention is directed towards a process for producing a superior tasting pharmaceutical composition having porous granules produced through in situ gas generation using effervescence-producing ingredients. The method disclosed herein is especially suitable for producing superior tasting antacid tablets as well as superior tasting calcium supplements.
Type:
Grant
Filed:
May 12, 1992
Date of Patent:
April 12, 1994
Assignee:
Merrell Dow Pharmaceuticals Inc.
Inventors:
Deepak S. Phadke, Melissa P. Neddermeyer
Abstract: The present invention is directed to a new class of piperidinyl medicinal agents which are useful as antithrombotic agents and as serotonin 5HT.sub.2 antagonists.
Type:
Grant
Filed:
March 5, 1992
Date of Patent:
March 8, 1994
Assignee:
Merrell Dow Pharmaceuticals Inc.
Inventors:
Albert A. Carr, Richard C. Dage, John E. Koerner, Tung Li, Francis P. Miller, Thaddeus R. Nieduzak
Abstract: The present invention pertains to a new class of compounds which can be characterized as 1,4-disubstituted piperidinyl compounds useful as antiarrhythmics, analgesics, and serotonin 5HT.sub.2 antagonists.
Type:
Grant
Filed:
February 14, 1992
Date of Patent:
February 15, 1994
Assignee:
Merrell Dow Pharmaceuticals Inc.
Inventors:
Albert A. Carr, John E. Koerner, Richard C. Dage, Tung Li
Abstract: This invention relates to certain conjugates of folates and antifolates with difluoroglutamic acid which are useful in the treatment of patients suffering from certain neoplastic diseases including leukemia, melanomas, carcinomas, sarcomas and mixed neoplasias.
Type:
Grant
Filed:
April 12, 1990
Date of Patent:
February 15, 1994
Assignees:
The Regents of the University of Michigan, Health Research, Inc., Merrell Dow Pharmaceuticals Inc.
Inventors:
Philippe Bey, James K. Coward, John J. McGuire
Abstract: The present invention relates to certain bis[4-(2,6-dialkyl)phenol]silane derivatives which are useful as inhibitors of LDL lipid peroxidation and as antiatherosclerotic agents.