Abstract: Substituted imidazoles attached through a methylene bridge to novel substituted phenyl derivatives of the Formula I, are useful as angiotensin II antagonists.
Type:
Grant
Filed:
August 13, 1991
Date of Patent:
February 2, 1993
Assignee:
Merck & Co., Inc.
Inventors:
William J. Greenlee, Arthur A. Patchett, David Hangauer, Thomas F. Walsh, Kenneth J. Fitch, Ralph A. Rivero, Daljit S. Dhanoa
Abstract: A dispenser for liquids, e.g., ophthalmic liquids, is provided with a movable top that rotates to uncover an aperture and to expose a recessed dispensing tip.
Abstract: Substituted triazoles attached through a methylene bridge to novel substituted phenyl derivatives of the Formula I, are useful as angiotensin II antagonists.
Type:
Grant
Filed:
August 13, 1991
Date of Patent:
January 5, 1993
Assignee:
Merck & Co., Inc.
Inventors:
William J. Greenlee, Arthur A. Patchett, David Hangauer, Wallace Ashton, Kenneth J. Fitch, Thomas F. Walsh, Ralph A. Rivero, Daljit S. Dhanoa
Abstract: Substituted heterocycles attached through a methylene bridge to novel substituted indole or dihydroindole derivative of the Formula I are useful as angiotensin II antagonists.
Type:
Grant
Filed:
June 5, 1991
Date of Patent:
December 29, 1992
Assignee:
Merck & Co., Inc.
Inventors:
Scott Bagley, William J. Greenlee, Daljit S. Dhanoa, Arthur A. Patchett
Abstract: Intermediates are described for preparing conformationally constrained tricyclic thienothiopyran compounds that are topically effective carbonic anhydrase inhibitors useful in the treatment of ocular hypertension and glaucoma associated therewith.
Type:
Grant
Filed:
October 15, 1991
Date of Patent:
December 29, 1992
Assignee:
Merck & Co., Inc.
Inventors:
John J. Baldwin, Gerald S. Ponticello, Kenneth L. Shepard, Theresa M. Williams
Abstract: Substituted pyrimidines, pyrimidinones and pyridopyrimidines of formula (I) are as angiotensin II antagonists useful in the treatment of hypertension, ocular hypertension and certain CNS ailments: ##STR1## wherein K is --N(R.sup.8a)--C(.dbd.M) or --N.dbd.C(R.sup.8b) where M is O or NR.sup.22.
Type:
Grant
Filed:
March 27, 1991
Date of Patent:
November 24, 1992
Assignee:
Merck & Co., Inc.
Inventors:
Eric E. Allen, William J. Greenlee, Malcolm MacCoss, Arthur A. Patchett
Abstract: There are disclosed new substituted imidazo-fused 5-membered ring heterocyclic compounds and derivatives thereof which are useful as angiotensin II antagonists.
Type:
Grant
Filed:
April 25, 1990
Date of Patent:
November 17, 1992
Assignee:
Merck & Co., Inc.
Inventors:
William J. Greenlee, David B. R. Johnston, Malcolm MacCoss, Nathan B. Mantlo, Arthur A. Patchett, Prasun K. Chakravarty, Thomas F. Walsh
Abstract: Substituted heterocycles attached through a methylene bridge to novel substituted phenyl derivatives of the Formula I are useful as angiotensin II antagonists.
Type:
Grant
Filed:
May 7, 1991
Date of Patent:
November 10, 1992
Assignee:
Merck & Co., Inc.
Inventors:
Prasun K. Chakravarty, Malcolm MacCoss, Nathan Mantlo, Thomas F. Walsh
Abstract: Substituted 1-(2H)-isoquinolinones of the structural formula: ##STR1## are angiotensin II antagonists which are useful in the treatment of hypertension and congestive heart failure.
Type:
Grant
Filed:
May 10, 1991
Date of Patent:
November 10, 1992
Assignee:
Merck & Co., Inc.
Inventors:
Prasun K. Chakravarty, William J. Greenlee, Nathan B. Mantlo, Arthur A. Patchett, Dooseop Kim
Abstract: A sterile packaging assembly (100) for dispensing a liquid in drops comprises a main body (101) of plastic material, having a top portion (103) with an outside thread for receiving a screw cap (104), and containing a flow rate restriction system (105) for controlling drop formation. The flow rate restriction system is positioned substantially on the axis of the main body and is held in position by a constricted portion (106) of the top portion (103) of the main body. The invention is particularly applicable to sterile packaging of pharmaceutical substances such as eye drops.
Abstract: A sterile packaging assembly (100) for dispensing a liquid in drops comprises a main body (101) of plastic material, having a top portion (103) with an outside thread for receiving a screw cap (104), the top portion ending in an elongate neck, constituting a dispensing portion which is surmounted by a closure head (110) that can be torn off in order to define a dispensing orifice (111) on first utilization of the packaging assembly. The invention is particularly applicable to sterile packaging of pharmaceutical substances such as eye drops.
Abstract: Substituted quinolines of the formula (I), are angiotensin II antagonists, ##STR1## and useful in the treatment of hypertension, ocular hypertension and certain CNS disorders.
Type:
Grant
Filed:
April 5, 1991
Date of Patent:
October 20, 1992
Assignee:
Merck & Co., Inc.
Inventors:
William J. Greenlee, David B. R. Johnston, Malcolm MacCoss
Abstract: Substituted Imidazo-fused 6-membered heterocycles of structural formula: ##STR1## wherein A, B, C, and D are independently carbon atoms or nitrogen atoms are angiotensin II antagonists useful in the treatment of hypertension and congestive heart failure.
Type:
Grant
Filed:
February 24, 1992
Date of Patent:
October 20, 1992
Assignee:
Merck & Co., Inc.
Inventors:
Prasun K. Chakravarty, William J. Greenlee, Nathan B. Mantlo, Arthur A. Patchett, Thomas F. Walsh
Abstract: Topical administration of a cholinomimetic agent, such as pilocarpine, in combination with a cholinergic M.sub.3 receptor antagonist, such as 4-diphenyl-acetoxy-N-methylpiperidine, to the eye of a mammal reduces intraocular pressure without the concommitant miotic effect that normally occurs with administration of a cholinomimetic agent along.
Abstract: Peptide analogues of human humoral hypercalcemic factor (hHCF) that contain a lactam bridge act as inhibitors of the naturally occurring peptide. A lactam bridge between Lys and Asp situated five residues (inclusive) apart confers rigidity to that region of the peptide, and enhances the helical nature and metabolic stability of the peptide analogue.
Abstract: Compounds of structural formula (I): ##STR1## are squalene synthestase inhibitors useful in inhibiting the biosynthesis of cholesterol in the treatment of hypercholesterolemia and related disorders.
Type:
Grant
Filed:
May 17, 1991
Date of Patent:
August 4, 1992
Assignee:
Merck & Co., Inc.
Inventors:
Alfred W. Alberts, Gregory D. Berger, James D. Bergstrom