Abstract: Novel angiotensin II receptor antagonists of the formula ##STR1## wherein X, X.sub.1, X.sub.2, R.sub.1, R.sub.2, R.sub.3, R.sub.4 and R.sub.5 are as defined herein, are disclosed. These compounds are useful, for example, in the treatment of hypertension, congestive heart failure and cardiac hypertrophy.
Abstract: Compounds of the formula ##STR1## wherein R.sub.1 is an N-heterocyclic group as defined herein, are disclosed. These compounds are inhibitors of renin and therefore useful as cardiovascular agents.
Abstract: Novel compounds having the formula ##STR1## wherein ##STR2## are disclosed. These compounds have potassium channel activating activity and are useful, for example, as cardiovascular agents, especially as antiischemic agents.
Type:
Grant
Filed:
February 27, 1991
Date of Patent:
August 18, 1992
Assignee:
E. R. Squibb & Sons, Inc.
Inventors:
Karnail Atwal, Gary J. Grover, Kyoung S. Kim
Abstract: In accordance with the present invention an improved tablet composition for drugs or active ingredients prone to poor tabletting properties is disclosed. The improved composition comprises a premixture, consisting essentially of between about 85 and 99.9 percent by weight of the active ingredient and between about 0.1 and 15 percent by weight of citric acid, and one or more other formulation ingredients added to premixture. The present invention also involves the process for making such compositions and products therefrom.
Type:
Grant
Filed:
May 28, 1991
Date of Patent:
August 11, 1992
Assignee:
E. R. Squibb & Sons, Inc.
Inventors:
Andrew B. Dennis, Peter Timmins, Himadri Sen
Abstract: Rhenium tris dioxime complexes are useful in the synthesis of boronic acid adducts of rhenium dioxime complexes which are useful as radiotherapeutic agents.
Type:
Grant
Filed:
August 28, 1989
Date of Patent:
June 2, 1992
Assignee:
E. R. Squibb & Sons, Inc.
Inventors:
Silvia Jurisson, Karen E. Linder, Lynn C. Francesconi
Abstract: A novel pharmaceutical composition and method is disclosed for the treatment of cardiovascular diseases, e.g. myocardial ischemia and/or arrhythmia. The method and composition include an effective amount of a compound of the formula ##STR1## wherein X, Y, R, R.sub.1, A, A', m, n, p, p' and B are as defined herein.
Type:
Grant
Filed:
January 26, 1990
Date of Patent:
May 26, 1992
Assignee:
E. R. Squibb & Sons, Inc.
Inventors:
John Krapcho, James L. Bergey, Gary J. Grover
Abstract: Novel compounds having the general formula ##STR1## wherein A and A' are amino acid residues linked by a peptidal bond to the nucleus, are disclosed. These compounds are CNS agents with anxiogenic activity.
Abstract: Novel intermediates for preparing 2-oxo-1-[[(substituted sulfonyl)-amino]carbonyl]azetidines are disclosed. These intermediates have the formula ##STR1## wherein Prot is as defined herein.
Type:
Grant
Filed:
September 27, 1990
Date of Patent:
April 21, 1992
Assignee:
E. R. Squibb & Sons, Inc.
Inventors:
Jollie D. Godfrey, Jr., Richard H. Mueller
Abstract: Novel compounds of the formula ##STR1## wherein X is sulfur or oxygen, R.sub.2 is aryl or heterocyclo and R.sub.1 is as defined herein, are disclosed. Compounds of formula I possess calcium channel activating activity.
Abstract: A novel antibiotic substance, janthinocin, is prepared by cultivation of a strain of the microorganism Janthinobacterium lividum, ATCC No. 53,857.
Type:
Grant
Filed:
July 31, 1989
Date of Patent:
January 14, 1992
Assignee:
E. R. Squibb & Sons, Inc.
Inventors:
Joseph O'Sullivan, John E. McCullough, Janice H. Del Mar
Abstract: Novel calcium channel blockers having the formula ##STR1## wherein X is oxygen or sulfur and wherein R, R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6 are as defined herein, are disclosed. These compounds are useful, for example, as anti-ischemic agents.
Abstract: Boronic acid adducts of technetium-.sup.99m imine-dioxime complexes are useful for imaging the myocardium, hepatobiliary system, brain and blood pool in humans and other mammalian species.
Abstract: Novel compounds are disclosed having the formula ##STR1## and R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6 and R.sub.7 are as defined herein. These compounds are useful, for example, as cardiovascular agents and especially as anti-ischemic agents.
Abstract: A process is disclosed for providing benzazepine intermediates of the formulae ##STR1## wherein R.sub.3, R.sub.4 and Y are as defined herein, which intermediates are useful in a process for the preparation of pharmaceutically useful benzazepine derivatives.
Type:
Grant
Filed:
November 29, 1989
Date of Patent:
October 1, 1991
Assignee:
E. R. Squibb & Sons, Inc.
Inventors:
Wen-Sen Li, John K. Thottathil, Michael Murphy
Abstract: An improved process for preparation of compounds of the formula ##STR1## as disclosed. These compounds are useful as intermediates in the preparation of boronic acid adducts of technetium 99m dioxime complexes of the formula.sup.99m Tc X(Y).sub.3 Zwhich are useful as imaging agents.
Abstract: Cultivation of a strain of the microorganism Dactylosporangium sp. A.T.C.C. No. 53693, yields the antibiotic substance EM5586 which contains the novel useful components dactylocycline A and dactylocycline B.
Type:
Grant
Filed:
December 24, 1987
Date of Patent:
June 18, 1991
Assignee:
E. R. Squibb & Sons, Inc.
Inventors:
Carol A. Aklonis, Helen A. Ax, Donald R. Kirsch, Joseph O'Sullivan, Adrienne Tymiak, J. Scott Wells
Abstract: Novel compounds of the formula ##STR1## and tautomers thereof, wherein at least one of R.sub.2, R.sub.3 and R.sub.4 is a strong electron withdrawing group, are disclosed. These compounds possess potassium channel activating activity and, as such, are useful as antihypertensive agents. Advantageously, the compounds of the present invention have shown less cardiac effects than known potassium channel activators.Also disclosed is a process for preparing these and other compounds.
Type:
Grant
Filed:
May 8, 1989
Date of Patent:
April 30, 1991
Assignee:
E. R. Squibb & Sons, Inc.
Inventors:
Karnail Atwal, John R. McCullough, Gary J. Grover
Abstract: In accordance with the present invention a novel composite compression and support dressing is disclosed. This dressing comprises an extensible bandage having a stretchable hydrocolloid adhesive composition laminated thereto.
Abstract: Novel compounds of the formula ##STR1## and tautomers thereof are disclosed. These compounds possess potassium channel blocking activity and, as such, are useful as antiarrhythmic agents.