Paul Dowd - Pittsburgh PA Christopher Kaufman - Dravosburg PA Robert H. Abeles - Newton Centre MA
Assignee:
University of Pittsburgh - Pittsburgh PA
International Classification:
C07C 6104
US Classification:
562506
Abstract:
The subject invention relates to novel cyclopropanone hydrate derivatives of the structural formula ##STR1## wherein R. sub. 1 and R. sub. 2 are selected from the group consisting of --H, --(CH. sub. 2). sub. n -- where n is an integer between 1 and 20, preferably 2 and 10, --COCH. sub. 2 NH. sub. 2, and ##STR2## and R. sub. 3 and R. sub. 4 selected from the group consisting of --H, --OH, 13 NH. sub. 2, --CN, --COOR. sub. 5, --COOH, --SH, --(CH. sub. 2). sub. n OH, --(CH. sub. 2). sub. n NH. sub. 2, --(CH. sub. 2). sub. n COOH, --(CH. sub. 2). sub. n COOR. sub. 5, --CCH. sub. 3 OH (CH. sub. 2). sub. n COOH, halogen and C. sub. 7 -C. sub. 10 arakyls, where n is an integer between 1 and 20, preferably 1 and 10, and R. sub. 5 is an alkyl radical having between 1 and 20, preferably 1 and 10, carbon atoms; and to a process for the synthesis thereof.
David Taub - Metuchen NJ Robert H. Abeles - Newton Centre MA Arthur A. Patchett - Westfield NJ
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
C07K 506 C07K 508 A61K 3702 C07C10110
US Classification:
514 18
Abstract:
Described are 3-halovinylglycines and their amino acid dipeptide and oligopeptide conjugates, a new class of efficient antibacterial agents, pharmaceutical compositions containing them as active ingredients, and methods of synthesis. The compounds are thought to interfere in bacterial cell wall synthesis.
David Taub - Metuchen NJ Robert H. Abeles - Newton Centre MA Arthur A. Patchet - Westfield NJ
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
C07C10106
US Classification:
562574
Abstract:
Described bare 3-halovinylglycines and their amino acid dipeptide and oligopeptide conjugates, a new class of efficient antibacterial agents, pharmaceutical compositions containing them as active ingredients, and methods of synthesis. The compounds are thought to interfere in bacterial cell wall synthesis.
Fluorine And Chlorine Statine Or Statone Containing Peptides And Method Of Use
Robert H. Abeles - Waltham MA Michael H. Gelb - Seattle WA
Assignee:
Sandoz Ltd. - Basle
International Classification:
A61K 3702 C07K 510 C07K 706 C07K 708
US Classification:
514 18
Abstract:
A peptide optionally in isosteric form wherein a methylene group in the backbone chain is disubstituted, one or both substituents being fluorine and/or chlorine, in free form or in pharmaceutically acceptable salt form, such as a compound of formula I ##STR1## wherein the substituents have various significances, or an isosteric form thereof, is useful as an enzyme inhibitor. In particular, as a renin inhibitor, it is useful in the prophylaxis or treatment of hypertension and congestive heart failure. It is prepared by a process comprising the step of coupling two corresponding peptide residues optionally in isosteric form, or precursors thereof, and if required appropriately converting any resultant compound in precursor form.
Robert Abeles 1963 graduate of Webster Groves High School in Webster groves, MO is on Classmates.com. See pictures, plan your class reunion and get caught up with Robert and other high school alumni