Abstract: Renin-inhibiting aminomethyl peptides of the formula ##STR1## in which A is H, an alkyl radical, a sulphonyl radical or an amino-protecting group,B, D, E and F each independently is a direct bond or an amino-organo-carbonyl group,R.sup.1 is an optionally substituted alkyl or aryl radical,R.sup.2 is H, alkyl or acyl,R.sup.3 is H, alkyl, aryl or acyl, andR.sup.4 is alkyl, alkoxy, aryl or amino,and physiologically acceptable salts thereof.
Type:
Grant
Filed:
August 17, 1989
Date of Patent:
April 23, 1991
Assignee:
Bayer Aktiengesellschaft
Inventors:
Rolf Henning, Gunter Benz, Johannes-Peter Stasch, Andreas Knorr, Wolfgang Bender
Abstract: The invention relates to novel peptides and their acid addition salts, suppressing the function of the immune system, pharmaceutical compositions containing these peptides as well as to a process for preparing these peptides and compositions. The peptides are represented by formulae (1) to (16): ##STR1## The novel peptides are useful for the therapy of diseases where a decrease in the activity of the immune system is desirable.
Type:
Grant
Filed:
June 13, 1989
Date of Patent:
April 16, 1991
Assignee:
Richter Gedeon Vegyeszeti Gyar R. T.
Inventors:
Istvan Schon, Olga Nyeki, Lajos Kisfaludy, deceased, Laszlo Denes, Gyorgy Hajos, Laszlo Szporny
Abstract: A particularly preferred peptide has the amino acid sequence ##STR1## and is combined with a carrier effective to promote passage of the peptide through a patient's skin for an antinociceptive composition useful for relieving pain in a patient experiencing burning pain or hyperesthesia. Topical application of the composition has been found dramatically to reduce such pain in most individuals treated for periods of from about 5-24 hours, and continued control of the pain can be had by daily doses.
Abstract: Novel peptides having inhibitor activity toward the binding of motor neurons to s-laminin are disclosed which are selected from the group consisting ofAEKQLREQVGDQYQTVRALAEand fragments thereof containing the essential sequence LRE.
Type:
Grant
Filed:
July 19, 1989
Date of Patent:
March 26, 1991
Assignee:
Washington University
Inventors:
Dale D. Hunter, Joshua R. Sanes, John P. Merlie, Steven P. Adams
Abstract: A novel hexapeptide is provided having the following structure:Tyr-D-Ala-Gly-Phe-Leu-Glualso provided is a proposed medicinal preparation for treatment of erosive and ulcerative lesions of the gastrointestinal tract comprised of an active principle, said hexapeptide, and a pharmaceutical carrier.
Type:
Grant
Filed:
February 3, 1989
Date of Patent:
March 26, 1991
Inventors:
Valentin A. Vinogradov, Mikhail I. Titov, Vladimir M. Polonsky, Nikolai V. Korobov, Anatoly S. Sokolov, Maria L. Yakusheva, Zhanna D. Bespalova, Mikhail V. Ovchinnikov, Boris L. Pekelis
Abstract: A method for cleaving polypeptides at their methionine residue(s) by mean of reaction with cyanogen bromide wherein a solution of guanidium chloride into hydrochloric acid is employed as reaction medium.
Type:
Grant
Filed:
February 13, 1989
Date of Patent:
October 2, 1990
Assignee:
Istituto di Ricerca Cesare Serono SpA
Inventors:
Umberto Canosi, Gabriele De Fazio, Stefano Villa
Abstract: Disclosed is a human TNF derivative with a reduced tendency to cause adverse side effects that is obtained by replacing the 31st and 32nd arginine residues from the N-terminal of the amino acid sequence of human TNF, which has a potential for causing serious adverse effects, with asparagine residue and threoine residue, respectively, as well as a method of preparing the same utilizing recombinant DNA technology.