Bradykinin peptides with modifications at the N terminus
US5597803A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | Jan 17, 1995 |
| Grant date | Jan 28, 1997 |
| Priority date | — |
| Expiry date | Jan 17, 2015 |
Classification
- Technology area (CPC Y)Emerging Cross-Sectional Technologies
- CPC primaryY02P20/55
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
Peptides of the formula I EQU Z-P-A-B-C-E-F-K-(D)Q-G-M-F'-I (I) and the physiologically tolerated salts thereof, are described. They have an excellent bradykinin-antagonistic action. They are obtained by reacting reacting a fragment with a C-terminal free carboxyl group or its activated derivative with a corresponding fragment with an N-terminal free amino group or assembling the peptide stepwise, where appropriate eliminating in the compound obtained in this way one or more protective groups introduced temporarily to protect other functionalities, and where appropriate converting the compounds of the formula I obtained in this way into the physiologically tolerated salt thereof.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.