Bile acid derivatives, process for their preparation and use of these compounds as pharmaceuticals
US5250524A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | Dec 4, 1991 |
| Grant date | Oct 5, 1993 |
| Priority date | — |
| Expiry date | Dec 4, 2011 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC07J41/0094
- WIPO fieldOrganic fine chemistry
- WIPO sectorChemistry
Abstract
The invention relates to bile acid derivatives of the formula I EQU G1--X--G2 (I) in which PA1 G1 and G2 are bile acid radicals or modified bile acid radicals in the form of the free acids, the esters or amides, the salt forms and also the forms derivatized on the alcohol groups and PA1 X is a bridge group or a single covalent bond, it being possible for G1 and G2 to be optionally bonded via X. The compounds according to the invention have a high affinity for the specific bile acid transport system of the small intestine and inhibit bile acid absorption in a concentration-dependent and competitive manner.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.