摘要:
The present invention is directed to compounds according to the formula (R 2 R 3 )-A 1 -c (A 2 -A 3 -A 4 -A 5 -A 6 -A 7 -A 8 -A 9 )-A 10 -R 1 , and pharmaceutically acceptable salts thereof that act as ligands for one or more of the melanocortin receptors, to methods of using such compounds to treat mammals and to pharmaceutical compositions comprising said compounds.
摘要:
The invention relates to a process for the preparation of injectable pharmaceutical compositions for the sustained release of somatostatin analogues and to pharmaceutical compositions prepared according to the process. In a preferred aspect the process comprises the steps of combining lanreotide acetate and acetic acid, lyophilizing the resulting mixture only once, and hydrating the lyophilizate. Acetic acid may be added to a desired pH during the final step of the process.
摘要:
The present invention relates to improvements in compositions containing peptides that are ligands of one or more of the melanocortin receptors (MC-R), or pharmaceutically acceptable salts thereof, methods for preparing such compositions, and method of using such compositions to treat mammals. In particular, the present invention relates to a pharmaceutical composition comprising a pamoate salt of Ac-Arg-cyclo(Cys-D-Ala-His-D-Phe-Arg-Trp-Cys)-NH 2 which is a ligand of the melanocortin receptor subtype 4 (MC4-R), and in which, after subcutaneous or intramuscular administration to a subject, the peptide forms a depot at physiological pH that is slowly dissolved and released into the body fluid and bloodstream. The present invention may further comprise an organic component such as dimethylacetamide (DMA) or polyethylene glycol (PEG) with an average molecular weight of lower than 1000.
摘要:
The present invention is directed to a compound according to the formula: €ƒ€ƒ€ƒ€ƒ€ƒ€ƒ€ƒ€ƒ Ac-Arg-c(Cys-D-Ala-His-D-Phe-Arg-Trp-Cys)-NH 2 and pharmaceutically-acceptable salts thereof. This compound acts as a ligand for one or more of the melanocortin receptors. The invention also relates to methods of using this compound to treat mammals and to pharmaceutical compositions comprising said compound.
摘要:
The present invention relates to a solid pharmaceutical composition including the active principle 6-oxo-6,7,8,9,10,11-hexahydrocyclohepta[c]chromen-3-yl sulfamate. The present invention also relates to polymorphs of the 6-oxo-6,7,8,9,10,11-hexahydrocyclohepta[c]chromen-3-yl sulfamate compound.
摘要:
The invention concerns the use of stannylenes and germylenes of general formula (1) wherein: M represents a tin or germanium atom; L1 and L2 independently represent a group of formula: -E14(R14)(R'14)(R''14), -E15(R15)(R'15) or -E16(R16), or together form a chain of formula -L'1-A-L'2; A represents a saturated or unsaturated chain comprising one, two or three elements of group 14; L'1 and L'2, represent, independently, a group of formula: -E14(R14)(R'14)-, E15(R15)- or -E16-; E14 is an element of group 14; E15 is an element of group 15; E16 is an element of group 16; R14, R'14, R''14, R15, R'15 and R16 represent variable groups as polymerisation catalysts of heterocycles.
摘要:
The invention relates to the use of at least one botulism neurotoxin for the production of a medicament for treating or preventing the pain induced by a medicament used to treat the AIDS virus.
摘要:
There is provided a novel series of analogues of glucose-dependent insulinotropic polypeptide, pharmaceutical compositions containing said compounds, and the use of said compounds as GIP- receptor agonists or antagonists for treatment of GIP -receptor mediated conditions, such as non- insulin dependent diabetes mellitus and obesity.