Melanocortin receptor ligands
    71.
    发明公开
    Melanocortin receptor ligands 有权
    黑皮质素受体配体

    公开(公告)号:EP2548568A2

    公开(公告)日:2013-01-23

    申请号:EP12188784.8

    申请日:2006-07-10

    申请人: IPSEN PHARMA

    IPC分类号: A61K38/04

    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.

    摘要翻译: 本发明涉及作为配体的根据式(R2R3)-A1-c(A2-A3-A4-A5-A6-A7-A8-A9)-A10-R1的化合物及其药学上可接受的盐, 一种或多种黑皮质素受体,使用此类化合物治疗哺乳动物的方法以及包含所述化合物的药物组合物。

    PHARMACEUTICAL COMPOSITIONS OF MELANOCORTIN RECEPTOR LIGANDS
    75.
    发明公开
    PHARMACEUTICAL COMPOSITIONS OF MELANOCORTIN RECEPTOR LIGANDS 有权
    黑色素受体配体的药物组合物

    公开(公告)号:EP2501225A1

    公开(公告)日:2012-09-26

    申请号:EP10830850.3

    申请日:2010-11-15

    IPC分类号: A01N25/00

    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.

    摘要翻译: 本发明涉及一种在含有对一种或多种黑皮质素受体的(MC-R)的配体的肽的组合物的改进,或它们的药学上可接受的盐,用于制备这样的组合物,和使用这样的组合物治疗哺乳动物的方法的方法。 特别地,本发明涉及包含交流基-Arg-环的双羟萘酸盐(CYS-d-ALA-的His-d-苯丙氨酸 - 精氨酸 - 色氨酸 - 半胱氨酸)的药物组合物-NH 2,其是黑皮质素的配体 受体亚型4(MC4-R),并且其中在对受试者进行皮下或肌内给药后,所述肽在生理pH下形成贮库,其缓慢溶解并释放到体液和血流中。 本发明可以进一步包含有机组分,例如平均分子量低于1000的二甲基乙酰胺(DMA)或聚乙二醇(PEG)。