发明名称 N-acylthiourea and N-acylurea inhibitors of the Hedgehog protein signalling pathway
摘要 The present invention relates to the use of acylthiourea or acylurea derivatives for the treatment of pathologies involving a tissue dysfunction associated with a deregulation of the Hedgehog protein signalling pathway, and also to novel acylthiourea or acylurea derivatives as such, to their use as a medicinal product, and to pharmaceutical compositions containing them.
申请公布号 US9073835(B2) 申请公布日期 2015.07.07
申请号 US200912988975 申请日期 2009.04.16
申请人 Centre National De La Recherche Scientifique;Universite De Strasbourg 发明人 Ruat Martial;Faure Hélène;Traiffort Elisabeth;Schoenfelder Angèle;Mann André;Taddei Maurizio;Solinas Antonio;Manetti Fabrizio
分类号 C07C275/54;C07C335/26;C07D213/81;C07D209/08;C07D209/14;C07D235/14;C07D307/68;C07D317/68;C07D319/18;C07D333/38;C07D471/04;C07D513/04;C07D235/18;C07C335/08 主分类号 C07C275/54
代理机构 Alston & Bird LLP 代理人 Alston & Bird LLP
主权项 1. A method for manufacturing a drug, said method comprising mixing at least one pharmaceutically acceptable excipient and at least one compound with the following formula (I): wherein: R1, R2 and R3, which are identical or different and independent of each other, represent a hydrogen or a halogen atom, a hydroxyl radical, an alkyl, perfluoroalkyl, alkoxy, alkylthio or nitrile group, or a substituted alkoxy group; X represents a sulfur or oxygen atom; Y represents a a —NH—(C═O)—R6, or —(C═O)—NH—R6 group, wherein R6 represents a non-substituted aryl group; an aryl group comprising one or more substituents selected from a halogen atom and an alkyl, alkoxy or mono- or dialkylamino radical; a mono- or polycyclic heteroaryl group; a linear or branched alkyl radical; or a saturated or unsaturated mono- or polycyclic hydrocarbon group; R4 and R5, which are identical or different and independent of each other, represent a hydrogen or a halogen atom, or an alkoxy, alkylthio, alkyl, perfluoroalkyl, nitrile or nitro group.
地址 Paris FR