[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/wiki29\/2021\/11\/29\/sabcomeline-wikipedia\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/wiki29\/2021\/11\/29\/sabcomeline-wikipedia\/","headline":"Sabcomeline \u2013 Wikipedia","name":"Sabcomeline \u2013 Wikipedia","description":"before-content-x4 Sabcomeline (Memric; SB-202.026) ist ein selektives M1 Rezeptor-Partialagonist, der zur Behandlung der Alzheimer-Krankheit entwickelt wurde.[1] Es schaffte es in","datePublished":"2021-11-29","dateModified":"2021-11-29","author":{"@type":"Person","@id":"https:\/\/wiki.edu.vn\/wiki29\/author\/lordneo\/#Person","name":"lordneo","url":"https:\/\/wiki.edu.vn\/wiki29\/author\/lordneo\/","image":{"@type":"ImageObject","@id":"https:\/\/secure.gravatar.com\/avatar\/44a4cee54c4c053e967fe3e7d054edd4?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/44a4cee54c4c053e967fe3e7d054edd4?s=96&d=mm&r=g","height":96,"width":96}},"publisher":{"@type":"Organization","name":"Enzyklop\u00e4die","logo":{"@type":"ImageObject","@id":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","url":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","width":600,"height":60}},"image":{"@type":"ImageObject","@id":"https:\/\/en.wikipedia.org\/wiki\/Special:CentralAutoLogin\/start?type=1x1","url":"https:\/\/en.wikipedia.org\/wiki\/Special:CentralAutoLogin\/start?type=1x1","height":"1","width":"1"},"url":"https:\/\/wiki.edu.vn\/wiki29\/2021\/11\/29\/sabcomeline-wikipedia\/","wordCount":1881,"articleBody":"     (adsbygoogle = window.adsbygoogle || []).push({});before-content-x4Sabcomeline (Memric; SB-202.026) ist ein selektives M1 Rezeptor-Partialagonist, der zur Behandlung der Alzheimer-Krankheit entwickelt wurde.[1]  Es schaffte es in klinische Phase-III-Studien, bevor es aufgrund schlechter Ergebnisse abgebrochen wurde.Siehe auch[edit]Verweise[edit]^ Loudon JM, Bromidge SM, Brown F, et al.  (Dezember 1997). \u201eSB 202026: ein neuartiger muskarinischer Partialagonist mit funktioneller Selektivit\u00e4t f\u00fcr M1-Rezeptoren\u201c. The Journal of Pharmacology and Experimental Therapeutics. 283 (3): 1059\u201368.  PMID 9399977.       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