<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(12)</volume><submitter>Kuduk SD</submitter><pubmed_abstract>Selective activation of the M1 muscarinic receptor via positive allosteric modulation represents an approach to treat the cognitive decline in patients with Alzheimer's disease. A series of amides were examined as a replacement for the carboxylic acid moiety in a class of quinolizidinone carboxylic acid M1 muscarinic receptor positive allosteric modulators, and leading pyran 4o and cyclohexane 5c were found to possess good potency and in vivo efficacy.</pubmed_abstract><journal>ACS medicinal chemistry letters</journal><pagination>1070-4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4025801</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification of amides as carboxylic Acid surrogates for quinolizidinone-based m1 positive allosteric modulators.</pubmed_title><pmcid>PMC4025801</pmcid><pubmed_authors>Koeplinger KA</pubmed_authors><pubmed_authors>Greshock TJ</pubmed_authors><pubmed_authors>Ray WJ</pubmed_authors><pubmed_authors>Bilodeau MT</pubmed_authors><pubmed_authors>Ma L</pubmed_authors><pubmed_authors>Kuduk SD</pubmed_authors><pubmed_authors>Seager MA</pubmed_authors><pubmed_authors>Hartman GD</pubmed_authors><pubmed_authors>Chang RK</pubmed_authors><pubmed_authors>Wittmann M</pubmed_authors><pubmed_authors>Thompson CD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of amides as carboxylic Acid surrogates for quinolizidinone-based m1 positive allosteric modulators.</name><description>Selective activation of the M1 muscarinic receptor via positive allosteric modulation represents an approach to treat the cognitive decline in patients with Alzheimer's disease. A series of amides were examined as a replacement for the carboxylic acid moiety in a class of quinolizidinone carboxylic acid M1 muscarinic receptor positive allosteric modulators, and leading pyran 4o and cyclohexane 5c were found to possess good potency and in vivo efficacy.</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Dec</publication><modification>2025-04-04T08:41:43.792Z</modification><creation>2019-03-27T01:28:29Z</creation></dates><accession>S-EPMC4025801</accession><cross_references><pubmed>24900430</pubmed><doi>10.1021/ml300280g</doi></cross_references></HashMap>