Synthesis and Structure-Activity Studies of a Series of 1-Oxa-8-Azaspiro(4.5)decanes as M1 Muscarinic Agonists.

Chemical and Pharmaceutical Bulletin - Japan
doi 10.1248/cpb.43.842
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Pharmaceutical Society of Japan

Related search

4-Benzyl-8-Phenyl-1-Thia-4-Azaspiro[4.5]decan-3-One

Acta Crystallographica Section E Structure Reports Online
2012English

8-Methyl-4-Morpholinoethyl-1-Thia-4-Azaspiro[4.5]decan-3-One

Acta Crystallographica Section E Structure Reports Online
2008English

Synthesis, Biological Evaluation and Molecular Modeling of 1-Oxa-4-Thiaspiro- And 1,4-Dithiaspiro[4.5]decane Derivatives as Potent and Selective 5-Ht1a Receptor Agonists

European Journal of Medicinal Chemistry
MedicineOrganic ChemistryDrug DiscoveryPharmacology
2017English

A Stereoselective Synthesis of a 3,4,5-Substituted Piperidine of Interest as a Selective Muscarinic (M1) Receptor Agonist

Synlett
Organic Chemistry
2015English

Synthesis and Structure-Activity Relationships of 3, 8-Diazabicyclo[4.2.0]octane Ligands, Potent Nicotinic Acetylcholine Receptor Agonists

English

Diastereoselective Synthesis of Optically Active C2-Substituted Spiro(4.5)decanes: Two Key Intermediates for Spirovetivane Sesquiterpenes.

Chemical and Pharmaceutical Bulletin
MedicineDrug DiscoveryChemistry
1997English

Structure-Activity Relationship Studies on a Series of Novel, Substituted 1-Benzyl-5-Phenyltetrazole P2X7 Antagonists

English

Negative Cooperativity in Binding of Muscarinic Receptor Agonists and GDP as a Measure of Agonist Efficacy

British Journal of Pharmacology
Pharmacology
2011English

M1 Muscarinic Receptor Activation Mediates Cell Death in M1-Hek293 Cells

PLoS ONE
Multidisciplinary
2013English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy