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xanomeline
Known as:
(3-O-hexyloxy)-TZTP
, 3-(3-O-hexyl-1,2,5-thiadiazol-4-yl)-1,2,5,6-tetrahydro-1-methylpyridine
National Institutes of Health
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Related topics
Related topics
7 relations
Narrower (2)
LY 246708
xanomeline tartrate
Broader (5)
Muscarinic Agonists
Parasympathomimetic Agents
Psychotropic Drugs
Pyridines
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Classics in Chemical Neuroscience: Xanomeline.
Aaron M. Bender
,
Carrie K Jones
,
C. Lindsley
ACS Chemical Neuroscience
2017
Corpus ID: 3462779
Xanomeline (1) is an orthosteric muscarinic acetylcholine receptor (mAChR) agonist, often referred to as M1/M4-preferring, that…
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Review
2014
Review
2014
Activation of M1 and M4 muscarinic receptors as potential treatments for Alzheimer’s disease and schizophrenia
Daniel J. Foster
,
D. Choi
,
Jeffrey P. Conn
,
J. M. Rook
Neuropsychiatric Disease and Treatment
2014
Corpus ID: 18822599
Alzheimer’s disease (AD) and schizophrenia (SZ) are neurological disorders with overlapping symptomatology, including both…
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Review
2013
Review
2013
Allosteric modulation of the M1 muscarinic acetylcholine receptor: improving cognition and a potential treatment for schizophrenia and Alzheimer's disease.
B. Melancon
,
J. Tarr
,
Joseph D. Panarese
,
M. Wood
,
C. Lindsley
Drug Discovery Today
2013
Corpus ID: 25992747
Highly Cited
2010
Highly Cited
2010
Intrinsic versus Idiosyncratic Drug-Induced Hepatotoxicity—Two Villains or One?
R. Roth
,
P. Ganey
Journal of Pharmacology and Experimental…
2010
Corpus ID: 7883537
“Intrinsic” and “idiosyncratic” drug-induced liver injury reactions are commonly thought to arise by different modes of action…
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Review
2006
Review
2006
Xanomeline and the antipsychotic potential of muscarinic receptor subtype selective agonists.
N. Mirza
,
D. Peters
,
R. G. Sparks
CNS drug reviews
2006
Corpus ID: 6235562
Binding studies initially suggested that the muscarinic agonist, xanomeline, was a subtype selective muscarinic M(1) receptor…
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Highly Cited
2005
Highly Cited
2005
The highly efficacious actions of N-desmethylclozapine at muscarinic receptors are unique and not a common property of either typical or atypical antipsychotic drugs: is M1 agonism a pre-requisite…
M. Davies
,
Beth A. Compton-Toth
,
S. Hufeisen
,
H. Meltzer
,
B. Roth
Psychopharmacology
2005
Corpus ID: 33594018
RationaleRecent studies have suggested that the salutary actions of clozapine in schizophrenia may be due to selective activation…
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Review
2004
Review
2004
Cholinergic targets for cognitive enhancement in schizophrenia: focus on cholinesterase inhibitors and muscarinic agonists
J. Friedman
Psychopharmacology
2004
Corpus ID: 13439923
RationaleAlterations in the central cholinergic system of patients with schizophrenia such as reduced numbers of muscarinic and…
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Highly Cited
2001
Highly Cited
2001
The muscarinic receptor agonist xanomeline has an antipsychotic-like profile in the rat.
K. Stanhope
,
N. Mirza
,
+11 authors
A. Wyatt
Journal of Pharmacology and Experimental…
2001
Corpus ID: 2934695
The muscarinic receptor agonist xanomeline was examined and compared with the antipsychotics clozapine and/or haloperidol in the…
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Highly Cited
1999
Highly Cited
1999
The assessment of antagonist potency under conditions of transient response kinetics.
A. Christopoulos
,
A. Parsons
,
M. Lew
,
E. El-Fakahany
European Journal of Pharmacology
1999
Corpus ID: 38296847
Highly Cited
1997
Highly Cited
1997
Brain proton magnetic resonance spectroscopy (1H-MRS) in Alzheimer's disease: changes after treatment with xanomeline, an M1 selective cholinergic agonist.
A. Satlin
,
N. Bodick
,
W. Offen
,
P. Renshaw
American Journal of Psychiatry
1997
Corpus ID: 26485288
OBJECTIVE Higher than normal cellular levels of the phospholipid catabolic intermediate glycerophosphocholine have been found in…
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