(Q57074627)

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A rationale for the design and synthesis of m1 selective muscarinic agonists

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title

A rationale for the design and synthesis of m1 selective muscarinic agonists (English)

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author name string

H. Tecle

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1

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T. Mirzadegan

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2

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W.H. Moos

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3

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D.W. Moreland

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4

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M.R. Pavia

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5

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R.D. Schwarz

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6

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R.E. Davis

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7

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English

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publication date

August 1992

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published in

Bioorganic & Medicinal Chemistry Letters

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volume

2

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issue

8

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page(s)

821-826

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cites work

Identification of a family of muscarinic acetylcholine receptor genes

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https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2980538-7

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7 January 2021

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Muscarinic receptor subtypes

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https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2980538-7

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7 January 2021

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Muscarinic receptor subtypes. Physiology and clinical implications

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https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2980538-7

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7 January 2021

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Identification and localization of muscarinic acetylcholine receptor proteins in brain with subtype-specific antibodies

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https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2980538-7

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7 January 2021

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Muscarinic receptor subtypes: M1 and M2 biochemical and functional characterization

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https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2980538-7

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7 January 2021

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Predicting the biologically active conformations of short polypeptides

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https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2980538-7

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7 January 2021

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Muscarinic cholinergic agonists and antagonists of the 3-(3-alkyl-1,2,4-oxadiazol-5-yl)-1,2,5,6-tetrahydropyridine type. Synthesis and structure-activity relationships

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https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2980538-7

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7 January 2021

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Synthesis and muscarinic activities of 1,2,4-thiadiazoles.

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https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2980538-7

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7 January 2021

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Synthesis and muscarinic activity of quinuclidinyl- and (1-azanorbornyl)pyrazine derivatives

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2980538-7

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7 January 2021

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10.1016/S0960-894X(00)80538-7

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(Q57074627)

A rationale for the design and synthesis of m1 selective muscarinic agonists

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