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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 189 (1961), S. 671-673 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The muscarinic activity of muscarine is considerably reduced in the isomers in which the CH3, CH2NMea or OH groups are inverted4. If the quaternary N group and the ether O of (III), lying almost in a plane, form the chief two centres for drug-receptor association (the OH group acting as a secondary ...
    Type of Medium: Electronic Resource
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