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Collect. Czech. Chem. Commun. 1999, 64, 1980-1992
https://doi.org/10.1135/cccc19991980

Truxillic Acid Derivatives, Neuromuscular Blocking Agents with Very High Affinity for the Allosteric Binding Site of Muscarinic Acetylcholine Receptors

Marek Urbanskýa,*, Jan Proškab, Jan Říčnýc and Pavel Drašara

a Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Flemingovo nám. 2, 166 10 Prague 6, Czech Republic
b Research Institute for Pharmacy and Biochemistry, Kouřimská 17, 130 60 Prague 3, Czech Republic
c Institute of Physiology, Academy of Sciences of the Czech Republic, Vídeňská 1083, 142 20 Prague 4, Czech Republic

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  • Sokolova Anastasiya, Pavlova Alla, Komarova Nina, Ardashov Oleg, Shernyukov Andrey, Gatilov Yuriy, Yarovaya Olga, Tolstikova Tat’yana, Salakhutdinov Nariman: Synthesis and analgesic activity of new α-truxillic acid derivatives with monoterpenoid fragments. Med Chem Res 2016, 25, 1608. <https://doi.org/10.1007/s00044-016-1593-z>
  • Urbansky Marek, Proska Jan, Ricny Jan, Drasar Pavel: ChemInform Abstract: Truxillic Acid Derivatives, Neuromuscular Blocking Agents with Very High Affinity for the Allosteric Binding Site of Muscarinic Acetylcholine Receptors. ChemInform 2000, 31. <https://doi.org/10.1002/chin.200014201>
  • Zlotos D.P, Buller S, Tränkle C, Mohr K: Bisquaternary caracurine V derivatives as allosteric modulators of ligand binding to M2 acetylcholine receptors. Bioorganic & Medicinal Chemistry Letters 2000, 10, 2529. <https://doi.org/10.1016/S0960-894X(00)00509-6>