Abstract
THE molecule of d-tubocurarine chloride contains two phenolic hydroxy groups as well as two methoxy groups attached to the aromatic nucleus1. The hydroxy groups can be alkylated ; when they are methylated, the resulting dimethyl ether differs in a striking way from d-tubocurarine chloride in its pharmacological properties2.
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COLLIER, H., PARIS, S. & WOOLF, L. Pharmacological Activities in Different Rodent Species of d-Tubocurarine Chloride and the Dimethyl Ether of d-Tubocurarine Iodide. Nature 161, 817–819 (1948). https://doi.org/10.1038/161817a0
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DOI: https://doi.org/10.1038/161817a0
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