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- W1796356094 abstract "Using extended Huckel theory molecular orbital calculations, the preferred conformations of acetylcholine, L-(+)-muscarine, and D-(-)-muscarone have been predicted from total-energy minimization as a function of geometry. The calculations for muscarine and acetylcholine reveal a preferred conformation strikingly similar to conformations reported in the literature based upon crystal X-ray analysis. A comparison of calculated preferred conformations of L-(+)-muscarine and D-(-)-muscarone leads to the observation that the heteroatoms in the two molecules bear spatial relationships similar to each other. It is concluded that D-(-)-muscarone approaches the muscarinic receptor with the opposite face than does L-(+)-muscarine. From a consideration of the calculations on the three compounds, a complementary pattern of forces representing the muscarinic receptor is proposed." @default.
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- W1796356094 date "1967-09-01" @default.
- W1796356094 modified "2023-10-12" @default.
- W1796356094 title "Molecular orbital calculation of preferred conformations of acetylcholine, muscarine, and muscarone." @default.
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