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Liesegang ring formation during the supramolecular hydrogelation of the chiral drug methocarbamol

Alexander Alexandrovich Bredikhin 1
Alexander Alexandrovich Bredikhin
, 
Zemfira Azal'evna Bredikhina 1
Zemfira Azal'evna Bredikhina
, 
Alexander Vladimirovich Pashagin 1
Alexander Vladimirovich Pashagin
10.1016/j.mencom.2011.04.010
Published 2011-04-28
Communication , Volume 21, Issue 3, 144-145
9
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Bredikhin A. A., Bredikhina Z. A., Pashagin A. V. Liesegang ring formation during the supramolecular hydrogelation of the chiral drug methocarbamol // Mendeleev Communications. 2011. Vol. 21. No. 3. pp. 144-145.
GOST all authors (up to 50) Copy
Bredikhin A. A., Bredikhina Z. A., Pashagin A. V. Liesegang ring formation during the supramolecular hydrogelation of the chiral drug methocarbamol // Mendeleev Communications. 2011. Vol. 21. No. 3. pp. 144-145.
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TY - JOUR
DO - 10.1016/j.mencom.2011.04.010
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.04.010
TI - Liesegang ring formation during the supramolecular hydrogelation of the chiral drug methocarbamol
T2 - Mendeleev Communications
AU - Bredikhin, Alexander Alexandrovich
AU - Bredikhina, Zemfira Azal'evna
AU - Pashagin, Alexander Vladimirovich
PY - 2011
DA - 2011/04/28
PB - Mendeleev Communications
SP - 144-145
IS - 3
VL - 21
ER -
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@article{2011_Bredikhin,
author = {Alexander Alexandrovich Bredikhin and Zemfira Azal'evna Bredikhina and Alexander Vladimirovich Pashagin},
title = {Liesegang ring formation during the supramolecular hydrogelation of the chiral drug methocarbamol},
journal = {Mendeleev Communications},
year = {2011},
volume = {21},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.04.010},
number = {3},
pages = {144--145},
doi = {10.1016/j.mencom.2011.04.010}
}
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Bredikhin, Alexander Alexandrovich, et al. “Liesegang ring formation during the supramolecular hydrogelation of the chiral drug methocarbamol.” Mendeleev Communications, vol. 21, no. 3, Apr. 2011, pp. 144-145. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.04.010.

Abstract

The chiral drug methocarbamol, which is prone to spontaneous resolution, is an effective molecular hydrogelator as both an enantiomer and a racemate; the samples of methocarbamol having an intermediate enantiomeric composition generate clearly visible periodic structures (Liesegang rings) during the gelation process.

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