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Figure 2
A superposition of the mol­ecular conformations of clindamycin mol­ecules, showing the planar central carboxamide groups. The overlay was made by making a least-squares fit through the planar carboxamide atoms of (I)[link]. The labels and r.m.s deviations (Å) of the carboxamide atoms are as follows: clin­da­mycin hydrochloride monohydrate ethanol solvate, (II)[link], 0.025; 1YJN, (III), 0.050; lincomycin hydro­chloride, (IV), 0.025; clin­da­mycin 2-phosphate hydrate, (V), 0.091 (even though there are three mol­ecules in the asymmetric unit and their overlay is almost exact, only one mol­ecule is represented here). Disordered atoms C151/C161/C171 of (I)[link] and C161/C171 of (II)[link] and all H atoms have been omitted for clarity.

Journal logoSTRUCTURAL
CHEMISTRY
ISSN: 2053-2296
Volume 66| Part 2| January 2010| Pages o97-o100
doi:10.1107/S0108270110000958
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