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Polymorph VI of 4-amino-N-(2-pyrid­yl)benzene­sulfonamide, C11H11N3O2S, is monoclinic (space group P21/n). The asymmetric unit contains two different tautomeric forms. The structure displays N—H...N and N—H...O hydrogen bonding. The two independent mol­ecules form two separate two- and three-dimensional hydrogen-bonded networks which inter­penetrate. The observed patterns of hydrogen bonding are analogous to those in polymorph I of sulfathia­zole.

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The structure of the title compound (systematic name: 2-{2-[1-(4-chloro­benzo­yl)-5-meth­oxy-2-methyl-1H-indol-3-yl]acet­oxy}­acetic acid monohydrate, C21H18ClNO6·H2O) contains one-dimensional infinite hydrogen-bonded chains. Mol­ecules of acemetacin, a nonsteroidal anti-inflammatory drug, and water are linked by three independent O—H...O bonds. The central unit in each chain consists of a sequence of alternating centrosymmetric R44(12) and R44(18) rings, which are edge-fused. Each ring links two acemetacin and two water mol­ecules. A comparison with seven related structures reveals that mol­ecules of acemetacin, indomethacin and their analogues can adopt two principal conformations.

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N-H...O bonding in a form of 5-butyl-5-ethyl­barbituric acid (systematic name: 5-butyl-5-ethyl-1,3-diazinane-2,4,6-trione), C10H16N2O3, produces two distinct one-dimensional motifs, viz. tape and ladder. Both are different from the ribbon chain motif observed in two previously reported polymorphs of the same compound.
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