FIELD: medicine, pharmaceutics.
SUBSTANCE: invention relates to a novel crystalline form of an inhibitor of the sodium-dependent glucose cotransporter SGLT2 of formula , characterised by a powder X-ray diffraction pattern (XRDP) with the application of CuKα1 radiation, including peaks at 11.2, 12.9, 15.5, 17.8, 19.1, 20.0 and 20.7 degrees 2θ (±0.1 degree 2θ), spectrum of Raman scattering, including peaks at 353, 688, 825, 1178, 1205, 1212, 1608, 2945, 3010 and 3063 cm-1, as well as an endotherm, obtained by the method of differential scanning calorimetry (DSC), at 136°C, its obtaining by re-crystallisation from ethanol or methanol by the addition of water and based on it pharmaceutical compositions for treating diseases, the pathogenesis of which requires the inhibition of the sodium-dependent glucose cotransporter 2 (SGLT2).
EFFECT: claimed is the novel crystalline form of the biologically active substance with low hygroscopicity.
33 cl, 8 dwg, 5 tbl, 12 ex
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Authors
Dates
2015-11-27—Published
2011-06-10—Filed