Abstract
Co-crystal forming abilities of the two anti-HIV drugs lamivudine and zidovudine were studied. A study of five crystal structures was carried out to investigate the general applicability of the retrosynthetic approach in the design of new cocrystals. This analysis of co-crystals and salt structures showed a complete to partial success, and in one case, a total failure to obtain the predicted synthon. Both screening strategies and retrosynthetic methods may be appropriate for the discovery of new active pharmaceutical ingredients co-crystals. © 2009 American Chemical Society.
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CITATION STYLE
Bhatt, P. M., Azim, Y., Thakur, T. S., & Desiraju, G. R. (2009). Co-crystals of the anti-HIV drugs lamivudine and zidovudine. Crystal Growth and Design, 9(2), 951–957. https://doi.org/10.1021/cg8007359
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