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Original Articles

Hydrogen bonding and sodium coordination in the crystal structure of tetrasodium (3-((2,4-dinitrophenyl)amino)-1-hydroxypropane-1,1-diyl)-bis-phosphonate pentahydrate – a N-substituted Pamidronate

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Pages 215-220 | Received 20 Jul 2018, Accepted 19 Oct 2018, Published online: 30 Nov 2018

References

  • Widler, L.; Jaeggi, K. A.; Glatt, M.; Müller, K.; Bachmann, R.; Bisping, M.; Born, A.-R.; Cortesi, B.; Guiglia, G.; Jeker, H.; Klein, R.; Ramseier, U.; Schmidt, J.; Schreiber, G.; Seltenmeyer, Y.; Green, J. R. Highly Potent Geminal Bisphonates. From Pamidronate Disodium (Aredia) to Zoledronic Acid (Zometa). J. Med. Chem. 2002, 45, 3721–3738 and references therein.
  • Meyers, P. A.; Healey, J. H.; Chou, A. J.; Wexler, L. H.; Merola, P. R.; Morris, C. D.; Laquaglia, M. P.; Kellick, M. G.; Abramson, S. J.; Gorlick, R. Addition of Pamidronate to Chemotherapy for the Treatment of Osteosarcoma. Cancer 2011, 117, 1736–1744. https://doi.org/10.1002/cncr.25744.
  • Ebetino, F. H.; Hogan, A.-M. L.; Sun, S.; Tsoumpra, M. K.; Duan, X.; Triffitt, J. T.; Kwaasi, A. A.; Dunford, J. E.; Barnett, B. L.; Oppermann, U.; et al. The Relationship Between the Chemistry and Biological Activity of the Bisphosphonates. Bone 2011, 49, 20–33. https://doi.org/10.1016/j.bone.2011.03.774.
  • Stahl, K.; Treppendahl, S. P.; Preikschat, H.; Fischer, E. Sodium 3-ammonio-1-Hydroxypropylidene-1.1-bisphosphonate Monohydrate. Acta Crystallogr. 2005, E61, m132–m134.
  • Vega, D.; Fernandez, D.; Ellena, J. A. Disodium Pamidronate. Acta Crystallogr. 2002, C58, m77–m80.
  • Puhl, M. 1-Hydroxy-1,1-bisphosphonosäure-funktionalisierte Farbstoffe: Synthese, NMR-spektroskopische und analytische Untersuchungen, Ph.D. Thesis, Heinrich-Heine-Universität Düsseldorf, 2002.
  • Reiss, G. J.; van Megen, M.; Frank, W. Hydrogen Bonds and van der Waals Forces as Tools for the Construction of a Herringbone Pattern in the Crystal Structure of Hexane-1,6-diaminium Hexane-1,6-diyl bis(Hydrogen Phosphonate). Acta Crystallogr. 2017, E73, 76–80 and references therein.
  • Deacon, G. B.; Forsyth, C. M.; Greenhill, N. B.; Junk, P. C.; Wang, J. Coordination Polymers of Increasing Complexity Derived from Alkali Metal Cations and (4-Amino-1-hydroxybutylidine)-1,1-bisphosphonic Acid (Alendronic Acid): The Competitive Influences of Coordination and Supramolecular Interactions. Crystal Growth Design 2015, 15, (9), 4646–4662.
  • ChrysalisPro Software System for Data Collection and Reduction. United Kingdom: Rigaku Oxford Diffraction. https://www.rigaku.com/en/products/smc/chrysalis.
  • Sheldrick, G. M. A short history of SHELX. Acta Crystallogr. 2008, A64, 112–122. DOI:10.1107/S0108767307043930.
  • DIAMOND, version 4.3.2, Crystal and Molecular Structure Visualization. Germany: CHRYSTAL IMPACT, Dr. H. Putz & Dr. K. Brandenburg GbR, 2017.

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