Conformational pseudo-polymorphism and hydrogen bonding: benzthiazide anhydrate and monohydrate, an antihypertensive drug (Articolo in rivista)

Type
Label
  • Conformational pseudo-polymorphism and hydrogen bonding: benzthiazide anhydrate and monohydrate, an antihypertensive drug (Articolo in rivista) (literal)
Anno
  • 2003-01-01T00:00:00+01:00 (literal)
Alternative label
  • Prabakaran P., Umadevi B., Panneerselvam P., Muthiah P.T., Bocelli G., Righi L. (2003)
    Conformational pseudo-polymorphism and hydrogen bonding: benzthiazide anhydrate and monohydrate, an antihypertensive drug
    in Crystal engineering
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Prabakaran P., Umadevi B., Panneerselvam P., Muthiah P.T., Bocelli G., Righi L. (literal)
Pagina inizio
  • 487 (literal)
Pagina fine
  • 489 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 5 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Titolo
  • Conformational pseudo-polymorphism and hydrogen bonding: benzthiazide anhydrate and monohydrate, an antihypertensive drug (literal)
Abstract
  • Studies on hydrogen-bonding patterns. The conformation and the hydrogen-bonding patterns of a benzthiazide molecule in anhydrate and monohydrate forms which heve been recently considered for sustematic studies due to many industrial applications such a drug polymorphs in pharmaceutical.Unespectedly the conformation of benzthiazide molecule significantly differs in the two crystal forms leading to a conformational \"pseudo-polymorphism\". The two molecules reveals, respectively, a J-like folded as ell as extended type conformations that have critical torsional flexibility along the C-C-S-C bonds and novel H-bonded sulfonamide motifs. (literal)
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