2011
DOI: 10.1016/j.carres.2011.07.003
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Investigation of the binding of roxatidine acetate hydrochloride with cyclomaltoheptaose (β-cyclodextrin) using IR and NMR spectroscopy

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Cited by 12 publications
(8 citation statements)
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“…Furthermore, there is a broad band in the 3200–3650 cm –1 area that can be attributed to the N–H or, to a lesser extent, O–H stretching vibrations (the latter might originate from the moisture or residually protonated carboxylate groups). , The presence of carboxylate groups coordinated to Co­(II) centers is accounted for by the strong bands appearing at 1610 and 1654 cm –1 for antisymmetric stretching vibrations and a broad absorption occurring at 1378 cm –1 for the symmetric stretching vibration. Moreover, a C–O bending vibration contributes to the band at 1105 cm –1 . The FT-IR spectral features are in good agreement with the molecular structure of Co­(II)-TMU-63 established by single-crystal X-ray diffraction.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Furthermore, there is a broad band in the 3200–3650 cm –1 area that can be attributed to the N–H or, to a lesser extent, O–H stretching vibrations (the latter might originate from the moisture or residually protonated carboxylate groups). , The presence of carboxylate groups coordinated to Co­(II) centers is accounted for by the strong bands appearing at 1610 and 1654 cm –1 for antisymmetric stretching vibrations and a broad absorption occurring at 1378 cm –1 for the symmetric stretching vibration. Moreover, a C–O bending vibration contributes to the band at 1105 cm –1 . The FT-IR spectral features are in good agreement with the molecular structure of Co­(II)-TMU-63 established by single-crystal X-ray diffraction.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, a C−O bending vibration contributes to the band at 1105 cm −1 . 70 The FT-IR spectral features are in good agreement with the molecular structure of Co(II)-TMU-63 established by single-crystal X-ray diffraction.…”
Section: Resultsmentioning
confidence: 99%
“…By contrast, aromatic ring containing compounds ordinarily show binding constants an order of magnitude lower. 11,43 The lack of the cross-peaks of terminal methyl moiety of the gemini tail and βCD cavity provides indirect evidence that the drug may interact with βCDg, further indicating the biological benefit of the complexation. 15,16 The apparent lack of observable interactions between the drug and βCDg host indicates that a noninclusion ternary complex is formed.…”
Section: Molecular Pharmaceuticsmentioning
confidence: 99%
“…The peak around 1655 cm −1 is attributed to the O–H bending vibration of adsorbed water and hydroxyl groups in β -CD molecule. The absorption peak around 1033 cm −1 is stretching vibration of C–O–C and C–O bonds in the hole 28 43 44 45 . Moreover, new weak distinct peaks appeared around 1255 cm −1 and 3700 cm −1 .…”
Section: Resultsmentioning
confidence: 99%