Both 1 H NMR and 13 C NMR spectra were assigned to a series of acyclovir ester and amide prodrugs. Assignments were based on spectral comparison with compounds of similar structure.
NMR spectral data for ester prodrugs of ganciclovir
β Scribed by Hongwu Gao; Ashim K. Mitra
- Book ID
- 101341285
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 63 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
A series of 9-[(1,3-dihydroxy-2-propoxy)methyl]guanine mono-and diesters, 2a-i, 3a-d and 4a-d, were synthesized as potential prodrugs of ganciclovir and both 1 H NMR and 13 C NMR spectra were assigned to these esters based on spectral comparison with compounds of similar structure.
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Alkyl esters of ketorolac were synthesized as potential prodrugs for transdermal delivery and evaluated to determine the relationship between their skin permeation characteristics and their physicochemical properties. Solubility of the prodrugs in various vehicles was determined at room temperature