| Literature DB >> 4009430 |
Abstract
New dihydropyridine in equilibrium pyridinium salt-type redox carrier systems were developed in which the drug is linked via the ring nitrogen atom of nicotinamide. The rate of oxidation of the dihydropyridine forms, and thus the overall and brain-specific distribution of the corresponding 3-carbamoyl-1-carbamoylalkyl-drug quaternary salts, depends on the number of methylene groups separating the ring nitrogen and the carbamoyl function linked to the drug.Entities:
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Year: 1985 PMID: 4009430 DOI: 10.1002/jps.2600740304
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534