JPET Introducing ALZET?ew Model 2006 Pump

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by FELLOWS, E. J.
Right arrow Articles by LIVINGSTON, A. E.
Right arrow Search for Related Content
PubMed
Right arrow Articles by FELLOWS, E. J.
Right arrow Articles by LIVINGSTON, A. E.
Journal of Pharmacology And Experimental Therapeutics, Vol. 73, Issue 1, 27-32, 1941
Copyright © 1941 by American Society for Pharmacology and Experimental Therapeutics


THE LOCAL ANESTHETIC ACTIVITY OF CERTAIN DERIVATIVES OF agr AND beta-NAPHTHOL

EDWIN J. FELLOWS 1, RAYMOND W. CUNNINGHAM 1, and A. E. LIVINGSTON 1

1 From the Department of Pharmacology, Temple University School of Medicine, Philadelphia, Pennsylvania

1. In the present experiments the hydrochlorides of agr-morpholino methyl-beta naphthol (I), agr-piperidino methyl-beta-naphthol (II), beta-piperidino methyl agr-naphthyl p-aminobenzoate (III), beta-morpholino methyl agr-naphthyl p-aminobenzoate (IV), agr-morpholino methyl beta-naphthyl p-aminobenzoate (V), agr-piperidino-methyl beta-naphthyl benzoate (VI) and agr-piperidino methyl-beta-naphthyl p-aminobenzoate (VII) were found to produce local anesthesia.

2. Compounds I and II produced marked anesthesia intracutaneously in guinea-pigs but caused irritation. Compound II also was more toxic than procaine subcutaneously in guinea pigs. Compounds III, IV and V are very unstable in solution and produce anesthesia of poor depth and variable duration.

3. Compounds VI and VII produced marked anesthesia and VII was found to have an extremely low subcutaneous toxicity. Both compounds produced irritation in corneal and intradermal tests.

Submitted on May 6, 1941







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1941 by the American Society for Pharmacology and Experimental Therapeutics.