Biological activities of some 5-substituted N,N-dimethyltryptamines, α-methyltryptamines, and gramines
✍ Scribed by Beng T. Ho; William M. McIsaac; Rong An; Robert T. Harris; K. E. Walker; Patricia M. Kralik; Mauno M. Airaksinen
- Book ID
- 104759602
- Publisher
- Springer
- Year
- 1970
- Tongue
- English
- Weight
- 565 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0033-3158
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✦ Synopsis
Three series of derivatives of N,N-dimcthyltryptamine, ~r tryptamine and gramine bearing substituents of varying electronic nature on the C-5 position were tested for acute toxicity, effect on barbiturate sleeping time, antireserpine effect, swim maze, variable interval conditioned behavior, and inhibition of monoamine oxidase. No correlation could be made between the electronic effects and their pharmacological activities. It was thus suggested that there exist different pharmacological receptors for the tryptamines and gramines.
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## Abstract Chemical synthesis and biological activities of a new α‐melanotropin derivative are described. __N__^α^‐(5‐Bromovaleryl)‐__N__^α^‐deacetyl‐α‐melanotropin contains the 5‐bromopentanoyl group as a chemical ‘handle’ in place of the acetyl group of the natural hormone. The synthesis involve