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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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Melanotropin Receptors I. Synthesis and
✍ Rudolf Wunderlin; Panagiota Minakakis; Aung Tun-Kyi; Shub Dev Sharma; Robert Sch 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 German ⚖ 699 KB

## 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