CENTRAL STIMULANT ACTIONS OF ALPHA-ALKYL SUBSTITUTED TRYPTAMINES IN MICE.
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Body Temperature↗
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Results for “Tryptamines”
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THE EFFECTS OF ALPHA-ALKYL SUBSTITUTED TRYPTAMINES ON 5-HYDROXYTRYPTAMINE UPTAKE BY BLOOD PLATELETS.
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5-Hydroxytryptophan↗
INTERFERING SUBSTANCES BY DETERMINATION OF POISONS IN AUTOPSY MATERIAL. IV. TRYPTAMINE.
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Alkaloids↗
INTERACTION BETWEEN THE TRYPTAMINE AND THE MONOAMINE OXIDASE IN THE DIGESTIVE AND THE CENTRAL NERVOUS SYSTEMS.
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Biochemical Phenomena↗
[INDOLE DERIVATIVES. SYNTHESIS OF BETA-ALKYL- AND BETA-ARYL-TRYPTAMINES].
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Chemistry, Pharmaceutical↗
[COMPARATIVE STUDY OF TRYPTAMINE BLOCKING AGENTS].
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Guinea Pigs↗
PARGYLINE HYDROCHLORIDE, HYPERTENSION, URINARY TRYPTAMINE, AND VASCULAR REFLEXES.
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Blood Pressure↗
[COMPARATIVE AUXIN EFFECT OF TRYPTAMINE AND SEROTONIN].
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Indoleacetic Acids↗
A STUDY OF THE POTENTIATION OF TRYPTAMINE BY MONOAMINE OXIDASE INHIBITORS IN THE DOG.
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Blood↗
THE MELTING POINT AND STRUCTURE OF TRYPTAMINE.
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Chemical Phenomena↗
Tryptolines. Formation from tryptamines and 5-MTHF by human platelets.
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Adult↗
[On the basically substituted tryptamines and tryptophols. 1. Synthesis of in 1-position substituted derivateves].
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Chemistry, Pharmaceutical↗
[Synthesis and antiserotonin activity of various substituted tryptamines].
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Animals↗
[Basic substituted tryptamines and tryptophols. 3. Pharmacologic studies on 1- and 2-position of basic substituted derivatives].
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Animals↗
[Receptor affinity of ecliptic fixed tryptamine and serotonin analogs].
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Blood Platelets↗
Mass spectrometric and nuclear magnetic resonance confirmation of a 3,3-spirocyclic indole derivative formed from melatonin and related acyl tryptamines.
When melatonin is reacted with pentafluoropropionic anhydride for selected ion monitoring or electron capture gas chromatographic analysis a volatile product results. Examination of the product by combined gas chromatography mass spectrometry has established that the molecular weight of 360 corresponds to the addition of one molecule of pentafluoropropionic acid followed by dehydration. Further spectroscopic and chemical examination using mass spectrometry and nuclear magnetic resonance with isotopic labelling has established that the product is a 3,3-spirocyclic indole derivative. Several analogous compounds were also examined and their mass spectra studied.
Indoles↗
[Synthesis of new substituted tryptamines].
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Chemical Phenomena↗
[Synthesis and incorporation of a 14C-and 3H-labeled 4-dimethylallyl-tryptophan and a 14C-labeled 4-dimethylallyl-tryptamine as well as incorporation of a 14C-labelled Dimethylallyl-pyrophosphate].
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Carbon Isotopes↗