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Felipe Augusto Dörr

2 papers in the library · 74 citations · publishing 2009-2013

Papers

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Tryptamine and dimethyltryptamine inhibit indoleamine 2,3 dioxygenase and increase the tumor-reactive effect of peripheral blood mononuclear cells.

Cell biochemistry and function July 2013 Melissa Cavalheiro Tourino, Edson Mendes De Oliveira, Luziane Potrich Bellé et al.

Indoleamine 2,3-dioxygenase (IDO) is an interferon-γ (IFN-γ)-induced tryptophan-degrading enzyme, producing kynurenine (KYN) that participates in the mechanism of tumor immune tolerance. Thus, IDO inhibition has been considered a strategy for anticancer therapy. The aim of this study was to identify whether the metabolites originated from the competitive routes of tryptophan metabolism, such as...

DOI: 10.1002/cbf.2980 (opens in new tab) Full text (opens in new tab) Immune escape Kynurenine pathway Tolerance Tryptophan metabolism +1

Gas chromatographic analysis of dimethyltryptamine and β‐carboline alkaloids in ayahuasca, an amazonian psychoactive plant beverage

Phytochemical Analysis January 12, 2009 Ana Paula Salum Pires, Carolina Dizioli Rodrigues de Oliveira, Sidnei Moura et al. 74 citations

Abstract Introduction Ayahuasca is obtained by infusing the pounded stems of Banisteriopsis caapi in combination with the leaves of Psychotria viridis . P . viridis is rich in the psychedelic indole N , N ‐dimethyltryptamine, whereas B . caapi contains substantial amounts of β ‐carboline alkaloids, mainly harmine, harmaline and tetrahydroharmine, which are monoamine‐oxidase inhibitors. Because...

DOI: 10.1002/pca.1110 (opens in new tab) Ayahuasca Harmine Harmaline Gas chromatography +2