Literature DB >> 29274489

Branching tryptamines as a tool to tune their antiproliferative activity.

Rinat F Salikov1, Konstantin P Trainov1, Irina K Belousova2, Aleksandr Yu Belyy1, Ulyana Sh Fatkullina3, Regina V Mulyukova3, Liana F Zainullina4, Yulia V Vakhitova4, Yury V Tomilov5.   

Abstract

The influence of a series of tryptamine derivatives on the viability of normal (HEK293) and tumor (HepG2, Jurkat and SH-SY5Y) cells has been evaluated. All tryptamines tested were three different substitution types: C- and N-branching, and indole benzylation. All the derivations enhance the activity of compounds separately, although the effects of different substitutions were not additive. Thus, combinations of C- and N-branchings as well as C-branching and indole benzylation gave little or no increase in activity.
Copyright © 2017 Elsevier Masson SAS. All rights reserved.

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Keywords:  Branching amines; Cyclopropylketone arylhydrazones; Cytotoxicity; MAO degradation; Rearrangement; Tryptamine derivatives

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Year:  2017        PMID: 29274489     DOI: 10.1016/j.ejmech.2017.12.028

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  1 in total

1.  Potent, Selective, Water Soluble, Brain-Permeable EP2 Receptor Antagonist for Use in Central Nervous System Disease Models.

Authors:  Radhika Amaradhi; Avijit Banik; Shabber Mohammed; Vidyavathi Patro; Asheebo Rojas; Wenyi Wang; Damoder Reddy Motati; Ray Dingledine; Thota Ganesh
Journal:  J Med Chem       Date:  2020-01-16       Impact factor: 7.446

  1 in total

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