Results 1 to 10 of about 288,590 (166)

Clinical Persistence of Chlamydia trachomatis Sexually Transmitted Strains Involves Novel Mutations in the Functional αββα Tetramer of the Tryptophan Synthase Operon [PDF]

open access: yesmBio, 2019
Clinical persistence of Chlamydia trachomatis (Ct) sexually transmitted infections (STIs) is a major public health concern. In vitro persistence is known to develop through interferon gamma (IFN-γ) induction of indoleamine 2,3-dioxygenase (IDO), which ...
Naraporn Somboonna   +4 more
doaj   +3 more sources

Indole contributes to tetracycline resistance via the outer membrane protein OmpN in Vibrio splendidus [PDF]

open access: yes, 2020
As an interspecies and interkingdom signaling molecule, indole has recently received attention for its diverse effects on the physiology of both bacteria and hosts. In this study, indole increased the tetracycline resistance of Vibrio splendidus.
Guo, Ming   +6 more
core   +1 more source

Synthesis of Bis(3‐indolyl)methanes Mediated by Potassium tert‐Butoxide

open access: yesChemistryOpen, 2023
The indole moiety is an important N‐heterocycle found in natural products, and a key structural component of many value‐added chemicals including pharmaceuticals. In particular, bis(3‐indolyl)methanes (BIMs) are an important subgroup of indoles, composed
A. Sofia Santos   +5 more
doaj   +1 more source

Bisindolyl Maleimides and Indolylmaleimide Derivatives—A Review of Their Synthesis and Bioactivity

open access: yesPharmaceuticals, 2023
The evolution of bisindolyl maleimides and indolyl maleimide derivatives and their unique biological activities have stimulated great interest in medicinal chemistry programs.
Louise N. Cooney   +5 more
doaj   +1 more source

The Emergence of Insect Odorant Receptor-Based Biosensors

open access: yesBiosensors, 2020
The olfactory receptor neurons of insects and vertebrates are gated by odorant receptor (OR) proteins of which several members have been shown to exhibit remarkable sensitivity and selectivity towards volatile organic compounds of significant importance ...
Jonathan D. Bohbot, Sefi Vernick
doaj   +1 more source

Relation between Mood and the Host-Microbiome Co-Metabolite 3-Indoxylsulfate: Results from the Observational Prospective NutriNet-Santé Study

open access: yesMicroorganisms, 2021
Gut microbiota metabolizes tryptophan into indole, which can influence brain and behavior. Indeed, some oxidized derivatives of indole, formed in the liver, have neuroactive properties, and indole overproduction by the gut microbiota induces an anxio ...
Catherine Philippe   +8 more
doaj   +1 more source

From sequence-defined macromolecules to macromolecular pin codes [PDF]

open access: yes, 2020
Dynamic sequence-defined oligomers carrying a chemically written pin code are obtained through a strategy combining multicomponent reactions with the thermoreversible addition of 1,2,4-triazoline-3,5-diones (TADs) to indole substrates.
Badi, Nezha   +4 more
core   +1 more source

2-[3-(4-Chlorophenyl)-5-(4-fluorophenyl)-4,5-dihydro-1H-pyrazol-1-yl]-8H-indeno[1,2-d]thiazole

open access: yesIUCrData, 2019
The title molecule, C25H17ClFN3S, contains indenothiazolyl (A), pyrazolyl (B), fluorophenyl (C) and chlorophenyl (D) groups. The dihedral angles between the ring planes A/B, B/C and B/D are 14.2 (1), 83.0 (1) and 6.5 (2)°, respectively.
Gamal A. El-Hiti   +4 more
doaj   +1 more source

α-Glucosidase Inhibitors Based on Oleanolic Acid for the Treatment of Immunometabolic Disorders

open access: yesApplied Sciences, 2023
Using oleanolic acid as a starting compound, a series of new oleanane-type triterpenic derivatives were synthesized via O-acylation (with nicotinic, isonicotinic, and methoxycinnamic acid acyl chlorides), N-amidation (with cyclic- or polyamines), the ...
Anastasiya V. Petrova   +6 more
doaj   +1 more source

Indole diterpenoid natural products as the inspiration for new synthetic methods and strategies. [PDF]

open access: yes, 2017
Indole terpenoids comprise a large class of natural products with diverse structural topologies and a broad range of biological activities. Accordingly, indole terpenoids have and continue to serve as attractive targets for chemical synthesis.
Corsello, Michael A   +2 more
core   +1 more source

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