Results 11 to 20 of about 29,916 (207)

A ferrocene redox-active triazolium macrocycle that binds and senses chloride [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2012
A ferrocene bis(triazole) macrocycle was synthesised in good yield by the Eglinton coupling of an acyclic bis(alkyne) precursor and characterised in the solid state by X-ray crystallography. Alkylation gives the corresponding triazolium macrocycle, which
Nicholas G. White, Paul D. Beer
doaj   +3 more sources

Supramolecular complexes of dihydroazolopyrimidines with macrocyclic receptors: synthesis, rapid analysis, and evaluation [PDF]

open access: yesBeilstein Journal of Organic Chemistry
One of the main challenges limiting the medical use of dihydroazolopyrimidine derivatives is their poor water solubility. However, this problem can be significantly reduced by binding to supramolecular receptors.
Daria Miasnikova   +8 more
doaj   +2 more sources

Performance evaluation of flexible macrocycle docking in AutoDock [PDF]

open access: yes, 2022
Macrocycles represent an important class of ligands, both in natural products and designed drugs. In drug design, macrocyclizations can impart specific ligand conformations and contribute to passive permeation by encouraging intramolecular H-bonds ...
Matthew, Holcomb   +3 more
core   +2 more sources

Threading a linear molecule through a macrocycle thanks to boron [PDF]

open access: yes, 2023
Two BODIPYs and one boron beta-diketonate were threaded through a macrocycle bearing a 2,2’-biphenol unit, showing thus the ability of boron to act as a gathering atom.
Fabienne, Berrée   +7 more
core   +2 more sources

Artificial Macrocycles [PDF]

open access: yesSynlett, 2018
Artificial macrocycles recently became popular as a novel research field in drug discovery. As opposed to their natural twins, artificial macrocycles promise to have better control on synthesizability and control over their physicochemical properties resulting in druglike properties. Very few synthetic methods allow for the convergent, fast but diverse
Abdelraheem   +3 more
openaire   +2 more sources

Photosensitizers Mediated Photodynamic Inactivation against Fungi

open access: yesNanomaterials, 2021
Superficial and systemic fungal infections are essential problems for the modern health care system. One of the challenges is the growing resistance of fungi to classic antifungals and the constantly increasing cost of therapy.
Daniel Ziental   +4 more
doaj   +1 more source

A DNA-Encoded Macrocycle Library that Resembles Natural Macrocycles [PDF]

open access: yes, 2019
Herein we perform a seven-step chemical synthesis of a DNA-encoded macrocycle library (DEML) on DNA. Inspired by polyketide and mixed peptide-polyketide natural products, the library was designed to incorporate rich backbone diversity ...
Dennis G., Gillingham   +4 more
core   +2 more sources

Crystal structure of cyclo-tris(μ-3,4,5,6-tetrafluoro-o-phenylene-κ2C1:C2)trimercury–tetracyanoethylene (1/1)

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
The title compound, [Hg3(C6F4)3]·C6N4, contains one molecule of tetracyanoethylene B per one molecule of mercury macrocycle A, i.e., A•B, and crystallizes in the monoclinic space group C2/c.
Raúl Castañeda   +2 more
doaj   +1 more source

Computational Site Saturation Mutagenesis of Canonical and Non-Canonical Amino Acids to Probe Protein-Peptide Interactions

open access: yesFrontiers in Molecular Biosciences, 2022
Technologies for discovering peptides as potential therapeutics have rapidly advanced in recent years with significant interest from both academic and pharmaceutical labs.
Jeffrey K. Holden   +4 more
doaj   +1 more source

Spectral manifestation of substitution of out-of-plane ligands in metallophtalocyanines

open access: yesEPJ Web of Conferences, 2017
In our study, we demonstrate the splitting effect of long-wavelength bands in absorption spectra (excitation of fluorescence) of the series of Zn(II), Ti(IV), Zr(IV) and Hf(IV) phthalocyanines at low temperatures.
Starukhin A.   +6 more
doaj   +1 more source

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