Refine
Has Fulltext
- no (3)
Document Type
- Article (3) (remove)
Language
- English (3)
Is part of the Bibliography
- yes (3)
Keywords
- anthracene (3) (remove)
Institute
Leishmaniasis is a vector-borne disease caused by protozoal Leishmania parasites. Previous studies have shown that endoperoxides (EP) can selectively kill Leishmania in host cells.
Therefore, we studied in this work a set of new anthracene-derived EP (AcEP) together with their non-endoperoxidic analogs in model systems of Leishmania tarentolae promastigotes (LtP) and J774 macrophages for their antileishmanial activity and selectivity.
The mechanism of effective compounds was explored by studying their reaction with iron (II) in chemical systems and in Leishmania. The correlation of structural parameters with activity demonstrated that in this compound set, active compounds had a LogP(OW) larger than 3.5 and a polar surface area smaller than 100 angstrom(2).
The most effective compounds (IC50 in LtP < 2 mu M) with the highest selectivity (SI > 30) were pyridyl-/tert-butyl-substituted AcEP.
Interestingly, also their analogs demonstrated activity and selectivity. In mechanistic studies, it was shown that EP were activated by iron in chemical systems and in LtP due to their EP group.
However, the molecular structure beyond the EP group significantly contributed to their differential mitochondrial inhibition in Leishmania.
The identified compound pairs are a good starting point for subsequent experiments in pathogenic Leishmania in vitro and in animal models.
Programmable oils feature tunable viscosity and therefore possess potential for technical improvements and innovative solutions in many lubricated applications. Herein, we describe the first assessment of the variability of rheological properties of light-programmable 9-anthracene ester-terminated polydimethylsiloxanes (PDMS-As), including implications that arise with UV-light as an external trigger. We applied a modified rheometer setup that enables the monitoring of dynamic moduli during exposure to UV-light. The reversible dimerization of anthracene esters is used to either link PDMS chains by UV-A radiation (365 nm) or cleave chains by UV-C radiation (254 nm) or at elevated temperatures (>130 degrees C). Thermal cleavage fully restores the initial material properties, while the photochemical cleavage of dimers occurs only to a limited extent. Prolonged UV radiation causes material damage and in turn reduces the range of programmable rheological properties. The incomplete cleavage contributes to a gradual buildup of viscosity over a course of several switching cycles, which we suggest to result from chain length-dependent reaction kinetics. Material property gradients induced during radiation due to attenuation of the light beam upon its passing through the oil layer have to be considered, emphasizing the need for proper mixing protocols during the programming step. The material in focus shows integrated photorheology and is suggested to improve the performance of silicone oils in friction systems.
In this paper, we report on the fluorescence behaviour of three regioisomers which consist of two 9-anthracenyl fluorophores and of differently substituted dithiodicyanoethene moieties. These isomeric fluorescent probes show different quantum yields (phi(f)). In these probes, an oxidative photoinduced electron transfer (PET) from the excited 9-anthracenyl fluorophore to the dithiodicyanoethene unit quenches the fluorescence. This quenching process is accelerated by an intramolecular charge transfer (ICT) of the push-pull pi-electron system of the dithiodicyanoethene group. The acceleration of the PET depends on the strength of the ICT unit. The higher the dipole moment of the ICT unit, the stronger the observed fluorescence quenching. To the best of our knowledge, this is the first report of a regioisomeric influence on an oxidative PET by an ICT.