Molecular binding behaviors and thermodynamics of ferrocenyl dimethylaminium derivatives by anionic pillar[5]arene

2015 ◽  
Vol 13 (44) ◽  
pp. 10808-10812 ◽  
Author(s):  
Cui-Fang Zhang ◽  
Sheng-Hua Li ◽  
Cai-Cai Zhang ◽  
Yu Liu

A novel anionic water-soluble pillar[5]arene (4C-WP5A) was synthesized via a convenient synthetic strategy of the direct cyclization of a functionalized hydroquinone monomer.

2015 ◽  
Vol 51 (30) ◽  
pp. 6621-6624 ◽  
Author(s):  
Junwei Ma ◽  
Hongmei Deng ◽  
Suxiang Ma ◽  
Jian Li ◽  
Xueshun Jia ◽  
...  

Complexation of paraquat derivatives and bis(N-mono-substituted bipyridine) cations by a negatively charged carboxylato-biphen[3]arene in water is described.


2005 ◽  
Vol 71 (2) ◽  
Author(s):  
Nicola Angelini ◽  
Norberto Micali ◽  
Valentina Villari ◽  
Placido Mineo ◽  
Daniele Vitalini ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2530
Author(s):  
Martin Studenovský ◽  
Anna Rumlerová ◽  
Libor Kostka ◽  
Tomáš Etrych

Recently, the antitumor potential of benzimidazole anthelmintics, such as mebendazole and its analogues, have been reported to have minimal side effects, in addition to their well-known anti-parasitic abilities. However, their administration is strongly limited owing to their extremely poor solubility, which highly depletes their overall bioavailability. This study describes the design, synthesis, and physico-chemical properties of polymer-mebendazole nanomedicines for drug repurposing in cancer therapy. The conjugation of mebendazole to water-soluble and biocompatible polymer carrier was carried out via biodegradable bond, relying on the hydrolytic action of lysosomal hydrolases for mebendazole release inside the tumor cells. Five low-molecular-weight mebendazole derivatives, differing in their inner structure, and two polymer conjugates differing in their linker structure, were synthesized. The overall synthetic strategy was designed to enable the modification and polymer conjugation of most benzimidazole-based anthelmintics, such as albendazole, fenbendazole or albendazole, besides the mebendazole. Furthermore, the described methodology may be suitable for conjugation of other biologically active compounds with a heterocyclic N-H group in their molecules.


2020 ◽  
Vol 4 (2) ◽  
pp. 555-566 ◽  
Author(s):  
Nathan R. Paisley ◽  
Christopher M. Tonge ◽  
Don M. Mayder ◽  
Kyle A. Thompson ◽  
Zachary M. Hudson

Spectrally tunable, two-photon active benzothiadiazole-based fluorescent materials are realized by a simple synthetic strategy. Deep red emission from two-photon absorption, and incorporation into water-soluble polymer dots are achieved.


2016 ◽  
Vol 14 (46) ◽  
pp. 10804-10811 ◽  
Author(s):  
Kui Wang ◽  
Jian-Hua Cui ◽  
Si-Yang Xing ◽  
Hong-Xi Dou

A unique regioselective recognition of N-methyl-N′-(naphthalen-2-ylmethyl)-4,4′-bipyridinium bromide iodide using a p-sulfonatocalix[4]arene was found.


2017 ◽  
Vol 71 ◽  
pp. 351-362 ◽  
Author(s):  
José M. Landeros ◽  
Fernando Belmont-Bernal ◽  
Alma Teresa Pérez-González ◽  
Mario Israel Pérez-Padrón ◽  
Patricia Guevara-Salazar ◽  
...  

2008 ◽  
Vol 2008 ◽  
pp. 1-10 ◽  
Author(s):  
M. David Maree ◽  
Eberhard W. Neuse ◽  
Elizabeth Erasmus ◽  
Jannie C. Swarts

The general synthetic strategy towards water-soluble biodegradable drug carriers and the properties that they must have are discussed. The syntheses of water-soluble biodegradable copolymers of lysine and aspartic acid as potential drug-delivering devices, having amine-functionalised side chains are then described. Covalent anchoring of carboxylic acid derivatives of the antineoplastic ferrocene and photodynamically active phthalocyanine moieties to the amine-containing drug carrier copolymers under mild coupling conditions has been achieved utilising the coupling reagent O-benzotriazolyl-N,N,N′,N′-tetramethyluronium hexafluorophosphate to promote formation of the biodegradable amide bond. Even though the parent antineoplastic ferrocene and phthalocyanine derivatives are themselves insoluble in water at pH < 7, the new carrier-drug conjugates that were obtained are well water-soluble.


2020 ◽  
Vol 18 (39) ◽  
pp. 7899-7906
Author(s):  
Jonathan Martinelli ◽  
Rogelio Jiménez-Juárez ◽  
Diego Alberti ◽  
Simonetta Geninatti Crich ◽  
Kristina Djanashvili

The advantage of a solid-phase synthetic strategy with DEAM-PS resin is applied for a clean and efficient preparation of water-soluble DOTA derivatives conjugated with phenylboronic functional groups.


Author(s):  
J. G. Robertson ◽  
D. F. Parsons

The extraction of lipids from tissues during fixation and embedding for electron microscopy is widely recognized as a source of possible artifact, especially at the membrane level of cell organization. Lipid extraction is also a major disadvantage in electron microscope autoradiography of radioactive lipids, as in studies of the uptake of radioactive fatty acids by intestinal slices. Retention of lipids by fixation with osmium tetroxide is generally limited to glycolipids, phospholipids and highly unsaturated neutral lipids. Saturated neutral lipids and sterols tend to be easily extracted by organic dehydrating reagents prior to embedding. Retention of the more saturated lipids in embedded tissue might be achieved by developing new cross-linking reagents, by the use of highly water soluble embedding materials or by working at very low temperatures.


Sign in / Sign up

Export Citation Format

Share Document