Organoselenium compounds beyond antioxidants DOI
Ritu Mamgain, Garima Mishra,

Saumya Kriti

et al.

Future Medicinal Chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 1 - 23

Published: Dec. 22, 2024

Organoselenium chemistry has become a significant field due to its role in synthesizing numerous biologically active and therapeutic compounds. In early phase, researchers focused on designing organoselenium compounds with antioxidant properties were quite successful. last two decades, synthetic chemists shifted their focus toward synthesis of biological properties, moving beyond traditional properties. The review includes study organo-selenium as anticancer, antimicrobial, antiviral, antidiabetic, antithyroid, anti-inflammatory therapies, contributing disease treatment. This covers the medicinal applications over past 10 years, thus making it valuable resource for chemistry.

Language: Английский

Design, synthesis and biological evaluation of artesunate-Se derivatives as anticancer agents by inducing GPX4-mediated ferroptosis DOI

Meilin Ren,

Simin Liang,

Sitong Lin

et al.

Bioorganic Chemistry, Journal Year: 2024, Volume and Issue: 152, P. 107733 - 107733

Published: Aug. 16, 2024

Language: Английский

Citations

1

A prospective therapeutic strategy: GPX4-targeted ferroptosis mediators DOI

Jia-Yu Qian,

Chao-Yuan Lou,

Yili Chen

et al.

European Journal of Medicinal Chemistry, Journal Year: 2024, Volume and Issue: 281, P. 117015 - 117015

Published: Oct. 30, 2024

Language: Английский

Citations

1

Selenylated Analogs of Tacrine: Synthesis, in Silico and in Vitro Studies of Toxicology and Antioxidant Properties DOI
Manoela Sacramento,

Roberto B. Morais,

Ariana Silveira Lima

et al.

Chemistry - An Asian Journal, Journal Year: 2024, Volume and Issue: unknown

Published: July 10, 2024

We present our results on the synthesis and preliminary in silico vitro studies of toxicology antioxidant properties selenylated analogs Tacrine. Initially, we synthesized 2-aminobenzonitriles containing an organic selenium moiety, resulting sixteen compounds with various substituents linked to portion derived from diorganyl diselenide. These were then used as substrates reactions cyclic ketones, presence 1.4 equivalents trifluoroboroetherate a Lewis acid, synthesize Tacrine yields ranging 20 % 87 %. In explored computational parameters related activity hepatotoxicity. elucidated effects its hybrid (TSe) neutralizing ABTS radicals, scavenging DPPH reducing iron ions. Additionally, acute oral toxicity one compound was evaluated.

Language: Английский

Citations

0

Visible-light-promoted selenylation/cyclization of o-(1-alkynyl) benzoates to access seleno-substituted isocoumarins DOI

Mei-Lin Ren,

Xi-Rui Gong,

Yanyan Chen

et al.

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(36), P. 7327 - 7331

Published: Jan. 1, 2024

A simple and efficient method to access 4-selenyl-isocoumarin derivatives through visible-light-promoted selenylation/cyclization of o -(1-alkynyl) benzoates has been developed.

Language: Английский

Citations

0

Synthesis and application of new selanylfullerene derivatives as photosensitizers for photodynamic therapy DOI
Letiére C. Soares,

Josimar Vargas,

Bruno B. Ravanello

et al.

Chemistry - An Asian Journal, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 16, 2024

This study aims to describe the synthesis of a new class selanylfullerene derivatives in convergent strategy route, affording desired products few steps and good yields. C

Language: Английский

Citations

0

Synthesis and Antiosteoporotic Characterization of Diselenyl Maleimides: Discovery of a Potent Agent for the Treatment of Osteoporosis by Targeting RANKL DOI
Bin Li, Yao Wu,

Linkun Ying

et al.

Journal of Medicinal Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 19, 2024

To discover new osteoclast-targeting antiosteoporosis agents, we identified forty-six diselenyl maleimides, which were efficiently prepared using a novel, simple, and metal-free method at room temperature in short reaction time. Among them,

Language: Английский

Citations

0

Phenylseleno trifluoromethoxylation of alkenes DOI Creative Commons
Clément Delobel, Armen Panossian, Gilles Hanquet

et al.

Beilstein Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 20, P. 2434 - 2441

Published: Sept. 26, 2024

Trifluoromethoxylated molecules and selenylated compounds find a wide range of interesting applications, but separately. In order to combine the potential these two motifs propose new class compounds, we have developed an electrophilic phenylseleno trifluoromethoxylation alkenes, which leads β-selenylated trifluoromethoxylated or, upon subsequent reduction, ones.

Language: Английский

Citations

0

Selenium(II)‐Nitrogen Exchange (SeNEx) Chemistry: A Good Chemistry Suitable for Nanomole‐Scale Parallel Synthesis, DNA‐encoded Library Synthesis, and Bioconjugation DOI
Wei Hou,

Shaoneng Hou,

Yuang Gu

et al.

ChemBioChem, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 9, 2024

The continuous development of click reactions with new connecting linkage is crucial for advancing the frontiers chemistry. Selenium-nitrogen exchange (SeNEx) chemistry, a versatile chemistry in represents an all-encompassing term nucleophilic substitution events that replace nitrogen at electrophilic selenium(II) center, enabling flexible and efficient assembly linkages around Se(II) core. Several SeNEx chemistries have been developed inspired by biochemical reaction between Ebselen cysteine residue, demonstrated significant potential on-plate nanomole-scale parallel synthesis, selenium-containing DNA-encoded library (SeDEL) as well peptide protein bioconjugation. This concept aims to present origins, advancements, applications selenium(II)-nitrogen while also outlining directions future research this field.

Language: Английский

Citations

0

Recent advances of selenized tubulin inhibitors in cancer therapy DOI
Yang Zhao, Long Yan,

Yuan Xu

et al.

Bioorganic & Medicinal Chemistry Letters, Journal Year: 2024, Volume and Issue: unknown, P. 130037 - 130037

Published: Nov. 1, 2024

Language: Английский

Citations

0

ACE inhibitory peptides and flavor compounds from Se-enriched Bacillus natto fermented chickpea DOI Creative Commons
Ying Xu,

Jiarui Che,

Yang Wang

et al.

LWT, Journal Year: 2024, Volume and Issue: 215, P. 117190 - 117190

Published: Dec. 11, 2024

Language: Английский

Citations

0