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1.
Adv Mater ; 36(13): e2311102, 2024 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-38100677

RESUMO

The electronic structure and geometric configuration of catalysts play a crucial role to design novel perovskite-type catalysts for oxygen reduction reaction (ORR). Nowadays, many studies are more concerned with the influence of electronic structure and ignore the geometric effect, which plays a nonnegligible role in enhancing catalytic performances. Herein, this work regulates the MnO6 octahedral tilting degree of LaMnO3 by modulating the concentration of Y3+, excluding the electronic effect from the valence state of manganese. Plotting the MnO6 octahedral tilting degree as a function of concentration of Y3+ produces a volcano-shaped plot. The octahedral tilting can reduce the Mn-O covalency, generating more highly active Mn3+ and oxygen vacancies during ORR process. The specific activity has a positive correlation with octahedral tilting degree. Meanwhile, the octahedral tilting stabilizes Mn-O interactions during ORR process and promote stability. Based on experimental results and DFT calculations, octahedral tilting alters the rate-determining step (RDS) and decrease the energy barrier. Subsequent extended experiment confirms that octahedral tilting is the key factor to affect the catalytic performances.

2.
Chem Biol Drug Des ; 97(3): 565-571, 2021 03.
Artigo em Inglês | MEDLINE | ID: mdl-32914538

RESUMO

A series of indirubin derivatives hydrochloride were obtained using a convenient and mild method from indirubin. The newly synthesized compounds and their derivatives were characterized by 1 H NMR, 13 C NMR, and MS. Furthermore, we tested their IDO1 enzyme inhibitory activity and anti-proliferative activities in K562 tumor cells. The experimental results revealed that some of the compounds showed potential anti-enzyme and anti-tumor activity. Among of them, compound 4b exhibited certain inhibitory activity on IDO1 (IC50 : 29.52 µmol/L), and compound 4a displayed activity similar to indirubin in K562 tumor cells (IC50 : 24.96 µmol/L). This type of indirubin derivative is expected to have the potential to act as an immunologically active anti-tumor drug, indicating that further research will be worthwhile.


Assuntos
Antineoplásicos/síntese química , Antineoplásicos/metabolismo , Antineoplásicos/farmacologia , Sítios de Ligação , Linhagem Celular Tumoral , Proliferação de Células/efeitos dos fármacos , Inibidores Enzimáticos/química , Inibidores Enzimáticos/farmacologia , Humanos , Indolamina-Pirrol 2,3,-Dioxigenase/antagonistas & inibidores , Indolamina-Pirrol 2,3,-Dioxigenase/metabolismo , Indóis/química , Indóis/metabolismo , Indóis/farmacologia , Simulação de Acoplamento Molecular , Relação Estrutura-Atividade
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