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1.
J Org Chem ; 87(12): 7955-7967, 2022 06 17.
Artigo em Inglês | MEDLINE | ID: mdl-35653697

RESUMO

An efficient TfOH-catalyzed cascade C-H/N-H annulation of indole-2-carboxamides with benzoquinones has been developed for the synthesis of tetracyclic indolo[2,3-c]quinolinones. This reaction exhibits excellent chemo-/regioselectivity, achieving functionalization of the C-3 of indole and N-H of the amide moiety to form the new C-C and C-N bonds. Various expected products were synthesized from readily available starting materials in good to high yields with a wide substrate scope and good functional group tolerance. Among all synthetic products, 3d showed the most potent cytotoxicity toward the 4T1 cancer cell line with an IC50 value of 0.62 ± 0.05 µM. In vivo study demonstrated that 3d remarkably suppressed 4T1 xenograft tumor growth without body weight loss.


Assuntos
Quinolonas , Benzoquinonas , Catálise , Humanos , Indóis/química , Quinolonas/farmacologia
2.
Food Chem ; 455: 139814, 2024 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-38824735

RESUMO

Persimmon (Diospyros kaki) leaf is widely used as a tea substitute in East Asia, offering potential health benefits. Although studies have highlighted their effects on hyperpigmentation disorders, the active components remain unidentified. This study introduces a novel approach combining LC-MS/MS-based molecular networking with AlphaFold2-enabled virtual screening to expedite the identification of bioactive components in persimmon leaf. A total of 105 compounds were identified by MS/MS analysis. Further, virtual screening identified five flavonoids with potential anti-melanogenic properties. Bioassays confirmed myricetin, quercetin, and kaempferol inhibited melanogenesis in human melanocytes in a dose-dependent manner. Biolayer interferometry assays revealed strong binding affinity between these flavonols and hsTYR, with KD values of 23.26 ± 11.77 for myricetin, 12.43 ± 0.37 for quercetin, and 14.99 ± 3.80 µM for kaempferol. Molecular dynamics simulations provided insights into the binding interactions of these flavonols with hsTYR, particularly highlighting the essential role of the 3-OH group on the C-ring. This study elucidates the bioactive components responsible for the anti-melanogenic effects of persimmon leaf, supporting their use in product development.


Assuntos
Diospyros , Extratos Vegetais , Folhas de Planta , Espectrometria de Massas em Tandem , Diospyros/química , Folhas de Planta/química , Humanos , Extratos Vegetais/química , Extratos Vegetais/farmacologia , Melanócitos/efeitos dos fármacos , Melanócitos/metabolismo , Melanócitos/química , Flavonoides/química , Flavonoides/farmacologia , Melaninas/química , Melaninas/metabolismo , Cromatografia Líquida , Espectrometria de Massa com Cromatografia Líquida
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