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1.
Phytochemistry ; 135: 135-143, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-27989370

RESUMO

Four dimeric chalcone derivatives, 8″,9″-dihydrowelwitschin H, uvarins A-C, a naphthalene derivative, 2-hydroxy-3-methoxy-6-(4'- hydroxyphenyl)naphthalene, and the known dimeric chalcones, dependensin and welwitschin E, flavonoids, a cyclohexane oxide derivative, an aromatic aldehyde were isolated from the roots of Uvaria siamensis (Annonaceae). The structures of the compounds were elucidated by spectroscopic analysis, as well as by comparison with literature data. The isolated compounds with a sufficient amount for biological assays were evaluated for their antimalarial, antimycobacterial, and cytotoxic activities. The dimeric chalcones 8″,9″-dihydrowelwitschin H, uvarins B and C, dependensin and welwitschin E showed strong antiplasmodial activity with IC50 values of 3.10, 3.02, 3.09, 4.21 and 3.99 µg/mL, respectively. A possible biosynthesis pathway of the dimeric chalcones is discussed.


Assuntos
Antimaláricos/isolamento & purificação , Antimaláricos/farmacologia , Chalconas/farmacologia , Raízes de Plantas/química , Uvaria/química , Antibacterianos/farmacologia , Antimaláricos/química , Chalconas/química , Chalconas/isolamento & purificação , Flavonoides/química , Flavonoides/isolamento & purificação , Flavonoides/farmacologia , Concentração Inibidora 50 , Estrutura Molecular
2.
Planta Med ; 79(1): 83-6, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23180340

RESUMO

Two new C-benzylated dihydrochalcone derivatives, 4,2',4'-trihydroxy-6'-methoxy-3'(2''-hydroxybenzyl)dihydrochalcone (1) and 2',4'-dihydroxy-4,6'-dimethoxy-3'(2''-hydroxybenzyl)dihydrochalcone (2), along with six known flavonoid derivatives (3-8), a known dihydrochalcone dimer (9), three known aromatic esters (10-12), and one known aromatic amide (13), were isolated from the leaves of Melodorum siamensis. The structures of the compounds were elucidated by spectroscopic analysis, mainly 1D and 2D NMR techniques (1H, 13C, COSY, HMQC, and HMBC), as well as by comparison with literature data. The isolated compounds with a sufficient amount for biological assays were evaluated for their antimalarial, antimycobactirial, and cytotoxic activities. Compounds 1, 2, and 13 exhibited strong cytotoxicity against human tumor cell lines KB and NCI-H187, with IC50 values in the range of 0.66-7.16 µg/mL.


Assuntos
Annonaceae/química , Antibacterianos/isolamento & purificação , Antimaláricos/isolamento & purificação , Antineoplásicos/isolamento & purificação , Compostos de Benzil/isolamento & purificação , Chalconas/isolamento & purificação , Citotoxinas/isolamento & purificação , Antibacterianos/química , Antibacterianos/farmacologia , Antimaláricos/química , Antimaláricos/farmacologia , Antineoplásicos/química , Antineoplásicos/farmacologia , Compostos de Benzil/química , Compostos de Benzil/farmacologia , Linhagem Celular Tumoral , Chalconas/química , Chalconas/farmacologia , Citotoxinas/química , Citotoxinas/farmacologia , Humanos , Concentração Inibidora 50 , Estrutura Molecular , Folhas de Planta/química
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