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New limonophyllines A-C from the stem of Atalantia monophylla and cytotoxicity against cholangiocarcinoma and HepG2 cell lines.
Sombatsri, Aonnicha; Thummanant, Yutthapong; Sribuhom, Thurdpong; Boonmak, Jaursup; Youngme, Sujittra; Phusrisom, Suphanthip; Kukongviriyapan, Veerapol; Yenjai, Chavi.
Afiliação
  • Sombatsri A; Natural Products Research Unit, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, 40002, Thailand.
  • Thummanant Y; Natural Products Research Unit, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, 40002, Thailand.
  • Sribuhom T; Natural Products Research Unit, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, 40002, Thailand.
  • Boonmak J; Materials Chemistry Research Center, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, 40002, Thailand.
  • Youngme S; Materials Chemistry Research Center, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, 40002, Thailand.
  • Phusrisom S; Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand.
  • Kukongviriyapan V; Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand.
  • Yenjai C; Natural Products Research Unit, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, 40002, Thailand. chayen@kku.ac.th.
Arch Pharm Res ; 41(4): 431-437, 2018 Apr.
Article em En | MEDLINE | ID: mdl-29546611
ABSTRACT
Three new limonoids, limonophyllines A-C (1, 4 and 5), along with two known limonoids (2 and 3) and 11 acridone alkaloids (6-16) were isolated from the stems of Atalantia monophylla. All isolates were evaluated against cholangiocarcinoma, KKU-M156, and HepG2 cancer cell lines. Compounds 12, 14 and 16 displayed cytotoxicity against KKU-M156 cell line with IC50 ranging from 3.39 to 4.1 µg/mL while cytotoxicity against HepG2 cell line with IC50 ranging from 1.43 to 8.4 µg/mL. The structures of all isolated compounds were established by spectroscopic methods including 1D and 2D NMR, IR and mass spectrometry.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Colangiocarcinoma / Rutaceae / Citotoxinas / Limoninas / Antineoplásicos Fitogênicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Colangiocarcinoma / Rutaceae / Citotoxinas / Limoninas / Antineoplásicos Fitogênicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article