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Five undescribed aryltetralin lignans with cytotoxic activities from the fruits of Cleistanthus eberhardtii.
Nguyen, Lam Hong; Nguyen, Thi Hue; Tran, Viet Hung; Litaudon, Marc; Nguyen, Van Thanh; Doan, Thi Mai Huong; Pham, Van Cuong.
Afiliação
  • Nguyen LH; Institute of Marine Biochemistry of the Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Caugiay, Hanoi, Viet Nam; Hanoi University of Pharmacy, 13 Le Thanh Tong, Hoankiem, Hanoi, Viet Nam.
  • Nguyen TH; Institute of Marine Biochemistry of the Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Caugiay, Hanoi, Viet Nam.
  • Tran VH; Institute of Drug Quality Control - Ho Chi Minh City, 200 Co Bac Street, Co Giang Ward, District 1, Ho Chi Minh City, Viet Nam.
  • Litaudon M; Institut de Chimie des Substances Naturelles, CNRS-ICSN, UPR 2301, Université Paris-Saclay, 91198 Gif-sur-Yvette, France.
  • Nguyen VT; Institute of Marine Biochemistry of the Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Caugiay, Hanoi, Viet Nam.
  • Doan TMH; Institute of Marine Biochemistry of the Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Caugiay, Hanoi, Viet Nam; Graduate University of Science and Technology, VAST, 18 Hoang Quoc Viet, Caugiay, Hanoi, Viet Nam. Electronic address: huongdm@imbc.vast.vn.
  • Pham VC; Institute of Marine Biochemistry of the Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Caugiay, Hanoi, Viet Nam; Graduate University of Science and Technology, VAST, 18 Hoang Quoc Viet, Caugiay, Hanoi, Viet Nam. Electronic address: phamvc@imbc.vast.vn.
Fitoterapia ; 173: 105826, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38219842
ABSTRACT
Five undescribed lignans, cleiseberharnins A-D (1-4), cleiseberharside A (5) were isolated from the fruits of Cleistanthus eberhartii (Phyllanthaceae), together with six known aryltetralin lignans, cleistantoxin (6), picroburseranin (7), neocleistantoxin (8), 7-hydroxypicropolygamain (9), cleisindoside D (10), and cleisindoside A (11). Their structures and relative configurations were established by analysis of HRESIMS and NMR data, and quantum chemical calculations of JH,H coupling constants. The absolute configurations of 1-5 were determined by analysis of their experimental CD spectra and comparison with calculated electronic circular dichroism (ECD) spectra. All compounds (1-11) were evaluated for their cytotoxicity against KB, MCF-7, HepG-2, and Lu-1 human cancer cell lines. Among the tested compounds, compounds 6 and 7 showed strong activity against KB, MCF7, HepG2 and Lu-1 cell lines with IC50 values in the range of 0.02-0.62 µM. Compound 1 showed activity against three cancer cell lines KB, HepG2, and Lu-1 with IC50 values of 6.98, 7.61 and 11.75 µM, respectively. Compound 2 exhibited a selective inhibition with moderate cytotoxicity against Lu-1 with IC50 value of 15.30 µM. Compounds 4, 5 and 9 showed moderate activity against the three cancer cell lines with IC50 values in the range of 8.73-19.70 µM.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Lignanas / Malpighiales / Antineoplásicos / Antineoplásicos Fitogênicos Limite: Humans Idioma: En Revista: Fitoterapia Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Lignanas / Malpighiales / Antineoplásicos / Antineoplásicos Fitogênicos Limite: Humans Idioma: En Revista: Fitoterapia Ano de publicação: 2024 Tipo de documento: Article