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Cytotoxic homoisoflavonoids from the bulbs of Bellevalia flexuosa.
El-Elimat, Tamam; Rivera-Chávez, José; Burdette, Joanna E; Czarnecki, Austin; Alhawarri, Maram B; Al-Gharaibeh, Mohammad; Alali, Feras; Oberlies, Nicholas H.
Afiliação
  • El-Elimat T; Department of Medicinal Chemistry and Pharmacognosy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan. Electronic address: telimat@just.edu.jo.
  • Rivera-Chávez J; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, North, Carolina, 27402, United States.
  • Burdette JE; Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, Chicago, IL 60612, United States.
  • Czarnecki A; Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, Chicago, IL 60612, United States.
  • Alhawarri MB; Department of Medicinal Chemistry and Pharmacognosy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan.
  • Al-Gharaibeh M; Department of Natural Resources and Environment, Faculty of Agriculture, Jordan University of Science and Technology, Irbid 22110, Jordan.
  • Alali F; Faculty of Pharmacy, Qatar University, Doha 2713, Qatar.
  • Oberlies NH; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, North, Carolina, 27402, United States.
Fitoterapia ; 127: 201-206, 2018 Jun.
Article em En | MEDLINE | ID: mdl-29471027
ABSTRACT
Four new homoisoflavonoids, 7-O-methyl-8-demethoxy-3'-hydroxy-3,9-dihydropunctatin (4), 6-hydroxy-8-demethoxy-4'-O-methyl-3,9-dihydropunctatin (8), 7,4'-O-dimethyl-8-demethoxy-3,3'-dihydroxy-3,9-dihydropunctatin (13), and 7-O-methyl-3-hyroxy-3,9-dihydropunctatin (14) were identified from a chloroform extract of the bulbs of Bellevalia flexuosa, along with 13 known analogues. The structures were determined by analysis of HRMS and NMR data, while ECD spectroscopy enabled the assignment of the absolute configurations of the new compounds 4, 8, 13 and 16. The cytotoxic activities of the isolated compounds (1-17) were evaluated using a panel of human cancer cell lines. Compounds 2 and 7 were the most potent against the MDA-MB-435 (melanoma) cancer cell line with IC50 values of 1.6 and 2.0 µM, respectively, and were essentially equipotent against the OVCAR3 (ovarian) cancer cell line with IC50 values of 9.5 and 10.8 µM, respectively. However, compound 7, with an IC50 value of 3.6 µM, was the most potent against the MDA-MB-231 (breast) cancer cell line.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Raízes de Plantas / Asparagaceae / Isoflavonas / Antineoplásicos Fitogênicos Limite: Humans Idioma: En Revista: Fitoterapia Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Raízes de Plantas / Asparagaceae / Isoflavonas / Antineoplásicos Fitogênicos Limite: Humans Idioma: En Revista: Fitoterapia Ano de publicação: 2018 Tipo de documento: Article