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New isoflavones from Gynandriris sisyrinchium and their antioxidant and cytotoxic activities.
Al-Qudah, Mahmoud A; Saleh, Ayman M; Al-Jaber, Hala I; Tashtoush, Hasan I; Lahham, Jamil N; Abu Zarga, Musa H; Afifi, Fatma U; Abu Orabi, Sultan T.
Affiliation
  • Al-Qudah MA; Department of Chemistry, Faculty of Science, Yarmouk University, Irbid, Jordan. Electronic address: mahmoud.qudah@yu.edu.jo.
  • Saleh AM; Department of Basic Medical Sciences, King Saud Bin Abdulaziz University for Health Sciences, and King Abdullah International Medical Research Center (KAIMRC), Riyadh, Saudi Arabia.
  • Al-Jaber HI; Department of Applied Sciences, Faculty of Engineering Technology, Al-Balqa Applied University, Marka, Jordan. Electronic address: rhhjaber@yahoo.com.
  • Tashtoush HI; Department of Chemistry, Faculty of Science, Yarmouk University, Irbid, Jordan.
  • Lahham JN; Department of Biological Sciences, Faculty of Science, Yarmouk University, Irbid, Jordan.
  • Abu Zarga MH; Department of Chemistry, Faculty of Science, The University of Jordan, Amman, Jordan.
  • Afifi FU; Department of Pharmaceutical Sciences, Faculty of Pharmacy, The University of Jordan, Amman, Jordan.
  • Abu Orabi ST; Department of Chemistry, Faculty of Science, Yarmouk University, Irbid, Jordan.
Fitoterapia ; 107: 15-21, 2015 Dec.
Article in En | MEDLINE | ID: mdl-26410237
ABSTRACT
Chemical investigation of Gynandriris sisyrinchium (L.) Parl growing in Jordan resulted in the isolation and characterization of a total of twelve compounds two of which are reported here for the first time in nature. These new compounds included the isoflavones; 3'-methyl tenuifone (2) and gynandrinone (5). In addition, ten known compounds including; ß-sitosterol (1), 7,3'-dimethoxy-5,6,4'-trihydroxyisoflavone (3), iristectorigenin (4), hispidulin (6), galangustin (7), 6-hydroxybiochanin A (8), ursolic acid (9), ladanetin (10), 4'-O-methylgenistein (11) and ß-sitosterol glucoside (12) are also reported here for the first time from G. sisyrinchium. The isolated compounds were characterized by different spectroscopic methods including NMR (1D and 2D), UV, IR and MS (HRESIMS and EIMS). The antioxidant and cytotoxic activities of isoflavones 2, 3 and 5 were investigated. Compound 3 showed the highest antioxidant activity (IC50=17.3µg/mL), as compared to compounds 5 and 2 (IC50=26.7 and 51.7µg/mL, respectively). The cytotoxic activity against the human promyelocytic leukemia HL-60 cells revealed that compound 2 was the most active (40µM). The results indicate that the cytotoxicity of compound 2 is mediated by apoptosis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Iridaceae / Isoflavones / Antineoplastic Agents, Phytogenic / Antioxidants Limits: Humans Country/Region as subject: Asia Language: En Journal: Fitoterapia Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Iridaceae / Isoflavones / Antineoplastic Agents, Phytogenic / Antioxidants Limits: Humans Country/Region as subject: Asia Language: En Journal: Fitoterapia Year: 2015 Document type: Article