New flavonol glycoside from Scabiosa prolifera L. aerial parts with in vitro antioxidant and cytotoxic activities

被引:16
作者
Al-Qudah, Mahmoud A. [1 ]
Otoom, Noor K. [1 ]
Al-Jaber, Hala I. [2 ]
Saleh, Ayman M. [3 ,4 ]
Abu Zarga, Musa H. [5 ]
Afifi, Fatma U. [6 ]
Abu Orabi, Sultan T. [5 ]
机构
[1] Yarmouk Univ, Dept Chem, Fac Sci, Irbid, Jordan
[2] Al Balqa Appl Univ, Dept Phys & Basic Sci, Fac Engn Technol, Amman, Jordan
[3] King Saud Bin Abdulaziz Univ Hlth Sci, Coll Appl Med Sci, Dept Clin Lab Sci, Jeddah, Saudi Arabia
[4] KAIMRC, Jeddah, Saudi Arabia
[5] Univ Jordan, Dept Chem, Sch Sci, Amman, Jordan
[6] Univ Jordan, Dept Pharmaceut Sci, Sch Pharm, Amman, Jordan
关键词
Scabiosa prolifera; Dipsacaceae; kaempferol-3-O-(4; 6-di-E-p-coumaroyl)--D-galactopyranoside; antioxidant activity; cytotoxic activity; PHENOLIC-COMPOUNDS; OLEANOLIC ACID; GROWING WILD; CONSTITUENTS; DIPSACACEAE; SAPONINS; LEAVES; PLANTS;
D O I
10.1080/14786419.2017.1305377
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Phytochemical investigation of the chemical constituents of the aerial parts of Scabiosa prolifera L. led to the isolation of one new flavonol glycoside, kaempferol-3-O-(4,6-di-E-p-coumaroyl)-- D-galactopyranoside (1), along with ten other known compounds including luteolin-7-O-(2-O-ethyl--glucopyranoside), -sitosterol, -sitosterylglucoside, ursolic acid, corosolic acid, ursolic acid 3-O--D-arabinopyranoside, apigenin, methyl--D-glucopyranoside, luteolin-7-O--glucopyranoside and isoorientin. The structures of all isolated compounds were established using chemical methods and spectroscopic methods including IR, UV, NMR (1D and 2D) and HRESIMS. All compounds were isolated for the first time from the plant. The antioxidant and cytotoxic activities of compounds 1 and 2 were also investigated. [GRAPHICS]
引用
收藏
页码:2865 / 2874
页数:10
相关论文
共 43 条
[1]  
Agrawal P.K., 1989, CARBON 13 NMR FLAVON
[2]   NMR-SPECTROSCOPY IN THE STRUCTURAL ELUCIDATION OF OLIGOSACCHARIDES AND GLYCOSIDES [J].
AGRAWAL, PK .
PHYTOCHEMISTRY, 1992, 31 (10) :3307-3330
[3]  
Akimaliev A. A., 1989, Chemistry of Natural Compounds, V25, P174, DOI 10.1007/BF00598405
[4]  
AL-EISAWI D M, 1982, Mitteilungen der Botanischen Staatssammlung Muenchen, V18, P79
[5]   New terpenes from Salvia palaestina Benth. and Salvia syriaca L. growing wild in Jordan [J].
Al-Jaber, Hala I. ;
Abrouni, Khadeja K. ;
Al-Qudah, Mahmuod A. ;
Abu Zarga, Musa H. .
JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2012, 14 (07) :618-625
[6]  
Al-Qudah MA, 2016, JORDAN J CHEM, V11, P99
[7]   New isoflavones from Gynandriris sisyrinchium and their antioxidant and cytotoxic activities [J].
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. .
FITOTERAPIA, 2015, 107 :15-21
[8]   Flavonoid and phenolic compounds from Salvia palaestina L. growing wild in Jordan and their antioxidant activities [J].
Al-Qudah, Mahmoud A. ;
Al-Jaber, Hala I. ;
Abu Zarga, Musa H. ;
Abu Orabi, Sultan T. .
PHYTOCHEMISTRY, 2014, 99 :115-120
[9]  
Almeida Ana P., 2006, Rev. bras. farmacogn., V16, P485, DOI 10.1590/S0102-695X2006000400008
[10]  
[Anonymous], 1999, HDB NATURAL FLAVONOI