Tyrosinase Inhibitory Activity of Chemical Constituents of Euphorbia macrostegia

被引:0
|
作者
Ozlem Demirkiran
Gulacti Topcu
Ali Azarpira
M. Iqbal Choudhary
机构
[1] Trakya University,D.O.E. Great Lakes Bioenergy Research Center
[2] Department of Pharmacognosy,Department of Chemistry, College of Sciences
[3] Faculty of Pharmacy,undefined
[4] Bezmialem Vakif University,undefined
[5] Faculty of Pharmacy,undefined
[6] Department of Pharmacognosy,undefined
[7] H.E.J. Research Institute of Chemistry,undefined
[8] International Center for Chemical Sciences,undefined
[9] University of Karachi,undefined
[10] University of Wisconsin-Madison,undefined
[11] King Said University,undefined
来源
关键词
Boiss; long chain fatty acids; flavonoid glycosides; tyrosinase inhibitory activity; 2-(4-hydroxyphenyl)ethylhentriacontanoate;
D O I
暂无
中图分类号
学科分类号
摘要
The chloroform extract of the aerial parts of E. macrostegia has yielded a new compound, 2-(4-hydroxyphenyl)-ethylhentriacontanoate (1), along with hentriacontan-1-ol (2), lupenone (3), cycloart-22-ene-3,25-diol (4), 3,3′,4′-tri-O-methylellagic acid (5), cleomiscosin (6), and glucoclioniasterol (stigmast-5-en-3-O-β-glucopyranoside) (7), and from the ethyl acetate extract of aerial parts of the plant isoquercetin (8), quercetin-3-O-α-arabinofuranoside (avicularin) (9), and rutin (10) have been isolated. Compounds 1–10 were tested for their tyrosinase inhibitory activity, and 2 exhibited an IC50 value of 71.4 μM, almost comparable to standard kojic acid (IC50 58.2 μM). Compounds 1–4 also showed good activity with IC50 values of 77.2, 78.6, 71.4, and 77.5 μM, respectively.
引用
收藏
页码:810 / 813
页数:3
相关论文
共 50 条
  • [21] Chemical Constituents of Euphorbia sororia
    Palida Abulizi
    Yuanyuan Cong
    Mirensha Yakupu
    Atikanmu Wahepu
    Chemistry of Natural Compounds, 2014, 50 : 908 - 909
  • [22] Constituents of the pollen of Crocus sativus L. and their tyrosinase inhibitory activity
    Li, CY
    Wu, TS
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2002, 50 (10) : 1305 - 1309
  • [23] Phenolic Constituents from the Heartwood of Artocapus altilis and their Tyrosinase Inhibitory Activity
    Mai Ha Khoa Nguyen
    Hai Xuan Nguyen
    Mai Thanh Thi Nguyen
    Nhan Trung Nguyen
    NATURAL PRODUCT COMMUNICATIONS, 2012, 7 (02) : 185 - 186
  • [24] Chemical synthesis and tyrosinase inhibitory activity of rhododendrol glycosides
    Iwadate, Takehiro
    Kashiwakura, Yutaka
    Masuoka, Noriyoshi
    Yamada, Yoichi
    Nihei, Ken-ichi
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2014, 24 (01) : 122 - 125
  • [25] Chemical constituents of Piper aduncum and their inhibitory effects on soluble epoxide hydrolase and tyrosinase
    Bui Thi Thuy Luyen
    Nguyen Phuong Thao
    Widowati, Wahyu
    Fauziah, Nurul
    Maesaroh, Maesaro
    Herlina, Tati
    Kim, Young Ho
    MEDICINAL CHEMISTRY RESEARCH, 2017, 26 (01) : 220 - 226
  • [26] Chemical Constituents from Typhonium giganteum Rhizome and Their Antioxidant, Tyrosinase Inhibitory Activities
    Shu, Penghua
    Zhang, Lingxiang
    Liu, Wanrong
    Fei, Yingying
    Sun, Mengyuan
    Lou, Yueyue
    Liu, Anqi
    Yu, Mengzhu
    Li, Junping
    Wei, Xialan
    Sun, Na
    RECORDS OF NATURAL PRODUCTS, 2021, 15 (01) : 53 - 58
  • [27] Chemical constituents of Piper aduncum and their inhibitory effects on soluble epoxide hydrolase and tyrosinase
    Bui Thi Thuy Luyen
    Nguyen Phuong Thao
    Wahyu Widowati
    Nurul Fauziah
    Maesaro Maesaroh
    Tati Herlina
    Young Ho Kim
    Medicinal Chemistry Research, 2017, 26 : 220 - 226
  • [28] Identification of chemical constituents from the bark of Larix kaempferi and their tyrosinase inhibitory effect
    Kakumu, Yuya
    Yamauchi, Kosei
    Mitsunaga, Tohru
    HOLZFORSCHUNG, 2019, 73 (07) : 637 - 643
  • [29] Mushroom tyrosinase inhibitory activity of esculetin isolated from seeds of Euphorbia lathyris L.
    Masamoto, Y
    Ando, H
    Murata, Y
    Shimoishi, Y
    Tada, M
    Takahata, K
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2003, 67 (03) : 631 - 634
  • [30] Chemical constituents from Euphorbia hirta
    Li, En-Tao
    Liu, Kuan-Hui
    Zang, Ming-Hui
    Zhang, Xue-Lan
    Jiang, Hai-Qiang
    Zhou, Hong-Lei
    Wang, De-Yun
    Liu, Jia-Guo
    Hu, Yuan-Liang
    Wu, Yi
    BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2015, 62 : 204 - 207