Cytotoxic and anti-inflammatory resorcinol and alkylbenzoquinone derivatives from the leaves of Ardisia sieboldii

Author:

Shahinozzaman Md12,Ishii Takahiro3,Halim Mohammad A.45,Hossain Md Amzad6,Islam Md Tofazzal7,Tawata Shinkichi23

Affiliation:

1. Department of Bioscience and Biotechnology, Faculty of Agriculture , University of the Ryukyus , Okinawa , Japan

2. PAK Research Center , University of the Ryukyus , Okinawa , Japan

3. Department of Bioscience and Biotechnology, Faculty of Agriculture , University of the Ryukyus , Senbaru 1, Nishihara-cho , Okinawa 903-0213 , Japan

4. Division of Computer Aided Drug Design , The Red-Green Research Centre , Dhaka 1219 , Bangladesh

5. Department of Physical Sciences , University of Arkansas-Fort Smith , Fort Smith , AR 72913 , USA

6. Subtropical Field Science Center, Faculty of Agriculture , University of the Ryukyus , Okinawa , Japan

7. Department of Biotechnology , Bangabandhu Sheikh Mujibur Rahman Agricultural University , Gazipur 1706 , Bangladesh

Abstract

Abstract Medicinal plants belonging to the genus Ardisia are traditionally used to cure various human diseases including inflammation and cancer. This study aimed to purify and characterize cytotoxic and anti-inflammatory compounds from Ardisia sieboldii leaves. Bioassay-guided chromatographic analyses yielded three compounds, 2-methyl-5-(8Z-heptadecenyl) resorcinol (1), 5-(8Z-heptadecenyl) resorcinol (2), and ardisiaquinone A (3), whereas liquid chromatography–electrospray ionisation–mass spectrometry chemical profiling revealed the presence of diverse resorcinol and alkylbenzoquinone derivatives in cytotoxic 70% methanol extracts. Chemical structures of 1 3 were confirmed by spectroscopic methods including 1H NMR (nuclear magnetic resonance), 13C NMR, and electrospray ionisation–mass spectrometry. Compounds 1 and 2 were purified from A. sieboldii for the first time, and all three compounds showed cytotoxicity against a panel of cancer cell lines and brine shrimps in a dose-response manner. Among them, compound 2 exhibited the highest cytotoxicity on cancer cells (IC50 values of 8.8–25.7 μM) as well as on brine shrimps (IC50 value of 5.1 μM). Compounds 1 3 exhibited anti-inflammatory effects through inhibiting protein denaturation (IC50 values of 5.8–9.6 μM), cyclooxygenase-2 activity (IC50 values of 34.5–60.1 μM), and nitrite formation in RAW 264.7 cells. Cytotoxic and anti-inflammatory activities of 1 3 demonstrated in this study deserve further investigation for considering their suitability as candidates or leads to develop anticancer and anti-inflammatory drugs.

Publisher

Walter de Gruyter GmbH

Subject

General Biochemistry, Genetics and Molecular Biology

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