Synthesis of xanthone derivatives based on α-mangostin and their biological evaluation for anti-cancer agents
- Bioorg Med Chem Lett. 2014 May 1;24(9):2062-5. doi: 10.1016/j.bmcl.2014.03.047.
- 1. College of Pharmacy and Gachon Institute of Pharmaceutical Sciences, Gachon University, Incheon 406-779, Republic of Korea.
- 2. College of Pharmacy, Korea University, Sejong 339-700, Republic of Korea.
- 3. College of Pharmacy and Medicinal Research Center (MRC), Chungbuk National University, Cheongju 361-763, Republic of Korea.
- 4. College of Pharmacy and Gachon Institute of Pharmaceutical Sciences, Gachon University, Incheon 406-779, Republic of Korea. Electronic address: [email protected].
- 5. College of Pharmacy, Korea University, Sejong 339-700, Republic of Korea. Electronic address: [email protected].
A xanthone-derived natural product, α-mangostin is isolated from various parts of the mangosteen, Garcinia mangostana L. (Clusiaceae), a well-known tropical fruit. Novel xanthone derivatives based on α-mangostin were synthesized and evaluated as anti-cancer agents by cytotoxicity activity screening using 5 human Cancer cell lines. Some of these analogs had potent to moderate inhibitory activities. The structure-activity relationship studies revealed that phenol groups on C3 and C6 are critical to anti-proliferative activity and C4 modification is capable to improve both anti-cancer activity and drug-like properties. Our findings provide new possibilities for further explorations to improve potency.