Planta Med 2013; 79(01): 37-44
DOI: 10.1055/s-0032-1327897
Natural Product Chemistry
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Suppression of Melanin Synthesis by the Phenolic Constituents of Sappanwood (Caesalpinia sappan)

Kaoru Mitani
1   Pharmacognosy and Chemistry of Natural Products, School of Pharmacy and Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan
,
Fumihide Takano
1   Pharmacognosy and Chemistry of Natural Products, School of Pharmacy and Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan
2   Nihon Pharmaceutical University, Saitama, Japan
,
Tetsuro Kawabata
1   Pharmacognosy and Chemistry of Natural Products, School of Pharmacy and Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan
,
Ahmed E. Allam
1   Pharmacognosy and Chemistry of Natural Products, School of Pharmacy and Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan
,
Mayumi Ota
1   Pharmacognosy and Chemistry of Natural Products, School of Pharmacy and Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan
,
Tomoya Takahashi
1   Pharmacognosy and Chemistry of Natural Products, School of Pharmacy and Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan
,
Nobuo Yahagi
1   Pharmacognosy and Chemistry of Natural Products, School of Pharmacy and Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan
,
Chikai Sakurada
2   Nihon Pharmaceutical University, Saitama, Japan
,
Shinji Fushiya
2   Nihon Pharmaceutical University, Saitama, Japan
,
Tomihisa Ohta
1   Pharmacognosy and Chemistry of Natural Products, School of Pharmacy and Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan
› Author Affiliations
Further Information

Publication History

received 16 May 2012
revised 29 September 2012

accepted 09 October 2012

Publication Date:
15 November 2012 (online)

Abstract

Sappanwood (Caesalpinia sappan Linn.) is used as an herbal medicine. It is sometimes used to treat skin damage or as a facial cleanser. In the present study, the methanol (MeOH) extract of sappanwood was found to inhibit melanin synthesis in cultured human melanoma HMV-II cells stimulated with forskolin, and six active compounds (15 and 7) were isolated from the extract along with a non-active compound (6). Compounds 27 were identified as sappanchalcone (2), 3′-deoxy-4-O-methylsappanol (3), brazilein, (4), brazilin (5), sappanol (6), and 4-O-methylsappanol (7). Compound 1 was a new compound, and its structure was determined to be (6aS,11bR)-7,11b-dihydro-6H-indeno[2,1-c]chromene-3,6a,10,11-tetrol by spectroscopic analyses. Among the six active compounds, brazilin (5) (EC50: 3.0 ± 0.5 µM) and 4-O-methylsappanol (7) (EC50: 4.6 ± 0.7 µM) strongly suppressed melanin synthesis in HMV-II cells. Bioactive compounds showed moderate cytotoxicities against HMV-II cells with IC50 values of 83.1 ± 4.0 µM (for 2), 72.0 µM ± 2.4 (for 3), 33.8 ± 1.1 µM (for 4), 18.4 ± 0.8 µM (for 5), and 20.2 ± 0.8 (for 7), respectively. Brazilin (5) selectively suppressed the expression of mRNAs for tyrosinase-related protein (TYRP) 2 and tyrosinase but did not influence the expression of TYRP1. These results suggest that brazilin (5) is a new class of melanin inhibitor and that sappanwood could be used as a cosmetic material.

Supporting Information

 
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