Abstract
Antioxidant-guided fractionation of Mammea americana L. seeds resulted in the identification of three new isoprenylated coumarins, mammea B/BA hydroxycyclo F (1 ), mammea E/BC (2 ), and mammea E/BD (3 ). In addition, twelve known isoprenylated coumarins, mammea A/AA (4 ), mammea A/AA cyclo D (5 ), mammea A/AA cyclo F (6 ), mammea A/AC cyclo D (7 ), mammea A/AD cyclo D (8 ), mammea B/BA (9 ), mammea B/BA cyclo F (10 ), mammea B/BB (11 ), mammea B/BC (12 ), mammea B/BD (13 ), mammea E/BA (14 ), and mammea E/BB (15 ), as well as two known flavanols, (+)-catechin (16 ) and (-)-epicatechin (17 ) were identified. The fifteen isoprenylated coumarins were screened for their cytotoxicity in the SW-480, HT-29, and HCT-116 human colon cancer cell lines and antioxidant capacities in the DPPH (1,1-diphenyl-2-picrylhydrazyl) free-radical assay. Compounds 1 - 15 exhibited significant cytotoxic activities in the SW-480, HT-29, and HCT-116 human colon cancer cell lines (IC50 ranges 13.9 - 88.1, 11.2 - 85.3, and 10.7 - 76.7 μM, in the three cell lines, respectively) at concentrations comparable to 5-fluorouracil (IC50 = 53.0, 46.1, and 45.1 μM), a drug frequently used for human colon cancer treatment. Compounds 2 - 4 , 9 , and 11 - 15 displayed high antioxidant activity in the DPPH assay (IC50 range 86 - 135 μM ), compounds 1 , 5 - 8 , and 10 , however, had no antioxidant activity (IC50 > 200 μg/mL) in the DPPH assay. The results of these assays were used to study the structure-activity relationships for this class of compounds. In the SW-480 cell line, the three new coumarins, 1 - 3 , also exhibited dose-dependent increases in sub-diploid cells by flow cytometry, indicating that they induce apoptosis.
Key words
Clusiaceae -
Mammea americana
- mamey - isoprenylated coumarin - cytotoxicity - antioxidant activity - SAR studies
References
1 Morton J F. Fruits of Warm Climates. Julia F Morton (self published) . Miami, Florida; 1987.: p. 304-7.
2 Kennard W C, Winters H F. Some fruits and nuts for the tropics. Miscellaneous Publication 801 . U.S. Department of Agriculture, Agricultural Research Service Washington, D.C.; 1960.: p. 85-6.
3 Crombie L, Games D E. Extractives of Mammea americana L. Part I. The 4-n -alkylcoumarins. Isolation and structure of mammea B/BA, B/BB, B/BC and C/BB. J Chem Soc (C) 1967: 2545-52
4 Crombie L, Games D E. Extractives of Mammea americana L. Part II. The 4-phenylcoumarins. Isolation and structure of mammea B/AA, A/A cyclo D, A/BA, A/AB and A/BB. J Chem Soc (C) 1967: 2553-9
5
Crombie L, Games D E, Haskins N J, Reed G F, Finnegan R A, Merkel K E.
Identification of new Mammea coumarins: Four 7,8-annulated relative of the mammea coumarins B/AA, B/AA, and two of the 6-acyl family, B/AA (isomammein) and B/AB.
Tetrahedron Lett.
1970;
46
3979-82
6 Crombie L, Games D E, Haskins N J, Reed G F. Extractives of Mammea americana L. Part III. Identification of new coumarin relatives of Mammea B/BA, B/BB, and B/BC having 5,6-annulation and higher oxidation records. J Chem Soc [Perkin I] 1972: 2241-8
7 Crombie L, Games D E, Haskins N J, Reed G F. Extractives of Mammea americana L. Part IV. Identification of new 7,8-annulated relates of the coumarins Mammea B/AA, A/AB, B/AA, and B/AB and new members of the 6-acyl family B/AA, B/AB, and B/AC. J Chem Soc [Perkin I] 1972: 2248-54
8 Crombie L, Games D E, Haskins N J, Reed G F. Extractives of Mammea americana L. Part V. The insecticidal compounds. J Chem Soc [Perkin I] 1972: 2255-60
9 Crombie L, Jones R C, Palmer C J. Synthesis of the Mammea coumarins. Part 1. The coumarins of the Mammea A, B, and C series. J Chem Soc [Perkin I] 1987: 317-31
10
Yang H, Protiva P, Cui B L, Ma C Y, Baggett S, Hequet V. et al .
New bioactive polyphenols from Theobroma grandiflorum (”Cupuaçu”).
J Nat Prod.
2003;
66
1501-4
11
Ma J, Luo X D, Protiva P, Yang H, Ma C Y, Basile M J. et al .
Bioactive novel polyphenols from the fruit of Manilkara zapota (sapodilla).
J Nat Prod.
2003;
66
983-6
12
Smith R C, Reeves J C, Dage R C, Schnettler R A.
Antioxidant properties of 2-imidazolones and 2-imidazolthiones.
Biochem Pharmacol.
1987;
36
1457-60
13
Darzynkiewicz Z, Bruno S, Del Bino G, Gorczyca W, Hotz M A, Lassota P. et al .
Features of apoptotic cells measured by flow cytometry.
Cytometry.
1992;
13
795-808
14
Morel C, Guilet D, Oger J, Seraphin D, Sevenet T, Wiart C. et al .
6-Acylcoumarins from Mesua racemosa
.
Phytochemistry.
1999;
50
1243-47
15
Mahidol C, Kaweetripob W, Prawat H, Ruchirawat S.
Mammea coumarins from the flowers of Mammea siamensis
.
J Nat Prod.
2002;
65
757-60
16
Bala K, Seshadri T.
Isolation and synthesis of some coumarin components of Mesua ferrea seed oil.
Phytochemistry.
1971;
10
1131-4
17
Guilet D, Helesbeux J J, Seraphin D, Sevenet T, Richomme P, Bruneton J.
Novel cytotoxic 4-phenylfruanocoumarins from Calophyllum dispar
.
J Nat Prod.
2001;
64
563-8
18
Thebtaranonth C, Imraporn S, Padungkul N.
Phenylcoumarins from Ochrocarpus siamensis
.
Phytochemistry.
1981;
20
2305-6
19
Kashman Y, Gustafson K R, Fuller R W, Cardellian JHC I I, McMahon J B, Currens M J. et al .
The calanolides. A novel HIV-Inhibitory class of coumarin derivatives from the tropical rainforest tree, Calophyllum lanigerum
.
J Med Chem.
1992;
35
2735-43
20
Patil A D, Freyer A J, Eggleston D S, Haltiwanger R C, Bean M F, Taylor P B. et al .
The inophyllums, novel inhibitors of HIV-1 reverse transcriptase isolated from the Malaysian tree, Calophyllum inophyllum Linn.
J Med Chem.
1993;
36
4131-8
21
Itoigawa M, Ito C, Tan H T-W, Kuchide M, Tokuda H, Nishino H. et al .
Cancer chemo-preventive agents, 4-phenylcoumarins from Calophyllum inophyllum
.
Cancer Lett.
2001;
169
15-9
22
Ito C, Itoigawa M, Mishina Y, Filho V C, Enjo F, Tokuda H. et al .
Chemical constituents of Calphyllum brasiliense . 2. Structure of three new coumarins and cancer chemopreventive activity of 4-substituted coumarins.
J Nat Prod.
2003;
66
368-71
23
Cao G, Sofic E, Prior R.
Antioxidant capacity of tea and common vegetables.
J Agric Food Chem.
1996;
44
3426-31
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