Plant Lycopersicon esculentum (Solanaceae) | Dr. Duke's Phytochemical and Ethnobotanical Databases

Common Names

Tomato

How this plant is used

Food

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List of plant chemicals.
Click on column headings to sort table by that column. *Unless otherwise noted all references are to (Duke, 1992)
Chemical Name	Plant Part	Low Parts Per Million	High Parts Per Million	Standard Deviation	Reference
1',2'-EPOXY-1',2'-DIHYDRO-BETA-EPSILON-PSEUDOCAROTENE	Fruit	not available	not available	not available	Duke, 1992 *
1',2'-EPOXY-1',2'-DIHYDRO-BETA-PSI-CAROTENE	Fruit	not available	not available	not available	Duke, 1992 *
1,2-EPOXY-1,2-DIHYDRO-PSI,PSI-CAROTENE	Fruit	not available	not available	not available	Duke, 1992 *
1-BUTYL-2-THIAZOL	Fruit	not available	not available	not available	Duke, 1992 *
1-O-FERULOYL-BETA-D-GLUCOSE	Fruit	not available	not available	not available	Duke, 1992 *
1-O-P-COUMAROYL-BETA-D-GLUCOSE	Fruit	not available	not available	not available	Duke, 1992 *
10,16-DIHYDROXY-DECANOIC-ACID	Fruit	not available	not available	not available	Duke, 1992 *
10,16-DIHYDROXY-HEXADECANOIC-ACID	Fruit	not available	not available	not available	Duke, 1992 *
16-HYDROXY-HEXADECANOIC-ACID	Fruit	not available	not available	not available	Duke, 1992 *
2,7-DIMETHYL-OCT-4-ENEDIOIC-ACID	Shoot	not available	1.2	not available	Duke, 1992 *
2,7-DIMETHYL-OCTA-2,4-DIENOIC-ACID	Shoot	not available	1.8	not available	Duke, 1992 *
2-BUTANONE	Fruit	not available	not available	not available	Duke, 1992 *
2-PENTANONE	Fruit	not available	not available	not available	Duke, 1992 *
2-PROPANONE	Fruit	not available	not available	not available	Duke, 1992 *
24-(R)-ETHYL-LOPHENOL	Seed	not available	not available	not available	Duke, 1992 *
24-METHYL-31-NOR-LANOST-9(11)-EN-3-BETA-OL	Seed	not available	not available	not available	Duke, 1992 *
24-METHYL-LOPHENOL	Seed	not available	not available	not available	Duke, 1992 *
24-METHYLENE-CYCLOARTANAL	Seed	not available	not available	not available	Duke, 1992 *
24-METHYLENE-CYCLOARTENAL	Plant	not available	not available	not available	Duke, 1992 *
3-BETA-HYDROXY-5-ALPHA-PREG-16-EN-20-ONE	Shoot	not available	not available	not available	Duke, 1992 *

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List of plant activities.
Click on column headings to sort table by that column. *Unless otherwise noted all references are to (Duke, 1992)
Activity	Chemical Count	Reference
Spasmogenic	3	Duke, 1992 *
Spermicide	2	Martindale's 28th
Spermigenic	2	Werbach, M. 1993. Healing with Food. Harper Collins, New York, 443 pp.
Sprout-Inhibitor	2	Duke, J.A.. Personal Communication.
Sunscreen	5	Lazarova*, G., Kostova, I., Neychev, H. 1992. Photodynamic damage prevention by some hydroxycoumarins. Fitoterapia 64(2): 134-136, 1993.
Suppository	1	Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Surfactant	1	Schulz, V, Hansel, R and Tyler, VE. 1998. Rational Phytotherapy - A Physician's Guide to Herbal Medicine. 3rd ed. 1st English Edition. Translated by Terry C. Telger. Springer Verlag, Heidelberg. 306 pp.
Sweetener	3	Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp.
Sympathomimetic	1	Duke, 1992 *
Tachycardic	1	Duke, 1992 *
Teratogenic	5	Duke, 1992 *
Teratologic	2	Duke, 1992 *
Termiticide	3	Duke, 1992 *
Testosteronigenic	1	Werbach, M. 1993. Healing with Food. Harper Collins, New York, 443 pp.
Thymoprotective	1	Pizzorno, J.E. and Murray, M.T. 1985. A Textbook of Natural Medicine. John Bastyr College Publications, Seattle, Washington (Looseleaf).
Thyrotropic	1	Davies, S., and Stewart, A. 1990. Nutritional Medicine. Avon Books, New York. 509pp.
TNF-alpha-Inhibitor	3	Duke, 1992 *
TOPO-2-Inhibitor	1	Duke, 1992 *
Topoisomerase-I-Inhibitor	3	Santti, R., Makela, S., Strauss, L., Korman, J., Kostian, M. L. 1998. Phytoestrogens: Potential Endocrine Disruptors in Males. Toxicol Ind Health, 14: 223-237.
Topoisomerase-II-Inhibitor	3	Constantinou, A., Mehta, R., Runyan, C., Rao, K., Vaughan, A., Moon, R. 1995. Flavonoids as DNA Topoisomerase Antagonists and Poisons: Structure-Activity Relationships. J Natural Products, 58: 217-225.