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Biological Activity Antimalarial

List of activity chemicals.
Click on column headings to sort table by that column. *Unless otherwise noted all references are to (Duke, 1992)
Chemical Name Dosage Reference
(-)-CORYDALMINE IC50=840-2840 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
(-)-CURINE IC50=353 uM Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
(-)-CYCLEAPELTINE IC50=0.03-0.04 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
(-)-DICENTRINE IC50=1260-2550 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
(-)-ISOLAURELINE IC50=1610-2560 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
(-)-NOR-DICENTRINE IC50=470-1030 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
(-)-ROEMEROLINE IC50=1,780-3,150 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
(-)-TETRAHYDROSTEPHABINE IC50=1,940-2,230 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
(-)-THAICANINE IC50=550-1,610 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
(-)-XYLOPINE IC50=440-2,270 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
(8',9'-DIHYDROXY)-3-FARNESYLINDOLE IC50=2.8 ug/ml Duke, 1992 *
1(S)-HYDROXY-ALPHA-BISABOLOLOXIDE IC50=5.09 ug/ml Duke, 1992 *
1,2-DI-O-ACETYLCORINE IC50=1 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
1-BETA-HYDROPEROXYISOBILIN IC50=1 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
1-DEACETYLKHIVORIN IC50=10 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
1-HYDROXYBENZOISOCHROMAN IC50=2.7 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
1-O-ACETYLNORPLUVIININE IC50=28.3-34.2 ug/ml Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
10'-HYDROXYUSAMBARENSINE IC50=0.2-0.5 uM Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
10,12-PEROXYCALAMENENE IC50=2.3 uM Rukunga, G. and Simons, A. J. 2006. The Potential of Plants as a Source of Antimalarial Agents - A Review. Africa Herbal Antimalaria Meeting. PlantaPhile Publications, Berlin. 72 pp.
11-BETA-ACETOXYGEDUNIN IC50=3.11 ug/ml Duke, 1992 *
List of Activity Plants.
Click on column headings to sort table by that column.
Plant Name Common Name Chemical Count Total Parts Per Million
Ligustrum lucidum Chinese Privet; Glossy Privet; Ligustri Fructus; Privet; White Waxtree 4 402, 001.5000000596
Limnophila rugosa not available 1 0
Limonia acidissima Elephant Apple; Manzana De Elefante; Wood-Apple 1 0
Lippia dulcis Sweet Herb 1 0
Liquidambar orientalis Oriental Storax; Oriental Styrax 1 0
Liquidambar styraciflua American Styrax; Sweetgum 2 0
Lithocarpus attenuata not available 1 0
Lithocarpus polystachya not available 1 1.600000023841858
Ludwigia adscendens Ascending ludwigia 1 0
Ludwigia parviflora not available 1 0
Ludwigia perennis Perennial ludwigia 1 0
Luffa aegyptiaca Luffa; Smooth Loofah; Vegetable Sponge 1 0
Luisia indivisa not available 1 0
Lupinus albus White Lupine 1 0
Lycium chinense Wolfberry; Chinese Boxthorn; Chinese Matrimony Vine; Chinese Wolfberry; Gou Qi (Chin.); Lyciet de Chine (Fr.); Chinesischer Bocksdorn (Ger.); Daun Koki (Indones.); Spina Santa Cinese (Ital.); Kuko (Jap.); Kaukichai (Malays.) 2 0
Lycopersicon esculentum Tomato 3 24, 000
Lycopus europeus European Bugle 2 0
Lycopus lucidus not available 1 0
Lycopus virginicus Bugle 1 0
Lycoris radiata Spider Lily 1 0