Skip to main content

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Biological Activity Antimalarial

Select a Results View:

Download these results as:
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 Sort descending Dosage Reference
KORUNDAMINE-A IC50=1.1 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.
KORUPENSAMINE-A IC50=0.02-0.6 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.
KORUPENSAMINE-B IC50=0.2-0.4 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.
KORUPENSAMINE-E IC50=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.
LAPACHOL not available Duke, 1992 *
LAPINONE not available Duke, 1992 *
LICOCHALCONE-A not available Duke, 1992 *
LIMACINE IC50=0.05-0.79 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.
LIMONIN IC50=>100 ug/ml Khalid, S.A., Farouk, A., Geary**, T.G., and Jensen, J.B. 1985. Potential Antimalarial Candidates From African Plants: An In Vitro Approach Using Plasmodium falciparum*. Journal of Ethnopharmacology, 15: 201-209, 1986.
LUPEOL IC50=46.8 ug/ml Khalid, S.A., Farouk, A., Geary**, T.G., and Jensen, J.B. 1985. Potential Antimalarial Candidates From African Plants: An In Vitro Approach Using Plasmodium falciparum*. Journal of Ethnopharmacology, 15: 201-209, 1986.
LYCORINE IC50=0.3-0.7 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.
MAACKIAIN EC50=10 ug/ml Chanphen, R., Thebtaranonth, Y., Wanauppathamkul, S., and Yuthavong, Y. 1998. Antimalarial Principles from Artemisia indica. J. Nat. Prod., 61 (9):1146-1147.
MACRALSTONINE IC50=8.9 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.
MACROCARPAMINE IC50=0.4-32.6 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.
MELDENIN IC50=5.2 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.
METHYLANGOLENSATE IC50=5 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.
MUZANZAGENIN IC50=16-163 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.
MYRTENAL IC50=5-50 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.
MYRTENOL IC50=5-50 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.
N-ISOBUTYLDECA-2,4-DIENAMIDE IC50=5-5.4 ug/ml Duke, 1992 *
Download these results as:
List of Activity Plants.
Click on column headings to sort table by that column.
Plant Name Sort descending Common Name Chemical Count Total Parts Per Million
Spinacia oleracea Spinach 2 189
Spondianthus preussii not available 1 12, 000
Stellaria media Chickweed; Common Chickweed 1 0
Stemonoporus affinis not available 1 0
Stemonoporus canaliculatus not available 1 0
Stemonoporus cordifolius not available 1 0
Stemonoporus oblongifolius not available 1 0
Stemonoporus petiolaris not available 1 0
Stemonoporus reticulatus not available 1 0
Stephania glabra Indian Tape-Vine 4 0
Stephania japonica Japanese Tape-Vine 2 0
Stephania tetrandra Stephania 1 0
Stevia rebaudiana Ca-A-E; Sweet Leaf of Paraguay; Stevia 5 237
Strychnos nux-vomica Nux-Vomica; Stychnine 3 1, 940
Sweetia panamensis Billy Webb; Cascara Amarga 1 0
Swertia chirata Chirata; Chiretta 2 0
Symplocos racemosa not available 1 0
Syncarpia glomulifera not available 1 12, 000
Syncarpia laurifolia not available 1 12, 000
Syringa vulgaris Lilac 2 0