Plant Calendula officinalis (Asteraceae) | Dr. Duke's Phytochemical and Ethnobotanical Databases

Common Names

Calendula; Pot-Marigold

How this plant is used

Generally Recognized as Safe

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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	Activity Count	Plant Part	Low Parts Per Million	High Parts Per Million	Standard Deviation	Reference
ASCORBIC-ACID	112	Flower	1330.0	3100.0	0.12	Duke, 1992 *
AUROCHROME	0	Flower	not available	not available	not available	Duke, 1992 *
AUROXANTHIN	0	Flower	not available	not available	not available	Duke, 1992 *
BETA-AMYRIN	9	Flower	not available	not available	not available	Duke, 1992 *
BETA-SITOSTEROL	47	Flower	not available	not available	not available	Duke, 1992 *
BREIN	0	Flower	not available	not available	not available	Duke, 1992 *
CAFFEIC-ACID	102	Plant	not available	not available	not available	Duke, 1992 *
CALCIUM	28	Leaf	not available	30400.0	0.82	Duke, 1992 *
CALENDINE	0	Flower	not available	100.0	not available	Duke, 1992 *
CALENDOL	0	Plant	not available	not available	not available	Duke, 1992 *
CALENDRIN	0	Plant	not available	not available	not available	Duke, 1992 *
CALENDULADIOL	0	Flower	not available	not available	not available	Duke, 1992 *
CALENDULOSIDES	0	Root	not available	not available	not available	Duke, 1992 *
CAMPESTANOL	0	Shoot	not available	not available	not available	Duke, 1992 *
CAMPESTEROL	2	Flower	not available	not available	not available	Duke, 1992 *
CAROTENOIDS	0	Flower	not available	30000.0	not available	Duke, 1992 *
CARYOPHYLLENE	31	Flower	not available	not available	not available	Duke, 1992 *
CERYL-ALCOHOL	0	Flower	not available	not available	not available	Duke, 1992 *
CHLOROGENIC-ACID	77	Flower	not available	not available	not available	Duke, 1992 *
CHOLEST-7-EN-3-BETA-OL	0	Sprout Seedling	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
Phagocytotic	2	Duke, 1992 *
Phospholipase-Inhibitor	1	Duke, 1992 *
Phytoalexin	1	Nigg, H.N. and Seigler, D.S., eds. 1992. Phytochemical Resources for Medicine and Agriculture. Plenum Press, New York. 445 pp.
Piscicide	1	ANON. 1948-1976. The Wealth of India raw materials. Publications and Information Directorate, CSIR, New Delhi. 11 volumes.
PKC-Inhibitor	1	Duke, 1992 *
Plasmodicide	1	Neuwinger, H. D. 1996. African Ethnobotany - Poisons and Drugs. Chapman & Hall, New York. 941 pp.
Prebiotic	1	Duke, 1992 *
Probiotic	1	Duke, 1992 *
Probiotigenic	1	Duke, 1992 *
Proliferant	1	Duke, 1992 *
Prooxidant	3	Duke, 1992 *
Propecic	3	Duke, 1992 *
Prostaglandigenic	3	Duke, 1992 *
Prostaglandin-Synthesis-Inhibitor	3	Duke, 1992 *
Protein-Kinase-C-Inhibitor	1	Naim, M., Zehavi, U., Nagy, S., and Rouseff, R.L. Hydroxycinnamic Acids as Off-Flavor Precursors in Citrus Fruits and Their Products. Phenolic Compounds in Food and Their Effects on Health, Ch.14.
Protisticide	2	Meckes, M., Calzada, F., Tapia-Contreras, A., Cedillo-Rivera, R. 1999. Antiprotozoal Properties of Helianthemum glomeratum. Phytotherapy Research, 13(2): 102-105.
Psychotropic	1	Uchida, U., Ohta, H., Niwa, M., Mori, A., Nonaka, G-i., Nishioka, I., and Zaki, M. 1989. Prolongation of Life Span of Stroke-Prone Spontaneously Hypertensive Rats (SHRSP) Ingesting Persimmon Tannin. Chem. Pharm. Bull. 38(4): 1049-1052, 1990.
PTK-Inhibitor	1	Duke, 1992 *
Quinone-Reductase-Inducer	3	Duke, 1992 *
Radioprotective	1	Duke, 1992 *