Calendula officinalis Linn. |
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Botanical Name |
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Calendula officinalis Linn. |
English
Name |
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Marigold. Calendula. Common Calendula. English or Pot Marigold and Mary Bud |
Family |
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Asteraceae |
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General Info
Description |
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An aromatic, erect, annual herb, up to 60 cm in height. Stems angular, glandular, hairy; leaves 2.5-7.5 cm long, alternate, sessile, spatulate or oblancleolate, dentate with widely spaced teeth, and hairy; lower spathulate, entire, upper lanceolate, with cordate-amplexicaul base; flower-heads terminal, heterogamous, light yellow to deep orange; ray florets fertile; achenes 1.0-1.5 cm long, boat-shaped, faintly ribbed. |
Herb Effects |
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Organic extract causes a reduction of reverse transcriptase activity accounting for its anti-HIV action (Kalvatchev), antiprotozoal and antispamodic (plant); antibacterial (essential oil and flower); reduces fever, diaphoretic, antiemetic and carminative; stimulant, bitter, tonic, sudorific, febrifuge, carminative,
anti-emetic and anthelmintic (florets). |
Chemistry
Active Ingredients |
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Calenduline, oleanolic acid glycosides, alpha and beta-amyrin, gamma-taraxasterol, taraxasterol, brein, faradiol, lupeol, erythrodiol, arnidiol, calenduladiol, coflodiol, manilladiol, stigmasterol, beta-sitosterol and campesterol flower); iso-rhamnetin. |
Chemistry
of Active Ingredients |
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Name |
CAS# |
IUPAC Name |
Formula |
Structure |
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Oleanolic acid |
508-02-1 |
10-hydroxy-2,2,6a,6b ,9,9,12a-heptamethyl -1,3,4,5,6,6a,7,8,8a ,10,11,12,
13,14b-t etradecahydropicene- 4a-carboxylic acid |
C30H48O3 |
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alpha-Amyrin |
638-95-9 |
4,4,6a,6b,8a,11,12,1 4b-octamethyl-2,3,4a ,5,6,7,8,9,10,11,12, 12a,14,14a
-tetrade cahydro-1H-picen-3-o l |
C30H50O |
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beta-Amyrin |
559-70-6 |
4,4,6a,6b,8a,11,11,1 4b-octamethyl-1,2,3, 4a,5,6,7,8,9,10,12,1 2a,14,14a-
tetradec ahydropicen-3-ol |
C30H50O |
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Taraxasterol |
1059-14-9 |
4,4,6a,6b,8a,12,14b- heptamethyl-11-methy lidene-1,2,3,4a,5,6, 6a,7,8,9,1
0,12,12a ,13,14,14a-hexadecah ydropicen-3-ol |
C30H50O |
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Faradiol |
Not Available |
4,4,6a,6b,8a,11,12,1 4b-octamethyl-1,2,3, 4,4a,5,6,6a,6a,6b,7, 8,8a,9,12,
12a,13,1 4,14a,14b-icosahydro picene-3,8-diol |
C30H50O2 |
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Lupeol |
Not Available |
Not Available |
C30H50O |
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Erythrodiol |
545-48-2 |
8a-(hydroxymethyl)-4 ,4,6a,6b,11,11,14b-h eptamethyl-1,2,3,4a, 5,6,7,8,9,
10,12,12 a,14,14a-tetradecahy dropicen-3-ol |
C30H50O2 |
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Arnidiol |
Not Available |
4,4,6a,6b,8a,12,14b- heptamethyl-11-methy lidene-2,3,4,4a,5,6, 6a,6a,6b,7
,8,8a,9, 10,12,12a,13,14,14a, 14b-icosahydro-1H-pi cene-3,8-diol |
C30H50O2 |
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Calenduladiol |
10070-48-1 |
Not Available |
C30H50O2 |
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Stigmasterol |
4736-55-4 |
17-(4-ethyl-1,5-dime thyl-hex-2-enyl)-10, 13-dimethyl-1,2,4,5, 6,7,8,9,10
,11,12,1 3,14,15,16,17-hexade cahydrocyclopenta[a] phenanthren-3-one |
C29H48O |
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Beta-sitosterol |
5779-62-4 |
17-(5-ethyl-6-methyl -heptan-2-yl)-10,13- dimethyl-2,3,4,7,8,9 ,11,12,14,
15,16,17 -dodecahydro-1H-cycl openta[a]phenanthren -3-ol |
C29H50O |
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Campesterol |
474-62-4 |
17-(5,6-dimethylhept an-2-yl)-10,13-dimet hyl-2,3,4,7,8,9,11,1 2,14,15,16
,17-dode cahydro-1H-cyclopent a[a]phenanthren-3-ol |
C28H48O |
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Pharmacology
Medicinal Use |
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HIV, wounds (plant); eye diseases (flower infusion);in ointments for treating wounds, malignant ulcers, frost-bite and skin-damage, and scars; in dental pharmacology and for fumigation amenorrhea, cancer, conjunctivitis, corns, as a depurative agent, in fever, influenza, Hodgkin's disease, internal ulcers, vomiting, sore muscles, sprains, minor burns. |
Contraindication |
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Do not use during pregnancy. |
Reference |
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Stary, Medicinal Herbs and Plants.
Chandel et al., Biodiversity in Medicinal and Aromatic Plants in India.
The Himalaya Drug Company.
Grieve M. A Modern Herbal (1931) (www.botanical.com).
Johnson T. CRC Ethnobotany Desk Reference. |
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