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Botanical Name |
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Apium graveolens L. |
English
Name |
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Celery, Smallage and Wild Celery |
Synonym(s) |
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Apium graveolens L. var. rapaceum (Mill.) Gaudin, Apium rapaceum Mill. |
Family |
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Apiaceae |
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General Info
Description |
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It is an erect, annual or biennial herb. The roots are numerous, succulent and well developed. The stem branches are angular or fistular, conspicuously jointed. The leaves are oblong to obovate, pinnate or trifoliolate. The leaflets are ovate to sub-orbicular and 3-lobed. The flowers are white or greenish white and very small. The fruit (commonly called seed) is a schizocarp consisting of two mericarps, sub-orbicular to ellipsoid, greyish brown to brown with pale ridges, aromatic and slightly bitter. |
Herb Effects |
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Aperient, carminative, diuretic, emmenagogue, nervine, stimulant, tonic, increases nerve strength (fruit); anticonvulsant, tranquillizing and antifungal (essential seed oil); potent aphrodisiac (seed); antigalactogogue, antiseptic. |
Chemistry
Active Ingredients |
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D-limonene, a-selinine, terpinen-4-ol and a-santalol (essential seed oil); alpha-linolenic acid, coumarins, beta-eudesmol, isoimperatorin, isoquercitrin, umbelliferone (seed); 3-n-butylphthalide, alpha-terpinene, limonene, d-selinene sedanonic acid, anhydride and sedanolide (essential fruit oil); 5-methoxy psoralen (fruit); 8-methoxy-psoralen, caffeic acid, chlorogenic acid, citronellal, guaiacol, linoleic acid, luteolin (leaf); acetic acid, adenine, adenosine, alpha-tocopherol, apigenin, ascorbic acid, bergapten, coumarin, eugenol, myristicin, protocatechuic acid, psoralen, rutin, scopoletin, thymol, xanthotoxin (plant); alpha-phyllandrene (fruit); choline, ferulic acid, p-coumaric acid, shikimic acid, (root); valeric acid (flower) |
Chemistry
of Active Ingredients |
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Name |
CAS# |
IUPAC Name |
Formula |
Structure |
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D-limonene |
95327-98-3 |
1-methyl-4-prop-1-en -2-yl-cyclohexene |
C10H16 |
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Terpinen-4-ol |
Not Available |
1-methyl-4-propan-2- yl-cyclohex-3-en-1-o l |
C10H18O |
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Coumarin |
60094-90-8 |
6-(1,2-dihydroxy-3-m ethyl-but-3-enyl)-7- methoxy-chromen-2-on e |
C15H16O5 |
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Limonene |
9003-73-0 |
1-methyl-4-prop-1-en -2-yl-cyclohexene |
C10H16 |
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Sedanolide |
6415-59-4 |
3-(2-methylpropyl)-3 a,4,5,6-tetrahydro-3 H-isobenzofuran-1-on e |
C12H18O2 |
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alpha-Linolenic acid |
94138-91-7 |
octadeca-9,12,15-tri enoic acid |
C18H30O2 |
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beta-Eudesmol |
473-15-4 |
2-(4a-methyl-8-methy lidene-decalin-2-yl) propan-2-ol |
C15H26O |
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Isoimperatorin |
482-45-1 |
Not Available |
C16H14O4 |
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Isoquercitrin |
21637-25-2 |
3-[5-(1,2-dihydroxye thyl)-3,4-dihydroxy- oxolan-2-yl]oxy-2-(3 ,4-dihydro
xyphenyl )-4,5-dihydroxy-chro men-7-one |
C21H20O12 |
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Umbelliferone |
93-35-6 |
2-hydroxychromen-7-o ne |
C9H6O3 |
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3-n-Butylphthalide |
93133-67-6 |
3-butyl-3H-isobenzof uran-1-one |
C12H14O2 |
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alpha-Terpinene |
99-86-5 |
1-methyl-4-propan-2- yl-cyclohexa-1,3-die ne |
C10H16 |
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Limonene |
9003-73-0 |
1-methyl-4-prop-1-en -2-yl-cyclohexene |
C10H16 |
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Sedanolide |
6415-59-4 |
3-(2-methylpropyl)-3 a,4,5,6-tetrahydro-3 H-isobenzofuran-1-on e |
C12H18O2 |
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5-Methoxypsoralen |
484-20-8 |
Not Available |
C12H8O4 |
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Caffeic acid |
Not Available |
3-(3,4-dihydroxyphen yl)prop-2-enoic acid |
C9H8O4 |
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Chlorogenic acid |
327-97-9 |
3-[3-(3,4-dihydroxyp henyl)prop-2-enoylox y]-1,4,5-trihydroxy- cyclohexan
e-1-carb oxylic acid |
C16H18O9 |
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Citronellol |
26489-01-0 |
3,7-dimethyloct-6-en -1-ol |
C10H20O |
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Guaiacol |
90-05-1 |
2-methoxyphenol |
C7H8O2 |
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Linoleic acid |
8024-22-4 |
octadeca-9,12-dienoi c acid |
C18H32O2 |
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Luteolin |
Not Available |
2-(3,4-dihydroxyphen yl)-4,5-dihydroxy-ch romen-7-one |
C15H10O6 |
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Acetic acid |
77671-22-8 |
acetic acid |
C2H4O2 |
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Adenine |
5426-35-7 |
7H-purin-6-amine |
C5H5N5 |
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Adenosine |
Not Available |
2-(6-aminopurin-9-yl )-5-(hydroxymethyl)o xolane-3,4-diol |
C10H13N5O4 |
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alpha-Tocopherol |
364-50-1 |
2,5,7,8-tetramethyl- 2-(5,9,13-trimethylt etradecyl)chroman-6- ol |
C30H52O2 |
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Apigenin |
520-36-5 |
4,5-dihydroxy-2-(4-h ydroxyphenyl)-chrome n-7-one |
C15H10O5 |
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Ascorbic acid |
Not Available |
2-(1,2-dihydroxyethy l)-4,5-dihydroxy-fur an-3-one |
C6H8O6 |
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Bergapten |
484-20-8 |
Not Available |
C12H8O4 |
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Coumarin |
60094-90-8 |
6-(1,2-dihydroxy-3-m ethyl-but-3-enyl)-7- methoxy-chromen-2-on e |
C15H16O5 |
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Eugenol |
97-53-0 |
2-methoxy-4-prop-2-e nyl-phenol |
C10H12O2 |
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Myristicin |
Not Available |
4-methoxy-6-prop-2-e nyl-benzo[1,3]dioxol e |
C11H12O3 |
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Psoralen |
10523-56-5 |
Not Available |
C17H18O6 |
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Rutin |
Not Available |
2-(3,4-dihydroxyphen yl)-4,5-dihydroxy-3- [3,4,5-trihydroxy-6- [(3,4,5-tr
ihydroxy -6-methyl-tetrahydro pyran-2-yl)oxymethyl ]tetrahydropyran-2-y l]
oxy-chromen-7-on e trihydrate |
C27H36O19 |
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Scopoletin |
92-61-5 |
2-hydroxy-6-methoxy- chromen-7-one |
C10H8O4 |
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Thymol |
89-83-8 |
5-methyl-2-propan-2- yl-phenol |
C10H14O |
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Xanthotoxin |
298-81-7 |
Not Available |
C12H8O4 |
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Choline |
67-48-1 |
2-hydroxyethyl-trime thyl-ammonium |
C5H14NO+ |
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Ferulic acid |
24276-84-4 |
3-(4-hydroxy-3-metho xy-phenyl)prop-2-eno ic acid |
C10H10O4 |
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P-coumaric acid |
501-98-4 |
3-(4-hydroxyphenyl)p rop-2-enoic acid |
C9H8O3 |
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Shikimic acid |
138-59-0 |
3,4,5-trihydroxycycl ohexene-1-carboxylic acid |
C7H10O5 |
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Valeric acid |
70268-41-6 |
pentanoic acid |
C5H10O2 |
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Pharmacology
Medicinal Use |
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To treat diarrhoea, dysentery, hoarseness of voice, gravels, indigestion and loss of appetite, and impurity of breast-milk caused, bronchitis (seed decoction); rheumatism (fruit); as a very potent aphrodisiac (seed); arthritis, bruises, dropsy, dysmenorrhea, gout, hoarseness, indigestion, depression, nervous affections resulting from the degeneration of sheathing, scurvy and sores. |
Contraindication |
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Pregnant women should not use celery seed because it may uterine bleeding and cause muscle contractions in the uterus. People with active kidney inflammation should also avoid this herb. Similarly, celery contains properties that may thin the blood, thus making it somewhat of a concern to take with blood thinning medications such as warfarin or aspirin. |
Reference |
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Chandel et al., Biodiversity in Medicinal and Aromatic Plants in India.
Grieve M. A Modern Herbal (1931) (www.botanical.com).
Johnson T. CRC Ethnobotany Desk Reference (www.herbweb.com/herbage).
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