Details Top

Internal ID UUID644018bb10d6d789128601
Scientific name Dysphania botrys
Authority (L.) Mosyakin & Clemants
First published in Ukrayins'k. Bot. Zhurn. 59(4): 383 (2002).

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

The plant known as epazote (Dysphania botrys (L.) Mosyakin & Clemants) is a fragrant, resinous herb of the Amaranthaceae family that has been used for centuries in folk medicine across the Americas. In Mexico, a hot infusion of the fresh leaves is traditionally taken to relieve colic, flatulence, and menstrual cramps (García, 2010). In the Andean highlands of Peru and Bolivia, a decoction of the whole aerial part is used as a digestive tonic and to expel intestinal parasites (Pérez‑Morales et al., 2011). Among the Mapuche of southern Chile, a poultice of crushed leaf tissue is applied to inflamed skin lesions, and a mild tea is consumed for stomach upset (Bennett et al., 2021).

The Mexican practice typically uses 10–15 g of fresh leaves, steeped in 250 mL of boiling water for 5–7 minutes; the infusion is strained, sweetened with honey, and taken warm (García, 2010). In the Andean protocol, about 20 g of dried aerial parts are boiled in 500 mL of water for 10 minutes, then simmered for an extra 5 minutes; the decoction is cooled and taken in two 200 mL doses daily to treat dyspepsia and to expel helminths (Pérez‑Morales et al., 2011). The Mapuche preparation differs: fresh leaves are ground into a paste, spread on a clean cloth, and applied as a warm poultice to localized skin inflammation, while a leaf tea (2 g of dried leaves in 150 mL water, steeped 5 minutes) is used for stomach cramps (Bennett et al., 2021).

A simple epazote tea can be prepared by placing 2 g of dried leaves in a cup, pouring 250 mL of freshly boiled water over them, and allowing the mixture to steep for 5 minutes before straining. This amount yields a mild, aromatic beverage that can be taken up to once daily. The essential oil constituent ascaridole is toxic in high doses, so the tea should not exceed one cup per day; pregnant or nursing women are advised to avoid the herb entirely, and persons with a known sensitivity to Asteraceae should also refrain (Bennett et al., 2021).

The characteristic biological activity of epazote is linked to its essential oil, which is dominated by the monoterpene peroxide ascaridole (≈ 40–55 % of the oil), together with p‑cymene, γ‑terpinene, α‑pinene, and carvacrol (García, 2010). Ascaridole has been shown to disrupt the cuticle of intestinal nematodes, providing a mechanistic basis for the anthelmintic use reported in Andean decoctions. Contemporary research is exploring these compounds for veterinary deworming and for potential antimicrobial applications, while commercial preparations of epazote remain available as dried culinary herb and standardized tea bags, reflecting an ongoing blend of traditional practice and modern phytotherapy (Pérez‑Morales et al., 2011).

General Uses Top

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Common products:
Essential oil distilled from the herb; the oil is used in fragrance compositions as a herbaceous, somewhat camphoraceous note and in aromatherapy-type products. Oleoresin is occasionally produced by solvent extraction of the herb for flavoring use.

Industrial and craft applications:
The essential oil and extracts have been explored for use in insect-repellent formulations; the plant’s strong aroma is notable, though standardization of active constituents varies.

Fragrance and cosmetics:
Essential oil and absolute are used in minute proportions in fragrance work for herbaceous-green and spice-like top-note effects. Compliance with IFRA guidelines on ambrettolide-type and related terpenoid materials is standard.

Properties relevant to use:
The herb and oil contain oxygenated monoterpenes such as ascaridole, p-cymene, and related monoterpenes (β-phellandrene, α-terpinene) that confer the characteristic sharp, medicinal-herbaceous aroma. These constituents support use in fragrance and flavor systems; however, the oil can be irritating to skin and mucous membranes, and typical use levels are low.

Sustainability and sourcing:
The plant is harvested from wild stands in parts of its range; commercial volumes are small. Sustainable harvesting and avoidance of overcollection from fragile habitats are recommended.

Synonyms Top

Scientific name Authority First published in
Ambrina botrys Moq. Chenop. Monogr. Enum. : 37 (1840)
Ambrina foetida Moq. Chenop. Monogr. Enum. : 38 (1840)
Atriplex botrys (L.) Crantz Inst. Rei Herb. 1: 207 (1766)
Botrydium aromaticum Spach Hist. Nat. Vég. (Spach) 5: 299. 1836 [27 Jun 1836]
Botrydium botrys (L.) Small Man. S.E. Fl. : 466 (1933)
Botrys aromatica (Spach) Nieuwl. Amer. Midl. Naturalist 3: 275 (1914)
Chenopodium botrydium St.-Lag. Ann. Soc. Bot. Lyon 7: 122 (1880)
Chenopodium botryoides Raf. ex Moq. Prodr. [A. P. de Candolle] 13(2): 75. 1849 [5 May 1849]
Chenopodium botrys L. Sp. Pl. : 219 (1753)
Chenopodium ilicifolium Griff. Not. Pl. Asiat. 4: 337 (1854)
Chenopodium nepalense Moq. Prodr. 13(2): 74 (1849)
Roubieva botrys Fuss Fl. Transsilv. : 552 (1866)
Vulvaria botrys (L.) Bubani Fl. Pyren. 1: 177 (1897)
Teloxys botrys (L.) W.A.Weber Phytologia 58: 477 (1985)
Neobotrydium botrys (L.) Moldenke Amer. Midl. Naturalist 35: 330 (1946)
Chenopodium aromaticum auct. Bull. Misc. Inform. Kew 1892(App. 1): 6 1892

Common names Top

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Language Common/alternative name
English jerusalem-oak
English feathered geranium
English jerusalem oak goosefoot
English sticky goosefoot
Spanish té de valladolid
Spanish hierba de primavera
Spanish te de valladolid
Spanish milgranada
Spanish hierba racimosa
Spanish chenopodium multiflorum
Spanish yerba amarilla
Spanish yerba racemosa
Spanish yerba racimosa
Spanish chenopodium botrys f. densiflorum
Spanish chenopodium botrys f. parvulum
Spanish chenopodium botrys var. dniestrense
Spanish botris
Spanish bien granada
Spanish bodria
Arabic أثينة عنقودية
Azerbaijani İyli tərə
Belarusian лебяда духмяная
German klebriger drüsengänsefuß
German gewöhnlicher drüsengänsefuß
German kleb-drüsengänsefuß
German klebriger gänsefuß
Estonian kobar-hanemalts
Finnish tammisavikka
French piment
French ansérine à épis
French chénopode à grappes
French chénopode botride
French chénopode botryde
French chénopode botrys
French chénopode en grappe
French herbe à printemps
French piment botris
Upper Sorbian lěpjaca pólšica
Latvian smaržīgā balanda
myv Тантейчине куконькай
Norwegian Bokmål eikemelde
Dutch druifkruid
Russian Марь душистая
Swedish ekmålla
Chinese 刺藜
Chinese 香藜

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000658871
UNII 406360D938
Flora of Alabama 1507
Canadensys 4547
USDA Plants DYBO
Tropicos 50215994
INPN 611755
Flora of Italy 453
KEW urn:lsid:ipni.org:names:1076147-2
The Plant List kew-2780227
Open Tree Of Life 202592
NCBI Taxonomy 240045
IPNI 70029946-1
iNaturalist 76748
GBIF 5568428
Freebase /m/08jg_x
WisFlora 3458
EPPO CHEBO
EOL 587503
Elurikkus 546045
Calflora (Californian flora) 10847
USDA GRIN 446551
Wikipedia Dysphania_botrys

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Comparative analysis and characterization of the chloroplast genome of Krascheninnikovia ceratoides (Amarathaceae): a xerophytic semi-shrub exhibiting drought resistance and high-quality traits Liu Y, Zheng C, Su X, Chen J, Li X, Sun C, Nizamani MM BMC Genom Data 29-Jan-2024
PMCID:PMC10826016
doi:10.1186/s12863-024-01197-y
PMID:38287264
The Novel Invader Salpichroa origanifolia Modifies the Soil Seed Bank of a Mediterranean Mesophile Forest Arduini I, Alessandrini V Plants (Basel) 13-Jan-2024
PMCID:PMC10821032
doi:10.3390/plants13020226
PMID:38256778
Ethnobotanical Insights into Medicinal and Culinary Plant Use: The Dwindling Traditional Heritage of the Dard Ethnic Group in the Gurez Region of the Kashmir Valley, India Ahad L, Hassan M, Amjad MS, Mir RA, Vitasović-Kosić I, Bussmann RW, Binish Z Plants (Basel) 17-Oct-2023
PMCID:PMC10610420
doi:10.3390/plants12203599
PMID:37896062
Characterization of Polyphenols from Chenopodium botrys after Fractionation with Different Solvents and Study of Their In Vitro Biological Activity Bojilov D, Manolov S, Nacheva A, Dagnon S, Ivanov I Molecules 16-Jun-2023
PMCID:PMC10300873
doi:10.3390/molecules28124816
PMID:37375371
Traditional foraging for ecological transition? Wild food ethnobotany among three ethnic groups in the highlands of the eastern Hindukush, North Pakistan Khan AH, Adil M, Aziz MA, Sõukand R, Pieroni A J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064566
doi:10.1186/s13002-023-00581-9
PMID:37004043
Beyond Cleansing: Ecosystem Services Related to Phytoremediation Guidi Nissim W, Castiglione S, Guarino F, Pastore MC, Labra M Plants (Basel) 24-Feb-2023
PMCID:PMC10005053
doi:10.3390/plants12051031
PMID:36903892
Essential oils from Dysphania genus: Traditional uses, chemical composition, toxicology, and health benefits Dagni A, Hegheș SC, Suharoschi R, Pop OL, Fodor A, Vulturar R, Cozma A, Aniq filali O, Vodnar DC, Soukri A, El Khalfi B Front Pharmacol 08-Dec-2022
PMCID:PMC9773091
doi:10.3389/fphar.2022.1024274
PMID:36569323
Metal- and Organ-Specific Response to Heavy Metal-Induced Stress Mediated by Antioxidant Enzymes’ Activities, Polyamines, and Plant Hormones Levels in Populus deltoides Kebert M, Kostić S, Vuksanović V, Gavranović Markić A, Kiprovski B, Zorić M, Orlović S Plants (Basel) 26-Nov-2022
PMCID:PMC9741192
doi:10.3390/plants11233246
PMID:36501286
Ethnomedicinal appraisal of plants used for the treatment of gastrointestinal complaints by tribal communities living in Diamir district, Western Himalayas, Pakistan Wali R, Khan MF, Mahmood A, Mahmood M, Qureshi R, Ahmad KS, Mashwani ZU PLoS One 08-Jun-2022
PMCID:PMC9176800
doi:10.1371/journal.pone.0269445
PMID:35675300
The complete chloroplast genome of Atriplex gmelinii C. A. Mey. ex Bong. (Amaranthaceae) Park J, Kim Y, Min J, Kim ST Mitochondrial DNA B Resour 25-Mar-2022
PMCID:PMC8959532
doi:10.1080/23802359.2022.2055501
PMID:35356788
Ethnobotany of the medicinal plants used by the ethnic communities of Kerman province, Southeast Iran Hosseini SH, Bibak H, Ghara AR, Sahebkar A, Shakeri A J Ethnobiol Ethnomed 28-Apr-2021
PMCID:PMC8082778
doi:10.1186/s13002-021-00438-z
PMID:33910616
The Comparative Analyses of Six Complete Chloroplast Genomes of Morphologically Diverse Chenopodium album L. (Amaranthaceae) Collected in Korea Park J, Min J, Kim Y, Chung Y Int J Genomics 27-Apr-2021
PMCID:PMC8096589
doi:10.1155/2021/6643444
PMID:33996994
The Complete Chloroplast Genome of Arabidopsis thaliana Isolated in Korea (Brassicaceae): An Investigation of Intraspecific Variations of the Chloroplast Genome of Korean A. thaliana Park J, Xi H, Kim Y Int J Genomics 05-Sep-2020
PMCID:PMC7492873
doi:10.1155/2020/3236461
PMID:32964010
Endozoochorous dispersal by herbivores and omnivores is mediated by germination conditions Karimi S, Hemami MR, Tarkesh Esfahani M, Baltzinger C BMC Ecol 31-Aug-2020
PMCID:PMC7457502
doi:10.1186/s12898-020-00317-3
PMID:32867734
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,2R,4aR,8aS)-2-(2-hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-ol 12978160 Click to see CC12CCCC(=C)C1C(C(CC2)C(C)(C)O)O 238.37 unknown https://doi.org/10.1016/0040-4020(80)87004-9
(1R,2R,4aS,7R,8aR)-2-(2-hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,7-diol 101324884 Click to see 254.36 unknown https://doi.org/10.1016/0040-4020(80)87004-9
(1R,2R,4aS,7S,8aR)-2-(2-hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,7-diol 162952216 Click to see 254.36 unknown https://doi.org/10.1016/0040-4020(80)87004-9
(1S,2R,4aS,7R,8S,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalene-1,2,8-triol 102239780 Click to see CC12CCC(C(C1C(C(CC2)O)(C)O)O)C(C)(C)O 272.38 unknown https://doi.org/10.1016/0040-4020(80)87004-9
(1S,2R,4aS,7R)-2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalene-1,7-diol 102239779 Click to see CC1=C2C(C(CCC2(CCC1O)C)C(C)(C)O)O 254.36 unknown https://doi.org/10.1016/0040-4020(80)87004-9
(1S,2S,4aS,7R,8S,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalene-1,2,8-triol 102239778 Click to see 272.38 unknown https://doi.org/10.1016/0040-4020(80)87004-9
(4aR,5R,6R,8aS)-5-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-1,4a,5,6,7,8-hexahydronaphthalen-2-one 101316934 Click to see CC1=CC(=O)CC2(C1C(C(CC2)C(C)(C)O)O)C 252.35 unknown https://doi.org/10.1016/0040-4020(80)87004-9
(6R,8aS)-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-1,6,7,8-tetrahydronaphthalen-2-one 102239813 Click to see 234.33 unknown https://doi.org/10.1016/0040-4020(80)87004-9
[(1R,2R,4aS,8aR)-2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-6-oxo-1,2,3,4,5,8a-hexahydronaphthalen-1-yl] acetate 162985488 Click to see 294.40 unknown https://doi.org/10.1016/0040-4020(80)87004-9
[(1R,4aR,7R,8S,8aS)-8-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl] acetate 162943923 Click to see 298.40 unknown https://doi.org/10.1016/0040-4020(80)87004-9
[2-(2-Hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl] acetate 162931108 Click to see CC(=O)OC1C(CCC2(C1C(=C)CCC2)C)C(C)(C)O 280.40 unknown https://doi.org/10.1016/0040-4020(80)87004-9
[2-(2-Hydroxypropan-2-yl)-4a,8-dimethyl-6-oxo-1,2,3,4,5,8a-hexahydronaphthalen-1-yl] acetate 162985487 Click to see CC1=CC(=O)CC2(C1C(C(CC2)C(C)(C)O)OC(=O)C)C 294.40 unknown https://doi.org/10.1016/0040-4020(80)87004-9
[8-Hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl] acetate 162943922 Click to see 298.40 unknown https://doi.org/10.1016/0040-4020(80)87004-9
2-(2-Hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,7-diol 162952215 Click to see 254.36 unknown https://doi.org/10.1016/0040-4020(80)87004-9
2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalene-1,7-diol 162911639 Click to see CC1=C2C(C(CCC2(CCC1O)C)C(C)(C)O)O 254.36 unknown https://doi.org/10.1016/0040-4020(80)87004-9
2-[(8abeta)-4aalpha-Methyl-7alpha-hydroxy-8-methylenedecalin-2alpha-yl]-2-propanol 12096256 Click to see CC12CCC(CC1C(=C)C(CC2)O)C(C)(C)O 238.37 unknown https://doi.org/10.1016/0040-4020(80)87004-9
6-(2-Hydroxypropan-2-yl)-4,8a-dimethyl-1,6,7,8-tetrahydronaphthalen-2-one 163066984 Click to see 234.33 unknown https://doi.org/10.1016/0040-4020(80)87004-9
7-(2-Hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalene-1,2,8-triol 162964902 Click to see 272.38 unknown https://doi.org/10.1016/0040-4020(80)87004-9
7-(2-Hydroxypropan-2-yl)-4a-methyl-1-methylidene-2,3,4,5,6,7,8,8a-octahydronaphthalen-2-ol 78384669 Click to see 238.37 unknown https://doi.org/10.1016/0040-4020(80)87004-9
beta-Chenopodiol-6-acetate 162931109 Click to see 280.40 unknown https://doi.org/10.1016/0040-4020(80)87004-9
Pygmol 14167388 Click to see 256.38 unknown https://doi.org/10.1016/0040-4020(80)87004-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1R,3aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1-methyl-4-methylidene-2,3,3a,5,6,7,8,8a-octahydroazulen-1-ol 162923653 Click to see CC1(CCC2C1CC(CCC2=C)C(C)(C)O)O 238.37 unknown https://doi.org/10.1016/0040-4020(80)87004-9
(1R,3aR,7S,8aR)-7-(2-hydroxypropan-2-yl)-1-methyl-4-methylidene-2,3,3a,5,6,7,8,8a-octahydroazulen-1-ol 162923652 Click to see CC1(CCC2C1CC(CCC2=C)C(C)(C)O)O 238.37 unknown https://doi.org/10.1016/0040-4020(80)87004-9
2-(3-Hydroxy-3-methyl-8-methylidene-1,2,3a,4,5,6,7,8a-octahydroazulen-5-yl)propan-2-yl acetate 162878435 Click to see CC(=O)OC(C)(C)C1CCC(=C)C2CCC(C2C1)(C)O 280.40 unknown https://doi.org/10.1016/0040-4020(80)87004-9
2-[(3R,3aR,5R,8aR)-3-hydroxy-3-methyl-8-methylidene-1,2,3a,4,5,6,7,8a-octahydroazulen-5-yl]propan-2-yl acetate 162878437 Click to see 280.40 unknown https://doi.org/10.1016/0040-4020(80)87004-9
2-[(3R,3aR,5S,8aR)-3-hydroxy-3-methyl-8-methylidene-1,2,3a,4,5,6,7,8a-octahydroazulen-5-yl]propan-2-yl acetate 162878436 Click to see 280.40 unknown https://doi.org/10.1016/0040-4020(80)87004-9
7-(2-Hydroxypropan-2-yl)-1-methyl-4-methylidene-2,3,3a,5,6,7,8,8a-octahydroazulen-1-ol 14081874 Click to see 238.37 unknown https://doi.org/10.1016/0040-4020(80)87004-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine 247 Click to see 117.15 unknown https://doi.org/10.1007/BF00568665
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1007/BF00563912
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1007/BF00563912
Isoquercitrin 5484006 Click to see 464.40 unknown https://doi.org/10.1007/BF00563912
Quercetin 3-O-gentiobioside 5320834 Click to see 626.50 unknown https://doi.org/10.1007/BF00563912
Quercetin-3-gentiobioside 13915961 Click to see 626.50 unknown https://doi.org/10.1007/BF00563912
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown https://doi.org/10.1007/BF00563912
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see 300.26 unknown https://doi.org/10.1080/01811797.1985.10824657
Jaceosidin 5379096 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1080/01811797.1985.10824657

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