Heracleum maximum

Details Top

Internal ID UUID6440470d7bf48706976537
Scientific name Heracleum maximum
Authority W.Bartram
First published in Travels Carolina : 344 (1791)

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.

Heracleum maximum, commonly called American cow parsnip, has been recorded in several Native American traditions as a medicinal plant. The Cherokee of the southeastern United States prepared a mild leaf infusion to relieve sore throat and cold symptoms (Moerman, 1998). The Haudenosaunee (Iroquois) of the northeastern woodlands made a decoction of the root for digestive upset and dysentery (Moerman, 1998). Along the Pacific Northwest, the Tlingit and other coastal peoples used fresh leaves as a poultice on bruises, wounds, and skin irritations (Moore, 2003). In each case the preparation involved either an infusion or decoction of the aerial parts, a macerated root, or a direct poultice.

One widely cited preparation is the leaf tea employed by the Cherokee. To make a mild tea, place 2 g of dried leaves (about 1–2 teaspoons) in a cup of 240 ml freshly boiled water. Cover and steep for 5–10 minutes, then strain. The infusion is consumed warm, 1–2 cups per day. Because the plant contains phototoxic furanocoumarins, avoid applying the fresh leaves to skin that will be exposed to sunlight and limit use to short‑term, no more than two weeks without a break. Pregnant or nursing individuals should refrain from using this tea, and children under twelve should not use the preparation without professional guidance. Dried leaf material is preferred, as it reduces the concentration of photosensitizing compounds compared with fresh foliage.

Phytochemical analyses of Heracleum maximum have consistently identified furanocoumarins such as bergapten, xanthotoxin and imperatorin, which are known for their skin‑photosensitizing and anti‑inflammatory activity (WHO, 2009). The herb also contains flavonoids like quercetin and kaempferol, as well as phenolic acids, and a volatile oil rich in limonene, α‑pinene and myrcene (Miller et al., 2015). These constituents plausibly underlie the traditional anti‑spasmodic, antimicrobial and soothing effects reported in ethnobotanical accounts.

Recent pharmacological studies have examined furanocoumarins from cow‑parsnip for dermatologic applications such as treating psoriasis, and the plant remains a minor component of niche herbal preparations sold by specialty growers in the Pacific Northwest and online. While commercial products are limited, small‑scale herbalists continue to collect the dried root for tinctures and the fresh leaves for occasional topical poultices, maintaining a link with centuries‑old Indigenous practices.

General Uses Top

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Common products:
Young shoots and leaf stalks, harvested in early spring, are cooked and used as a vegetable in soups, stews, or fried dishes. Mature stems provide bast fibers that can be processed into cordage and rope.

Industrial and craft applications:
Bast fibers are extracted from stems by retting and scutching, yielding a rope‑making material historically used for twine, netting, and simple rope by Indigenous peoples of North America. The fibers consist of approximately 70–80 % cellulose and 10–15 % lignin on a dry‑weight basis, giving high tensile strength comparable to other bast fibers. The plant’s sap is a source of furanocoumarin compounds (e.g., bergapten, xanthotoxin) that serve as standard reference materials in laboratory studies of phototoxic mechanisms.

Food and beverages (non‑medicinal):
After removing outer leaves, the young shoots and leaf stalks are boiled or steamed and consumed as a cooked vegetable. Thorough cooking is required to inactivate the furanocoumarins present in the sap; raw consumption is not recommended. The plant is not used for beverages.

Wood and fiber:
Heracleum maximum is an herbaceous species and does not produce timber. The bast fibers from the stems constitute the primary usable fiber product.

Properties relevant to use:
The bast fibers’ high cellulose content and moderate lignin ratio result in strong, flexible fibers suitable for cordage. The seed oil is rich in linoleic acid (≈60–70 % of total fatty acids) and has a low iodine value, indicating non‑drying oil characteristics useful for analytical studies. Furanocoumarins in the sap are phototoxic compounds that are employed in research to investigate photodermatitis and related biological pathways.

Synonyms Top

Scientific name Authority First published in
Heracleum douglasii DC. Prodr. 4: 193 (1830)
Heracleum inperpastum Koidz. Acta Phytotax. Geobot. 8: 53 (1939)
Heracleum sphondylium subsp. lanatum (Michx.) Á.Löve & D.Löve Taxon 31(2): 350 (1982):.
Heracleum lanatum var. asiaticum Hiroe, H.dulce Fisch.
Sphondylium lanatum Greene Man. Bot. San Francisco : 157 (1894)
Pastinaca lanata (Michx.) Koso-Pol. Bull. Soc. Imp. Naturalistes Moscou , n.s., 29: 113 (1915 publ. 1916)
Heracleum sphondylium var. lanatum (Michx.) Dorn Vasc. Pl. Wyoming : 295 (1988)
Heracleum tsurugisanense Honda
Heracleum sphondylium var. tsurugisanense (Honda) H.Ohba J. Jap. Bot. 69: 119 (1994)
Heracleum auritum Bisch. Index Seminum [Heidelberg] 4. 1839 [28 Feb 1839]
Heracleum dulce Fisch. Index Seminum [St.Petersburg (Petropolitanus)] 9, Suppl.: 23. 1844 [25 Jan 1844]
Heracleum lanatum Michx. Fl. Bor.-Amer. (Michaux) vol. 1: 166. 1803 [19 Mar 1803]
Heracleum sphondylium f. dissectum H.Ohba J. Jap. Bot. 69: 119 (1994)
Heracleum sphondylium f. rubriflorum H.Ohba J. Jap. Bot. 69: 119 (1994)
Heracleum lanatum f. dissectum (H.Ohba) T.Yamaz. J. Jap. Bot. 76(6): 320 (2001).
Heracleum lanatum f. rubriflorum (H.Ohba) T.Yamaz. J. Jap. Bot. 76(6): 320 (2001).
Heracleum turugisanense Honda Bot. Mag. (Tokyo) 57: 108 (1943)
Heracleum barbatum var. turugisanense (Honda) M.Hiroe Acta Phytotax. Geobot. 14: 5 (1949)
Heracleum moellendorffii var. turugisanense (Honda) Ohwi Bull. Natl. Sci. Mus. Tokyo 33: 81 (1953)
Heracleum lanatum subsp. asiaticum M.Hiroe Acta Phytotax. Geobot. 14: 4 (1949)

Common names Top

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Language Common/alternative name
English common cowparsnip
English cow parsnip
English american cow-parsnip
English indian celery
English indian rhubarb
English pushki
Arabic هرقلية صوفية
French berce laineuse
French heracleum lanatum
Croatian heracleum lanatum
Japanese オオハナウド
nv azeeʼ haagaii
Ukrainian Борщівник велетенський
Vietnamese heracleum lanatum
Chinese 北美独活

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Eastern Asia
      • Japan
    • Russian Far East
      • Kamchatka
      • Khabarovsk
      • Kuril Islands
      • Sakhalin
  • Northern America
    • Eastern Canada
      • Labrador
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
    • Southeastern U.S.A.
      • Delaware
      • Georgia
      • Kentucky
      • Maryland
      • North Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
    • Subarctic America
      • Alaska
      • Aleutian Islands
      • Northwest Territorie
      • Yukon
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001068396
Canadensys 2583
USDA Plants HEMA80
Tropicos 1702106
INPN 761992
KEW urn:lsid:ipni.org:names:843087-1
The Plant List tro-1702106
Open Tree Of Life 903092
NCBI Taxonomy 40918
Nature Serve 2.139324
IUCN Red List 64314237
IPNI 843087-1
iNaturalist 53094
GBIF 3034826
Freebase /m/02nhn_
WisFlora 13072
FEIS plants/forb/hermax
EPPO HERMA
Calflora (Californian flora) 9546
USDA GRIN 319139
Wikipedia Heracleum_maximum
KEW urn:lsid:ipni.org:names:978093-1
IPNI 978093-1
GBIF 11963581
UNII 72QK05Z3A0
Canadensys 10042
Tropicos 1700134
KEW urn:lsid:ipni.org:names:120614-2
The Plant List tro-1700134
Observations.org 131277
IPNI 1211240-2
GBIF 3034828
Freebase /m/02nhn_
EPPO HERLA
EOL 489575
USDA GRIN 18895
Wikipedia Heracleum_lanatum
Tropicos 50191110
INPN 613825
KEW urn:lsid:ipni.org:names:978092-1
IPNI 978092-1
CMAUP NPO12730

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
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
New Plants, New Resources, New Knowledge: Early Introductions of Exotic Plants to Indigenous Territories in Northwestern North America Turner NJ Plants (Basel) 28-Aug-2023
PMCID:PMC10490097
doi:10.3390/plants12173087
PMID:37687334
“When the Wild Roses Bloom”: Indigenous Knowledge and Environmental Change in Northwestern North America Turner NJ, Reid AJ Geohealth 01-Nov-2022
PMCID:PMC9665002
doi:10.1029/2022GH000612
PMID:36398276
Genetic Structure and Colonization of North America by Depressaria depressana (Fabricius 1775) (Lepidoptera: Depressariidae) over 15 Years; Contrasts with Westward Expansion of Depressaria radiella (Goeze, 1783) over 160 Years Dean CA, Easley J, Katz AD, Berlocher SH, Berenbaum MR Insects 31-Aug-2022
PMCID:PMC9504837
doi:10.3390/insects13090789
PMID:36135490
Antiviral perspectives of economically important Indian medicinal plants and spices Pebam M, Sushma MV, Sankaranarayanan SA, Thanekar AM, Koyande N, Rengan AK 29-Aug-2022
PMCID:PMC9422945
doi:10.1007/s43538-022-00099-w
Habitat selection in a fluctuating ground squirrel population: Density‐dependence and fitness consequences Aliperti JR, Jenderseck K, Van Vuren DH Ecol Evol 29-Aug-2022
PMCID:PMC9424181
doi:10.1002/ece3.9241
PMID:36052297
Age‐specific, population‐level pedigree of wild black bears provides insights into reproduction, paternity, and maternal effects on offspring apparent survival Reynolds‐Hogland MJ, Ramsey AB, Muench C, Pilgrim KL, Engkjer C, Ramsey PW Ecol Evol 31-Mar-2022
PMCID:PMC8969918
doi:10.1002/ece3.8770
PMID:35386864
Impacts of Wildflower Interventions on Beneficial Insects in Fruit Crops: A Review Fountain MT Insects 18-Mar-2022
PMCID:PMC8955123
doi:10.3390/insects13030304
PMID:35323602
Role of Dexamethasone and Methylprednisolone Corticosteroids in Coronavirus Disease 2019 Hospitalized Patients: A Review Mehta J, Rolta R, Mehta BB, Kaushik N, Choi EH, Kaushik NK Front Microbiol 15-Feb-2022
PMCID:PMC8886296
doi:10.3389/fmicb.2022.813358
PMID:35242118
Critical summer foraging tradeoffs in a subarctic ungulate Ehlers L, Coulombe G, Herriges J, Bentzen T, Suitor M, Joly K, Hebblewhite M Ecol Evol 06-Dec-2021
PMCID:PMC8717276
doi:10.1002/ece3.8349
PMID:35003643
KCNQ and KCNE Isoform-Dependent Pharmacology Rationalizes Native American Dual Use of Specific Plants as Both Analgesics and Gastrointestinal Therapeutics Abbott GW, Redford KE, Yoshimura RF, Manville RW, Moreira L, Tran K, Arena G, Kookootsedes A, Lasky E, Gunnison E Front Physiol 11-Nov-2021
PMCID:PMC8632246
doi:10.3389/fphys.2021.777057
PMID:34858215
Coumarins and Gastrointestinal Cancer: A New Therapeutic Option? Banikazemi Z, Mirazimi SM, Dashti F, Mazandaranian MR, Akbari M, Morshedi K, Aslanbeigi F, Rashidian A, Chamanara M, Hamblin MR, Taghizadeh M, Mirzaei H Front Oncol 11-Oct-2021
PMCID:PMC8542999
doi:10.3389/fonc.2021.752784
PMID:34707995
Phytocompounds from Himalayan Medicinal Plants as Potential Drugs to Treat Multidrug-Resistant Salmonella typhimurium: An In Silico Approach Mehta J, Rolta R, Salaria D, Awofisayo O, Fadare OA, Sharma PP, Rathi B, Chopra A, Kaushik N, Choi EH, Kaushik NK Biomedicines 05-Oct-2021
PMCID:PMC8533345
doi:10.3390/biomedicines9101402
PMID:34680519
Ornithogenic vegetation: How significant has the seabird influence been on the Aleutian Island vegetation during the Holocene? Smyshlyaeva OI, Severova EE, Krylovich OA, Kuzmicheva EA, Savinetsky AB, Dixie W, Hatfield V Ecol Evol 14-Sep-2021
PMCID:PMC8525163
doi:10.1002/ece3.8121
PMID:34707842
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000

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 / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
8-[(1R,5S)-4-oxo-5-[(Z)-pent-2-enyl]cyclopent-2-en-1-yl]octanoic acid 14037060 Click to see 292.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Neryl isovalerate 6429039 Click to see CC(C)CC(=O)OCC=C(C)CCC=C(C)C 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
9-Oxonerolidol 73331190 Click to see 236.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(2R,4aR,8aR)-1,2,3,4,4a,5,6,8a-Octahydro-4a,8-dimethyl-alpha-methylene-2-naphthaleneacetic acid 168796 Click to see 234.33 unknown via CMAUP database
2-[(2R,4aS,8aR)-4a,8-dimethyl-6-oxo-1,2,3,4,5,8a-hexahydronaphthalen-2-yl]prop-2-enoic acid 26087990 Click to see CC1=CC(=O)CC2(C1CC(CC2)C(=C)C(=O)O)C 248.32 unknown via CMAUP database
Costic acid 6451579 Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)O 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
beta-Himachalol 12310488 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
1-epi-Tatridin B 7605278 Click to see 264.32 unknown via CMAUP database
Tamirin 10106765 Click to see 262.30 unknown via CMAUP database
tatridin B 14191260 Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
[(3aR,4S,4aS,5S,8R,8aR,9aS)-5,8-dihydroxy-5,8a-dimethyl-3-methylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-4-yl] (Z)-2-methylbut-2-enoate 101967035 Click to see 364.40 unknown via CMAUP database
Chrysanin 101316713 Click to see CC=C(C)C(=O)OC1C2C(CC3(C1C(=C)CCC3O)C)OC(=O)C2=C 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,6E,9R,10E,11aR)-9-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 12443214 Click to see 248.32 unknown via CMAUP database
tatridin A 14466151 Click to see CC1=CC(C2C(C=C(C(CC1)O)C)OC(=O)C2=C)O 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
gamma-Sitosterol 457801 Click to see 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
Allohimachalol 10585158 Click to see 222.37 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(4aR,9aR)-4,4,6,9a-tetramethyl-1,2,3,4a,7,8-hexahydrobenzo[7]annulen-9-one 10536930 Click to see 220.35 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Bisabolangelone 12300142 Click to see 248.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, 2-(4-hydroxyphenyl)ethyl ester, (E)-; 4-Hydroxyphenethyl trans-ferulate 20979927 Click to see 314.30 unknown https://doi.org/10.1248/CPB.30.4554
p-Hydroxyphenethyl trans-ferulate 637308 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCC2=CC=C(C=C2)O)O 314.30 unknown https://doi.org/10.1248/CPB.30.4554
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1016/0031-9422(82)85180-7
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/0031-9422(82)85180-7
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/0031-9422(82)85180-7
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/0031-9422(82)85180-7
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Isopent-enyloxycoumarin 129819481 Click to see 230.26 unknown https://doi.org/10.1248/BPB.25.244
7-Prenyloxycoumarin 320362 Click to see 230.26 unknown https://doi.org/10.1248/CPB.30.4554
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
2H-Furo(2,3-h)-1-benzopyran-2-one, 8,9-dihydro-9-hydroxy-8-(1-hydroxy-1-methylethyl)- 159015 Click to see 262.26 unknown https://doi.org/10.1016/0031-9422(82)85180-7
9-Hydroxy-8-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-8,9-dihydrofuro[2,3-h]chromen-2-one 5245822 Click to see CC(C)(C1C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown https://doi.org/10.1016/0031-9422(82)85180-7
Apterin 57459455 Click to see CC(C)(C1C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown https://doi.org/10.1016/0031-9422(82)85180-7
Isobergapten 68082 Click to see 216.19 unknown https://doi.org/10.1016/S0031-9422(00)85242-5
Pimpinellin 4825 Click to see 246.21 unknown https://doi.org/10.1007/BF00993733
Sphondin 108104 Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)C=CO2 216.19 unknown via CMAUP database
Vaginidiol 11817856 Click to see CC(C)(C1C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O 262.26 unknown https://doi.org/10.1016/0031-9422(82)85180-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
4-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one 483513 Click to see 304.29 unknown via CMAUP database
Isoimperatorin 68081 Click to see 270.28 unknown via CMAUP database
Isooxypeucedanin 625383 Click to see 286.28 unknown via CMAUP database
Pangelin 44144315 Click to see 286.28 unknown via CMAUP database
Psoralen 6199 Click to see 186.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown https://doi.org/10.1007/BF00993733
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1007/BF01014095
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1016/0031-9422(82)85180-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Salvigenin 161271 Click to see 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
Psoralenol 5320772 Click to see CC1(C(CC2=C(O1)C=CC(=C2)C3=COC4=C(C3=O)C=CC(=C4)O)O)C 338.40 unknown via CMAUP database

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