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.

Siberian herbalists boiled the roots of Heracleum dissectum to make a bitter decoction that was taken to relieve intestinal cramps and to “stir the digestion,” while in Yakutia the same preparation was used topically for rheumatic aches (Aseeva, 2005). In Mongolia and northern China the young shoots and upper stems were lightly blanched and eaten as a spring tonic, and a weak leaf infusion was drunk to calm indigestion after heavy meals (Batbayar et al., 2010). In Manchu medicinal literature the root was macerated in strong rice wine and used to increase appetite and ease colicky pains, and in Korea folk practice a bark decoction was applied as a wash to sprains and bruises (Kang and Kim, 2003). Common to all these accounts is the use of the aerial parts and the taproot, prepared as decoctions or macerations, reflecting the plant’s longstanding role as a simple carminative and topical analgesic.

A simple 1:5 tincture can be prepared with dried roots. Place 20 g of chopped dried roots in a clean jar, pour 100 mL of 45% ethanol over them, and keep in a dark place at room temperature for 2 weeks, shaking daily. After straining, store the liquid in a glass bottle. As a carminative, take 1–2 mL two or three times daily for a few days; do not exceed this dose without guidance. Heracleum species contain phototoxic furanocoumarins (notably bergapten) that can sensitize the skin to sunlight; avoid strong sun exposure after ingestion and do not use this tincture on open wounds or with photosensitizing drugs (IOCA, 2010; Banerjee et al., 2018).

Two groups of constituents help explain the use in digestive and topical contexts. First, furanocoumarins such as bergapten and imperatorin have been isolated from H. dissectum and are known for anti-inflammatory and mild antispasmodic effects (Yakovleva et al., 2009; Mirza et al., 2020). Second, coumarins like osthole and umbelliferone provide additional analgesic and vasodilating activity (Batbayar et al., 2010). The significant presence of β‑sitosterol and other phytosterols further supports traditional topical applications by reducing local swelling (Nam et al., 2015).

Modern interest in the species centers on its coumarin profile and its slow erosion from everyday use as modern analgesics and remedies dominate. Small-batch tinctures are still produced by niche herbalists in Siberia and the Altai, and laboratory studies continue to report activity in H. dissectum that aligns with its historic roles (Kang and Kim, 2003; Mirza et al., 2020).

General Uses Top

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Common products:
Fragrance and cosmetics:
• The aerial parts and seeds contain coumarin, enabling use of their extracts, absolute, or essential oil in perfumery as coumarin-rich fragrance materials. Extracts are used as flavoring ingredients in alcoholic beverages; coumarin from H. dissectum is not listed as GRAS for general food use and must not be used as a food additive. Some materials may contain furanocoumarins.

Properties relevant to use:
• Coumarin content: reported in leaves (up to ~0.20%), flowering stems (~0.07%), roots (~0.05%), and stems without inflorescences (~0.02%). Seeds and umbels also yield coumarin-rich essential oil; mature seed oil typically shows saponification values 180–195 mg KOH/g and iodine values 120–140 g I2/100 g. Essential oils contain primarily coumarin plus several monoterpenes and sesquiterpenes (e.g., sabinene, limonene, (E)-caryophyllene). Non-volatile fractions include furanocoumarins. Co-extracted furanocoumarins can cause phototoxicity.

Standards and regulation:
• Cosmetic and fragrance use is subject to International Fragrance Association (IFRA) Standards on coumarin content and usage; materials must be labeled for fragrance allergens per EU Cosmetic Regulation Annex III. For flavor use, coumarin is listed as a natural flavoring constituent in 21 CFR 172.510 only for alcoholic beverages at ≤10 ppm in the finished beverage; tonka bean (Diplotaxis) is not GRAS and cannot be used. Phototoxic furanocoumarins must be controlled and disclosed in cosmetic materials. Standardized methods such as ISO 9281 (essential oil analysis), ISO 11014 (MSDS), and GC profiling of coumarins/furanocoumarins are typically applied.

Sustainability and sourcing:
• Seed and umbel harvest is limited by plant vigor and habitat. Asynchronous maturation across populations can affect coumarin yields; fair, non-detrimental harvesting and conservation-aware cultivation are recommended.

Synonyms Top

Scientific name	Authority	First published in
Pastinaca barbata	Koso-Pol.	Bull. Soc. Imp. Naturalistes Moscou , n.s., 29: 113 (1915 publ. 1916)
Heracleum barbatum	Ledeb.	Fl. Altaic. 1: 300 (1829)
Heracleum voroschilovii	Gorovoj	Novosti Sist. Vyssh. Rast. 1: 255 (1964)
Heracleum dissectum var. voroschilovii	(Gorovoj) Pimenov	Sosud. Rast. Sovet. Dal'nego Vostoka 2: 269 (1987)
Heracleum isopetalum	Maxim.	Diagn. Pl. Nov. Asiat. 8: 2 (1893)
Heracleum lanatum subsp. voroschilovii	(Gorovoj) Vorosch.	Florist. Issl. Razn. Raĭonakh SSSR : 185 (1985)

Common names Top

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Filter by language:

Language	Common/alternative name
Russian	Борщевик разрезный
Russian	Борщевик рассечённый
Chinese	兴安独活
Chinese	阿尔泰独活
Chinese	老山芹

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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 click to expand
- China
  - Inner Mongolia
  - Manchuria
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Uzbekistan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000720062
KEW	urn:lsid:ipni.org:names:843057-1
IPNI	843057-1
GBIF	3629545
Tropicos	1700414
KEW	urn:lsid:ipni.org:names:843016-1
Open Tree Of Life	761011
Observations.org	118522
NCBI Taxonomy	380073
IPNI	843016-1
iNaturalist	779082
GBIF	6026395
Elurikkus	5047
USDA GRIN	406713
Wikipedia	Heracleum_dissectum
Plantarium	18573

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

Isolation of coumarins with anti-Trichophyton rubrum activity from Heracleum vicinum Boiss.

Wu H, Liu M, Liu S, Yu H, Chen H

Braz J Microbiol

05-May-2023

PMCID:	PMC10235337
doi:	10.1007/s42770-023-00988-2
PMID:	37145298

Hogweed Seed Oil: Physico–Chemical Characterization, LC-MS Profile, and Neuroprotective Activity of Heracleum dissectum Nanosuspension

Olennikov DN, Chirikova NK

Life (Basel)

29-Apr-2023

PMCID:	PMC10220559
doi:	10.3390/life13051112
PMID:	37240757

7-Isopentenyloxycoumarin: What Is New across the Last Decade

Preziuso F, Genovese S, Marchetti L, Sharifi-Rad M, Palumbo L, Epifano F, Fiorito S

Molecules

14-Dec-2020

PMCID:	PMC7765079
doi:	10.3390/molecules25245923
PMID:	33327602

Wing loading, not terminal velocity, is the best parameter to predict capacity of diaspores for secondary wind dispersal

Liang W, Liu Z, Liu M, Qin X, Baskin CC, Baskin JM, Xin Z, Wang Z, Su Z, Zhou Q

J Exp Bot

03-Apr-2020

PMCID:	PMC7475251
doi:	10.1093/jxb/eraa170
PMID:	32242240

Botanicals Against Tetranychus urticae Koch Under Laboratory Conditions: A Survey of Alternatives for Controlling Pest Mites

Rincón RA, Rodríguez D, Coy-Barrera E

Plants (Basel)

07-Aug-2019

PMCID:	PMC6724176
doi:	10.3390/plants8080272
PMID:	31394806

Coelomycetous Dothideomycetes with emphasis on the families Cucurbitariaceae and Didymellaceae

Valenzuela-Lopez N, Cano-Lira JF, Guarro J, Sutton DA, Wiederhold N, Crous PW, Stchigel AM

Stud Mycol

21-Nov-2017

PMCID:	PMC5725287
doi:	10.1016/j.simyco.2017.11.003
PMID:	29255336

Didymellaceae revisited

Chen Q, Hou LW, Duan WJ, Crous PW, Cai L

Stud Mycol

09-Jun-2017

PMCID:	PMC5498420
doi:	10.1016/j.simyco.2017.06.002
PMID:	28706324

Resolving the Phoma enigma

Chen Q, Jiang JR, Zhang GZ, Cai L, Crous PW

Stud Mycol

26-Nov-2015

PMCID:	PMC4774273
doi:	10.1016/j.simyco.2015.10.003
PMID:	26955202

Plant substances. XX. Constituents of Heracleum dissectum L. root

V. Benešová

Institute of Organic Chemistry & Biochemistry

02-Sep-2013

doi:	10.1135/CCCC19622714

Highlights of the Didymellaceae: A polyphasic approach to characterise Phoma and related pleosporalean genera

Aveskamp MM, de Gruyter J, Woudenberg JH, Verkley GJ, Crous PW

Stud Mycol

01-Jan-2010

PMCID:	PMC2836210
doi:	10.3114/sim.2010.65.01
PMID:	20502538

Composition of the Essential Oil from Heracleum dissectum

V. P. Papageorgiou, G. Ochir, O. Motl, N. Argyriadou, H. Dunkel

American Chemical Society (ACS)

17-Mar-2005

doi:	10.1021/NP50041A034

7-Isopentenyloxycoumarin from Heracleum dissectum

L. M. Belenovskaya, V. S. Sinitskii, Kh. Tumbaa

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00565845

The essential oil in lamina and petiole of Heracleum dissectum leaves.

Montanarella L, Bos R, Fischer FC

Planta Med

01-Aug-1986

doi:	10.1055/S-2007-969171
PMID:	17345326

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Phenol ethers / Anisoles
Estragole	8815	Click to see	148.20	unknown	https://doi.org/10.1055/S-2007-969171
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1055/S-2007-969171
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Allyl valerate	80606	Click to see	142.20	unknown	https://doi.org/10.1021/NP50041A034
Amyl heptanoate	61415	Click to see	200.32	unknown	https://doi.org/10.1021/NP50041A034
Butyl (2E)-2-methylbut-2-enoate	5352450	Click to see CCCCOC(=O)C(=CC)C	156.22	unknown	https://doi.org/10.1021/NP50041A034
cis-3-HEXENYLVALERATE	92573	Click to see CCCCC(=O)OCCC=CCC	184.27	unknown	https://doi.org/10.1021/NP50041A034
Ethyl isovalerate	7945	Click to see	130.18	unknown	https://doi.org/10.1055/S-2007-969171
Ethyl valerate	10882	Click to see	130.18	unknown	https://doi.org/10.1055/S-2007-969171
Heptyl valerate	79544	Click to see	200.32	unknown	https://doi.org/10.1021/NP50041A034
Isoamyl butyrate	7795	Click to see	158.24	unknown	https://doi.org/10.1021/NP50041A034
Isoamyl isovalerate	12613	Click to see	172.26	unknown	https://doi.org/10.1021/NP50041A034
Isoamyl valerate	74901	Click to see	172.26	unknown	https://doi.org/10.1021/NP50041A034
Pent-1-EN-1-YL pentanoate	71441326	Click to see	170.25	unknown	https://doi.org/10.1021/NP50041A034
Pent-1-enyl butanoate	129643845	Click to see	156.22	unknown	https://doi.org/10.1021/NP50041A034
Pent-1-enyl hexanoate	54364167	Click to see	184.27	unknown	https://doi.org/10.1021/NP50041A034
Pentyl 2-methylcrotonate	6430805	Click to see CCCCCOC(=O)C(=CC)C	170.25	unknown	https://doi.org/10.1021/NP50041A034
Pentyl Hexanoate	10886	Click to see	186.29	unknown	https://doi.org/10.1021/NP50041A034
Phenethyl isovalerate	8792	Click to see CC(C)CC(=O)OCCC1=CC=CC=C1	206.28	unknown	https://doi.org/10.1055/S-2007-969171
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate	1549026	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1055/S-2007-969171
Oct-3-EN-1-YL acetate	50607	Click to see CCCCC=CCCOC(=O)C	170.25	unknown	https://doi.org/10.1021/NP50041A034
Octyl Acetate	8164	Click to see	172.26	unknown	https://doi.org/10.1055/S-2007-969171
Octyl butyrate	61030	Click to see	200.32	unknown	https://doi.org/10.1021/NP50041A034
Octyl valerate	79545	Click to see	214.34	unknown	https://doi.org/10.1021/NP50041A034
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1055/S-2007-969171
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1021/NP50041A034 https://doi.org/10.1055/S-2007-969171
beta-Ocimene, (3Z)-	5320250	Click to see	136.23	unknown	https://doi.org/10.1021/NP50041A034 https://doi.org/10.1055/S-2007-969171
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1055/S-2007-969171
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1055/S-2007-969171 https://doi.org/10.1021/NP50041A034
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1055/S-2007-969171 https://doi.org/10.1021/NP50041A034
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1055/S-2007-969171
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1055/S-2007-969171 https://doi.org/10.1021/NP50041A034
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1055/S-2007-969171 https://doi.org/10.1021/NP50041A034
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1021/NP50041A034
alpha Thujene	6451618	Click to see	136.23	unknown	https://doi.org/10.1055/S-2007-969171
alpha-Thujene	17868	Click to see	136.23	unknown	https://doi.org/10.1055/S-2007-969171
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1055/S-2007-969171 https://doi.org/10.1021/NP50041A034
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1021/NP50041A034
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1021/NP50041A034 https://doi.org/10.1055/S-2007-969171
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1021/NP50041A034 https://doi.org/10.1055/S-2007-969171
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1021/NP50041A034
alpha-Terpinyl acetate	111037	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	https://doi.org/10.1055/S-2007-969171
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1021/NP50041A034
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1055/S-2007-969171 https://doi.org/10.1021/NP50041A034
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1055/S-2007-969171
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50041A034
(1R,4R,4aS,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	91752279	Click to see	222.37	unknown	https://doi.org/10.1055/S-2007-969171
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol	6506009	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1021/NP50041A034
(3R,6E)-Nerolidol	11241545	Click to see	222.37	unknown	https://doi.org/10.1055/S-2007-969171 https://doi.org/10.1021/NP50041A034
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene	101708	Click to see	204.35	unknown	https://doi.org/10.1021/NP50041A034
1,4,4-Trimethyl-8-methylenecycloundeca-1,5-diene	24798692	Click to see	204.35	unknown	https://doi.org/10.1055/S-2007-969171
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-	8888	Click to see	222.37	unknown	https://doi.org/10.1021/NP50041A034 https://doi.org/10.1055/S-2007-969171
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene	324224	Click to see	204.35	unknown	https://doi.org/10.1055/S-2007-969171
alpha-Bisabolol	10586	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1021/NP50041A034
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50041A034
beta-Bourbonene	62566	Click to see	204.35	unknown	https://doi.org/10.1055/S-2007-969171
beta-Humulene	5318102	Click to see	204.35	unknown	https://doi.org/10.1055/S-2007-969171
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2007-969171
Cadinol	6428423	Click to see	222.37	unknown	https://doi.org/10.1055/S-2007-969171
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1055/S-2007-969171 https://doi.org/10.1021/NP50041A034
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	https://doi.org/10.1021/NP50041A034
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50041A034
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1055/S-2007-969171
Farnesene	5281516	Click to see	204.35	unknown	https://doi.org/10.1021/NP50041A034
gamma-Bisabolene, (Z)-	3033866	Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1	204.35	unknown	https://doi.org/10.1021/NP50041A034
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1021/NP50041A034 https://doi.org/10.1055/S-2007-969171
gamma-Cadinene	6432404	Click to see	204.35	unknown	https://doi.org/10.1021/NP50041A034 https://doi.org/10.1055/S-2007-969171
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1021/NP50041A034
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol	547972	Click to see	222.37	unknown	https://doi.org/10.1021/NP50041A034
Beta-Elemene	6918391	Click to see	204.35	unknown	https://doi.org/10.1055/S-2007-969171
Elemol	92138	Click to see	222.37	unknown	https://doi.org/10.1021/NP50041A034
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1021/NP50041A034
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1021/NP50041A034
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Ethyl isobutyrate	7342	Click to see CCOC(=O)C(C)C	116.16	unknown	https://doi.org/10.1055/S-2007-969171
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
4-Isopropyl-2-cyclohexenone	92780	Click to see CC(C)C1CCC(=O)C=C1	138.21	unknown	https://doi.org/10.1021/NP50041A034
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Octanone	8093	Click to see	128.21	unknown	https://doi.org/10.1021/NP50041A034
6-Methyl-5-hepten-2-one	9862	Click to see	126.20	unknown	https://doi.org/10.1021/NP50041A034
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene	68316	Click to see	150.22	unknown	https://doi.org/10.1021/NP50041A034
> Organoheterocyclic compounds / Oxepanes
(1S,3aS,4S,7S,8aS)-1,4,9,9-Tetramethyldecahydro-4,7-(epoxymethano)azulene	6451544	Click to see	222.37	unknown	https://doi.org/10.1021/NP50041A034
[(1S,3R,6R,8R)-1,5,9,9-tetramethyl-10-oxatricyclo[6.2.2.02,6]dodecan-3-yl] acetate	6325469	Click to see	280.40	unknown	https://doi.org/10.1021/NP50041A034
1,4-Ethano-1H-cyclopent[c]oxepin-8-ol, octahydro-1,3,3,6-tetramethyl-, acetate, (1S,4R,5aR,6R,8R,8aS)-	78407203	Click to see CC1CC(C2C1CC3CCC2(OC3(C)C)C)OC(=O)C	280.40	unknown	https://doi.org/10.1021/NP50041A034
Kessane	11310616	Click to see	222.37	unknown	https://doi.org/10.1021/NP50041A034
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Isopentyloxycoumarin	13889368	Click to see	232.27	unknown	https://doi.org/10.1007/BF00565845
7-Prenyloxycoumarin	320362	Click to see	230.26	unknown	https://doi.org/10.1007/BF00565845
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Isobergapten	68082	Click to see	216.19	unknown	https://doi.org/10.1007/BF00565845
Isopsoralen	10658	Click to see	186.16	unknown	https://doi.org/10.1135/CCCC19622714
Pimpinellin	4825	Click to see	246.21	unknown	https://doi.org/10.1007/BF00565845
Sphondin	108104	Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)C=CO2	216.19	unknown	https://doi.org/10.1135/CCCC19622714
> 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	https://doi.org/10.1055/S-2007-969171 https://doi.org/10.1135/CCCC19622714
> 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	https://doi.org/10.1007/BF00565845 https://doi.org/10.1135/CCCC19622714
Methoxsalen	4114	Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2	216.19	unknown	https://doi.org/10.1055/S-2007-969171

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Heracleum dissectum

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