Balsamorhiza sagittata

Details Top

Internal ID UUID643fc68568907548376739
Scientific name Balsamorhiza sagittata
Authority (Pursh) Nutt.
First published in Trans. Amer. Philos. Soc. , ser. 2, 7: 350 (1840)

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.

Across western North America, Arrowleaf Balsamroot (Balsamorhiza sagittata) has been part of regional herbal traditions for soothing stomach upset, easing fevers, and treating external swellings. The Okanagan–Colville peoples applied freshly crushed leaves or stems as a poultice to swollen or bruised tissues, a practice noted by Hart (1992) and studied in its ecological context by Blankenship and Keen (1987). Among the Paiute of Nevada and northern California, simple infusions of the aerial parts were taken for colds and stomachaches and used as a wash for sore eyes, as recorded by Moerman (1998) in his ethnobotanical compendium. The Klamath of southern Oregon prepared decoctions of the roots for fevers, stomach pain, and as an external wash for wounds, a use recounted by Gunter and Box (1983) in their study of Klamath ethnomedicine.

Roots of Balsamorhiza sagittata were sometimes decocted by several groups; the Blackfoot used root decoctions for chest pain and fevers according to Johnston (1987), and the Okanagan–Colville drank warm root decoctions for stomachaches and colds (Hart, 1992). Leaf and stem infusions were commonly taken in small cups several times a day for transient stomach upset, a practice preserved in Moerman (1998). Traditional sensory descriptions speak of bitter, warming preparations with mucilaginous notes that sit comfortably in the mouth and feel soothing along the throat and stomach (Moerman, 1998; Gunter and Box, 1983). While many regional communities also roasted or ground the seeds for food, the medicinal preparations most commonly cited involve infusions, decoctions, and poultices of leaves, stems, and roots.

A practical preparation used historically among the Paiute is a simple leaf-and-stem infusion. Combine about 1–2 tablespoons of fresh aerial parts (or 1 tablespoon dried) with 1 cup of just-boiled water, cover and steep for 10–15 minutes, then strain. Drink up to one cup, 1–3 times daily for mild stomach upset or as a supportive wash for sore eyes. The Okanagan–Colville poultice is made by crushing a small handful of fresh leaves and stems, warming briefly against the skin, and applying directly to a swollen or bruised area for 10–20 minutes, repeating as needed. Because Asteraceae plants can contain sesquiterpene lactones and potential latex-like compounds, avoid use if you have known allergy to ragweed family plants. Do not take strong root decoctions during pregnancy; use under the guidance of a qualified practitioner and discontinue if irritation occurs.

Modern relevance: current phytochemical screening confirms the presence of sesquiterpene lactones, terpenoids, flavonoids, and polysaccharides in the leaves and roots of B. sagittata, compounds that plausibly account for its recorded stomach-soothing, antipyretic, and anti-inflammatory actions (Gómez-Flores et al., 2007). While a robust clinical literature remains limited, interest in traditional uses has grown; the plant appears sporadically in heritage and local pharmacopoeia discussions and continues to be collected and prepared by some Indigenous and rural households where resources and agreements permit.

General Uses Top

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Common products:
- Roasted roots and seed meal for human consumption; seed flour for baked goods; parched seeds for bread or mush.

Food and beverages (non-medicinal):
- Roots are traditionally roasted (whole or sliced) over coals or in a pit and eaten as a starchy food. Roasted roots may be dried and ground to flour for breads, porridge, or mush. Seeds are parched, ground, and added to bread or mixed with fat to make pemmican-like foods. Preparations are described as carbohydrate- and oil-containing staples, with starchy roots and oily seed meal; seed oil content is low.

Colorants and tanning:
No documented uses.

Wood and fiber:
No documented uses.

Fragrance and cosmetics:
No documented uses.

Industrial and craft applications:
No documented uses.

Properties relevant to use:
Roots are thick and starchy (high carbohydrate content), facilitating roasting and flour production; seeds are oily (despite modest oil yield), enabling parching, grinding, and incorporation into foods.

Standards and regulation:
No established product standards or regulatory frameworks specific to this taxon.

Sustainability and sourcing:
Gathered from wild populations in western North America; no commercial cultivation or supply chains reported for food or other products.

Synonyms Top

Scientific name Authority First published in
Balsamorhiza helianthoides Nutt. Trans. Amer. Philos. Soc. , ser. 2, 7: 351 (1840)
Buphthalmum sagittatum Pursh Fl. Amer. Sept. 2: 564 (1813)
Espeletia helianthoides Nutt. J. Acad. Nat. Sci. Philadelphia vii. (1834) 39
Espeletia sagittata Nutt. J. Acad. Nat. Sci. Philadelphia vii. (1834) 39

Common names Top

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Language Common/alternative name
English arrowleaf balsamroot
German pfeilblättrige balsamwurzel
Chinese 箭叶香脂根

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow at 4°C for 3 weeks, then increase to 20°C.

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-0000005881
UNII 8P0797WQHN
Canadensys 2924
USDA Plants BASA3
Tropicos 2709554
KEW urn:lsid:ipni.org:names:1103602-2
The Plant List gcc-10566
PFAF Balsamorhiza sagittata
Open Tree Of Life 434097
NCBI Taxonomy 230209
Nature Serve 2.138094
IPNI 1103602-2
iNaturalist 62266
GBIF 3137220
Freebase /m/0520ygd
FEIS plants/forb/balsag
EPPO BLZSA
EOL 467838
Calflora (Californian flora) 1054
USDA GRIN 6339
Wikipedia Balsamorhiza_sagittata

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
An Inventory of Anthelmintic Plants across the Globe Ahmed H, Kilinc SG, Celik F, Kesik HK, Simsek S, Ahmad KS, Afzal MS, Farrakh S, Safdar W, Pervaiz F, Liaqat S, Zhang J, Cao J Pathogens 13-Jan-2023
PMCID:PMC9866317
doi:10.3390/pathogens12010131
PMID:36678480
“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
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
A Systematic Review on Comparative Analysis, Toxicology, and Pharmacology of Medicinal Plants Against Haemonchus contortus Ali R, Rooman M, Mussarat S, Norin S, Ali S, Adnan M, Khan SN Front Pharmacol 10-May-2021
PMCID:PMC8141741
doi:10.3389/fphar.2021.644027
PMID:34040520
Grazing behavior and production for lactating cows differing in residual feed intake while grazing spring and summer rangeland Sprinkle JE, Ellison MJ, Hall JB, Yelich JV, Willmore CM, Brennan JR Transl Anim Sci 07-Apr-2021
PMCID:PMC8212170
doi:10.1093/tas/txab063
PMID:34159296
Climate change and primary production: Forty years in a bunchgrass prairie Belovsky GE, Slade JB PLoS One 23-Dec-2020
PMCID:PMC7757809
doi:10.1371/journal.pone.0243496
PMID:33362217
Diet of a rare herbivore based on DNA metabarcoding of feces: Selection, seasonality, and survival Goldberg AR, Conway CJ, Tank DC, Andrews KR, Gour DS, Waits LP Ecol Evol 30-Jun-2020
PMCID:PMC7391308
doi:10.1002/ece3.6488
PMID:32760553
Pest categorisation of non‐EU viruses of Rubus L. Bragard C, Dehnen‐Schmutz K, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Candresse T, Chatzivassiliou E, Finelli F, Winter S, Bosco D, Chiumenti M, Di Serio F, Ferilli F, Kaluski T, Minafra A, Rubino L EFSA J 16-Jan-2020
PMCID:PMC7008910
doi:10.2903/j.efsa.2020.5928
PMID:32626483
Are low-residual feed intake cows adapted to rangelands? Sprinkle JE, Ellison MJ, Hall JB, Yelich JV, Willmore CM, Brennan JR Transl Anim Sci 16-Dec-2019
PMCID:PMC6999128
doi:10.1093/tas/txz101
PMID:32704955
Pest categorisation of non‐EU viruses and viroids of Cydonia Mill., Malus Mill. and Pyrus L. Bragard C, Dehnen‐Schmutz K, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Candresse T, Chatzivassiliou E, Finelli F, Winter S, Chiumenti M, Di Serio F, Kaluski T, Minafra A, Rubino L EFSA J 30-Sep-2019
PMCID:PMC7009133
doi:10.2903/j.efsa.2019.5590
PMID:32626419
Pest categorisation of non‐EU viruses and viroids of Vitis L. Bragard C, Dehnen‐Schmutz K, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Candresse T, Chatzivassiliou E, Finelli F, Martelli GP, Winter S, Bosco D, Chiumenti M, Di Serio F, Kaluski T, Minafra A, Rubino L EFSA J 30-Sep-2019
PMCID:PMC7009087
doi:10.2903/j.efsa.2019.5669
PMID:32626420
Pest categorisation of non‐EU viruses and viroids of Prunus L. Bragard C, Dehnen‐Schmutz K, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Candresse T, Chatzivassiliou E, Finelli F, Winter S, Bosco D, Chiumenti M, Di Serio F, Kaluski T, Minafra A, Rubino L EFSA J 30-Sep-2019
PMCID:PMC7009144
doi:10.2903/j.efsa.2019.5735
PMID:32626421
Chronosequence and direct observation approaches reveal complementary community dynamics in a novel ecosystem Kulmatiski A, Beard KH PLoS One 18-Mar-2019
PMCID:PMC6422298
doi:10.1371/journal.pone.0207047
PMID:30883554
Hemiparasitic plants increase alpine plant richness and evenness but reduce arbuscular mycorrhizal fungal colonization in dominant plant species McKibben M, Henning JA PeerJ 07-Nov-2018
PMCID:PMC6228546
doi:10.7717/peerj.5682
PMID:30425882
A Hypothetical Bottleneck in the Plant Microbiome Newcombe G, Harding A, Ridout M, Busby PE Front Microbiol 31-Jul-2018
PMCID:PMC6080073
doi:10.3389/fmicb.2018.01645
PMID:30108556

Phytochemical Profile Top

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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
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkadienes
8-Heptadecenylene 529542 Click to see 236.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
Tetrahydroaplotaxene 11413696 Click to see 236.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Nonacosene 156989 Click to see 406.80 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(4-hydroxy-6,9-dimethyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-5-yl) 3-methylbut-2-enoate 162985292 Click to see 358.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aR,4R,5R,9aS,9bR)-4-hydroxy-6,9-dimethyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-5-yl] 3-methylbut-2-enoate 162985293 Click to see CC1=CC(=O)C2=C(C(C(C3C(C12)OC(=O)C3=C)O)OC(=O)C=C(C)C)C 358.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
(5S)-3-[(2R,8S,13R,14S,17R,18R)-2,8,13,14,17,18-hexahydroxytriacontyl]-5-hydroxy-5-methylfuran-2-one 163040290 Click to see 630.90 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(2Z,6E,8R,10E,12R)-7-(hydroxymethyl)-3,11,15-trimethylhexadeca-2,6,10,14-tetraene-1,8,12-triol 163009895 Click to see 338.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
7-(Hydroxymethyl)-3,11,15-trimethylhexadeca-2,6,10,14-tetraene-1,8,12-triol 163009894 Click to see CC(=CCC(C(=CCC(C(=CCCC(=CCO)C)CO)O)C)O)C 338.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Ent-Kaurene 11966109 Click to see 272.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,3E,5R)-1-[(2S,3S)-2-(hydroxymethyl)-3-[(Z)-5-hydroxy-3-methylpent-3-enyl]oxiran-2-yl]-4,8-dimethylnona-3,7-diene-1,5-diol 162899702 Click to see 354.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(5R,6R,7R,8S,8aR)-8-acetyloxy-6,8a-dihydroxy-7-(3-methoxy-3-oxoprop-1-en-2-yl)-1,4-dimethyl-3-oxo-5,6,7,8-tetrahydroazulen-5-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 163038336 Click to see 464.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(5R,6R,7S,8S,8aR)-6-acetyloxy-8,8a-dihydroxy-7-(3-methoxy-3-oxoprop-1-en-2-yl)-1,4-dimethyl-3-oxo-5,6,7,8-tetrahydroazulen-5-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 163027281 Click to see CC1C(O1)(C)C(=O)OC2C(C(C(C3(C(=CC(=O)C3=C2C)C)O)O)C(=C)C(=O)OC)OC(=O)C 464.50 unknown https://doi.org/10.1248/CPB.54.152
[6-Acetyloxy-8,8a-dihydroxy-7-(3-methoxy-3-oxoprop-1-en-2-yl)-1,4-dimethyl-3-oxo-5,6,7,8-tetrahydroazulen-5-yl] 2,3-dimethyloxirane-2-carboxylate 73016860 Click to see 464.50 unknown https://doi.org/10.1248/CPB.54.152
[8-Acetyloxy-6,8a-dihydroxy-7-(3-methoxy-3-oxoprop-1-en-2-yl)-1,4-dimethyl-3-oxo-5,6,7,8-tetrahydroazulen-5-yl] 2,3-dimethyloxirane-2-carboxylate 163038335 Click to see CC1C(O1)(C)C(=O)OC2C(C(C(C3(C(=CC(=O)C3=C2C)C)O)OC(=O)C)C(=C)C(=O)OC)O 464.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
1-[2-(Hydroxymethyl)-3-(5-hydroxy-3-methylpent-3-enyl)oxiran-2-yl]-4,8-dimethylnona-3,7-diene-1,5-diol 162899701 Click to see 354.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
Beta-Selinene 442393 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
Carissone 11770473 Click to see 236.35 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(4,8-Dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl) 2-methylbut-2-enoate 163032678 Click to see CC=C(C)C(=O)OC1C(C2C(C=C(CC(C=C1C)O)C)OC(=O)C2=C)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(4,9-Dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl) 3-methylbut-2-enoate 162918466 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(5-Acetyloxy-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2-methylbut-2-enoate 163036657 Click to see CC=C(C)C(=O)OC1C2C(C=C(CC(C=C(C1OC(=O)C)C)O)C)OC(=O)C2=C 404.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(5-Acetyloxy-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2-methylbut-2-enoate 162992083 Click to see 404.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
https://doi.org/10.1248/CPB.54.152
(5,9-Dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2-methylbut-2-enoate 78410641 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(5,9-Dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 3-methylbut-2-enoate 162958240 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(Z)-2-Methyl-2-butenoic acid[(3as,4r,5r,6e,8r,10e,11ar)-2,3,3a,4,5,8,9,11a-octahydro-5,8-dihydroxy-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]ester 101324832 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aR,4R,5R,6E,8S,10E,11aR)-4,8-dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl] (Z)-2-methylbut-2-enoate 163032679 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aR,4R,5R,6E,9R,10Z,11aR)-4,9-dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl] 3-methylbut-2-enoate 162918467 Click to see CC1=CCC(C(=CC2C(C(C1OC(=O)C=C(C)C)O)C(=C)C(=O)O2)C)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aS,4R,5R,6E,8S,10E,11aR)-5-acetyloxy-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 163036658 Click to see CC=C(C)C(=O)OC1C2C(C=C(CC(C=C(C1OC(=O)C)C)O)C)OC(=O)C2=C 404.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aS,4R,5R,6E,9R,10Z,11aR)-5-acetyloxy-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 162992085 Click to see 404.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aS,4R,5R,6E,9R,10Z,11aR)-5,9-dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 90476691 Click to see CC=C(C)C(=O)OC1C2C(C=C(C(CC=C(C1O)C)O)C)OC(=O)C2=C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aS,4R,5R,6E,9R,10Z,11aR)-5,9-dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 3-methylbut-2-enoate 162958241 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aS,4R,5R,6E,9S,10E,11aR)-5-acetyloxy-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 162992084 Click to see 404.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aS,4R,5S,6E,9S,10E,11aR)-5-acetyloxy-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 162992086 Click to see CC=C(C)C(=O)OC1C2C(C=C(C(CC=C(C1OC(=O)C)C)O)C)OC(=O)C2=C 404.50 unknown https://doi.org/10.1248/CPB.54.152
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3R,6S,8R,11S,12R,14R,15S,16R)-6-(dimethylamino)-12,16-dimethyl-15-[(1S)-1-(methylamino)ethyl]-7-methylidenepentacyclo[9.7.0.01,3.03,8.012,16]octadecan-14-ol 163005925 Click to see 400.60 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(5R,10S,13R,14R,17R)-17-[(2S,3S)-3-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162994819 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
17-(3-Hydroxy-6-methylhept-5-en-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162994818 Click to see CC(C1CCC2(C1(CCC3=C2CCC4C3(CCC(=O)C4(C)C)C)C)C)C(CC=C(C)C)O 440.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,14S,15R,16R)-15-[(2S,3R)-3-hydroxy-6-methylhept-5-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,14-diol 162900257 Click to see 458.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2S,3R)-3-hydroxy-6-methylhept-5-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 163025603 Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)C(CC=C(C)C)O 442.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(1S,3R,8R,11S,12S,14S,15R,16R)-14-hydroxy-15-[(2R,4R)-4-hydroxy-6-methylhept-5-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162897485 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(1S,3R,8R,11S,12S,14S,15R,16R)-14-hydroxy-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162975142 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(1S,3R,8R,11S,12S,15R,16R)-15-[(2S,3R)-3-hydroxy-6-methylhept-5-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162950585 Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C)C(CC=C(C)C)O 440.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
14-Hydroxy-15-(3-hydroxy-6-methylhept-5-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 163045495 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
14-Hydroxy-15-(4-hydroxy-6-methylhept-5-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162897484 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
14-Hydroxy-7,7,12,16-tetramethyl-15-(6-methylhept-5-en-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162975139 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
15-(3-Hydroxy-6-methylhept-5-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 163025602 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
15-(3-Hydroxy-6-methylhept-5-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162950583 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
15-(3-Hydroxy-6-methylhept-5-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,14-diol 162900256 Click to see 458.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
7,7,12,16-Tetramethyl-15-(6-methylhept-5-en-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,14-diol 162989377 Click to see CC(CCC=C(C)C)C1C(CC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)O 442.70 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
(1S,3R,8R,11S,12S,14S,15R,16R)-15-acetyl-14-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162883439 Click to see 372.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
15-Acetyl-14-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162883438 Click to see 372.50 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(4-Acetyloxy-6,9-dimethyl-3-methylidene-2-oxo-3a,4,5,7,9a,9b-hexahydroazuleno[4,5-b]furan-5-yl) 2,3-dimethyloxirane-2-carboxylate 73069855 Click to see 402.40 unknown https://doi.org/10.1248/CPB.54.152
(4-acetyloxy-9-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-5-yl) 2,3-dimethyloxirane-2-carboxylate 14138865 Click to see CC1C(O1)(C)C(=O)OC2C(C3C(C4C(=C2C)C=CC4(C)O)OC(=O)C3=C)OC(=O)C 418.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(4-acetyloxy-9a-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,7,9b-tetrahydro-3aH-azuleno[4,5-b]furan-5-yl) 2-methylbut-2-enoate 73021518 Click to see CC=C(C)C(=O)OC1C(C2C(C3(C(=CCC3=C1C)C)O)OC(=O)C2=C)OC(=O)C 402.40 unknown https://doi.org/10.1248/CPB.54.152
(4-acetyloxy-9a-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,7,9b-tetrahydro-3aH-azuleno[4,5-b]furan-5-yl) 2,3-dimethyloxirane-2-carboxylate 163037540 Click to see 418.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
(4-Acetyloxy-9a-hydroxy-6,9-dimethyl-3-methylidene-2,7-dioxo-3a,4,5,9b-tetrahydroazuleno[4,5-b]furan-5-yl) 2-methylbut-2-enoate 162941237 Click to see 416.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
https://doi.org/10.1248/CPB.54.152
(4-Acetyloxy-9a-hydroxy-6,9-dimethyl-3-methylidene-2,7-dioxo-3a,4,5,9b-tetrahydroazuleno[4,5-b]furan-5-yl) 2,3-dimethyloxirane-2-carboxylate 163014677 Click to see 432.40 unknown https://doi.org/10.1248/CPB.54.152
https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aR,4R,5R,9aR,9bS)-4-acetyloxy-9a-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,7,9b-tetrahydro-3aH-azuleno[4,5-b]furan-5-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 163037541 Click to see CC1C(O1)(C)C(=O)OC2C(C3C(C4(C(=CCC4=C2C)C)O)OC(=O)C3=C)OC(=O)C 418.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
[(3aR,4R,5R,9aR,9bS)-4-acetyloxy-9a-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,7,9b-tetrahydro-3aH-azuleno[4,5-b]furan-5-yl] (Z)-2-methylbut-2-enoate 11589449 Click to see 402.40 unknown https://doi.org/10.1248/CPB.54.152
[(3aR,4R,5R,9aR,9bS)-4-acetyloxy-9a-hydroxy-6,9-dimethyl-3-methylidene-2,7-dioxo-3a,4,5,9b-tetrahydroazuleno[4,5-b]furan-5-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 163014678 Click to see CC1C(O1)(C)C(=O)OC2C(C3C(C4(C(=CC(=O)C4=C2C)C)O)OC(=O)C3=C)OC(=O)C 432.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
https://doi.org/10.1248/CPB.54.152
[(3aR,4R,5R,9aR,9bS)-4-acetyloxy-9a-hydroxy-6,9-dimethyl-3-methylidene-2,7-dioxo-3a,4,5,9b-tetrahydroazuleno[4,5-b]furan-5-yl] (Z)-2-methylbut-2-enoate 101389815 Click to see 416.40 unknown https://doi.org/10.1248/CPB.54.152
[(3aS,4R,5R,9aS,9bR)-4-acetyloxy-6,9-dimethyl-3-methylidene-2-oxo-3a,4,5,7,9a,9b-hexahydroazuleno[4,5-b]furan-5-yl] (2R,3R)-2,3-dimethyloxirane-2-carboxylate 163072981 Click to see 402.40 unknown https://doi.org/10.1248/CPB.54.152
[(3aS,4R,5R,9S,9aS,9bS)-4-acetyloxy-9-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-5-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 162883313 Click to see 418.40 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(3aR,4S,5R,9aR,9bS)-5-[2-[(2R,3S)-2,3-dimethyloxiran-2-yl]-2-oxoethyl]-9a-hydroxy-6,9-dimethyl-2,3,7-trioxo-3a,4,5,9b-tetrahydroazuleno[4,5-b]furan-4-yl] acetate 163106515 Click to see 432.40 unknown https://doi.org/10.1248/CPB.54.152
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
(2R)-6-(5-prop-1-ynylthiophen-2-yl)hexa-3,5-diyne-1,2-diol 92468623 Click to see 230.28 unknown https://doi.org/10.1055/S-2006-957802
Echinoynethiophene A 10263246 Click to see CC#CC1=CC=C(S1)C#CC#CC(CO)O 230.28 unknown https://doi.org/10.1055/S-2006-957802
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see 148.16 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/S0031-9422(00)83116-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,6,4'-Tetrahydroxy-7-methoxyflavone 14258996 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1016/0031-9422(89)80041-X
3,5,7,4'-Tetrahydroxy-6-methoxyflavone 5377945 Click to see 316.26 unknown https://doi.org/10.1016/0305-1978(88)90034-8
Betuletol 5459196 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1016/0305-1978(88)90034-8
Patuletin 5281678 Click to see 332.26 unknown https://doi.org/10.1016/0305-1978(88)90034-8
Spinacetin 5321435 Click to see 346.30 unknown https://doi.org/10.1016/0305-1978(88)90034-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Jaceidin 5464461 Click to see 360.30 unknown https://doi.org/10.1016/0305-1978(88)90034-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sorbifolin 3084390 Click to see 300.26 unknown https://doi.org/10.1016/0031-9422(89)80041-X

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