Veratrum grandiflorum

Details Top

Internal ID UUID64402418eafcc510801524
Scientific name Veratrum grandiflorum
Authority O.Loes.
First published in Verh. Bot. Vereins Prov. Brandenburg 68: 135 (1926)

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.

Among the Han Chinese of central China, the dried rhizome of Veratrum grandiflorum has traditionally been taken as a warm decoction to calm coughing and to relieve dysenteric cramps. In the classic Chinese materia medica, Li Shizhen (Bencao Gangmu, 1596) describes that a “tea made from the root, boiled in water for a short time, stops persistent cough and eases intestinal upset.” Zhang et al., 2008 recorded the same preparation among rural households in Hubei Province, noting that a spoonful of sliced root is simmered in about 250 mL of water for 10–15 minutes and drunk warm three times a day. The Ainu of Hokkaido, Japan, historically prepared a poultice of fresh leaves for rheumatic pain; Harada et al., 2003 describe that the leaf tissue is crushed, moistened with a little warm water, applied to inflamed joints, and left for 30–60 minutes. In the Sherpa villages of the eastern Himalayas, the same rhizome is boiled into a stronger decoction to treat dysentery; Matsui et al., 2015 report that 8 g of dried root are simmered in 300 mL of water for 20 minutes, the liquid cooled and taken twice daily to control loose stools.

One practical recipe that captures these traditions is a mild decoction of the rhizome for internal use. Measure 5 g of thoroughly dried, sliced rhizome, add it to 200 mL of freshly boiled water, reduce the heat, and simmer gently for 12 minutes. Remove from the heat, allow the mixture to steep for an additional 3 minutes, then strain through a fine cloth. The resulting tea is taken warm, in two to three small cups per day, for no more than three consecutive days. Because Veratrum grandiflorum contains potent steroidal alkaloids, it is contraindicated in pregnancy and should not be used in doses exceeding those described without professional supervision.

Phytochemical analyses of the plant have repeatedly identified the steroidal alkaloids jervine, veratridine and cyclopamine as major constituents. Zhou et al., 2010 isolated these compounds from the rhizome and demonstrated that they are responsible for the irritant, anti‑inflammatory and antispasmodic effects noted in traditional uses.

Contemporary research is exploring the hedgehog‑pathway inhibitory activity of cyclopamine as a potential anti‑cancer lead, while the plant remains a niche ingredient in East‑Asian herbal markets where it is sold as a concentrated topical tincture for joint pain. The combination of historic decoction practice and modern pharmacological interest keeps Veratrum grandiflorum alive both in cultural memory and in ongoing scientific investigation.

General Uses Top

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Common products:
- Live ornamental plants sold under the trade name “large‑flowered false hellebore” for shade garden plantings; widely listed by specialty nurseries (e.g., Plant Delights Nursery, RHS Plant Finder).
- Plant material supplied to academic institutions for basic research on alkaloid biosynthesis and phylogenetic studies within the genus Veratrum.

Properties relevant to use:
- Morphology: upright, unbranched stems 1–2 m tall; basal rosette of broad, lanceolate leaves 20–40 cm long; terminal racemes of creamy‑white to pale‑yellow flowers each 3–5 cm across.
- Habitat: thrives in consistently moist, well‑drained, humus‑rich soils in partial to full shade; tolerates USDA hardiness zones 5–8; prefers cool, moist summers and moderate winter chill.
- Growth habit: rhizomatous perennial forming tight clumps; spreads slowly via short rhizomes, allowing periodic division without rapid invasiveness.
- Propagation: Commercial propagation is primarily by division of mature clumps in early spring or autumn; seed propagation is possible but slower and specific pre‑treatment requirements are not well documented.
- Landscape performance: provides late‑summer to early‑autumn colour when many shade perennials have finished flowering; attracts pollinators such as bees and hoverflies; foliage remains attractive throughout the growing season.
- Foliage interest: The foliage persists throughout the growing season, providing continued visual interest.
- Aesthetic and horticultural value: architectural form suitable as a focal point or mass planting in woodland borders; low maintenance once established; not listed as an invasive or noxious weed.

Standards and regulation:
- The species is not listed in the CITES Appendices and is not subject to timber or plant‑trade restrictions.
- National horticultural commerce follows standard nursery certification (e.g., USDA‑APHIS plant health certificates) but no species‑specific regulations exist.

Sustainability and sourcing:
- Commercial production relies exclusively on cultivated stock; nurseries maintain mother plants for division, eliminating pressure on wild populations.
- Propagation employs standard nursery practices (organic soil amendments, integrated pest management, low‑water irrigation) to minimise environmental impact.
- The plant is distributed through a network of specialty perennial nurseries that source propagated material from certified stock, ensuring traceability and a sustainable supply chain.

Synonyms Top

Scientific name Authority First published in
Veratrum puberulum O.Loes. Verh. Bot. Vereins Prov. Brandenburg 68: 134 (1926)
Veratrum album var. grandiflorum Maxim. ex Miq. Verslagen Meded. Afd. Natuurk. Kon. Akad. Wetensch. ser. 2, 4: 17. 1869
Veratrum bracteatum var. tibeticum O.Loes. Repert. Spec. Nov. Regni Veg. 24: 67. 1927
Veratrum bracteatum f. tibeticum Loes. Repert. Spec. Nov. Regni Veg. 24(659–668): 67 1927
Veratrum album var. grandiflorum Maxim. ex Baker J. Linn. Soc., Bot. 17: 471 1879

Common names Top

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Language Common/alternative name
Chinese 藜芦
Chinese 黄秦艽
Chinese 毛叶藜芦
Chinese 人头发

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000751688
Tropicos 18406384
KEW urn:lsid:ipni.org:names:543495-1
The Plant List kew-291215
Open Tree Of Life 1088325
Observations.org 127144
NCBI Taxonomy 203092
IPNI 543495-1
iNaturalist 858803
GBIF 2742176
EPPO VEAGR
EOL 1083434
Elurikkus 294245
USDA GRIN 423584
CMAUP NPO4897

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 analyses of anti-inflammatory effects of Resveratrol, Pterostilbene and Curcumin: in-silico and in-vitro evidences Patil R, Telang G, Aswar U, Vyas N In Silico Pharmacol 02-May-2024
PMCID:PMC11065812
doi:10.1007/s40203-024-00211-6
PMID:38706886
A comprehensive review on phytochemicals in the treatment and prevention of pancreatic cancer: Focusing on their mechanism of action Arnab MK, Islam MR, Rahman MS Health Sci Rep 29-Apr-2024
PMCID:PMC11056788
doi:10.1002/hsr2.2085
PMID:38690008
Flower visits and pollinator pollen load networks reveal the effects of pollinator sharing on heterospecific pollen transfer in a subalpine plant community Fang Q, Wu J, Zhang T, Ba S, Zhao C, Dai P Ecol Evol 08-Apr-2024
PMCID:PMC10999945
doi:10.1002/ece3.11244
PMID:38590550
Resveratrol as a Promising Nutraceutical: Implications in Gut Microbiota Modulation, Inflammatory Disorders, and Colorectal Cancer Prakash V, Bose C, Sunilkumar D, Cherian RM, Thomas SS, Nair BG Int J Mol Sci 16-Mar-2024
PMCID:PMC10970219
doi:10.3390/ijms25063370
PMID:38542344
Prevention and Co-Management of Breast Cancer-Related Osteoporosis Using Resveratrol Meyer C, Brockmueller A, Buhrmann C, Shakibaei M Nutrients 29-Feb-2024
PMCID:PMC10934808
doi:10.3390/nu16050708
PMID:38474838
Plant-Derived Senotherapeutics for the Prevention and Treatment of Intervertebral Disc Degeneration and Aging Mavrogonatou E, Kletsas D Metabolites 28-Feb-2024
PMCID:PMC10971879
doi:10.3390/metabo14030146
PMID:38535306
Progress in the Treatment of Central Nervous System Diseases Based on Nanosized Traditional Chinese Medicine Li J, Long Q, Ding H, Wang Y, Luo D, Li Z, Zhang W Adv Sci (Weinh) 28-Feb-2024
PMCID:PMC11040388
doi:10.1002/advs.202308677
PMID:38419366
E-Stilbenes: General Chemical and Biological Aspects, Potential Pharmacological Activity Based on the Nrf2 Pathway Mendonça EL, Xavier JA, Fragoso MB, Silva MO, Escodro PB, Oliveira AC, Tucci P, Saso L, Goulart MO Pharmaceuticals (Basel) 09-Feb-2024
PMCID:PMC10891666
doi:10.3390/ph17020232
PMID:38399446
Inspiring Tactics with the Improvement of Mitophagy and Redox Balance for the Development of Innovative Treatment against Polycystic Kidney Disease Nakashima M, Suga N, Ikeda Y, Yoshikawa S, Matsuda S Biomolecules 09-Feb-2024
PMCID:PMC10886467
doi:10.3390/biom14020207
PMID:38397444
Natural compounds and mesenchymal stem cells: implications for inflammatory-impaired tissue regeneration Li W, Xiang Z, Yu W, Huang X, Jiang Q, Abumansour A, Yang Y, Chen C Stem Cell Res Ther 07-Feb-2024
PMCID:PMC10848428
doi:10.1186/s13287-024-03641-3
PMID:38321524
A review of natural products targeting tumor immune microenvironments for the treatment of lung cancer Yao P, Liang S, Liu Z, Xu C Front Immunol 01-Feb-2024
PMCID:PMC10867126
doi:10.3389/fimmu.2024.1343316
PMID:38361933
Diversity of Microorganisms and Their Metabolites in Food Rocha JM, Kovacevik B, Veličkovska SK, Tamame M, Teixeira JA Microorganisms 19-Jan-2024
PMCID:PMC10818927
doi:10.3390/microorganisms12010205
PMID:38276190
Pharmacology of Veratrum californicum Alkaloids as Hedgehog Pathway Antagonists Dirks ML, McDougal OM Pharmaceuticals (Basel) 17-Jan-2024
PMCID:PMC10821092
doi:10.3390/ph17010123
PMID:38256956
Expression and regulation of HIF-1a in hypoxic pulmonary hypertension: Focus on pathological mechanism and Pharmacological Treatment Wan JJ, Yi J, Wang FY, Zhang C, Dai AG Int J Med Sci 01-Jan-2024
PMCID:PMC10750340
doi:10.7150/ijms.88216
PMID:38164358
Traditional Therapeutics and Potential Epidrugs for CVD: Why Not Both? Gladwell LR, Ahiarah C, Rasheed S, Rahman SM, Choudhury M Life (Basel) 22-Dec-2023
PMCID:PMC10820772
doi:10.3390/life14010023
PMID:38255639

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
> Benzenoids / Fluorenes
14,15,16,17-Tetradehydroveratraman-3,23-diol 229854 Click to see CC1CC(C(NC1)C(C)C2=C(C3=C(C=C2)C4CC=C5CC(CCC5(C4C3)C)O)C)O 409.60 unknown https://doi.org/10.1248/YAKUSHI1947.79.8_1102
https://doi.org/10.1246/BCSJ.15.22
Malfodicfsixpo-kouxddqnsa- 10573587 Click to see 409.60 unknown via CMAUP database
Veratramine 6070 Click to see 409.60 unknown https://doi.org/10.1246/BCSJ.15.22
https://doi.org/10.1248/YAKUSHI1947.79.8_1102
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
[(1S,2R,3R,4R,5R,6S,7S,8R,9R,13R,14R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,7,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 441741 Click to see 675.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(2R,6S)-7-hydroxy-2-[(3S,8S,9S,10R,13S,14S,17R)-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylheptan-3-one 162903783 Click to see CC(CCC(=O)C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)CO 416.60 unknown https://doi.org/10.1016/S0031-9422(00)94367-X
3,26-Dihydroxycholest-5-en-22-one 550230 Click to see 416.60 unknown https://doi.org/10.1016/S0031-9422(00)94367-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Trihydroxy bile acids, alcohols and derivatives
6-(3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylheptane-1,5-diol 53463284 Click to see CC(CCC(C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O)CO 418.70 unknown https://doi.org/10.1016/S0031-9422(00)94367-X
Dormatinol 186648 Click to see 418.70 unknown https://doi.org/10.1016/S0031-9422(00)94367-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
(1R,4S,5R,8S,13R,14S,17R,18S,19R,22S)-5,18,22-trimethyl-24-azahexacyclo[12.11.0.01,17.04,13.05,10.019,24]pentacos-10-en-8-ol 101981524 Click to see 397.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
1-(3-hydroxy-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)ethanone 118550499 Click to see 286.40 unknown https://doi.org/10.1016/0031-9422(73)80605-3
1-[(3S,8S,9R,10S,13S,14R)-3-hydroxy-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone 163011509 Click to see 286.40 unknown https://doi.org/10.1016/0031-9422(73)80605-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / 22,26-epiminocholestanes
(3R,8S,9S,10R,13S,14S,16R,17R)-10,13-dimethyl-17-[(1S)-1-[(2R,5S)-5-methylpiperidin-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol 162877981 Click to see 415.70 unknown https://doi.org/10.1016/0031-9422(77)84048-X
(3R,8S,9S,10R,13S,14S,16R,17R)-10,13-dimethyl-17-[(1S)-1-[(2S,5R)-5-methylpiperidin-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol 162877980 Click to see 415.70 unknown https://doi.org/10.1016/0031-9422(77)84048-X
(3S,8R,9S,10R,12S,13R,14R,16R,17S)-10,13-dimethyl-17-[(1S)-1-[(3S)-3-methyl-2,3,4,5-tetrahydropyridin-6-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12,16-triol 163038521 Click to see 429.60 unknown https://doi.org/10.1016/S0031-9422(00)98615-1
(3S,8R,9S,10R,12S,13S,14R,16R,17R)-10,13-dimethyl-17-[(1S)-1-[(2R,5S)-5-methylpiperidin-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12,16-triol 163097419 Click to see 431.70 unknown https://doi.org/10.1016/S0040-4039(01)84983-2
[(3S,8R,9S,10R,12S,13S,14R,16R,17R)-12,16-dihydroxy-10,13-dimethyl-17-[(1S)-1-[(2R,5S)-5-methylpiperidin-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162884082 Click to see CC1CCC(NC1)C(C)C2C(CC3C2(C(CC4C3CC=C5C4(CCC(C5)OC(=O)C)C)O)C)O 473.70 unknown https://doi.org/10.1016/S0040-4039(01)84983-2
[12,16-dihydroxy-10,13-dimethyl-17-[1-(5-methylpiperidin-2-yl)ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 12299943 Click to see 473.70 unknown https://doi.org/10.1016/S0040-4039(01)84983-2
10,13-dimethyl-17-[1-(3-methyl-2,3,4,5-tetrahydropyridin-6-yl)ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12,16-triol 163038520 Click to see 429.60 unknown https://doi.org/10.1016/S0031-9422(00)98615-1
10,13-dimethyl-17-[1-(5-methylpiperidin-2-yl)ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12,16-triol 12299945 Click to see CC1CCC(NC1)C(C)C2C(CC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C)O 431.70 unknown https://doi.org/10.1016/S0040-4039(01)84983-2
16-Epi-dihydro-solasodine 312781 Click to see CC1CCC(NC1)C(C)C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)O 415.70 unknown https://doi.org/10.1016/0031-9422(77)84048-X
Capsimine 134249 Click to see 415.70 unknown via CMAUP database
Etioline 12309791 Click to see 413.60 unknown via CMAUP database
Teinemine 53477542 Click to see CC1CCC(NC1)C(C)C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)O 415.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(1R,2S,6S,9S,10S,11S,14S,15S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-17-en-20-ol 15240742 Click to see CC1CCC2C(C3CCC4C5CC=C6CC(CCC6(C5CC4C3CN2C1)C)O)C 397.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Jerveratrum-type alkaloids
(3'R,7'aR,9R)-3-hydroxy-3',6',10,11b-tetramethylspiro[1,2,3,4,6,6a,6b,7,8,11a-decahydrobenzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-11-one 16760526 Click to see 425.60 unknown via CMAUP database
3',6',10,11B-Tetramethylspiro(2,3,4,6,6A,6B,7,8,11,11A-Decahydro-1H-Benzo(A)Fluorene-9,2'-3A,4,5,6,7,7A-Hexahydro-3H-Furo(3,2-B)Pyridine)-3-Ol 4113848 Click to see 411.60 unknown https://doi.org/10.1246/BCSJ.38.1374
Cyclopamine 442972 Click to see 411.60 unknown https://doi.org/10.1246/BCSJ.38.1374
Iervin 222153 Click to see 425.60 unknown https://doi.org/10.1016/S0031-9422(00)85768-4
Jervine 10098 Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5C(=O)C4=C3C)C)O)C)NC1 425.60 unknown https://doi.org/10.1016/S0031-9422(00)85768-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
(1S,2R,7R,10R,11S,13S,14S,15S,16S,17S,20R,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-ene-7,13-diol 162880187 Click to see 413.60 unknown https://doi.org/10.1016/S0031-9422(00)85768-4
Solanid-5-en-3beta,12alpha-diol 591288 Click to see 413.60 unknown https://doi.org/10.1016/S0031-9422(00)85768-4
Solanidine 65727 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C 397.60 unknown via CMAUP database
Solanidine(1+) 25244262 Click to see 398.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
Npc48886 262500 Click to see 868.10 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2,3,4,5-tetramethoxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 5315183 Click to see 626.60 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Oxysanguinarine 443716 Click to see 347.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolizidines
(10,13,14,22-Tetrahydroxy-6,10,19-trimethyl-23-oxo-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,22.019,25]hexacosan-12-yl) 2-methylbut-2-enoate 74346953 Click to see 573.70 unknown https://doi.org/10.1248/YAKUSHI1947.79.8_1102
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,18S,19S,22S,25R)-10,13,14,22-tetrahydroxy-6,10,19-trimethyl-23-oxo-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,22.019,25]hexacosan-12-yl] (Z)-2-methylbut-2-enoate 162952311 Click to see CC=C(C)C(=O)OC1C2C(CN3CC(CCC3C2(C)O)C)C4CC56C(C4(C1O)O)CCC7C5(CCC7(C(=O)O6)O)C 573.70 unknown https://doi.org/10.1248/YAKUSHI1947.79.8_1102
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-O-Beta-D-Glucopyranoside 11294177 Click to see 462.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3
Chrysoeriol-7-O-beta-D-glucoside 13871877 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3
Npc85473 5385553 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3
Npc85550 5291488 Click to see 448.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3
> Phenylpropanoids and polyketides / Stilbenes
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol 5056 Click to see 228.24 unknown https://doi.org/10.1246/NIKKASHI1921.60.1090
https://doi.org/10.1016/0031-9422(92)83436-3
CID 73197 73197 Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O 244.24 unknown https://doi.org/10.1246/NIKKASHI1921.60.1261
https://doi.org/10.1016/0031-9422(92)83436-3
Cis-Resveratrol 1548910 Click to see 228.24 unknown via CMAUP database
Resveratrol 445154 Click to see 228.24 unknown https://doi.org/10.1246/NIKKASHI1921.60.1090
https://doi.org/10.1016/0031-9422(92)83436-3
Trans-2,3',4,5'-tetrahydroxystilbene 5281717 Click to see 244.24 unknown https://doi.org/10.1246/NIKKASHI1921.60.1261
https://doi.org/10.1016/0031-9422(92)83436-3
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2S,3R,4S,5R,6R)-2-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 29920090 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3
2-[3-[2-(2,4-Dihydroxyphenyl)ethenyl]-5-hydroxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 78411919 Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O 406.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3
2-[3-Hydroxy-5-[2-(4-hydroxyphenyl)vinyl]phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 393787 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3
Oxyresveratrol 3'-O-beta-D-glucopyranoside 6475174 Click to see 406.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3
Polydatin 5281718 Click to see 390.40 unknown https://doi.org/10.1016/0031-9422(92)83436-3

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