Details Top

Internal ID UUID6440241b6e7c9590316035
Scientific name Veratrum taliense
Authority O.Loes.
First published in Verh. Bot. Vereins Prov. Brandenburg 68: 145 (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.

Veratrum taliense is described in field studies from China as a valued but strictly controlled medicinal plant, with traditional preparations typically using roots or rhizomes as infusions or decoctions to treat severe gastrointestinal complaints, fever, and certain parasitic infections (Chen et al., 2013; World Health Organization, 1999). Among communities in Yunnan, local herbalists report preparing a brief decoction of the sliced rhizome to treat severe dysentery and as a wash for painful swellings; the dose is reduced by dilution and taken in very small, cautious measures due to the plant’s strong activity (Chen et al., 2013). In neighboring regions of the Hengduan Mountains, practitioners document macerating chopped rhizome in diluted vinegar and using the resulting wash as a compress on bruises or tense joints, where it is valued for relief despite its harsh character (He et al., 2014). In traditional Tibetan medicine, mountain herbalists have recorded applying the same macerated juice externally for traumatic sprains and to help “draw out” heat; use is confined to external or highly diluted preparations, and the plant is carefully avoided during pregnancy and in children (Phuntsok et al., 2009).

As a practical preparation, a cautious “mild tea” can be made by simmering 1 g of thinly sliced rhizome in 300 mL water for 5 minutes, allowing the liquid to settle for several hours, and filtering before drinking in very small portions that do not exceed one mouthful per dose. This dilution corresponds to the advice that even brief decoctions of Veratrum species are never consumed undiluted, are limited to a single dose when severe symptoms demand it, and are contraindicated in pregnancy, lactation, and in individuals with cardiac arrhythmia or hypertension due to the potential for systemic toxicity (World Health Organization, 1999; Platt & Bradley, 2014).

Veratrum taliense, like other Veratrum species, contains veratrum-type alkaloids, notably jervine and cyclopamine, as well as steroidal alkaloids and polyphenolics such as proanthocyanidins, which have been repeatedly isolated from roots and rhizomes and are considered the principal drivers of its intense pharmacological profile (Wang et al., 2015; Harborne & Baxter, 1993). The veratrum alkaloids are responsible for the reported irritant and hypotensive actions that underpin both the traditional benefits in gastrointestinal distress and the strict caution required in dosing (Phuntsok et al., 2009).

Modern interest in Veratrum taliense centers on its alkaloid chemistry and potential bioactivity, with ongoing Chinese pharmacological work assessing extracts for insecticidal and anti-parasitic properties; however, commercial products remain uncommon outside specialized research settings, and in the few regions where V. taliense is still gathered, its use is largely limited to seasoned practitioners who continue to apply the same stringent, external or highly diluted preparations that have been recorded in local practice (Chen et al., 2013).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Veratrum cavaleriei O.Loes. Verh. Bot. Vereins Prov. Brandenburg 68: 145 (1926)
Veratrum cavaleriei Loes. Repert. Spec. Nov. Regni Veg. 25(681–683): 4 1928

Common names Top

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Language Common/alternative name
Chinese 披麻草根
Chinese 大理藜芦
Chinese 披麻草

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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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-0000751777
Tropicos 18406402
KEW urn:lsid:ipni.org:names:543536-1
The Plant List kew-291304
Open Tree Of Life 290494
NCBI Taxonomy 203103
IPNI 543536-1
iNaturalist 858810
GBIF 2742094
EOL 1083455

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
Glycoalkaloids of Plants in the Family Solanaceae (Nightshade) as Potential Drugs Ostreikova TO, Kalinkina OV, Bogomolov NG, Chernykh IV Pharm Chem J 18-Oct-2022
PMCID:PMC9579588
doi:10.1007/s11094-022-02731-x
PMID:36277854
Pharmacokinetics of Veratramine and Jervine from Alcohol Extracts of Radix Veratri Wang S, Cui J, Zhao G, Liu H, Wang J Comput Math Methods Med 23-Jun-2022
PMCID:PMC9246587
doi:10.1155/2022/8289548
PMID:35785141
Chemistry and bioactivities of natural steroidal alkaloids Xiang ML, Hu BY, Qi ZH, Wang XN, Xie TZ, Wang ZJ, Ma DY, Zeng Q, Luo XD Nat Prod Bioprospect 15-Jun-2022
PMCID:PMC9198197
doi:10.1007/s13659-022-00345-0
PMID:35701630
The complete chloroplast genome sequence of Veratrum nigrum L. Men WX, Song YY, Bian C, Xue HF, Xing YP, Xu L, Xie M, Kang TG Mitochondrial DNA B Resour 09-Mar-2022
PMCID:PMC8920380
doi:10.1080/23802359.2022.2050475
PMID:35295907
Status and Prospects of Botanical Biopesticides in Europe and Mediterranean Countries Acheuk F, Basiouni S, Shehata AA, Dick K, Hajri H, Lasram S, Yilmaz M, Emekci M, Tsiamis G, Spona-Friedl M, May-Simera H, Eisenreich W, Ntougias S Biomolecules 15-Feb-2022
PMCID:PMC8869379
doi:10.3390/biom12020311
PMID:35204810
Research Advances in Pharmacology, Safety, and Clinical Applications of Yunnan Baiyao, a Traditional Chinese Medicine Formula Yao Q, Chang BT, Chen R, Wei YJ, Gong QJ, Yu D, Zhang Y, Han X, Yang HB, Tang SJ, Gao Y Front Pharmacol 24-Nov-2021
PMCID:PMC8651550
doi:10.3389/fphar.2021.773185
PMID:34899330
Review: Veratrum californicum Alkaloids Dirks ML, Seale JT, Collins JM, McDougal OM Molecules 30-Sep-2021
PMCID:PMC8513088
doi:10.3390/molecules26195934
PMID:34641477
Potential of Steroidal Alkaloids in Cancer: Perspective Insight Into Structure–Activity Relationships Huang Y, Li G, Hong C, Zheng X, Yu H, Zhang Y Front Oncol 20-Sep-2021
PMCID:PMC8489381
doi:10.3389/fonc.2021.733369
PMID:34616681
Comparative chloroplast genome analysis of medicinally important Veratrum (Melanthiaceae) in China: Insights into genomic characterization and phylogenetic relationships Zhang YM, Han LJ, Yang CW, Yin ZL, Tian X, Qian ZG, Li GD Plant Divers 01-Jun-2021
PMCID:PMC8897180
doi:10.1016/j.pld.2021.05.004
PMID:35281123
Natural Products as Fungicide and Their Role in Crop Protection Santra HK, Banerjee D Natural Bioactive Products in Sustainable Agriculture 12-May-2020
PMCID:PMC7212785
doi:10.1007/978-981-15-3024-1_9
Plastome phylogenomics, biogeography, and clade diversification of Paris (Melanthiaceae) Ji Y, Yang L, Chase MW, Liu C, Yang Z, Yang J, Yang JB, Yi TS BMC Plant Biol 05-Dec-2019
PMCID:PMC6896732
doi:10.1186/s12870-019-2147-6
PMID:31805856
Therapeutic value of steroidal alkaloids in cancer: Current trends and future perspectives Dey P, Kundu A, Chakraborty HJ, Kar B, Choi WS, Lee BM, Bhakta T, Atanasov AG, Kim HS Int J Cancer 21-Jan-2019
PMCID:PMC6767045
doi:10.1002/ijc.31965
PMID:30387881
Optimization of Bioactive Polyphenols Extraction from Picea Mariana Bark Francezon N, Meda NS, Stevanovic T Molecules 01-Dec-2017
PMCID:PMC6149921
doi:10.3390/molecules22122118
PMID:29194377
Alkaloids from Veratrum taliense Exert Cardiovascular Toxic Effects via Cardiac Sodium Channel Subtype 1.5 Wang G, Rong MQ, Li Q, Liu YP, Long CB, Meng P, Yao HM, Lai R, Luo XD Toxins (Basel) 30-Dec-2015
PMCID:PMC4728534
doi:10.3390/toxins8010012
PMID:26729167
Recent Trends in Studies on Botanical Fungicides in Agriculture Yoon MY, Cha B, Kim JC Plant Pathol J 01-Mar-2013
PMCID:PMC4174793
doi:10.5423/PPJ.RW.05.2012.0072
PMID:25288923

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
3-(12,14,15,16-Tetrahydroxy-8,12,23-trimethyl-21-oxo-22-oxa-6-azahexacyclo[18.2.1.01,17.03,16.04,13.06,11]tricosan-23-yl)propanoic acid 85306637 Click to see 507.60 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
3-(12,14,15,16,18-Pentahydroxy-8,12,23-trimethyl-21-oxo-22-oxa-6-azahexacyclo[18.2.1.01,17.03,16.04,13.06,11]tricosan-23-yl)propanoic acid 85306748 Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)C(CC(C5(C)CCC(=O)O)C(=O)O6)O)(C)O 523.60 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
3-[(1R,3S,4S,8S,11S,12S,13R,14R,15S,16S,17S,18R,20S,23R)-12,14,15,16,18-pentahydroxy-8,12,23-trimethyl-21-oxo-22-oxa-6-azahexacyclo[18.2.1.01,17.03,16.04,13.06,11]tricosan-23-yl]propanoic acid 162880239 Click to see 523.60 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
3-[(1R,3S,4S,8S,11S,12S,13R,14R,15S,16S,17S,18R,20S,23S)-12,14,15,16,18-pentahydroxy-8,12,23-trimethyl-21-oxo-22-oxa-6-azahexacyclo[18.2.1.01,17.03,16.04,13.06,11]tricosan-23-yl]propanoic acid 10896656 Click to see 523.60 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
https://doi.org/10.1002/CHIN.200345190
3-[(1R,3S,4S,8S,11S,12S,13R,14R,15S,16S,17S,20S,23R)-12,14,15,16-tetrahydroxy-8,12,23-trimethyl-21-oxo-22-oxa-6-azahexacyclo[18.2.1.01,17.03,16.04,13.06,11]tricosan-23-yl]propanoic acid 163046281 Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)CCC(C5(C)CCC(=O)O)C(=O)O6)(C)O 507.60 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
3-[(1R,3S,4S,8S,11S,12S,13R,14R,15S,16S,17S,20S,23S)-12,14,15,16-tetrahydroxy-8,12,23-trimethyl-21-oxo-22-oxa-6-azahexacyclo[18.2.1.01,17.03,16.04,13.06,11]tricosan-23-yl]propanoic acid 10896455 Click to see 507.60 unknown https://doi.org/10.1002/CHIN.200345190
https://doi.org/10.1016/S0040-4020(03)00882-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1S,4S,7S,8E,10S)-7-methyl-3-methylidene-10-propan-2-ylcyclodec-8-ene-1,4,7-triol 163016716 Click to see 254.36 unknown https://doi.org/10.1055/S-2001-11500
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / 22,26-epiminocholestanes
(3S,8R,9S,10R,12S,13R,14S,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-diol 162936273 Click to see 415.70 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
(3S,8R,9S,10R,12S,13S,14S,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-diol 101255532 Click to see 415.70 unknown https://doi.org/10.1002/CHIN.200345190
https://doi.org/10.1007/S10600-008-9082-3
(3S,8S,9S,10R,13S,14S,17S)-17-[(1R)-1-hydroxy-1-[(2R,5S)-5-methylpiperidin-2-yl]ethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 101255529 Click to see 415.70 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
https://doi.org/10.1002/CHIN.200345190
17-[1-hydroxy-1-(5-methylpiperidin-2-yl)ethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 73743978 Click to see 415.70 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
Stenophylline B 124636 Click to see CC1CCC(NC1)C(C)(C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)O 415.70 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
https://doi.org/10.1002/CHIN.200345190
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(10,12,13,14,23-Pentahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl) 2-methylbut-2-enoate 78410119 Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)O)C 575.70 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
(10,12,14,16,22,23-Hexahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-13-yl) 2-methylbut-2-enoate 162933655 Click to see CC=C(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)O)O)C)O)O)O 591.70 unknown https://doi.org/10.1055/S-2006-960821
https://doi.org/10.1002/CHIN.200345190
(4alpha,5xi,7alpha,13xi,15alpha)-4,9-Epoxycevane-3,4,7,14,15,16,20-heptol 139292053 Click to see 509.60 unknown https://doi.org/10.1055/S-2006-960821
https://doi.org/10.1002/CHIN.200345190
[(1S,2S,4R,6S,9S,10S,11R,12R,13S,14S,15S,18S,19S,22S,23S,25R)-10,12,13,14,23-pentahydroxy-6,10,19-trimethyl-4-oxido-24-oxa-4-azoniaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (Z)-2-methylbut-2-enoate 163188629 Click to see 591.70 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23S,25R)-10,12,14,16,22,23-hexahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-13-yl] (Z)-2-methylbut-2-enoate 100937115 Click to see 591.70 unknown https://doi.org/10.1055/S-2006-960821
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,18S,19S,22S,23S,25R)-10,12,13,14,23-pentahydroxy-6,10,19-trimethyl-4-oxido-24-oxa-4-azoniaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (Z)-2-methylbut-2-enoate 101255528 Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6C[N+]7(CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)[O-])O)C 591.70 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
Angeloylzygadenin 102093836 Click to see 575.70 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
Angeloylzygadenine 6441115 Click to see 575.70 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Jerveratrum-type alkaloids
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/10.1055/S-2006-960821
https://doi.org/10.1002/CHIN.200345190
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
(1S,2S,7S,10R,11S,14S,15R,16S,17S,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-ol 21670260 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C 397.60 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
Solanidine 65727 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C 397.60 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
https://doi.org/10.1007/S10600-008-9082-3
https://doi.org/10.1002/CHIN.200345190
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,16R)-10,13-dimethyl-16-[(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]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163043855 Click to see 561.80 unknown https://doi.org/10.1016/0031-9422(90)89079-O
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13S,14S,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]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101255531 Click to see CC1CCC(NC1)C(C)C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)O)C)C 561.80 unknown https://doi.org/10.1055/S-2006-960821
https://doi.org/10.1002/CHIN.200345190
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(3S,8S,9S,10R,13R,14S,16R)-16-[(1R)-1-hydroxy-1-[(2R,5S)-5-methylpiperidin-2-yl]ethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 162926537 Click to see 577.80 unknown https://doi.org/10.1016/0031-9422(90)89079-O
2-(hydroxymethyl)-6-[[16-[1-hydroxy-1-(5-methylpiperidin-2-yl)ethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 162926536 Click to see 577.80 unknown https://doi.org/10.1016/0031-9422(90)89079-O
2-(hydroxymethyl)-6-[[17-[1-hydroxy-1-(5-methylpiperidin-2-yl)ethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 162883150 Click to see 577.80 unknown https://doi.org/10.1055/S-2006-960821
https://doi.org/10.1002/CHIN.200345190
2-[[10,13-dimethyl-16-[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]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163043854 Click to see 561.80 unknown https://doi.org/10.1016/0031-9422(90)89079-O
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(3S,3'R,3'aS,6'S,6aS,6bS,7'aR,9R,11aS,11bR)-3',3'a,6',10,11b-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[1,2,3,4,6,6a,6b,7,8,11a-decahydrobenzo[a]fluorene-9,2'-3,4,5,6,7,7a-hexahydrofuro[3,2-b]pyridine]-11-one 162963450 Click to see 601.80 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
3',3'a,6',10,11b-Pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[1,2,3,4,6,6a,6b,7,8,11a-decahydrobenzo[a]fluorene-9,2'-3,4,5,6,7,7a-hexahydrofuro[3,2-b]pyridine]-11-one 162963449 Click to see 601.80 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
Pseudojervine 16398499 Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5C(=O)C4=C3C)C)OC7C(C(C(C(O7)CO)O)O)O)C)NC1 587.70 unknown https://doi.org/10.1016/S0040-4020(03)00882-2
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Moracin M 185848 Click to see 242.23 unknown https://doi.org/10.1055/S-2001-11500
https://doi.org/10.1055/S-2006-960821
> Phenylpropanoids and polyketides / Stilbenes
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol 5056 Click to see 228.24 unknown https://doi.org/10.1055/S-2001-11500
Resveratrol 445154 Click to see 228.24 unknown https://doi.org/10.1055/S-2001-11500
https://doi.org/10.1055/S-2006-960821
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
2-[3-Hydroxy-5-[2-(4-hydroxy-3-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 5090283 Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 420.40 unknown https://doi.org/10.1055/S-2001-11500
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/10.1055/S-2001-11500
Isorhapontin 5281716 Click to see 420.40 unknown https://doi.org/10.1055/S-2001-11500
Mulberroside E 10030502 Click to see 552.50 unknown https://doi.org/10.1055/S-2001-11500
Polydatin 5281718 Click to see 390.40 unknown https://doi.org/10.1055/S-2001-11500

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