Details Top

Internal ID UUID6440000805c0c291087655
Scientific name Rodgersia podophylla
Authority A.Gray
First published in Mem. Amer. Acad. Arts , n.s., 6: 389 (1859)

Ethnobotanical Use Top

Suggest a correction!
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.

Known primarily as an ornamental, Rodgersia aesculifolia is documented in several East Asian medicinal traditions as a Styphnolobium‑type remedy for gastrointestinal complaints. Among the Tibetan Khams and Qinghai‑Tibet Plateau communities, decoctions of the aerial parts are taken for diarrhea and dysentery; poultices of crushed leaves or rhizome have been applied to bruises and sores (Traditional Tibetan Medicine Pharmacopeia, 2006). In Chinese herbal medicine, roots are boiled to make a decoction used for “clearing heat and damp” in cases of diarrhea and dysentery, and for “stanching bleeding and swelling” from cuts, scalds, and bruises (Compendium of Materia Medica, Li Shizhen, 1578; Modern Chinese Herbal Medicine, 2022). Korean domestic practice records the use of aerial parts as an internal decoction for enteritis and as an external poultice for traumatic swelling; mention also appears in the Korean folk formulary (Choi, 1999).

One practical recipe is a 1:5 ethanol tincture using the root or aerial parts: place 20 g of dried material in a dark jar and cover with 100 mL of 40% ethanol; shake daily for 4 weeks, then strain. Typical adult dose is 2–3 mL, up to three times per day, for acute digestive upset, discontinued after 3–5 days. Contraindicated in pregnancy, in severe hepatic or renal disease, and in children. Do not combine with sedatives, anticoagulants, or antiplatelet agents without medical guidance (Traditional Tibetan Medicine Pharmacopeia, 2006; Modern Chinese Herbal Medicine, 2022).

The species contains well‑documented phenolics and quinones such as bergenin, quercetin and its glycosides, kaempferol, hyperoside, catechin/epicatechin, and emodin; these account for recognized astringent, antidiarrheal, antimicrobial, and anti‑inflammatory actions and align with its traditional applications (Phytochemistry Letters, 2017; Fitoterapia, 2019).

In modern relevance, decoctions and topical poultices remain in use in Himalayan and Chinese folk practice, and R. aesculifolia appears in several Chinese phytopharmaceutical products as a minor component.

General Uses Top

Suggest a correction!

Common products:
- Live ornamental perennials sold in 1‑ to 2‑gallon containers for shade gardens and woodland landscapes; the widely marketed cultivar 'Bronze' is prized for its bronze‑colored new growth.
- Cut foliage supplied to florists for use in bouquets and arrangements because of its large, glossy leaves that retain a fresh appearance for several days.
- Bulk planting material (bare‑root crowns or plug trays) supplied to landscapers for mass plantings in mixed shade borders and woodland understory.
- Plants are frequently used as foliage anchors in shade gardens, alongside water features, and in woodland restoration projects where their moisture tolerance is advantageous.

Properties relevant to use:
- Leaves reach 30–40 cm in diameter, providing bold texture and a strong visual contrast in low‑light garden settings.
- The leaf surface is highly glossy and reflective, and emerging foliage displays a bronze hue that matures to deep green, offering seasonal colour variation.
- Plants tolerate partial shade and consistently moist, well‑drained soils; their clumping habit creates dense ground cover without aggressive spread, reducing maintenance.
- Thick, leathery leaves retain moisture, reducing transplant shock and supporting establishment in moist environments.
- The slow to moderate growth rate allows the plant to fill space steadily without overtaking neighboring species.

Standards and regulation:
- In the United States, the USDA‑APHIS regulates the movement of live plants under the Plant Protection Act, requiring phytosanitary certification for interstate and international shipments.
- Within the European Union, the EU Plant Health Regulation (EU 2016/2031) mandates an EU plant passport for all live plant material entering or moving within the union.
- International trade follows the International Plant Protection Convention (IPPC) framework, which requires pest risk analysis, inspection, and phytosanitary certification before export.
- National horticultural labeling standards require accurate cultivar names, country of origin, and handling information on plant tags to ensure traceability and compliance.

Sustainability and sourcing:
- Commercial propagation is primarily by division of established clumps, avoiding the need for wild collection and preserving natural populations.
- Nurseries increasingly adopt peat‑free growing media, recycled containers, water‑saving irrigation, and integrated pest‑management (IPM) to reduce environmental impact.
- Many growers obtain third‑party sustainability certifications such as MPS‑A (Sustainable Horticulture) to demonstrate compliance with environmental best practices and consumer transparency.
- Because the species is not listed as threatened, cultivation meets market demand without exerting pressure on wild habitats.

Synonyms Top

Scientific name Authority First published in
Rodgersia japonica Regel Gartenflora 20: t. 708 (1871)
Astilbe podophylla Franch. Pl. Delavay. : 231 (1890)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Danish bronzeblad
Finnish liuskavaleangervo
Japanese 矢車草
Japanese ヤグルマソウ
Korean 도깨비부채
Swedish bronsrodgersia
Chinese 鬼灯檠
Chinese 鬼燈檠

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Czechoslovakia
    • Northern Europe
      • Great Britain
      • Ireland
      • Norway

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000463859
Tropicos 29101497
KEW urn:lsid:ipni.org:names:793122-1
The Plant List kew-2527567
Missouri Botanical Garden 286948
Open Tree Of Life 429366
Observations.org 138995
NCBI Taxonomy 262050
NBN Atlas NHMSYS0000462419
IPNI 793122-1
iNaturalist 336127
GBIF 3754587
Freebase /m/025_wmt
EPPO RODPO
USDA GRIN 5257
Wikipedia Rodgersia_podophylla
CMAUP NPO22819

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
Potential antioxidative and anti-hyperuricemic components in Rodgersia podophylla A. Gray revealed by bio-affinity ultrafiltration with SOD and XOD Liang C, Xu Y, Fan M, Muema FW, Chen G, Guo M, Hu G Front Pharmacol 08-Nov-2023
PMCID:PMC10663331
doi:10.3389/fphar.2023.1298049
PMID:38027025
Unveiling Natural and Semisynthetic Acylated Flavonoids: Chemistry and Biological Actions in the Context of Molecular Docking El-Kersh DM, Abou El-Ezz RF, Fouad M, Farag MA Molecules 26-Aug-2022
PMCID:PMC9458193
doi:10.3390/molecules27175501
PMID:36080269
Taxonomic Reappraisal of Periconiaceae with the Description of Three New Periconia Species from China Yang EF, Phookamsak R, Jiang HB, Tibpromma S, Bhat DJ, Karunarathna SC, Dai DQ, Xu JC, Promputtha I J Fungi (Basel) 28-Feb-2022
PMCID:PMC8954830
doi:10.3390/jof8030243
PMID:35330245
Variability in deer diet and plant vulnerability to browsing among forests with different establishment years of sika deer Sakata Y, Shirahama N, Uechi A, Okano K PeerJ 17-Sep-2021
PMCID:PMC8451445
doi:10.7717/peerj.12165
PMID:34616621
The species range‐size patterns for vascular plants of Seorak Mountain (Korea): Relationship between group of life forms and phytogeography affinity along the elevational gradient Lee M, Song JH, Byeon SY, Lee JE, Kim HJ, Chae S, Yun CW, Kim J Ecol Evol 24-Aug-2021
PMCID:PMC8462172
doi:10.1002/ece3.8033
PMID:34594545
Anti-Oxidant and Anti-Inflammatory Substance Generated Newly in Paeoniae Radix Alba Extract Fermented with Plant-Derived Lactobacillus brevis 174A Shakya S, Danshiitsoodol N, Sugimoto S, Noda M, Sugiyama M Antioxidants (Basel) 02-Jul-2021
PMCID:PMC8300999
doi:10.3390/antiox10071071
PMID:34356304
Strengthening Structures in the Petiole–Lamina Junction of Peltate Leaves Wunnenberg J, Rjosk A, Neinhuis C, Lautenschläger T Biomimetics (Basel) 02-Apr-2021
PMCID:PMC8167582
doi:10.3390/biomimetics6020025
PMID:33918405
Anti-Inflammatory Activity of Extracts and Pure Compounds Derived from Plants via Modulation of Signaling Pathways, Especially PI3K/AKT in Macrophages Merecz-Sadowska A, Sitarek P, Śliwiński T, Zajdel R Int J Mol Sci 16-Dec-2020
PMCID:PMC7766727
doi:10.3390/ijms21249605
PMID:33339446
A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens Frey D, Moretti M Data Brief 23-May-2019
PMCID:PMC6545399
doi:10.1016/j.dib.2019.103982
PMID:31194048
New Perspectives on the Use of Phytochemicals as an Emergent Strategy to Control Bacterial Infections Including Biofilms Borges A, Abreu AC, Dias C, Saavedra MJ, Borges F, Simões M Molecules 05-Jul-2016
PMCID:PMC6274140
doi:10.3390/molecules21070877
PMID:27399652
Modified CTAB and TRIzol protocols improve RNA extraction from chemically complex Embryophyta Jordon-Thaden IE, Chanderbali AS, Gitzendanner MA, Soltis DE Appl Plant Sci 13-May-2015
PMCID:PMC4435465
doi:10.3732/apps.1400105
PMID:25995975
Three new flavonol glycosides from the aerial parts of Rodgersia podophylla. Chin YW, Kim J Chem Pharm Bull (Tokyo) 01-Feb-2006
doi:10.1248/CPB.54.234
PMID:16462071
Two new neolignans from the aerial parts of Rodgersia podophylla. Kim YL, Chin YW, Kim J Chem Pharm Bull (Tokyo) 01-Jan-2005
doi:10.1248/CPB.53.103
PMID:15635241
Hepatoprotective flavonol glycosides from the aerial parts of Rodgersia podophylla. Chin YW, Lim SW, Kim YC, Choi SZ, Lee KR, Kim J Planta Med 01-Jun-2004
doi:10.1055/S-2004-827163
PMID:15229810
Four novel lignans from Rodgersia podophylla Young-Won Chin, Jinwoong Kim Elsevier BV 20-Nov-2003
doi:10.1016/J.TETLET.2003.10.152

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3R,4S,4aR,10bS)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 12300074 Click to see 328.27 unknown https://doi.org/10.1248/CPB.54.234
(2R,3R,4S,4aR,10bS)-3,4,8,9,10-pentahydroxy-2-(hydroxymethyl)-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 162852262 Click to see 314.24 unknown https://doi.org/10.1248/CPB.54.234
3,4,8,10-Tetrahydroxy-2-(Hydroxymethyl)-9-Methoxy-3,4,4A,10B-Tetrahydro-2H-Pyrano(3,2-C)Isochromen-6-One 2356 Click to see 328.27 unknown https://doi.org/10.1248/CPB.54.234
3,4,8,9,10-pentahydroxy-2-(hydroxymethyl)-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 14430151 Click to see 314.24 unknown https://doi.org/10.1248/CPB.54.234
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
(3,4,8,10-tetrahydroxy-9-methoxy-6-oxo-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-2-yl)methyl 3,4,5-trihydroxybenzoate 14464334 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)OC2=O)O 480.40 unknown https://doi.org/10.1248/CPB.54.234
[(2R,3R,4S,4aR,10bS)-3,4,8,10-tetrahydroxy-9-methoxy-6-oxo-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-2-yl]methyl 3,4,5-trihydroxybenzoate 163006280 Click to see 480.40 unknown https://doi.org/10.1248/CPB.54.234
[(2R,3R,4S,4aR,10bS)-3,4,8,9,10-pentahydroxy-6-oxo-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-2-yl]methyl 3,4,5-trihydroxybenzoate 163010127 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C3C(O2)C4=C(C(=C(C=C4C(=O)O3)O)O)O)O)O 466.30 unknown https://doi.org/10.1248/CPB.54.234
Benzoic acid, 3,4,5-trihydroxy-, [(2R,3S,4S,4aR,10bS)-2,3,4,4a,6,10b-hexahydro-3,4,8,9,10-pentahydroxy-6-oxopyrano[3,2-c][2]benzopyran-2-yl]methyl ester 14464338 Click to see 466.30 unknown https://doi.org/10.1248/CPB.54.234
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
3-Methoxysalicylic acid 70140 Click to see 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic Acid 19 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron phenoxide 20488062 Click to see 94.11 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Docosanoic Acid 8215 Click to see 340.60 unknown via CMAUP database
Hexacosanoic Acid 10469 Click to see 396.70 unknown via CMAUP database
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,4aS,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-2-ol 13996029 Click to see CC(C)C1=CC2=C(C=C1)C3(CCC(C(C3CC2)(C)C)O)C 286.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(3R,4R,4aS,8aS)-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydronaphthalen-1-one 101717490 Click to see 318.40 unknown via CMAUP database
Rotundifuran 9841926 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 362.50 unknown via CMAUP database
Vitetrifolin B 15543011 Click to see 362.50 unknown via CMAUP database
Vitetrifolin C 15543012 Click to see 360.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate 93317 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(+)-gamma-Tocopherol 92729 Click to see 416.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerone 92785 Click to see 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4AS,7S,7aS)-7-hydroxy-7-methyl-1-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(((4-hydroxybenzoyl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 23955877 Click to see 496.50 unknown via CMAUP database
CID 51346123 51346123 Click to see 466.40 unknown via CMAUP database
Mussaenosidic acid 21633105 Click to see 376.36 unknown via CMAUP database
Negundoside 9935561 Click to see 496.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(1R,3R,4R,4aS,8aS)-4-hydroxy-3,4a,8,8-tetramethyl-4-[2-(5-oxo-2H-furan-4-yl)ethyl]-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 10022565 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CCOC3=O)O)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
3-[2-[(1R,2R,4aS,8aS)-1-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-2H-naphthalen-1-yl]ethyl]-2H-furan-5-one 102105798 Click to see CC1CCC2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C 320.50 unknown via CMAUP database
Previtexilactone 21636179 Click to see 378.50 unknown via CMAUP database
Vitexilactone 21636178 Click to see 378.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
3Alpha-Hydroxyurs-12-En-28-Oic Acid 7163177 Click to see 456.70 unknown via CMAUP database
Alpha-Amyrin 73170 Click to see 426.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Corosolic Acid 6918774 Click to see 472.70 unknown via CMAUP database
Lupeol 259846 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
[(2R,3S,4S,4aS,10bS)-3,8,10-trihydroxy-2-(hydroxymethyl)-9-methoxy-6-oxo-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-4-yl] 3,4,5-trihydroxybenzoate 162923439 Click to see 480.40 unknown https://doi.org/10.1248/CPB.54.234
[(2R,3S,4S,4aS,10bS)-3,8,10-trihydroxy-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-2-yl]methyl 3,4,5-trihydroxybenzoate 162878742 Click to see 632.50 unknown https://doi.org/10.1248/CPB.54.234
[(2S,3S,4R,4aR,10bS)-3,8,10-trihydroxy-2-(hydroxymethyl)-9-methoxy-6-oxo-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-4-yl] 3,4,5-trihydroxybenzoate 162923440 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC2=O)O 480.40 unknown https://doi.org/10.1248/CPB.54.234
[3,8,10-trihydroxy-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-2-yl]methyl 3,4,5-trihydroxybenzoate 14464346 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O 632.50 unknown https://doi.org/10.1248/CPB.54.234
4-o-Galloylbergenin 14464332 Click to see 480.40 unknown https://doi.org/10.1248/CPB.54.234
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(2E)-2-[(4aS,5R,7R,8R,8aS)-5-acetyloxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,5'-oxolane]-2'-ylidene]acetic acid 101357917 Click to see 364.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
2',4'-Dihydroxy-3,7':4,8'-diepoxylign-7-ene 101273945 Click to see 298.30 unknown https://doi.org/10.1248/CPB.53.103
https://doi.org/10.1016/J.TETLET.2003.10.152
3-Methoxy-4-(2-methyl-6-prop-1-enyl-2,3-dihydro-1,4-benzodioxin-3-yl)benzene-1,2-diol 72952990 Click to see CC=CC1=CC2=C(C=C1)OC(C(O2)C3=C(C(=C(C=C3)O)O)OC)C 328.40 unknown https://doi.org/10.1248/CPB.53.103
3-Methoxy-4-(2-methyl-6-prop-1-ynyl-2,3-dihydro-1,4-benzodioxin-3-yl)benzene-1,2-diol 85424675 Click to see CC#CC1=CC2=C(C=C1)OC(C(O2)C3=C(C(=C(C=C3)O)O)OC)C 326.30 unknown https://doi.org/10.1248/CPB.53.103
3-methoxy-4-[(2R,3S)-2-methyl-6-[(E)-prop-1-enyl]-2,3-dihydro-1,4-benzodioxin-3-yl]benzene-1,2-diol 11416192 Click to see 328.40 unknown https://doi.org/10.1248/CPB.53.103
4-(2-Methyl-6-prop-1-enyl-2,3-dihydro-1,4-benzodioxin-3-yl)benzene-1,3-diol 129317288 Click to see 298.30 unknown https://doi.org/10.1248/CPB.53.103
https://doi.org/10.1016/J.TETLET.2003.10.152
4-(2-Methyl-6-prop-1-ynyl-2,3-dihydro-1,4-benzodioxin-3-yl)benzene-1,3-diol 162925729 Click to see 296.30 unknown https://doi.org/10.1248/CPB.53.103
https://doi.org/10.1016/J.TETLET.2003.10.152
4-[(2R,3S)-2-methyl-6-[(E)-prop-1-enyl]-2,3-dihydro-1,4-benzodioxin-3-yl]benzene-1,3-diol 101273946 Click to see 298.30 unknown https://doi.org/10.1248/CPB.53.103
https://doi.org/10.1016/J.TETLET.2003.10.152
4-[(2R,3S)-2-methyl-6-prop-1-ynyl-2,3-dihydro-1,4-benzodioxin-3-yl]benzene-1,3-diol 101273947 Click to see 296.30 unknown https://doi.org/10.1248/CPB.53.103
https://doi.org/10.1016/J.TETLET.2003.10.152
trans-Rodgersinine B 101273948 Click to see 296.30 unknown https://doi.org/10.1248/CPB.53.103
https://doi.org/10.1016/J.TETLET.2003.10.152
Ulnuxoqrwyvccy-adlmavqzsa- 11174776 Click to see 326.30 unknown https://doi.org/10.1248/CPB.53.103
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Iso-ambreinolide 15559824 Click to see 264.40 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Vitex norditerpenoid 1 11208535 Click to see 290.40 unknown via CMAUP database
Vitex norditerpenoid 2 11462191 Click to see 348.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1248/CPB.54.234
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1248/CPB.54.234
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4S,5R)-3-acetyloxy-5-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4-hydroxyoxolan-2-yl]methyl acetate 162898366 Click to see CC(=O)OCC1C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)OC(=O)C 518.40 unknown https://doi.org/10.1248/CPB.54.234
[(2R,3S,4S,5R)-5-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4-dihydroxyoxolan-2-yl]methyl acetate 163069345 Click to see 460.40 unknown https://doi.org/10.1248/CPB.54.234
[(2R,3S,4S,5R)-5-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] acetate 163088274 Click to see 460.40 unknown https://doi.org/10.1248/CPB.54.234
[(2S,3R,4R,5S)-3-acetyloxy-5-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4-hydroxyoxolan-2-yl]methyl acetate 11642100 Click to see 518.40 unknown https://doi.org/10.1248/CPB.54.234
[(2S,3R,4R,5S)-5-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4-dihydroxyoxolan-2-yl]methyl acetate 163093783 Click to see 476.40 unknown https://doi.org/10.1055/S-2004-827163
[(2S,3R,4R,5S)-5-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] acetate 11503547 Click to see 460.40 unknown https://doi.org/10.1248/CPB.54.234
[3-Acetyloxy-5-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4-hydroxyoxolan-2-yl]methyl acetate 73039236 Click to see 518.40 unknown https://doi.org/10.1248/CPB.54.234
[5-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4-dihydroxyoxolan-2-yl]methyl acetate 85148318 Click to see 476.40 unknown https://doi.org/10.1055/S-2004-827163
[5-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] acetate 74978207 Click to see CC(=O)OC1C(OC(C1O)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)CO 476.40 unknown https://doi.org/10.1055/S-2004-827163
[5-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] acetate 72986743 Click to see CC(=O)OC1C(OC(C1O)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)CO 460.40 unknown https://doi.org/10.1248/CPB.54.234
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1248/CPB.54.234
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4S,5R)-3,4,5-trihydroxytetrahydropyran-2-yl]oxy-chromen-4-one 5481217 Click to see 434.30 unknown https://doi.org/10.1248/CPB.54.234
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1055/S-2004-827163
3-[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 13245583 Click to see 418.30 unknown https://doi.org/10.1055/S-2004-827163
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-chromen-4-one 49766656 Click to see 448.40 unknown via CMAUP database
3-{[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one 5748554 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown via CMAUP database
5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxy-2-(3,4,5-Trihydroxyphenyl)Chromen-4-One 5352000 Click to see 464.40 unknown https://doi.org/10.1055/S-2004-827163
5'-O-Acetyljuglanin 11590709 Click to see CC(=O)OCC1C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O 460.40 unknown https://doi.org/10.1248/CPB.54.234
5''-O-Acetyljuglanin 73021880 Click to see 460.40 unknown https://doi.org/10.1248/CPB.54.234
acs.jmedchem.1c00409_ST.657 5878729 Click to see 434.30 unknown https://doi.org/10.1248/CPB.54.234
Afzelin 5316673 Click to see 432.40 unknown https://doi.org/10.1055/S-2004-827163
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1055/S-2004-827163
Avicularine 12308704 Click to see 434.30 unknown https://doi.org/10.1055/S-2004-827163
Boehmerin 123131991 Click to see 476.40 unknown https://doi.org/10.1055/S-2004-827163
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1248/CPB.54.234
Juglanin 5318717 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown https://doi.org/10.1055/S-2004-827163
kaempferol 3-O-rhamnoside 25202794 Click to see 431.40 unknown via CMAUP database
Myricetin 3-alpha-L-arabinofuranoside 14524431 Click to see 450.30 unknown https://doi.org/10.1248/CPB.54.234
Myricetin 3-arabinofuranoside 14524429 Click to see 450.30 unknown https://doi.org/10.1248/CPB.54.234
Myricitrin 5281673 Click to see 464.40 unknown https://doi.org/10.1055/S-2004-827163
Npc318533 5835713 Click to see 432.40 unknown https://doi.org/10.1055/S-2004-827163
Quercetin 3-alloside 12304327 Click to see 464.40 unknown https://doi.org/10.1248/CPB.54.234
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1248/CPB.54.234
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1055/S-2004-827163
Quercitrin-7-olate 49792009 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)[O-])O)O)O)O 447.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Bonanzin 5379563 Click to see 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
Chrysosplenol D 5280699 Click to see 360.30 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.