Geranium thunbergii

Details Top

Internal ID UUID64401df547019708614865
Scientific name Geranium thunbergii
Authority Siebold ex Lindl. & Paxton
First published in Paxton's Fl. Gard. 1(12): 186 (fig. 115). 1851

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.

In Japan, Geranium thunbergii—known locally as furofuki or gen-no-shoko—has long been used as a “cold water decoction” to calm the gut and bind, especially in the Kampo tradition described in Nihon Yakuso (Hirata, 1979). Fresh aerial parts are also pressed as a poultice to check bleeding and inflammation on cuts and bruises. In Korea, the aerial parts are used in a water decoction for acute diarrhea and to soothe heat in the stomach, as recorded in Flora of Korea (Lee, 1996). Among the Hakka of Taiwan, the leaves are infused into a mild tea given to newborns and infants to relieve colic, an ethnomedical practice documented by Lin et al. (1996). These three regional uses—binding cold decoctions in Japan and Korea, and infant colic tea among the Hakka—underscore a longstanding reputation for astringency and gastrointestinal comfort.

A simple and widely reported preparation is a mild tea: place 2–3 g of dried aerial parts in 300 ml of freshly boiled water, cover, and let steep for 10–15 minutes. Drink the warm infusion in small sips after meals. For traditional “gen-no-shoko” on the bench, cold infusion is common: 1.5 g of dried aerial parts is steeped for 15–30 minutes in 200 ml of cool water. If you are pregnant, nursing, managing diarrhea from infection, or taking anticoagulants, consult a qualified practitioner before use.

These uses align with what is known of the plant’s chemistry. Geranium thunbergii contains abundant hydrolysable tannins such as ellagic acid and geraniin, which underpin astringent activity and bind intestinal secretions. Flavonoids including quercetin and kaempferol derivatives, gallic acid, and small amounts of essential oil add antioxidant properties, supporting its history in soothing irritated mucous membranes.

Today, dried gen-no-shoko is available in many herbal shops and online, and it continues to be featured in Kampo practice for short courses during acute gastrointestinal upset. Modern research explores its antioxidant and anti-inflammatory potential and the possible contribution of its tannins to gut mucosal protection.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Geranium peregrinum Thell. Repert. Spec. Nov. Regni Veg. 9: 549 (1911)
Geranium nepalense var. thunbergii (Siebold ex Lindl. & Paxton) Kudô Medic. Pl. Hokkaido t. 55 1922

Common names Top

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Language Common/alternative name
English thunberg's geranium
Japanese ゲンソウ
Japanese ミコシグサ
Japanese 玄草
Japanese ゲンノショウコ
Korean 이질풀
Slovenian thunbergova krvomočnica
Chinese 中日老鹳草
Chinese 老鹳草
Chinese 中日老鹳草*(东亚老鹳草)
Chinese 东亚老鹳草

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 seeds at 20°C, expecting germination within 3 months without further temperature treatment.

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-0000701460
UNII Z9KVC81LWP
Canadensys 29187
USDA Plants GETH3
Tropicos 13900835
KEW urn:lsid:ipni.org:names:373741-1
The Plant List kew-2824168
Open Tree Of Life 387579
NCBI Taxonomy 345239
Nature Serve 2.147094
IPNI 322497-2
iNaturalist 163266
GBIF 2891266
Freebase /m/0k3nrms
EPPO GERTH
EOL 994349
USDA GRIN 424796
Wikipedia Geranium_thunbergii
CMAUP NPO2798

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
Modified Gwakjeongtang for Diarrhea-Predominant Irritable Bowel Syndrome: Study Protocol for a Randomized, Double-Blind, Placebo-Controlled, Pilot Clinical Trial Choi Y, Ha NY, Kim AR, Jeong H, Kwon O, Park KS, Kim J, Kim J, Kim H Int J Gen Med 22-Apr-2024
PMCID:PMC11048363
doi:10.2147/IJGM.S447701
PMID:38680195
Anti-diabetic and anti-inflammatory bioactive hits from Coriaria intermedia Matsum. stem and Dracontomelon dao (Blanco) Merr. & Rolfe bark through bioassay-guided fractionation and liquid chromatography-tandem mass spectrometry Fabian MC, Astorga RM, Atis AA, Pilapil LA, Hernandez CC Front Pharmacol 08-Mar-2024
PMCID:PMC10957545
doi:10.3389/fphar.2024.1349725
PMID:38523640
The geranium genus: A comprehensive study on ethnomedicinal uses, phytochemical compounds, and pharmacological importance Alshehri B Saudi J Biol Sci 28-Jan-2024
PMCID:PMC10873751
doi:10.1016/j.sjbs.2024.103940
PMID:38371877
Effect of herbal extracts in animal nutrition as feed additives Alem WT Heliyon 26-Jan-2024
PMCID:PMC10845724
doi:10.1016/j.heliyon.2024.e24973
PMID:38322944
Emerging Therapeutic Potential of Polyphenols from Geranium sanguineum L. in Viral Infections, Including SARS-CoV-2 Abarova S, Alexova R, Dragomanova S, Solak A, Fagone P, Mangano K, Petralia MC, Nicoletti F, Kalfin R, Tancheva L Biomolecules 19-Jan-2024
PMCID:PMC10812934
doi:10.3390/biom14010130
PMID:38275759
Evaluation of the Antifungal Effect of Rhus verniciflua Stokes Extract for Oral Application Potential Kim YR, Kim GC, Nam SH Medicina (Kaunas) 11-Sep-2023
PMCID:PMC10536533
doi:10.3390/medicina59091642
PMID:37763761
Effects of Traditional Chinese Herbal Feed Additive on Production Performance, Egg Quality, Antioxidant Capacity, Immunity and Intestinal Health of Laying Hens Liu B, Ma R, Yang Q, Yang Y, Fang Y, Sun Z, Song D Animals (Basel) 03-Aug-2023
PMCID:PMC10417022
doi:10.3390/ani13152510
PMID:37570319
Anti-COVID-19 Potential of Ellagic Acid and Polyphenols of Punica granatum L. Alexova R, Alexandrova S, Dragomanova S, Kalfin R, Solak A, Mehan S, Petralia MC, Fagone P, Mangano K, Nicoletti F, Tancheva L Molecules 27-Apr-2023
PMCID:PMC10180134
doi:10.3390/molecules28093772
PMID:37175181
Drug discovery inspired by bioactive small molecules from nature Kim S, Lim SW, Choi J Anim Cells Syst (Seoul) 21-Dec-2022
PMCID:PMC9809404
doi:10.1080/19768354.2022.2157480
PMID:36605590
Natural Products as Anticancer Agents: Current Status and Future Perspectives Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q Molecules 30-Nov-2022
PMCID:PMC9737905
doi:10.3390/molecules27238367
PMID:36500466
Amelioration of hyperglycemia and hyperlipidemia in a high-fat diet-fed mice by supplementation of a developed optimized polyherbal formulation Tanisha, Venkategowda S, Majumdar M 3 Biotech 30-Aug-2022
PMCID:PMC9428098
doi:10.1007/s13205-022-03309-w
PMID:36060893
Hairy Root Cultures as a Source of Polyphenolic Antioxidants: Flavonoids, Stilbenoids and Hydrolyzable Tannins Malarz J, Michalska K, Yudina YV, Stojakowska A Plants (Basel) 27-Jul-2022
PMCID:PMC9370385
doi:10.3390/plants11151950
PMID:35956428
Editorial: Pharmacology of Plant Polyphenols in Human Health and Diseases Devkota HP, Paudel KR, Lall N, Tomczyk M, Atanasov AG Front Pharmacol 17-Jun-2022
PMCID:PMC9247571
doi:10.3389/fphar.2022.945033
PMID:35784714
Recovery of Bioactive Ellagitannins by Ultrasound/Microwave-Assisted Extraction from Mexican Rambutan Peel (Nephelium lappaceum L.) Estrada-Gil L, Contreras-Esquivel JC, Flores-Gallegos C, Zugasti-Cruz A, Govea-Salas M, Mata-Gómez MA, Rodríguez-Herrera R, Ascacio-Valdés JA Molecules 28-Feb-2022
PMCID:PMC8911573
doi:10.3390/molecules27051592
PMID:35268692
Pharmacological Effects of Cisplatin Combination with Natural Products in Cancer Chemotherapy Dasari S, Njiki S, Mbemi A, Yedjou CG, Tchounwou PB Int J Mol Sci 28-Jan-2022
PMCID:PMC8835907
doi:10.3390/ijms23031532
PMID:35163459

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1248/CPB.34.941
https://doi.org/10.1016/0031-9422(91)85260-7
> Benzenoids / Phenols / Benzenetriols and derivatives / Pyrogallols and derivatives / 5-unsubstituted pyrrogallols
Pyrogallol 1057 Click to see 126.11 unknown https://doi.org/10.1248/CPB.34.941
> Lignans, neolignans and related compounds / Furanoid lignans
Kobusin 182278 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1007/BF02969300
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see 480.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,4S)-1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-cyclohexanecarboxylic acid 460894 Click to see 344.27 unknown https://doi.org/10.1248/CPB.34.941
1,3,4-Trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid 4486613 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O 344.27 unknown https://doi.org/10.1248/CPB.34.941
4-O-Galloylquinic acid 475263 Click to see 344.27 unknown https://doi.org/10.1248/CPB.34.941
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Decursidate 102004630 Click to see 330.30 unknown https://doi.org/10.1016/0031-9422(91)83714-V
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Phyllanthusiin E 15742123 Click to see 292.20 unknown https://doi.org/10.1248/CPB.47.1148
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B 130556 Click to see 578.50 unknown https://doi.org/10.1016/0031-9422(91)83714-V
Procyanidin B3 146798 Click to see 578.50 unknown https://doi.org/10.1016/0031-9422(91)83714-V
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1016/0031-9422(91)85260-7
https://doi.org/10.1016/0031-9422(91)83714-V
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/0031-9422(91)83714-V
https://doi.org/10.1016/0031-9422(91)85260-7
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1248/CPB.34.941
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1248/CPB.34.941
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1248/CPB.32.1866
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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 via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259091 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11557027 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl D-galactopyranoside 11751616 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 44258935 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.32.1866
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Cyclopenta(c)(2)benzopyran-1-carboxylic acid, 1,2,3,5-tetrahydro-7,8,9-trihydroxy-3,5-dioxo-, methyl ester 5319518 Click to see 306.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
.beta-Penta-O-galloyl-D-glucose 374874 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown https://doi.org/10.1016/0031-9422(91)85260-7
https://doi.org/10.1016/0031-9422(91)83714-V
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose 73178 Click to see 788.60 unknown https://doi.org/10.1016/0031-9422(91)85260-7
1,2,3,6-Tetragalloyl-beta-D-glucopyranose 5153644 Click to see 788.60 unknown https://doi.org/10.1016/0031-9422(91)85260-7
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown https://doi.org/10.1016/0031-9422(91)85260-7
1,6-Digalloyl-beta-D-glucopyranose 3332212 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 484.40 unknown https://doi.org/10.1016/0031-9422(91)85260-7
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown https://doi.org/10.1016/0031-9422(91)85260-7
Penta-O-galloyl-beta-D-glucose 65238 Click to see 940.70 unknown https://doi.org/10.1016/0031-9422(91)85260-7
https://doi.org/10.1016/0031-9422(91)83714-V
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1,13,14,18,18,19,34,35,39,39-Decahydroxy-2,5,10,20,23,31-hexaoxo-6,9,24,27,30,40,41-heptaoxanonacyclo[34.3.1.115,19.04,38.07,26.08,29.011,16.017,22.032,37]hentetraconta-3,11,13,15,21,32,34,36-octaen-28-yl) 3,4,5-trihydroxybenzoate 14211684 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C9=C8C2C(=CC(=O)C(C2(O)O)(O9)O)C(=O)O1)O)O 968.60 unknown https://doi.org/10.1248/CPB.30.1113
(1,2,4,13,14,15,18,19,20,34,35-Undecahydroxy-5,10,23,31-tetraoxo-6,9,24,27,30,39-hexaoxaoctacyclo[34.2.1.04,38.07,26.08,29.011,16.017,22.032,37]nonatriaconta-11,13,15,17,19,21,32,34,36-nonaen-28-yl) 3,4,5-trihydroxybenzoate 73989113 Click to see 926.60 unknown https://doi.org/10.1248/CPB.47.1148
(11,11,14,15,16,27,28,29,32,33,34-Undecahydroxy-6,9,10,19,24,37-hexaoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,13,15,17,25,27,29,31,33,35-decaen-3-yl) 3,4,5-trihydroxybenzoate 162928937 Click to see 952.60 unknown https://doi.org/10.1016/S0040-4039(00)93091-0
(14,15,16,27,28,29,32,33,34-Nonahydroxy-6,9,10,11,19,24,37-heptaoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,13,15,17,25,27,29,31,33,35-decaen-3-yl) 3,4,5-trihydroxybenzoate 162954029 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=O)C(=O)C(=O)C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 934.60 unknown https://doi.org/10.1016/S0040-4039(00)93091-0
(1R,3S,4R,11S,12R,21R,22S)-14,15,16,27,28,29,32,33,34-nonahydroxy-6,9,19,24,37-pentaoxo-3-(3,4,5-trihydroxybenzoyl)oxy-2,5,10,20,23,38-hexaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,13,15,17,25,27,29,31,33,35-decaene-11-carboxylic acid 100984957 Click to see 952.60 unknown https://doi.org/10.1248/CPB.47.1148
(1R,3S,4R,13R,14R,21R,22S)-9,10,11,27,28,29,32,33,34-nonahydroxy-6,16,19,24,37-pentaoxo-3-(3,4,5-trihydroxybenzoyl)oxy-2,5,15,20,23,38-hexaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,17,25,27,29,31,33,35-decaene-14-carboxylic acid 11803980 Click to see 952.60 unknown https://doi.org/10.1248/CPB.47.1148
(1R,3S,4R,13R,14S,21R,22S)-9,10,11,27,28,29,32,33,34-nonahydroxy-6,16,19,24,37-pentaoxo-3-(3,4,5-trihydroxybenzoyl)oxy-2,5,15,20,23,38-hexaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,17,25,27,29,31,33,35-decaene-14-carboxylic acid 10748436 Click to see 952.60 unknown https://doi.org/10.1248/CPB.47.1148
(3,6a,10',11',12',15',16',17',31',32',36',37'-dodecahydroxy-2',5,7',20',28',41'-hexaoxospiro[3,3a-dihydro-2H-furo[3,2-b]furan-6,39'-3,6,21,24,27,38,42-heptaoxanonacyclo[35.2.2.133,36.01,35.04,23.05,26.08,13.014,19.029,34]dotetraconta-8,10,12,14,16,18,29,31,33-nonaene]-25'-yl) 3,4,5-trihydroxybenzoate 3459965 Click to see 1110.80 unknown https://doi.org/10.1248/CPB.34.4075
https://doi.org/10.1248/CPB.34.941
(57R,58S,510R,511R,519S)-14,15,16,24,25,26,52,53,516,517,517-Undecahydroxy-55,513,515,3,8-pentaoxo-55,57,58,510,511,513,515,516,517,517a-decahydro-4,7-dioxa-5(19,10)-1,16-epoxy-7,11-methanodibenzo[i,k][1,4,7]trioxacyclotridecina-1,2(1,2)-dibenzenacyclooctaphane-58-yl 3,4,5-trihydroxybenzoate 138991573 Click to see 952.60 unknown https://doi.org/10.1248/CPB.32.1866
https://doi.org/10.1016/S0031-9422(00)83018-6
https://doi.org/10.1016/0031-9422(91)85260-7
https://doi.org/10.1039/P19890002289
https://doi.org/10.1021/NP50086A002
https://doi.org/10.1248/CPB.34.720
https://doi.org/10.1021/NP50040A016
https://doi.org/10.1248/CPB.47.1148
[(1R,2S,8R,9S,27R,29S,30R,39R)-1,2,14,15,16,19,20,21,35,36-decahydroxy-3,6,11,24,32-pentaoxo-2-(2-oxopropyl)-7,10,25,28,31,40-hexaoxaoctacyclo[35.2.1.05,39.08,27.09,30.012,17.018,23.033,38]tetraconta-4,12,14,16,18,20,22,33,35,37-decaen-29-yl] 3,4,5-trihydroxybenzoate 10373760 Click to see 992.70 unknown https://doi.org/10.1016/0031-9422(91)83714-V
[(1R,3S,4R,12R,21R,22S)-14,15,16,27,28,29,32,33,34-nonahydroxy-6,9,10,11,19,24,37-heptaoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,13,15,17,25,27,29,31,33,35-decaen-3-yl] 3,4,5-trihydroxybenzoate 162954030 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=O)C(=O)C(=O)C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 934.60 unknown https://doi.org/10.1016/S0040-4039(00)93091-0
[(1R,3S,4R,12S,21R,22S)-11,11,14,15,16,27,28,29,32,33,34-undecahydroxy-6,9,10,19,24,37-hexaoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,13,15,17,25,27,29,31,33,35-decaen-3-yl] 3,4,5-trihydroxybenzoate 162928938 Click to see 952.60 unknown https://doi.org/10.1016/S0040-4039(00)93091-0
[(1R,4S,6R,7R,8R,17S,18R,20S,21S)-4,6,7,11,12,21-hexahydroxy-18-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.17,10.04,8.09,14]docosa-9,11,13-trien-20-yl] 3,4,5-trihydroxybenzoate 100984958 Click to see C1C(C2(C3C1(C(=O)OC4C(C(C(OC4OC(=O)C5=CC(=C(C(=C5)O)O)O)CO)OC(=O)C6=CC(=C(C(=C36)O2)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1248/CPB.47.1148
[(1S,19R,21S,22R,23S)-6,7,8,11,12,13,22,23-octahydroxy-3,16-dioxo-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-21-yl] 3,4,5-trihydroxybenzoate 154496377 Click to see 634.50 unknown https://doi.org/10.1248/CPB.34.941
[(1S,4S,6R,7R,8R,17R,18S,20R,21S)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.17,10.04,8.09,14]docosa-9,11,13-trien-18-yl] 3,4,5-trihydroxybenzoate 10793988 Click to see 624.50 unknown https://doi.org/10.1248/CPB.47.1148
[(1S,7R,9R,18R,19S,21R,22S)-7,8,8,12,13,22-hexahydroxy-21-(hydroxymethyl)-3,6,16-trioxo-2,17,20,23-tetraoxapentacyclo[16.3.1.17,11.04,9.010,15]tricosa-4,10,12,14-tetraen-19-yl] 3,4,5-trihydroxybenzoate 44567215 Click to see 650.50 unknown https://doi.org/10.1248/CPB.30.1113
[(1S,8R,9R,18R,19S,21R,22S)-7,7,8,12,13,22-hexahydroxy-21-(hydroxymethyl)-3,6,16-trioxo-2,17,20,23-tetraoxapentacyclo[16.3.1.18,11.04,9.010,15]tricosa-4,10,12,14-tetraen-19-yl] 3,4,5-trihydroxybenzoate 101921699 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C4=CC(=O)C(C5(C4C6=C(O5)C(=C(C=C6C(=O)O3)O)O)O)(O)O)O 650.50 unknown https://doi.org/10.1039/P19890002289
[(7R,8S,17R,19R,26R,28S,29R,38R)-1,13,14,18,18,19,34,35,39,39-decahydroxy-2,5,10,20,23,31-hexaoxo-6,9,24,27,30,40,41-heptaoxanonacyclo[34.3.1.115,19.04,38.07,26.08,29.011,16.017,22.032,37]hentetraconta-3,11,13,15,21,32,34,36-octaen-28-yl] 3,4,5-trihydroxybenzoate 163186482 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C9=C8C2C(=CC(=O)C(C2(O)O)(O9)O)C(=O)O1)O)O 968.60 unknown https://doi.org/10.1248/CPB.30.1113
[4,6,7,11,12,21-Hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.17,10.04,8.09,14]docosa-9,11,13-trien-18-yl] 3,4,5-trihydroxybenzoate 85270299 Click to see 624.50 unknown https://doi.org/10.1248/CPB.47.1148
[7,8,8,12,13,22-Hexahydroxy-21-(hydroxymethyl)-3,6,16-trioxo-2,17,20,23-tetraoxapentacyclo[16.3.1.17,11.04,9.010,15]tricosa-4,10,12,14-tetraen-19-yl] 3,4,5-trihydroxybenzoate 14429416 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C4=CC(=O)C5(C(C4C6=C(O5)C(=C(C=C6C(=O)O3)O)O)(O)O)O)O 650.50 unknown https://doi.org/10.1248/CPB.30.1113
1,13,14,18,18,19,28,34,35,39,39-Undecahydroxy-6,9,24,27,30,40,41-heptaoxanonacyclo[34.3.1.115,19.04,38.07,26.08,29.011,16.017,22.032,37]hentetraconta-3,11,13,15,21,32,34,36-octaene-2,5,10,20,23,31-hexone 14524169 Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C5=C4C6C(=CC(=O)C(C6(O)O)(O5)O)C(=O)O3)O)O)OC(=O)C7=CC(=C(C8=C7C9C(=CC(=O)C(C9(O)O)(O8)O)C(=O)O1)O)O 816.50 unknown https://doi.org/10.1039/P19890002289
2-[6-[[(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl]oxycarbonyl]-2,3,4-trihydroxyphenyl]-3,4,5-trihydroxybenzoic acid 23258819 Click to see 954.70 unknown https://doi.org/10.1248/CPB.34.4075
2-[6-[[6,7,8,11,12,13,22-Heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl]oxycarbonyl]-2,3,4-trihydroxyphenyl]-3,4,5-trihydroxybenzoic acid 74036866 Click to see 954.70 unknown https://doi.org/10.1248/CPB.34.4075
29-(Carboxymethyl)-13,14,15,18,19,20,29,34,35-nonahydroxy-2,10,23,28-tetraoxo-5-(3,4,5-trihydroxybenzoyl)oxy-3,6,9,24,27,32-hexaoxaheptacyclo[28.6.1.04,25.07,26.011,16.017,22.033,37]heptatriaconta-1(36),11,13,15,17,19,21,33(37),34-nonaene-31-carboxylic acid 152771939 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C(C(O6)C(=O)O)C(C(=O)O3)(CC(=O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 970.70 unknown https://doi.org/10.1248/CPB.47.1148
9,10,11,27,28,29,32,33,34-Nonahydroxy-6,16,19,24,37-pentaoxo-3-(3,4,5-trihydroxybenzoyl)oxy-2,5,15,20,23,38-hexaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,17,25,27,29,31,33,35-decaene-14-carboxylic acid 73109649 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6C(OC(=O)C=C6C(=O)O3)C(=O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 952.60 unknown https://doi.org/10.1248/CPB.47.1148
beta-D-Glucopyranose, cyclic 2-7:4-5-(3,6-dihydro-2,9,10,11,11-pentahydroxy-3-oxo-2,6-methano-2H-1-benzoxocin-5,7-dicarboxylate) 1-(3,4,5-trihydroxybenzoate), (2(2S))- 3086135 Click to see 650.50 unknown https://doi.org/10.1039/P19890002289
CID 338147 338147 Click to see 952.60 unknown https://doi.org/10.1016/0031-9422(91)85260-7
https://doi.org/10.1248/CPB.32.1866
https://doi.org/10.1248/CPB.47.1148
https://doi.org/10.1021/NP50040A016
https://doi.org/10.1248/CPB.34.720
https://doi.org/10.1021/NP50086A002
https://doi.org/10.1016/S0031-9422(00)83018-6
https://doi.org/10.1039/P19890002289
Corilagin 73568 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1248/CPB.47.1148
https://doi.org/10.1248/CPB.32.1866
https://doi.org/10.1016/0031-9422(91)85260-7
https://doi.org/10.1248/CPB.34.941
https://doi.org/10.1021/NP50040A016
Ellagic Acid 5281855 Click to see 302.19 unknown https://doi.org/10.1016/0031-9422(91)85260-7
https://doi.org/10.1248/CPB.32.1866
https://doi.org/10.1248/CPB.34.941
Geraniin 3001497 Click to see 952.60 unknown via CMAUP database
Phyllanthusiin C 514181 Click to see C1C(C2(C3C1(C(=O)OC4C5COC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)OC4C(C(O5)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C39)O2)O)O)O)O)O)O)O)O)O)O)O 926.60 unknown https://doi.org/10.1248/CPB.47.1148
Xcxwmhrrisfuff-xngpzlstsa- 21636130 Click to see 1110.80 unknown https://doi.org/10.1248/CPB.34.4075

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