Details Top

Internal ID UUID643fe7460cce9839300864
Scientific name Phyllanthus amarus
Authority Schumach. & Thonn.
First published in Beskr. Guin. Pl. : 421 (1827)

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 Mapuche of southern Chile, Bennett et al., 2021 record the use of Phyllanthus amarus as a bitter leaf infusion for fevers, with whole-plant decoctions taken for urinary complaints. Across the Indian subcontinent, Naidu and Shukla, 2004 report whole-plant decoctions and infusions as a hepato‑protective “stonebreaker,” traditionally employed for jaundice and gallstone pains; Singh, 1989 lists identical preparations for jaundice and as a febrifuge. In Bangladesh and West Africa, Hossan et al., 2015 and Ahmad et al., 2008 describe infusions or decoctions of the aerial parts for fever, dysentery, and liver ailments; in the Caribbean and northern South America, Etnobiología and Caribbean ethnobotanical surveys note poultices of crushed leaves for skin irritations and ulcers. In Chinese ethnomedicine the whole herb (que bei mu) is prepared as a “Yejuhua tea” to clear liver heat and dampness, documented by Yang, 2012.

One practical recipe for a mild leaf infusion is to place 2–3 g of dried aerial parts in 200 mL freshly boiled water, cover, and steep 10–15 minutes; strain and drink 1–2 cups daily for short‑term fever relief. For a standard 1:5 ethanolic tincture of the dried herb, macerate 20 g material in 100 mL 45–50% ethanol for 2–3 weeks with daily agitation, strain, and store in amber glass; typical adult dose is 2–4 mL up to three times daily. Avoid during pregnancy and lactation; discontinue if digestive upset, dizziness, or rash occur, and consult a clinician if you take anticoagulants or prescription medications, as herb–drug interactions are possible.

Key constituents documented for Phyllanthus amarus include gallic acid, ellagic acid, phyllanthin, hypophyllanthin, corilagin, rutin, and quercetin. These phenolics and lignans align with the plant’s longstanding use as a hepato‑protective febrifuge.

Modern relevance: contemporary research continues to investigate hepatoprotective and anti‑inflammatory activity, and standardized extracts are widely available as dietary supplements, while traditional infusions and decoctions remain in active use across tropical communities.

General Uses Top

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Common products:
No commercial products from Phyllanthus amarus are widely reported in accessible technical or commercial literature. Absence of entries in standard commodity or trade databases indicates a lack of established trade goods.

Industrial and craft applications:
No documented industrial or craft applications are recorded.

Food and beverages (non-medicinal):
No established food or beverage products, food additives, or processing uses are documented in primary references.

Colorants and tanning:
No documented uses as a dye or tannin source are reported.

Wood and fiber:
No timber, bast fiber, or other fiber uses are documented.

Fragrance and cosmetics:
No fragrance, essential oil, or cosmetic ingredient uses are documented.

Properties relevant to use:
No standardized physical or chemical properties relevant to commercial use are reported.

Standards and regulation:
No specific standards or regulatory frameworks are associated with Phyllanthus amarus as a commodity ingredient.

Sustainability and sourcing:
No sustainable sourcing, cultivation, or trade information is documented for commercial use.

Synonyms Top

Scientific name Authority First published in
Phyllanthus amarus var. baronianus Leandri Notul. Syst. (Paris) 7: 183. 1939
Phyllanthus nanus Hook.f. Fl. Brit. India 5: 298 (1887)
Phyllanthus niruri var. amarus (Schumach. & Thonn.) Leandri Fl. Madagasc. 111: 73. 1958
Phyllanthus niruri var. scabrellus (Webb) Müll.Arg. Linnaea 32: 43 (1863)
Phyllanthus scabrellus Webb Niger Fl. : 175 (1849)
Phyllanthus swartzii Kostel. Allg. Med.-Pharm. Fl. 5: 1771 (1836)
Diasperus nanus (Hook.f.) Kuntze Revis. Gen. Pl. 2: 601 (1891)
Phyllanthus niruri var. genuinus Müll.Arg. Prodr. 15(2): 406 (1866)
Phyllanthus amarus subsp. sanyaensis P.T.Li & Y.T.Zhu J. S. China Agric. Univ. 17(3): 118 (1996).
Phyllanthus niruroides var. madagascariensis Leandri Notul. Syst. (Paris) 7: 184. 1939
Phyllanthus niruri var. baronianus (Leandri) Leandri Fl. Madagasc. 111: 74 1958

Common names Top

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Language Common/alternative name
English carry me seed
tcy ನೆಲನೆಲ್ಲಿ
Vietnamese chó đẻ thân xanh
Chinese 小返魂
Chinese 月下珠
Chinese 珠子草
Chinese 霸贝菜
Chinese 苦味叶下珠
Chinese 苦味叶下珠‘(珠子f)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Mozambique
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mauritania
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre
    • Western Indian Ocean
      • Aldabra
      • Chagos Archipelago
      • Comoros
      • Madagascar
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Oman
      • Saudi Arabia
      • Yemen
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Maldives
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • South China Sea
      • Thailand
    • Malesia
      • Borneo
      • Christmas Island
      • Cocos (keeling) Islands
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
    • Papuasia
      • New Guinea
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • Western Australia
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Alabama
      • Florida
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
      • Marshall Islands
      • Wake Island
    • South-central Pacific
      • Cook Islands
      • Line Islands
      • Marquesas
      • Society Islands
      • Tuamotu
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji
      • Gilbert Islands
      • Howland-baker Islands
      • Nauru
      • New Caledonia
      • Niue
      • Phoenix Islands
      • Samoa
      • Tokelau-manihiki
      • Tonga
      • Tuvalu
      • Vanuatu
      • Wallis-Futuna Islands
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Aruba
      • Bahamas
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Turks-caicos Islands
      • Windward Islands
    • Central America
      • Belize
      • Central American Pacific
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Chile North
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000270441
UNII 5578I1KA35
Florida Plant Atlas 1430
Flora of Alabama 5386
USDA Plants PHAM5
Tropicos 12800250
INPN 445642
KEW urn:lsid:ipni.org:names:326408-2
The Plant List kew-153315
Open Tree Of Life 1039186
Observations.org 198824
NCBI Taxonomy 293060
Nature Serve 2.132169
IPNI 326408-2
iNaturalist 166747
GBIF 5382589
EPPO PYLAM
EOL 1153243
Elurikkus 531938
USDA GRIN 401814
Wikipedia Phyllanthus_amarus
PaleoBotany 69637

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
Knowledge and practices of traditional management of child malnutrition and associated pathologies in Benin Vissoh AC, Klotoé JR, Fah L, Agbodjento E, Koudokpon H, Togbe E, Saïdou S, Dougnon V J Ethnobiol Ethnomed 02-May-2024
PMCID:PMC11064319
doi:10.1186/s13002-024-00684-x
PMID:38693543
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Alpha-Glucosidase Inhibition, Antioxidant Activities, and Molecular Docking Study of Krom Luang Chumphon Khet Udomsak, a Thai Traditional Remedy Limcharoen T, Chaniad P, Chonsut P, Punsawad C, Juckmeta T, Konyanee A, Rais IR, Sangkaew S Adv Pharmacol Pharm Sci 30-Apr-2024
PMCID:PMC11074829
doi:10.1155/2024/1322310
PMID:38716223
Mitigating digestive disorders: Action mechanisms of Mediterranean herbal active compounds Kmail A Open Life Sci 18-Apr-2024
PMCID:PMC11032100
doi:10.1515/biol-2022-0857
Overview of Research on Leishmaniasis in Africa: Current Status, Diagnosis, Therapeutics, and Recent Advances Using By-Products of the Sargassaceae Family Abdoul-Latif FM, Oumaskour K, Abdallah N, Ainane A, Houmed Aboubaker I, Merito A, Mohamed H, Ainane T Pharmaceuticals (Basel) 18-Apr-2024
PMCID:PMC11054980
doi:10.3390/ph17040523
PMID:38675483
Unraveling potential neuroprotective mechanisms of herbal medicine for Alzheimer’s diseases through comprehensive molecular docking analyses Alsenani F Saudi J Biol Sci 15-Apr-2024
PMCID:PMC11053229
doi:10.1016/j.sjbs.2024.103998
PMID:38681227
Exploring the antioxidant potential of endophytic fungi: a review on methods for extraction and quantification of total antioxidant capacity (TAC) Asomadu RO, Ezeorba TP, Ezike TC, Uzoechina JO 3 Biotech 05-Apr-2024
PMCID:PMC10997672
doi:10.1007/s13205-024-03970-3
PMID:38585410
Harmony in Motion: Unraveling the Nexus of Sports, Plant-Based Nutrition, and Antioxidants for Peak Performance Ayaz A, Zaman W, Radák Z, Gu Y Antioxidants (Basel) 04-Apr-2024
PMCID:PMC11047508
doi:10.3390/antiox13040437
PMID:38671884
Mitigation Potential of Herbal Extracts and Constituent Bioactive Compounds on Salmonella in Meat-Type Poultry Orimaye OE, Ekunseitan DA, Omaliko PC, Fasina YO Animals (Basel) 03-Apr-2024
PMCID:PMC11011123
doi:10.3390/ani14071087
PMID:38612326
Storage and time course effects on the quality of oil extracted from Phyllanthus amarus Schumach and Annona muricata Linn and their antidiabetic potentials Ogunjinmi OE, Oriyomi VO, Olaogun RA, Gbadegesin AT BioTechnologia (Pozn) 29-Mar-2024
PMCID:PMC11020154
doi:10.5114/bta.2024.135641
PMID:38633891
Acute and Subchronic Toxicological Study of the Cocktail Extract from Curcuma xanthorrhiza Roxb, Phyllanthus niruri L. and Morinda citrifolia L. Rosidah I, Renggani TN, Firdausi N, Ningsih S, Yunianto P, Permatasari D, Pongtuluran OB, Bahua H, Efendi J, Kusumastuti SA, Nuralih, El Muttaqien S, Nizar, Kusumaningrum S, Agustini K J Toxicol 27-Mar-2024
PMCID:PMC10990647
doi:10.1155/2024/9445226
PMID:38571743
Impact of Heavy Metal Pollution in the Environment on the Metabolic Profile of Medicinal Plants and Their Therapeutic Potential Asiminicesei DM, Fertu DI, Gavrilescu M Plants (Basel) 21-Mar-2024
PMCID:PMC10976221
doi:10.3390/plants13060913
PMID:38592933
Suppression of P2X4 and P2X7 by Lactobacillus rhamnosus vitaP1: effects on hangover symptoms Kwon JE, Hong W, Jeon H, Kim CS, Kim H, Kang SC AMB Express 15-Mar-2024
PMCID:PMC10942966
doi:10.1186/s13568-024-01685-5
PMID:38491208
A metagenomic investigation of phytoplasma diversity in Australian vegetable growing regions Rodrigues Jardim B, Gambley C, Tran-Nguyen LT, Webster C, Kehoe M, Kinoti WM, Bond S, Davis R, Jones L, Pathania N, Sharman M, Chapman T, Rodoni BC, Constable FE Microb Genom 06-Mar-2024
PMCID:PMC10999746
doi:10.1099/mgen.0.001213
PMID:38446015
Biogenic synthesis of levofloxacin-loaded copper oxide nanoparticles using Cymbopogon citratus: A green approach for effective antibacterial applications Jabeen A, Khan A, Ahmad P, Khalid A, Ibrahim Wizrah MS, Anjum Z, Alotibi S, Aloufi BH, Alanazi AM, Jefri OA, Ismail MA Heliyon 28-Feb-2024
PMCID:PMC10945134
doi:10.1016/j.heliyon.2024.e27018
PMID:38501012

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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Laurenquinone B 24750385 Click to see 394.40 unknown https://doi.org/10.1016/0031-9422(94)00836-I
> 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/10.1016/0031-9422(93)85545-3
> Lignans, neolignans and related compounds / Aryltetralin lignans
(-)-Nirtetralin 13989913 Click to see COCC1CC2=CC3=C(C(=C2C(C1COC)C4=CC(=C(C=C4)OC)OC)OC)OCO3 430.50 unknown https://doi.org/10.1055/S-2005-871258
(+/-)-Hypophyllanthin 71749431 Click to see 430.50 unknown https://doi.org/10.1055/S-2005-871258
https://doi.org/10.1021/NP50092A008
https://doi.org/10.1002/PCA.2800040507
(1S,2R,3S)-1-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2,3-bis(methoxymethyl)-1,2,3,4-tetrahydronaphthalene 162910470 Click to see 416.50 unknown https://doi.org/10.1055/S-2005-871258
(5R,6S,7R)-5-(3,4-dimethoxyphenyl)-4-methoxy-6,7-bis(methoxymethyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole 51534489 Click to see 430.50 unknown https://doi.org/10.1055/S-2005-871258
1-(3,4-Dimethoxyphenyl)-6,7-dimethoxy-2,3-bis(methoxymethyl)-1,2,3,4-tetrahydronaphthalene 13318863 Click to see 416.50 unknown https://doi.org/10.1055/S-2005-871258
9-(3,4-Dimethoxyphenyl)-4-methoxy-7,8-bis(methoxymethyl)-6,7,8,9-tetrahydrobenzo[g][1,3]benzodioxole 3425009 Click to see 430.50 unknown https://doi.org/10.1055/S-2005-871258
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
4-[3-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-2-(methoxymethyl)butyl]-1,2-dimethoxybenzene 101522 Click to see 418.50 unknown https://doi.org/10.1055/S-2005-871258
6-(3-((3,4-Dimethoxyphenyl)methyl)-4-methoxy-2-(methoxymethyl)butyl)-4-methoxy-1,3-benzodioxole 13989914 Click to see 432.50 unknown https://doi.org/10.1055/S-2005-871258
6-[(2R,3R)-3-[(3,4-dimethoxyphenyl)methyl]-4-methoxy-2-(methoxymethyl)butyl]-4-methoxy-1,3-benzodioxole 13989915 Click to see COCC(CC1=CC(=C(C=C1)OC)OC)C(CC2=CC3=C(C(=C2)OC)OCO3)COC 432.50 unknown https://doi.org/10.1055/S-2005-871258
Phyllanthin 358901 Click to see COCC(CC1=CC(=C(C=C1)OC)OC)C(CC2=CC(=C(C=C2)OC)OC)COC 418.50 unknown https://doi.org/10.1002/PCA.2800040507
https://doi.org/10.1021/NP50092A008
https://doi.org/10.1055/S-2005-871258
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
4-O-Galloylquinic acid 475263 Click to see 344.27 unknown https://doi.org/10.1016/0031-9422(94)00836-I
> Organoheterocyclic compounds / Azaspirodecane derivatives
(1S,2S,7R,14R)-14-hydroxy-12-oxa-6-azatetracyclo[5.5.2.01,9.02,6]tetradec-9-en-11-one 162851224 Click to see 221.25 unknown https://doi.org/10.1016/0031-9422(96)00345-7
Epibubbialine 11830997 Click to see 221.25 unknown https://doi.org/10.1016/0031-9422(96)00345-7
Isobubbialine 102003051 Click to see 221.25 unknown https://doi.org/10.1016/0031-9422(96)00345-7
> Organoheterocyclic compounds / Indolizidines
(8S)-4-methoxy-14-oxa-7-azatetracyclo[6.6.1.01,11.02,7]pentadeca-9,11-dien-13-one 122236592 Click to see COC1CCN2C(C1)C34CC2C=CC3=CC(=O)O4 247.29 unknown https://doi.org/10.1016/0031-9422(96)00345-7
2-Allosecurinine 267769 Click to see 217.26 unknown https://doi.org/10.1016/0031-9422(96)00345-7
4-Methoxy-14-oxa-7-azatetracyclo[6.6.1.01,11.02,7]pentadeca-9,11-dien-13-one 571784 Click to see 247.29 unknown https://doi.org/10.1016/0031-9422(96)00345-7
CID 10868614 10868614 Click to see COC1CCN2C(C1)C34CC2C=CC3=CC(=O)O4 247.29 unknown https://doi.org/10.1016/0031-9422(96)00345-7
Phyllanthine 193552 Click to see COC1CCN2C(C1)C34CC2C=CC3=CC(=O)O4 247.29 unknown https://doi.org/10.1016/0031-9422(96)00345-7
Securinine 442872 Click to see 217.26 unknown https://doi.org/10.1016/0031-9422(96)00345-7
> Organoheterocyclic compounds / Naphthofurans
4-Ethenyl-6,9-dihydroxy-4-methyl-3-methylidene-3a,9b-dihydrobenzo[g][1]benzofuran-5-one 162969758 Click to see CC1(C2C(C3=C(C=CC(=C3C1=O)O)O)OCC2=C)C=C 272.29 unknown https://doi.org/10.1016/0031-9422(94)00836-I
> 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(92)90071-W
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin 9882981 Click to see 306.27 unknown https://doi.org/10.1016/0031-9422(93)85545-3
Flavan-3,3',4',5,5',7-hexol 1249 Click to see 306.27 unknown https://doi.org/10.1016/0031-9422(93)85545-3
Gallocatechin 65084 Click to see 306.27 unknown https://doi.org/10.1016/0031-9422(93)85545-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/0031-9422(93)85545-3
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/10.1016/0031-9422(93)85545-3
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1016/0031-9422(93)85545-3
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/0031-9422(93)85545-3
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/0031-9422(93)85545-3
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown https://doi.org/10.1016/0031-9422(93)85545-3
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(93)85545-3
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1,13,14,15,18,19,20,34,35,39,39-Undecahydroxy-2,5,10,23,31-pentaoxo-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-28-yl) 3,4,5-trihydroxybenzoate 115063 Click to see 952.60 unknown https://doi.org/10.1016/0031-9422(93)85545-3
(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/10.1016/0031-9422(94)00836-I
(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/10.1016/0031-9422(94)00836-I
(3S,4S)-4-[(Z)-1-carboxy-3-[[(1R,19R,21S,22R,23R)-6-(6-carboxy-2,3,4-trihydroxyphenoxy)-7,8,11,12,13,22-hexahydroxy-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]oxy]-3-oxoprop-1-en-2-yl]-5,6,7-trihydroxy-1-oxo-3,4-dihydroisochromene-3-carboxylic acid 16170982 Click to see 1138.80 unknown https://doi.org/10.1016/0031-9422(94)00836-I
(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/10.1016/S0166-3542(02)00213-9
https://doi.org/10.1016/0031-9422(93)85545-3
[(1'R,3S,3aS,4'R,5'S,6R,6aS,23'R,25'S,26'R,35'R,36'S,37'R)-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 162886694 Click to see 1110.80 unknown https://doi.org/10.1016/0031-9422(94)00836-I
[(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(92)90071-W
[(1R,2S)-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 5320535 Click to see CC(=O)CC1(C(=O)C=C2C3C1(OC4=C3C(=CC(=C4O)O)C(=O)OC5C6C(C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC5OC(=O)C9=CC(=C(C(=C9)O)O)O)OC2=O)O)O 992.70 unknown https://doi.org/10.1016/0031-9422(92)90071-W
[(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/10.1016/0031-9422(94)00836-I
[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 4318491 Click to see 650.50 unknown https://doi.org/10.1016/0031-9422(94)00836-I
12,13,17,18,18,32,33,42,43-Nonahydroxy-5,8,23,26,28,35,40,46,49-nonaoxadecacyclo[23.19.3.114,17.130,34.02,41.03,37.06,24.07,27.010,15.016,21]nonatetraconta-1(44),2(41),10,12,14,20,30,32,34(48),42-decaene-4,9,19,22,29,36,39,45-octone 152771996 Click to see C1C2C3C4=C(C(=C(C=C4C(=O)OCC5C6C(C(C(O5)OC(=O)C7=CC(=C(C(=C7)OC2=O)O)O)OC(=O)C8=CC(=C(C9=C8C2C(=CC(=O)C(C2(O9)O)(O)O)C(=O)O6)O)O)OC3=O)O)O)OC1=O 922.60 unknown https://doi.org/10.1080/10575639308043836
2-[(4R,5S,7R,25S,26R,29R,30R,31S)-13,14,15,18,19,20,29,31,35,36-decahydroxy-2,10,23,28,32-pentaoxo-5-(3,4,5-trihydroxybenzoyl)oxy-3,6,9,24,27,33-hexaoxaheptacyclo[28.7.1.04,25.07,26.011,16.017,22.034,38]octatriaconta-1(37),11,13,15,17,19,21,34(38),35-nonaen-29-yl]acetic acid 163005208 Click to see 970.70 unknown https://doi.org/10.1016/0031-9422(94)00836-I
2-[13,14,15,18,19,20,29,31,35,36-Decahydroxy-2,10,23,28,32-pentaoxo-5-(3,4,5-trihydroxybenzoyl)oxy-3,6,9,24,27,33-hexaoxaheptacyclo[28.7.1.04,25.07,26.011,16.017,22.034,38]octatriaconta-1(37),11,13,15,17,19,21,34(38),35-nonaen-29-yl]acetic acid 163005207 Click to see 970.70 unknown https://doi.org/10.1016/0031-9422(94)00836-I
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/10.1016/0031-9422(94)00836-I
Amariin 73989733 Click to see 968.60 unknown https://doi.org/10.1016/0031-9422(93)85545-3
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/10.1016/0031-9422(94)00836-I
CID 338147 338147 Click to see 952.60 unknown https://doi.org/10.1016/0031-9422(93)85545-3
https://doi.org/10.1016/S0166-3542(02)00213-9
CID 5482103 5482103 Click to see 968.60 unknown https://doi.org/10.1016/0031-9422(93)85545-3
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/10.1016/S0166-3542(02)00213-9
https://doi.org/10.1016/0031-9422(93)85545-3
Corilagin (Standard) 5089683 Click to see 634.50 unknown https://doi.org/10.1016/0031-9422(93)85545-3
Geraniin 3001497 Click to see 952.60 unknown https://doi.org/10.1016/0031-9422(93)85545-3

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