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Acalypha indica

Acalypha indica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Acalypha indica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644039ca20e58197741226
Scientific name Acalypha indica
Authority L.
First published in Sp. Pl. : 1003 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Acalypha somalensis Pax Bot. Jahrb. Syst. 19: 100 (1894)
Acalypha somalium Müll.Arg. Bremen Abh. 7: 27 (1880)
Acalypha spicata Forssk. Fl. Aegypt.-Arab. : 161 (1775)
Ricinocarpus deciduus Kuntze Revis. Gen. Pl. 2: 617 (1891)
Ricinocarpus indicus Kuntze Revis. Gen. Pl. 2: 618 (1891)
Acalypha canescens Wall. Numer. List [Wallich] n. 7785. 1847
Acalypha caroliniana Blanco Fl. Filip. : 748 (1837)
Cupamenis indica Raf. Sylva Tellur. : 67 (1838)
Acalypha chinensis Benth. Fl. Hongk. 303. 1861 (1861)
Acalypha ciliata Wall. Numer. List [Wallich] n. 7779 J. 1847
Acalypha cupamenii Dragend. Heilpfl. 380. 1898 (1898)
Acalypha decidua Forssk. Fl. Aegypt.-Arab. : 161 (1775)
Acalypha fimbriata Baill. Recueil Observ. Bot. 1: 272 (1861)
Acalypha indica var. bailloniana (Müll.Arg.) Hutch. Fl. Trop. Afr. 6(1): 904. 1912

Common names Top

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Language Common/alternative name
Spanish ricinocarpus baillonianus
Arabic برطم
Arabic حرامي الذبل
Arabic أكاليفة
Arabic عطارد ثلاثي
Bengali মুক্তাঝুরি
dv ވަށްފުފުޅި
Persian آکالیفا هندی
Hindi खोकली
Indonesian akar kucing
Indonesian anting-anting
Indonesian kucing-kucingan
Indonesian kucing galak
jv kucing galak (tetuwuhan)
Kannada ಕುಪ್ಪಿಗಿಡ
mad Ḍâng-ḍângset
mad tompong parot
mad pa'-cepplo'
Malayalam കുപ്പമേനി
Malay pokok kucing galak
Burmese ကြောင်ရိုသေပင်
Oriya ଇନ୍ଦ୍ରମାରିସ
Russian Акалифа индийская
Sinhala කුප්පමේනිය
Tamil குப்பை மேனி
Tamil குப்பி
Tamil அரிமஞ்சரி
Tamil குப்பைமேனி
Tamil மார்ஜலமோகினி
Tamil பூனைவணங்கி
Telugu మురిపిండి
Telugu కుప్పింటాకు
Telugu పిప్పింటాకు
Telugu హరిత మంజరి
Telugu హరితమంజరి
Thai กัญชาแมว
Vietnamese tai tượng Ấn
Chinese 印度鐵莧
Chinese 熱帶鐵莧菜
Chinese 印度铁苋
Chinese 热带铁苋菜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
      • Djibouti
      • Eritrea
      • Ethiopia
      • Socotra
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Zaïre
    • Western Indian Ocean
      • Chagos Archipelago
      • Comoros
      • Madagascar
      • Mauritius
      • Réunion
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Oman
      • Saudi Arabia
    • China
      • Hainan
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Laccadive Islands
      • Maldives
      • Nepal
      • Pakistan
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Nicobar Nicobar
      • South China Sea
      • Thailand
      • Vietnam
    • Malesia
      • Christmas Island
      • Cocos (keeling) Islands
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • Southwestern Pacific
      • Samoa
  • Southern America
    • Caribbean
      • Cuba
      • Leeward Islands
      • Puerto Rico
      • Windward Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000953231
UNII Y34S6V2PSH
USDA Plants ACIN12
Tropicos 12800113
INPN 629004
Flora of Italy 10347
KEW urn:lsid:ipni.org:names:337497-1
The Plant List kew-713
Plantarium 31
Open Tree Of Life 3910628
Observations.org 129122
NCBI Taxonomy 478095
Nature Serve 2.138052
IPNI 337497-1
iNaturalist 157894
GBIF 3056259
Freebase /m/080njgk
EPPO ACCIN
EOL 1145503
USDA GRIN 400002
Wikipedia Acalypha_indica

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
Ceria nanoparticles: biomedical applications and toxicity N/A J Zhejiang Univ Sci B 10-May-2024
PMCID:PMC11087188
doi:10.1631/jzus.B2300854
PMID:38725338
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
Larvicidal, Ovicidal, and Repellent Activities of Leucas stachydiformis (Hochst. ex Benth.) Briq Essential Oil against Anopheles arabiensis Fikru S, Tolossa K, Lindemann P, Bucar F, Asres K J Trop Med 29-Mar-2024
PMCID:PMC10997417
doi:10.1155/2024/1051086
PMID:38586242
Biosynthesis and assessment of antibacterial and antioxidant activities of silver nanoparticles utilizing Cassia occidentalis L. seed Arya A, Tyagi PK, Bhatnagar S, Bachheti RK, Bachheti A, Ghorbanpour M Sci Rep 27-Mar-2024
PMCID:PMC10973378
doi:10.1038/s41598-024-57823-3
PMID:38538702
Acalypha indica induced acute oxidative haemolysis and methaemoglobinaemia: two case reports Maddumabandara K, Rajaratnam A, Ishfak M, Samarakoon N, Ellepola K, Bowattage S J Med Case Rep 19-Mar-2024
PMCID:PMC10949590
doi:10.1186/s13256-024-04481-8
PMID:38500232
New Alien Plant Taxa for Italy and Europe: An Update Musarella CM, Laface VL, Angiolini C, Bacchetta G, Bajona E, Banfi E, Barone G, Biscotti N, Bonsanto D, Calvia G, Cambria S, Capuano A, Caruso G, Crisafulli A, Del Guacchio E, Di Gristina E, Domina G, Fanfarillo E, Fascetti S, Fiaschi T, Galasso G, Mascia F, Mazzacuva G, Mei G, Minissale P, Motti R, Perrino EV, Picone RM, Pinzani L, Podda L, Potenza G, Rosati L, Stinca A, Tavilla G, Villano C, Wagensommer RP, Spampinato G Plants (Basel) 24-Feb-2024
PMCID:PMC10934091
doi:10.3390/plants13050620
PMID:38475466
Metal Nanoparticles: Advanced and Promising Technology in Diabetic Wound Therapy Zheng Q, Chen C, Liu Y, Gao J, Li L, Yin C, Yuan X Int J Nanomedicine 26-Jan-2024
PMCID:PMC10826594
doi:10.2147/IJN.S434693
PMID:38293611
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Green and cost-effective biofabrication of copper oxide nanoparticles: Exploring antimicrobial and anticancer applications Gebreslassie YT, Gebremeskel FG Biotechnol Rep (Amst) 12-Jan-2024
PMCID:PMC10835232
doi:10.1016/j.btre.2024.e00828
PMID:38312482
Macrofungal Mediated Biosynthesis of Silver Nanoparticles and Evaluation of Its Antibacterial and Wound-Healing Efficacy Vijayakumar G, Kim HJ, Jo JW, Rangarajulu SK Int J Mol Sci 10-Jan-2024
PMCID:PMC10815654
doi:10.3390/ijms25020861
PMID:38255936
Plant-mediated synthesis of silver nanoparticles: unlocking their pharmacological potential–a comprehensive review Dhir R, Chauhan S, Subham P, Kumar S, Sharma P, Shidiki A, Kumar G Front Bioeng Biotechnol 09-Jan-2024
PMCID:PMC10803431
doi:10.3389/fbioe.2023.1324805
PMID:38264582
Spotlight on therapeutic efficiency of green synthesis metals and their oxide nanoparticles in periodontitis Kiarashi M, Mahamed P, Ghotbi N, Tadayonfard A, Nasiri K, Kazemi P, Badkoobeh A, Yasamineh S, Joudaki A J Nanobiotechnology 05-Jan-2024
PMCID:PMC10770920
doi:10.1186/s12951-023-02284-5
PMID:38183090
Integrated Network Pharmacology Approach to Evaluate Bioactive Phytochemicals of Acalypha indica and Their Mechanistic Actions to Suppress Target Genes of Tuberculosis Harakeh S, Niyazi HA, Niyazi HA, Abdalal SA, Mokhtar JA, Almuhayawi MS, Alkuwaity KK, Abujamel TS, Slama P, Haque S ACS Omega 29-Dec-2023
PMCID:PMC10795024
doi:10.1021/acsomega.3c05589
PMID:38250414
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
Phytochemicals as Immunomodulatory Molecules in Cancer Therapeutics Paudel S, Mishra N, Agarwal R Pharmaceuticals (Basel) 26-Nov-2023
PMCID:PMC10746110
doi:10.3390/ph16121652
PMID:38139779

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2R,3R)-2-hydroxy-4-methoxy-1-methyl-6-oxo-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2H-pyridine-3-carbonitrile 102286666 Click to see CN1C(C(C(=CC1=O)OC)(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 360.32 unknown https://doi.org/10.1016/0031-9422(82)80022-8
https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
(2S,3R)-2-hydroxy-4-methoxy-6-oxo-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2-dihydropyridine-3-carbonitrile 102286667 Click to see COC1=CC(=O)NC(C1(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 346.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
(Z)-4-cyano-3-methoxy-N-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-3-enamide 102286670 Click to see CNC(=O)CC(=C(C#N)OC1C(C(C(C(O1)CO)O)O)O)OC 332.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
2-hydroxy-4-methoxy-1-methyl-6-oxo-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2H-pyridine-3-carbonitrile 435918 Click to see CN1C(C(C(=CC1=O)OC)(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 360.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
https://doi.org/10.1016/0031-9422(82)80022-8
4-cyano-3-methoxy-N-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-3-enamide 163028032 Click to see CNC(=O)CC(=C(C#N)OC1C(C(C(C(O1)CO)O)O)O)OC 332.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R)-2-hydroxy-4-methoxy-1-methyl-6-oxo-3-[(2R,3R,4S,5S,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy-2H-pyridine-3-carbonitrile 163193083 Click to see CN1C(C(C(=CC1=O)OC)(C#N)OC2C(C(C(C(O2)O)O)O)O)O 346.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
(2R,3R)-2-hydroxy-4-methoxy-6-oxo-3-[(2R,3R,4S,5S,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy-1,2-dihydropyridine-3-carbonitrile 162876865 Click to see COC1=CC(=O)NC(C1(C#N)OC2C(C(C(C(O2)O)O)O)O)O 332.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
(2S,3R)-2-hydroxy-4-methoxy-1-methyl-6-oxo-3-[(2R,3R,4S,5S,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy-2H-pyridine-3-carbonitrile 163010766 Click to see CN1C(C(C(=CC1=O)OC)(C#N)OC2C(C(C(C(O2)O)O)O)O)O 346.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
(2S,3R)-2-hydroxy-4-methoxy-1-methyl-6-oxo-3-[(2R,3R,4S,5S,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy-2H-pyridine-3-carboxamide 163102167 Click to see CN1C(C(C(=CC1=O)OC)(C(=O)N)OC2C(C(C(C(O2)O)O)O)O)O 364.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
(2S,3R)-2-hydroxy-4-methoxy-1-methyl-6-oxo-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2H-pyridine-3-carboxamide 102286669 Click to see CN1C(C(C(=CC1=O)OC)(C(=O)N)OC2C(C(C(C(O2)CO)O)O)O)O 378.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
(2S,3R)-2-hydroxy-4-methoxy-6-oxo-3-[(2R,3R,4S,5S,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy-1,2-dihydropyridine-3-carbonitrile 163192864 Click to see COC1=CC(=O)NC(C1(C#N)OC2C(C(C(C(O2)O)O)O)O)O 332.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
2-hydroxy-4-methoxy-1-methyl-6-oxo-3-(3,4,5,6-tetrahydroxyoxan-2-yl)oxy-2H-pyridine-3-carbonitrile 163010765 Click to see CN1C(C(C(=CC1=O)OC)(C#N)OC2C(C(C(C(O2)O)O)O)O)O 346.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
2-hydroxy-4-methoxy-1-methyl-6-oxo-3-(3,4,5,6-tetrahydroxyoxan-2-yl)oxy-2H-pyridine-3-carboxamide 163102166 Click to see CN1C(C(C(=CC1=O)OC)(C(=O)N)OC2C(C(C(C(O2)O)O)O)O)O 364.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
2-Hydroxy-4-methoxy-6-oxo-3-(3,4,5,6-tetrahydroxyoxan-2-yl)oxy-1,2-dihydropyridine-3-carbonitrile 162876864 Click to see COC1=CC(=O)NC(C1(C#N)OC2C(C(C(C(O2)O)O)O)O)O 332.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
4-Methoxy-1-methyl-5-(3,4,5,6-tetrahydroxyoxan-2-yl)oxypyridin-2-one 162865158 Click to see CN1C=C(C(=CC1=O)OC)OC2C(C(C(C(O2)O)O)O)O 303.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
4-methoxy-1-methyl-5-[(2R,3R,4S,5S,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]oxypyridin-2-one 162865159 Click to see CN1C=C(C(=CC1=O)OC)OC2C(C(C(C(O2)O)O)O)O 303.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
> Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes
(1R,3S,5R,6S,7S,8R,10R)-1-acetyl-6,7-dihydroxy-5-(hydroxymethyl)-14-methoxy-11-methyl-2,4,9-trioxa-11-azatricyclo[8.4.0.03,8]tetradec-13-en-12-one 162947184 Click to see CC(=O)C12C(N(C(=O)C=C1OC)C)OC3C(C(C(OC3O2)CO)O)O 359.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
1-Acetyl-6,7-dihydroxy-5-(hydroxymethyl)-14-methoxy-11-methyl-2,4,9-trioxa-11-azatricyclo[8.4.0.03,8]tetradec-13-en-12-one 162947183 Click to see CC(=O)C12C(N(C(=O)C=C1OC)C)OC3C(C(C(OC3O2)CO)O)O 359.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.12.011
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Decursidate 102004630 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(C2=CC=C(C=C2)O)O)O 330.30 unknown https://doi.org/10.1002/JCCS.199700075
> 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 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 https://doi.org/10.1016/J.FITOTE.2006.04.007
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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 https://doi.org/10.1002/JCCS.199700075
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 162927229 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)C)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
3-[(2S,5R,6R)-4,5-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 44391816 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12313332 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
Biorobin 15944778 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
Clitorin 11592917 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
Isoquercetin 5280804 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 https://doi.org/10.1002/JCCS.199700075
Kaempferol 3-(2''-rhamnosylrutinoside) 74978013 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)C)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
Kaempferol 3-O-rhamnosyl-rhamnosyl-glucoside 157009737 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)C)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
https://doi.org/10.1002/JCCS.199700075
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1002/JCCS.199700075
> Phenylpropanoids and polyketides / Tannins
[(1S,4R,6R,7R,8R,17R,18S,20R,21S)-4,6,7,12,13,21-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 162917555 Click to see C1C(C2(C3C1(C(=O)OC4C(OC(C(C4O)OC(=O)C5=C(C(=CC(=C35)O2)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)CO)O)O)O 624.50 unknown https://doi.org/10.1002/JCCS.199700075
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate 4628122 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/10.1002/JCCS.199700075
[4,6,7,12,13,21-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 162917554 Click to see C1C(C2(C3C1(C(=O)OC4C(OC(C(C4O)OC(=O)C5=C(C(=CC(=C35)O2)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)CO)O)O)O 624.50 unknown https://doi.org/10.1002/JCCS.199700075
1,2,3,6-Tetragalloyl-beta-D-glucopyranose 5153644 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)O 788.60 unknown https://doi.org/10.1002/JCCS.199700075
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/J.FITOTE.2006.04.007
https://doi.org/10.1002/JCCS.199700075
NP-003686 73178 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)O 788.60 unknown https://doi.org/10.1002/JCCS.199700075
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3S,4S)-4-[(Z)-1-Carboxy-3-[[(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]oxy]-3-oxoprop-1-en-2-yl]-5,6,7-trihydroxy-1-oxo-3,4-dihydroisochromene-3-carboxylic acid 14483070 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)OC(=O)C(=CC(=O)O)C6C(OC(=O)C7=CC(=C(C(=C67)O)O)O)C(=O)O 970.70 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
(3S)-4-[(Z)-1-carboxy-3-[[(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]oxy]-3-oxoprop-1-en-2-yl]-5,6,7-trihydroxy-1-oxo-3,4-dihydroisochromene-3-carboxylic acid 6325895 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)OC(=O)C(=CC(=O)O)C6C(OC(=O)C7=CC(=C(C(=C67)O)O)O)C(=O)O 970.70 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
(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 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(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 952.60 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
(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 5089683 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/10.1002/JCCS.199700075
[(1R,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 101933032 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/10.1016/J.FITOTE.2006.04.007
[(1S,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 14887888 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/10.1002/JCCS.199700075
[(7S,8R,9R,11S,12R,21R)-1,8,17,18,22,22-hexahydroxy-9-(hydroxymethyl)-2,5,14-trioxo-6,10,13,23-tetraoxapentacyclo[17.3.1.04,21.07,12.015,20]tricosa-3,15,17,19-tetraen-11-yl] 3,4,5-trihydroxybenzoate 163187062 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)O)OC(=O)C4=CC(=O)C5(C(C4C6=C(O5)C(=C(C=C6C(=O)O3)O)O)(O)O)O 650.50 unknown https://doi.org/10.1002/JCCS.199700075
[1,8,17,18,22,22-Hexahydroxy-9-(hydroxymethyl)-2,5,14-trioxo-6,10,13,23-tetraoxapentacyclo[17.3.1.04,21.07,12.015,20]tricosa-3,15,17,19-tetraen-11-yl] 3,4,5-trihydroxybenzoate 162998013 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)O)OC(=O)C4=CC(=O)C5(C(C4C6=C(O5)C(=C(C=C6C(=O)O3)O)O)(O)O)O 650.50 unknown https://doi.org/10.1002/JCCS.199700075
2-[(4R,5S,7R,8R,9S,12S,13S,14S)-8,14,18,19-tetrahydroxy-7-(hydroxymethyl)-2,11,15-trioxo-5-(3,4,5-trihydroxybenzoyl)oxy-3,6,10,16-tetraoxatetracyclo[11.7.1.04,9.017,21]henicosa-1(20),17(21),18-trien-12-yl]acetic acid 163188905 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)O)OC(=O)C(C4C(C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)CC(=O)O 652.50 unknown https://doi.org/10.1002/JCCS.199700075
2-[(4R,5S,7R,8R,9S,12S,13S)-8,17,18-trihydroxy-7-(hydroxymethyl)-2,11,14-trioxo-5-(3,4,5-trihydroxybenzoyl)oxy-3,6,10,15-tetraoxatetracyclo[11.6.1.04,9.016,20]icosa-1(19),16(20),17-trien-12-yl]acetic acid 162999508 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)O)OC(=O)C(C4C5=C(C(=C(C=C5C(=O)O3)O)O)OC4=O)CC(=O)O 622.40 unknown https://doi.org/10.1002/JCCS.199700075
2-[(5R,7R)-13,14,15,18,19,20,31,35,36-nonahydroxy-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 134694193 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(C(=O)O3)CC(=O)O)C(C(=O)O6)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 954.70 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
2-[8,14,18,19-Tetrahydroxy-7-(hydroxymethyl)-2,11,15-trioxo-5-(3,4,5-trihydroxybenzoyl)oxy-3,6,10,16-tetraoxatetracyclo[11.7.1.04,9.017,21]henicosa-1(20),17(21),18-trien-12-yl]acetic acid 162995825 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)O)OC(=O)C(C4C(C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)CC(=O)O 652.50 unknown https://doi.org/10.1002/JCCS.199700075
2-[8,17,18-Trihydroxy-7-(hydroxymethyl)-2,11,14-trioxo-5-(3,4,5-trihydroxybenzoyl)oxy-3,6,10,15-tetraoxatetracyclo[11.6.1.04,9.016,20]icosa-1(19),16(20),17-trien-12-yl]acetic acid 162999507 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)O)OC(=O)C(C4C5=C(C(=C(C=C5C(=O)O3)O)O)OC4=O)CC(=O)O 622.40 unknown https://doi.org/10.1002/JCCS.199700075
CID 250397 250397 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(C(=O)O3)CC(=O)O)C(C(=O)O6)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 954.70 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
CID 338147 338147 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(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 952.60 unknown https://doi.org/10.1016/J.FITOTE.2006.04.007
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/J.FITOTE.2006.04.007
https://doi.org/10.1002/JCCS.199700075
repandusinic acid A 147900 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)OC(=O)C(=CC(=O)O)C6C(OC(=O)C7=CC(=C(C(=C67)O)O)O)C(=O)O 970.70 unknown https://doi.org/10.1002/JCCS.199700075
Wutxioakrfkqhk-bwpkhyersa- 21672436 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)OC(=O)C(=CC(=O)O)C6C(OC(=O)C7=CC(=C(C(=C67)O)O)O)C(=O)O 970.70 unknown https://doi.org/10.1002/JCCS.199700075

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