Phyllanthus niruri - Unknown
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Details Top

Internal ID UUID643fe7866cba7552092315
Scientific name Phyllanthus niruri
Authority L.
First published in Sp. Pl. : 981 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Nymphanthus niruri (L.) Lour. Fl. Cochinch. : 545 (1790)
Phyllanthus kirganelia Blanco Fl. Filip., ed. 2 : 480 (1845)
Niruris annua Raf. Sylva Tellur. : 91 (1838)
Phyllanthus lathyroides f. decoratus Standl. & Steyerm. Fieldiana, Bot. 24(6): 152 1949
Diasperus niruri (L.) Kuntze Revis. Gen. Pl. 2: 600 (1891)

Common names Top

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Language Common/alternative name
English stonebreaker
English gale of the wind
English seed-under-leaf
English medicinal herbs
Spanish niruris annua
Spanish quebra pedra
Spanish nymphanthus niruri
Spanish niruris indica
Spanish diasperus rosellus
Spanish diasperus lathyroides
Spanish chanca piedra
Azerbaijani diasperus niruri
bjn hambin hambin buah
Bengali ঔষধি গুল্ম
Bengali ভুঁই আমলা
dtp soronipon
dtp piasau-piasau
Persian فیلانتوس نیروری
Gujarati ભોંઆમલી
Hindi भुंई आमला
ht dèyè do
Indonesian daun susu-susu
Indonesian meniran
Indonesian dukung anak
Kannada ನೆಲನೆಲ್ಲಿ
min sidukuang
min sidukuang anak
Malayalam കിരുട്ടാർ നെല്ലി
Malayalam കീഴാർനെല്ലി
Malayalam കീഴാർ നെല്ലി
Marathi भुईआवळी
Malay pokok dukung anak
Malay dukung anak
Oriya ଭୂଇଁ ଅଅଁଳା
Punjabi ਹਜ਼ਾਰਦਾਣੀ
Portuguese quebra-pedra
Kinyarwanda uruheza
Tamil கீழாநெல்லி
Telugu నేల ఉసిరి
Thai ลูกใต้ใบ
Chinese 珠子草
Chinese 坝贝菜
Chinese 小返魂
Chinese 霸贝菜
Chinese 月下珠
Chinese 蜜柑草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Phyllanthus niruri subsp. lathyroides (Kunth) G.L.Webster Contr. Gray Herb. 176: 52 (1955)
Phyllanthus niruri subsp. niruri Unknown

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • South-central U.S.A.
      • Texas
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Puerto Rico
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000271623
UNII NSN3MQO38G
USDA Plants PHNI2
Tropicos 12800264
INPN 611776
KEW urn:lsid:ipni.org:names:194900-2
The Plant List kew-154454
Open Tree Of Life 399363
NCBI Taxonomy 296034
Nature Serve 2.140609
IPNI 194900-2
iNaturalist 166755
GBIF 5381945
Freebase /m/02qcbl4
EPPO PYLNI
EOL 1152757
USDA GRIN 28124
Wikipedia Phyllanthus_niruri
PaleoBotany 20885

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
The Biological Active Substances of Taraxacum officinale and Arctium lappa from the Siberian Federal District Frolova AS, Fokina AD, Milentyeva IS, Asyakina LK, Proskuryakova LA, Prosekov AY Int J Mol Sci 13-Mar-2024
PMCID:PMC10970438
doi:10.3390/ijms25063263
PMID:38542237
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
Evaluation of packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
Effects of silymarin use on liver enzymes and metabolic factors in metabolic dysfunction-associated steatotic liver disease: a systematic review and meta-analysis Malik A, Malik M, Qureshi S Can Liver J 26-Feb-2024
PMCID:PMC10946183
doi:10.3138/canlivj-2023-0021
PMID:38505782
HIV/AIDS in Indonesia: current treatment landscape, future therapeutic horizons, and herbal approaches Jocelyn, Nasution FM, Nasution NA, Asshiddiqi MH, Kimura NH, Siburian MH, Rusdi ZY, Munthe AR, Chairenza I, Ginting Munthe MC, Sianipar P, Gultom SP, Simamora D, Uswanas IR, Salim E, Khairunnisa K, Syahputra RA Front Public Health 14-Feb-2024
PMCID:PMC10899510
doi:10.3389/fpubh.2024.1298297
PMID:38420030
Plant-Origin Components: New Players to Combat Antibiotic Resistance in Klebsiella pneumoniae Luna-Pineda VM, Rodríguez-Martínez G, Salazar-García M, Romo-Castillo M Int J Mol Sci 10-Feb-2024
PMCID:PMC10888558
doi:10.3390/ijms25042134
PMID:38396811
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Therapeutic approaches for chronic hepatitis C: a concise review Nawaz A, Manzoor A, Ahmed S, Ahmed N, Abbas W, Mir MA, Bilal M, Sheikh A, Ahmad S, Jeelani I, Nakagawa T Front Pharmacol 12-Jan-2024
PMCID:PMC10811011
doi:10.3389/fphar.2023.1334160
PMID:38283838
An update about beneficial effects of medicinal plants in aquaculture: A review Dadras F, Velisek J, Zuskova E Vet Med (Praha) 26-Dec-2023
PMCID:PMC10828785
doi:10.17221/96/2023-VETMED
PMID:38303995
Evaluation of Salicylic Acid and Methyl Jasmonate as Elicitors in Phyllanthus acuminatus Hairy Roots by Non-Targeted Analysis Using High-Resolution Mass Spectrometry Benavides K, Sánchez-Kopper A, Jiménez-Quesada K, Perez R, Garro-Monge G Molecules 22-Dec-2023
PMCID:PMC10780090
doi:10.3390/molecules29010080
PMID:38202663
Organic and Biogenic Nanocarriers as Bio-Friendly Systems for Bioactive Compounds’ Delivery: State-of-the Art and Challenges Petrovic SM, Barbinta-Patrascu ME Materials (Basel) 07-Dec-2023
PMCID:PMC10744464
doi:10.3390/ma16247550
PMID:38138692
Physiological mechanism of action and partial separation of herbicide–active compounds from the Diaporthe sp. extract on Amaranthus tricolor L. Manichart N, Laosinwattana C, Somala N, Teerarak M, Chotsaeng N Sci Rep 31-Oct-2023
PMCID:PMC10618292
doi:10.1038/s41598-023-46201-0
PMID:37907593
Harnessing Nature’s Gifts: Salix nigra and Its Potential for Combating Hepatitis C Virus (HCV) Bibi S, Nisar M, Rafique S, Waqas M, Zahoor M, Idrees M, Nazir N, Ihsan M, Salmen SH, Alharbi SA, Khan A, Al-Harrasi A ACS Omega 30-Oct-2023
PMCID:PMC10653063
doi:10.1021/acsomega.3c06193
PMID:38024752
The Green Synthesis of Silver Nanoparticles from Avena fatua Extract: Antifungal Activity against Fusarium oxysporum f.sp. lycopersici Qureshi AK, Farooq U, Shakeel Q, Ali S, Ashiq S, Shahzad S, Tariq M, Seleiman MF, Jamal A, Saeed MF, Manachini B Pathogens 16-Oct-2023
PMCID:PMC10609796
doi:10.3390/pathogens12101247
PMID:37887762
Hepatoprotective effects of bioactive compounds from traditional herb Tulsi (Ocimum sanctum Linn) against galactosamine-induced hepatotoxicity in rats Kamel FO, Karim S, Bafail DA, Aldawsari HM, Kotta S, Ilyas UK Front Pharmacol 04-Oct-2023
PMCID:PMC10582332
doi:10.3389/fphar.2023.1213052
PMID:37860117

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 / Benzenesulfonamides
N-Butylbenzenesulfonamide 19241 Click to see CCCCNS(=O)(=O)C1=CC=CC=C1 213.30 unknown https://doi.org/10.1515/ZNB-2006-0111
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1515/ZNB-2006-0111
https://doi.org/10.1021/NP50056A033
https://doi.org/10.1248/CPB.37.2531
https://doi.org/10.1021/NP0497245
https://doi.org/10.1016/0031-9422(92)80352-F
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown https://doi.org/10.1080/14786410903335232
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
2,3,5,6-Tetrahydroxybenzyl acetate 86054418 Click to see CC(=O)OCC1=C(C(=CC(=C1O)O)O)O 214.17 unknown https://doi.org/10.1007/S10600-005-0011-4
> Benzenoids / Benzene and substituted derivatives / Biphenols
2,4,5-Trihydroxy-3-(4,6,7-trihydroxy-3-oxo-1,3-dihydroisobenzofuran-5-yl)-benzoic acid methyl ester 129819533 Click to see COC(=O)C1=CC(=C(C(=C1O)C2=C(C3=C(COC3=O)C(=C2O)O)O)O)O 364.26 unknown https://doi.org/10.1007/S10600-005-0011-4
> Lignans, neolignans and related compounds / Aryltetralin lignans
(+-)-Nirtetralin 182644 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-2007-969635
(+/-)-Hypophyllanthin 71749431 Click to see COCC1CC2=CC(=C3C(=C2C(C1COC)C4=CC(=C(C=C4)OC)OC)OCO3)OC 430.50 unknown https://doi.org/10.1055/S-2006-961520
https://doi.org/10.1039/P19820000999
https://doi.org/10.1016/0378-8741(85)90026-1
https://doi.org/10.1021/NP50124A006
(1S,2R,3R)-1-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2,3-bis(methoxymethyl)-1,2,3,4-tetrahydronaphthalene 13318864 Click to see COCC1CC2=CC(=C(C=C2C(C1COC)C3=CC(=C(C=C3)OC)OC)OC)OC 416.50 unknown https://doi.org/10.1055/S-2006-947224
(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 COCC1CC2=CC3=C(C(=C2C(C1COC)C4=CC(=C(C=C4)OC)OC)OC)OCO3 430.50 unknown https://doi.org/10.1021/NP50124A006
https://doi.org/10.1055/S-2006-961520
(5S,6R,7R)-5-(1,3-benzodioxol-5-yl)-6,7-bis(methoxymethyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole 162913797 Click to see COCC1CC2=CC3=C(C=C2C(C1COC)C4=CC5=C(C=C4)OCO5)OCO3 384.40 unknown https://doi.org/10.1021/NP050288B
(7S,8R,9S)-9-(3,4-dimethoxyphenyl)-4-methoxy-7,8-bis(methoxymethyl)-6,7,8,9-tetrahydrobenzo[g][1,3]benzodioxole 163002996 Click to see COCC1CC2=CC(=C3C(=C2C(C1COC)C4=CC(=C(C=C4)OC)OC)OCO3)OC 430.50 unknown https://doi.org/10.1007/BF03171072
1-(3,4-Dimethoxyphenyl)-6,7-dimethoxy-2,3-bis(methoxymethyl)-1,2,3,4-tetrahydronaphthalene 13318863 Click to see COCC1CC2=CC(=C(C=C2C(C1COC)C3=CC(=C(C=C3)OC)OC)OC)OC 416.50 unknown https://doi.org/10.1055/S-2006-947224
5-(1,3-Benzodioxol-5-yl)-6,7-bis(methoxymethyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole 73089421 Click to see COCC1CC2=CC3=C(C=C2C(C1COC)C4=CC5=C(C=C4)OCO5)OCO3 384.40 unknown https://doi.org/10.1021/NP050288B
5-(3,4-Dimethoxyphenyl)-6,7-bis(methoxymethyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole 137796378 Click to see COCC1CC2=CC3=C(C=C2C(C1COC)C4=CC(=C(C=C4)OC)OC)OCO3 400.50 unknown https://doi.org/10.1055/S-2006-961520
5-[(1S,2R,3R)-6,7-dimethoxy-2,3-bis(methoxymethyl)-1,2,3,4-tetrahydronaphthalen-1-yl]-1,3-benzodioxole 21722954 Click to see COCC1CC2=CC(=C(C=C2C(C1COC)C3=CC4=C(C=C3)OCO4)OC)OC 400.50 unknown https://doi.org/10.1055/S-2007-969635
9-(3,4-Dimethoxyphenyl)-4-methoxy-7,8-bis(methoxymethyl)-6,7,8,9-tetrahydrobenzo[g][1,3]benzodioxole 3425009 Click to see COCC1CC2=CC(=C3C(=C2C(C1COC)C4=CC(=C(C=C4)OC)OC)OCO3)OC 430.50 unknown https://doi.org/10.1007/BF03171072
https://doi.org/10.1055/S-2006-947224
https://doi.org/10.1515/ZNB-2006-0111
Hypophyllanthin 182140 Click to see COCC1CC2=CC(=C3C(=C2C(C1COC)C4=CC(=C(C=C4)OC)OC)OCO3)OC 430.50 unknown https://doi.org/10.1055/S-2006-947224
https://doi.org/10.1055/S-2007-969635
https://doi.org/10.1515/ZNB-2006-0111
Lintetralin 11361584 Click to see COCC1CC2=CC(=C(C=C2C(C1COC)C3=CC4=C(C=C3)OCO4)OC)OC 400.50 unknown https://doi.org/10.1055/S-2006-961520
https://doi.org/10.1021/NP50055A004
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
4-[(2R,3R)-3-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-2-(methoxymethyl)butyl]-1,2-dimethoxybenzene 9953821 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/10.1055/S-2006-947224
4-[3-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-2-(methoxymethyl)butyl]-1,2-dimethoxybenzene 101522 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/10.1007/BF03171072
https://doi.org/10.1055/S-2006-947224
5-[(2S,3S)-3-[(3,4-dimethoxyphenyl)methyl]-4-methoxy-2-(methoxymethyl)butyl]-1,2,3-trimethoxybenzene 162975867 Click to see COCC(CC1=CC(=C(C=C1)OC)OC)C(CC2=CC(=C(C(=C2)OC)OC)OC)COC 448.50 unknown https://doi.org/10.1016/S0040-4020(01)81005-X
5-[(2S,3S)-3-[(3,4-dimethoxyphenyl)methyl]-4-methoxy-2-(methoxymethyl)butyl]-3-methoxybenzene-1,2-diol 162875644 Click to see COCC(CC1=CC(=C(C=C1)OC)OC)C(CC2=CC(=C(C(=C2)OC)O)O)COC 420.50 unknown https://doi.org/10.1016/S0040-4020(01)81005-X
5-[3-(1,3-Benzodioxol-5-ylmethyl)-4-methoxy-2-(methoxymethyl)butyl]-1,3-benzodioxole 73200963 Click to see COCC(CC1=CC2=C(C=C1)OCO2)C(CC3=CC4=C(C=C3)OCO4)COC 386.40 unknown https://doi.org/10.1021/NP050288B
5-[3-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-2-(methoxymethyl)butyl]-1,2,3-trimethoxybenzene 162975866 Click to see COCC(CC1=CC(=C(C=C1)OC)OC)C(CC2=CC(=C(C(=C2)OC)OC)OC)COC 448.50 unknown https://doi.org/10.1016/S0040-4020(01)81005-X
5-[3-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-2-(methoxymethyl)butyl]-3-methoxybenzene-1,2-diol 162875643 Click to see COCC(CC1=CC(=C(C=C1)OC)OC)C(CC2=CC(=C(C(=C2)OC)O)O)COC 420.50 unknown https://doi.org/10.1016/S0040-4020(01)81005-X
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-2006-961520
CID 11575632 11575632 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-2007-969635
Cubebin dimethyl ether 15939540 Click to see COCC(CC1=CC2=C(C=C1)OCO2)C(CC3=CC4=C(C=C3)OCO4)COC 386.40 unknown https://doi.org/10.1021/NP050288B
Nirphyllin 5491556 Click to see COCC(CC1=CC2=C(C(=C1)OC)OCO2)C(CC3=CC(=C(C(=C3)OC)O)OC)COC 448.50 unknown https://doi.org/10.1021/NP50061A004
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/10.1055/S-2006-961520
https://doi.org/10.1016/0378-8741(85)90026-1
https://doi.org/10.1021/NP50124A006
https://doi.org/10.1007/BF03171072
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown https://doi.org/10.1055/S-2006-961520
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Triacontanol 68972 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 438.80 unknown https://doi.org/10.1016/0378-8741(85)90026-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Triacontanal 3084375 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC=O 436.80 unknown https://doi.org/10.1016/0378-8741(85)90026-1
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols / Bactoprenols
(2Z,6Z,10Z,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol 13559232 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97901-9
Farnesylfarnesol 54290761 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97901-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(6S,10S)-6,10,14-trimethylpentadecan-2-one 1810797 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown https://doi.org/10.1515/ZNB-2006-0111
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown https://doi.org/10.1515/ZNB-2006-0111
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP0497245
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP0497245
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP0497245
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(2S,3S,5R)-4-(acetoxymethyl)-5-[(2R,3R,4S,5S,6R)-3,5-diacetoxy-6-(acetoxymethyl)-4-hydroxy-tetrahydropyran-2-yl]oxy-3-hydroxy-4-[(E)-3-phenylprop-2-enoyl]oxy-tetrahydrofuran-2-yl]methyl (E)-3-phenylprop-2-enoate 6476125 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(O2)COC(=O)C=CC3=CC=CC=C3)O)(COC(=O)C)OC(=O)C=CC4=CC=CC=C4)OC(=O)C)O)OC(=O)C 770.70 unknown https://doi.org/10.1021/NP9600560
Niruriside 70697928 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC=CC=C3)O)OC(=O)C=CC4=CC=CC=C4)COC(=O)C)OC(=O)C)O)OC(=O)C 770.70 unknown https://doi.org/10.1021/NP9600560
> Organoheterocyclic compounds / Azaspirodecane derivatives
(1S,2R,7R,14S)-14-hydroxy-12-oxa-6-azatetracyclo[5.5.2.01,9.02,6]tetradec-9-en-11-one 135034108 Click to see C1CC2C34CC(C(N2C1)CC3=CC(=O)O4)O 221.25 unknown https://doi.org/10.1016/0031-9422(96)00345-7
14-Hydroxy-12-oxa-6-azatetracyclo[5.5.2.01,9.02,6]tetradec-9-en-11-one 494942 Click to see C1CC2C34CC(C(N2C1)CC3=CC(=O)O4)O 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/10.1055/S-2007-969635
Phyllanthine 193552 Click to see COC1CCN2C(C1)C34CC2C=CC3=CC(=O)O4 247.29 unknown https://doi.org/10.1055/S-2007-969635
> Organoheterocyclic compounds / Pyrrolizidines
(1R,8R,11S,13R)-11-methoxy-2-oxa-9-azatetracyclo[6.5.1.01,5.09,13]tetradeca-4,6-dien-3-one 154496030 Click to see COC1CC2C34CC(N2C1)C=CC3=CC(=O)O4 233.26 unknown https://doi.org/10.1055/S-2007-969635
6,10b-Methano-10bH-furo[2,3-c]pyrrolo[1,2-a]azepin-2(6H)-one, 8,9,10,10a-tetrahydro- 494791 Click to see C1CC2C34CC(N2C1)C=CC3=CC(=O)O4 203.24 unknown https://doi.org/10.1016/0031-9422(96)00345-7
Norsecurinine 11106439 Click to see C1CC2C34CC(N2C1)C=CC3=CC(=O)O4 203.24 unknown https://doi.org/10.1016/0031-9422(96)00345-7
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Phyllnirurin 179963 Click to see CC1C(OC2=C1C=C(C=C2OC)CCCO)C3=CC4=C(C=C3)OCO4 342.40 unknown https://doi.org/10.1021/NP50061A004
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162846471 Click to see CC(=CCC1=C2C(=CC=C1)C(=O)CC(O2)C3=CC=C(C=C3)O)C 308.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.024
(2S)-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 163022156 Click to see CC(=CCC1=C2C(=CC=C1)C(=O)CC(O2)C3=CC=CC=C3)C 292.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.024
4'-Hydroxy-8-prenylflavanone 24829257 Click to see CC(=CCC1=C2C(=CC=C1)C(=O)CC(O2)C3=CC=C(C=C3)O)C 308.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.024
8-Prenylflavanone 17861867 Click to see CC(=CCC1=C2C(=CC=C1)C(=O)CC(O2)C3=CC=CC=C3)C 292.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.024
Nirurinetin 178813 Click to see CC(=CCC1=C(C(=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O)O)C 356.40 unknown https://doi.org/10.1021/NP50036A008
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(92)80352-F
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(92)80352-F
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1016/0031-9422(92)80352-F
(-)-Epicatechingallate 367141 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1016/0031-9422(92)80352-F
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate 1287 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1016/0031-9422(92)80352-F
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1016/0031-9422(92)80352-F
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin 9882981 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/10.1016/0031-9422(92)80352-F
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/10.1016/0031-9422(92)80352-F
Flavan-3,3',4',5,5',7-hexol 1249 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/10.1016/0031-9422(92)80352-F
Gallocatechin 65084 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/10.1016/0031-9422(92)80352-F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S)-6,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-5-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 163186806 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C(C4=C3C(=O)CC(O4)C5=CC=C(C=C5)O)CC=C(C)C)O)O)O)O)O)O)O)O 664.60 unknown https://doi.org/10.1021/NP50036A008
6,7-Dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-5-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 125896 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C(C4=C3C(=O)CC(O4)C5=CC=C(C=C5)O)CC=C(C)C)O)O)O)O)O)O)O)O 664.60 unknown https://doi.org/10.1021/NP50036A008
Nirurin 42608097 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C(C4=C3C(=O)CC(O4)C5=CC=C(C=C5)O)CC=C(C)C)O)O)O)O)O)O)O)O 664.60 unknown https://doi.org/10.1021/NP50036A008
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 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 448.40 unknown https://doi.org/10.1055/S-2007-969635
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/10.1515/ZNB-2006-0111
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 125528541 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/10.1055/S-2007-969635
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 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 448.40 unknown https://doi.org/10.1055/S-2007-969635
3-[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 162949761 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)OC5C(C(C(C(O5)CO)O)O)O 610.50 unknown https://doi.org/10.1515/ZNB-2006-0111
3-[3,4-Dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 13845899 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)OC5C(C(C(C(O5)CO)O)O)O 610.50 unknown https://doi.org/10.1515/ZNB-2006-0111
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 14825575 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 596.50 unknown https://doi.org/10.1021/NP0497245
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2007-969635
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/10.1515/ZNB-2006-0111
Quercetin 3-alloside 12304327 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/10.1055/S-2007-969635
Quercetin 3-sambubioside 5487635 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 596.50 unknown https://doi.org/10.1021/NP0497245
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2R)-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one 154496535 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=O)CC(OC3=C2)C4=CC(=C(C=C4)O)O)O)O)O)O 434.40 unknown https://doi.org/10.1055/S-0028-1097589
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5,7-Dihydroxy-2-(4-methoxyphenyl)-4-oxochromene-6-sulfonic acid 11494293 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)S(=O)(=O)O)O 364.30 unknown https://doi.org/10.1515/ZNB-2006-0111
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O 292.20 unknown https://doi.org/10.1016/0031-9422(92)80352-F
https://doi.org/10.1515/ZNB-2006-0111
(2R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-2-carboxylic acid 163020001 Click to see C1C(C(=O)C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O)C(=O)O 292.20 unknown https://doi.org/10.1248/CPB.37.2531
7,8,9-Trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-2-carboxylic acid 76333823 Click to see C1C(C(=O)C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O)C(=O)O 292.20 unknown https://doi.org/10.1248/CPB.37.2531
Brevifolincarboxylic acid 9838995 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O 292.20 unknown https://doi.org/10.1016/0031-9422(92)80352-F
https://doi.org/10.1515/ZNB-2006-0111
ethyl (2R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-2-carboxylate 162887636 Click to see CCOC(=O)C1CC2=C(C1=O)OC(=O)C3=CC(=C(C(=C23)O)O)O 320.25 unknown https://doi.org/10.1248/CPB.37.2531
Ethyl 7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-2-carboxylate 76326537 Click to see CCOC(=O)C1CC2=C(C1=O)OC(=O)C3=CC(=C(C(=C23)O)O)O 320.25 unknown https://doi.org/10.1248/CPB.37.2531
methyl (1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylate 163033643 Click to see COC(=O)C1CC(=O)C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O 306.22 unknown https://doi.org/10.1248/BPB.30.382
https://doi.org/10.1515/ZNB-2006-0111
Methyl brevifolincarboxylate 5319518 Click to see COC(=O)C1CC(=O)C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O 306.22 unknown https://doi.org/10.1248/BPB.30.382
https://doi.org/10.1515/ZNB-2006-0111
https://doi.org/10.1248/BPB.29.177
> Phenylpropanoids and polyketides / Tannins
[(1R,4S,9R,18R,19R,21S,22S)-11,12,13-trihydroxy-3,6,7,8,16-pentaoxo-21,22-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,17,20-trioxatetracyclo[16.3.1.04,9.010,15]docosa-10,12,14-trien-19-yl]methyl 3,4,5-trihydroxybenzoate 162913611 Click to see C1C2C(C3=C(C(=C(C=C3C(=O)OC4C(OC(C(C4OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)OC(=O)C6=CC(=C(C(=C6)O)O)O)COC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)O)C(=O)C(=O)C1=O 938.70 unknown https://doi.org/10.1016/0031-9422(92)80352-F
[11,12,13-Trihydroxy-3,6,7,8,16-pentaoxo-21,22-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,17,20-trioxatetracyclo[16.3.1.04,9.010,15]docosa-10,12,14-trien-19-yl]methyl 3,4,5-trihydroxybenzoate 12443323 Click to see C1C2C(C3=C(C(=C(C=C3C(=O)OC4C(OC(C(C4OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)OC(=O)C6=CC(=C(C(=C6)O)O)O)COC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)O)C(=O)C(=O)C1=O 938.70 unknown https://doi.org/10.1016/0031-9422(92)80352-F
[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/10.1021/NP0497245
1,2,4,6-Tetragalloyl-beta-D-glucopyranose 14464350 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)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown https://doi.org/10.1016/0031-9422(92)80352-F
1,2,4,6-Tetragalloylglucose 11297287 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)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown https://doi.org/10.1016/0031-9422(92)80352-F
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/10.1021/NP0497245
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(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/10.1021/NP50056A033
(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/10.1007/S10600-005-0011-4
https://doi.org/10.1515/ZNB-2006-0111
https://doi.org/10.1248/CPB.37.2531
(9,10,11,27,28,29,32,33,34-Nonahydroxy-6,14,15,16,19,24,37-heptaoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,17,25,27,29,31,33,35-decaen-3-yl) 3,4,5-trihydroxybenzoate 162939436 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6C(=CC(=O)C(=O)C6=O)C(=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/10.1016/0031-9422(92)80352-F
[(1R,19S,21S,22S,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 5316067 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/10.1007/S10600-005-0011-4
[(1R,3S,4R,13S,21R,22S)-9,10,11,27,28,29,32,33,34-nonahydroxy-6,14,15,16,19,24,37-heptaoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,17,25,27,29,31,33,35-decaen-3-yl] 3,4,5-trihydroxybenzoate 162939437 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6C(=CC(=O)C(=O)C6=O)C(=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/10.1016/0031-9422(92)80352-F
[(1S,19R,21S,22R,23R)-6,7,8,11,12,13,23-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-22-yl] 3,4,5-trihydroxybenzoate 14284664 Click to see C1C2C(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(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1016/0031-9422(92)80352-F
[3,4,5-Trihydroxy-6-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,8,9,10-pentahydroxy-6-oxobenzo[c]chromene-1-carboxylate 72788642 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C4=C3C5=C(C(=C(C=C5C(=O)O4)O)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1021/NP0497245
[6,7,8,11,12,13,23-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-22-yl] 3,4,5-trihydroxybenzoate 14284662 Click to see C1C2C(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(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1016/0031-9422(92)80352-F
1-O-galloyl-6-O-luteoyl-alpha-D-glucose 11296628 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C4=C3C5=C(C(=C(C=C5C(=O)O4)O)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1021/NP0497245
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/10.1021/NP50056A033
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/10.1007/S10600-005-0011-4
https://doi.org/10.1248/CPB.37.2531
https://doi.org/10.1515/ZNB-2006-0111
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1248/CPB.37.2531
https://doi.org/10.1021/NP50056A033
Isocorilagin 10077799 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/10.1515/ZNB-2006-0111

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