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Epilobium hirsutum

Epilobium hirsutum - Unknown
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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 UUID644019e67ef72814010616
Scientific name Epilobium hirsutum
Authority L.
First published in Sp. Pl. : 347 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Chamaenerion grandiflorum Moench Methodus : 677 (1794)
Chamaenerion hirsutum Scop. Fl. Carniol. , ed. 2, 1: 270 (1771)
Epilobium amplexicaule Lam. Fl. Franç. 3: 479 (1779)
Epilobium aquaticum Thuill. Fl. Env. Paris , ed. 2: 191 (1799)
Epilobium dubium Borbás Értek. Természettud. Köréb. Magyar Tud. Akad. 16: 6 (1879)
Epilobium foliosum Hochst. Flora 24(1, Intelligenzbl.): 30. 1841
Epilobium grandiflorum Weber Prim. Fl. Holsat. : 30 (1780)
Epilobium himalense Royle Ill. Bot. Himal. Mts. : 211 (1835)
Epilobium hirsutum f. alboroseum D.C.McClint. Garden (London, 1975+) 105: 502 (1980)
Epilobium hirsutum var. laetum Wall. ex C.B.Clarke Fl. Brit. India 2: 584 1879
Epilobium hirsutum f. minor Gančev Fl. Narodna Republ. Bulg. 7: 496. 1979
Epilobium hirsutum f. minus Gančev Fl. Nar. Republ. Bulgariya 7: 496 (1979)
Epilobium hirsutum var. sericeum Benth. ex C.B.Clarke Fl. Brit. India 2: 584 1879
Epilobium hirsutum var. villosissimum W.D.J.Koch Syn. Fl. Germ. Helv. 240 1835
Epilobium incanum Pers. Syn. Pl. 1: 410 (1805)
Epilobium mirei Quézel Bull. Soc. Hist. Nat. Afrique N. 48: 90 (1957)
Epilobium nassirelinulci Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 51: 57 (1886)
Epilobium ramosum Huds. Fl. Angl. : 141 (1762)
Epilobium serratum Jacquem. ex C.B.Clarke Fl. Brit. India 2: 588 (1879)
Epilobium tomentosum Vent. Descr. Pl. Nouv. : t. 90 (1802)
Epilobium velutinum Nevski Trudy Bot. Inst. Akad. Nauk S.S.S.R., Ser. 1, Fl. Sist. Vyssh. Rast. 4: 312 (1937).
Epilobium villosum Thunb. Prodr. Pl. Cap. : 75 (1794)
Epilobium hirsutum var. tomentosum (Vent.) Boiss. Fl. Orient. 2: 746 1872
Epilobium hirsutum var. villosum (Thunb.) H.Hara J. Jap. Bot. 18: 178 1942
Epilobium nassirelmulci Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 51: 57 (1886)

Common names Top

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Language Common/alternative name
English great willowherb
English great hairy willowherb
English hairy willowherb
Spanish epilobium laetum
Spanish epilobium nassirelinulcii
Spanish epilobium peradnatum
Spanish epilobium ramosum
Spanish epilobium sericeum
Spanish epilobium serratum
Spanish epilobium tomentosum
Spanish epilobium velutinum
Spanish epilobium villosum
Spanish chamaenerion hirsutum
Spanish epilobio velludo
Spanish epilobium amplexicaule
Spanish epilobium himalense
Spanish epilobium grandiflorum
Spanish epilobium aquaticum
Spanish epilobium incanum
Arabic سنفية مشعرة
Azerbaijani tükcüklü yağıotu
Belarusian скрыпень касматы
Bulgarian влакнеста върбовка
Czech vrbovka chlupatá
Czech vrbovka huňatá
Welsh helyglys pêr
Danish lodden dueurt
German zottiges weidenröschen
German behaartes weidenröschen
Estonian karvane pajulill
Basque goilora
Persian علف فر پشمالو
Finnish karvahorsma
French epilobe a grandes fleurs
French epilobe hérissé
French Épilobe hérissé
French Épilobe hirsute
French Épilobe à grandes fleurs
Irish lus na tríonóide
Hebrew ערברבה שעירה
Croatian runjava vrbolika
Upper Sorbian wjelowe zelo
Upper Sorbian kosmičkata wjerbinka
Hungarian borzas füzike
Japanese オオアカバナ
Cornish helygles meur
Lithuanian plaukuotoji ožkarožė
Malayalam എപ്പിലോബിയം ഹിർസുതം
Norwegian Bokmål stormjølke
Dutch harig wilgenroosje
Dutch harig wilgeroosje
Polish wierzbownica kosmata
Romanian răchițică pufoasă
Slovak vŕbovka chlpatá
Swedish rosendunört
Chinese 柳葉菜
Chinese 鸡脚参
Chinese 水朝阳花
Chinese 柳叶菜花
Chinese 柳叶菜根
Chinese 柳叶菜

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Canary Islands
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
    • South Tropical Africa
      • Angola
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Namibia
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Burundi
      • Central African Republic
      • Rwanda
      • Zaïre
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
      • Yemen
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Russian Far East
      • Primorye
    • Siberia
      • Altay
      • West Siberia
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • Nepal
      • Pakistan
      • West Himalaya
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
      • Oregon
      • Washington
    • Southeastern U.S.A.
      • Kentucky
      • Maryland
    • Southwestern U.S.A.
      • Utah
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000669196
Canadensys 6776
USDA Plants EPHI
Tropicos 23200135
INPN 96180
Flora of Italy 3375
KEW urn:lsid:ipni.org:names:611919-1
The Plant List kew-2790521
Open Tree Of Life 266692
Observations.org 6732
NCBI Taxonomy 210355
NBN Atlas NBNSYS0000003536
Nature Serve 2.160682
IUCN Red List 164347
IPNI 611919-1
iNaturalist 84517
GBIF 3189172
Freebase /m/03cn20w
WisFlora 3525
EPPO EPIHI
EOL 582985
Elurikkus 4566
USDA GRIN 417511
Wikipedia Epilobium_hirsutum
CMAUP NPO20489

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
Fractionation and phytochemical composition of an ethanolic extract of Ziziphus nummularia leaves: antioxidant and anticancerous properties in human triple negative breast cancer cells Abdallah R, Shaito AA, Badran A, Baydoun S, Sobeh M, Ouchari W, Sahri N, Eid AH, Mesmar JE, Baydoun E Front Pharmacol 09-Feb-2024
PMCID:PMC10885810
doi:10.3389/fphar.2024.1331843
PMID:38405665
Nature-Inspired Designs in Wind Energy: A Review Omidvarnia F, Sarhadi A Biomimetics (Basel) 01-Feb-2024
PMCID:PMC10886931
doi:10.3390/biomimetics9020090
PMID:38392136
Investigation of Epilobium hirsutum L. Optimized Extract’s Anti-Inflammatory and Antitumor Potential Vlase AM, Toiu A, Gligor O, Muntean D, Casian T, Vlase L, Filip A, Bȃldea I, Clichici S, Decea N, Moldovan R, Toma VA, Virag P, Crișan G Plants (Basel) 11-Jan-2024
PMCID:PMC10819739
doi:10.3390/plants13020198
PMID:38256751
Manipulating network connectance by altering plant attractiveness Russo L, Stout JC PeerJ 09-Nov-2023
PMCID:PMC10640842
doi:10.7717/peerj.16319
PMID:38025756
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Multispecies fish tracking across newly created shallow and deep habitats in a forward-restored lake van Leeuwen CH, de Leeuw JJ, van Keeken OA, Volwater JJ, Seljee F, van Aalderen R, van Emmerik WA, Bakker ES Mov Ecol 27-Jul-2023
PMCID:PMC10373381
doi:10.1186/s40462-023-00405-1
PMID:37501192
Exploring the Use of Indigenous Wild Vegetables by the Basotho People of Southern Africa: A Comprehensive Review of the Literature and Nutritional Analysis of Selected Species Tshikororo RR, Ajao AA, Moteetee AN Foods 20-Jul-2023
PMCID:PMC10378859
doi:10.3390/foods12142763
PMID:37509855
Comparison of Biological and Genetic Characteristics between Two Most Common Broad-Leaved Weeds in Paddy Fields: Ammannia arenaria and A. multiflora (Lythraceae) Gao Y, Li S, Yuan G, Fang J, Shen G, Tian Z Biology (Basel) 30-Jun-2023
PMCID:PMC10375975
doi:10.3390/biology12070936
PMID:37508367
Fertilizer and herbicide alter nectar and pollen quality with consequences for pollinator floral choices Russo L, Ruedenauer F, Gronert A, Van de Vreken I, Vanderplanck M, Michez D, Klein A, Leonhardt S, Stout JC PeerJ 12-Jun-2023
PMCID:PMC10269573
doi:10.7717/peerj.15452
PMID:37334137
New Data on Native and Alien Vascular Flora of Sicily (Italy): New Findings and Updates Cambria S, Azzaro D, Caldarella O, Aleo M, Bazan G, Guarino R, Torre G, Cristaudo AE, Ilardi V, La Rosa A, Laface VL, Luchino F, Mascia F, Minissale P, Sciandrello S, Tosetto L, Tavilla G Plants (Basel) 23-Apr-2023
PMCID:PMC10181230
doi:10.3390/plants12091743
PMID:37176800
Chemical Characterization and Biological Evaluation of Epilobium parviflorum Extracts in an In Vitro Model of Human Malignant Melanoma Kyriakou S, Tragkola V, Paraskevaidis I, Plioukas M, Trafalis DT, Franco R, Pappa A, Panayiotidis MI Plants (Basel) 09-Apr-2023
PMCID:PMC10146124
doi:10.3390/plants12081590
PMID:37111814
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Tephrosia toxicaria (Sw.) Pers. extracts: Screening by examining aedicidal action under laboratory and field conditions along with its antioxidant, antileishmanial, and antimicrobial activities Sá GC, da Silva LB, Bezerra PV, da Silva MA, Inacio CL, Paiva WD, e Silva VP, Cordeiro LV, Oliveira JW, Silva MS, Lima ED, Moreira FJ, Rocha HA, Barra PB, Ximenes MD, Uchôa AF PLoS One 11-Jan-2023
PMCID:PMC9833590
doi:10.1371/journal.pone.0275835
PMID:36630475
Ethnopharmacobotany and Diversity of Mediterranean Endemic Plants in Marmilla Subregion, Sardinia, Italy Cocco E, Maccioni D, Sanjust E, Falconieri D, Farris E, Maxia A Plants (Basel) 18-Nov-2022
PMCID:PMC9695302
doi:10.3390/plants11223165
PMID:36432894
Medicinal plants used by rural communities in the arid zone of Viesca and Parras Coahuila in northeast Mexico Torres-León C, Rebolledo Ramírez F, Aguirre-Joya JA, Ramírez-Moreno A, Chávez-González ML, Aguillón-Gutierrez DR, Camacho-Guerra L, Ramírez-Guzmán N, Hernández Vélez S, Aguilar CN Saudi Pharm J 12-Nov-2022
PMCID:PMC9845112
doi:10.1016/j.jsps.2022.11.003
PMID:36685306

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
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 15939858 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown via CMAUP database
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown via CMAUP database
Thermospine 638234 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
Caulophylline 670971 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Mamanine 3085182 Click to see C1CCN2CC(CC(C2C1)CO)C3=CC=CC(=O)N3 262.35 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(+)-12alpha-Hydroxysophocarpine 44408595 Click to see C1CC2CN3C(C4C2N(C1)CCC4)C(C=CC3=O)O 262.35 unknown via CMAUP database
(1R,2R,5S,9S,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 10659287 Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4 264.36 unknown via CMAUP database
(1R,2R,9R,13R,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 21586634 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-] 264.36 unknown via CMAUP database
(1R,2R,9R,17S)-7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 21763818 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
(5beta,6beta,7beta,11alpha)-Matridin-15-one 638232 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
5,9-Dihydroxymatrine 14274649 Click to see C1CC2C3CC(CN4C3C(CCC4)(CN2C(=O)C1)O)O 280.36 unknown via CMAUP database
5alpha-Hydroxysophocarpine 15385686 Click to see C1CC2C3CC=CC(=O)N3CC4(C2N(C1)CCC4)O 262.35 unknown via CMAUP database
9alpha-Hydroxy-13,14-didehydromatridine-15-one 12133310 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O 262.35 unknown via CMAUP database
9alpha-Hydroxymatrine 15385684 Click to see C1CC2C3CC(CN4C3C(CCC4)CN2C(=O)C1)O 264.36 unknown via CMAUP database
Allomatrine 7000681 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
Isomatrine 5271984 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
Matridin-15-one, 12,13-didehydro- 3041752 Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
Matrine 91466 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
Sophocarpine 115269 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
Sophoranol 12442899 Click to see C1CC2C3CCCN4C3C(CCC4)(CN2C(=O)C1)O 264.36 unknown via CMAUP database
Sophoridine 165549 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
Lupanine 91471 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1007/BF00570720
https://doi.org/10.1002/(SICI)1096-9888(199706)32:6<645::AID-JMS518>3.0.CO;2-P
https://doi.org/10.1016/S0031-9422(97)00370-1
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 3,5-dihydroxy-4-methoxybenzoate 5319726 Click to see COC1=C(C=C(C=C1O)C(=O)OC)O 198.17 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
> 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/10.1007/BF00570720
https://doi.org/10.1002/(SICI)1096-9888(199706)32:6<645::AID-JMS518>3.0.CO;2-P
https://doi.org/10.1016/S0031-9422(97)00370-1
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3R,4S,5R,6R)-2,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxy-tetrahydropyran-4-yl] 3,4,5-trihydroxybenzoate 471118 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)CO)O 484.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
2,3-Bis-O-(3,4,5-trihydroxybenzoyl)hexopyranose 14213991 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)CO)O 484.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
6-O-(3,4,5-Trihydroxybenzoyl)-alpha-D-glucopyranose 11968480 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
6-O-Galloylglucose 128839 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC(C(C(C(C=O)O)O)O)O 332.26 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
galloyl(-2)[galloyl(-3)]b-Man 163082172 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)CO)O 484.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Glucogallin, beta 250398 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1002/(SICI)1096-9888(199706)32:6<645::AID-JMS518>3.0.CO;2-P
https://doi.org/10.1016/S0031-9422(97)00370-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate 21636205 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)CO)O)O)O)(C)C)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O 1251.40 unknown via CMAUP database
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Hemiacetals
3,4,5-Trihydroxy-4-methoxycyclohexa-1,5-diene-1-carboxylic acid 162513630 Click to see COC1(C(C=C(C=C1O)C(=O)O)O)O 202.16 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
3,4,5-Trihydroxy-5-methoxycyclohexa-1,3-diene-1-carboxylic acid 54690297 Click to see COC1(CC(=CC(=C1O)O)C(=O)O)O 202.16 unknown https://doi.org/10.1007/BF00570720
> Organoheterocyclic compounds / Azoles / Imidazoles
2,4-Dimethylimidazole 70259 Click to see CC1=CN=C(N1)C 96.13 unknown via CMAUP database
4-Methylimidazole 13195 Click to see CC1=CN=CN1 82.10 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Kushecarpin B 10831417 Click to see COC1C2C(C3(CCC(=O)C=C3O1)OC)OC4=CC5=C(C=C24)OCO5 346.30 unknown via CMAUP database
Kushecarpin C 10496772 Click to see COC1C2C(C3(CCC(=O)C=C3O1)O)OC4=CC5=C(C=C24)OCO5 332.30 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Kushecarpin A 10495761 Click to see COC1C2C(C3(CCC(=O)C=C3O1)O)OC4=C2C=CC(=C4)OC 318.32 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
Sophoramine 169014 Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4 244.33 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(3S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate 6920044 Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-] 216.24 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
(+)-Isokuraramine 101665417 Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO 222.28 unknown via CMAUP database
(+)-Kuraramine 46187187 Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO 222.28 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines
(4Z)-4-ethylidene-8-[4-hydroxy-2-(methoxymethyl)phenyl]-13-oxa-6-azatetracyclo[6.5.0.03,11.06,10]tridecan-7-one 5319437 Click to see CC=C1CN2C3CC(C2=O)(C4CC1C3CO4)C5=C(C=C(C=C5)O)COC 355.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2,4-Dihydroxy-5-prenylphenyl)-5,6-methylenedioxybenzofuran 15953774 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=CC3=CC4=C(C=C3O2)OCO4)C 338.40 unknown via CMAUP database
2'-Hydroxy-4'-methoxy-5,6-methylenedioxy-2-phenylbenzofuran 44260109 Click to see COC1=CC(=C(C=C1)C2=CC3=CC4=C(C=C3O2)OCO4)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1002/(SICI)1096-9888(199706)32:6<645::AID-JMS518>3.0.CO;2-P
https://doi.org/10.1016/S0031-9422(97)00370-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S,2''S)-6-lavandulyl-5,7,2',4'-tetrahydroxylflavanone 118975901 Click to see CC(=CCC(CC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 424.50 unknown via CMAUP database
(2S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one 38351420 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)OC)O)C 370.40 unknown via CMAUP database
Kushenol V 10572194 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3O)O)OC)O)C 386.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-5-methoxy-2,3-dihydrochromen-4-one 44584091 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O 472.50 unknown via CMAUP database
(2R,3S)-2-(2,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-((R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl)chroman-4-one 102004822 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 454.50 unknown via CMAUP database
(2S)-2-(2,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-(1-methylethenyl)hexyl]-4H-1-benzopyran-4-one 44563159 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O 442.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 6565899 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 26209050 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 438.50 unknown via CMAUP database
(2S)-2'-methoxykurarinone 11982641 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 452.50 unknown via CMAUP database
(2S)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 14258999 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC(=C(C=C3)O)OC)C 370.40 unknown via CMAUP database
(2S)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one 44563122 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O 426.50 unknown via CMAUP database
(2S)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 60039901 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 452.50 unknown via CMAUP database
(2S)-7,2'-dihydroxy-8-lavandulyl-5-methoxyflavanone 42607847 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C 422.50 unknown via CMAUP database
(2S)-7,4'-dihydroxy-8-lavandulyl-5-methoxyflavanone 42608062 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=C(C=C3)O)C(=C)C)C 422.50 unknown via CMAUP database
(2S)-euchrenone a7 44593508 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C 340.40 unknown via CMAUP database
(2S)-Isoxanthohumol 9928523 Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=C(C=C3)O)C 354.40 unknown via CMAUP database
7,2',4'-Trihydroxy-8-lavandulyl-5-methoxyflavanone 11982640 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 438.50 unknown via CMAUP database
8-Prenylnaringenin 480764 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown via CMAUP database
CID 102004745 102004745 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C 492.60 unknown via CMAUP database
Flavenochromane A 11351168 Click to see CC1(CCC2=CC(=C(C=C2O1)O)C3C(C(=O)C4=C(O3)C5=C(C=C4O)OC(CC5)(C)C)O)C 440.50 unknown via CMAUP database
Isobavachin 193679 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C 324.40 unknown via CMAUP database
Kurarinol 44563198 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O 456.50 unknown via CMAUP database
Kushenol A 44563121 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C 408.50 unknown via CMAUP database
Kushenol E 127234 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C 424.50 unknown via CMAUP database
Kushenol I 20832634 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 454.50 unknown via CMAUP database
Kushenol L 21721878 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC=C(C)C)O)C 440.50 unknown via CMAUP database
Kushenol M 180948 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC(CC=C(C)C)C(=C)C)O)C 508.60 unknown via CMAUP database
Kushenol S 10854625 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C 340.40 unknown via CMAUP database
KushenolK 44428630 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O 472.50 unknown via CMAUP database
leachianone A 44593449 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 438.50 unknown via CMAUP database
Leachianone G 5275227 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C 356.40 unknown via CMAUP database
Sophoraflavanone G 72936 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Licoflavonol 5481964 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
8-Prenylkaempferol 5318624 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 354.40 unknown via CMAUP database
Flavenochromane B 11327657 Click to see CC1(CCC2=C3C(=C4C(=C2O1)CCC(O4)(C)C)C(=O)C(=C(O3)C5=CC=C(C=C5)O)O)C 422.50 unknown via CMAUP database
Flavenochromane C 11451469 Click to see CC1(CCC2=C3C(=C(C=C2O1)OC)C(=O)C(=C(O3)C4=CC=C(C=C4)O)O)C 368.40 unknown via CMAUP database
Isoanhydroicaritin 5322079 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C 368.40 unknown via CMAUP database
Kushenol C 5481237 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 438.50 unknown via CMAUP database
Kushenol G 44259516 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O 456.50 unknown via CMAUP database
Sophoflavescenol 9929189 Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1002/(SICI)1096-9888(199706)32:6<645::AID-JMS518>3.0.CO;2-P
https://doi.org/10.1016/S0031-9422(97)00370-1
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1002/(SICI)1096-9888(199706)32:6<645::AID-JMS518>3.0.CO;2-P
https://doi.org/10.1016/S0031-9422(97)00370-1
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1002/(SICI)1096-9888(199706)32:6<645::AID-JMS518>3.0.CO;2-P
https://doi.org/10.1016/S0031-9422(97)00370-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2S,3S,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 44258914 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
6-[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 14058644 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 494.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Kaempferol 3-glucuronide 5318759 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Kaempferol-3-O-glucuronoside 14185731 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Miquelianin (Quercetin 3-O-glucuronide) 13258914 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Myricetin 3-glucuronide 44259442 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 494.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Myricetin 3-O-glucuronide 5487413 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 494.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Quercetin 3-glucuronide 12004528 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
> 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/10.1016/S0031-9422(97)00370-1
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/10.1016/S0031-9422(97)00370-1
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 44259215 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
4',5,7-Trihydroxy-3-(alpha-D-arabinopyranosyloxy)flavone 11625890 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 418.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one 14749097 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 418.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
5,7-dihydroxy-3-[(2R,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 162915549 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 450.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
5,7-dihydroxy-3-[(3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 22878721 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 450.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Afzelin 5316673 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 432.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
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 https://doi.org/10.1007/BF00570720
https://doi.org/10.1016/S0031-9422(97)00370-1
Juglanin 5318717 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Kaempferol-3-O-rhamnoside 5835713 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 432.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Myricetin 3-beta-D-glucopyranoside 12311099 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Myricetin 3-galactoside 5491408 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
https://doi.org/10.1016/S0021-9673(01)87147-8
Myricetin 3-rhamnoside 5352000 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)O 464.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Myricetin-3-O-xyloside 21477996 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 450.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Myricitrin 5281673 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)O 464.40 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Quercetin-3-O-arabinoside 12309865 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
Quercitrin 5280459 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/10.1016/S0021-9673(01)87147-8
https://doi.org/10.1016/S0031-9422(97)00370-1
Reynoutrin 5878729 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5318902 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 562.50 unknown via CMAUP database
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain-3-O-glucosyl-6''-O-malonate 23724669 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5=CC6=C(C=C25)OCO6 532.40 unknown via CMAUP database
(-)-Variabilin 442828 Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O 300.30 unknown via CMAUP database
(+)-Maackiain 161298 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown via CMAUP database
(+)-Medicarpin 73067 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol 6326060 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown via CMAUP database
(6aR,11aR)-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8,9-diol 361910 Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC(=C(C=C4O3)O)O 286.28 unknown via CMAUP database
(6aR,11aR)-8-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 21676223 Click to see COC1=C(C=C2C(=C1)C3COC4=C(C3O2)C=CC(=C4)O)O 286.28 unknown via CMAUP database
(6aS,12aS)-6abeta,12abeta-Dihydro-3-methoxy-6H-[1,3]dioxolo[5,6]benzofuro[3,2-c][1]benzopyran 373519 Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5 298.29 unknown via CMAUP database
CID 44428627 44428627 Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O 300.30 unknown via CMAUP database
Maackiain 91510 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown via CMAUP database
Pterocarpin 1715306 Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5 298.29 unknown via CMAUP database
Trifolirhizin 442827 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3',4',7-Trihydroxyisoflavone 5284648 Click to see C1=CC(=C(C=C1C2=COC3=C(C2=O)C=CC(=C3)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
Flavescenone A 101238023 Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC4=C(C=C3O)OCO4)O)C 384.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
Alpinumisoflavone 5490139 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C 336.30 unknown via CMAUP database
Flavescenone B 101238024 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC4=C(C=C3O)OCO4)O)C 382.40 unknown via CMAUP database
Lupalbigenin 10001388 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C 406.50 unknown via CMAUP database
Luteone 5281797 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C=C(C=C3)O)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3'-Hydroxy-4'-methoxy-7-(6-O-(beta-D-xylopyranosyl)-beta-D-glucopyranosyloxy)isoflavone 73603980 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 578.50 unknown via CMAUP database
3'-Hydroxy-4'-methoxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 73603978 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O 578.50 unknown via CMAUP database
3'-Hydroxydaidzin 68607439 Click to see C1=CC(=C(C=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
3'-Methoxy-4'-hydroxy-7-(6-O-(beta-D-xylopyranosyl)-beta-D-glucopyranosyloxy)isoflavone 73603979 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 578.50 unknown via CMAUP database
3'-Methoxy-4'-hydroxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 102131642 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O 578.50 unknown via CMAUP database
3',4'-(Epoxymethanoxy)-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 102131643 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC6=C(C=C5)OCO6)O)O)O)O)(CO)O 576.50 unknown via CMAUP database
Ambonin 20055730 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC=C(C=C5)O)O)O)O)O)(CO)O 548.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
Koparin 5318834 Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A 5280373 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown via CMAUP database
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Kuraridine 44428631 Click to see CC(=CCC(CC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=C(C=C(C=C2)O)O)O)C(=C)C)C 438.50 unknown via CMAUP database
Xanthohumol 639665 Click to see CC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=C(C=C2)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
Sophodibenzoside A 73603983 Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)O)O 582.50 unknown via CMAUP database
Sophodibenzoside B 73603972 Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)O)O 582.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,6-Trigalloyl-beta-D-glucopyranose 3357644 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)O 636.50 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
1,2,6-Trigalloylglucose 440308 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)O 636.50 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
1,6-bis-O-galloyl-beta-D-glucose 440221 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/S0031-9422(97)00370-1
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/S0031-9422(97)00370-1
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2R,3R,4S,5R,6R)-2,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoate 163033014 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(OC2O)CO)O)OC(=O)C3=CC(=C(C(=C3OC4=C(C5=C6C(=C4)C(=O)OC7=C6C(=CC(=C7O)O)C(=O)O5)O)O)O)O 784.50 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
[(3R,5R,6R)-2,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoate 163033013 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(OC2O)CO)O)OC(=O)C3=CC(=C(C(=C3OC4=C(C5=C6C(=C4)C(=O)OC7=C6C(=CC(=C7O)O)C(=O)O5)O)O)O)O 784.50 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
[2,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoate 163033012 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(OC2O)CO)O)OC(=O)C3=CC(=C(C(=C3OC4=C(C5=C6C(=C4)C(=O)OC7=C6C(=CC(=C7O)O)C(=O)O5)O)O)O)O 784.50 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
1'-Monodecarboxyvaloneic acid dilactone 10410181 Click to see C1=CC(=C(C(=C1O)O)O)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O 426.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
3,4,5-Trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzamide 163032352 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)OC5=C(C(=C(C=C5C(=O)N)O)O)O 469.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
https://doi.org/10.1002/(SICI)1096-9888(199706)32:6<645::AID-JMS518>3.0.CO;2-P
6,7,8,17,18-Pentahydroxy-3,10,15,22-tetraoxahexacyclo[14.6.2.02,11.04,9.013,23.020,24]tetracosa-1(23),2(11),4(9),5,7,12,16(24),17,19-nonaene-14,21-dione 21635780 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC5=C(C(=C43)OC2=O)OC6=C(O5)C(=C(C(=C6)O)O)O 424.30 unknown https://doi.org/10.1016/S0031-9422(97)00370-1
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/10.1002/(SICI)1096-9888(199706)32:6<645::AID-JMS518>3.0.CO;2-P
https://doi.org/10.1016/S0031-9422(97)00370-1
Sanguisorbic acid 71308268 Click to see C1=C(C=C(C(=C1O)O)OC2=C(C(=C(C(=C2C(=O)O)C3=C(C(=C(C=C3C(=O)O)O)O)O)O)O)O)C(=O)O 506.30 unknown https://doi.org/10.1007/BF00565955
Valoneic acid dilactone 10151874 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)OC5=C(C(=C(C=C5C(=O)O)O)O)O 470.30 unknown https://doi.org/10.1002/(SICI)1096-9888(199706)32:6<645::AID-JMS518>3.0.CO;2-P
https://doi.org/10.1016/S0031-9422(97)00370-1

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