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Ribes nigrum

Ribes nigrum - 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 UUID643ff8da9a5b9752227825
Scientific name Ribes nigrum
Authority L.
First published in Sp. Pl. : 201 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Ribes aconitifolium hort. ex K.Koch Dendrologie 1: 661 (1869)
Ribes apiifolium hort. ex K.Koch Dendrologie 1: 661 (1869)
Ribes bactonii Lavallée Énum. Arbres : 121 (1877)
Ribes olidum Moench Methodus : 683 (1794)
Ribesium nigrum Medik. Philos. Bot. 1: 120 (1789)
Botryocarpium nigrum (L.) Spach Hist. Nat. Vég. (Spach) 6: 158. 1838 [Jan 1838 publ. 10 Mar 1838] ; vide Holub in Folia Geobot. &Phytotax., Praha, ii. 404 (1967)
Grossularia nigra Mill. ex Steud. Nomencl. Bot. [Steudel], ed. 2. 1: 708. 1840
Botrycarpum obtusilobum Opiz Seznam 22 1852
Ribes pauciflorum Turcz. ex Ledeb. Spisok Rast. Gerb. Fl. S.S.S.R. 10: 69 (1936)
Botrycarpum nigrum A.Rich. Bot. Med. ii. 490.
Ribes nigrum var. europaeum Jancz. Mém. Soc. Phys. Genève 35(3): 348, f. 77 1907
Ribes nigrum var. pauciflorum (Turcz. ex Ledeb.) Jancz. Mém. Soc. Phys. Genève 35(3): 348, f. 78 1907
Ribes cyathiforme Pojarkova Trudy Prikl. Bot. 22(3): 349 (1929)

Common names Top

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Language Common/alternative name
English black currant
English european black currant
English blackcurrant
Spanish casis
Spanish grosella negra
Spanish grosellero negro
Arabic كشمش أسود
Arabic الكشمش الأسود
Arabic كشمش اسود
Azerbaijani qara qarağat
Azerbaijani ribes cyathiforme
Azerbaijani ribes nigrum f. chlorocarpum
Azerbaijani ribes nigrum var. chlorocarpum
Azerbaijani ribes nigrum var. sibiricum
Azerbaijani ribes olidum
azb قارا قاراغات
ba Ҡарағат
Belarusian Парэчкі чорныя
Bulgarian Касис
Bulgarian черно френско грозде
Bulgarian касис
Bengali ব্ল্যাককারেন্ট
Tibetan སིལ་ཏོག་ཅིག་གི་མིང་།
bxr Үхэр нюдэн
Catalan riber negre
Catalan cassís
Catalan grosella negra
Catalan groseller negre
Czech rybíz černý
Czech černý rybíz
Czech meruzalka černá
Welsh llwyn cwrens duon
Danish solbær-busk
Danish solbær
Danish solbærbusk
German schwarze johannisbeere
German cassis
German ahlbeere
German kakelbeere
Esperanto nigra ribo
Esperanto ribo nigra
Estonian must sõstar
Estonian mustasõstrapõõsas
Estonian mustsõstar
Basque andere-mahats beltz
Persian انگورفرنگی سیاه
Finnish mustaherukka
Finnish mustaviinimarja
French groseillier noir
French cassissier
French cassissier d'europe
French groseiller noir
frr solbei
Irish cuirín dubh
Galician groselleira negra
Manx berrish ghoo
Hebrew ענבי שועל
Croatian crni ribiz
Upper Sorbian Čorny januškowc
Upper Sorbian Čorna janska jahodka
Upper Sorbian Čorny janski jahodowc
Hungarian fekete ribiszke
Hungarian fekete ribizli
Armenian Հաղարջենի սև
Indonesian anggur hitam
io kasiso
Icelandic sólber
Italian ribes nero
Italian cassis
Japanese クロスグリ
Japanese カシス
Japanese クロフサスグリ
Japanese ブラックカラント
Japanese ブラッククラント
Japanese 黒すぐり
Japanese 黒スグリ
jv anggur ireng
Georgian შავი მოცხარი
Kazakh Қарлыған
Korean 블랙커런트
lb schwaarz kréischel
Lithuanian juodasis serbentas
Lithuanian juodieji serbentai
Latvian upene
Latvian melnā upene
Latvian upenes
mhr Шоптырвондер
mt kassisa
Norwegian Bokmål solbær
Norwegian Bokmål solbærbusk
Dutch zwarte bes
Dutch zwarte bessen
Norwegian Nynorsk solbær
Oriya ଜାମୁକୋଳି
os Сау хъæлæрдзы
Punjabi ਬਲੈਕਕਰੰਟ
pam blackcurrant
Polish porzeczka czarna
Polish czarna porzeczka
Portuguese groselha preta
Portuguese groselha-preta
Portuguese cassis
Quechua yananara
Romanian coacăz negru
Russian Смородина чёрная
Russian Смородина черная
Russian Черная смородина
Russian Чёрная смородина
Yakutian Моонньоҕон
Yakutian Моонньоҕон, сэппэрээк
se Čáhppesjieret
se Čáhppesjierit
se sáhppesjieret
Slovak ríbezľa čierna
Slovak čierna ríbezľa
Serbian crna ribizla
Swedish svart vinbär
Swedish svartvinbär
Swedish tistron
Swedish svarta vinbär
Thai แบล็กเคอร์แรนต์
Turkish siyah frenk üzümü
Turkish kuş üzümü
tyv Инек-караа
udm Сьӧд сутэр
Ukrainian Смородина чорна
Ukrainian Чорна смородина
vec Ùa spinèla
vep Čigičaine
Vietnamese lý chua đen
Chinese 黑果茶藨
Chinese 黑加仑
Chinese 黑茶藨子
Chinese 黑茶镳子（黑穗醋栗、黑果镳）
Chinese 哈日一哈达
Chinese 旱葡萄
Chinese 茶藨子
Chinese 黑豆
Chinese 黑加侖
Chinese 黑加侖子
Chinese 黑醋栗

Subspecies (abbr. subsp./ssp.) Top

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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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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
  • Asia-temperate
    • China
      • Inner Mongolia
      • Manchuria
      • Xinjiang
    • Eastern Asia
      • Korea
    • Middle Asia
      • Kazakhstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Magadan
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya
    • Western Asia
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • 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
      • Bulgaria
      • Italy
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • France
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Minnesota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Vermont

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000405161
UNII AL9P010789
Canadensys 6077
USDA Plants RINI
Tropicos 29100051
INPN 117766
Flora of Italy 1872
KEW urn:lsid:ipni.org:names:792873-1
The Plant List kew-2426569
Open Tree Of Life 248647
Observations.org 7316
NCBI Taxonomy 78511
NBN Atlas NBNSYS0000003515
Nature Serve 2.150329
IPNI 792873-1
iNaturalist 54430
GBIF 2986192
Freebase /m/0174rt
WisFlora 4813
EPPO RIBNI
EOL 583204
Elurikkus 6858
US Library of Congress sh85045792
USDA GRIN 31845
Wikipedia Blackcurrant
CMAUP NPO1751

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
Nose of dog, eye of elk, and wolf’s liver: exploring the interconnectedness of Indigenous health and foraging among the Dukha reindeer herders of Mongolia Hatcherson J Int J Circumpolar Health 18-Apr-2024
PMCID:PMC11028006
doi:10.1080/22423982.2024.2343454
PMID:38634711
Current Uses of Bromelain in Children: A Narrative Review Locci C, Chicconi E, Antonucci R Children (Basel) 21-Mar-2024
PMCID:PMC10969483
doi:10.3390/children11030377
PMID:38539412
Polyphenol-rich black currant and cornelian cherry juices ameliorate metabolic syndrome induced by a high-fat high-fructose diet in Wistar rats Paunovic M, Milosevic M, Mitrovic-Ajtic O, Velickovic N, Micic B, Nedic O, Todorovic V, Vucic V, Petrovic S Heliyon 11-Mar-2024
PMCID:PMC10999883
doi:10.1016/j.heliyon.2024.e27709
PMID:38590904
Effects of Thermosonication on the Antioxidant Capacity and Physicochemical, Bioactive, Microbiological, and Sensory Qualities of Blackcurrant Juice Qiu X, Su J, Nie J, Zhang Z, Ren J, Wang S, Pei Y, Li X Foods 06-Mar-2024
PMCID:PMC10931099
doi:10.3390/foods13050809
PMID:38472922
Safety evaluation of the food enzyme β‐fructofuranosidase from the non‐genetically modified Saccharomyces cerevisiae strain NCYC R693 Lambré C, Barat Baviera JM, Bolognesi C, Cocconcelli PS, Crebelli R, Gott DM, Grob K, Lampi E, Mengelers M, Mortensen A, Rivière G, Steffensen I, Tlustos C, Van Loveren H, Vernis L, Zorn H, Herman L, Roos Y, Aguilera J, Andryszkiewicz M, Cavanna D, Liu Y, Marini E, Pesce F, di Piazza G, Chesson A EFSA J 27-Feb-2024
PMCID:PMC10897736
doi:10.2903/j.efsa.2024.8616
PMID:38415018
The Complete Mitochondrial Genome of Paeonia lactiflora Pall. (Saxifragales: Paeoniaceae): Evidence of Gene Transfer from Chloroplast to Mitochondrial Genome Tang P, Ni Y, Li J, Lu Q, Liu C, Guo J Genes (Basel) 14-Feb-2024
PMCID:PMC10888214
doi:10.3390/genes15020239
PMID:38397228
Specific Antimicrobial Activities Revealed by Comparative Evaluation of Selected Gemmotherapy Extracts Héjja M, Mihok E, Alaya A, Jolji M, György É, Meszaros N, Turcus V, Oláh NK, Máthé E Antibiotics (Basel) 13-Feb-2024
PMCID:PMC10885950
doi:10.3390/antibiotics13020181
PMID:38391567
Dihydromyrcenol Modulates Involucrin Expression through the Akt Signaling Pathway Yang S, Kang W, Choi D, Roh J, Park T Int J Mol Sci 13-Feb-2024
PMCID:PMC10889318
doi:10.3390/ijms25042246
PMID:38396923
Use of Aureobasidium in a sustainable economy Rensink S, van Nieuwenhuijzen EJ, Sailer MF, Struck C, Wösten HA Appl Microbiol Biotechnol 13-Feb-2024
PMCID:PMC10864419
doi:10.1007/s00253-024-13025-5
PMID:38349550
Coloration in Flow: The Potential of In Situ Coloration of Casein Fibers to Mitigate Environmental Impact of Traditional Dyeing Methods Houghton JA, Tidder A, Stenton M, Blackburn RS ACS Sustain Chem Eng 29-Jan-2024
PMCID:PMC10865441
doi:10.1021/acssuschemeng.3c07437
PMID:38362531
In Vitro Antibacterial and Antioxidative Activity and Polyphenolic Profile of the Extracts of Chokeberry, Blackcurrant, and Rowan Berries and Their Pomaces Meremäe K, Raudsepp P, Rusalepp L, Anton D, Bleive U, Roasto M Foods 28-Jan-2024
PMCID:PMC10855937
doi:10.3390/foods13030421
PMID:38338557
The Role of Natural Extracts in the Management of Infantile Hemangiomas and Vascular Tumors Roca IC, Cojocaru E, Rusu CD, Trandafir LM, Săveanu CI, Lupu VV, Butnariu LI, Ţarcă V, Moscalu M, Bernic J, Lupu A, Ţarcă E Pediatric Health Med Ther 06-Jan-2024
PMCID:PMC10778175
doi:10.2147/PHMT.S439537
PMID:38213420
Structural Studies of Mexican Husk Tomato (Physalis ixocarpa) Fruit Cutin Arrieta-Baez D, Quezada Huerta C, Rojas-Torres GS, Perea-Flores MD, Mendoza-León HF, Gómez-Patiño MB Molecules 28-Dec-2023
PMCID:PMC10780591
doi:10.3390/molecules29010184
PMID:38202766
Antiarthritic and Anti-Inflammatory Properties of Cannabis sativa Essential Oil in an Animal Model Kabdy H, Azraida H, Agouram F, Oufquir S, Laadraoui J, Baslam A, Aitbaba A, Ouazzani ME, Elyazouli L, Aboufatima R, Garzoli S, Chait A Pharmaceuticals (Basel) 22-Dec-2023
PMCID:PMC10819254
doi:10.3390/ph17010020
PMID:38256854
Wild Edible Fruits as a Source of Food and Medicine: A Study among Tribal Communities of Southern Khyber Pakhtunkhwa Ul Abidin SZ, Khan R, Ahmad M, Cuerrier A, Zafar M, Ullah A, Khan J, Saeed A, Al-Qahtani WH, Kazi M Plants (Basel) 21-Dec-2023
PMCID:PMC10780817
doi:10.3390/plants13010039
PMID:38202347

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 / Harmala alkaloids
Flazine methyl ether 131751427 Click to see COCC1=CC=C(O1)C2=C3C(=CC(=N2)C(=O)O)C4=CC=CC=C4N3 322.30 unknown https://doi.org/10.1515/ZNC-1994-9-1002
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown https://doi.org/10.1002/(SICI)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see C1=CC(=C(C=C1O)C(=O)O)O 154.12 unknown https://doi.org/10.1002/(SICI)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1002/(SICI)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
> 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/BF02273935
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1007/BF02273935
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
2-Naphthol 8663 Click to see C1=CC=C2C=C(C=CC2=C1)O 144.17 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
3,4-Dehydrolarreatricin 25775479 Click to see CC1=C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 282.30 unknown via CMAUP database
4-[(2S,3R,5S)-5-(4-hydroxyphenyl)-3-methyl-4-methylideneoxolan-2-yl]phenol 73213070 Click to see CC1C(OC(C1=C)C2=CC=C(C=C2)O)C3=CC=C(C=C3)O 282.30 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
4,4'-(3,4-Dimethyl-2,5-dihydrofuran-2alpha,5beta-diyl)bis(2-methoxyphenol) 73213069 Click to see CC1=C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C 342.40 unknown via CMAUP database
4,4'-(3alpha-Methyl-4-methylenetetrahydrofuran-2alpha,5beta-diyl)bis(2-methoxyphenol) 73213151 Click to see CC1C(OC(C1=C)C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC 342.40 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown https://doi.org/10.1007/BF02273935
https://doi.org/10.1016/0031-9422(92)80196-L
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatrienes
(Z,Z)-Heptadeca-1,8,11-triene 5352709 Click to see CCCCCC=CCC=CCCCCCC=C 234.40 unknown https://doi.org/10.1021/JF0512095
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isolariciresinol, (+)- 160521 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1016/J.FOODCHEM.2012.03.133
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(2R,3R)-2,3-bis[(4-hydroxy-3-methoxyphenyl)(113C)methyl](113C)butane-1,4-diol 11646293 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O 365.40 unknown https://doi.org/10.1016/J.FOODCHEM.2012.03.133
https://doi.org/10.1207/S15327914NC5402_5
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Larreatricin 26389403 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown via CMAUP database
Meso-3,3'-Didemethoxynectandrin B 14213224 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
(-)-alpha-Conidendrin 72506 Click to see COC1=C(C=C2C(C3COC(=O)C3CC2=C1)C4=CC(=C(C=C4)O)OC)O 356.40 unknown https://doi.org/10.1016/J.FOODCHEM.2012.03.133
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(6R,9S)-Roseoside 11165077 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown via CMAUP database
[(E)-1-cyano-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-1-enyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 102372418 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC(=CCOC2C(C(C(C(O2)CO)O)O)O)C#N)O 437.40 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
[(E)-2-cyano-4-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 5320164 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(=CCOC2C(C(C(C(O2)CO)O)O)O)C#N)O 451.40 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
[(E)-2-cyano-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 11972424 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(=CCOC2C(C(C(C(O2)CO)O)O)O)C#N)O 451.40 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
[(E)-2-cyano-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 11972423 Click to see C1=CC(=CC=C1C=CC(=O)OCC(=CCOC2C(C(C(C(O2)CO)O)O)O)C#N)O 421.40 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
[2-Cyano-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 73157792 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(=CCOC2C(C(C(C(O2)CO)O)O)O)C#N)O 451.40 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
[2-Cyano-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl] 3-(4-hydroxyphenyl)prop-2-enoate 73157791 Click to see C1=CC(=CC=C1C=CC(=O)OCC(=CCOC2C(C(C(C(O2)CO)O)O)O)C#N)O 421.40 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[R,(+)]-3,7-Dimethyl-7-octen-1-ol acetate 36690979 Click to see CC(CCCC(=C)C)CCOC(=O)C 198.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
7-Octen-1-ol, 3,7-dimethyl-, (S)- 81263 Click to see CC(CCCC(=C)C)CCO 156.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1016/0031-9422(91)83454-S
Octadeca-9,12,15-trienoic acid 5282822 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1016/0031-9422(91)83454-S
Stearidonic acid 5312508 Click to see CCC=CCC=CCC=CCC=CCCCCC(=O)O 276.40 unknown https://doi.org/10.1016/0009-3084(92)90079-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown via CMAUP database
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-beta-Phellandrene 442484 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Humulene 5318102 Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
2-[(3S,4aR,6aS,10aS,10bR)-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-yl]acetaldehyde 14845520 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)CC=O)C)C)C 306.50 unknown https://doi.org/10.1021/JF0347517
Isoarborinol 12305182 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1021/JF001245Y
https://doi.org/10.1016/S0040-4039(00)00954-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 25180961 Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C 360.50 unknown https://doi.org/10.1021/JF001245Y
https://doi.org/10.1016/S0021-9673(98)00673-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,4S)-1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-cyclohexanecarboxylic acid 460894 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O 344.27 unknown https://doi.org/10.1016/S0031-9422(00)80722-0
3-O-Feruloylquinic acid 9799386 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)O)(C(=O)O)O)O 368.30 unknown https://doi.org/10.1016/S0031-9422(00)80722-0
Chlorogenic Acid 1794427 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 https://doi.org/10.1002/(SICI)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
https://doi.org/10.1016/S0031-9422(00)80722-0
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 https://doi.org/10.1016/S0031-9422(00)80722-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-O-beta-D-glucosyl-4-coumaric acid 9840292 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1021/JF0347517
Lavandoside 13916049 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 356.32 unknown https://doi.org/10.1016/S0031-9422(00)80722-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Heptoses
(3R,4S,5R,6R)-3,4,5,6,7-pentahydroxy-1-(3,4,5-trihydroxyphenyl)heptane-1,2-dione 21120298 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)C(=O)C(C(C(C(CO)O)O)O)O 332.26 unknown https://doi.org/10.1016/S0031-9422(00)80722-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Sorbicillamine B 136264441 Click to see CC=CC=CC(=C1C2C3(C(=C4C(=O)CC(N=C4C(C3(OC2(C(=O)C(=C1O)C)C)O)(C)O)C=CC)O)C)O 511.60 unknown https://doi.org/10.1021/JF0486850
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
5,9,10-Trihydroxy-7-(3-hydroxy-3-methylbutyl)-8-(3-methylbut-2-enyl)furo[2,3-c]xanthen-6-one 162937039 Click to see CC(=CCC1=C(C2=C(C(=C1O)O)OC3=C(C2=O)C(=CC4=C3C=CO4)O)CCC(C)(C)O)C 438.50 unknown https://doi.org/10.1016/S0031-9422(00)80722-0
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5R)-5-[(Z)-hex-4-en-2-ynyl]oxolan-2-one 162852891 Click to see CC=CC#CCC1CCC(=O)O1 164.20 unknown https://doi.org/10.1016/S0031-9422(00)80722-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
Caffeoylglucose 129629071 Click to see C1=CC(=C(C=C1C=CC(=O)C(=O)C(C(C(C(CO)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1021/JF0347517
https://doi.org/10.1016/S0031-9422(00)80722-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-Propenoic acid, 3-(4-hydroxyphenyl)-, methyl ester 92203 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
1-Caffeoyl-beta-D-glucose 5281761 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O)O 342.30 unknown https://doi.org/10.1021/JF0347517
https://doi.org/10.1016/S0031-9422(00)80722-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1002/(SICI)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1002/(SICI)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1002/(SICI)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
2-(3,4,5-trihydroxyphenyl)-8-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-4-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 5152777 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C(=C7)O)O)O)O)C8=CC(=C(C(=C8)O)O)O)O)O)O)C9=CC(=C(C(=C9)O)O)O)O 914.80 unknown https://doi.org/10.1016/0031-9422(92)80050-O
Gallocatechin-(4alpha->8)-epigallocatechin 442682 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80050-O
Gallocatechin-(4alpha->8)-gallocatechin-(4alpha->8)-gallocatechin 71664720 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C(=C7)O)O)O)O)C8=CC(=C(C(=C8)O)O)O)O)O)O)C9=CC(=C(C(=C9)O)O)O)O 914.80 unknown https://doi.org/10.1016/0031-9422(92)80050-O
Prodelphinidin B 5089687 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80050-O
Prodelphinidin B3 13831068 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown via CMAUP database
> 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)80196-L
https://doi.org/10.1016/0731-7085(91)80128-V
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/10.1016/0731-7085(91)80128-V
https://doi.org/10.1016/0031-9422(92)80196-L
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1016/0031-9422(92)80196-L
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)80196-L
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
> 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)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
https://doi.org/10.1021/JF0010228
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/10.1016/S0021-9673(97)01061-3
https://doi.org/10.1021/JF0010228
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)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
https://doi.org/10.1021/JF991274C
https://doi.org/10.1021/JF0010228
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-1-benzopyran-1-ium-3-yl 6-O-[(2Z)-3-(4-hydroxyphenyl)prop-2-enoyl]-beta-D-glucopyranoside 118797966 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 595.50 unknown via CMAUP database
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenium-3-yl 6-O-[(2Z)-3-(4-hydroxyphenyl)prop-2-enoyl]-beta-D-glucopyranoside 72193639 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O 611.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256715 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1021/JF001245Y
https://doi.org/10.1016/S0021-9673(98)00673-6
3-[(6-O-alpha-L-Rhamnopyranosyl-beta-D-glucopyranosyl)oxy]-4',5,7-trihydroxy-3',5'-dimethoxyflavylium 101942241 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)OC)O)OC)O)O)O)O)O)O)O)O 639.60 unknown via CMAUP database
Cyanidin 3-(2G-glucosylrutinoside) 56671053 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O 757.70 unknown https://doi.org/10.1021/JF0347517
Cyanidin 3-O-xyloside 87948385 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(O4)CO)O)O)O)O)O)O 419.40 unknown https://doi.org/10.1021/JF0486850
Cyanidin 3-O-xylosyl-rutinoside 74976932 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)OC6C(C(C(CO6)O)O)O)O)O)O)O)O 727.60 unknown https://doi.org/10.1021/JF0486850
https://doi.org/10.1021/JF0347517
Delphinidin 3-O-glucoside cation 443650 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 465.40 unknown via CMAUP database
Keracyanin cation 441674 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown https://doi.org/10.1021/JF0347517
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
Oenin 443652 Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 493.40 unknown via CMAUP database
Pelargonidin 3-glucoside ion 443648 Click to see C1=CC(=CC=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O 433.40 unknown via CMAUP database
Pelargonidin 3-O-rutinoside 443917 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC=C(C=C5)O)O)O)O)O)O)O)O)O 579.50 unknown via CMAUP database
Peonidin 3-O-galactoside 11454027 Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O 463.40 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
Peonidin 3-O-rutinoside 90470732 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O)O)O 609.60 unknown via CMAUP database
Peonidin-3-glucoside 443654 Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O 463.40 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
Petunidin 3-glucoside 443651 Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 479.40 unknown https://doi.org/10.1021/JF0486850
Petunidin 3-rutinoside 101949843 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)OC)O)O)O)O)O)O)O)O)O)O 625.60 unknown via CMAUP database
Tulipanin 5492231 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O)O)O 611.50 unknown https://doi.org/10.1016/S0021-9673(98)00673-6
https://doi.org/10.1021/JF0512095
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Cannabiscitrin 5486615 Click to see C1=C(C=C(C(=C1O)O)OC2C(C(C(C(O2)CO)O)O)O)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O 480.40 unknown https://doi.org/10.1021/JF0347517
> 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/S0031-9422(01)00441-1
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(01)00441-1
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162942602 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
3-(3,4-Dihydroxyphenyl)-7-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-one 137199988 Click to see CC1=CC2=C3C(=CC(=O)C=C3OC(=C2OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O1 486.40 unknown https://doi.org/10.1016/S0040-4039(00)00954-0
3-(3,4-Dihydroxyphenyl)-7-methyl-4-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-one 137199990 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=O)C=C5C4=C3C=C(O5)C)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 632.60 unknown https://doi.org/10.1016/S0040-4039(00)00954-0
3-[[6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-galactopyranosyl]oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one 73803273 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)O 626.50 unknown https://doi.org/10.1021/JF0347517
3-beta-D-Arabinopyranosyloxy-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-1-benzopyrylium 101603499 Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O 435.40 unknown via CMAUP database
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162856353 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)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 642.50 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
5,7-Dihydroxy-2-(3,4,5-trihydroxyphenyl)-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162856352 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)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 642.50 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12358426 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 via CMAUP database
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 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/10.1016/S0031-9422(01)00441-1
7-Methyl-3-(3,4,5-trihydroxyphenyl)-4-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-one 137199991 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=O)C=C5C4=C3C=C(O5)C)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O)O 648.60 unknown https://doi.org/10.1016/S0040-4039(00)00954-0
7-Methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxyphenyl)-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-one 137199989 Click to see CC1=CC2=C3C(=CC(=O)C=C3OC(=C2OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C(=C5)O)O)O)O1 502.40 unknown https://doi.org/10.1016/S0040-4039(00)00954-0
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/10.1016/S0031-9422(01)00441-1
https://doi.org/10.1021/JF0347517
delphinidin 3-O-beta-D-glucoside betaine 165559 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C=C3C(=CC(=O)C=C3O2)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1016/S0040-4039(00)00954-0
https://doi.org/10.1016/S0021-9673(98)00673-6
https://doi.org/10.1021/JF001245Y
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 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/10.1021/JF0347517
https://doi.org/10.1016/S0031-9422(01)00441-1
https://doi.org/10.1081/JLC-100100418
kaempferol 3-O-beta-L-glucopyranoside 9911508 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 via CMAUP database
malvidin 3-O-rutinoside 90657906 Click to see CC1CC(C(C(C1O)O)O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=O)C=C(C4=C3)O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O 636.60 unknown https://doi.org/10.1016/S0021-9673(98)00673-6
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(01)00441-1
myricetin 3-O-alpha-L-glucopyranoside 72551451 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 via CMAUP database
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(01)00441-1
Myricetin 3-rutinoside 44259428 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)O 626.50 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
Pyranocyanin D 101198724 Click to see C1=CC(=CC=C1C2=CC3=C4C(=CC(=[OH+])C=C4OC(=C3OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O2)O 565.50 unknown via CMAUP database
Pyranodelphinin D 101198725 Click to see C1=CC(=CC=C1C2=CC3=C4C(=CC(=[OH+])C=C4OC(=C3OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C(=C6)O)O)O)O2)O 581.50 unknown via CMAUP database
Quercetin-3-gentiobioside 13915961 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(01)00441-1
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 https://doi.org/10.1016/S0031-9422(01)00441-1
https://doi.org/10.1021/JF0347517
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/10.1021/JF0347517
https://doi.org/10.1081/JLC-100100418
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-7-[(2S,3S,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 129010093 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1002/(SICI)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
Naringin 442428 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1002/(SICI)1099-1565(199603)7:2<97::AID-PCA286>3.0.CO;2-M
> Phenylpropanoids and polyketides / Macrolides and analogues
6-Hydroxy-5,7,8-trimethyl-2,10,19-trioxa-15-azatetracyclo[10.5.1.15,8.015,18]nonadec-12-ene-3,9-dione 85189098 Click to see CC1C(C2(CC(=O)OC3CCN4C3C(=CC4)COC(=O)C1(O2)C)C)O 351.40 unknown https://doi.org/10.1016/0031-9422(92)80050-O
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
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/10.1300/J065V02N04_03

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