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Syzygium cumini

Syzygium cumini - 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 UUID643fee1ef3d4f445857172
Scientific name Syzygium cumini
Authority (L.) Skeels
First published in Bull. Bur. Pl. Industr. U.S.D.A. 248: 25 (1912)

Description Top

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Synonyms Top

Scientific name Authority First published in
Jambolifera chinensis Spreng. Syst. Veg. 2: 216 (1825)
Jambolifera coromandelica Houtt. Nat. Hist. 2(2): 275 (1774)
Myrtus corticosa Spreng. Syst. Veg. 2: 488 (1825)
Myrtus cumini L. Sp. Pl. : 471 (1753)
Myrtus obovata Spreng. Syst. Veg. 2: 486 (1825)
Syzygium brachiatum Miq. Fl. Ned. Ind. 1(1): 460 (1855)
Syzygium caryophyllifolium (Lam.) DC. Prodr. 3: 260 (1828)
Syzygium cumini var. tsoi (Merr. & Chun) H.T.Chang & R.H.Miao Acta Bot. Yunnan. 4: 22 (1982)
Syzygium fruticosum DC. Prodr. 3: 260 (1828)
Syzygium jambolanum (Lam.) DC. Prodr. 3: 259 (1828)
Syzygium obovatum DC. Prodr. 3: 259 (1828)
Syzygium obtusifolium Kostel. Allg. Med.-Pharm. Fl. 4: 1532 (1835)
Syzygium pseudojambolana Miq. Fl. Ned. Ind. 1(1): 458 (1855)
Syzygium tenue (Wall. ex Duthie) N.P.Balakr. Bull. Bot. Surv. India 22: 175 (1980 publ. 1982)
Syzygium cumini var. caryophyllifolium (Lam.) K.K.Khanna Fl. Bihar, Analysis : 199 (2001)
Syzygium cumini var. obtusifolium (Roxb.) K.K.Khanna Fl. Bihar, Analysis : 202 (2001)
Calyptranthes capitellata Buch.-Ham. ex Wall. Numer. List : n.º 3560B (1831)
Calyptranthes caryophyllifolia (Lam.) Willd. Ann. Bot. (Usteri) 17: 22 (1796)
Calyptranthes cumini Pers. Syn. Pl. 2: 32 (1806)
Calyptranthes cuminodora Stokes Bot. Mat. Med. 3: 67 (1812)
Calyptranthes jambolana Willd. Ann. Bot. (Usteri) 17: 23 (1796)
Calyptranthes jambolifera Stokes Bot. Mat. Med. 3: 68 (1812)
Calyptranthes oneillii Lundell Bull. Torrey Bot. Club 64: 554 (1937)
Calyptranthes tenuis Buch.-Ham. ex Wall. Numer. List : n.º 3570 (1831)
Caryophyllus corticosus Stokes Bot. Mat. Med. 3: 75 (1812)
Caryophyllus jambos Stokes Bot. Mat. Med. 3: 73 (1812)
Syzygium jambolanum var. acuminata O.Berg Linnaea 27: 339. 1856
Syzygium jambolanum var. elliptica O.Berg Linnaea 27: 339. 1856
Syzygium jambolanum var. obovata O.Berg Linnaea 27: 339. 1856
Eugenia brachiata Roxb. Fl. Ind. ed. 1832 , 2: 488 (1832)
Eugenia calyptrata Roxb. ex Wight & Arn. Prodr. Fl. Ind. Orient. : 329 (1834)
Eugenia caryophyllifolia Lam. Encycl. 3: 198 (1789)
Eugenia cumini (L.) Druce Rep. Bot. Exch. Club Soc. Brit. Isles 3: 418 (1913 publ. 1914)
Eugenia djouat Perr. Mém. Soc. Linn. Paris 3: 116 (1825)
Eugenia fruticosa Roxb. Hort. Bengal. 37. 1814
Eugenia jambolana Lam. Encycl. 3: 198 (1789)
Eugenia jambolana var. caryophyllifolia (Lam.) Duthie Fl. Brit. India 2: 499 (1879)
Eugenia jambolana var. obtusifolia Duthie Fl. Brit. India 2: 500. 1879
Eugenia jambolifera Roxb. ex Wight & Arn. Prodr. Fl. Ind. Orient. : 329 (1834)
Eugenia obovata Poir. Encycl. , Suppl. 3: 124 (1813)
Eugenia obtusifolia Roxb. Fl. Ind. ed. 1832 , 2: 485 (1832)
Eugenia odorata Wight Ill. Ind. Bot. 2: 16 (1841)
Eugenia tenuis Duthie Fl. Brit. India 2: 500 (1879)
Eugenia tsoi Merr. & Chun Sunyatsenia 2: 291 (1935)
Syzygium cumini var. caryophyllifolia (Duthie) R.R.Stewart Kew Bull. 29(2): 444. 1974 [1 Oct 1974]
Syzygium jambolanum var. axillare Gamble Fl. Madras 1: 482 (1919)
Calyptranthes pedunculata Forsyth f.
Eugenia fruticosa (DC.) Roxb.

Common names Top

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Language Common/alternative name
English java plum
English jambul
English jamun
English black plum
English jambolan
Spanish jambolifera pedunculata
Spanish arbol yambul
Spanish Árbol yambul
Spanish yambolan
Arabic شجرة البامبوزيا
Arabic الجامبول
Arabic الرياعة الكمونية
ban juwet
bcl duhat
bho जामुन
Bengali কালোজাম
Bengali জামঃ
Bengali জাম
Czech hřebíčkovec šabrejový
German jambulbaum
dv ދަނބު
Persian درخت جمبو
Persian جمبو
Finnish jaavanjambolaani
French jamblon
French jamelonier
gom जांबळ
Gujarati જાંબુ (વૃક્ષ)
Hebrew ימבולנה
Hindi जामुन
hif jaamun
Indonesian duwet
Indonesian jambu keling
Indonesian jamblang
ilo lungboy
ilo lumboy
Japanese ムラサキフトモモ
Japanese ドゥハット
jv dhuwet
Kannada ನೇರಳೆ
Korean 염부
Korean 염부수
Korean 자문
Korean 잠부
Korean 염부나무
koi Джамболан
kv Джамболан
lbe Джамболан
lbe Жамболан
mad dhuwâ'
mai जामुन
min jambu kaliang
Malayalam jambul
Malayalam ജാമുൻ
Malayalam ഞാവൽ
Marathi जांभुळ
Marathi जांभूळ
mrj Джамболан
Malay pokok jambu keling
Nepali जामुन
Dutch roosappel
Dutch jambolan
Oriya ଜାମୁକୋଳି
Oriya ଜାମୁ କୋଳି
Punjabi ਜਾਮਣ
Polish czapetka kuminowa
Punjab جامنوں
Pashto جامنو
Portuguese azeitona-preta
Portuguese azeitona-roxa
Portuguese jambolão
Portuguese jamelao
Portuguese jamelão
Russian Сизигиум ямболан
Russian Ямболан
Russian Джамболан
sa जम्बूफलम्
sat ᱠᱩᱫ
sd ڄمون
Sinhala මාදං
su jamblang
Tamil நாவல் மரம்
Tamil நாவல்
tcy ನೇರೊಳು
Telugu గిన్నె చెట్టు
Telugu జంబు
Telugu నేరేడు
Thai หว้า
udm Джамболан
Ukrainian Джамболан
Urdu جامن
Vietnamese trâm mốc
Chinese 野冬青果
Chinese 乌楣
Chinese 乌墨
Chinese 蒲桃
Chinese 海南蒲桃
Chinese 羊屎果
Chinese 羊屎果树皮
Chinese 堇寶蓮
Chinese 乌墨（海南蒲桃）
Chinese 云南獐牙菜
Chinese 堇宝莲叶
Chinese 蒲桃子
Chinese 西洋果
Chinese 长萼乌墨
Chinese 閻浮樹
Chinese 阎浮树

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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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • West Tropical Africa
      • Guinea
      • Guinea-Bissau
    • Western Indian Ocean
      • Comoros
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Nepal
      • Pakistan
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • South-central Pacific
      • Cook Islands
      • Marquesas
      • Society Islands
      • Tuamotu
    • Southwestern Pacific
      • Fiji
      • New Caledonia
      • Vanuatu
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • El Salvador
      • Guatemala
      • Honduras
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000318521
UNII AQ5VSC4CK4
Florida Plant Atlas 338
USDA Plants SYCU
Tropicos 22102113
INPN 447410
KEW urn:lsid:ipni.org:names:601603-1
The Plant List kew-199476
Open Tree Of Life 380002
NCBI Taxonomy 260142
Nature Serve 2.161374
IUCN Red List 49487196
IPNI 601603-1
iNaturalist 169518
GBIF 3183840
Freebase /m/068kf5
EPPO SYZCU
EOL 2508660
USDA GRIN 36128
Wikipedia Syzygium_cumini
CMAUP NPO9138

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
Folk Knowledge and Perceptions about the Use of Wild Fruits and Vegetables–Cross-Cultural Knowledge in the Pipli Pahar Reserved Forest of Okara, Pakistan Jabeen S, Arshad F, Harun N, Waheed M, Alamri S, Haq SM, Vitasović-Kosić I, Fatima K, Chaudhry AS, Bussmann RW Plants (Basel) 14-Mar-2024
PMCID:PMC10974405
doi:10.3390/plants13060832
PMID:38592859
An Alarming Decline in the Nutritional Quality of Foods: The Biggest Challenge for Future Generations’ Health Bhardwaj RL, Parashar A, Parewa HP, Vyas L Foods 14-Mar-2024
PMCID:PMC10969708
doi:10.3390/foods13060877
PMID:38540869
Functional pH-Sensitive Film Containing Purple Sweet Potato Anthocyanins for Pork Freshness Monitoring and Cherry Preservation Ke F, Liu D, Qin J, Yang M Foods 28-Feb-2024
PMCID:PMC10930767
doi:10.3390/foods13050736
PMID:38472849
The Standardization of Daruharidradi Ghanavati Chawre SV, Waykar PA, Shinde VS, Gulhane JD Int J Appl Basic Med Res 20-Feb-2024
PMCID:PMC10947755
doi:10.4103/ijabmr.ijabmr_363_23
PMID:38504835
Magnetic iron oxide-based nanozymes: from synthesis to application Ghazzy A, Nsairat H, Said R, Sibai OA, AbuRuman A, Shraim AS, Al hunaiti A Nanoscale Adv 19-Feb-2024
PMCID:PMC10929596
doi:10.1039/d3na00903c
PMID:38482039
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
Characterization and toxicological potential of Alternaria alternata associated with post-harvest fruit rot of Prunus avium in China Ahmad T, Xing F, Cao C, Liu Y Front Microbiol 06-Feb-2024
PMCID:PMC10877066
doi:10.3389/fmicb.2024.1273076
PMID:38380098
Green Synthesis of Narrow-Size Silver Nanoparticles Using Ginkgo biloba Leaves: Condition Optimization, Characterization, and Antibacterial and Cytotoxic Activities Ni Q, Zhu T, Wang W, Guo D, Li Y, Chen T, Zhang X Int J Mol Sci 05-Feb-2024
PMCID:PMC10856183
doi:10.3390/ijms25031913
PMID:38339192
Yams (Dioscorea spp.) in shellmounds and swiddens: ancient history in Babitonga Bay, Santa Catarina State, southern Brazil da Silva Souza DA, da Bandeira DR, Peroni N J Ethnobiol Ethnomed 02-Feb-2024
PMCID:PMC10836009
doi:10.1186/s13002-024-00653-4
PMID:38308263
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Antimicrobial and Synergistic Effects of Syzygium cumini, Moringa oleifera, and Tinospora cordifolia Against Different Candida Infections Adelakun AO, Awosika A, Adabanya U, Omole AE, Olopoda AI, Bello ET Cureus 24-Jan-2024
PMCID:PMC10808863
doi:10.7759/cureus.52857
PMID:38274587
Analyzing the Antihyperglycemic Effect of Cissus quadrangularis and Bacopa monnieri on 3T3-L1 Cell Lines R K, S M, IGK I, J S, S V Cureus 21-Jan-2024
PMCID:PMC10877220
doi:10.7759/cureus.52661
PMID:38380214
Nanocellulose, the Green Biopolymer Trending in Pharmaceuticals: A Patent Review Garcia KR, Beck RC, Brandalise RN, dos Santos V, Koester LS Pharmaceutics 21-Jan-2024
PMCID:PMC10819157
doi:10.3390/pharmaceutics16010145
PMID:38276515
Potential Effects of Essential Oil from Plinia cauliflora (Mart.) Kausel on Leishmania: In Vivo, In Vitro, and In Silico Approaches Holanda VN, Brito TG, de Oliveira JR, da Cunha RX, da Silva AP, da Silva WV, Araújo TF, Tavares JF, dos Santos SG, Figueiredo RC, Lima VL Microorganisms 19-Jan-2024
PMCID:PMC10819817
doi:10.3390/microorganisms12010207
PMID:38276192
Relationship between Cumulative Temperature and Light Intensity and G93 Parameters of Isoprene Emission for the Tropical Tree Ficus septica Oku H, Iqbal A, Oogai S, Inafuku M, Mutanda I Plants (Basel) 15-Jan-2024
PMCID:PMC10820733
doi:10.3390/plants13020243
PMID:38256797

Phytochemical Profile Top

Add a new one!
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 / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> 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/10.1016/S0031-9422(01)00365-X
https://doi.org/10.1055/S-0028-1097868
https://doi.org/10.1002/(SICI)1099-1573(199811)12:7<488::AID-PTR344>3.0.CO;2-0
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[2-(1,2-Dihydroxyethyl)-5-hydroxy-4-(3,4,5-trihydroxybenzoyl)oxyoxolan-3-yl] 3,4,5-trihydroxybenzoate;[2,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate;[4,5,6-trihydroxy-1-oxo-3-(3,4,5-trihydroxybenzoyl)oxyhexan-2-yl] 3,4,5-trihydroxybenzoate 163192237 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.C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC2C(CO)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O.C1=C(C=C(C(=C1O)O)O)C(=O)OC(C=O)C(C(C(CO)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O 1453.10 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
2,3-di-O-galloyl--d-glucose 21146989 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC(C=O)C(C(C(CO)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O 484.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
2,3,5-Trihydroxy-6-(hydroxymethyl)oxan-4-yl 3,4,5-trihydroxybenzoate 15608603 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2O)O)CO)O 332.26 unknown https://doi.org/10.1055/S-0028-1097868
3-O-galloyl-beta-d-glucose 102303744 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2O)O)CO)O 332.26 unknown https://doi.org/10.1055/S-0028-1097868
6-O-galloyl-beta-D-glucose 5317463 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/10.1055/S-0028-1097868
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown https://doi.org/10.1055/S-0028-1097868
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/10.1055/S-0028-1097868
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
https://doi.org/10.1055/S-0028-1097868
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1021/NP50028A031
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6S,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol 101492046 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)O)O 344.40 unknown https://doi.org/10.1080/14786410802038697
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 234817 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1080/14786410802038697
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol 23159121 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)O)O 344.40 unknown https://doi.org/10.1080/14786410802038697
5-[(3S,3aR,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,3-dimethoxyphenol 102034302 Click to see COC1=CC(=CC(=C1OC)O)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 386.40 unknown https://doi.org/10.1080/14786410802038697
5-[(3S,3aR,6S,6aR)-3-(3,4-dihydroxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]benzene-1,2,3-triol 162878411 Click to see C1C2C(COC2C3=CC(=C(C(=C3)O)O)O)C(O1)C4=CC(=C(C=C4)O)O 346.30 unknown https://doi.org/10.1080/14786410802038697
5-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,3-dimethoxyphenol 132492668 Click to see COC1=CC(=CC(=C1OC)O)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 388.40 unknown https://doi.org/10.1080/14786410802038697
5-[3-(1,3-Benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,3-dimethoxyphenol 163020895 Click to see COC1=CC(=CC(=C1OC)O)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 386.40 unknown https://doi.org/10.1080/14786410802038697
5-[3-(3,4-Dihydroxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]benzene-1,2,3-triol 162878410 Click to see C1C2C(COC2C3=CC(=C(C(=C3)O)O)O)C(O1)C4=CC(=C(C=C4)O)O 346.30 unknown https://doi.org/10.1080/14786410802038697
5-[3-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,3-dimethoxyphenol 163043364 Click to see COC1=CC(=CC(=C1OC)O)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 388.40 unknown https://doi.org/10.1080/14786410802038697
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1080/14786410802038697
> Lignans, neolignans and related compounds / Lignan lactones
(3S,3aS,6S,6aR)-3-(3,4-dihydroxyphenyl)-6-(3,4,5-trihydroxyphenyl)-3,3a,6,6a-tetrahydro-1H-furo[3,4-c]furan-4-one 163014479 Click to see C1C2C(C(O1)C3=CC(=C(C=C3)O)O)C(=O)OC2C4=CC(=C(C(=C4)O)O)O 360.30 unknown https://doi.org/10.1080/14786410802038697
(3S,3aS,6S,6aR)-3-(3,4-dihydroxyphenyl)-6-(4-hydroxy-3-methoxyphenyl)-3,3a,6,6a-tetrahydro-1H-furo[3,4-c]furan-4-one 162994857 Click to see COC1=C(C=CC(=C1)C2C3COC(C3C(=O)O2)C4=CC(=C(C=C4)O)O)O 358.30 unknown https://doi.org/10.1080/14786410802038697
3-(3,4-dihydroxyphenyl)-6-(3,4,5-trihydroxyphenyl)-3,3a,6,6a-tetrahydro-1H-furo[3,4-c]furan-4-one 163014478 Click to see C1C2C(C(O1)C3=CC(=C(C=C3)O)O)C(=O)OC2C4=CC(=C(C(=C4)O)O)O 360.30 unknown https://doi.org/10.1080/14786410802038697
3-(3,4-dihydroxyphenyl)-6-(4-hydroxy-3-methoxyphenyl)-3,3a,6,6a-tetrahydro-1H-furo[3,4-c]furan-4-one 162994856 Click to see COC1=C(C=CC(=C1)C2C3COC(C3C(=O)O2)C4=CC(=C(C=C4)O)O)O 358.30 unknown https://doi.org/10.1080/14786410802038697
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(-)-leukotoxin B 5281128 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)O 296.40 unknown https://doi.org/10.1002/JSFA.2740430111
(9Z)-(12S,13R)-12,13-Epoxyoctadecenoic acid 6449780 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)O 296.40 unknown https://doi.org/10.1002/JSFA.2740430111
Malvalic acid 10416 Click to see CCCCCCCCC1=C(C1)CCCCCCC(=O)O 280.40 unknown https://doi.org/10.1002/JSFA.2740430111
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1002/JSFA.2740430111
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1002/JSFA.2740430111
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1002/JSFA.2740430111
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1002/JSFA.2740430111
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown https://doi.org/10.1002/JSFA.2740430111
Sterculic acid 12921 Click to see CCCCCCCCC1=C(C1)CCCCCCCC(=O)O 294.50 unknown https://doi.org/10.1002/JSFA.2740430111
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1002/JSFA.2740430111
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,4aR,4bS,7R,10aR)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-ol 22216597 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1O)C)(C)C=C)C 288.50 unknown via CMAUP database
3-Acetoxy-8(17),13E-labdadien-15-oic acid 13858192 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCC(C2(C)C)OC(=O)C)C 362.50 unknown via CMAUP database
3-Oxoanticopalic Acid 13858184 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCC(=O)C2(C)C)C 318.40 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Alepterolic acid 13858188 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCC(C2(C)C)O)C 320.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 302.50 unknown via CMAUP database
Sandaracopimaradienediol 12313649 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown via CMAUP database
Sandaracopimaric acid 221580 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> 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 https://doi.org/10.1021/NP50028A031
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1021/NP50028A031
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/NP50028A031
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(1R,3R,6R)-3,7,7-trimethylbicyclo[4.1.0]heptane 98052623 Click to see CC1CCC2C(C1)C2(C)C 138.25 unknown via CMAUP database
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP50028A031
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/NP50028A031
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/NP50028A031
Bicyclo[2.2.1]heptane, 1,3,3-trimethyl-, (1S,4R)- 10877186 Click to see CC1(CC2(CCC1C2)C)C 138.25 unknown via CMAUP database
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1021/NP50028A031
Bornyl acetate, (-)- 93009 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1021/NP50028A031
> 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
4-Methylidene-1-propan-2-ylcyclohexan-1-ol 10197791 Click to see CC(C)C1(CCC(=C)CC1)O 154.25 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/NP50028A031
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1021/NP50028A031
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50028A031
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP50028A031
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/NP50028A031
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50028A031
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/NP50028A031
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/NP50028A031
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP50028A031
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1021/NP50028A031
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1007/BF03036544
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0378-8741(88)90142-0
https://doi.org/10.1007/BF03036544
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
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/10.1016/S0031-9422(01)00365-X
> Organoheterocyclic compounds / Furofurans
(3aR,4S,6aS)-4-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 163070534 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COCC3CO2 280.32 unknown https://doi.org/10.1080/14786410802038697
4-(3,4,5-Trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 163070533 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COCC3CO2 280.32 unknown https://doi.org/10.1080/14786410802038697
> Organoheterocyclic compounds / Pteridines and derivatives / Pterins and derivatives / Folic acids and derivatives / Folic acids
2-[[4-[(2-amino-4-oxo-1H-pteridin-6-yl)methylamino]benzoyl]amino]pentanedioic acid 3405 Click to see C1=CC(=CC=C1C(=O)NC(CCC(=O)O)C(=O)O)NCC2=CN=C3C(=N2)C(=O)N=C(N3)N 441.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 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/10.1016/S0031-9422(01)00365-X
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/S0367-326X(02)00009-6
https://doi.org/10.1016/S0031-9422(01)00365-X
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/10.1016/S0367-326X(02)00009-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3R,4R,5R,6S)-2-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(1R,2R,3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl]oxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 5316222 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5CC(C(C(C5O)O)O)CO)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 755.70 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
6-beta-D-Glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 369636 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1021/NP300417Q
Swertisin 124034 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1021/NP300417Q
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2S,3S,4R,5R,6S)-6-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 159521681 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(01)00365-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4R,5R,6S)-5-acetyloxy-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4-hydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 101204094 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)OC(=O)C 658.50 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
[(2S,3R,4S,5R,6S)-6-[2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 23955895 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)OC(=O)C 520.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
[(2S,3R,4S,5R,6S)-6-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 44715599 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)OC(=O)C 506.40 unknown https://doi.org/10.1016/S0367-326X(02)00009-6
https://doi.org/10.1016/S0031-9422(01)00365-X
[(2S,3R,4S,5S,6S)-6-[2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 163079131 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)OC(=O)C 520.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
[(2S,3R,4S,5S,6S)-6-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 162954905 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)OC(=O)C 506.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
[(2S,3S,4R,5R,6S)-5-acetyloxy-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4-hydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 163087151 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)OC(=O)C 658.50 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
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(01)00365-X
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/10.1016/S0031-9422(01)00365-X
2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 154496989 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 44259504 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)O 478.40 unknown via CMAUP database
4''-O-Acetylmyricitrin 74978302 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)OC(=O)C 506.40 unknown https://doi.org/10.1016/S0367-326X(02)00009-6
https://doi.org/10.1016/S0031-9422(01)00365-X
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162873125 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/S0367-326X(99)00013-1
Eujambin 21159144 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)OC(=O)C 658.50 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
Eujambolin 74095102 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)OC(=O)C 520.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
Mearnsetin 3-O-(4''-O-acetyl)-alpha-L-rhamnopyranoside 44259506 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)OC(=O)C 520.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
Mearnsetin 3-rhamnoside; Myricetin 4'-methyl ether-3-O-rhamnoside 15560174 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
Mearnsitrin 6918652 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)OC)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
Myricetin 3-acetylrhamnoside 44259449 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)OC(=O)C 506.40 unknown https://doi.org/10.1016/S0367-326X(02)00009-6
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(01)00365-X
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(01)00365-X
https://doi.org/10.1016/S0367-326X(02)00009-6
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/S0031-9422(01)00365-X
> Phenylpropanoids and polyketides / Stilbenes
3-Methoxy-5-(2-phenylethenyl)phenol 182229 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database
3,5-Dimethoxystilbene 5316874 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11S,12R,15R)-3,4,5,13,21,22,23-heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 3,4,5-trihydroxy-2-[(5,12,13-trihydroxy-3,9-dioxo-2,10-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaen-6-yl)oxy]benzoate 70693253 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3OC4=C(C5=C6C(=C4)C(=O)OC7=C(C(=CC(=C67)OC5=O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1086.70 unknown https://doi.org/10.1021/NP300417Q
3-O-methylellagic acid 13915428 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O)O 316.22 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
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/10.1016/S0031-9422(01)00365-X
Iso-Oenothein C 66554347 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3OC4=C(C=C5C6=C4OC(=O)C7=CC(=C(C(=C76)OC5=O)O)O)O)O)O)O)O)CO)O 784.50 unknown https://doi.org/10.1021/NP300417Q
Oenothein C 9962370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3OC4=C(C5=C6C(=C4)C(=O)OC7=C6C(=CC(=C7O)O)C(=O)O5)O)O)O)O)O)CO)O 784.50 unknown https://doi.org/10.1021/NP300417Q

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