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Syzygium cumini

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
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)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Syzygium cumini, commonly called jamun or black plum, has a long history of use in traditional medicine across South Asia, West Africa, and Latin America. Among the Ayurvedic practitioners of northern India, dried leaves are steeped in hot water to produce a mild tea that is prescribed for type‑2 diabetes and for soothing stomach upset (Sharma et al., 2015). In the Yoruba communities of southwestern Nigeria, a decoction of fresh leaves is taken to reduce fever and to treat malaria‑related chills (Bhat et al., 2018). In Brazil, the fruit pulp and the bark are macerated in alcohol to create a tincture that is used as a topical poultice for skin infections and as an internal remedy for urinary tract infections (Kumar et al., 2020). These preparations all rely on infusions or decoctions of the leaf, bark, or fruit, and they illustrate the plant’s versatility across cultures.

A simple, safe tea can be made at home with dried jamun leaves. Use about 5 g (roughly one tablespoon) of dried leaves and 250 ml of boiling water. Pour the hot water over the leaves, cover, and let steep for 10 minutes. Strain, allow the tea to cool slightly, and drink 2–3 cups per day. This dosage is well within the limits reported in traditional use and is unlikely to cause adverse effects in most adults. However, because the leaves contain bioactive compounds that can lower blood sugar, people with diabetes on medication should monitor their glucose levels, and pregnant or nursing women should consult a healthcare provider before regular consumption.

The pharmacological activity of Syzygium cumini is largely attributed to its rich content of flavonoids and phenolic acids. Ellagic acid, quercetin, catechins, and gallic acid are abundant in the leaves and bark, while the fruit pulp is high in anthocyanins. These compounds have been shown to possess antioxidant, anti‑inflammatory, and antidiabetic properties in laboratory studies, providing a biochemical basis for the traditional uses described above.

Modern research continues to validate the traditional claims. Recent clinical trials have confirmed the hypoglycemic effect of jamun leaf extracts in patients with impaired glucose tolerance, and preclinical studies demonstrate anti‑inflammatory activity that supports the use of leaf decoctions for fever and wound healing. Commercially, jamun leaf tea is now available in health‑food stores and online, and many communities still prepare the plant’s decoctions and tinctures for everyday ailments, keeping the ethnobotanical heritage alive.

General Uses Top

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Common products:
- Edible fruit products (fresh, canned, jams, jellies, syrups), fruit beverages, and non-alcoholic concentrates.
- Seed flour for bakery mixes and traditional cakes.
Industrial and craft applications:
- Wood for light construction, furniture, cabinetry, agricultural implements, and tool handles.
- Bark as a source of tannins for leather dyeing/tanning, producing brown hues on protein fibers.
Food and beverages (non-medicinal):
- Fruit: processing into fruit pulp, juice, squash, syrup, jams, jellies, preserves; also used in mixed-fruit beverages and sorbets.
- Seed: dried and milled seed flour used in bakery products and traditional cakes; sometimes combined with rice or wheat flour.
Colorants and tanning:
- Bark: hydrolyzable tannins extracted for leather dyeing and tanning, yielding brown shades; also used for dyeing textiles and protein fibers.
Wood and fiber:
- Wood: medium-density hardwood with straight to interlocked grain, used in furniture, paneling, tool handles, sports goods, light construction, and as fuelwood; suitable for turning and joinery.
- Fiber: fiber from the fruit pericarp can be processed into biodegradable composites or fillers; mechanical properties vary with matrix and processing.
Fragrance and cosmetics:
- Fruit aroma is occasionally used as a natural flavoring in beverages and foods; not widely reported as a cosmetic fragrance ingredient.
Properties relevant to use:
- Wood: medium density, typically moderate dimensional stability; tannin class (hydrolyzable).
- Seed flour: starch-rich with measurable amylose/amylopectin ratios enabling binding and thickening in bakery matrices.
- Fruit characteristics: high sugar and acid content supporting jam/jelly setting and beverage stability; viable seed content enabling propagation and continuity of fruit supply.
Standards and regulation:
- Fruit products for consumption follow national food-safety regulations (e.g., national food codes for canned fruits and juices) and Good Manufacturing Practice standards.
Sustainability and sourcing:
- Seed utilization reduces waste from fruit processing. Wood is sourced from planted and secondary-growth stands; local bark/tannin collection can be sustainable with careful harvesting practices.

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.
Jambolifera pedunculata Houtt. Nat. Hist. 2(2): 273 (1774)

Common names Top

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Language Common/alternative name
English java plum
English jambul
English jamun
English black plum
English jambolan
English jambolan plum
Spanish arbol yambul
Spanish Árbol yambul
Spanish yambolan
Spanish myrtus corticosa
Spanish calyptranthes capitellata
Spanish calyptranthes cumini
Spanish calyptranthes cuminodora
Spanish calyptranthes jambolifera
Spanish caryophyllus corticosus
Spanish eugenia jambolifera
Spanish jambolifera pedunculata
Spanish eugenia cumini
Spanish eugenia obtusifolia
Spanish jambolifera coromandelica
Spanish myrtus obovata
Spanish syzygium caryophyllifolium
Spanish syzygium jambolanum
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
Estonian jambolani-nelgipuu
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
Khmer pring
Kannada ನೇರಳೆ
Korean 염부
Korean 염부수
Korean 자문
Korean 잠부
Korean 염부나무
koi Джамболан
ks کُل ماچھ
ks کِلمِش
kv Джамболан
lbe Джамболан
lbe Жамболан
Latvian džambolāna
Latvian jambolāna
Latvian javas plūme
Latvian duvets
Latvian džāmbhūls
Latvian džāms
Latvian džāmūns
Latvian hambolana
Latvian indijas upenes
Latvian malabaras plūme
Latvian nāvals
Latvian ņāvals
Latvian žamelau
Latvian melnā plūme
mad dhuwâ'
mai जामुन
Malagasy rotra
Malagasy robary
Malagasy voamaritampona
min jambu kaliang
Malayalam jambul
Malayalam ജാമുൻ
Malayalam ഞാവൽ
Marathi जांभुळ
Marathi जांभूळ
mrj Джамболан
Malay pokok jambu keling
mwl jamelon
Burmese သပြေဖြူ
Nepali जामुन
Dutch roosappel
Dutch jambolan
Dutch eugenia cumini
Oriya ଜାମୁକୋଳି
Oriya ଜାମୁ କୋଳି
Punjabi ਜਾਮਣ
Polish czapetka kuminowa
Punjab جامنوں
Punjab جامݨ
Pashto جامنو
Portuguese azeitona-preta
Portuguese azeitona-roxa
Portuguese jambolão
Portuguese jamelao
Portuguese jamelão
Portuguese eugenia jambolana
Russian Сизигиум ямболан
Russian Ямболан
Russian Джамболан
sa जम्बूफलम्
sat ᱠᱩᱫ
sd ڄمون
Sinhala මාදං
Slovenian klinčevec
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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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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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
Anti-diabetic, anti-pancreatic lipase, and anti-protein glycation potential of Irvingia gabonensis stem bark extracts: in vitro and in silico studies Omonkhua AA, Otitolaiye C, Aguebor-Ogie B, Elekofehinti O, Okello E, Onoagbe I, Okonofua F In Silico Pharmacol 14-May-2024
PMCID:PMC11091014
doi:10.1007/s40203-024-00219-y
PMID:38751710
On-farm crop diversity, conservation, importance and value: a case study of landraces from Western Ghats of Karnataka, India Puneeth GM, Gowthami R, Katral A, Laxmisha KM, Vasudeva R, Singh GP, Archak S Sci Rep 10-May-2024
PMCID:PMC11087530
doi:10.1038/s41598-024-61428-1
PMID:38730080
Study of medicinal plants used in ethnoveterinary medical system in riverine areas of Punjab, Pakistan Umair M, Altaf M, Ahsan T, Bussmann RW, Abbasi AM, Gatasheh MK, Elrobh M J Ethnobiol Ethnomed 07-May-2024
PMCID:PMC11077875
doi:10.1186/s13002-024-00686-9
PMID:38715115
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Demonstration of the synergistic effect of biochar and Trichoderma harzianum on the development of Ralstonia solanacearum in eggplant Ahmad CA, Akhter A, Haider MS, Abbas MT, Hashem A, Avila-Quezada GD, Abd_Allah EF Front Microbiol 25-Apr-2024
PMCID:PMC11079429
doi:10.3389/fmicb.2024.1360703
PMID:38725679
Host Plant Modulated Physio-Biochemical Process Enhances Adaptive Response of Sandalwood (Santalum album L.) under Salinity Stress Verma K, Kumar A, Kumar R, Kumar N, Kumar A, Bhardwaj AK, Verma RC, Sharma P Plants (Basel) 22-Apr-2024
PMCID:PMC11054670
doi:10.3390/plants13081162
PMID:38674572
Prebiotic Systems Containing Anthocyanin-Rich Pomegranate Flower Extracts with Antioxidant and Antidiabetic Effects Gościniak A, Rosiak N, Szymanowska D, Miklaszewski A, Cielecka-Piontek J Pharmaceutics 10-Apr-2024
PMCID:PMC11054034
doi:10.3390/pharmaceutics16040526
PMID:38675187
Access restrictions to forest resources, rather than COVID-19 bans, drive the selection of firewood species for bonfires during Festas Juninas in northeastern Brazil Araújo IV, Centeno-Alvarado D, Ramos MA J Ethnobiol Ethnomed 04-Apr-2024
PMCID:PMC10996119
doi:10.1186/s13002-024-00677-w
PMID:38575934
Essential Oils: Chemistry and Food Applications Rodilla JM, Rosado T, Gallardo E Foods 01-Apr-2024
PMCID:PMC11011311
doi:10.3390/foods13071074
PMID:38611379
From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach Ahmed SS, Rahman MO PLoS One 29-Mar-2024
PMCID:PMC10980240
doi:10.1371/journal.pone.0301348
PMID:38551991
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
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
Green synthesis of cadmium oxide nanoparticles (CdO-NPS) using syzygium cumini: exploring industrial applications of CdO NPs as a corrosion inhibitor of mild steel in the acidic environment Sivalingam S, Kavirajwar J, Seethalakshmi K, Gayathri J, Roniboss A RSC Adv 06-Mar-2024
PMCID:PMC10915717
doi:10.1039/d4ra00560k
PMID:38454945
Use of Callistemon citrinus as a gastroprotective and anti-inflammatory agent on indomethacin-induced gastric ulcers in obese rats Piñón-Simental JS, Ayala-Ruiz LA, Ortega-Pérez LG, Magaña-Rodríguez OR, Meléndez-Herrera E, Aguilera-Méndez A, Rios-Chavez P PeerJ 28-Feb-2024
PMCID:PMC10908265
doi:10.7717/peerj.17062
PMID:38435992
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

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 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 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 1453.10 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
2,3-di-O-galloyl--d-glucose 21146989 Click to see 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 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 332.26 unknown https://doi.org/10.1055/S-0028-1097868
Methyl Gallate 7428 Click to see 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 136.23 unknown https://doi.org/10.1021/NP50028A031
> Lignans, neolignans and related compounds / Furanoid lignans
(+-)-Pinoresinol 234817 Click to see 358.40 unknown https://doi.org/10.1080/14786410802038697
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 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]benzene-1,2-diol 23159121 Click to see 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 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 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 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 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 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 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 358.30 unknown https://doi.org/10.1080/14786410802038697
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(9Z)-11-((2R,3S)-3-Pentyl-2-oxiranyl)-9-undecenoic acid 5281128 Click to see 296.40 unknown https://doi.org/10.1002/JSFA.2740430111
Malvalic acid 10416 Click to see 280.40 unknown https://doi.org/10.1002/JSFA.2740430111
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1002/JSFA.2740430111
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1002/JSFA.2740430111
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1002/JSFA.2740430111
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1002/JSFA.2740430111
Vernolic acid, cis-(+)- 6449780 Click to see 296.40 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 200.32 unknown https://doi.org/10.1002/JSFA.2740430111
Sterculic acid 12921 Click to see 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 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown https://doi.org/10.1002/JSFA.2740430111
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(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 288.50 unknown via CMAUP database
3-Acetoxy-8(17),13E-labdadien-15-oic acid 13858192 Click to see 362.50 unknown via CMAUP database
3-Oxoanticopalic Acid 13858184 Click to see 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 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 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
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 136.23 unknown https://doi.org/10.1021/NP50028A031
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1021/NP50028A031
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
Myrcene 31253 Click to see 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 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1021/NP50028A031
(1R,3R,6R)-3,7,7-trimethylbicyclo[4.1.0]heptane 98052623 Click to see 138.25 unknown via CMAUP database
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1021/NP50028A031
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1021/NP50028A031
Bicyclo[2.2.1]heptane, 1,3,3-trimethyl-, (1S,4R)- 10877186 Click to see 138.25 unknown via CMAUP database
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1021/NP50028A031
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1021/NP50028A031
D-Borneol 6552009 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 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
d-beta-Phellandrene 442484 Click to see 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 136.23 unknown https://doi.org/10.1021/NP50028A031
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(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-Cadinene 441005 Click to see 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
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1021/NP50028A031
Humulene 5281520 Click to see 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 456.70 unknown https://doi.org/10.1007/BF03036544
Oleanolic Acid 10494 Click to see 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 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 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 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 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 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
5-Hydroxy-2-(4-Hydroxyphenyl)-7-Methoxy-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One 369636 Click to see 446.40 unknown https://doi.org/10.1021/NP300417Q
Swertisin 124034 Click to see 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 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 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 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 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-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-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 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 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 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 626.50 unknown https://doi.org/10.1016/S0367-326X(99)00013-1
5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxy-2-(3,4,5-Trihydroxyphenyl)Chromen-4-One 5352000 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
Eujambin 21159144 Click to see 658.50 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
Eujambolin 74095102 Click to see 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 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 478.40 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
Myricetin 3-acetylrhamnoside 44259449 Click to see 506.40 unknown https://doi.org/10.1016/S0367-326X(02)00009-6
Myricitrin 5281673 Click to see 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 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 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 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 302.19 unknown https://doi.org/10.1016/S0031-9422(01)00365-X
Iso-Oenothein C 66554347 Click to see 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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