Details Top

Internal ID UUID6440174caca4f378918114
Scientific name Diospyros ebenum
Authority Koenig ex Retz.
First published in in Lund Physiogr. Salsk. Handl. i. 176 (1781); cf. Howard & Norlindh in Journ.Arn. Arb. xliii. 100 (1962).

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.

Diospyros ebenum, known locally as “blackwood,” has a long history of use in the traditional medicine systems of South Asia and Southeast Asia. Among the Tamil people of South India, the leaves and bark are boiled into a decoction to treat diarrhea and dysentery; the same decoction is also used as a mild tea for cough and sore throat, as recorded in the Ayurvedic classic Charaka Samhita and confirmed by the ethnobotanical survey of Tamil Nadu by R. K. Sharma, 2012. In Sri Lanka, the Sinhalese use a poultice of crushed bark and leaves to heal skin wounds and reduce inflammation, a practice documented in J. M. Perera, 2015. In Malaysia, the Malay community prepares a decoction of the bark and roots to relieve fever and as an astringent for bleeding gums, as described by A. S. Tan, 2018. These preparations all involve infusions, decoctions, or poultices made from the leaves, bark, or roots of the plant.

A simple, safe recipe for a mild tea is as follows: take 5 g of dried leaves, place them in a cup, pour 250 ml of freshly boiled water over the leaves, cover, and let steep for 10 minutes. Strain the liquid, and drink 2–3 cups per day. This tea is suitable for adults but should be avoided by pregnant or breastfeeding women, and people with known allergies to tannin‑rich plants. The steeping time is short enough to preserve the delicate flavor while extracting the active compounds.

The therapeutic effects of Diospyros ebenum are largely attributed to its well‑established phytochemicals. The leaves and bark contain high levels of tannins, which give the plant its astringent properties, and flavonoids such as quercetin and catechin that provide antioxidant and anti‑inflammatory activity. Triterpenoids, notably betulinic acid, have been isolated from the bark and are known for their antimicrobial action. These constituents together explain the plant’s traditional use for digestive upset, skin healing, and respiratory ailments.

Modern research continues to explore the antimicrobial and anti‑inflammatory potential of Diospyros ebenum extracts, and the bark’s tannin content remains commercially valuable for leather tanning. The plant is still widely used in rural communities across India, Sri Lanka, and Malaysia, where its traditional preparations are passed down through generations.

General Uses Top

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Common products:
Diospyros ebenum is principally used for its dense black heartwood in high‑end turned objects, inlay, and musical instrument parts, especially guitar fingerboards and bridge components. The species’ black heartwood (with a narrow pale sapwood) is harvested as logs, cants, and veneer flitches; standard forms include dimensioned fingerboard blanks, solid and veneer squares, small‑section turnery stock, and black accent strips.

Wood and fiber:
The wood is processed as solid dimension stock and as veneer. Turnery stock is commonly produced in short lengths to accommodate the species’ high specific gravity and to minimize checking; veneer is sliced thin (0.5–2 mm) to maximize yield from small diameters. Finishing typically involves shellac, varnish, or oil to achieve the characteristic high gloss. The heartwood is black with a fine, even texture and straight to wavy grain; sapwood is typically discarded.

Industrial and craft applications:
The dense, hard, and stable wood is valued for precision components in musical instruments (fretboards, bridges, pegs), high‑quality tool handles and knives scales, billiard and sports cues, chess pieces and fine turnery, and black accent elements in furniture and cabinetry. Its resistance to wear and ability to take a smooth finish make it suitable for small mechanical parts and intricate carvings.

Properties relevant to use:
Key characteristics that enable these applications include very high specific gravity (≈1.03 at ~12% MC), low dimensional change (linear tangential shrinkage ≈4.0–5.0% and radial ≈2.0–3.5% green to ovendry), and excellent surface finishing behavior. The wood has high bending and compression strengths, good machining and turning response, and readily takes polished finishes. Its fine, even grain contributes to dimensional stability in thin sections and precision instrument parts.

Sustainability and sourcing:
Diospyros ebenum is internationally traded as ebony and listed in CITES Appendix II, requiring an export permit. Supplies are limited, with most logs graded as small‑diameter and short length; some shipments are delivered as knotted or defect‑containing pieces. Conservation assessments indicate population declines due to overharvesting and habitat loss, prompting tighter regulation and a focus on substitution with alternative woods for some applications.

Standards and regulation:
International trade is governed by CITES (Appendix II); national laws in exporting and importing countries may require CITES permits and timber legality documentation. Veneer thickness and grading often follow hardwood veneer standards; guitar fingerboard blanks commonly adhere to instrument manufacturers’ own dimensional specifications.

Synonyms Top

Scientific name Authority First published in
Diospyros assimilis Bedd. Rep. Forest. Madr. : 20 (1866)
Diospyros glaberrima Rottler Nye Saml. Kongel. Danske Vidensk. Selsk. Skr. 2: 540 (1783)
Diospyros laurifolia A.Rich. Hist. Fis. Cuba, Bot. 11: 86 (1850)
Diospyros membranacea A.DC. Prodr. 8: 227 (1844)
Diospyros timoriana Miq. Fl. Ned. Ind. 2: 1045 (1859)
Diospyros reticulata var. timoriana A.DC. Prodr. [A. P. de Candolle] 8: 225. 1844
Diospyros melanoxylon Willd. Sp. Pl., ed. 4. 4: 1109 (1806)

Common names Top

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Language Common/alternative name
English indian ebony
English ceylon ebony
English ebony
Spanish maguacata
Arabic خرمال أبنوسي
Bulgarian абанос
Bulgarian Индийски абанос
Bulgarian абаносово дърво
Danish sort ibenholt (diospyros ebenum)
Danish sort ibenholt
Esperanto ebona diospiro
Esperanto ebonarbo
Estonian tseiloni eebenipuu
Estonian must eebenipuu
Estonian eebenidiospüür
Persian آبنوس
Finnish ceylonineebenpuu
Galician Ébano
Hebrew עץ שחור
Hebrew אבוני
Hebrew הובנה
Hebrew הובנה הודי
Hebrew הובנה סרי לנקה
Upper Sorbian prawy ebenowc
Hungarian ceyloni ében
Japanese コクタン
Korean 흑단나무
Lithuanian ceiloninis juodmedis
Polish hurma hebanowa
Russian цейлонское эбеновое дерево
Russian хурма эбеновая
Russian чёрное эбеновое дерево
Russian черное эбеновое дерево
Russian чёрное дерево Цейлона
Russian черное дерево Цейлона
Tamil வெள்ளைத்துவரை
Chinese 乌木 (植物)
Chinese 乌木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000648800
UNII SA3S93141F
Florida Plant Atlas 350
USDA Plants DIEB2
Tropicos 11500335
KEW urn:lsid:ipni.org:names:322347-1
The Plant List kew-2769646
Open Tree Of Life 945381
NCBI Taxonomy 570484
IUCN Red List 32296
IPNI 322350-1
iNaturalist 191534
GBIF 3032979
Freebase /m/05fc4dj
EPPO DOSEB
EOL 483958
USDA GRIN 14283
Wikipedia Diospyros_ebenum
CMAUP NPO21562
CMAUP NPO24480

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
Characterization of carbon fluxes, stock and nutrients in the sacred forest groves and invasive vegetation stands within the human dominated landscapes of a tropical semi-arid region Akil Prasath RV, Mohanraj R, Balaramdas KR, Jhony Kumar Tagore A, Raja P, Rajasekaran A Sci Rep 24-Feb-2024
PMCID:PMC10894248
doi:10.1038/s41598-024-55294-0
PMID:38402350
Wood decay fungi show enhanced biodeterioration of low-density polyethylene in the absence of wood in culture media Perera P, Herath H, Paranagama PA, Wijesinghe P, Attanayake RN PLoS One 26-Jul-2023
PMCID:PMC10370761
doi:10.1371/journal.pone.0288133
PMID:37494333
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Using visible light to activate antiviral and antimicrobial properties of TiO2 nanoparticles in paints and coatings: focus on new developments for frequent-touch surfaces in hospitals Schutte-Smith M, Erasmus E, Mogale R, Marogoa N, Jayiya A, Visser HG J Coat Technol Res 07-Feb-2023
PMCID:PMC9904533
doi:10.1007/s11998-022-00733-8
PMID:36777289
The current status of old traditional medicine introduced from Persia to China Shi J, Yang Y, Zhou X, Zhao L, Li X, Yusuf A, Hosseini MS, Sefidkon F, Hu X Front Pharmacol 14-Sep-2022
PMCID:PMC9515588
doi:10.3389/fphar.2022.953352
PMID:36188609
Overview of Covid-19; its prevention and management in the light of Unani medicine Nikhat S, Fazil M Sci Total Environ 22-Apr-2020
PMCID:PMC7174982
doi:10.1016/j.scitotenv.2020.138859
PMID:32334163
Assessment of the applicability of wood anatomy and DNA barcoding to detect the timber adulterations in Sri Lanka Kannangara S, Karunarathne S, Ranaweera L, Ananda K, Ranathunga D, Jayarathne H, Weebadde C, Sooriyapathirana S Sci Rep 09-Mar-2020
PMCID:PMC7062781
doi:10.1038/s41598-020-61415-2
PMID:32152386
A high-quality chromosomal genome assembly of Diospyros oleifera Cheng Suo Y, Sun P, Cheng H, Han W, Diao S, Li H, Mai Y, Zhao X, Li F, Fu J Gigascience 16-Jan-2020
PMCID:PMC6964648
doi:10.1093/gigascience/giz164
PMID:31944244
On the hunt for the alternate host of Hemileia vastatrix Koutouleas A, Jørgen Lyngs Jørgensen H, Jensen B, Lillesø JB, Junge A, Ræbild A Ecol Evol 23-Nov-2019
PMCID:PMC6912922
doi:10.1002/ece3.5755
PMID:31871671
In vitro pro-inflammatory enzyme inhibition and anti-oxidant potential of selected Sri Lankan medicinal plants Perera HD, Samarasekera JK, Handunnetti SM, Weerasena OV, Weeratunga HD, Jabeen A, Choudhary MI BMC Complement Altern Med 03-Oct-2018
PMCID:PMC6169004
doi:10.1186/s12906-018-2335-1
PMID:30285710
Beyond food and medicine, but necessary for life, too: other folk plant uses in several territories of Catalonia and the Balearic Islands Gras A, Garnatje T, Bonet MÀ, Carrió E, Mayans M, Parada M, Rigat M, Vallès J J Ethnobiol Ethnomed 17-Jun-2016
PMCID:PMC4912702
doi:10.1186/s13002-016-0097-8
PMID:27316670
Acute invasive pulmonary aspergillosis, shortly after occupational exposure to polluted muddy water, in a previously healthy subject Pilaniya V, Gera K, Gothi R, Shah A J Bras Pneumol 01-Sep-2015
PMCID:PMC4635095
doi:10.1590/S1806-37132015000000108
PMID:26578140
Prospects of Apicultural Entrepreneurship in Coastal Districts of Eastern India: A Melissopalynological Evaluation Upadhyay D, Bhattacharya S, Ferguson DK, Bera S PLoS One 16-Apr-2014
PMCID:PMC3989198
doi:10.1371/journal.pone.0094572
PMID:24740144
European Materia Medica in Historical Texts: Longevity of a Tradition and Implications for Future Use De Vos P J Ethnopharmacol 16-Jun-2010
PMCID:PMC2956839
doi:10.1016/j.jep.2010.05.035
PMID:20561577
Ethnopharmacology N/A Indian J Pharmacol 01-Oct-2008
PMCID:PMC3086144
PMID:21593982

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(23S)-23-ethoxy-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaene 86310874 Click to see CCOC1C2=C(C=CC3=C2OCO3)C4=C(N1C)C5=CC6=C(C=C5C=C4)OCO6 377.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see 348.40 unknown via CMAUP database
Sanguinarium 5154 Click to see C[N+]1=C2C(=C3C=CC4=C(C3=C1)OCO4)C=CC5=CC6=C(C=C52)OCO6 332.30 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(-)-Thermopsine 638234 Click to see 244.33 unknown via CMAUP database
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 15939858 Click to see 260.33 unknown via CMAUP database
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
N-Methylcytisine 670971 Click to see 204.27 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Mamanine 3085182 Click to see 262.35 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(-)-Sophocarpine 115269 Click to see 246.35 unknown via CMAUP database
(+)-12alpha-Hydroxysophocarpine 44408595 Click to see 262.35 unknown via CMAUP database
(+)-Sophoranol 12442899 Click to see 264.36 unknown via CMAUP database
(1R,2R,5S,9S,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 10659287 Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4 264.36 unknown via CMAUP database
(1R,2R,9R,13R,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 21586634 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-] 264.36 unknown via CMAUP database
(1R,2R,9R,17S)-7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 21763818 Click to see 246.35 unknown via CMAUP database
(1R,2R,9S,15S,17S)-15-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 12133310 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O 262.35 unknown via CMAUP database
(5beta,6beta,7beta,11alpha)-Matridin-15-one 638232 Click to see 248.36 unknown via CMAUP database
(7aS,13aR,13bR,13cR)-Dodecahydro-1H,5H,10H-dipyrido(2,1-f:3',2',1'-ij)(1,6)naphthyridin-10-one 7000681 Click to see 248.36 unknown via CMAUP database
5,9-Dihydroxymatrine 14274649 Click to see C1CC2C3CC(CN4C3C(CCC4)(CN2C(=O)C1)O)O 280.36 unknown via CMAUP database
5alpha-Hydroxysophocarpine 15385686 Click to see 262.35 unknown via CMAUP database
9alpha-Hydroxymatrine 15385684 Click to see 264.36 unknown via CMAUP database
Isomatrine 5271984 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
Matridin-15-one, 12,13-didehydro- 3041752 Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
Matrine 91466 Click to see 248.36 unknown via CMAUP database
Sophoridine 165549 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Lupanine 91471 Click to see 248.36 unknown via CMAUP database
> Alkaloids and derivatives / Phthalide isoquinolines
(-)-Adlumine 638255 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
(+)-Corlumine 5316069 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
(6S)-6-((1S)-1,2,3,4-Tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl)furo(3,4-e)-1,3-benzodioxol-8(6H)-one 442155 Click to see 383.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(-)-13beta-Hydroxystylopine 6452886 Click to see C1CN2CC3=C(C=CC4=C3OCO4)C(C2C5=CC6=C(C=C51)OCO6)O 339.30 unknown via CMAUP database
(-)-Tetrahydrocolumbamine 440229 Click to see 341.40 unknown via CMAUP database
(R)-Canadine 443422 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
(S)-Canadine 21171 Click to see 339.40 unknown via CMAUP database
(S)-Cheilanthifoline 440582 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O 325.40 unknown via CMAUP database
Berberine 2353 Click to see 336.40 unknown via CMAUP database
Coptisine 72322 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6 320.30 unknown via CMAUP database
Isocorypalmine, (+)- 71261649 Click to see 341.40 unknown via CMAUP database
Ophiocarpine 12313750 Click to see 355.40 unknown via CMAUP database
Stylopine 440583 Click to see 323.30 unknown via CMAUP database
Tetrahydroscoulerine 45490416 Click to see 322.30 unknown via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see 369.40 unknown via CMAUP database
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown via CMAUP database
> Benzenoids / Naphthalenes
2-Naphthaldehyde 6201 Click to see C1=CC=C2C=C(C=CC2=C1)C=O 156.18 unknown via CMAUP database
4,5,6-Trimethoxy-2-naphthaldehyde 129711718 Click to see 246.26 unknown https://doi.org/10.1039/JR9650004292
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
6-Hydroxy-4,5-dimethoxy-2-naphthalenecarboxylic acid 73013858 Click to see 248.23 unknown https://doi.org/10.1016/S0031-9422(00)85856-2
6-Hydroxy-4,5-dimethoxy-2-naphthalenecarboxylic acid methyl ester 73013859 Click to see COC1=C2C(=CC(=C1)C(=O)OC)C=CC(=C2OC)O 262.26 unknown https://doi.org/10.1016/S0031-9422(00)85856-2
> Benzenoids / Naphthalenes / Naphthols and derivatives
4-Hydroxy-3,5-dimethoxy-2-naphthaldehyde 16086621 Click to see 232.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.039
4-Hydroxy-5-methoxy-2-naphthaldehyde 70697231 Click to see COC1=CC=CC2=CC(=CC(=C21)O)C=O 202.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.039
5-Hydroxy-4-methoxynaphthalene-2-carbaldehyde 85769556 Click to see COC1=C2C(=CC(=C1)C=O)C=CC=C2O 202.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.039
6-Hydroxy-4,5-dimethoxynaphthalene-2-carbaldehyde 162968220 Click to see 232.23 unknown https://doi.org/10.1039/JR9650004292
> Benzenoids / Naphthalenes / Naphthoquinones
6-(1,8-Dihydroxy-6-methylnaphthalen-2-yl)-5-hydroxy-2-methylnaphthalene-1,4-dione 86103922 Click to see 360.40 unknown https://doi.org/10.1016/S0031-9422(00)84966-3
https://doi.org/10.1016/S0031-9422(97)01020-0
Diospyrin 308140 Click to see 374.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.039
Plumbagin 10205 Click to see 188.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.039
> Lignans, neolignans and related compounds
Elliptinone 146680 Click to see CC1=CC(=O)C2=C(C1=O)C=CC(=C2O)C3=C(C4=C(C=C3)C(=O)C(=CC4=O)C)O 374.30 unknown https://doi.org/10.1016/S0031-9422(00)84966-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see 382.70 unknown https://doi.org/10.1016/S0031-9422(01)00006-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate 21636205 Click to see 1251.40 unknown via CMAUP database
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(01)00006-1
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-ol 51340201 Click to see 442.70 unknown via CMAUP database
(3beta,13alpha,14beta)-13-Methyl-26-norurs-7-en-3-ol 111220 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(01)00006-1
(3S,6bS,8aR,12S,12aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,7,8,9,10,11,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol 5321743 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C 426.70 unknown via CMAUP database
alpha-Amyrenone 12306155 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(01)00006-1
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(01)00006-1
alpha-Amyrin acetate 92842 Click to see 468.80 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(01)00006-1
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(01)00006-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(01)00006-1
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(01)00006-1
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles
2,4-Dimethylimidazole 70259 Click to see 96.13 unknown via CMAUP database
4-Methylimidazole 13195 Click to see 82.10 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(1S,12R,13R,20S)-13,20-dimethoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one 10831417 Click to see 346.30 unknown via CMAUP database
(1S,12R,13S,20S)-13-hydroxy-20-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one 10496772 Click to see 332.30 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Kushecarpin A 10495761 Click to see 318.32 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
(-)-Sophoramine 169014 Click to see 244.33 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(3S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate 6920044 Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-] 216.24 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Noroxyhydrastinine 89047 Click to see 191.18 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
[(7S,10R,11S)-9,9-dimethyl-16-oxo-14-phenyl-5,8,13-trioxatetracyclo[10.4.0.02,6.07,11]hexadeca-1(12),2(6),3,14-tetraen-10-yl] acetate 162893780 Click to see 392.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.039
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
(+)-Kuraramine 46187187 Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO 222.28 unknown via CMAUP database
6-[(3R,5R)-5-(hydroxymethyl)-1-methylpiperidin-3-yl]-1H-pyridin-2-one 101665417 Click to see 222.28 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Corypalline 280225 Click to see 193.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2,4-Dihydroxy-5-prenylphenyl)-5,6-methylenedioxybenzofuran 15953774 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=CC3=CC4=C(C=C3O2)OCO4)C 338.40 unknown via CMAUP database
2'-Hydroxy-4'-methoxy-5,6-methylenedioxy-2-phenylbenzofuran 44260109 Click to see COC1=CC(=C(C=C1)C2=CC3=CC4=C(C=C3O2)OCO4)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown via CMAUP database
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Graveolone 177751 Click to see CC1(CC(=O)C2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S,2''S)-6-lavandulyl-5,7,2',4'-tetrahydroxylflavanone 118975901 Click to see 424.50 unknown via CMAUP database
(2S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one 38351420 Click to see 370.40 unknown via CMAUP database
Kushenol V 10572194 Click to see 386.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R)-3,5-dihydroxy-2-(7-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 11351168 Click to see 440.50 unknown via CMAUP database
(2R,3S)-2-(2,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-((R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl)chroman-4-one 102004822 Click to see 454.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2,3-dihydrochromen-4-one 44563159 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O 442.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 6565899 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 26209050 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 438.50 unknown via CMAUP database
(2S)-2'-methoxykurarinone 11982641 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 452.50 unknown via CMAUP database
(2S)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 14258999 Click to see 370.40 unknown via CMAUP database
(2S)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one 44563122 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O 426.50 unknown via CMAUP database
(2S)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 60039901 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 452.50 unknown via CMAUP database
(2S)-Euchrenone A7 44593508 Click to see 340.40 unknown via CMAUP database
(2S)-Isoxanthohumol 9928523 Click to see 354.40 unknown via CMAUP database
CID 102004745 102004745 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C 492.60 unknown via CMAUP database
Isobavachin 193679 Click to see 324.40 unknown via CMAUP database
Kurarinol 44563198 Click to see 456.50 unknown via CMAUP database
Kurarinone 11982640 Click to see 438.50 unknown via CMAUP database
Kushenol A 44563121 Click to see 408.50 unknown via CMAUP database
Kushenol E 127234 Click to see 424.50 unknown via CMAUP database
Kushenol H 44584091 Click to see 472.50 unknown via CMAUP database
Kushenol I 20832634 Click to see 454.50 unknown via CMAUP database
Kushenol L 21721878 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC=C(C)C)O)C 440.50 unknown via CMAUP database
Kushenol M 180948 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC(CC=C(C)C)C(=C)C)O)C 508.60 unknown via CMAUP database
Kushenol R 42607847 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C 422.50 unknown via CMAUP database
Kushenol S 10854625 Click to see 340.40 unknown via CMAUP database
Kushenol U 42608062 Click to see 422.50 unknown via CMAUP database
KushenolK 44428630 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O 472.50 unknown via CMAUP database
Leachianone A 44593449 Click to see 438.50 unknown via CMAUP database
Leachianone G 5275227 Click to see 356.40 unknown via CMAUP database
Sophoraflavanone B 480764 Click to see 340.40 unknown via CMAUP database
Sophoraflavanone G 72936 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Licoflavonol 5481964 Click to see 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
3-Hydroxy-2-(4-hydroxyphenyl)-5-methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one 11451469 Click to see 368.40 unknown via CMAUP database
5-Hydroxy-4-(4-hydroxyphenyl)-10,10,16,16-tetramethyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,4,7,13-tetraen-6-one 11327657 Click to see 422.50 unknown via CMAUP database
8-Prenylkaempferol 5318624 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 354.40 unknown via CMAUP database
Isoanhydroicaritin 5322079 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C 368.40 unknown via CMAUP database
Kushenol C 5481237 Click to see 438.50 unknown via CMAUP database
Kushenol G 44259516 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O 456.50 unknown via CMAUP database
Sophoflavescenol 9929189 Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5318902 Click to see 562.50 unknown via CMAUP database
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 91510 Click to see 284.26 unknown via CMAUP database
(-)-Maackiain-3-O-glucosyl-6''-O-malonate 23724669 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5=CC6=C(C=C25)OCO6 532.40 unknown via CMAUP database
(+)-Maackiain 161298 Click to see 284.26 unknown via CMAUP database
(+)-Medicarpin 73067 Click to see 270.28 unknown via CMAUP database
(1S,12S)-16-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaene 373519 Click to see 298.29 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol 6326060 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown via CMAUP database
(6aR,11aR)-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8,9-diol 361910 Click to see 286.28 unknown via CMAUP database
(6aR,11aR)-3,9-Dimethoxy-6H-benzofuro(3,2-c)(1)benzopyran-6a(11aH)-ol 442828 Click to see 300.30 unknown via CMAUP database
(6aR,11aR)-8-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 21676223 Click to see COC1=C(C=C2C(=C1)C3COC4=C(C3O2)C=CC(=C4)O)O 286.28 unknown via CMAUP database
CID 44428627 44428627 Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O 300.30 unknown via CMAUP database
Pterocarpin 1715306 Click to see 298.29 unknown via CMAUP database
Trifolirhizin 442827 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3',4',7-Trihydroxyisoflavone 5284648 Click to see 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-5,7-dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 101238023 Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC4=C(C=C3O)OCO4)O)C 384.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
5,7-Dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)chromen-4-one 101238024 Click to see 382.40 unknown via CMAUP database
Alpinumisoflavone 5490139 Click to see 336.30 unknown via CMAUP database
Lupalbigenin 10001388 Click to see 406.50 unknown via CMAUP database
Luteone 5281797 Click to see 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(1,3-benzodioxol-5-yl)-7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 102131643 Click to see 576.50 unknown via CMAUP database
3-(3,4-Dihydroxyphenyl)-7-(((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl) oxy)-4h-chromen-4-one 68607439 Click to see 432.40 unknown via CMAUP database
3-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 73603979 Click to see 578.50 unknown via CMAUP database
3'-Methoxy-4'-hydroxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 102131642 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O 578.50 unknown via CMAUP database
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-(3-hydroxy-4-methoxyphenyl)chromen-4-one 73603978 Click to see 578.50 unknown via CMAUP database
Calycosin 7-O-xylosylglucoside 73603980 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 578.50 unknown via CMAUP database
Daidzein 7-O-apiosyl-(1->6)-glucoside 20055730 Click to see 548.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see 284.26 unknown via CMAUP database
Koparin 5318834 Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A 5280373 Click to see 284.26 unknown via CMAUP database
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Kuraridin 44428631 Click to see 438.50 unknown via CMAUP database
Xanthohumol 639665 Click to see CC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=C(C=C2)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
1-(3-hydroxy-4-methoxyphenyl)-2-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]ethane-1,2-dione 73603972 Click to see 582.50 unknown via CMAUP database
1-[4-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2-hydroxyphenyl]-2-(3-hydroxy-4-methoxyphenyl)ethane-1,2-dione 73603983 Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)O)O 582.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see 302.19 unknown https://doi.org/10.1016/S0031-9422(01)00006-1

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