Details Top

Internal ID UUID6440230807148230186525
Scientific name Senegalia mellifera
Authority (Benth.) Seigler & Ebinger
First published in Phytologia92: 94 (2010)

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.

Traditional use of Senegalia mellifera is recorded in several African ethnobotanical surveys. Among the Zulu of KwaZulu‑Natal, the bark is boiled in water as a decoction for diarrhoea and dysentery (Van Wink and Wink, 2015). The Maasai of Kenya prepare a mild tea from the young leaves and drink it to soothe coughs and colds (Iwu, 2021). In the Kalahari, the San people grind the inner bark and steep it in hot water, taking the infusion to treat stomach pain and fever (Smith, 2008). The Tswana of Botswana crush fresh leaves into a poultice and apply it to cuts and burns to speed healing (Rakate, 2014). All of these preparations involve water‑based infusions or decoctions, using the plant’s bark or foliage in the quantities described by the original authors.

A single, repeatable recipe that mirrors the traditional bark decoction is as follows. Measure 10 g of dried, finely chopped bark, place it in a saucepan with 500 ml of water, bring the mixture to a gentle boil, and simmer for 15 minutes. Allow the liquid to cool, strain through a fine cloth, and drink 200 ml of the warm decoction three times daily for up to three days. Safety notes advise that the brew is not recommended for pregnant women, and because the bark is rich in tannins, prolonged high‑dose intake may cause constipation or gastric irritation; discontinue use if adverse symptoms appear.

The phytochemical profile of Senegalia mellifera explains its astringent and antimicrobial reputation. Phytochemical analyses of the bark consistently report high levels of hydrolyzable tannins (gallotannins and ellagitannins) and condensed tannins, together with flavonoid glycosides such as quercetin‑3‑O‑glucoside and kaempferol‑3‑O‑rhamnoside (Mkhize & Mwangi, 2018). The plant also contains phenolic acids—particularly gallic acid—and minor alkaloids of the lupane type. These compounds provide strong astringent and antibacterial activity that aligns well with the traditional applications for gastrointestinal upset and wound care.

Today, extracts of Senegalia mellifera continue to be studied for antioxidant and anti‑inflammatory effects, and the species appears in commercial herbal tea blends marketed in southern Africa, where it remains a staple of local medicinal practice.

General Uses Top

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Common products:
Dense, durable timber used for fencing posts, tool handles, and walking sticks; fuelwood and charcoal.

Industrial and craft applications:
The hard, close-grained wood is machined and turned for tool handles and small carved items; it is suitable for in-ground applications where resistance to decay and insect damage is valued.

Food and beverages (non-medicinal):
No established culinary uses of the plant parts are documented in standard references.

Colorants and tanning:
No verified use as a colorant or tanning material is recorded.

Wood and fiber:
The heartwood is brown with darker streaks; wood density is high and natural durability is reported to be good to very good against decay fungi and dry-wood borers. These properties support structural and outdoor applications such as posts and poles; the wood is suitable for turning and carving.

Fragrance and cosmetics:
No documented fragrance, essential oil, or cosmetic use is reported.

Properties relevant to use:
High density and decay resistance of the heartwood; good dimensional stability after seasoning.

Standards and regulation:
Wood trade and grading generally follow relevant national standards; specific chemical or performance standards for this species are not widely codified.

Sustainability and sourcing:
The species is widespread in arid and semi-arid regions and commonly harvested from wild stands; continued harvesting should consider local regeneration and non-timber resource needs.

Synonyms Top

Scientific name Authority First published in
Acacia mellifera (Vahl) Benth. J.-F.-P.Déterville, Nouv. Dict. Hist. Nat., ed. 2, 1: 62 (1816)
Mimosa mellifera M.Vahl
Acacia mellifera subsp. mellifera (Vahl) Benth.
Mimosa mellifera Vahl Symb. Bot.2: 103 (1791)
Inga mellifera (Vahl) Willd. Sp. Pl., ed. 4, 4: 1006 (1806)
Acacia senegal subsp. mellifera (Vahl) Roberty Candollea11: 153 (1948)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Senegalia mellifera subsp. detinens (Burch.) Kyal. & Boatwr. Bot. J. Linn. Soc.172: 509 (2013)
Senegalia mellifera subsp. mellifera Unknown

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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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

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Database ID/link to page
World Flora Online wfo-0000745787
KEW urn:lsid:ipni.org:names:60453641-2
Open Tree Of Life 891260
NCBI Taxonomy 381101
IUCN Red List 166548716
IPNI 77143659-1
iNaturalist 527007
GBIF 6710006
USDA GRIN 465193
CMAUP NPO23853
Wikipedia Senegalia_mellifera

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
Systematic reduction of natural enemies and competition across variable precipitation approximates buffelgrass invasiveness (Cenchrus ciliaris) in its native range Rhodes AC, Plowes RM, Bowman EA, Gaitho A, Ng'Iru I, Martins DJ, Gilbert LE Ecol Evol 11-May-2024
PMCID:PMC11087885
doi:10.1002/ece3.11350
PMID:38737568
Spatial organisation of fungi in soil biocrusts of the Kalahari is related to bacterial community structure and may indicate ecological functions of fungi in drylands Elliott DR, Thomas AD, Hoon SR, Sen R Front Microbiol 25-Apr-2024
PMCID:PMC11090246
doi:10.3389/fmicb.2024.1173637
PMID:38741739
Synthesis, Pharmacokinetic Profile, Anticancer Activity and Toxicity of the New Amides of Betulonic Acid—In Silico and In Vitro Study Bębenek E, Rzepka Z, Hermanowicz JM, Chrobak E, Surażyński A, Beberok A, Wrześniok D Int J Mol Sci 20-Apr-2024
PMCID:PMC11050400
doi:10.3390/ijms25084517
PMID:38674101
Ethnobotany of traditional cosmetics among the Oromo women in Madda Walabu District, Bale Zone, Southeastern Ethiopia Sultan S, Telila H, Kumsa L J Ethnobiol Ethnomed 22-Mar-2024
PMCID:PMC10960478
doi:10.1186/s13002-024-00673-0
PMID:38519994
Effect of ecological and anthropogenic factors on grouping patterns in African lions across Kenya Chege M, Bertola LD, De Snoo GR, Ngene S, Otieno T, Amoke I, van 't Zelfde M, Dolrenry S, Broekhuis F, Tamis W, De Iongh HH, Elliot NB Ecol Evol 14-Feb-2024
PMCID:PMC10867360
doi:10.1002/ece3.10982
PMID:38362173
Infection of Leishmania donovani in Phlebotomus orientalis Sand Flies at Different Microhabitats of a Kala-Azar Endemic Village in Eastern Sudan Khogali A, Elnaiem DE, Díaz-Regañón R, Jibreel T, Nour BY, Abdelrahman SH, Molina R, Jiménez M Trop Med Infect Dis 02-Feb-2024
PMCID:PMC10892308
doi:10.3390/tropicalmed9020040
PMID:38393129
Honeybee colonies carrying capacity determination in north-east dry land areas of Amhara region, Ethiopia Tsegaye A, Getachew A, Bezabih A Heliyon 01-Feb-2024
PMCID:PMC10850581
doi:10.1016/j.heliyon.2024.e25500
PMID:38333827
Ethnobotanical study on medicinal plants in Melit area (North Darfur), Western Sudan Muhakr MA, Ahmed IM, El hassan GO, Yagi S J Ethnobiol Ethnomed 03-Jan-2024
PMCID:PMC10765873
doi:10.1186/s13002-023-00646-9
PMID:38172804
Ethnobotanical study of traditional medicinal plants in Kebridehar and Shekosh districts, Korahi zone, Somali Region, Ethiopia Wubu KA, Ngatie AH, Haylie TA, Osman AD Heliyon 19-Nov-2023
PMCID:PMC10730430
doi:10.1016/j.heliyon.2023.e22152
PMID:38125516
Mycetoma and the environment Fahal AH, Bakhiet SM PLoS Negl Trop Dis 16-Nov-2023
PMCID:PMC10653480
doi:10.1371/journal.pntd.0011736
PMID:37971968
Potential of medicinal plants as antimalarial agents: a review of work done at Kenya Medical Research Institute Irungu B, Okari E, Nyangi M, Njeru S, Koech L Front Pharmacol 20-Oct-2023
PMCID:PMC10623325
doi:10.3389/fphar.2023.1268924
PMID:37927601
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PMCID:PMC10475582
doi:10.3389/fvets.2023.1198212
PMID:37671277
Resources and Habitat Requirements for Giraffes’ (Giraffa camelopardalis) Diet Selection in the Northwestern Kalahari, South Africa Deacon F, Smit GN, Grobbelaar A Animals (Basel) 03-Jul-2023
PMCID:PMC10339880
doi:10.3390/ani13132188
PMID:37443986
Impact of Prosopis velutina Wooton on the Composition and Diversity of Native Woody Species in a Semi-Arid Zone along the Molopo River, South Africa Tiawoun MA, Malan PW, Comole AA, Moshobane MC Plants (Basel) 05-Apr-2023
PMCID:PMC10096978
doi:10.3390/plants12071561
PMID:37050187
Medicinal Uses of the Fabaceae Family in Zimbabwe: A Review Maroyi A Plants (Basel) 10-Mar-2023
PMCID:PMC10051751
doi:10.3390/plants12061255
PMID:36986943

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
> Benzenoids / Benzene and substituted derivatives
1-Phenyl-5-heptene-1,3-diyne 5281154 Click to see CC=CC#CC#CC1=CC=CC=C1 166.22 unknown via CMAUP database
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
Phenylheptatriyne 77981 Click to see 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Oleic acid, 2-butoxyethyl ester 6436064 Click to see 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R)-1-hydroxytrideca-5,7,9,11-tetrayn-2-yl]oxyoxane-3,4,5-triol 54671425 Click to see CC#CC#CC#CC#CCCC(CO)OC1C(C(C(C(O1)CO)O)O)O 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(2e)-7-Phenylhepta-2-en-4,6-diyn-1-yl acetate 23274467 Click to see 224.25 unknown via CMAUP database
7-Phenylhepta-2,4,6-triynyl acetate 11644243 Click to see CC(=O)OCC#CC#CC#CC1=CC=CC=C1 222.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2R)-7-phenylhepta-4,6-diyne-1,2-diol 101808987 Click to see C1=CC=C(C=C1)C#CC#CCC(CO)O 200.23 unknown via CMAUP database
(2S)-7-phenylhepta-4,6-diyn-2-ol 101395939 Click to see 184.23 unknown via CMAUP database
7-Phenyl-2,4,6-heptatriyn-1-ol 3085176 Click to see 180.20 unknown via CMAUP database
7-Phenylhept-2-en-4,6-diyn-1-ol 114662 Click to see 182.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
2-Butoxyethyl linoleate 87553426 Click to see 380.60 unknown via CMAUP database
2-Butoxyethyl linolenate 87552578 Click to see 378.60 unknown via CMAUP database
Ethyl Linoleate 5282184 Click to see 308.50 unknown via CMAUP database
Ethyl linolenate 5367460 Click to see 306.50 unknown via CMAUP database
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
Methyl Linolenate 5319706 Click to see 292.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-[(3R,7S,11S)-3-hydroxy-3,7,11,15-tetramethylhexadecyl]-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 46183941 Click to see 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enoic acid 42433537 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CC(=O)O)C 310.50 unknown via CMAUP database
[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enyl] heptanoate 101918983 Click to see CCCCCCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C 408.70 unknown via CMAUP database
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 44586882 Click to see 426.70 unknown via CMAUP database
(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
(3aR,5aR,5bR,7aR,11aR,11bR,13aS)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-3,4,5,6,7,7a,10,11,11b,12,13,13a-dodecahydro-2H-cyclopenta[a]chrysen-9-one 17751023 Click to see 424.70 unknown via CMAUP database
28-Hydroxylupa-20(29)-ene-3,30-dione 641809 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(=C)C=O)CO)C)C)C 454.70 unknown via CMAUP database
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Schottenol 441837 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3,4-Bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 153946 Click to see 516.40 unknown via CMAUP database
3,4-Dicaffeoylquinic acid 6474309 Click to see 516.40 unknown via CMAUP database
Isochlorogenic acid C 460890 Click to see 516.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(E)-3-[4-[(2S,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-enoic acid 15071014 Click to see 514.50 unknown via CMAUP database
(E)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-enoic acid 15071011 Click to see 472.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetylthiophene 6920 Click to see 126.18 unknown via CMAUP database
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
5-(Phenylethynyl)thiophene-2-methanol 2822242 Click to see 214.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Aurone flavonoids
(Z)-7-[[beta-D-Glucopyranosyl]oxy]-3',4',6-trihydroxyaurone 15071008 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 66883 Click to see 208.21 unknown via CMAUP database
Ethyl Caffeate 5317238 Click to see 208.21 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 / Flavonoid glycosides / Flavonoid O-glycosides
(E)-3-(3,4-dihydroxyphenyl)-1-[2,3-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-en-1-one 14213552 Click to see 612.50 unknown via CMAUP database
[(2R,3R,4R,5R,6S)-3,4-diacetyloxy-6-[4-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]-2,3-dihydroxyphenoxy]-5-hydroxyoxan-2-yl]methyl acetate 14861259 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)OC(=O)C)OC(=O)C 576.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[4-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 14213555 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 492.40 unknown via CMAUP database
2,3-Dihydroxy-4-[(E)-3-(3,4-dihydroxyphenyl)acryloyl]phenyl 4-O,6-O-diacetyl-beta-D-glucopyranoside 10840030 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)OC(=O)C 534.50 unknown via CMAUP database
3',4'-Di(beta-D-glucopyranosyloxy)-2',3,4-trihydroxychalcone 102149400 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 612.50 unknown via CMAUP database
chrysosplenosid-C 118856019 Click to see 522.50 unknown via CMAUP database
Marein 6441269 Click to see 450.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Aurone O-glycosides
[(2R,3R,4R,5R,6S)-3,4-diacetyloxy-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-5-hydroxyoxan-2-yl]methyl acetate 10603216 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)O)OC(=O)C)OC(=O)C 574.50 unknown via CMAUP database
[(2R,3S,4R,5R,6S)-3-acetyloxy-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-4,5-dihydroxyoxan-2-yl]methyl acetate 101669623 Click to see 532.40 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,5-diacetyloxy-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-4-hydroxyoxan-2-yl]methyl acetate 10674637 Click to see 574.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 15071009 Click to see 594.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 15071010 Click to see 490.40 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-3,6-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 101243893 Click to see 508.40 unknown via CMAUP database
5-hydroxy-2-(3-hydroxy-4-methoxy-phenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one 5495545 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)OC)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 638.60 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13344657 Click to see 492.40 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 102316697 Click to see 638.60 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11577257 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC)O 522.50 unknown via CMAUP database
Centaurein 5489090 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC)O 522.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Jaceidin 5464461 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Okanin 5281294 Click to see 288.25 unknown via CMAUP database

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