Details Top

Internal ID UUID643fd6c430dc2463172368
Scientific name Piliostigma thonningii
Authority (Schumach.) Milne-Redh.
First published in Hooker's Icon. Pl.35: t. 3460 (1947)

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.

Piliostigma thonningii, a small savanna tree of the legume family, is recorded in West and East African traditional medicine as a source of several simple preparations. In Ghana the leaves are commonly infused into a light tea that is taken to calm a cough or to soothe a sore throat (Burkill, 1995). Across Nigeria the bark is boiled in water to make a stronger decoction used for the relief of fever and malaria‑like symptoms, and the same decoction is also given to children with diarrhoea (Burkill, 1995). In Kenya the fresh leaves are pounded into a moist paste and applied as a poultice to cuts, sores or inflammatory skin lesions, a practice that is noted among the Maasai of the Rift Valley (Kokwaro, 1976). All three reports describe the plant parts exactly – leaves for infusions or poultices, bark for decoctions – and each cites the same species name, confirming that the therapeutic traditions refer to Piliostigma thonningii and not a related plant (Ayodele and Aderogba, 2021).

For a practical, mild preparation, a simple leaf tea can be made by steeping one tablespoon of dried, roughly crushed leaves in 250 ml of freshly boiled water for five to ten minutes, then straining. The resulting infusion is usually drunk warm, up to two cups a day. The same amount of dried bark can be simmered in 500 ml of water for fifteen minutes to produce a decoction that is taken in small doses (about 100 ml) three times daily for fever. While the preparations are generally considered safe for healthy adults, they should be avoided by pregnant or nursing women because reliable safety data for these uses are lacking, and anyone with a known allergy to legumes should discontinue use if any irritation occurs.

Phytochemical studies of the leaves and bark have consistently identified flavonoids such as quercetin and kaempferol, condensed and hydrolyzable tannins, saponins, and triterpenoids including lupeol and betulinic acid. These classes of compounds are well‑documented in the species and provide a plausible biochemical basis for the observed antimicrobial, anti‑inflammatory and antipyretic actions reported in traditional preparations.

Recent laboratory work has shown that extracts of Piliostigma thonningii inhibit the growth of several bacterial strains and display modest antiplasmodial activity in vitro, encouraging further pharmacological investigation. In rural markets the dried bark and leaf material are still sold for home‑made teas and poultices, and a few small‑scale herbal enterprises are beginning to package standardized leaf extracts for sale, indicating that the traditional uses continue to find a place alongside modern research.

General Uses Top

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Common products:
- Heartwood and sapwood used as timber for construction, furniture, tool handles, poles, and for fuel wood and charcoal.
- Bark harvested for tannin extraction, providing a natural leather‑tanning agent.
- Bark yields a red‑brown natural dye used in textile coloration, especially on protein fibers.
- Gum exuded from the bark is collected for use as a natural adhesive.

Industrial and craft applications:
- Timber is processed into structural members, flooring and furniture components for local and regional markets.
- Bark tannins are employed in industrial leather tanning, improving durability and water resistance of leather.
- The bark dye is applied in textile dyeing of wool, silk and cotton, giving a stable brown hue.
- Gum is incorporated into small‑scale adhesive formulations for wood‑working and paper repair.

Colorants and tanning:
- The bark contains condensed tannins (≈10–15 % of dry weight) that provide efficient leather tanning through cross‑linking of collagen.
- A separate fraction of the bark yields flavonoid/anthocyanin pigments that produce a red‑brown dye suitable for natural textile coloration.

Wood and fiber:
- Wood is a dense hardwood with average density 0.78–0.85 g cm⁻³, offering high strength and decay resistance, suitable for construction, furniture and tool handles.
- No significant bast‑fiber or other fiber uses are reported for this species.

Properties relevant to use:
- High wood density and durability support structural performance.
- Condensed tannin chemistry (proanthocyanidins) yields strong leather‑tanning capacity.
- Bark gum consists of water‑soluble polysaccharides (e.g., arabinogalactan) that provide tack in adhesive mixes.
- Dye pigments are stable under typical textile‑dyeing pH conditions.

Standards and regulation:
- Harvesting and export of timber are regulated by national forestry legislation (e.g., Kenya’s Forests Act, Tanzania’s Forest Management Guidelines) requiring permits and sustainable‑management plans.
- Tannin extracts are classified as industrial chemicals under national chemical‑safety legislation, with labeling and handling requirements.

Sustainability and sourcing:
- Commercial use relies on wild‑harvested material; the species is not widely cultivated.
- Sustainable harvesting practices (selective cutting, limited bark stripping, reforestation) and monitoring by FAO and regional forestry agencies are recommended to prevent over‑exploitation.

Synonyms Top

Scientific name Authority First published in
Bauhinia thonningii Schum.
Bauhinia abyssinica A.Rich. Tent. Fl. Abyss.1: 253 (1847)
Bauhinia articulata Oliv. Fl. Trop. Afr.2: 290 (1871)
Bauhinia pyrrhocarpa Hochst. Flora27: 99 (1844)
Bauhinia tamarindacea Delile F.Cailliaud, Voy. Méroé: 34 (1826)
Bauhinia thonningii Schumach. Beskr. Guin. Pl.: 203 (1827)
Piliostigma pyrrhocarpum (Hochst.) Hochst. Flora29: 598 (1846)
Bauhinia reticulata var. rubiginosa A.Chev. Explor. Bot. Afrique Occ. Franç.1: 217 (1920)

Common names Top

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Language Common/alternative name
Hausa cancali

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Namibia
      • Northern Provinces
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Rwanda
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000170413
Tropicos 13060937
KEW urn:lsid:ipni.org:names:514346-1
Open Tree Of Life 276253
NCBI Taxonomy 653098
IPNI 514346-1
iNaturalist 592162
GBIF 2953141
USDA GRIN 315117
CMAUP NPO17288

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
Comprehensive Review of Epidemiology and Treatment of Snakebite Envenomation in West Africa: Case of Benin Dossou AJ, Fandohan AB, Omara T, Chippaux JP J Trop Med 08-Apr-2024
PMCID:PMC11018376
doi:10.1155/2024/8357312
PMID:38623180
Woody Species Composition, Structure, and Status of Regeneration in Pugnido Forest, Gambella Region, Western Ethiopia Masresha G, Melkamu Y, Mulu G Scientifica (Cairo) 04-Apr-2024
PMCID:PMC11008979
doi:10.1155/2024/3961434
PMID:38605976
The complete chloroplast genome and phylogenetic analysis of Bauhinia glauca subsp. hupehana (Craib) T. C. Chen 1988 Ke QL, Li RY, Cai SS, Tang MQ, Cui LC, Lai CD, Li YH Mitochondrial DNA B Resour 11-Mar-2024
PMCID:PMC10930098
doi:10.1080/23802359.2024.2324928
PMID:38476838
Evaluation of packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
Identification of Novel Flavonoids and Ansa-Macrolides with Activities against Leishmania donovani through Natural Product Library Screening Phan TN, Lee H, Baek KH, No JH Pathogens 28-Feb-2024
PMCID:PMC10974828
doi:10.3390/pathogens13030213
PMID:38535556
Ethnobotanical study of wild edible plants in Dibatie district, Metekel zone, Benishangul Gumuz Regional State, western Ethiopia Anbessa B, Lulekal E, Getachew P, Hymete A J Ethnobiol Ethnomed 27-Feb-2024
PMCID:PMC10900549
doi:10.1186/s13002-024-00671-2
PMID:38413982
Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A J Ethnobiol Ethnomed 22-Feb-2024
PMCID:PMC10885532
doi:10.1186/s13002-024-00651-6
PMID:38389077
Data on fungal abundance and diversity in copper and cobalt contaminated tailing soils in Kitwe, Zambia Dusengemungu L, Gwanama C, Mubemba B Data Brief 12-Dec-2023
PMCID:PMC10770708
doi:10.1016/j.dib.2023.109951
PMID:38186741
Antihypertensive potential of the stem bark of Canarium schweinfurthii Engl. (Burseraceae) in wistar rats: UPLC-ESI-QToF-MS/MS-based prediction of antihypertensive phytochemicals Mbosso Teinkela JE, Nguemfo EL, Fokou Nzodjou T, Bogning Zangueu C, Kalinski JC, Tsakem B, Assob Nguedia JC, Siwe Noundou X Heliyon 04-Nov-2023
PMCID:PMC10663920
doi:10.1016/j.heliyon.2023.e21841
PMID:38027816
Medicinal plants of the upper Aswa River catchment of northern Uganda - a cultural crossroads Masters ET J Ethnobiol Ethnomed 27-Oct-2023
PMCID:PMC10605377
doi:10.1186/s13002-023-00620-5
PMID:37884931
Cytotoxicity, acute and sub-chronic toxicities of the leaves of Bauhinia thonningii (Schumach.) Milne-Redh. (Caesalpiniaceae) Matieta VY, Mbaveng AT, Nouemsi GR, Tankeo SB, Kamsu GT, Nayim P, Lannang AM, Çelik İ, Efferth T, Kuete V BMC Complement Med Ther 27-Sep-2023
PMCID:PMC10523748
doi:10.1186/s12906-023-04172-9
PMID:37752510
In-vitro antibacterial, antioxidant and anti-inflammatory and In-silico ADMET, molecular docking study on Hardwickia binata phytocompunds with potential inhibitor of skin cancer protein Manimegalai P, Selvam K, Prakash P, Kirubakaran D, Shivakumar MS, SenthilNathan S In Silico Pharmacol 23-Sep-2023
PMCID:PMC10517914
doi:10.1007/s40203-023-00163-3
PMID:37750071
Ethnomedicinal Knowledge of Plants Used in Nonconventional Medicine in the Management of Diabetes Mellitus in Kinshasa (Democratic Republic of the Congo) Chiribagula Valentin B, Ndjolo Philippe O, Mboni Henry M, Mushagalusa Kasali F Evid Based Complement Alternat Med 20-Sep-2023
PMCID:PMC10533323
doi:10.1155/2023/4621883
PMID:37771953
Indigenous medicinal plants used in folk medicine for malaria treatment in Kwara State, Nigeria: an ethnobotanical study Evbuomwan IO, Stephen Adeyemi O, Oluba OM BMC Complement Med Ther 16-Sep-2023
PMCID:PMC10504731
doi:10.1186/s12906-023-04131-4
PMID:37716985
Ethnobotanical study of nutraceutical plants used to manage opportunistic infections associated with HIV/AIDS in Acholi sub-region, Northern Uganda Ikinyom N, Lamwaka AV, Malagala AT, Ndyomugyenyi EK Trop Med Health 01-Sep-2023
PMCID:PMC10472741
doi:10.1186/s41182-023-00540-w
PMID:37658427

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
Latifoline 5281736 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C3(C(C(=O)OC3C)C)O 393.40 unknown https://doi.org/10.1016/0031-9422(96)00367-6
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol 13966170 Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C 304.50 unknown via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 11870275 Click to see 302.50 unknown via CMAUP database
(4aS,10aS)-1,2,3,4,4a,9,10,10a-Octahydro-4a-methyl-1-methylene-7-(1-methylethyl)phenanthrene 44268166 Click to see 254.40 unknown via CMAUP database
(4aS,9R,10aS)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 21764434 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C 286.50 unknown via CMAUP database
2-[(4bS,8aS)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propan-2-ol 101586702 Click to see 286.50 unknown via CMAUP database
7-Dehydroabietanone 11289118 Click to see 284.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see 300.40 unknown via CMAUP database
Abietatriene 6432211 Click to see 270.50 unknown via CMAUP database
Anticopalic acid 11808890 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C 304.50 unknown via CMAUP database
Ethyl abietate 61182 Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C 330.50 unknown via CMAUP database
Isopimara-7,15-diene 13969536 Click to see 272.50 unknown via CMAUP database
methyl (E)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate 11290126 Click to see 318.50 unknown via CMAUP database
Pimarol 12314285 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
Sandaracopimaradiene 443469 Click to see 272.50 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 / Diterpenoids / Kaurane diterpenoids
(1S,4S,5S,9S,10R,13R,14R)-14-hydroxy-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 21629512 Click to see 320.50 unknown https://doi.org/10.1002/(SICI)1097-458X(199712)35:12<896::AID-OMR150>3.0.CO;2-S
16-Hydroxy-(-)-kauranoic acid 494329 Click to see 320.50 unknown https://doi.org/10.1002/(SICI)1097-458X(199712)35:12<896::AID-OMR150>3.0.CO;2-S
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 101280203 Click to see 456.70 unknown via CMAUP database
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-8,19-dihydroxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-5-one 101280208 Click to see 456.70 unknown via CMAUP database
(1S,6R,8S,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 21672660 Click to see 456.70 unknown via CMAUP database
(3S,6R,8S,11R,12S,15S,16R,19S,21R)-8,19-dimethoxy-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene 101280202 Click to see 470.80 unknown via CMAUP database
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol 101121169 Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 460.70 unknown via CMAUP database
21-Episerratenediol 12309682 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown via CMAUP database
3beta-Methoxy-21-oxoserratene 14830066 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C 454.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one 3034666 Click to see 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 12943207 Click to see 410.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasta-3,5-dien-7-one 12444466 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
6,7-dihydroxy-7,7a-dihydro-6H-1-benzofuran-2-one 324687 Click to see 168.15 unknown https://doi.org/10.1021/NP50046A036
Griffonilide 100341 Click to see C1=CC2=CC(=O)OC2C(C1O)O 168.15 unknown https://doi.org/10.1021/NP50046A036
> Organoheterocyclic compounds / Naphthopyrans
(3S,4aR,6aS,10aS,10bR)-3-ethenyl-3,7,7,10a-tetramethyl-1,2,4a,5,6,6a,8,9,10,10b-decahydrobenzo[f]chromene 102594798 Click to see 276.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
5-Hydroxy-2-(4-hydroxyphenoxy)-7-methoxy-6-methylchromen-4-one 10615140 Click to see 314.29 unknown https://doi.org/10.1016/0031-9422(96)00367-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see 270.28 unknown via CMAUP database
Strobopinin 442520 Click to see 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/0031-9422(96)00367-6
Rhamnetin 5281691 Click to see 316.26 unknown https://doi.org/10.1021/NP50046A036
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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/10.1016/0031-9422(96)00367-6
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1016/0031-9422(96)00367-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-methoxy-6,8-dimethyl-4H-1-benzopyran-4-one 10783637 Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)C)O 344.30 unknown https://doi.org/10.1016/0031-9422(96)00367-6
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-methoxy-6,8-dimethyl-4H-1-benzopyran-4-one 44259654 Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)C)O 328.30 unknown https://doi.org/10.1016/0031-9422(96)00367-6
6-C-Methylquercetin 3-methyl ether 44259678 Click to see 330.29 unknown https://doi.org/10.1016/0031-9422(96)00367-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-5-hydroxy-3,7-dimethoxy-6-methyl-4H-1-benzopyran-4-one 10545366 Click to see 344.30 unknown https://doi.org/10.1016/0031-9422(96)00367-6
2-(3,4-Dihydroxyphenyl)-5-hydroxy-3,7-dimethoxy-6,8-dimethyl-4H-1-benzopyran-4-one 10642123 Click to see 358.30 unknown https://doi.org/10.1016/0031-9422(96)00367-6
6-C-Methylquercetin 3,7,3'-trimethyl ether 44259693 Click to see 358.30 unknown https://doi.org/10.1016/0031-9422(96)00367-6
6,8-Di-C-methylkaempferol 3,7-dimethyl ether 14353450 Click to see 342.30 unknown https://doi.org/10.1016/0031-9422(96)00367-6
Tectochrysin 5281954 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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