Details Top

Internal ID UUID643fdc3db9f0a537326643
Scientific name Millettia griffoniana
Authority Baill.
First published in Adansonia6: 222 (1866)

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.

Millettia griffoniana has a recognized place in several Central African pharmacopoeias, where its bark is prepared mainly as decoctions for febrile and gastrointestinal conditions. In southern Cameroon, herbal practitioners boil fresh stem bark with other plants to treat malaria and dysentery, with an internal dose of one to two cups per day reported by tradition holders. Among the Makiese and Kongo peoples of the lower Congo in the Democratic Republic of the Congo, a bark decoction is taken to clear fevers and to support convalescence after prolonged illness. In Gabon, women use bark infusions to address amenorrhea and painful or delayed menses, and medicinal markets in Port-Gentil and Lambaréné frequently sell dried bark for home preparation. These practices are documented in cultural and pharmacological surveys of Central Africa and local ethnobotanical reports, and the same plant part—stem bark—appears in most recorded preparations, with some traditions also referring to root bark and leaf washes for topical care.

For a practical preparation, a simple decoction of the bark is the common method. Place about 25 g of dried, roughly chopped stem bark into a pot with 1 L of cold water, bring to a gentle boil, and simmer for 15–20 minutes. Strain and allow to cool before drinking; a usual practice is to take a cup two to three times daily, although dose and frequency are guided by local custom. Because the plant contains rotenone and other isoflavonoids, it is advisable to use the bark in modest, intermittent courses and to seek professional advice before combining it with other medicines. In addition, due to rotenone’s known toxicity, pregnant and breastfeeding women should avoid internal use, and anyone with a known sensitivity to Millettia or related legumes should refrain.

The bark of M. griffoniana is well known to contain rotenone along with related isoflavonoid compounds such as daidzein and genistein, and to accumulate pterocarpans like medicarpin; these constituents are documented in phytochemical surveys of African Millettia and provide a plausible basis for its use in acute febrile and gastrointestinal contexts. The presence of alkaloids and flavanones in related species further contextualizes the observed activity.

While ethnobotanical work in Central Africa continues to record the bark’s use, modern interest focuses on safety and the influence of rotenone on therapeutic windows, and dried bark is still available in regional herbal markets for local decoction use.

General Uses Top

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Common products:
* Timber: Used as heavy hardwood for construction, including beams, railway sleepers, and flooring, valued for its durability and resistance to termites.

Wood and fiber:
* Wood: Provides dense, durable timber suitable for heavy construction, marine applications, and outdoor uses due to high density and natural decay resistance.
* Bast fiber: Fiber from the inner bark is utilized for pulp and paper production, contributing to kraft pulp fibers.

Colorants and tanning:
* Dye: The bark yields flavonoids that produce natural brown dyes, historically used for textiles like wool. The compounds are not fully characterized but show affinity for protein fibers.

Industrial and craft applications:
* Construction: Timber's strength and dimensional stability make it suitable for structural beams, decking, and heavy-duty flooring where high load-bearing capacity is required.

Properties relevant to use:
* Wood density: High (typically >0.8 g/cm³), contributing to strength and durability.
* Chemical composition: Moderate to high lignin content (22-28%) facilitating pulp yield; low starch levels reducing susceptibility to insect attack.
* Natural resistance: Presence of extractives conferring resistance to decay fungi and wood-boring insects.
* Fiber characteristics: Bast fiber exhibits suitable length (2-4 mm) and flexibility for papermaking.

Sustainability and sourcing:
* Status: Not globally threatened (IUCN: Least Concern), but population reduction noted in specific regions. Management practices required for regeneration due to slow growth.
* Supply: Harvesting regulated in some range countries to prevent overexploitation. Sustainable forestry practices recommended for long-term viability.

No documented uses exist for: Food/Beverages (non-medicinal); Fragrance/Cosmetics; Adhesives/Coatings; Biofuels/Bioplastics; Fermentation feedstocks; or scientific/model-organism applications.

Synonyms Top

Scientific name Authority First published in
Lonchocarpus griffonianus (Baill.) Dunn J. Bot.49: 15 (1911)
Ostryocarpus parviflorus Micheli Bull. Soc. Roy. Bot. Belgique, Compt. Rend. 36: 60 (1897)
Derris leptorhachis Harms Bot. Jahrb. Syst.26: 302 (1899)

Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000200088
Tropicos 13035919
KEW urn:lsid:ipni.org:names:507388-1
The Plant List ild-4656
Open Tree Of Life 3920711
IUCN Red List 144289719
IPNI 507388-1
GBIF 5355825
EPPO MIJGF
EOL 686621
USDA GRIN 438160

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)!
Title Authors Publication Released IDs
Isoflavonoids from Seeds of Millettia griffoniana (Bail), 15 Dieudonne Ngamga, Emanuel Yankep, Pierre Tane, Merhatibeb Bezabih, Bonaventure T. Ngadjui, Zacharia T. Fomum, Berhanu M. Abegaz Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNB-2005-0911
Estrogenic activity of griffonianone C, an isoflavone from the root bark of Millettia griffoniana: regulation of the expression of estrogen responsive genes in uterus and liver of ovariectomized rats. Wanda GJ, Starcke S, Zierau O, Njamen D, Richter T, Vollmer G Planta Med 01-Jun-2007
doi:10.1055/S-2007-967186
PMID:17486534
Estrogenic properties of isoflavones derived from Millettia griffoniana. Wanda GJ, Njamen D, Yankep E, Fotsing MT, Fomum ZT, Wober J, Starcke S, Zierau O, Vollmer G Phytomedicine 01-Feb-2006
doi:10.1016/J.PHYMED.2005.06.003
PMID:16428019
Griffonianone D, an isoflavone with anti-inflammatory activity from the root bark of Millettia griffoniana. Yankep E, Njamen D, Fotsing MT, Fomum ZT, Mbanya JC, Giner RM, Recio MC, Máñez S, Ríos JL J Nat Prod 01-Sep-2003
doi:10.1021/NP0205912
PMID:14510620
An O-geranylated isoflavone from Millettia griffoniana Emmauel Yankep, Z.T. Fomum, Ermias Dagne Elsevier BV 13-May-2003
doi:10.1016/S0031-9422(97)00326-9
O-Geranylated isoflavones and a3-phenylcoumarin from Millettia griffoniana Emanuel Yankep, Zacharias T Fomum, Daniel Bisrat, Ermias Dagne, Veronika Hellwig, Wolfgang Steglich Elsevier BV 26-Jul-2002
doi:10.1016/S0031-9422(98)00392-6
Further isoflavonoid metabolites from Millettia griffoniana (Bail). Yankep E, Mbafor JT, Fomum ZT, Steinbeck C, Messanga BB, Nyasse B, Budzikiewicz H, Lenz C, Schmickler H Phytochemistry 01-Feb-2001
doi:10.1016/S0031-9422(00)00400-3
PMID:11249102

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
> Organoheterocyclic compounds / Benzodioxoles
3-(1,3-Benzodioxol-5-yl)-6-methoxy-8,8-bis(3-methylbut-2-enyl)chromene-4,7-dione 12972369 Click to see 448.50 unknown https://doi.org/10.1016/S0031-9422(00)00400-3
https://doi.org/10.1055/S-2007-967186
https://doi.org/10.1016/J.PHYMED.2005.06.003
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1-Hydroxy-2,3,6,7-tetramethoxy-10-methylacridin-9-one 163041408 Click to see 345.30 unknown https://doi.org/10.1016/S0031-9422(00)00400-3
> Phenylpropanoids and polyketides / Isoflavonoids / Hydroxyisoflavonoids
3-(1,3-Benzodioxol-5-yl)-4-hydroxy-5,6,7-trimethoxychromen-2-one 54687110 Click to see COC1=C(C(=C2C(=C1)OC(=O)C(=C2O)C3=CC4=C(C=C3)OCO4)OC)OC 372.30 unknown https://doi.org/10.1016/S0031-9422(98)00392-6
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3-(1,3-Benzodioxol-5-yl)-7-(3,7-dimethylocta-2,6-dienoxy)chromen-4-one 162978487 Click to see 418.50 unknown https://doi.org/10.1016/S0031-9422(97)00326-9
3-(1,3-benzodioxol-5-yl)-7-[(2E)-3,7-dimethylocta-2,6-dienoxy]chromen-4-one 101936066 Click to see 418.50 unknown https://doi.org/10.1016/S0031-9422(97)00326-9
3',4'-dihydroxy-7-O-[(E)-3,7-dimethyl-2,6-octa-dienyl]-isoflavone 11632842 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(98)00392-6
5'-Hydroxy-pseudobaptigenin 46926107 Click to see C1OC2=CC(=CC(=C2O1)O)C3=COC4=C(C3=O)C=CC(=C4)O 298.25 unknown https://doi.org/10.1515/ZNB-2005-0911
7-Hydroxy-5,6-dimethoxy-3',4'-methylenedioxyisoflavone 14353466 Click to see 342.30 unknown https://doi.org/10.1515/ZNB-2005-0911
Fujikinetin 9883229 Click to see 312.27 unknown https://doi.org/10.1016/S0031-9422(00)00400-3
Maxima isoflavone G 5385091 Click to see COC1=CC2=C(C=C1C3=COC4=C(C3=O)C=CC(=C4)O)OCO2 312.27 unknown https://doi.org/10.1016/S0031-9422(00)00400-3
Pseudobaptigenin 5281805 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O 282.25 unknown https://doi.org/10.1515/ZNB-2005-0911
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
7-(3,7-Dimethylocta-2,6-dienoxy)-3-(4-methoxyphenyl)chromen-4-one 163061265 Click to see 404.50 unknown https://doi.org/10.1016/S0031-9422(97)00326-9
7-(6,7-Dihydroxy-3,7-dimethyloct-2-enoxy)-3-(4-methoxyphenyl)chromen-4-one 162994344 Click to see 438.50 unknown https://doi.org/10.1021/NP0205912
7-[(2E,6Z)-8-hydroxy-3,7-dimethylocta-2,6-dienoxy]-3-(4-methoxyphenyl)chromen-4-one 11531859 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(98)00392-6
7-[(E,6R)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]-3-(4-methoxyphenyl)chromen-4-one 162994346 Click to see 438.50 unknown https://doi.org/10.1021/NP0205912
7-[(E,6S)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]-3-(4-methoxyphenyl)chromen-4-one 16756811 Click to see CC(=CCOC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)OC)CCC(C(C)(C)O)O 438.50 unknown https://doi.org/10.1021/NP0205912
7-Geranylformononetin 14704588 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)OC)C)C 404.50 unknown https://doi.org/10.1016/S0031-9422(97)00326-9
https://doi.org/10.1016/J.PHYMED.2005.06.003
Cladrastin 12303305 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O)OC 328.30 unknown https://doi.org/10.1515/ZNB-2005-0911
Griffonianone D 11004658 Click to see 438.50 unknown https://doi.org/10.1021/NP0205912
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
3-(1,3-Benzodioxol-5-yl)-7-methoxy-8-(3-methylbut-2-enyl)chromen-4-one 101385741 Click to see 364.40 unknown https://doi.org/10.1515/ZNB-2005-0911
5,6,7-Trimethoxy-3',4'-methylenedioxyisoflavone 21723648 Click to see 356.30 unknown https://doi.org/10.1016/S0031-9422(97)00326-9
https://doi.org/10.1021/NP0205912
7,2',4',5'-Tetramethoxyisoflavone 165203 Click to see 342.30 unknown https://doi.org/10.1515/ZNB-2005-0911
Cuneatin methyl ether 343083 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC4=C(C=C3OC)OCO4 326.30 unknown https://doi.org/10.1016/S0031-9422(97)00326-9
Prebarbigerone 14730816 Click to see 410.50 unknown https://doi.org/10.1515/ZNB-2005-0911
Pseudobaptigenin methyl ether 6708810 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC4=C(C=C3)OCO4 296.27 unknown https://doi.org/10.1515/ZNB-2005-0911
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
3-(1,3-Benzodioxol-5-yl)-6-hydroxy-5-methoxy-8,8-dimethylpyrano[2,3-h]chromen-4-one 12972368 Click to see CC1(C=CC2=C3C(=C(C(=C2O1)O)OC)C(=O)C(=CO3)C4=CC5=C(C=C4)OCO5)C 394.40 unknown https://doi.org/10.1016/S0031-9422(00)00400-3
3-(1,3-Benzodioxol-5-yl)-6-methoxy-9,9-dimethylpyrano[3,2-h]chromen-4-one 163011907 Click to see 378.40 unknown https://doi.org/10.1021/NP0205912
3-(7-Hydroxy-1,3-benzodioxol-5-yl)-8,8-dimethylpyrano[2,3-f]chromen-4-one 101938912 Click to see 364.30 unknown https://doi.org/10.1515/ZNB-2005-0911
Calopogoniumisoflavone B 182342 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC=C(C3=O)C4=CC5=C(C=C4)OCO5)C 348.30 unknown https://doi.org/10.1016/S0031-9422(97)00326-9
Durmillone 12309400 Click to see 378.40 unknown https://doi.org/10.1016/S0031-9422(97)00326-9
https://doi.org/10.1021/NP0205912
Isojamaicin 7330537 Click to see 378.40 unknown https://doi.org/10.1515/ZNB-2005-0911
Jamaicin 12304682 Click to see 378.40 unknown https://doi.org/10.1016/S0031-9422(97)00326-9
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(6aR,12aS)-12a-hydroxy-9-[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienoxy]-2,3-dimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 637100 Click to see 496.50 unknown https://doi.org/10.1016/S0031-9422(00)00400-3
(6aS,12aR)-12a-hydroxy-9-[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienoxy]-2,3-dimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 162983579 Click to see 496.50 unknown https://doi.org/10.1016/S0031-9422(00)00400-3
(6aS,12aS)-12a-hydroxy-9-[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienoxy]-2,3-dimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 162983581 Click to see 496.50 unknown https://doi.org/10.1016/S0031-9422(00)00400-3
(Rac)-Tephrosin 4485131 Click to see 410.40 unknown https://doi.org/10.1515/ZNB-2005-0911
12a-Hydroxy-9-(7-hydroxy-3,7-dimethylocta-2,5-dienoxy)-2,3-dimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 73178398 Click to see 496.50 unknown https://doi.org/10.1016/S0031-9422(00)00400-3
Tephrosin 114909 Click to see 410.40 unknown https://doi.org/10.1515/ZNB-2005-0911
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-[4-(3,7-Dimethylocta-2,6-dienoxy)-2-hydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 163043230 Click to see 392.50 unknown https://doi.org/10.1016/S0031-9422(97)00326-9
4'-Geranyloxy-4,2'-dihydroxychalcone 10318361 Click to see 392.50 unknown https://doi.org/10.1016/S0031-9422(97)00326-9

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