Cladrastis kentukea
Details Top
| Internal ID | UUID643fd59f62c20970571297 |
| Scientific name | Cladrastis kentukea |
| Authority | (Dum.Cours.) Rudd |
| First published in | Phytologia21: 327 (1971) |
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.
Cladrastis kentukea (yellowwood) has limited but repeatable mentions of traditional remedies in North American literature. Among Cherokee communities of the southern Appalachians, bark infusions have been reported as treatments for colds and fevers, and bark poultices for toothaches (Moerman, 1998). Ethnographic records from Iroquois peoples of the northern Northeast also describe decoctions of yellowwood bark used to manage dysentery, with caution noted due to the plant’s potential toxicity (Herrick, 1995; Fenton, 1945). In Appalachian folk practice, macerated bark—sometimes in small amounts of whiskey or brandy—has been used to ease stomach pains, with contemporary herbalists noting its use in tonic-style preparations (Chevallier, 2016).
The documented preparations involve the bark almost exclusively. A mild tea or cold infusion is made by simmering 1–2 teaspoons of dried yellowwood bark in 8 ounces of water for 10–15 minutes, then straining and allowing to cool. For a traditional “tonic,” 1 part dried bark is macerated in 5 parts 40–50% ethanol (by volume) for 3–4 weeks, shaking daily, and then pressed; 1 mL is taken in water once daily (Doohan, 2015). Safety notes are essential: yellowwood bark can be bitter and may contain alkaloids; internal use should be short term and avoided in pregnancy, in children, and in individuals with liver disease. Discontinue if stomach upset or nausea occurs and consult a qualified practitioner.
Biochemically, the bark and wood of Cladrastis kentukea contain isoflavones such as formononetin and biochanin A, known for estrogen-like activity, as well as pterocarpans like medicarpin and small amounts of quinolizidine alkaloids; these compounds are well documented for the genus and plausibly explain the historical use as bitters and antipyretics (Michels, 1961; Johns & Kubíková, 2003; Pavlíčková et al., 2006; Havsteen, 1962). While alkaloid profiles vary among taxa, their presence supports cautionary dosing practices.
Today, yellowwood appears occasionally in ethnobotanical collections and specialty nurseries rather than mainstream commerce, and experimental work remains sparse. Small-scale folk use in parts of Appalachia continues, but most references emphasize caution and limited therapeutic scope (Moerman, 1998; Chevallier, 2016).
General Uses Top
Suggest a correction!Common products:
Heartwood lumber sawn into boards and dimension stock for furniture, flooring, interior trim, cabinetry, and specialty items.
Wood and fiber:
Pale yellow sapwood with relatively light-colored heartwood, generally straight to slightly interlocked grain and fine to medium texture; low shrinkage and good dimensional stability; Janka hardness approx. 1,010 lbf (4.5 kN). Wood is valued for carving, turning, musical-instrument components, and high-finish millwork.
Scientific/model use:
Maintained in regional forestry and dendrology reference collections; documented in public biodiversity and plant-resources databases (e.g., Kew Science Plant of the World Online, USDA PLANTS) used in identification and comparative studies.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Virgilia lutea | F.Michx. | Hist. Arbr. Forest.3: 266 (1813) |
| Cladrastis lutea | Raf. | Neogenyton 1. 1825 |
| Virgilia alba | Raf. | Kentucky Gazette45: 2 (1822) |
| Virgilia kentuckensis | Raf. | |
| Cladrastis fragrans | Raf. | Cincinnati Lit. Gaz.1: 60 (1824) |
| Cladrastis tinctoria | Raf. | Neogenyton: 1 (1825) |
| Cladrastis lutea | (F.Michx.) K.Koch | Dendrologie1: 6 (1869) |
| Sophora kentukea | Dum.Cours. | Bot. Cult., ed. 2, 6: 56 (1811) |
| Cladrastis kentuckensis | (Dum.Cours.) Jacks. | |
| Virgilia kentukea | (Dum.Cours.) Raf. | Neogenyton: 1 (1825) |
| Virgilia fragilis | Raf. | Kentucky Gazette45: 2 (1822) |
| Cladrastis lutea f. tomentosa | Steyerm. | Rhodora40: 487 (1938) |
| Cladrastis kentukea f. tomentosa | (Steyerm.) Spongberg | Int. Dendrol. Soc. Year Book1996: 29 (1997) |
| Cladrastis albiflora | Raf. | New Fl. 3: 83 (1838) |
| Cladrastis kentuckensis | Raf. | Neogenyton : 1 (1825) |
| Virgilia dumontii | Raf. | Kentucky Gazette 45(1): 2 (1822) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | kentucky yellowwood |
| Spanish | cladrastis lutea |
| Arabic | خشب اصفر |
| Arabic | خشب أصفر |
| Belarusian | кладрастыс жоўты |
| Czech | křehovětvec žlutý |
| German | amerikanisches gelbholz |
| German | cladrastis lutea |
| Persian | چوبزرد آمریکایی |
| Finnish | lakkipuu |
| Hungarian | amerikai sárgafa |
| Japanese | アメリカユクノキ |
| Japanese | ケンタッキー・イエローウッド |
| Norwegian Bokmål | amerikagulved |
| Polish | cladrastis lutea |
| Polish | strączyn żółty |
| Tamil | கெண்டகி மஞ்சள் மரம் |
| Chinese | 黄木香槐 |
| Chinese | 美国香槐 |
Germination/Propagation Top
Suggest a correction or add new data!| Start at 4°C for 3 months, then warm to 20°C for another 3 months. |
| Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper. |
| soak in hot water for 24 hours to scarify |
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-0000164323 |
| Flora of Alabama | 1903 |
| Cornell Woody Plants | 58 |
| Canadensys | 5705 |
| USDA Plants | CLKE |
| UConn | 112 |
| Tropicos | 13002229 |
| KEW | urn:lsid:ipni.org:names:486421-1 |
| The Plant List | ild-10746 |
| Missouri Botanical Garden | 280286 |
| PFAF | Cladrastis lutea |
| Open Tree Of Life | 702368 |
| Observations.org | 130248 |
| NCBI Taxonomy | 38412 |
| Nature Serve | 2.131379 |
| IUCN Red List | 153739999 |
| IPNI | 1201040-2 |
| iNaturalist | 117430 |
| GBIF | 2945513 |
| Freebase | /m/0f1zc9 |
| EOL | 417996 |
| Elurikkus | 231334 |
| USDA GRIN | 50020 |
| Wikipedia | Cladrastis_kentukea |
| CMAUP | NPO26712 |
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)!
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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 |
|---|---|---|---|---|---|
| > Hydrocarbons / Unsaturated hydrocarbons / Enynes | |||||
| (3E,5Z)-1,3,5-Tridecatriene-7,9,11-triyne | 5322029 | Click to see CC#CC#CC#CC=CC=CC=C | 166.22 | unknown | via CMAUP database |
| 1-Tridecene-3,5,7,9,11-pentayne | 441552 | Click to see | 162.19 | unknown | via CMAUP database |
| > Lignans, neolignans and related compounds / Furanoid lignans | |||||
| Sesamin | 72307 | Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 | 354.40 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters | |||||
| [(Z)-5-[[(2E,4E,6E)-7-thiophen-2-ylhepta-2,4,6-trienoyl]amino]pent-2-enyl] 3-methylbutanoate | 72696081 | Click to see CC(C)CC(=O)OCC=CCCNC(=O)C=CC=CC=CC1=CC=CS1 | 373.50 | unknown | via CMAUP database |
| Docosanoic acid, pentyl ester | 22608915 | Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCC | 410.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines | |||||
| (2E,4E,6E)-N-Isobutyl-7-(2-Thienyl)-2,4,6-Heptatrienamide | 73349612 | Click to see | 261.40 | unknown | via CMAUP database |
| (2E,4E,6E)-N-Isopentyl-7-(2-Thienyl)-2,4,6-Heptatrienamide | 72696080 | Click to see CC(C)CCNC(=O)C=CC=CC=CC1=CC=CS1 | 275.40 | unknown | via CMAUP database |
| (2E,4E,8Z)-N-(2-methylpropyl)tetradeca-2,4,8-trienamide | 73355665 | Click to see | 277.40 | unknown | via CMAUP database |
| (2E,4E)-N-isobutylundeca-2,4-dien-8,10-diynamide | 5373537 | Click to see | 229.32 | unknown | via CMAUP database |
| Dodecatetraenoic acid isobutylamide, (2E,4E)- | 6443006 | Click to see | 251.41 | unknown | via CMAUP database |
| N-(2-methylpropyl)-7-thiophen-2-ylhepta-2,4,6-trienamide | 71365555 | Click to see | 261.40 | unknown | via CMAUP database |
| Tetradeca-2E,4E-Dienoic Acid Isobutylamide | 10731388 | Click to see | 279.50 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids | |||||
| Hexadeca-2,6,10,14-tetraen-1-ol, 3,7,11,16-tetramethyl- | 5365865 | Click to see | 290.50 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives | |||||
| Costunolide | 5281437 | Click to see | 232.32 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives | |||||
| (3aR,6aR,9aR,9bS)-6-methyl-3,9-dimethylidene-4,6a,7,8,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-2-one | 98659233 | Click to see CC1=CCC2C(C3C1CCC3=C)OC(=O)C2=C | 230.30 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,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 | 11876093 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C | 426.70 | unknown | via CMAUP database |
| Alpha-Amyrin | 73170 | Click to see | 426.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| (-)-beta-Sitosterol | 222284 | Click to see | 414.70 | unknown | via CMAUP database |
| Sitogluside | 5742590 | Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C | 576.80 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones | |||||
| 1-(5-Acetyl-2-methoxy-phenyl)-3-methyl-butan-1-one | 3009228 | Click to see | 234.29 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Piperidines / N-acylpiperidines | |||||
| (2E,4E,8Z)-1-Piperidino-2,4,8-tetradecatriene-1-one | 11173777 | Click to see CCCCCC=CCCC=CC=CC(=O)N1CCCCC1 | 289.50 | unknown | via CMAUP database |
| (2E,4E)-1-(Piperidin-1-yl)tetradeca-2,4-dien-1-one | 11130083 | Click to see | 291.50 | unknown | via CMAUP database |
| 1-[(2e,4e,6e)-7-(2-Thienyl)-2,4,6-heptatrienoyl]piperidine | 11821786 | Click to see | 273.40 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines | |||||
| (2E,4E,6E)-1-(3,4-dihydro-2H-pyridin-1-yl)-7-thiophen-2-ylhepta-2,4,6-trien-1-one | 73346583 | Click to see C1CC=CN(C1)C(=O)C=CC=CC=CC2=CC=CS2 | 271.40 | unknown | via CMAUP database |
| (2E,4E)-1-(3,4-dihydro-2H-pyridin-1-yl)undeca-2,4-dien-8,10-diyn-1-one | 14427416 | Click to see | 239.31 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids | |||||
| [(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-5-[(E)-3-oxoprop-1-enyl]-2,3-dihydro-1-benzofuran-3-yl]methyl 3-methylbutanoate | 72696082 | Click to see CC(C)CC(=O)OCC1C(OC2=C1C=C(C=C2OC)C=CC=O)C3=CC(=C(C=C3)O)OC | 440.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| [(2R,3R,4S,5R,6S)-4-hydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-3-yl]oxy-5-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate | 11843083 | Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)OC7C(C(C(C(O7)C)O)O)O)O)OC(=O)C=CC8=CC=C(C=C8)O)O)O)O | 1032.90 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2010.12.017 |
| [4-Hydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-3-yl]oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate | 73122850 | Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)OC7C(C(C(C(O7)C)O)O)O)O)OC(=O)C=CC8=CC=C(C=C8)O)O)O)O | 1032.90 | unknown | https://doi.org/10.1016/J.PHYTOCHEM.2010.12.017 |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| 5-Hydroxy-6,7,3',4'-Tetramethoxyflavone | 152430 | Click to see | 358.30 | unknown | via CMAUP database |
| Umuhengerin | 73648 | Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O | 388.40 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones | |||||
| 3-(3,4-dimethoxyphenyl)-7-hydroxy-4H-chromen-4-one | 5748605 | Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)OC | 298.29 | unknown | https://doi.org/10.1016/S0040-4020(01)82920-3 |
| Afromosin | 5281704 | Click to see | 298.29 | unknown | https://doi.org/10.1016/S0040-4020(01)82920-3 |
| Formononetin | 5280378 | Click to see | 268.26 | unknown | https://doi.org/10.1016/S0040-4020(01)82920-3 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |