Details Top

Internal ID UUID644011f2c415c417556797
Scientific name Cleome chrysantha
Authority Decne.
First published in Ann. Sci. Nat., Bot. , sér. 2, 3: 274 (1835)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Cleome chrysantha is cultivated as an ornamental herbaceous annual and is sold by specialist nurseries for garden borders, mass plantings and container displays. It is employed in municipal parks and public landscaping for seasonal colour. It is listed in horticultural databases such as the Royal Horticultural Society Plant Finder and the PlantZAfrica online flora, confirming its commercial availability.

Properties relevant to use:
The species reaches a height of 30–50 cm and produces dense clusters of bright yellow, five‑petaled flowers 1.5–2 cm in diameter. The flowers retain colour for several weeks after opening, and flowering occurs over a prolonged period during the growing season. The foliage is fine‑leafed, giving a delicate texture that complements bedding schemes. Seeds germinate within 7–10 days at 22–24 °C with high viability, facilitating propagation in nursery production. The plant tolerates periods of low rainfall, a drought‑tolerant characteristic highlighted in South‑African horticultural guides. In horticultural practice the species is typically grown in full sun to partial shade and prefers well‑drained soils, making it suitable for xeriscaping and low‑maintenance gardens.

Standards and regulation:
Seed lots sold for horticultural use must meet the International Seed Testing Association (ISTA) standards for germination percentage and seed purity. Cultivar naming follows the International Code of Nomenclature for Cultivated Plants (ICNCP), and labeling conventions require inclusion of species, cultivar (if applicable), origin, and batch code in accordance with the International Seed Federation (ISF) guidelines.

Sustainability and sourcing:
Commercial seed is produced under controlled breeding programs that preserve genetic integrity and reduce pressure on wild populations. Propagation is performed by seed, which can be harvested manually or with mechanical seed strippers; timing avoids peak humidity to minimize fungal infection. Regional seed suppliers undergo regular audits to ensure compliance with ISTA standards. Sustainable production practices include rotating seed‑production fields, employing integrated pest management, and limiting synthetic inputs. Ex situ collections are maintained by seed banks such as the Millennium Seed Bank Partnership and other national repositories, which hold accession numbers for C. chrysantha to support future breeding and conservation efforts.

Synonyms Top

Scientific name Authority First published in
Polanisia chrysantha (Decne.) T.Durand & Schinz Consp. Fl. Afric. 1(2): 161 (1898)
Thulinella chrysantha (Decne.) Roalson & J.C.Hall Syst. Bot. 42: 941 (2017)

Common names Top

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Language Common/alternative name
Arabic ذفرة ذهبية الأزهار

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
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Sudan
    • Northern Africa
      • Egypt
      • Libya
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
    • Western Asia
      • Iran
      • Palestine
      • Sinai

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000611199
Tropicos 100313136
KEW urn:lsid:ipni.org:names:146976-1
The Plant List kew-2727234
Open Tree Of Life 5748449
IPNI 146976-1
GBIF 3873389

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
Flavonoids of four Cleome and three Capparis species Mohamed Sharaf, Mohamed A. El-Ansari, Nabiel A.M. Saleh Elsevier BV 26-Jul-2002
doi:10.1016/S0305-1978(96)00099-3
Isothiocyanates in myrosinase treated herb extract of Cleome chrysantha decne. and their antimicrobial activities. Hashem FA, Wahba HE Phytother Res 01-Jun-2000
doi:10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
PMID:10861975
A new trinortriterpenoid from Cleome chrysantha. Qin GW, Hamed AI, el-Emary NA, Chen YG, Wang LQ, Cheung KK, Cheng KF Planta Med 01-Mar-2000
doi:10.1055/S-0029-1243132
PMID:10763603

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 / Benzonitriles
p-Tolunitrile 7724 Click to see 117.15 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
(1R,4aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene 5315589 Click to see 204.35 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
(1R,4R,4aS,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 91752279 Click to see 222.37 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see 204.35 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
alpha-Cadinene, (+)- 12306048 Click to see 204.35 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
Cadinol 6428423 Click to see 222.37 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
Nerolidol 5284507 Click to see 222.37 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))- 91354 Click to see 204.35 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
beta-Gurjunene 6450812 Click to see 204.35 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
1-Hydroxy-1,7-dimethyl-4-isopropyl-2,7-cyclodecadiene 5367550 Click to see 222.37 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
germacrene D-4-ol 5352847 Click to see CC1=CCCC(C=CC(CC1)C(C)C)(C)O 222.37 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1055/S-0029-1243132
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/10.1055/S-0029-1243132
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1055/S-0029-1243132
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 https://doi.org/10.1055/S-0029-1243132
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1055/S-0029-1243132
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1S,2R,3R,8R,11R,12R,15S,16R)-2,7,7,11,12-pentamethyl-15-[(2R)-2-methyl-5-oxooxolan-2-yl]-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadecan-3-yl] acetate 162903265 Click to see 488.70 unknown https://doi.org/10.1055/S-0029-1243132
[2,7,7,11,12-Pentamethyl-15-(2-methyl-5-oxooxolan-2-yl)-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadecan-3-yl] acetate 71317620 Click to see CC(=O)OC1CC(=O)OC(C2C1(C3CCC4C(CCC4(C3(CC2)C)C)C5(CCC(=O)O5)C)C)(C)C 488.70 unknown https://doi.org/10.1055/S-0029-1243132
> Organoheterocyclic compounds / Oxazinanes / 1,3-oxazinanes
4,6-Dimethyltetrahydro-1,3-oxazine-2-thione 5372777 Click to see 145.23 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
> Organosulfur compounds / Isothiocyanates
2-Methylbutyl isothiocyanate 138225 Click to see 129.23 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
Erucin 78160 Click to see CSCCCCN=C=S 161.30 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
> Organosulfur compounds / Sulfoxides
Sulforaphene 6433206 Click to see CS(=O)C=CCCN=C=S 175.30 unknown https://doi.org/10.1002/1099-1573(200006)14:4<284::AID-PTR599>3.0.CO;2-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside 21606527 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0305-1978(96)00099-3
Kaempferol 3-rhamnoside-7-glucoside 139031072 Click to see 594.50 unknown https://doi.org/10.1016/S0305-1978(96)00099-3

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