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Cleome brachycarpa

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644011f148aaf405910547
Scientific name Cleome brachycarpa
Authority Vahl ex DC.
First published in Prodr. 1: 240 (1824)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cleome brachycarpa var. angustifolia Gilg Annuario Reale Ist. Bot. Roma 6: 88 1896
Cleome brachycarpa f. diversifolia (Hochst. & Steud. ex T.Anderson) N.Terracc. Annuario Reale Ist. Bot. Roma 5: 114 1894
Cleome brachycarpa f. latifolia N.Terracc. Annuario Reale Ist. Bot. Roma 5: 114 1894
Cleome brevisiliqua Schult. & Schult.f. Syst. Veg., ed. 15 bis 7: 40 (1829)
Cleome diversifolia Hochst. & Steud. ex T.Anderson J. Proc. Linn. Soc., Bot. 5(Suppl. 1): 5 (1860)
Cleome moschata Stocks ex T.Anderson J. Proc. Linn. Soc., Bot. 5(Suppl. 1): 4 (1860)
Cleome parviflora R.Br. ex DC. Voy. Abyss. [Salt] Append. p. lxv. 1814 [Sep 1814] , nom. nud.
Cleome ruta Cambess. Voy. Inde 4: 19 (1841)
Cleome vahliana Fresen. Mus. Senckenberg. 2: 110 (1837)

Common names Top

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Language Common/alternative name
Arabic ذفرة قصيرة الثمار

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
    • Macaronesia
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Socotra
      • Somalia
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
    • West Tropical Africa
      • Mali
      • Mauritania
      • Niger
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Afghanistan
      • Iran
      • Sinai

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000611160
Tropicos 5900736
KEW urn:lsid:ipni.org:names:146948-1
The Plant List kew-2727199
Open Tree Of Life 517007
NCBI Taxonomy 1077933
IPNI 146948-1
iNaturalist 503294
GBIF 3871329
EPPO CLEBR

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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Title Authors Publication Released IDs
The Molecular Structure and Absolute Configuration of Brachycarpone, a New Trinortriterpenoid Dilactone from Cleome brachycarpa Viqar Uddin Ahmad, Khisal Ahmad Alvi, Masood A. Khan American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50044A009
Exudate flavonoids from aerial parts of four Cleome species Mohamed Sharaf, Ragaa M.A. Mansour, Nabiel A.M. Saleh Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(92)90084-Q
Cleocarpone, a triterpenoid from Cleome brachycarpa Viqar Uddin Ahmad, Sabiha Qazi, Nadeem Bin Zia, Changfu Xu, Jon Clardy Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85144-5
Deacetoxybrachycarpone, a trinortriterpenoid from Cleome brachycarpa Viqar Uddin Ahmad, Khisal Ahmad Alvi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81537-X

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1'R,4'S,5R,8R,9R,10R,13R,14R,17R)-1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethylspiro[2,5,6,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-3-one 163195156 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC45C6(CCC(O6)(O5)C(C)(C)O)C)C)C)C 472.70 unknown https://doi.org/10.1016/0031-9422(90)85144-5
(5R)-5-methyl-5-[(5R,8R,9R,10R,13R,14R,17S)-4,4,8,10,14-pentamethyl-3-oxo-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]oxolan-2-one 163195163 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(=O)O5)C)C)C)C 414.60 unknown https://doi.org/10.1016/S0031-9422(00)81537-X
1'-(2-hydroxypropan-2-yl)-4,4,4',8,10,14-hexamethylspiro[2,5,6,7,9,11,12,13,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,3'-2,7-dioxabicyclo[2.2.1]heptane]-3-one 14487122 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC45C6(CCC(O6)(O5)C(C)(C)O)C)C)C)C 472.70 unknown https://doi.org/10.1016/0031-9422(90)85144-5
5-Methyl-5-(4,4,8,10,14-pentamethyl-3-oxo-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl)oxolan-2-one 124222297 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(=O)O5)C)C)C)C 414.60 unknown https://doi.org/10.1016/S0031-9422(00)81537-X
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)81537-X
> 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-[(2S)-2-methyl-5-oxooxolan-2-yl]-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadecan-3-yl] acetate 101317834 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/10.1021/NP50044A009
[(1S,2R,3R,8R,11R,12R,15S,16S)-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 162903264 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/10.1016/S0031-9422(00)81537-X
[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/10.1016/S0031-9422(00)81537-X
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,2R,8R,11R,12R,15S,16R)-2,7,7,11,12-pentamethyl-15-[(2R)-2-methyl-5-oxooxolan-2-yl]-6-oxatetracyclo[9.7.0.02,8.012,16]octadecan-5-one 162952693 Click to see CC1(C2CCC3(C(C2(CCC(=O)O1)C)CCC4C3(CCC4C5(CCC(=O)O5)C)C)C)C 430.60 unknown https://doi.org/10.1016/S0031-9422(00)81537-X
2,7,7,11,12-Pentamethyl-15-(2-methyl-5-oxooxolan-2-yl)-6-oxatetracyclo[9.7.0.02,8.012,16]octadecan-5-one 162952692 Click to see CC1(C2CCC3(C(C2(CCC(=O)O1)C)CCC4C3(CCC4C5(CCC(=O)O5)C)C)C)C 430.60 unknown https://doi.org/10.1016/S0031-9422(00)81537-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Chrysosplenetin 5281608 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown https://doi.org/10.1016/0305-1978(92)90084-Q

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