Croton steenkampianus - Unknown
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Internal ID UUID644036f11d572672771012
Scientific name Croton steenkampianus
Authority Gerstner
First published in J. S. African Bot. 12: 38 (1946)

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Language Common/alternative name
Afrikaans maputalandkoorsbessie

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Tanzania
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Kwazulu-Natal
      • Northern Provinces

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000932431
Tropicos 12802912
KEW urn:lsid:ipni.org:names:343532-1
The Plant List kew-51245
Open Tree Of Life 1025277
NCBI Taxonomy 992676
IPNI 343532-1
iNaturalist 583080
GBIF 3058591
EOL 1146550
CMAUP NPO26587

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
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
Antimalarial Activity of Extract and Fractions of Sauropus androgynus (L.) Merr. Ekasari W, Fatmawati D, Khoiriah SM, Baqiuddin WA, Nisa HQ, Maharupini AA, Wahyuni TS, Oktarina RD, Suhartono E, Sahu RK Scientifica (Cairo) 08-Sep-2022
PMCID:PMC9477630
doi:10.1155/2022/3552491
PMID:36119646
Medicinal Plants for Mitigating Pain and Inflammatory-Related Conditions: An Appraisal of Ethnobotanical Uses and Patterns in South Africa Aremu AO, Pendota SC Front Pharmacol 22-Oct-2021
PMCID:PMC8569556
doi:10.3389/fphar.2021.758583
PMID:34744737
Antiprotozoal and Antitumor Activity of Natural Polycyclic Endoperoxides: Origin, Structures and Biological Activity Dembitsky VM, Ermolenko E, Savidov N, Gloriozova TA, Poroikov VV Molecules 28-Jan-2021
PMCID:PMC7865715
doi:10.3390/molecules26030686
PMID:33525706
Deciphering composition and connectivity of a natural product with the assistance of MS and 2D NMR Vinokur AI, White PB, Fotsing MT, Arderne C, Ndinteh DT, Vestling MM, Guzei IA Acta Crystallogr C Struct Chem 24-Oct-2017
PMCID:PMC5674227
doi:10.1107/S2053229617014966
PMID:29111532
In vitro and in vivo anti-malarial activity of plants from the Brazilian Amazon Lima RB, Rocha e Silva LF, Melo MR, Costa JS, Picanço NS, Lima ES, Vasconcellos MC, Boleti AP, Santos JM, Amorim RC, Chaves FC, Coutinho JP, Tadei WP, Krettli AU, Pohlit AM Malar J 18-Dec-2015
PMCID:PMC4683771
doi:10.1186/s12936-015-0999-2
PMID:26682750
Antimicrobial and acetylcholinesterase inhibitory activities of Buddleja salviifolia (L.) Lam. leaf extracts and isolated compounds. Pendota SC, Aderogba MA, Ndhlala AR, Van Staden J J Ethnopharmacol 09-Jul-2013
doi:10.1016/J.JEP.2013.04.047
PMID:23665162
Antibacterial Activity of Extracts of Three Croton Species Collected in Mpumalanga Region in South Africa Selowa S, Shai L, Masoko P, Mokgotho M, Magano S Afr J Tradit Complement Altern Med 30-Dec-2009
PMCID:PMC3021162
doi:10.4314/ajtcam.v7i2.50861
PMID:21304619
Plant-Derived Antimalarial Agents: New Leads and Efficient Phytomedicines. Part II. Non-Alkaloidal Natural Products Batista R, de Jesus Silva Júnior A, de Oliveira AB Molecules 13-Aug-2009
PMCID:PMC6254980
doi:10.3390/molecules14083037
PMID:19701144
Bioactive diterpenes and other constituents of Croton steenkampianus. Adelekan AM, Prozesky EA, Hussein AA, Ureña LD, van Rooyen PH, Liles DC, Meyer JJ, Rodríguez B J Nat Prod 01-Nov-2008
doi:10.1021/NP800333R
PMID:18855442
The major flavonoid of Dodonaea angustifolia. van Heerden FR, Viljoen AM, van Wyk BE Fitoterapia 01-Sep-2000
doi:10.1016/S0367-326X(00)00201-X
PMID:11449522

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 / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,2-Dihydroxy-6-methylanthraquinone 5319503 Click to see CC1=CC2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3O)O 254.24 unknown via CMAUP database
Anthragallol 11768 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)O)O 256.21 unknown via CMAUP database
Anthraquinone, 2-benzyl-1,3-dihydroxy- 630215 Click to see C1=CC=C(C=C1)CC2=C(C=C3C(=C2O)C(=O)C4=CC=CC=C4C3=O)O 330.30 unknown via CMAUP database
Damnacanthal 2948 Click to see COC1=C2C(=CC(=C1C=O)O)C(=O)C3=CC=CC=C3C2=O 282.25 unknown via CMAUP database
Morindone 442756 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3O)O)O 270.24 unknown via CMAUP database
Nordamnacanthal 160712 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)C=O)O 268.22 unknown via CMAUP database
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
Rubiadin 1-methyl ether 96191 Click to see CC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 268.26 unknown via CMAUP database
> Benzenoids / Indanes / Indanones
(2S)-2,6-dimethyl-1-oxo-2,3-dihydroindene-4-carboxylic acid 162916216 Click to see CC1CC2=C(C1=O)C=C(C=C2C(=O)O)C 204.22 unknown https://doi.org/10.1021/NP800333R
2,6-Dimethyl-1-oxo-2,3-dihydroindene-4-carboxylic acid 25157276 Click to see CC1CC2=C(C1=O)C=C(C=C2C(=O)O)C 204.22 unknown https://doi.org/10.1021/NP800333R
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
18-Nonadecene-4-yneoic acid 44203446 Click to see C=CCCCCCCCCCCCCC#CCCC(=O)O 292.50 unknown via CMAUP database
20-Henicosene-6-yneoic acid 44203444 Click to see C=CCCCCCCCCCCCCC#CCCCCC(=O)O 320.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
2,3-Di(nonadec-18-en-4-ynoyloxy)propyl nonadec-18-en-4-ynoate 44203468 Click to see C=CCCCCCCCCCCCCC#CCCC(=O)OCC(COC(=O)CCC#CCCCCCCCCCCCCC=C)OC(=O)CCC#CCCCCCCCCCCCCC=C 915.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids
(1S,3S,5R,7R,9S,13R,14S,15S)-14-hydroxy-2,2,5,9,13-pentamethyl-16-oxapentacyclo[11.2.1.01,3.07,11.07,15]hexadec-11-ene-6,10-dione 102031093 Click to see CC1CC2C(C23C4C(C(O3)(C=C5C4(C1=O)CC(C5=O)C)C)O)(C)C 330.40 unknown https://doi.org/10.1021/NP800333R
(5R,9S,13R)-14-hydroxy-2,2,5,9,13-pentamethyl-16-oxapentacyclo[11.2.1.01,3.07,11.07,15]hexadec-11-ene-6,10-dione 162939304 Click to see CC1CC2C(C23C4C(C(O3)(C=C5C4(C1=O)CC(C5=O)C)C)O)(C)C 330.40 unknown https://doi.org/10.1021/NP800333R
14-Hydroxy-2,2,5,9,13-pentamethyl-16-oxapentacyclo[11.2.1.01,3.07,11.07,15]hexadec-11-ene-6,10-dione 162939303 Click to see CC1CC2C(C23C4C(C(O3)(C=C5C4(C1=O)CC(C5=O)C)C)O)(C)C 330.40 unknown https://doi.org/10.1021/NP800333R
Steenkrotin A 25156985 Click to see CC1CC2C(C23C4C(C(O3)(C=C5C4(C1=O)CC(C5=O)C)C)O)(C)C 330.40 unknown https://doi.org/10.1021/NP800333R
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,4S,5R,6S,11R,14R,15S,18S,21R,22S,23R)-6,10,10,14,15,21,22-heptamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosane-9,25-dione 15240838 Click to see CC1CCC23CCC4(C5(CCC6C(C(=O)CCC6(C5C7C(C4(C2C1C)OC3=O)O7)C)(C)C)C)C 468.70 unknown via CMAUP database
(1S,2S,4S,5R,6S,9S,11R,14R,15S,18S,21R,22S,23R)-9-hydroxy-6,10,10,14,15,21,22-heptamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 15598293 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C7C(C4(C2C1C)OC3=O)O7)C)O)(C)C)C)C 470.70 unknown via CMAUP database
3-Hydroxy-11-ursen-28,13-olide 21606663 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C 454.70 unknown via CMAUP database
3beta-(Formyloxy)urs-12-ene-28-oic acid 21729656 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC=O)C)C)C2C1C)C)C(=O)O 484.70 unknown via CMAUP database
3beta-Hydroxy-27-(4-hydroxy-cis-cinnamoyloxy)oleana-12-ene-28-oic acid 102150860 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)COC(=O)C=CC6=CC=C(C=C6)O)C(=O)O)C 618.80 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Uncarinic acid E 10746421 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)COC(=O)C=CC6=CC=C(C=C6)O)C(=O)O)C 618.80 unknown via CMAUP database
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 via CMAUP database
Ursonic acid 9890209 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C(=O)O 454.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
(1R,3R,5S,6R,9R,13S,15S,16S)-6,16-dihydroxy-5-(2-hydroxypropan-2-yl)-3,9,13-trimethyl-7,8-dioxatetracyclo[7.5.2.01,11.06,15]hexadec-10-ene-2,12-dione 102031094 Click to see CC1CC(C2(C3C(C(C=C4C3(C1=O)CC(C4=O)C)(OO2)C)O)O)C(C)(C)O 380.40 unknown https://doi.org/10.1021/NP800333R
(1R,3R,6R,9R,13S,15S,16R)-6,16-dihydroxy-5-(2-hydroxypropan-2-yl)-3,9,13-trimethyl-7,8-dioxatetracyclo[7.5.2.01,11.06,15]hexadec-10-ene-2,12-dione 163189832 Click to see CC1CC(C2(C3C(C(C=C4C3(C1=O)CC(C4=O)C)(OO2)C)O)O)C(C)(C)O 380.40 unknown https://doi.org/10.1021/NP800333R
6,16-Dihydroxy-5-(2-hydroxypropan-2-yl)-3,9,13-trimethyl-7,8-dioxatetracyclo[7.5.2.01,11.06,15]hexadec-10-ene-2,12-dione 162981957 Click to see CC1CC(C2(C3C(C(C=C4C3(C1=O)CC(C4=O)C)(OO2)C)O)O)C(C)(C)O 380.40 unknown https://doi.org/10.1021/NP800333R
Steenkrotin B 25156986 Click to see CC1CC(C2(C3C(C(C=C4C3(C1=O)CC(C4=O)C)(OO2)C)O)O)C(C)(C)O 380.40 unknown https://doi.org/10.1021/NP800333R
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP800333R
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP800333R
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/J.JEP.2013.04.047
https://doi.org/10.1016/S0367-326X(00)00201-X
https://doi.org/10.1021/NP800333R
Tamarixetin 5281699 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1021/NP800333R

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