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Elaeodendron croceum

Elaeodendron croceum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64401936cc14e969866451
Scientific name Elaeodendron croceum
Authority DC.
First published in Prodr. 2: 11 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cassine crocea C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 467 (1845)
Crocoxylon croceum (Thunb.) N.Robson Bol. Soc. Brot. , sér. 2, 39: 41 (1965)
Crocoxylon excelsum Eckl. & Zeyh. Enum. Pl. Afric. Austral. [Ecklon & Zeyher] 1: 128. [Dec 1834-Mar 1835]
Elaeodendron capense Eckl. & Zeyh. Enum. Pl. Afric. Austral. : 127 (1835)
Elaeodendron verrucosum Kunth Index Seminum (B, Berolinensis) 1845: 12 (1845)
Elaeodendron zeyheri Turcz. Bull. Soc. Imp. Naturalistes Moscou 31(I): 452 (1858)
Salacia zeyheri Spreng. ex Harv. & Sond. Fl. Cap. 1: 230 (1860)
Ilex crocea Thunb. Prodr. Pl. Cap. : 32 (1794)

Common names Top

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Language Common/alternative name
Afrikaans bossaffraan

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
    • Middle Atlantic Ocean
      • Saint Helena
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000664930
Tropicos 6600485
Flora of Italy 12920
KEW urn:lsid:ipni.org:names:160659-1
Open Tree Of Life 5233481
NCBI Taxonomy 1004000
IUCN Red List 149513234
IPNI 160659-1
iNaturalist 557692
GBIF 3792084
USDA GRIN 447827

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
Medicinal Plants against Viral Infections: A Review of Metabolomics Evidence for the Antiviral Properties and Potentials in Plant Sources Adeosun WB, Loots DT Viruses 31-Jan-2024
PMCID:PMC10892737
doi:10.3390/v16020218
PMID:38399995
Plant-mediated synthesis of silver nanoparticles: unlocking their pharmacological potential–a comprehensive review Dhir R, Chauhan S, Subham P, Kumar S, Sharma P, Shidiki A, Kumar G Front Bioeng Biotechnol 09-Jan-2024
PMCID:PMC10803431
doi:10.3389/fbioe.2023.1324805
PMID:38264582
Osteoarthritis in the Elderly Population: Preclinical Evidence of Nutrigenomic Activities of Flavonoids Naselli F, Bellavia D, Costa V, De Luca A, Raimondi L, Giavaresi G, Caradonna F Nutrients 28-Dec-2023
PMCID:PMC10780745
doi:10.3390/nu16010112
PMID:38201942
How Poor Is Aphyllophoroid Fungi Diversity in the Boreal Urban Greenhouses of Eastern Europe? Shiryaev AG, Zmitrovich IV, Senator SA, Minogina EN, Tkachenko OB J Fungi (Basel) 17-Nov-2023
PMCID:PMC10672352
doi:10.3390/jof9111116
PMID:37998921
Fulvifomes wrightii (Hymenochaetales), a new species related to F. robiniae from Argentina and Paraguay Martínez M, Salvador-Montoya CA, de Errasti A, Popoff OF, Rajchenberg M Fungal Syst Evol 28-Jul-2023
PMCID:PMC10976966
doi:10.3114/fuse.2023.12.03
PMID:38550752
Phytochemicals: potential alternative strategy to fight Salmonella enterica serovar Typhimurium Almuzaini AM Front Vet Sci 16-May-2023
PMCID:PMC10228746
doi:10.3389/fvets.2023.1188752
PMID:37261108
The molecular interplay of known phytochemicals as Culex pipiens and Rift Valley fever virus inhibitors through molecular docking Abutaha N, AL-Mekhlafi FA, Wadaan MA, Moustafa Rady A, Baabbad AA, Al-Khalifa MS Saudi J Biol Sci 01-Mar-2023
PMCID:PMC10036733
doi:10.1016/j.sjbs.2023.103611
PMID:36970253
Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments Zhou Y, Wang D, Yan W Nutrients 18-Feb-2023
PMCID:PMC9967064
doi:10.3390/nu15041031
PMID:36839389
Bio-organic fertilizers improve Dendrocalamus farinosus growth by remolding the soil microbiome and metabolome Li S, Fan W, Xu G, Cao Y, Zhao X, Hao S, Deng B, Ren S, Hu S Front Microbiol 15-Feb-2023
PMCID:PMC9975161
doi:10.3389/fmicb.2023.1117355
PMID:36876063
Two new species of Hymenochaetaceae from tropical Asia and America Zhou M, Ji XH, Liu HG, Miller K, Yuan Y, Vlasák J Front Cell Infect Microbiol 19-Jan-2023
PMCID:PMC9892452
doi:10.3389/fcimb.2022.1100044
PMID:36741979
Canopy plant composition and structure of Cape subtropical dune thicket are predicted by the levels of fire exposure Strydom T, Kraaij T, Grobler BA, Cowling RM PeerJ 08-Nov-2022
PMCID:PMC9651048
doi:10.7717/peerj.14310
PMID:36389405
Antibacterial and Antioxidant Properties of Extracts of Yucca Baccata, a Plant of Northwestern Mexico, against Pathogenic Bacteria Morales-Figueroa GG, Pereo-Vega GD, Reyna-Murrieta ME, Pérez-Morales R, López-Mata MA, Sánchez-Escalante JJ, Tapia-Rodriguez MR, Ayala-Zavala JF, Juárez J, Quihui-Cota L Biomed Res Int 26-Oct-2022
PMCID:PMC9629963
doi:10.1155/2022/9158836
PMID:36337841
Neotropical Studies on Hymenochaetaceae: Unveiling the Diversity and Endemicity of Phellinotus Salvador-Montoya CA, Elias SG, Popoff OF, Robledo GL, Urcelay C, Góes-Neto A, Martínez S, Drechsler-Santos ER J Fungi (Basel) 22-Feb-2022
PMCID:PMC8950266
doi:10.3390/jof8030216
PMID:35330218
Metabolomic profile of medicinal plants with anti-RVFV activity More GK, Vervoort J, Steenkamp PA, Prinsloo G Heliyon 12-Feb-2022
PMCID:PMC8857432
doi:10.1016/j.heliyon.2022.e08936
PMID:35243061
Potential Benefits of Antiviral African Medicinal Plants in the Management of Viral Infections: Systematic Review Beressa TB, Deyno S, Mtewa AG, Aidah N, Tuyiringire N, Lukubye B, Weisheit A, Tolo CU, Ogwang PE Front Pharmacol 24-Dec-2021
PMCID:PMC8740180
doi:10.3389/fphar.2021.682794
PMID:35002686

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
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-1-(3-hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 15038288 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(93)85252-M
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-1-(3-hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 12980886 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(93)85252-M
(3S,4R,4aR,6aS,6aS,6bR,8aS,11R,12aR,14aS,14bR)-11-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-2,3,4,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydro-1H-picen-3-ol 162953158 Click to see CC1C2CCC3C(C2(CCC1O)C)CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C 430.70 unknown https://doi.org/10.1016/0031-9422(93)85252-M
(6aS,6bS,8aR,9S,12aR,14aR)-3,9-dihydroxy-4,6a,6b,8a,11,11,14a-heptamethyl-8,9,12,12a,13,14-hexahydro-7H-picene-2,10-dione 162883869 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5O)(C)C)C)C)C)C)O 450.60 unknown https://doi.org/10.1016/0031-9422(93)85252-M
(6aS,6bS,8aS,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,11,14a-heptamethyl-8,9,12,12a,13,14-hexahydro-7H-picene-2,10-dione 163060170 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5)(C)C)C)C)C)C)O 434.60 unknown https://doi.org/10.1016/0031-9422(93)85252-M
(6bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,14-diol 162986655 Click to see CC1(CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)O)C2C1)C)C)C 442.70 unknown https://doi.org/10.1080/14786410903052399
1-(3-Hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 14108935 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(93)85252-M
11-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-2,3,4,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydro-1H-picen-3-ol 162953157 Click to see CC1C2CCC3C(C2(CCC1O)C)CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C 430.70 unknown https://doi.org/10.1016/0031-9422(93)85252-M
3-hydroxy-4,6a,6b,8a,11,11,14a-heptamethyl-8,9,12,12a,13,14-hexahydro-7H-picene-2,10-dione 163060169 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5)(C)C)C)C)C)C)O 434.60 unknown https://doi.org/10.1016/0031-9422(93)85252-M
3,9-dihydroxy-4,6a,6b,8a,11,11,14a-heptamethyl-8,9,12,12a,13,14-hexahydro-7H-picene-2,10-dione 162883868 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5O)(C)C)C)C)C)C)O 450.60 unknown https://doi.org/10.1016/0031-9422(93)85252-M
30-Hydroxylup-20(29)-en-3-one 15038289 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(93)85252-M
Canophyllol 7330581 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(93)85252-M
Hennadiol 489919 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(93)85252-M
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
3,14-Dihydroxycard-20(22)-enolide 274159 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)O 374.50 unknown https://doi.org/10.1080/14786410903211912
Digitoxigenin 4369270 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)O 374.50 unknown https://doi.org/10.1080/14786410903211912
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
Glucodigitoxigenin 15558776 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)OC6C(C(C(C(O6)CO)O)O)O 536.70 unknown https://doi.org/10.1080/14786410903211912
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-[(1S,2R,5S,8S,10R,11R,15R)-8-hydroxy-11-methyl-15-[(1Z,2S)-1-(4-methyl-5-oxofuran-2-ylidene)propan-2-yl]-6,13-dioxo-14,16-dioxatetracyclo[8.6.0.02,8.011,15]hexadecan-5-yl]propan-2-yl acetate 44473750 Click to see CC1=CC(=CC(C)C23C(CC(=O)O2)(C4CC5(CC(=O)C(CCC5C4O3)C(C)(C)OC(=O)C)O)C)OC1=O 516.60 unknown https://doi.org/10.1016/0031-9422(93)85252-M
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Tingenin B 73147 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(C(C1=O)O)C 436.60 unknown https://doi.org/10.1016/0031-9422(93)85252-M
https://doi.org/10.1080/14786410903052399
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1016/0031-9422(93)85252-M
Hexitol 453 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1016/0031-9422(93)85252-M
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
(6bS,8aS,11R,12aR,14aR)-3,11-dihydroxy-4,6a,6b,8a,11,14a-hexamethyl-8,9,12,12a,13,14-hexahydro-7H-picene-2,10-dione 162921036 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5)(C)O)C)C)C)C)O 436.60 unknown https://doi.org/10.1080/14786410903052399
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(6aR,6bR,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 441687 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1080/14786410903052399
https://doi.org/10.1016/0031-9422(93)85252-M
Tingenone 101520 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1080/14786410903052399
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
CID 21881649 21881649 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(O2)C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)O 592.50 unknown https://doi.org/10.1016/0031-9422(93)85252-M
Ourateaproanthocyanidin A 9808627 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(O2)C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)O 592.50 unknown https://doi.org/10.1016/0031-9422(93)85252-M
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Egc-4'-O-ME 53463000 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O 320.29 unknown https://doi.org/10.1016/0031-9422(93)85252-M
3-methoxy-5,5-dimethyl-7,12a-dihydro-6aH-isochromeno[4,3-b]chromene-2,4,8,10-tetrol 15089250 Click to see CC1(C2=C(C(=C(C=C2C3C(O1)CC4=C(C=C(C=C4O3)O)O)O)OC)O)C 360.40 unknown https://doi.org/10.1016/0031-9422(93)85252-M
4'-Methyl-epigallocatechin 176920 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O 320.29 unknown https://doi.org/10.1016/0031-9422(93)85252-M
Elaeocyanidin 21676388 Click to see CC1(C2=C(C(=C(C=C2C3C(O1)CC4=C(C=C(C=C4O3)O)O)O)OC)O)C 360.40 unknown https://doi.org/10.1016/0031-9422(93)85252-M
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1080/14786410903052399
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1080/14786410903052399

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