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Strophanthus emini

Strophanthus emini - 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 UUID643fede11a314022888267
Scientific name Strophanthus emini
Authority Asch. ex Pax
First published in Bot. Jahrb. Syst. 15: 366 (1892)

Description Top

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Synonyms Top

Scientific name Authority First published in
Strophanthus fischeri Asch. & K.Schum. ex Holmes in Pharm. Journ. (1893) 868, nomen; et ex Franch. in Morot, Journ. de Bot. vii.(1893) 325,.
Strophanthus stuhlmannii Pax Ber. Deutsch. Pharm. Ges. 3: 44. 1893 (1893)
Strophanthus wittei Staner Ann. Soc. Sci. Bruxelles, Sér. B 52: 90 (1932)

Common names Top

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Language Common/alternative name
English emin's strophanthus

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
      • Tanzania
    • South Tropical Africa
      • Zambia
    • West-central Tropical Africa
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000317266
USDA Plants STEM4
Tropicos 1805576
KEW urn:lsid:ipni.org:names:81881-1
The Plant List kew-198216
Open Tree Of Life 375855
NCBI Taxonomy 52859
IPNI 81881-1
iNaturalist 544765
GBIF 3169611
Freebase /m/0wf1_ky
EOL 483911
USDA GRIN 35805
Wikipedia Strophanthus_eminii

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
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Taxonomic Novelties of Woody Litter Fungi (Didymosphaeriaceae, Pleosporales) from the Greater Mekong Subregion Ren G, Wanasinghe DN, de Farias AR, Hyde KD, Yasanthika E, Xu J, Balasuriya A, Chethana KW, Gui H Biology (Basel) 13-Nov-2022
PMCID:PMC9687740
doi:10.3390/biology11111660
PMID:36421373
Herbal remedies used by traditional healers to treat haemorrhoids in Tabora region, Tanzania Kacholi DS, Mvungi Amir H Pharm Biol 28-Oct-2022
PMCID:PMC9629089
doi:10.1080/13880209.2022.2136204
PMID:36307997
Screening of Traditionally Used Plants for In Vivo Antimalarial Activity in Mice Innocent E, Moshi MJ, Masimba PJ, Mbwambo ZH, Kapingu MC, Kamuhabwa A Afr J Tradit Complement Altern Med 07-Mar-2009
PMCID:PMC2816569
doi:10.4314/ajtcam.v6i2.57088
PMID:20209008
Brine Shrimp Toxicity Evaluation of Some Tanzanian Plants Used Traditionally for the Treatment of Fungal Infections Moshi MJ, van den Beukel CJ, Hamza OJ, Mbwambo ZH, Nondo RO, Masimba PJ, Matee MI, Kapingu MC, Mikx F, Verweij PE, van der Ven AJ Afr J Tradit Complement Altern Med 13-Nov-2006
PMCID:PMC2816448
doi:10.4314/ajtcam.v4i2.31211
PMID:20162095
Die Glykoside der Samen von <i>Strophanthus Eminii Asch et Pax.</i> 3. Mitteilung. Glykoside und Aglykone, 184. Mitteilung R. Zelnik, O. Schindler Wiley 26-Dec-2004
doi:10.1002/HLCA.19570400711
Die Glykoside der Samen von Strophanthus Eminii <i>Asch.</i> et <i>Pax</i>. Glykoside und Aglykone, 56. Mitteilung A. Lardon Wiley 26-Dec-2004
doi:10.1002/HLCA.19500330328
107. The glucosides of Strophanthus Emini I. D. Lamb, S. Smith Royal Society of Chemistry (RSC) 21-Apr-2004
doi:10.1039/JR9360000442

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 / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
3-(3,5,14-trihydroxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2H-furan-5-one 608378 Click to see CC12CCC(CC1(CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)O)O 390.50 unknown https://doi.org/10.1002/HLCA.19500330328
https://doi.org/10.1039/JR9360000442
3,5,14,19-Tetrahydroxycard-20(22)-enolide 544146 Click to see CC12CCC3C(C1(CCC2C4=CC(=O)OC4)O)CCC5(C3(CCC(C5)O)CO)O 406.50 unknown https://doi.org/10.1002/HLCA.19500330328
Periplogenin 10574 Click to see CC12CCC(CC1(CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)O)O 390.50 unknown https://doi.org/10.1039/JR9360000442
https://doi.org/10.1002/HLCA.19500330328
Strophanthidol 258412 Click to see CC12CCC3C(C1(CCC2C4=CC(=O)OC4)O)CCC5(C3(CCC(C5)O)CO)O 406.50 unknown https://doi.org/10.1002/HLCA.19500330328
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
3-[(2,6-Dideoxy-3-O-methylhexopyranosyl)oxy]-5,14,19-trihydroxycard-20(22)-enolide 574664 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)CO)OC)O 550.70 unknown https://doi.org/10.1002/HLCA.19500330328
https://doi.org/10.1002/HLCA.19570400711
3-[(3S,5S,8R,9S,10R,13R,14S,17R)-3-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-5,14-dihydroxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 162947448 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)O)OC)O 550.70 unknown https://doi.org/10.1002/HLCA.19500330328
https://doi.org/10.1039/JR9360000442
3-[(3S,5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-10,13-dimethyl-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 44445807 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)O)O)O 536.70 unknown https://doi.org/10.1002/HLCA.19570400711
3-[(3S,5S,8R,9S,10R,13R,14S,17S)-3-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-5,14-dihydroxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 162947449 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)O)OC)O 550.70 unknown https://doi.org/10.1039/JR9360000442
3-[(3S,5S,8R,9S,10R,13R,14S,17S)-5,14-dihydroxy-10,13-dimethyl-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 162971179 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)O)O)O 536.70 unknown https://doi.org/10.1002/HLCA.19570400711
3-[(3S,5S,8R,9S,10R,13R,14S,17S)-5,14-dihydroxy-3-[(2R,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 21575220 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)OC)O 534.70 unknown https://doi.org/10.1002/HLCA.19570400711
3-[5,14-dihydroxy-10,13-dimethyl-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 12304975 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)O)O)O 536.70 unknown https://doi.org/10.1002/HLCA.19570400711
3-[5,14-dihydroxy-3-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 120710 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)OC)O 534.70 unknown https://doi.org/10.1002/HLCA.19570400711
https://doi.org/10.1002/HLCA.19500330328
4-[(3S,5S,10R,13R,14S,17S)-5,14-Dihydroxy-3-[(2S,5R)-5-hydroxy-4-methoxy-6-methyl-oxan-2-YL]oxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[A]phenanthren-17-YL]-5H-furan-2-one 12305974 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)OC)O 534.70 unknown https://doi.org/10.1002/HLCA.19500330328
https://doi.org/10.1002/HLCA.19570400711
Card-20(22)-enolide, 3-[(2,6-dideoxy-3-O-methyl-beta-D-ribo-hexopyranosyl)oxy]-5,14-dihydroxy-19-oxo-, (3beta,5beta)- 539061 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)OC)O 548.70 unknown https://doi.org/10.1039/JR9360000442
Cymarine 441853 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)OC)O 548.70 unknown https://doi.org/10.1039/JR9360000442
Cymarol 12312886 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)CO)OC)O 550.70 unknown https://doi.org/10.1002/HLCA.19500330328
https://doi.org/10.1002/HLCA.19570400711
Emicymarin 554133 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)O)OC)O 550.70 unknown https://doi.org/10.1039/JR9360000442
https://doi.org/10.1002/HLCA.19500330328

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