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Euphorbia sapinii

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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 UUID64403b98d9570106236732
Scientific name Euphorbia sapinii
Authority De Wild.
First published in Ann. Mus. Congo Belge, Bot. , sér. 5, 2: 290 (1908)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 单刺大戟

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
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000964558
KEW urn:lsid:ipni.org:names:348153-1
The Plant List kew-82020
Open Tree Of Life 647129
NCBI Taxonomy 1281384
IPNI 348153-1
GBIF 3069585
EOL 1143972
CMAUP NPO24254

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
Two New Lanostane Triterpenoids from the Branches and Leaves of Polyalthia oblique Wang LK, Zheng CJ, Li XB, Chen GY, Han CR, Chen WH, Song XP Molecules 06-Jun-2014
PMCID:PMC6271888
doi:10.3390/molecules19067621
PMID:24914904
Terpenoids constituents of Euphorbia sapinii Apollinaire Tsopmo, Pierre Kamnaing Elsevier BV 25-Apr-2011
doi:10.1016/J.PHYTOL.2011.04.001

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 / Diterpenoids / Tigliane and ingenane diterpenoids
[(1S,4S,5R,6R,9S,10R,12R,14R)-6-acetyloxy-7-(acetyloxymethyl)-5-hydroxy-3,11,11,14-tetramethyl-15-oxo-4-tetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dienyl] (Z)-2-methylbut-2-enoate 162912364 Click to see CC=C(C)C(=O)OC1C(=CC23C1(C(C(=CC(C2=O)C4C(C4(C)C)CC3C)COC(=O)C)OC(=O)C)O)C 514.60 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
[6-Acetyloxy-7-(acetyloxymethyl)-5-hydroxy-3,11,11,14-tetramethyl-15-oxo-4-tetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dienyl] 2-methylbut-2-enoate 162912363 Click to see CC=C(C)C(=O)OC1C(=CC23C1(C(C(=CC(C2=O)C4C(C4(C)C)CC3C)COC(=O)C)OC(=O)C)O)C 514.60 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Taraxerol acetate 94225 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Taraxeryl acetate 5205968 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-17-[(2S)-6-methyl-5-methylideneheptan-2-yl]-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one 162996068 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2C(=O)CC4C3(CCC(C4(C)C)O)C)C)C 454.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
(3S,5R,8R,9S,10R,13R,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 101808640 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4(C)C)O)C)C)C 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
(3S,8R,9S,10R,13R,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,7,8,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 15730317 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2CC=C4C3(CCC(C4(C)C)O)C)C)C 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
24,25-Dihydrolanosterol 440560 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Euphol 441678 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Euphorbadienol 10863111 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Euphorbol 634628 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Friedelinol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Lanosta-8,24-dien-3-ol 856 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
> Lipids and lipid-like molecules / Saccharolipids
soldanelline B 70698165 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(C(OC2OC3C(C(OC(C3OC4C(C(C(C(O4)C)OC(=O)C(=CC)C)O)OC(=O)C(C)C(C)O)OC5C(C(C(OC5O1)C)O)O)CO)O)CO)O)OC(=O)C(C)CC 1137.30 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
17-(5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,5,8-triol 73190110 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2(C=CC4(C3(CCC(C4)O)C)O)O)C 430.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
Ergosta-6,22-diene-3beta,5alpha,8alpha-triol 15251535 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2(C=CC4(C3(CCC(C4)O)C)O)O)C 430.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
1-[(3R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]ethanone 162890256 Click to see CC(=O)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
4-Methylstigmasta-7,24(28)-dien-3-ol 625305 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
alpha1-Sitosterol 9548595 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.001
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Capparin B 24813533 Click to see COC1=CC2=C(C=C1)C(=C(N2)SC)C=O 221.28 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
6-Methoxyindoline-2,3-dione 10374972 Click to see COC1=CC2=C(C=C1)C(=O)C(=O)N2 177.16 unknown via CMAUP database
Capparin A 101457836 Click to see COC1=CC2=C(C=C1)C3(CN=C(S3)SC)C(=O)N2 280.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Oroxylin A 5320315 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin 5281703 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown via CMAUP database

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