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Euphorbia caerulescens

Euphorbia caerulescens - 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 UUID64403af520bc2611646436
Scientific name Euphorbia caerulescens
Authority Haw.
First published in Philos. Mag. Ann. Chem. 1: 276 (1827)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 浅蓝大戟
Chinese 莱迪恩大戟

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000961149
Tropicos 50271527
INPN 901922
KEW urn:lsid:ipni.org:names:345889-1
The Plant List kew-78782
Open Tree Of Life 136212
NCBI Taxonomy 1129976
IPNI 345889-1
iNaturalist 577767
GBIF 3067673
EPPO EPHCL
EOL 1145190
USDA GRIN 16351

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 new phorbol triester from the latices of Euphorbia frankiana and E. Coerulescens Fred J. Evans Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(77)80075-7
Irritant principles of the spurge family (Euphorbiaceae). XIII. Oligocyclic and macrocyclic diterpene esters from latices of some Euphorbia species utilized as source plants of honey. Sosath S, Ott HH, Hecker E J Nat Prod 01-Nov-1988
doi:10.1021/NP50060A003
PMID:3236005

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
[(1R,3R,4R,5R,7S,8S,9R,10E,12S,13S,14S)-9,13-diacetyloxy-3,6,6,10,14-pentamethyl-4-[(E)-2-methylbut-2-enoyl]oxy-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-8-yl] 2-methylbutanoate 44559781 Click to see CCC(C)C(=O)OC1C2C(C2(C)C)C(C(C(=O)C34CC(C(C3(O4)C=C(C1OC(=O)C)C)OC(=O)C)C)C)OC(=O)C(=CC)C 616.70 unknown https://doi.org/10.1021/NP50060A003
Ingol-7,8,12-acetate,ditiglate 44559778 Click to see CC=C(C)C(=O)OC1C(C(=O)C23CC(C(C2(O3)C=C(C(C(C4C1C4(C)C)OC(=O)C(=CC)C)OC(=O)C)C)O)C)C 572.70 unknown https://doi.org/10.1021/NP50060A003
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1R,2S,6R,10S,11R,13S,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] (E)-2-methylbut-2-enoate 6506231 Click to see CC=C(C)C(=O)OC12CC(C3(C(C1C2(C)C)C=C(CC4(C3C=C(C4=O)C)O)CO)O)C 430.50 unknown https://doi.org/10.1021/NP50060A003
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids / Phorbol esters
[(1R,2S,6R,10S,11R,12S,13S,15R)-8-(acetyloxymethyl)-1,6-dihydroxy-4,12,15-trimethyl-13-(2-methylbut-2-enoyloxy)-5-oxo-12-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl]methyl 2-methylbutanoate 162819099 Click to see CCC(C)C(=O)OCC1(C2C1(CC(C3(C2C=C(CC4(C3C=C(C4=O)C)O)COC(=O)C)O)C)OC(=O)C(=CC)C)C 572.70 unknown https://doi.org/10.1021/NP50060A003
[(1R,2S,6R,10S,11R,12S,13S,15R)-8-(acetyloxymethyl)-1,6-dihydroxy-4,12,15-trimethyl-13-[(Z)-2-methylbut-2-enoyl]oxy-5-oxo-12-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl]methyl 2-methylbutanoate 44559777 Click to see CCC(C)C(=O)OCC1(C2C1(CC(C3(C2C=C(CC4(C3C=C(C4=O)C)O)COC(=O)C)O)C)OC(=O)C(=CC)C)C 572.70 unknown https://doi.org/10.1021/NP50060A003
[(1S,2R,6R,10S,11R,13S,14R,15R)-13-acetyloxy-1,6-dihydroxy-4,12,12,15-tetramethyl-14-(3-methylbutanoyloxy)-5-oxo-8-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl]methyl (Z)-2-methylbut-2-enoate 162866423 Click to see CC=C(C)C(=O)OCC1=CC2C3C(C3(C(C(C2(C4C=C(C(=O)C4(C1)O)C)O)C)OC(=O)CC(C)C)OC(=O)C)(C)C 572.70 unknown https://doi.org/10.1016/0031-9422(77)80075-7
[13-Acetyloxy-1,6-dihydroxy-4,12,12,15-tetramethyl-14-(3-methylbutanoyloxy)-5-oxo-8-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl]methyl 2-methylbut-2-enoate 162866422 Click to see CC=C(C)C(=O)OCC1=CC2C3C(C3(C(C(C2(C4C=C(C(=O)C4(C1)O)C)O)C)OC(=O)CC(C)C)OC(=O)C)(C)C 572.70 unknown https://doi.org/10.1016/0031-9422(77)80075-7
12-Deoxy-phorbol-13-alpha-methylbutyrate-20-acetate 198036 Click to see CCC(C)C(=O)OC12CC(C3(C(C1C2(C)C)C=C(CC4(C3C=C(C4=O)C)O)COC(=O)C)O)C 474.60 unknown https://doi.org/10.1021/NP50060A003
12-Deoxyphorbol-13-isobutyrate-20-acetate 3035003 Click to see CC1CC2(C(C2(C)C)C3C1(C4C=C(C(=O)C4(CC(=C3)COC(=O)C)O)C)O)OC(=O)C(C)C 460.60 unknown https://doi.org/10.1021/NP50060A003
CID 360836 360836 Click to see CC1CC2(C(C2(C)C)C3C1(C4C=C(C(=O)C4(CC(=C3)CO)O)C)O)OC(=O)C 390.50 unknown https://doi.org/10.1021/NP50060A003
Prostratin 454217 Click to see CC1CC2(C(C2(C)C)C3C1(C4C=C(C(=O)C4(CC(=C3)CO)O)C)O)OC(=O)C 390.50 unknown https://doi.org/10.1021/NP50060A003

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