Euphorbia mellifera in Genus Euphorbia

Details Top

Internal ID	UUID64403b597ffe1906698624
Scientific name	Euphorbia mellifera
Authority	Aiton
First published in	Hort. Kew. 3: 493 (1789)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Tithymalus melliferus	Moench	Suppl. Meth. : 282 (1802)
Kobiosis mellifera	Raf.	Autik. Bot. : 94 (1840)
Euphorbia longifolia	Lam.	Encycl. 2: 417 (1788)
Euphorbia longifolia var. canariensis	(Boiss.) Oudejans	World Cat. Euphorb. Cum. Suppl. : 12 (1993)
Euphorbia mellifera var. canariensis	Boiss.	Prodr. 15(2): 108 1862

Common names Top

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Language	Common/alternative name
Spanish	tabaiba de monte
German	honiggebende wolfsmilch
Portuguese	alindres
Chinese	蜜大戟

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Canary Islands
  - Madeira

Europe click to expand
- Northern Europe
  - Great Britain

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000963305
Tropicos	12805446
KEW	urn:lsid:ipni.org:names:347318-1
The Plant List	kew-80838
Open Tree Of Life	523453
Observations.org	133952
NCBI Taxonomy	1091634
NBN Atlas	NBNSYS0200002173
IUCN Red List	102818634
IPNI	347318-1
iNaturalist	485518
GBIF	3069311
Freebase	/m/0jkzk
EPPO	EPHMF
EOL	1144419
USDA GRIN	454986
Wikipedia	Euphorbia_mellifera

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

Evolution and function of red pigmentation in land plants

Davies KM, Landi M, van Klink JW, Schwinn KE, Brummell DA, Albert NW, Chagné D, Jibran R, Kulshrestha S, Zhou Y, Bowman JL

Ann Bot

07-Sep-2022

PMCID:	PMC9670752
doi:	10.1093/aob/mcac109
PMID:	36070407

Research Progress on Natural Diterpenoids in Reversing Multidrug Resistance

Deng ZF, Bakunina I, Yu H, Han J, Dömling A, Ferreira MJ, Zhang JY

Front Pharmacol

28-Mar-2022

PMCID:	PMC8996378
doi:	10.3389/fphar.2022.815603
PMID:	35418870

Herbal Bioenhancers in Veterinary Phytomedicine

Yurdakok-Dikmen B, Turgut Y, Filazi A

Front Vet Sci

10-Oct-2018

PMCID:	PMC6191517
doi:	10.3389/fvets.2018.00249
PMID:	30364115

Hepatoprotective and Anti-Inflammatory Activities of the Cnidoscolus chayamansa (Mc Vaugh) Leaf Extract in Chronic Models

Pérez-González MZ, Siordia-Reyes AG, Damián-Nava P, Hernández-Ortega S, Macías-Rubalcava ML, Jiménez-Arellanes MA

Evid Based Complement Alternat Med

25-Jul-2018

PMCID:	PMC6083640
doi:	10.1155/2018/3896517
PMID:	30147729

Natural Products as Alternative Choices for P-Glycoprotein (P-gp) Inhibition

Dewanjee S, K. Dua T, Bhattacharjee N, Das A, Gangopadhyay M, Khanra R, Joardar S, Riaz M, De Feo V, Zia-Ul-Haq M

Molecules

25-May-2017

PMCID:	PMC6152721
doi:	10.3390/molecules22060871
PMID:	28587082

Morphological, Physiological and Proteomic Analyses Provide Insights into the Improvement of Castor Bean Productivity of a Dwarf Variety in Comparing with a High-Stalk Variety

Hu W, Chen L, Qiu X, Lu H, Wei J, Bai Y, He N, Hu R, Sun L, Zhang H, Shen G

Front Plant Sci

29-Sep-2016

PMCID:	PMC5040714
doi:	10.3389/fpls.2016.01473
PMID:	27746800

Biogeography of Mediterranean Hotspot Biodiversity: Re-Evaluating the 'Tertiary Relict' Hypothesis of Macaronesian Laurel Forests

Kondraskov P, Schütz N, Schüßler C, de Sequeira MM, Guerra AS, Caujapé-Castells J, Jaén-Molina R, Marrero-Rodríguez Á, Koch MA, Linder P, Kovar-Eder J, Thiv M

PLoS One

14-Jul-2015

PMCID:	PMC4501571
doi:	10.1371/journal.pone.0132091
PMID:	26173113

Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide

Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A

Biol Rev Camb Philos Soc

19-Mar-2013

PMCID:	PMC7161821
doi:	10.1111/brv.12029
PMID:	23506298

Madeiranes, a New Class of Pentacyclic Triterpenes: D‐Friedo‐madeir‐14‐en‐3β‐ol and ‐3‐one, D:C‐Friedomadeir‐7‐en‐3β‐ol and ‐3‐one

Maria‐José Umbelino Ferreira, Ana M. Lobo, Caroline A. O'Mahoney, David J. Williams, Hugo Wyler

Wiley

28-Dec-2004

doi:	10.1002/HLCA.19910740622

Euferol and melliferol: two novel triterpenoids from Euphorbia mellifera

M. Jos� U. Ferreira, Ana M. Lobo, Caroline A. O'Mahoney, David J. Williams, Hugo Wyler

Royal Society of Chemistry (RSC)

26-Apr-2004

doi:	10.1039/P19900000185

Triterpenes of Euphorbia polygonifolia

A.N. Starratt

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)85859-8

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 / Hopanoids
(21beta)-A'-Neogammacer-22(29)-en-3-one	11743121	Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C	424.70	unknown	https://doi.org/10.1016/S0031-9422(00)85859-8
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aR,6aR,6aS,8aR,12aS,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one	392170	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C	424.70	unknown	https://doi.org/10.1016/S0031-9422(00)85859-8
Taraxerone	92785	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C	424.70	unknown	https://doi.org/10.1016/S0031-9422(00)85859-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	102004740	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)85859-8
(3S,5R,10R,13S,14S)-17-[(1R)-1,5-dimethylhex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	472759	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)85859-8
Lanosterol	246983	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/S0031-9422(00)85859-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(3aR,5bR,7aR,11aR,11bR,13aS,13bS)-5b,8,8,11a-tetramethyl-3a-propan-2-yl-1,2,3,4,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydrocyclopenta[a]chrysen-9-one	101251715	Click to see CC(C)C12CCCC1C3CCC4C5(CCC(=O)C(C5CCC4(C3=CC2)C)(C)C)C	396.60	unknown	https://doi.org/10.1002/HLCA.19910740622
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(3beta,8alpha,9beta,10alpha,13alpha,14beta,17alpha,20S)-9-Methyl-19-norlanosta-5,24-dien-3-ol	14543445	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3(C2CC=C4C3CCC(C4(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1039/P19900000185
3beta-Cucurbita-5,24-dien-3-ol	634657	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3(C2CC=C4C3CCC(C4(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1039/P19900000185
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	145925700	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)85859-8
7,7,12,16-Tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadec-8-en-6-ol	162820419	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CC=C5C3(C4)CCC(C5(C)C)O)C)C	438.70	unknown	https://doi.org/10.1016/S0031-9422(00)85859-8
Cycloartenol	92110	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)85859-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
(3S,5R,8R,9R,13S,14R,17S)-4,4,9,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-3,5,6,7,8,11,12,15,16,17-decahydro-2H-cyclopenta[a]phenanthren-3-ol	14587400	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/10.1039/P19900000185
4,4,9,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-3,5,6,7,8,11,12,15,16,17-decahydro-2H-cyclopenta[a]phenanthren-3-ol	14587399	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/10.1039/P19900000185
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)85859-8
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)85859-8

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Euphorbia mellifera

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top