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Euphorbia officinarum

Euphorbia officinarum - 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 UUID64403b6ca973f062708912
Scientific name Euphorbia officinarum
Authority L.
First published in Sp. Pl. : 451 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tithymalus officinarum H.Karst. Deut. Fl. : 587 (1882)

Common names Top

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Language Common/alternative name
Chinese 印堂麒麟

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Euphorbia officinarum subsp. echinus (Hook.f. & Coss.) Vindt Trav. Inst. Sci. Chérifien, Sér. Bot. 19: 447 (1960)
Euphorbia officinarum subsp. officinarum Unknown

Varieties (abbr. var.) Top

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Name Authority First published in
Euphorbia officinarum var. beaumieriana (Hook.f. & Coss.) Maire Cat. Pl. Maroc 2: 461 (1932)

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
    • Northern Africa
      • Algeria
      • Morocco
      • Western Sahara
    • West Tropical Africa
      • Mauritania

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000963697
Tropicos 50286034
KEW urn:lsid:ipni.org:names:347573-1
The Plant List kew-81211
Open Tree Of Life 326310
Observations.org 326630
NCBI Taxonomy 1130835
IPNI 347573-1
iNaturalist 479929
GBIF 3067956
EOL 1144293
Elurikkus 361774
USDA GRIN 409965

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
The Role of Plant Latex in Virus Biology Merchán-Gaitán JB, Mendes JH, Nunes LE, Buss DS, Rodrigues SP, Fernandes PM Viruses 27-Dec-2023
PMCID:PMC10819414
doi:10.3390/v16010047
PMID:38257746
Feeding Ecology of the Cuvier’s Gazelle (Gazella cuvieri, Ogilby, 1841) in the Sahara Desert Herrera-Sánchez FJ, López O, Rodríguez-Siles J, Díaz-Portero MÁ, Arredondo Á, Sáez JM, Álvarez B, Cancio I, de Lucas J, Pérez J, Valenzuela G, Martínez-Valderrama J, Sánchez-Cerdá M, Qninba A, Virgós E, Calleja JA, Bartolomé J, Albanell E, Serrano E, Abáigar T, Gil-Sánchez JM Animals (Basel) 06-Feb-2023
PMCID:PMC9951649
doi:10.3390/ani13040567
PMID:36830354
Medicinal Chemistry of Anti-HIV-1 Latency Chemotherapeutics: Biotargets, Binding Modes and Structure-Activity Relationship Investigation Wang YK, Wei L, Hu W, Yu PX, Li Z, Yu HP, Li X Molecules 20-Dec-2022
PMCID:PMC9822059
doi:10.3390/molecules28010003
PMID:36615199
Biological Properties of Latex, Aqueous Extracts and Bee Products of Euphorbia officinarum L.: A Short Review Boutoub O, Ghadraoui LE, Miguel MG Molecules 24-Oct-2022
PMCID:PMC9656204
doi:10.3390/molecules27217200
PMID:36364025
Adnate Leaf-Base and the Origin of Ribs in Succulent Stems of Euphorbia L. Arévalo-Rodrigues G, Hurbath F, Prado E, Galvão I, Cordeiro I, Demarco D Plants (Basel) 15-Apr-2022
PMCID:PMC9027645
doi:10.3390/plants11081076
PMID:35448804
Antimicrobial Triterpenoids and Ingol Diterpenes from Propolis of Semi-Arid Region of Morocco Chimshirova R, Popova M, Chakir A, Valcheva V, Dimitrov S, Trusheva B, Romane A, Bankova V Molecules 28-Mar-2022
PMCID:PMC9000693
doi:10.3390/molecules27072206
PMID:35408603
3D-QSAR, ADME-Tox, and molecular docking of semisynthetic triterpene derivatives as antibacterial and insecticide agents Daoui O, Mazoir N, Bakhouch M, Salah M, Benharref A, Gonzalez-Coloma A, Elkhattabi S, Yazidi ME, Chtita S Struct Chem 23-Mar-2022
PMCID:PMC8941842
doi:10.1007/s11224-022-01912-4
PMID:35345415
Plant-Derived Protectants in Combating Soil-Borne Fungal Infections in Tomato and Chilli Arora H, Sharma A, Poczai P, Sharma S, Haron FF, Gafur A, Sayyed RZ J Fungi (Basel) 21-Feb-2022
PMCID:PMC8878687
doi:10.3390/jof8020213
PMID:35205967
Conventional Medicinal Uses, Phytoconstituents, and Biological Activities of Euphorbia officinarum L.: A Systematic Review Chamkhi I, Hnini M, Aurag J Adv Pharmacol Pharm Sci 06-Jan-2022
PMCID:PMC8758299
doi:10.1155/2022/9971085
PMID:35036919
Ethnopharmacological Survey and Comparative Study of the Healing Activity of Moroccan Thyme Honey and Its Mixture with Selected Essential Oils on Two Types of Wounds on Albino Rabbits Mekkaoui M, Assaggaf H, Qasem A, El-Shemi A, Abdallah EM, Bouidida EH, Naceiri Mrabti H, Cherrah Y, Alaoui K Foods 23-Dec-2021
PMCID:PMC8750595
doi:10.3390/foods11010028
PMID:35010154
Fungal diversity notes 1387–1511: taxonomic and phylogenetic contributions on genera and species of fungal taxa Boonmee S, Wanasinghe DN, Calabon MS, Huanraluek N, Chandrasiri SK, Jones GE, Rossi W, Leonardi M, Singh SK, Rana S, Singh PN, Maurya DK, Lagashetti AC, Choudhary D, Dai YC, Zhao CL, Mu YH, Yuan HS, He SH, Phookamsak R, Jiang HB, Martín MP, Dueñas M, Telleria MT, Kałucka IL, Jagodziński AM, Liimatainen K, Pereira DS, Phillips AJ, Suwannarach N, Kumla J, Khuna S, Lumyong S, Potter TB, Shivas RG, Sparks AH, Vaghefi N, Abdel-Wahab MA, Abdel-Aziz FA, Li GJ, Lin WF, Singh U, Bhatt RP, Lee HB, Nguyen TT, Kirk PM, Dutta AK, Acharya K, Sarma VV, Niranjan M, Rajeshkumar KC, Ashtekar N, Lad S, Wijayawardene NN, Bhat DJ, Xu RJ, Wijesinghe SN, Shen HW, Luo ZL, Zhang JY, Sysouphanthong P, Thongklang N, Bao DF, Aluthmuhandiram JV, Abdollahzadeh J, Javadi A, Dovana F, Usman M, Khalid AN, Dissanayake AJ, Telagathoti A, Probst M, Peintner U, Garrido-Benavent I, Bóna L, Merényi Z, Boros L, Zoltán B, Stielow JB, Jiang N, Tian CM, Shams E, Dehghanizadeh F, Pordel A, Javan-Nikkhah M, Denchev TT, Denchev CM, Kemler M, Begerow D, Deng CY, Harrower E, Bozorov T, Kholmuradova T, Gafforov Y, Abdurazakov A, Xu JC, Mortimer PE, Ren GC, Jeewon R, Maharachchikumbura SS, Phukhamsakda C, Mapook A, Hyde KD Fungal Divers 07-Dec-2021
PMCID:PMC8648402
doi:10.1007/s13225-021-00489-3
PMID:34899100
Comparative Study of the Antioxidant and Enzyme Inhibitory Activities of Two Types of Moroccan Euphorbia Entire Honey and Their Phenolic Extracts Boutoub O, El-Guendouz S, Manhita A, Dias CB, Estevinho LM, Paula VB, Carlier J, Costa MC, Rodrigues B, Raposo S, Aazza S, El Ghadraoui L, Miguel MG Foods 17-Aug-2021
PMCID:PMC8394845
doi:10.3390/foods10081909
PMID:34441685
Taxonomy and phylogeny of the basidiomycetous hyphomycete genus Hormomyces Mack J, Assabgui RA, Seifert KA Fungal Syst Evol 12-Feb-2021
PMCID:PMC8166209
doi:10.3114/fuse.2021.07.09
PMID:34124623
Floristic biodiversity, biogeographical significance, and importance of Morocco’s Arganeraie Biosphere Reserve Msanda F, Mayad EH, Furze JN Environ Sci Pollut Res Int 06-Jan-2021
PMCID:PMC7786145
doi:10.1007/s11356-020-11936-0
PMID:33405131
Identifying priority conservation areas in a Saharan environment by highlighting the endangered Cuvier’s Gazelle as a flagship species Herrera-Sánchez FJ, Gil-Sánchez JM, Álvarez B, Cancio I, de Lucas J, Arredondo Á, Díaz-Portero MÁ, Rodríguez-Siles J, Sáez JM, Pérez J, McCain E, Qninba A, Abáigar T Sci Rep 19-May-2020
PMCID:PMC7237411
doi:10.1038/s41598-020-65188-6
PMID:32427930

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)-4,8,9-triacetyloxy-3,6,6,10,14-pentamethyl-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-13-yl] 2-(4-methoxyphenyl)acetate 162817204 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1OC(=O)CC5=CC=C(C=C5)OC)O3)C)OC(=O)C)OC(=O)C)OC(=O)C)C 640.70 unknown https://doi.org/10.1016/J.BMC.2007.04.009
[(1R,3R,4R,5R,7S,8S,9R,10E,12S,13S,14S)-4,8,9-triacetyloxy-3,6,6,10,14-pentamethyl-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-13-yl] 2-phenylacetate 162817205 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1OC(=O)CC5=CC=CC=C5)O3)C)OC(=O)C)OC(=O)C)OC(=O)C)C 610.70 unknown https://doi.org/10.1016/J.BMC.2007.04.009
[(1R,3R,4R,5R,7S,8S,9R,10E,12S,13S,14S)-4,9-diacetyloxy-8-methoxy-3,6,6,10,14-pentamethyl-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-13-yl] 2-phenylacetate 162817203 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1OC(=O)CC5=CC=CC=C5)O3)C)OC(=O)C)OC)OC(=O)C)C 582.70 unknown https://doi.org/10.1016/J.BMC.2007.04.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2'S,3aR,3'aS,5R,6'S,7'S,7aR,7'aS)-2',6'-dihydroxy-3a,3'a,7',7a-tetramethyl-1-[(2R)-6-methylheptan-2-yl]spiro[2,3,6,7-tetrahydro-1H-indene-5,3'-2,4,5,6,7,7a-hexahydro-1H-indene]-4-one 44429427 Click to see CC1C(CCC2(C1CC(C23CCC4(C(CCC4(C3=O)C)C(C)CCCC(C)C)C)O)C)O 446.70 unknown https://doi.org/10.1016/J.BMC.2007.04.009
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(3S,4S,10S,13R)-4,10,13-trimethyl-17-[(2S)-6-methylheptan-2-yl]-2,3,4,5,6,7,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 162985838 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3CCC4C(C)CCCC(C)C)C 400.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.004
31-Norlanostenol 14845298 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCCC(C)C)C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.004
4,10,13,14-Tetramethyl-17-(6-methylheptan-2-yl)-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 14845297 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCCC(C)C)C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.004
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
4,14-Dimethylergosta-8,24(28)-dien-3-ol 634321 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.004
Obtusifoliol 65252 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.01.004

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