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Internal ID UUID64403afce867b105846894
Scientific name Euphorbia cheiradenia
Authority Boiss. & Hohen.
First published in Diagn. Pl. Orient. 12: 112 (1853)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tithymalus cheiradenius Klotzsch & Garcke Abh. Königl. Akad. Wiss. Berlin 1859: 98 (1860)
Tithymalus elwendicus (Stapf) Soják Cas. Nár. Mus., Odd. Prír. 140: 172 (1972)
Euphorbia bothriosperma Boiss. & Kotschy Cent. Euphorb. : 36 (1860)
Euphorbia elwendica Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 51: 45 (1886)
Euphorbia schizadenia Boiss. & Hohen. ex Boiss. Diagn. Pl. Orient. 12: 113 (1853)

Common names Top

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Language Common/alternative name
Arabic حلبلوب كيراديني
Arabic فربيون كيراديني

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
  • Asia-temperate
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000961351
Tropicos 50273144
KEW urn:lsid:ipni.org:names:346018-1
The Plant List kew-78970
Open Tree Of Life 943355
NCBI Taxonomy 1087799
IPNI 346018-1
GBIF 3067080
EPPO EPHCD
EOL 1145137
CMAUP NPO25151

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
Cadmium up Taking and Allocation in Wood Species Associated to Cacao Agroforestry Systems and Its Potential Role for Phytoextraction Galvis DA, Jaimes-Suárez YY, Rojas Molina J, Ruiz R, Carvalho FE Plants (Basel) 13-Aug-2023
PMCID:PMC10459764
doi:10.3390/plants12162930
PMID:37631142
Phytoremediation as an Effective Remedy for Removing Trace Elements from Ecosystems Mocek-Płóciniak A, Mencel J, Zakrzewski W, Roszkowski S Plants (Basel) 14-Apr-2023
PMCID:PMC10141480
doi:10.3390/plants12081653
PMID:37111876
From Western Asia to the Mediterranean Basin: Diversification of the Widespread Euphorbia nicaeensis Alliance (Euphorbiaceae) Stojilkovič V, Záveská E, Frajman B Front Plant Sci 23-Jun-2022
PMCID:PMC9262032
doi:10.3389/fpls.2022.815379
PMID:35812903
Phytoremediation of Heavy Metals: An Indispensable Contrivance in Green Remediation Technology Sabreena, Hassan S, Bhat SA, Kumar V, Ganai BA, Ameen F Plants (Basel) 06-May-2022
PMCID:PMC9104525
doi:10.3390/plants11091255
PMID:35567256
Formulation, characteristics and anti-bacterial effects of Euphorbia hirta L. mouthwash Iskandar B, Lukman A, Syaputra S, Al-Abrori UN, Surboyo MD, Lee CK J Taibah Univ Med Sci 17-Sep-2021
PMCID:PMC9073867
doi:10.1016/j.jtumed.2021.08.009
PMID:35592805
Phytoremediation: A Promising Approach for Revegetation of Heavy Metal-Polluted Land Yan A, Wang Y, Tan SN, Mohd Yusof ML, Ghosh S, Chen Z Front Plant Sci 30-Apr-2020
PMCID:PMC7203417
doi:10.3389/fpls.2020.00359
PMID:32425957
Phytosynthesis of Cu/rGO using Euphorbia cheiradenia Boiss extract and study of its ability in the reduction of organic dyes and 4‐nitrophenol in aqueous medium Fahiminia M, Shamabadi NS, Nasrollahzadeh M, Sajadi SM IET Nanobiotechnol 11-Dec-2018
PMCID:PMC8676669
doi:10.1049/iet-nbt.2018.5175
PMID:31051452
Apoptotic Effects of Linum album Extracts on AGS Human Gastric Adenocarcinoma Cells and ZNF703 Oncogene Expression Asl EA, Mehrabadi JF, Afshar D, Noorbazargan H, Tahmasebi H, Rahimi A Asian Pac J Cancer Prev 01-Jan-2018
PMCID:PMC6291028
doi:10.22034/APJCP.2018.19.10.2911
PMID:30362321
Microbial and Plant-Assisted Bioremediation of Heavy Metal Polluted Environments: A Review Ojuederie OB, Babalola OO Int J Environ Res Public Health 04-Dec-2017
PMCID:PMC5750922
doi:10.3390/ijerph14121504
PMID:29207531
A Checklist of the Flora of Shanjan Protected Area, East Azerbaijan Province, NW Iran Bibalani GH, Taheri E Afr J Tradit Complement Altern Med 03-Oct-2013
PMCID:PMC3847374
doi:10.4314/ajtcam.v10i6.1
PMID:24311859
Antimicrobial Activities of Some Euphorbia Species Kirbag S, Erecevit P, Zengin F, Guvenc AN Afr J Tradit Complement Altern Med 12-Aug-2013
PMCID:PMC3847420
doi:10.4314/ajtcam.v10i5.13
PMID:24311840
Three New Diterpenoids from <i>Euphorbia sororia</i> L. Yun Huang, Haji Akber Aisa Wiley 16-Jun-2010
doi:10.1002/HLCA.200900353
Effect of soil and physiographic factors on ecological plant groups in the eastern Elborz mountain rangeland of Iran Tatian M, Arzani H, Reihan MK, Bahmanyar MA, Jalilvand H 02-Jun-2010
PMCID:PMC7165600
doi:10.1111/j.1744-697X.2010.00178.x
PMID:32834830
Cheiradone: a vascular endothelial cell growth factor receptor antagonist Hussain S, Slevin M, Mesaik MA, Choudhary MI, Elosta AH, Matou S, Ahmed N, West D, Gaffney J BMC Cell Biol 29-Jan-2008
PMCID:PMC2248182
doi:10.1186/1471-2121-9-7
PMID:18230134
Chemistry and biological activity of secondary metabolites in Euphorbia from Iran. Jassbi AR Phytochemistry 01-Sep-2006
doi:10.1016/J.PHYTOCHEM.2006.06.030
PMID:16889806

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[(1S,2R,3S,4S,5S,7R,9S,12S,15R,16R)-4-acetyloxy-1-(acetyloxymethyl)-7,15-dihydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.03,7.012,16]hexadec-13-en-2-yl] benzoate 162934127 Click to see CC1CC2(C(C1OC(=O)C)C(C3(C(C=CC4C3C(C2=O)(OC4(C)C)C)O)COC(=O)C)OC(=O)C5=CC=CC=C5)O 570.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
[(1S,2S,3S,4S,5S,7R,9S,12R,15R,16R)-15-acetyloxy-1-(acetyloxymethyl)-4,7-dihydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.03,7.012,16]hexadec-13-en-2-yl] benzoate 163003313 Click to see CC1CC2(C(C1O)C(C3(C(C=CC4C3C(C2=O)(OC4(C)C)C)OC(=O)C)COC(=O)C)OC(=O)C5=CC=CC=C5)O 570.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
[15-Acetyloxy-1-(acetyloxymethyl)-4,7-dihydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.03,7.012,16]hexadec-13-en-2-yl] benzoate 163003312 Click to see CC1CC2(C(C1O)C(C3(C(C=CC4C3C(C2=O)(OC4(C)C)C)OC(=O)C)COC(=O)C)OC(=O)C5=CC=CC=C5)O 570.60 unknown https://doi.org/10.1002/HLCA.200900353
[4-Acetyloxy-1-(acetyloxymethyl)-7,15-dihydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.03,7.012,16]hexadec-13-en-2-yl] benzoate 162934126 Click to see CC1CC2(C(C1OC(=O)C)C(C3(C(C=CC4C3C(C2=O)(OC4(C)C)C)O)COC(=O)C)OC(=O)C5=CC=CC=C5)O 570.60 unknown https://doi.org/10.1002/HLCA.200900353
> Benzenoids / Phenanthrenes and derivatives
6-Oxopristimerol 11754914 Click to see CC1=C2C(=CC(=C1O)O)C3(CCC4(C5CC(CCC5(CCC4(C3=CC2=O)C)C)(C)C(=O)OC)C)C 480.60 unknown via CMAUP database
Zeylasterone 13945472 Click to see CC12CCC(CC1C3(CCC4(C5=CC(=C(C(=C5C(=O)C=C4C3(CC2)C)C(=O)O)O)O)C)C)(C)C(=O)OC 510.60 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
Anhydrosecoisolariciresinol 9974771 Click to see COC1=C(C=CC(=C1)CC2COCC2CC3=CC(=C(C=C3)O)OC)O 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Vierol 101297703 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)CO 306.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-D:B-Friedoolean-5-ene-3beta,29-diol 13918509 Click to see CC1(C(CCC2C1=CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)O)C 442.70 unknown via CMAUP database
20(29)-Lupene-1beta,3beta-diol 488250 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown via CMAUP database
3alpha,16beta-Dihydroxylupa-12-ene 44179020 Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C 442.70 unknown via CMAUP database
3alpha,16beta,28-Trihydroxylupa-20(29)-ene 44178931 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO 458.70 unknown via CMAUP database
3beta-Hydroperoxy-7beta,25-epoxy-D:B-friedooleanane-5-ene 101481671 Click to see CC1(CCC2(CCC3(C4C5C=C6C(C4(CCC3(C2C1)C)CO5)CCC(C6(C)C)OO)C)C)C 456.70 unknown via CMAUP database
3beta,16beta-Dihydroxylupa-12-ene 44178932 Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C 442.70 unknown via CMAUP database
Calenduladiol 461835 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C 442.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Glochidiol 13969554 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Paniculatadiol 101286253 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C 442.70 unknown via CMAUP database
Pristimerin 159516 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown via CMAUP database
Resinone 101316848 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2O)C)C)(C)C)C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids
16beta-Hydroxy-3,4-secolupane-20(29)-ene-3-oic acid 44179021 Click to see CC(C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CC(C4(C3C(CC4)C(=C)C)C)O)C)C 458.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1R,2R,3R,4S,5S,12R,15R,16R)-4,15-diacetyloxy-1-(acetyloxymethyl)-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.03,7.012,16]hexadec-13-en-2-yl] benzoate 163189084 Click to see CC1CC2(C(C1OC(=O)C)C(C3(C(C=CC4C3C(C2=O)(OC4(C)C)C)OC(=O)C)COC(=O)C)OC(=O)C5=CC=CC=C5)O 612.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
[(1R,2R,3R,4S,5S,7R,9S,12R,15R,16R)-4,15-diacetyloxy-1-(acetyloxymethyl)-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.03,7.012,16]hexadec-13-en-2-yl] benzoate 163002551 Click to see CC1CC2(C(C1OC(=O)C)C(C3(C(C=CC4C3C(C2=O)(OC4(C)C)C)OC(=O)C)COC(=O)C)OC(=O)C5=CC=CC=C5)O 612.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
[4,15-Diacetyloxy-1-(acetyloxymethyl)-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.03,7.012,16]hexadec-13-en-2-yl] benzoate 85202338 Click to see CC1CC2(C(C1OC(=O)C)C(C3(C(C=CC4C3C(C2=O)(OC4(C)C)C)OC(=O)C)COC(=O)C)OC(=O)C5=CC=CC=C5)O 612.70 unknown https://doi.org/10.1002/HLCA.200900353
> Organoheterocyclic compounds / Benzofurans
Isololiolide 11019783 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown via CMAUP database

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