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Euphorbia larica

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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 UUID64403b49067f2833642880
Scientific name Euphorbia larica
Authority Boiss.
First published in Cent. Euphorb. : 24 (1860)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tirucalia larica (Boiss.) P.V.Heath Calyx 5: 91 (1996)
Euphorbia masirahensis Ghaz. Novon 3: 258 (1993)

Common names Top

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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
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Yemen
    • Western Asia
      • Iran

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000962951
Tropicos 50111278
KEW urn:lsid:ipni.org:names:347061-1
The Plant List kew-80506
Open Tree Of Life 969006
NCBI Taxonomy 1031526
IPNI 347061-1
iNaturalist 334270
GBIF 3068607
EOL 1144559
Wikipedia Euphorbia_larica

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 Previously Unrecorded Fungal Species Isolated from Muui Island in Korea Shin S, Jeon H, Kim S, Noh HJ, Jo JW, Min K, Son H Mycobiology 27-Dec-2023
PMCID:PMC10763901
doi:10.1080/12298093.2023.2290766
PMID:38179114
Standardization of Euphorbia tithymaloides (L.) Poit. (Root) by Conventional and DNA Barcoding Methods Patil S, Imran M, Jaquline RS, Aeri V ACS Omega 04-Aug-2023
PMCID:PMC10433337
doi:10.1021/acsomega.3c02543
PMID:37599932
GC-MS Profiling and Biomedical Applications of Essential Oil of Euphorbia larica Boiss.: A New Report Shah M, Khan F, Ullah S, Mohanta TK, Khan A, Zainab R, Rafiq N, Ara H, Alam T, Rehman NU, Al-Harrasi A Antioxidants (Basel) 07-Mar-2023
PMCID:PMC10045896
doi:10.3390/antiox12030662
PMID:36978910
Pest categorisation of Fusarium brachygibbosum Bragard C, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Campese C, Czwienczek E, Maiorano A, Streissl F, Reignault PL EFSA J 12-Nov-2021
PMCID:PMC8590089
doi:10.2903/j.efsa.2021.6887
PMID:34804234
Plastome Evolution in the Hyperdiverse Genus Euphorbia (Euphorbiaceae) Using Phylogenomic and Comparative Analyses: Large-Scale Expansion and Contraction of the Inverted Repeat Region Wei N, Pérez-Escobar OA, Musili PM, Huang WC, Yang JB, Hu AQ, Hu GW, Grace OM, Wang QF Front Plant Sci 04-Aug-2021
PMCID:PMC8372406
doi:10.3389/fpls.2021.712064
PMID:34421963
Green-synthesized nanocatalysts and nanomaterials for water treatment: Current challenges and future perspectives Nasrollahzadeh M, Sajjadi M, Iravani S, Varma RS J Hazard Mater 07-Jul-2020
PMCID:PMC7606836
doi:10.1016/j.jhazmat.2020.123401
PMID:32763697
Comparative Chloroplast Genomics of Endangered Euphorbia Species: Insights into Hotspot Divergence, Repetitive Sequence Variation, and Phylogeny Khan A, Asaf S, Khan AL, Shehzad T, Al-Rawahi A, Al-Harrasi A Plants (Basel) 05-Feb-2020
PMCID:PMC7076480
doi:10.3390/plants9020199
PMID:32033491
Discriminatory power of rbcL barcode locus for authentication of some of United Arab Emirates (UAE) native plants Maloukh L, Kumarappan A, Jarrar M, Salehi J, El-wakil H, Rajya Lakshmi TV 3 Biotech 08-Jun-2017
PMCID:PMC5465043
doi:10.1007/s13205-017-0746-1
PMID:28597155
The Practice of Ethnomedicine in the Northern and Southern Provinces of Oman Divakar MC, Al-Siyabi A, Varghese SS, Rubaie MA Oman Med J 01-Jul-2016
PMCID:PMC4927734
doi:10.5001/omj.2016.49
PMID:27403235
An ethnobotanical survey on hormozgan province, Iran Safa O, Soltanipoor MA, Rastegar S, Kazemi M, Nourbakhsh Dehkordi K, Ghannadi A Avicenna J Phytomed 01-Jan-2013
PMCID:PMC4075690
PMID:25050260
Hydrocarbons from Euphorbia lathyris E. K. Nemethy, J. W. Otvos, M. Calvin Walter de Gruyter GmbH 11-Nov-2007
doi:10.1351/PAC198153061101
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
Flavonoids from Euphorbia larica, E. virgata, E. chamaesyce and E. magalanta Ayhan Ulubelen, Sevil Öksüz, Belkis Halfon, Yagoup Aynehchi, Tom J. Mabry American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50028A037

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163184988 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 6575009 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1351/PAC198153061101
https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Octacosyl docosanoate 13908827 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCCCCCC 733.30 unknown https://doi.org/10.1351/PAC198153061101
https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,8aR)-1-[(E)-6-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-4-methylhex-3-enyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 92966593 Click to see CC(=CCCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCC3C(=C)CCCC3(C)C 428.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
(1R,2R,4aS,8aS)-1-{(3E)-6-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-4-methylhex-3-en-1-yl}-2,5,5,8a-tetramethyldecahydronaphthalen-2-ol 86289515 Click to see CC(=CCCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCC3C(=C)CCCC3(C)C 428.70 unknown https://doi.org/10.1351/PAC198153061101
[(1R,3aR,5aR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 163187380 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
[(3S,6aR,8aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 5318302 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1351/PAC198153061101
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1351/PAC198153061101
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
https://doi.org/10.1351/PAC198153061101
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
https://doi.org/10.1351/PAC198153061101
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Nonacosan-10-one 441490 Click to see CCCCCCCCCCCCCCCCCCCC(=O)CCCCCCCCC 422.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
https://doi.org/10.1351/PAC198153061101
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/NP50028A037
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 125528541 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 154497089 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
https://doi.org/10.1021/NP50028A037
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP50028A037
Quercetin 3-alloside 12304327 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1021/NP50028A037
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1021/NP50028A037
https://doi.org/10.1016/J.PHYTOCHEM.2006.06.030

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