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Euphorbia condylocarpa

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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 UUID64403b01cf4a1435271260
Scientific name Euphorbia condylocarpa
Authority M.Bieb.
First published in Fl. Taur.-Caucas. 1: 377 (1808)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tithymalus amplexicaulis Klotzsch & Garcke Abh. Königl. Akad. Wiss. Berlin 1859: 80 (1860)
Tithymalus cardiophyllus Klotzsch & Garcke Abh. Königl. Akad. Wiss. Berlin 1859: 78 (1860)
Tithymalus condylocarpus Klotzsch & Garcke Abh. Königl. Akad. Wiss. Berlin 1859: 78 (1860)
Euphorbia amplexicaulis Ledeb. Fl. Ross. 3: 567 (1850)
Euphorbia cardiophylla Boiss. & Heldr. Diagn. Pl. Orient. 12: 107 (1853)

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
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Iraq
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000961452
Tropicos 12805531
KEW urn:lsid:ipni.org:names:346088-1
The Plant List kew-79065
Open Tree Of Life 630242
Observations.org 117764
NCBI Taxonomy 758543
IPNI 346088-1
GBIF 3070069
Freebase /m/0h_9vsq
EOL 1145099
Elurikkus 362386
Wikipedia Euphorbia_condylocarpa

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 Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
A Review on Plant-Mediated Synthesis of Bimetallic Nanoparticles, Characterisation and Their Biological Applications Berta L, Coman NA, Rusu A, Tanase C Materials (Basel) 13-Dec-2021
PMCID:PMC8705710
doi:10.3390/ma14247677
PMID:34947271
A new nanomagnetic Pd-Co bimetallic alloy as catalyst in the Mizoroki–Heck and Buchwald–Hartwig amination reactions in aqueous media Sobhani S, Zarei H, Sansano JM Sci Rep 23-Aug-2021
PMCID:PMC8382703
doi:10.1038/s41598-021-95931-6
PMID:34426594
Statistical evaluation of main extraction parameters in twenty plant extracts for obtaining their optimum total phenolic content and its relation to antioxidant and antibacterial activities Kadir DH Food Sci Nutr 06-May-2021
PMCID:PMC8269642
doi:10.1002/fsn3.2288
PMID:34262709
Laboratory analysis of Au–Pd bimetallic nanoparticles synthesized with Citrus limon leaf extract and its efficacy on mosquito larvae and non-target organisms Minal SP, Prakash S Sci Rep 10-Dec-2020
PMCID:PMC7728787
doi:10.1038/s41598-020-78662-y
PMID:33303823
Screening of plant-based natural compounds as a potential COVID-19 main protease inhibitor: an in silico docking and molecular dynamics simulation approach Majumder R, Mandal M J Biomol Struct Dyn 08-Sep-2020
PMCID:PMC7544942
doi:10.1080/07391102.2020.1817787
PMID:32897138
Bioactive metal oxide nanoparticles from some common fruit wastes and Euphorbia condylocarpa plant Mahmoudi G, Sufimahmoudi E, Sajadi SM Food Sci Nutr 31-Aug-2020
PMCID:PMC7590339
doi:10.1002/fsn3.1853
PMID:33133554
Phyto-Nanocatalysts: Green Synthesis, Characterization, and Applications Fierascu RC, Ortan A, Avramescu SM, Fierascu I Molecules 20-Sep-2019
PMCID:PMC6804184
doi:10.3390/molecules24193418
PMID:31547052
Saudi anti-human cancer plants database (SACPD): A collection of plants with anti-human cancer activities Al-Zahrani AA Oncol Rev 26-Mar-2018
PMCID:PMC5939832
doi:10.4081/oncol.2018.349
PMID:29774137
Palladium nanoparticle-decorated reduced graphene oxide sheets synthesized using Ficus carica fruit extract: A catalyst for Suzuki cross-coupling reactions Anasdass JR, Kannaiyan P, Raghavachary R, Gopinath SC, Chen Y PLoS One 21-Feb-2018
PMCID:PMC5821401
doi:10.1371/journal.pone.0193281
PMID:29466453
Synthesis paradigm and applications of silver nanoparticles (AgNPs), a review Beyene HD, Werkneh AA, Bezabh HK, Ambaye TG 24-Aug-2017
PMCID:PMC7148648
doi:10.1016/j.susmat.2017.08.001
Extraction of Sulfathiazole from Urine Samples Using Biosynthesized Magnetic Nanoparticles Maham M, Karami-Osboo R Iran J Pharm Res 01-Mar-2017
PMCID:PMC5603855
PMID:28979301
Green Synthesis, Characterization and Uses of Palladium/Platinum Nanoparticles Siddiqi KS, Husen A Nanoscale Res Lett 02-Nov-2016
PMCID:PMC5093107
doi:10.1186/s11671-016-1695-z
PMID:27807824
Optimal extraction method of phenolics from the root of Euphorbia condylocarpa Mahmoud Nasrollahzadeh, S. Mohammad Sajadi, Mehdi Maham, Peyman Salaryan, Ayesheh Enayati, S. Adnan Sajjadi, Khadijeh Naderi Springer Science and Business Media LLC 26-Jul-2011
doi:10.1007/S10600-011-9952-Y
A flavanone 7-glucoside fromEuphorbia condylocarpa Yu. V. Roshchin, A. L. Shinkarenko, É. T. Oganesyan Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564264

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(5S,10S,13S,14S)-4,4,10,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 138113753 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/10.1007/BF00564277
Lanosta-8,24-dien-3-ol 856 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/10.1007/BF00564277
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S10600-011-9952-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/S10600-011-9952-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 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/10.1007/BF00565849
Trifolin 5282149 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/10.1007/BF00565849
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-7-[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 163098391 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3(C(C(C(O3)CO)O)O)CO)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1007/BF00564264
4H-1-Benzopyran-4-one, 7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (2S)- 4441 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1007/S10600-011-9952-Y
7-[3,4-Dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 163098390 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3(C(C(C(O3)CO)O)O)CO)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1007/BF00564264
Naringin 442428 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1007/S10600-011-9952-Y

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