Dysphania multifida - Unknown
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Internal ID UUID644018bbcc5db957597232
Scientific name Dysphania multifida
Authority (L.) Mosyakin & Clemants
First published in Ukrayins'k. Bot. Zhurn. 59(4): 382 (2002).

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Synonyms Top

Scientific name Authority First published in
Roubieva microcarpa Phil. Anales Univ. Chile 110: 423 (1895)
Chenopodium microcarpum (Phil.) A.Tronc. Not. Mens. Mus. Nac. Hist. Nat. 21(250): 3 1977
Chenopodium multifidum L. Sp. Pl. : 220 (1753)
Chenopodium multifidum var. microcarpa (Phil.) Reiche Fl. Chile 6: 150 (1911)
Dysphania microcarpa (Phil.) Mosyakin & Clemants J. Bot. Res. Inst. Texas 2: 428 (2008)
Chenopodium multifidum f. spatulathum Aellen Amer. Midl. Naturalist 30: 50 1943
Orthosporum multifidum (L.) Kostel. Allg. Med.-Pharm. Fl. 4: 1434 (1835)
Teloxys multifida (L.) W.A.Weber Phytologia 58: 478 (1985)
Roubieva multifida (L.) Moq. Ann. Sci. Nat., Bot. , sér. 2, 1: 293 (1834)

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Language Common/alternative name
Welsh troed-yr-ŵydd sawrus
German ambrina pinnatisecta
German atriplex multifida
Swedish ullmålla

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000658883
Florida Plant Atlas 1942
Flora of Alabama 1508
USDA Plants DYMU
Tropicos 50215997
INPN 611760
Flora of Italy 456
KEW urn:lsid:ipni.org:names:1037855-2
The Plant List kew-2780238
Open Tree Of Life 496627
NCBI Taxonomy 1072223
IPNI 70029930-1
iNaturalist 76750
GBIF 5568361
Freebase /m/05p0lml
EPPO CHEMF
EOL 586721
Calflora (Californian flora) 10848
USDA GRIN 446555
Wikipedia Dysphania_multifida

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Essential oils from Dysphania genus: Traditional uses, chemical composition, toxicology, and health benefits Dagni A, Hegheș SC, Suharoschi R, Pop OL, Fodor A, Vulturar R, Cozma A, Aniq filali O, Vodnar DC, Soukri A, El Khalfi B Front Pharmacol 08-Dec-2022
PMCID:PMC9773091
doi:10.3389/fphar.2022.1024274
PMID:36569323
Biodiversity in Urban Areas: The Extraordinary Case of Appia Antica Regional Park (Rome, Italy) Iamonico D Plants (Basel) 15-Aug-2022
PMCID:PMC9414419
doi:10.3390/plants11162122
PMID:36015425
Resurrection of the genus Botrydium Spach (Chenopodiaceae), with a description of four new species from China, Peru and Burundi Zhang M, Zhu G Plant Divers 07-Dec-2016
PMCID:PMC6112192
doi:10.1016/j.pld.2016.10.005
PMID:30159484
Medicinal plants in the cultural landscape of a Mapuche-Tehuelche community in arid Argentine Patagonia: an eco-sensorial approach Molares S, Ladio A J Ethnobiol Ethnomed 26-Aug-2014
PMCID:PMC4150423
doi:10.1186/1746-4269-10-61
PMID:25159153
Phellandrene endoperoxides from the essential oil of Chenopodium multifidum J. De Pascual-T, I.S. Bellido, C. Torres, B.A. Sastre, M. Grande Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)85239-9
Δ5-Dehydro-1-hydroxycarvomenthols from the essential oil of Chenopodium multifidum J.De Pascual Teresa, C. Torres, M.S. González, M. Grande, I.S. Bellido Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97688-X

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 / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1016/0031-9422(81)85239-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-3-Carene 442461 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(81)85239-9
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(81)85239-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1R,2S,5S)-2-methyl-5-propan-2-ylcyclohex-3-ene-1,2-diol 26176656 Click to see CC(C)C1CC(C(C=C1)(C)O)O 170.25 unknown https://doi.org/10.1016/S0031-9422(00)97688-X
(1S,2R,5S)-2-methyl-5-propan-2-ylcyclohex-3-ene-1,2-diol 130830084 Click to see CC(C)C1CC(C(C=C1)(C)O)O 170.25 unknown https://doi.org/10.1016/S0031-9422(00)97688-X
(1S,2S,5S)-2-methyl-5-propan-2-ylcyclohex-3-ene-1,2-diol 26176657 Click to see CC(C)C1CC(C(C=C1)(C)O)O 170.25 unknown https://doi.org/10.1016/S0031-9422(00)97688-X
(4R,5S)-4-hydroxy-2-methyl-5-propan-2-ylcyclohex-2-en-1-one 44234541 Click to see CC1=CC(C(CC1=O)C(C)C)O 168.23 unknown https://doi.org/10.1016/0031-9422(81)85239-9
3-Hydroxy-p-menth-1-en-6-one 14106048 Click to see CC1=CC(C(CC1=O)C(C)C)O 168.23 unknown https://doi.org/10.1016/0031-9422(81)85239-9
5-p-Menthene-1,2-diol 14736609 Click to see CC(C)C1CC(C(C=C1)(C)O)O 170.25 unknown https://doi.org/10.1016/S0031-9422(00)97688-X
Acetic acid 4-isopropylcyclohexylmethyl ester 20155070 Click to see CC(C)C1CCC(CC1)COC(=O)C 198.30 unknown https://doi.org/10.1016/0031-9422(81)85239-9
trans-5-Hydroxy-p-menth-1(6)-en-2-one 6429209 Click to see CC1=CC(C(CC1=O)C(C)C)O 168.23 unknown https://doi.org/10.1016/0031-9422(81)85239-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxasteroids and derivatives
Inflatin A 53493985 Click to see CC12CCC3C(C1CCC4C25CCC(C(C4)C5)(CO)O)(COC(O3)C6=CC=C(C=C6)O)C 442.60 unknown https://doi.org/10.1016/0031-9422(81)85239-9
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
(1R,4S,7S)-5-methyl-7-propan-2-yl-2,3-dioxabicyclo[2.2.2]oct-5-ene 101408371 Click to see CC1=CC2C(CC1OO2)C(C)C 168.23 unknown https://doi.org/10.1016/0031-9422(81)85239-9
(1S,4R,7S)-5-methyl-7-propan-2-yl-2,3-dioxabicyclo[2.2.2]oct-5-ene 101408369 Click to see CC1=CC2C(CC1OO2)C(C)C 168.23 unknown https://doi.org/10.1016/0031-9422(81)85239-9
5-Methyl-7-propan-2-yl-2,3-dioxabicyclo[2.2.2]oct-5-ene 13969857 Click to see CC1=CC2C(CC1OO2)C(C)C 168.23 unknown https://doi.org/10.1016/0031-9422(81)85239-9

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