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Crepis foetida subsp. rhoeadifolia

Crepis foetida subsp. rhoeadifolia - 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 UUID643fd0e973f5b804123361
Scientific name Crepis foetida subsp. rhoeadifolia
Authority (M.Bieb.) Celak.
First published in Prodr. Fl. Böhmen : 190 (1871)

Description Top

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Common names Top

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Language Common/alternative name
Arabic سراغة نتنة نويع حمراء الأوراق
Czech škarda smrdutá mákolistá
German klatschmohn-stink-pippau
Finnish kaakonhaisukeltto
Polish pępawa makolistna

Varieties (abbr. var.) 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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000108143
Tropicos 2700638
INPN 133508
KEW urn:lsid:ipni.org:names:77181783-1
The Plant List gcc-66633
Open Tree Of Life 328687
Observations.org 125551
NCBI Taxonomy 310245
NBN Atlas NBNSYS0200003666
GBIF 5831060
EPPO CVPFR
USDA GRIN 70207

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
Electrical impedance spectroscopy (EIS) in plant roots research: a review Liu Y, Li D, Qian J, Di B, Zhang G, Ren Z Plant Methods 13-Nov-2021
PMCID:PMC8590265
doi:10.1186/s13007-021-00817-3
PMID:34774075
Beyond the Forest-Grassland Dichotomy: The Gradient-Like Organization of Habitats in Forest-Steppes Erdős L, Török P, Szitár K, Bátori Z, Tölgyesi C, Kiss PJ, Bede-Fazekas Á, Kröel-Dulay G Front Plant Sci 03-Mar-2020
PMCID:PMC7062704
doi:10.3389/fpls.2020.00236
PMID:32194608
Molecular phylogeny and taxonomy of Eurasian Neoerysiphe species infecting Asteraceae and Geranium Heluta V, Takamatsu S, Harada M, Voytyuk S Persoonia 08-Apr-2010
PMCID:PMC2890160
doi:10.3767/003158510X501696
PMID:20664762
Sesquiterpene lactones from Crepis rhoeadifolia W. Kisiel, B. Barszcz Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(96)00351-2

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
(E)-5-[(4aR,5S,8aS)-5-(hydroxymethyl)-2,5,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-enoic acid 163104399 Click to see CC1=C(C2(CCCC(C2CC1)(C)CO)C)CCC(=CC(=O)O)C 320.50 unknown https://doi.org/10.1016/0031-9422(96)00351-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3S,3aS,5R,6aR,8S,9R,9aR,9bS)-5,8-dihydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,6a,7,8,9,9a,9b-decahydroazuleno[4,5-b]furan-2-one 102247111 Click to see CC1C(CC2C1C3C(CC(C2=C)O)C(C(=O)O3)C)O 266.33 unknown https://doi.org/10.1016/0031-9422(96)00351-2
(3S,3aS,5R,6aR,8S,9S,9aR,9bS)-5,8-dihydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,6a,7,8,9,9a,9b-decahydroazuleno[4,5-b]furan-2-one 102247110 Click to see CC1C(CC2C1C3C(CC(C2=C)O)C(C(=O)O3)C)O 266.33 unknown https://doi.org/10.1016/0031-9422(96)00351-2
(3S,3aS,6aR,8S,9aR,9bS)-3-methyl-6,9-dimethylidene-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 21636137 Click to see CC1C2CCC(=C)C3CC(C(=C)C3C2OC1=O)OC4C(C(C(C(O4)CO)O)O)O 410.50 unknown https://doi.org/10.1016/0031-9422(96)00351-2
3-methyl-6,9-dimethylidene-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 73817502 Click to see CC1C2CCC(=C)C3CC(C(=C)C3C2OC1=O)OC4C(C(C(C(O4)CO)O)O)O 410.50 unknown https://doi.org/10.1016/0031-9422(96)00351-2
Azuleno(4,5-b)furan-2(3H)-one, decahydro-5,8-dihydroxy-3,9-dimethyl-6-methylene- 159226 Click to see CC1C(CC2C1C3C(CC(C2=C)O)C(C(=O)O3)C)O 266.33 unknown https://doi.org/10.1016/0031-9422(96)00351-2
Ixerin F 21636023 Click to see CC1C2CC(C(=C)C3CC(C(=C)C3C2OC1=O)OC4C(C(C(C(O4)CO)O)O)O)O 426.50 unknown https://doi.org/10.1016/0031-9422(96)00351-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Isosalicin 12304407 Click to see C1=CC=C(C(=C1)COC2C(C(C(C(O2)CO)O)O)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(96)00351-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Helicin 101799 Click to see C1=CC=C(C(=C1)C=O)OC2C(C(C(C(O2)CO)O)O)O 284.26 unknown https://doi.org/10.1016/0031-9422(96)00351-2

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