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Cousinia piptocephala

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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 UUID643fc7252dc05814923306
Scientific name Cousinia piptocephala
Authority Bunge
First published in Gatt. Cous. : 26 (1865)

Description Top

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Synonyms Top

Scientific name Authority First published in
Arctium piptocephalum Kuntze Revis. Gen. Pl. 1: 308 (1891)

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000012005
Tropicos 2728005
KEW urn:lsid:ipni.org:names:199195-1
The Plant List gcc-111628
Open Tree Of Life 167186
NCBI Taxonomy 254686
IPNI 199195-1
GBIF 3102690
EOL 6267287

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)!
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Title Authors Publication Released IDs
Isolation and Identification of Two Phenolic Compounds from a Moderately Cytotoxic Fraction of Cousinia verbascifolia Bunge Sajjadi SE, Ghanadian M, Haghighi M Adv Biomed Res 06-Jun-2017
PMCID:PMC5468789
doi:10.4103/2277-9175.190980
PMID:28626741
Bisabolene derivatives and sesquiterpene lactones from Cousinia species J.Alberto Marco, Juan F. Sanz, Remedios Albiach, A. Rustaiyan, Z. Habibi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)95002-7

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 / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(8-Hydroxy-3,6-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-9,2'-oxirane]-4-yl) 2-(hydroxymethyl)prop-2-enoate 182407 Click to see C=C1CC(C2C(C3C1CC(C34CO4)O)OC(=O)C2=C)OC(=O)C(=C)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(00)95002-7
[(3aR,4S,6aR,8S,9S,9aS,9bS)-9-(chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] 2-methylpropanoate 163018333 Click to see CC(C)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)(CCl)O)O 384.80 unknown https://doi.org/10.1016/S0031-9422(00)95002-7
[9-(Chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 14021482 Click to see C=C1CC(C2C(C3C1CC(C3(CCl)O)O)OC(=O)C2=C)OC(=O)C(=C)CO 398.80 unknown https://doi.org/10.1016/S0031-9422(00)95002-7
[9-(Chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] 2-methylpropanoate 163018332 Click to see CC(C)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)(CCl)O)O 384.80 unknown https://doi.org/10.1016/S0031-9422(00)95002-7
Chlorojanerin 182408 Click to see C=C1CC(C2C(C3C1CC(C3(CCl)O)O)OC(=O)C2=C)OC(=O)C(=C)CO 398.80 unknown https://doi.org/10.1016/S0031-9422(00)95002-7
Cynaropicrin 119093 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown https://doi.org/10.1016/S0031-9422(00)95002-7
Janerin 14021480 Click to see C=C1CC(C2C(C3C1CC(C34CO4)O)OC(=O)C2=C)OC(=O)C(=C)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(00)95002-7
Linichlorin A 182337 Click to see CC(=C)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)(CCl)O)O 382.80 unknown https://doi.org/10.1016/S0031-9422(00)95002-7
Saupirin 181128 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown https://doi.org/10.1016/S0031-9422(00)95002-7

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