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Tanacetum cadmeum

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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 UUID643fc61eeafcf420832955
Scientific name Tanacetum cadmeum
Authority (Boiss.) Heywood
First published in Notes Roy. Bot. Gard. Edinburgh 21: 58, in adnot. (1952)

Description Top

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Synonyms Top

Scientific name Authority First published in
Achillea speciosa Hayek Ann. Nat. Hofmus. Wien 20: 422. 1905

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Tanacetum cadmeum subsp. cadmeum (Boiss.) Heywood
Tanacetum cadmeum subsp. orientale Grierson Notes Roy. Bot. Gard. Edinburgh 33(2): 261 (1974)

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-0000002705
KEW urn:lsid:ipni.org:names:252258-1
The Plant List gcc-102603
Open Tree Of Life 3899212
IPNI 252258-1
GBIF 3118572
EOL 6232181

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)!
Title Authors Publication Released IDs
Isolation and structures of eudesmanolides from Tanacetum cadmeum ssp. cadmeum Zerrin Çalişkan, Nezhun Gören, William H. Watson Springer Science and Business Media LLC 04-May-2004
doi:10.1023/B:JOCC.0000026275.39368.FC

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
1-epi-tatridin B 7605278 Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
4-Hydroxy-6-methyl-3,10-dimethylidene-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-2,9-dione 556782 Click to see CC1=CC(C2C(CC(=C)C(=O)CC1)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
4,9-dihydroxy-6-methyl-3,10-dimethylidene-4,7,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-2-one 4437183 Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
Tamirin 10106765 Click to see CC1=CC(C2C(CC(=C)C(=O)CC1)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(1R,2S,5S,6S,9S,10R,13R)-10-hydroxy-5,9,13-trimethyl-3,14-dioxatetracyclo[7.5.0.01,13.02,6]tetradecan-4-one 102374952 Click to see CC1C2CCC3(C(CCC4(C3(C2OC1=O)O4)C)O)C 266.33 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
(3S,3aS,5aS,6R,9aR,9bS)-Decahydro-6,9a-dihydroxy-3,5a-dimethyl-9-methylenenaphtho[1,2-b]furan-2(3H)-one 14413453 Click to see CC1C2CCC3(C(CCC(=C)C3(C2OC1=O)O)O)C 266.33 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
10-Hydroxy-5,9,13-trimethyl-3,14-dioxatetracyclo[7.5.0.01,13.02,6]tetradecan-4-one 163000119 Click to see CC1C2CCC3(C(CCC4(C3(C2OC1=O)O4)C)O)C 266.33 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
3,5a,9-trimethyl-3a,4,5,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2,6-dione 3767748 Click to see CC1C2CCC3(C(=O)CCC(=C3C2OC1=O)C)C 248.32 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
6-Hydroxy-3,5a,9-trimethyl-3,3a,4,5,6,7,8,9b-octahydrobenzo[g][1]benzofuran-2-one 3807142 Click to see CC1C2CCC3(C(CCC(=C3C2OC1=O)C)O)C 250.33 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
Artemin 3678270 Click to see CC1C2CCC3(C(CCC(=C)C3(C2OC1=O)O)O)C 266.33 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
Artesin[sesquiterpene] 10422228 Click to see CC1C2CCC3(C(CCC(=C3C2OC1=O)C)O)C 250.33 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
Taurin 211707 Click to see CC1C2CCC3(C(=O)CCC(=C3C2OC1=O)C)C 248.32 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,4R,5E,9S,10Z,11aS)-4,9-dihydroxy-6,10-dimethyl-3-methylene-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-2(3H)-one 14466152 Click to see CC1=CC(C2C(C=C(C(CC1)O)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
4,9-Dihydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-2-one 72731791 Click to see CC1=CC(C2C(C=C(C(CC1)O)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Isofraxidin 5318565 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O 222.19 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1023/B:JOCC.0000026275.39368.FC

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