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Tanacetum artemisioides

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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 UUID643fcf43063f5874180063
Scientific name Tanacetum artemisioides
Authority Sch.Bip. ex Hook.f.
First published in Fl. Brit. India 3(8): 318 (1881)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chrysanthemum karakoramense Kitam. Acta Phytotax. Geobot. 19: 104 (1963)
Artemisia fasciculata Hook.f. & Thomson ex Hook.f. Fl. Brit. India 3(8): 318 (1881)

Common names Top

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Language Common/alternative name
Chinese 艾状菊蒿

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-0000088750
Tropicos 2735505
KEW urn:lsid:ipni.org:names:252234-1
The Plant List gcc-45080
Open Tree Of Life 7596067
IPNI 252234-1
GBIF 3118603
EOL 2904444

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
Two Ceramides from Tanacetum artemesioides Viqar U. Ahmad, Javid Hussain, Hidayat Hussain, Umar Farooq, Erum Akber, Sarfraz A. Nawaz, Muhammad I. Choudhary Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNB-2004-0316
Tanacetamide D: A New Ceramide from <i>Tanacetum artemisioides</i> Javid Hussain, Meamoona Munir, Zahid Hassan, Naseem Bano, Saima Arshad, Viqar Uddin Ahmad Wiley 11-Feb-2010
doi:10.1002/HLCA.200900204
The analgesic, anti-inflammatory and calcium antagonist potential of Tanacetum artemisioides. Bukhari IA, Khan RA, Gilani AU, Shah AJ, Hussain J, Ahmad VU Arch Pharm Res 01-Mar-2007
doi:10.1007/BF02977610
PMID:17424935
Tanacetamide C: One New Ceramide from Tanacetum artemisioides. J. Hussain, V. U. Ahmad, H. Hussain, Z. Hassan, A. Khan, U. Farooq Wiley 25-Oct-2005
doi:10.1002/CHIN.200547198

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 / Fatty Acyls / Fatty amides / N-acyl amines
(3S,4S)-3,4-dihydroxy-N-[(E,2R,3S,6R)-1,3,6-trihydroxypentadec-4-en-2-yl]pentacosanamide 102173277 Click to see CCCCCCCCCCCCCCCCCCCCCC(C(CC(=O)NC(CO)C(C=CC(CCCCCCCCC)O)O)O)O 670.10 unknown https://doi.org/10.1002/HLCA.200900204
3,4-dihydroxy-N-(1,3,6-trihydroxypentadec-4-en-2-yl)pentacosanamide 162981713 Click to see CCCCCCCCCCCCCCCCCCCCCC(C(CC(=O)NC(CO)C(C=CC(CCCCCCCCC)O)O)O)O 670.10 unknown https://doi.org/10.1002/HLCA.200900204
> Lipids and lipid-like molecules / Sphingolipids / Ceramides
(3S,4S)-3,4-dihydroxy-N-[(E,2R,3S,6R)-1,3,6-trihydroxynonacos-4-en-2-yl]dodecanamide 163074932 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(C=CC(C(CO)NC(=O)CC(C(CCCCCCCC)O)O)O)O 684.10 unknown https://doi.org/10.1002/CHIN.200547198
3,4-dihydroxy-N-(1,3,6-trihydroxynonacos-4-en-2-yl)dodecanamide 163074931 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(C=CC(C(CO)NC(=O)CC(C(CCCCCCCC)O)O)O)O 684.10 unknown https://doi.org/10.1002/CHIN.200547198
N-(1,3-dihydroxyhenicos-4-en-2-yl)-2-hydroxyhenicos-3-enamide 72968797 Click to see CCCCCCCCCCCCCCCCCC=CC(C(=O)NC(CO)C(C=CCCCCCCCCCCCCCCCC)O)O 664.10 unknown https://doi.org/10.1515/ZNB-2004-0316
N-(1,3-dihydroxyhenicos-4-en-2-yl)acetamide 72786619 Click to see CCCCCCCCCCCCCCCCC=CC(C(CO)NC(=O)C)O 383.60 unknown https://doi.org/10.1515/ZNB-2004-0316
N-[(E,2R,3S)-1,3-dihydroxyhenicos-4-en-2-yl]acetamide 11292035 Click to see CCCCCCCCCCCCCCCCC=CC(C(CO)NC(=O)C)O 383.60 unknown https://doi.org/10.1515/ZNB-2004-0316
> Lipids and lipid-like molecules / Sphingolipids / Ceramides / Long-chain ceramides
(E,2S)-N-[(E,2R,3S)-1,3-dihydroxyhenicos-4-en-2-yl]-2-hydroxyhenicos-3-enamide 11456573 Click to see CCCCCCCCCCCCCCCCCC=CC(C(=O)NC(CO)C(C=CCCCCCCCCCCCCCCCC)O)O 664.10 unknown https://doi.org/10.1515/ZNB-2004-0316
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1515/ZNB-2004-0316
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1515/ZNB-2004-0316
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1515/ZNB-2004-0316
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1515/ZNB-2004-0316
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Achillin 291264 Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C 246.30 unknown https://doi.org/10.1002/CHIN.200547198
Desacetoxymatricarin 167683 Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C 246.30 unknown https://doi.org/10.1002/CHIN.200547198
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-3,6,7,4'-tetramethoxyflavone 5318355 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC 358.30 unknown https://doi.org/10.1002/CHIN.200547198
Penduletin 5320462 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC 344.30 unknown https://doi.org/10.1007/BF02977610
https://doi.org/10.1002/CHIN.200547198
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3'-Demethylnobiletin 183466 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)O 388.40 unknown https://doi.org/10.1002/HLCA.200900204
5-o-Desmethylnobiletin 358832 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 388.40 unknown https://doi.org/10.1002/HLCA.200900204

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