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Seriphidium diffusum

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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 UUID643fcf45455ed737299073
Scientific name Seriphidium diffusum
Authority (Krasch. ex Poljakov) Y.R.Ling
First published in Bull. Bot. Res., Harbin 11(4): 16 (1991)

Description Top

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Synonyms Top

Scientific name Authority First published in
Artemisia diffusa Krasch. ex Poljakov Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 16: 399 (1954)

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000088869
KEW urn:lsid:ipni.org:names:962899-1
The Plant List gcc-45193
IPNI 962899-1
GBIF 3089871
EOL 5105683
Open Tree Of Life 96255

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
Flavonoid Aglycones from the Leaf Surfaces of Some Artemisia spp. (Compositae-Anthemideae) Karin M. Valant-Vetschera, Eckhard Wollenweber Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1995-5-604
Composition of the Volatile Oil of<i>Artemisia diffusa</i>Krasch. ex Poljak. Growing Wild in Iran Khatereh Khazraei-Alizadeh, Abdolhossein Rustaiyan Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.2001.9699656
Herniarin fromArtemisia diffusa V. A. Tarasov, Sh. Z. Kasymov, G. P. Sidyakin Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00595083
A sesquiterpene lactone from Artemisia diffusa A. Rustaiyan, H. Sigari, J. Jakupovic, M. Grenz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98075-0

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 / Bicyclic monoterpenoids
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1080/10412905.2001.9699656
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(1R,2R,5S,6S,9R,13R)-5,9,13-trimethyl-3,14-dioxatetracyclo[7.5.0.01,13.02,6]tetradecane-4,10-dione 162938058 Click to see CC1C2CCC3(C(=O)CCC4(C3(C2OC1=O)O4)C)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
(3S,3aR,4S,5aR,9bR)-4-hydroxy-3,5a,9-trimethyl-3a,4,5,7,8,9b-hexahydro-3H-benzo[g][1]benzofuran-2,6-dione 12314703 Click to see CC1C2C(CC3(C(=O)CCC(=C3C2OC1=O)C)C)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
(3S,3aS,5aR,6R,9bR)-6-hydroxy-3,5a,9-trimethyl-3,3a,4,5,6,7,8,9b-octahydrobenzo[g][1]benzofuran-2-one 7088143 Click to see CC1C2CCC3(C(CCC(=C3C2OC1=O)C)O)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
(3S,3aS,5aR,6R,9bR)-6-hydroxy-3,5a,9-trimethyl-3a,4,5,6,7,9b-hexahydro-3H-benzo[g][1]benzofuran-2,8-dione 101265856 Click to see CC1C2CCC3(C(CC(=O)C(=C3C2OC1=O)C)O)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
(3S,3aS,5aS,6R,9aR,9bR)-6,9a-dihydroxy-3,5a-dimethyl-9-methylidene-3,3a,4,5,6,7,8,9b-octahydrobenzo[g][1]benzofuran-2-one 163009013 Click to see CC1C2CCC3(C(CCC(=C)C3(C2OC1=O)O)O)C 266.33 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
(3S,3aS,5aS,6S,9aR,9bR)-6,9a-dihydroxy-3,5a-dimethyl-9-methylidene-3,3a,4,5,6,7,8,9b-octahydrobenzo[g][1]benzofuran-2-one 163009015 Click to see CC1C2CCC3(C(CCC(=C)C3(C2OC1=O)O)O)C 266.33 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
(3S,3aS,5aS,6S,9aR,9bS)-6,9a-dihydroxy-3,5a-dimethyl-9-methylidene-3,3a,4,5,6,7,8,9b-octahydrobenzo[g][1]benzofuran-2-one 14413452 Click to see CC1C2CCC3(C(CCC(=C)C3(C2OC1=O)O)O)C 266.33 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
3,5a,9-Trimethyl-3a,5,5a,9b-tetrahydronaphtho[1,2-b]furan-2,8(3H,4H)-dione 5156 Click to see CC1C2CCC3(C=CC(=O)C(=C3C2OC1=O)C)C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
4-hydroxy-3,5a,9-trimethyl-3a,4,5,7,8,9b-hexahydro-3H-benzo[g]benzofuran-2,6-dione 494703 Click to see CC1C2C(CC3(C(=O)CCC(=C3C2OC1=O)C)C)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
5,9,13-Trimethyl-3,14-dioxatetracyclo[7.5.0.01,13.02,6]tetradecane-4,10-dione 162938056 Click to see CC1C2CCC3(C(=O)CCC4(C3(C2OC1=O)O4)C)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
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/10.1016/S0031-9422(00)98075-0
6,11-alpha(H)-Santonin 7061081 Click to see CC1C2CCC3(C=CC(=O)C(=C3C2OC1=O)C)C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
Alkhanin 13944243 Click to see CC1C2CCC3(C(CC(=O)C(=C3C2OC1=O)C)O)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
Artemin 3678270 Click to see CC1C2CCC3(C(CCC(=C)C3(C2OC1=O)O)O)C 266.33 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
Santonin 221071 Click to see CC1C2CCC3(C=CC(=O)C(=C3C2OC1=O)C)C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,8R,11R,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 12305362 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
CID 348093 348093 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,4R,5S,8S,9S,12S,13S)-4,13-dihydroxy-5,9-dimethyl-11,14,15-trioxatetracyclo[11.2.1.01,5.08,12]hexadecan-10-one 162904238 Click to see CC1C2CCC3(C(CCC34CC(C2OC1=O)(OO4)O)O)C 298.33 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
(1S,5R)-2,2,4-trimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-one 14413455 Click to see CC1=CC(C2CC1OC2=O)(C)C 166.22 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
2,2,4-Trimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-one 14413456 Click to see CC1=CC(C2CC1OC2=O)(C)C 166.22 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
4,13-Dihydroxy-5,9-dimethyl-11,14,15-trioxatetracyclo[11.2.1.01,5.08,12]hexadecan-10-one 3810290 Click to see CC1C2CCC3(C(CCC34CC(C2OC1=O)(OO4)O)O)C 298.33 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
Tehranolide 6711941 Click to see CC1C2CCC3(C(CCC34CC(C2OC1=O)(OO4)O)O)C 298.33 unknown https://doi.org/10.1016/S0031-9422(00)98075-0
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxycoumarin 10748 Click to see COC1=CC2=C(C=C1)C=CC(=O)O2 176.17 unknown https://doi.org/10.1007/BF00595083
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1515/ZNC-1995-5-604
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1515/ZNC-1995-5-604
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown https://doi.org/10.1515/ZNC-1995-5-604

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