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Chrysanthemum ornatum

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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 UUID643fca50cec12109364508
Scientific name Chrysanthemum ornatum
Authority Hemsl.
First published in Bot. Mag. 130: t. 7965 (1904)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tanacetum ornatum Kitam. Mem. Coll. Sci. Kyoto Imp. Univ., Ser. B, Biol. xv. (Compos. Jap. II.) 352 (1
Dendranthema ornatum (Hemsl.) Kitam. Acta Phytotax. Geobot. 29: 166 (1978)
Chrysanthemum marginatum Raffill Gard. Chron. 1904, I. 51
Chrysanthemum sinense var. satsumense Yatabe Bot. Mag. Tokyo 5: 2, t. 20 (1891)
Chrysanthemum satsumense (Yatabe) Makino Ill. Fl. Jap. 46. 1948

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Chrysanthemum ornatum var. tokarense (M.Hotta & Hirai) H.Ohashi & Yonek. J. Jap. Bot. 79(3): 190 (2004)

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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-0000037366
Tropicos 2702270
KEW urn:lsid:ipni.org:names:193650-1
Open Tree Of Life 534931
NCBI Taxonomy 413248
IPNI 193650-1
GBIF 3091497
USDA GRIN 424270

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
How chrysanthemum (Chrysanthemum × grandiflorum) ‘Palisade White’ deals with long-term salt stress Bandurska H, Breś W, Tomczyk A, Zielezińska M, Borowiak K AoB Plants 02-Apr-2022
PMCID:PMC9089830
doi:10.1093/aobpla/plac015
PMID:35558162
Microsatellite polymorphism among Chrysanthemum sp. polyploids: the influence of whole genome duplication Wang H, Qi X, Gao R, Wang J, Dong B, Jiang J, Chen S, Guan Z, Fang W, Liao Y, Chen F Sci Rep 23-Oct-2014
PMCID:PMC4206843
doi:10.1038/srep06730
PMID:25339092
Next-Generation Sequencing of the Chrysanthemum nankingense (Asteraceae) Transcriptome Permits Large-Scale Unigene Assembly and SSR Marker Discovery Wang H, Jiang J, Chen S, Qi X, Peng H, Li P, Song A, Guan Z, Fang W, Liao Y, Chen F PLoS One 23-Apr-2013
PMCID:PMC3633874
doi:10.1371/journal.pone.0062293
PMID:23626799
Angeloylcumambrin-B, an antimicrobial sesquiterpene lactone from Chrysanthemum ornatum var. Spontaneum Mitsumasa Haruna, Makiko Kato, Kazuo Ito, Toshiaki Nikai, Hisayoshi Sugihara, Hiroyuki Muratat Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)83100-7

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 / Sesterterpenoids
(2',6-Dihydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7'-dioxospiro[4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-3,15'-8-oxatetracyclo[9.2.2.01,10.05,9]pentadec-12-ene]-4-yl) acetate 3108351 Click to see CC1=CCC2C1C3C(C(CC2(C)O)OC(=O)C)C4(CC56C=CC4(C5C7C(CCC6(C)O)C(=C)C(=O)O7)C)C(=O)O3 552.70 unknown https://doi.org/10.1016/0031-9422(81)83100-7
[(1'R,2'R,3S,3aR,4S,5'S,6R,6aR,9'S,9aR,9bR,10'S,11'R)-2',6-dihydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7'-dioxospiro[4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-3,15'-8-oxatetracyclo[9.2.2.01,10.05,9]pentadec-12-ene]-4-yl] acetate 162881546 Click to see CC1=CCC2C1C3C(C(CC2(C)O)OC(=O)C)C4(CC56C=CC4(C5C7C(CCC6(C)O)C(=C)C(=O)O7)C)C(=O)O3 552.70 unknown https://doi.org/10.1016/0031-9422(81)83100-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) 2-methylbut-2-enoate 5255772 Click to see CC=C(C)C(=O)OC1CC(C2CC=C(C2C3C1C(=C)C(=O)O3)C)(C)O 346.40 unknown https://doi.org/10.1016/0031-9422(81)83100-7
(6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) acetate 3809323 Click to see CC1=CCC2C1C3C(C(CC2(C)O)OC(=O)C)C(=C)C(=O)O3 306.40 unknown https://doi.org/10.1016/0031-9422(81)83100-7
[(3aR,4S,6R,6aR,9aR,9bR)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 10450322 Click to see CC=C(C)C(=O)OC1CC(C2CC=C(C2C3C1C(=C)C(=O)O3)C)(C)O 346.40 unknown https://doi.org/10.1016/0031-9422(81)83100-7
4,6-Dihydroxy-6,9-dimethyl-3-methylidene-3a,4,5,6,6a,7,9a,9b-octahydroazuleno[4,5-b]furan-2(3h)-one 99115 Click to see CC1=CCC2C1C3C(C(CC2(C)O)O)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1016/0031-9422(81)83100-7
cumambrin A 174867 Click to see CC1=CCC2C1C3C(C(CC2(C)O)OC(=O)C)C(=C)C(=O)O3 306.40 unknown https://doi.org/10.1016/0031-9422(81)83100-7
Cumambrin B 9992975 Click to see CC1=CCC2C1C3C(C(CC2(C)O)O)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1016/0031-9422(81)83100-7

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