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Ainsliaea uniflora

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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
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Details Top

Internal ID UUID643fc5e940a69880466659
Scientific name Ainsliaea uniflora
Authority Sch.Bip.
First published in Jahresber. Pollichia 18-19: 187 (1861)

Description Top

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Synonyms Top

Scientific name Authority First published in
Diaspananthus palmatus Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 186 (1866)
Diplactis alpina Raf. Fl. Tellur. 2: 45. 1837 [1836 publ. Jan-Mar 1837]
Diaspananthus uniflorus f. niveus M.Mizush. J. Jap. Bot. 30(3): 95 (1955)
Ainsliaea uniflora f. nivea (M.Mizush.) Yonek. J. Jap. Bot. 80(6): 330 (2005)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000001055
KEW urn:lsid:ipni.org:names:175781-1
Open Tree Of Life 744889
NCBI Taxonomy 418280
iNaturalist 901723
GBIF 3149515

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Sesquiterpene lactones from Diaspananthus uniflorus (SCH. BIP.) KITAM. SHIGERU ADEGAWA, TOSHIO MIYASE, AKIRA UENO Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.35.1479
Phylogeny and Biogeography of the Genus Ainsliaea (Asteraceae) in the Sino-Japanese Region based on Nuclear rDNA and Plastid DNA Sequence Data Mitsui Y, Chen ST, Zhou ZK, Peng CI, Deng YF, Setoguchi H Ann Bot 03-Nov-2007
PMCID:PMC2701833
doi:10.1093/aob/mcm267
PMID:17981878

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 / Eudesmanolides, secoeudesmanolides, and derivatives
6-Hydroxy-5a-methyl-3,9-dimethylidenedecahydronaphtho[1,2-b]furan-2(3h)-one 98958 Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C 248.32 unknown https://doi.org/10.1248/CPB.35.1479
Reynosin 482788 Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C 248.32 unknown https://doi.org/10.1248/CPB.35.1479
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 133640194 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1248/CPB.35.1479
Costunolide 5281437 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1248/CPB.35.1479
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3-methyl-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-8-yl) 3-methylbutanoate 73814573 Click to see CC1C2CCC(=C)C3CC(C(=C)C3C2OC1=O)OC(=O)CC(C)C 332.40 unknown https://doi.org/10.1248/CPB.35.1479
(3,6,9-Trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-8-yl) 3-methylbutanoate 85322231 Click to see CC(C)CC(=O)OC1CC2C(C1=C)C3C(CCC2=C)C(=C)C(=O)O3 330.40 unknown https://doi.org/10.1248/CPB.35.1479
(3aS,5S,6aR,8S,9aR,9bS)-5-hydroxy-3,6,9-trimethylidene-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 21629857 Click to see C=C1C2CC(C(=C)C2C3C(CC1O)C(=C)C(=O)O3)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown https://doi.org/10.1248/CPB.35.1479
(3aS,5S,6aR,8S,9aR,9bS)-5-hydroxy-3,6,9-trimethylidene-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 162853863 Click to see C=C1C2CC(C(=C)C2C3C(CC1O)C(=C)C(=O)O3)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown https://doi.org/10.1248/CPB.35.1479
(3aS,5S,6aR,9aR,9bS)-3,6,9-trimethylidene-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 21629859 Click to see C=C1CCC2C1C3C(CC(C2=C)OC4C(C(C(C(O4)CO)O)O)O)C(=C)C(=O)O3 408.40 unknown https://doi.org/10.1248/CPB.35.1479
(3aS,5S,6aR,9aR,9bS)-3,6,9-trimethylidene-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 162963225 Click to see C=C1CCC2C1C3C(CC(C2=C)OC4C(C(C(C(O4)CO)O)O)O)C(=C)C(=O)O3 408.40 unknown https://doi.org/10.1248/CPB.35.1479
(3aS,6aR,8S,9aR,9bS)-3,6,9-trimethylidene-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 162908328 Click to see C=C1CCC2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C 408.40 unknown https://doi.org/10.1248/CPB.35.1479
(3aS,6aR,8S,9S,9aS,9bS)-9-hydroxy-9-methyl-3,6-dimethylidene-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 162845179 Click to see CC1(C(CC2C1C3C(CCC2=C)C(=C)C(=O)O3)OC4C(C(C(C(O4)CO)O)O)O)O 426.50 unknown https://doi.org/10.1248/CPB.35.1479
(3aS,6aR,8S,9S,9aS,9bS)-9-hydroxy-9-methyl-3,6-dimethylidene-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 21629861 Click to see CC1(C(CC2C1C3C(CCC2=C)C(=C)C(=O)O3)OC4C(C(C(C(O4)CO)O)O)O)O 426.50 unknown https://doi.org/10.1248/CPB.35.1479
(3aS)-3a,4,5,6,6abeta,7,8,9,9abeta,9balpha-Decahydro-8alpha-(beta-D-glucopyranosyloxy)-3,6,9-tris(methylene)azuleno[4,5-b]furan-2(3H)-one 321680 Click to see C=C1CCC2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C 408.40 unknown https://doi.org/10.1248/CPB.35.1479
[(3S,3aS,6aR,8S,9aR,9bS)-3-methyl-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-8-yl] 3-methylbutanoate 21629856 Click to see CC1C2CCC(=C)C3CC(C(=C)C3C2OC1=O)OC(=O)CC(C)C 332.40 unknown https://doi.org/10.1248/CPB.35.1479
5-Hydroxy-3,6,9-trimethylidene-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 13855723 Click to see C=C1C2CC(C(=C)C2C3C(CC1O)C(=C)C(=O)O3)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown https://doi.org/10.1248/CPB.35.1479
9-Hydroxy-9-methyl-3,6-dimethylidene-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 73814576 Click to see CC1(C(CC2C1C3C(CCC2=C)C(=C)C(=O)O3)OC4C(C(C(C(O4)CO)O)O)O)O 426.50 unknown https://doi.org/10.1248/CPB.35.1479
Dehydrocostus lactone, (-)- 73174 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1248/CPB.35.1479
Dehydrocostuslactone 4426320 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1248/CPB.35.1479
Vernoflexuoside 442320 Click to see C=C1CCC2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C 408.40 unknown https://doi.org/10.1248/CPB.35.1479
Zaluzanin C isovalerate 10936430 Click to see CC(C)CC(=O)OC1CC2C(C1=C)C3C(CCC2=C)C(=C)C(=O)O3 330.40 unknown https://doi.org/10.1248/CPB.35.1479
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-2,5-bis(hydroxymethyl)oxolan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 21606609 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)CO)O)O 680.60 unknown https://doi.org/10.1248/CPB.35.1479

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