Elliottia paniculata

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Scientific Literature

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Details Top

Internal ID	UUID6440197ac4f8d480347363
Scientific name	Elliottia paniculata
Authority	(Siebold & Zucc.) Benth. & Hook.f.
First published in	Gen. Pl. 2: 598 (1876)

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Synonyms Top

Scientific name	Authority	First published in
Tripetaleia yakusimensis	Nakai	Bot. Mag. (Tokyo) 40: 485 (1926)
Tripetaleia paniculata f. albiflora	Y.Kimura	J. Jap. Bot. 16(1): 59. 1940 [Jan 1940]
Tripetaleia paniculata	Siebold & Zucc.	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 3(2): 732 (1843)
Elliottia paniculata f. albiflora	(Y.Kimura) Yonek.	J. Jap. Bot. 80: 327 (2005)

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	ホツツジ属
Japanese	ホツツジ
Swedish	trillingazalea

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Eastern Asia
  - Japan

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000666404
Tropicos	50333968
KEW	urn:lsid:ipni.org:names:328053-1
The Plant List	kew-2787640
Open Tree Of Life	606712
NCBI Taxonomy	75585
IPNI	328053-1
iNaturalist	636525
GBIF	7328332
EOL	11861395
USDA GRIN	316281

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

Taxonomy and phylogeny of Exobasidium pentasporium causing witches' broom of Rhododendron species

Shibata S, Hirooka Y

Mycoscience

20-Sep-2022

PMCID:	PMC10042312
doi:	10.47371/mycosci.2022.07.002
PMID:	37089520

[Studies on the constituents of Tripetaleia paniculata Sieb. et Zucc. V. On the constituents of the flowers and of the wood].

Yasue M, Sakakibara J, Ina H, Yanagisawa I

Yakugaku Zasshi

01-Dec-1974

doi:	10.1248/YAKUSHI1947.94.12_1634
PMID:	4476769

[Studies on the constituents of Tripetaleia paniculata Sieb. et Zucc. II. On the constituents of the leaves. (2)].

Yasue M, Sakakibara J, Ina H

Yakugaku Zasshi

01-Nov-1971

doi:	10.1248/YAKUSHI1947.91.11_1252
PMID:	5169134

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
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol	14521039	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O	552.60	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Grayanoids
Rhodojaponin III	21151017	Click to see CC1(C2C(O2)C3C1(C(CC45CC(C(C4O)CCC5C3(C)O)(C)O)O)O)C	368.50	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
Rhodojaponin-III	3035029	Click to see CC1(C2C(O2)C3C1(C(CC45CC(C(C4O)CCC5C3(C)O)(C)O)O)O)C	368.50	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
[(3S,6aR,8aR,12aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-yl] acetate	5321632	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
[(4aS,6aR,6aS,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-yl] acetate	138114876	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
Taraxerol	92097	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Galioside	185774	Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
Monotropein	73466	Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O	390.34	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4R,4aS,6aS,6aR,6bR,8aR,12aR,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol	154723954	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	https://doi.org/10.1248/YAKUSHI1947.91.11_1252
Acetyloleanolic acid	45050658	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C	498.70	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
Epifriedelanol	119242	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
Friedelinol	348029	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	https://doi.org/10.1248/YAKUSHI1947.91.11_1252
Maslinic Acid	73659	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
17-(5-ethyloctan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162967743	Click to see CCCC(CC)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	414.70	unknown	https://doi.org/10.1248/YAKUSHI1947.91.11_1252
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-alpha-hydroxysteroids
(3R,8R,9R,10S,13R,14R,17S)-17-[(2R,5S)-5-ethyloctan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162967745	Click to see CCCC(CC)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	414.70	unknown	https://doi.org/10.1248/YAKUSHI1947.91.11_1252
> 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/10.1248/YAKUSHI1947.94.12_1634
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
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/10.1248/YAKUSHI1947.94.12_1634
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/10.1248/YAKUSHI1947.94.12_1634
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal	107526	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
(2S,3R,4R)-2,3,4,5-tetrahydroxypentanal	66308	Click to see C(C(C(C(C=O)O)O)O)O	150.13	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
D-Xylose	135191	Click to see C1C(C(C(C(O1)O)O)O)O	150.13	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
DL-Xylose	644160	Click to see C(C(C(C(C=O)O)O)O)O	150.13	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
L-Arabinose	439195	Click to see C1C(C(C(C(O1)O)O)O)O	150.13	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin	69894	Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O	192.17	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
> 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/10.1248/YAKUSHI1947.94.12_1634
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Avicularin	5490064	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1248/YAKUSHI1947.94.12_1634

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Elliottia paniculata

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top