Rhododendron degronianum - Flower
Part: Flower
Author: Sorin

Rhododendron degronianum - Aerial parts
Part: Aerial parts
Author: Sorin

Rhododendron degronianum - Aerial parts
Part: Aerial parts
Author: Sorin

Rhododendron degronianum - Aerial parts
Part: Aerial parts
Author: Sorin

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Details Top

Internal ID UUID644072fd14433547040044
Scientific name Rhododendron degronianum
Authority Carrière
First published in Rev. Hort. (Paris) 41: 368 (1869)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rhododendron pentamerum (Maxim.) Nakai & Mastsum. Index Seminum (TI, Tokyo) 1915-1916: 24 (1916)
Rhododendron nakaii Komastsu Icon. Pl. Koisikav. 1: 145 (1913)
Azalea degroniana (Carrière) Makino J. Jap. Bot. 5: 8 (1928)
Rhododendron japonicum var. pentamerum (Maxim.) Hutch. Bot. Mag. 137: t. 8403 1911
Rhododendron metternichii var. pentamerum Maxim. Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 16(9): 22 1870

Common names Top

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Language Common/alternative name
Japanese アズマシャクナゲ
Polish różanecznik jakuszimański
Russian Рододендрон Дегрона
Swedish japansk rododendron

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Rhododendron degronianum var. amagianum (T.Yamaz) T.Yamaz Fl. Japan 3a: 42 (1993)
Rhododendron degronianum var. degronianum

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) 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-0000400778
KEW urn:lsid:ipni.org:names:332310-1
The Plant List kew-2419673
Open Tree Of Life 844322
NCBI Taxonomy 118364
IPNI 332310-1
iNaturalist 450795
iNaturalist 450796
GBIF 7327646
Freebase /m/0nc6kzl
EPPO RHODG
Elurikkus 588957
USDA GRIN 5074
Wikipedia Rhododendron_degronianum

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
[Studies on the constituents of leaves of Rhododendron degronianum Carr]. Kurihara T, Kikuchi M, Suzuki S, Toyoda E Yakugaku Zasshi 01-Dec-1976
doi:10.1248/YAKUSHI1947.96.12_1407
PMID:1035619

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 / Diterpenoids / Grayanoids / Leucothol and grayanotoxane diterpenoids
[(1R,3S,4S,6R,8S,9R,10S,13S,14S,16R)-3,4,6,9,14-pentahydroxy-5,5,9,14-tetramethyl-16-tetracyclo[11.2.1.01,10.04,8]hexadecanyl] acetate 162873374 Click to see CC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 412.50 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
Rhodotoxin 231125 Click to see CC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 412.50 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,4aS,6aR,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 162948456 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/YAKUSHI1947.96.12_1407
(3R,4aR,6aR,6bR,8aR,11S,12S,12aS,14aS,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 163022476 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
(3S,4aS,6aR,6bR,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 163185489 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
(3S,4aS,6aR,6bS,8aS,11S,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 162977494 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
(3S,4R,4aS,6aS,6aS,6bR,8aS,12aR,14aS,14bS)-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 162967122 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/YAKUSHI1947.96.12_1407
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
(4R,4aS,6aR,6aS,6bR,8aR,12aS,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 11870447 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/YAKUSHI1947.96.12_1407
[(3R,4aR,6aR,6bR,8aR,11S,12S,12aS,14aS,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate 162999321 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
[(3S,4aR,6aR,6bR,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 162928473 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
alpha-Amyrin acetate 293754 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
beta-Ursolic acid 220774 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/YAKUSHI1947.96.12_1407
Friedelan-3-one 244297 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/YAKUSHI1947.96.12_1407
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/YAKUSHI1947.96.12_1407
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407
Urs-12-ene-3,28-diol, (3beta)- 3266408 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1248/YAKUSHI1947.96.12_1407

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