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Eriobotrya deflexa

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440406345d84584981383
Scientific name Eriobotrya deflexa
Authority Nakai
First published in Bot. Mag. (Tokyo) 30: 18 (1916)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Eriobotrya deflexa var. buisanensis (Hayata) Hayata
Eriobotrya deflexa f. buisanensis (Hayata) Nakai ; 1916 18 1916
Eriobotrya deflexa f. koshunensis (Kaneh. & Sasaki) H.L.Li ; 1952 232 1952
Photinia deflexa Hemsl. Ann. Bot. (Oxford) 9: 153 (1895)
Photinia buisanensis Hayata Icon. Pl. Formosan. 3: 100 (1913)
Eriobotrya buisanensis (Hayata) Makino & Nemoto Fl. Japan : 464 (1931)
Eriobotrya deflexa var. koshunensis Kaneh. & Sasaki A catalogue of the government herbarium ; 1931 246 1931
Pyrus deflexa (Hemsl.) M.F.Fay & Christenh. Global Fl. 4: 101 (2018)
Rhaphiolepis deflexa (Hemsl.) B.B.Liu & J.Wen Front. Plant Sci. 10-1731: 10 (2020)
Eriobotrya buisanensis (Hayata) Kaneh. Formos. Trees : 213 (1918)

Common names Top

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Language Common/alternative name
Arabic بشملة منحنية
Russian Эриоботрия отклонённая
Chinese 台湾枇杷
Chinese 山枇杷
Chinese 猬脂
Chinese 臺灣枇杷

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-0001016266
Tropicos 27805484
KEW urn:lsid:ipni.org:names:724780-1
The Plant List rjp-6885
Open Tree Of Life 623252
IPNI 724780-1
iNaturalist 490705
GBIF 3024181
Freebase /m/0h66xbb
EPPO EIODF
EOL 229674
USDA GRIN 315469
Wikipedia Bronze_loquat

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
Monoterpene glycosides and triterpene acids from Eriobotrya deflexa. Lee TH, Lee SS, Kuo YC, Chou CH J Nat Prod 01-Jul-2001
doi:10.1021/NP0100237
PMID:11473413

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 / Triterpenoids
(1R,2R,4aS,6aS,6bR,10R,12aR)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-11-oxo-3,4,5,6,6a,7,8,8a,10,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid 470711 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(=O)C(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 486.70 unknown https://doi.org/10.1021/NP0100237
(4aS,6aS,6aS,6bR,10R,11R,12aS,14bR)-10,11-dihydroxy-12a-(hydroxymethyl)-2,2,6a,6b,9,9-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 182035 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)CO)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1021/NP0100237
1-Hydroxy-2-oxopomolic acid 10625284 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(C(=O)C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 502.70 unknown https://doi.org/10.1021/NP0100237
1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-11-oxo-3,4,5,6,6a,7,8,8a,10,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid 9870041 Click to see 486.70 unknown https://doi.org/10.1021/NP0100237
1,10,11-Trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 21325844 Click to see 488.70 unknown https://doi.org/10.1021/NP0100237
1,10,12-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-11-oxo-3,4,5,6,6a,7,8,8a,10,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid 76532587 Click to see 502.70 unknown https://doi.org/10.1021/NP0100237
1,11,12-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid 73077136 Click to see 502.70 unknown https://doi.org/10.1021/NP0100237
1Beta,2Alpha,19Alpha-Trihydroxy-3-Oxo-12-Ursen-28-Oic Acid 11730824 Click to see 502.70 unknown https://doi.org/10.1021/NP0100237
2-Oxopomolic Acid 44593379 Click to see 486.70 unknown https://doi.org/10.1021/NP0100237
2Alpha,19Alpha-Dihydroxy-3-Oxo-12-Ursen-28-Oic Acid 637229 Click to see 486.70 unknown https://doi.org/10.1021/NP0100237
2alpha,3alpha,19alpha-Trihydroxyolean-12-en-28-oic acid 11038273 Click to see 488.70 unknown https://doi.org/10.1021/NP0100237
Arjunic Acid 15385516 Click to see 488.70 unknown https://doi.org/10.1021/NP0100237
CID 73065833 73065833 Click to see 486.70 unknown https://doi.org/10.1021/NP0100237
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP0100237
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2S,3S,4S,5R,6R)-6-[[(2R,3S,4S,5R,6S)-6-[(3R)-3,7-dimethylocta-1,6-dien-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-5-hydroxy-2-methyl-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 10985547 Click to see 754.80 unknown https://doi.org/10.1021/NP0100237
[6-[[6-(3,7-Dimethylocta-1,6-dien-3-yloxy)-3,4,5-trihydroxyoxan-2-yl]methoxy]-5-hydroxy-2-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 73809251 Click to see 754.80 unknown https://doi.org/10.1021/NP0100237

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