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Pyrus ussuriensis

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 UUID64404d6e92956977394356
Scientific name Pyrus ussuriensis
Authority Maxim.
First published in Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 132 (1857)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Pyrus kunoriana Koidz. Acta Phytotax. Geobot. 3: 39 (1934)
Pyrus yukinourana Koidz. Acta Phytotax. Geobot. 4: 158 (1935)
Pyrus ugoensis Koidz. Acta Phytotax. Geobot. 8: 190 (1939)
Pyrus oncocarpa Koidz. Acta Phytotax. Geobot. 5: 49 (1936)
Pyrus invicibilis Koidz. Acta Phytotax. Geobot. 5: 50 (1936)
Pyrus koshiensis Koidz. Acta Phytotax. Geobot. 8: 190 (1939)
Pyrus kumaensis Koidz. Acta Phytotax. Geobot. 10: 59 (1941)
Pyrus oblongolanceolata Koidz. Acta Phytotax. Geobot. 10: 59 (1941)
Pyrus rufoferruginea Koidz. Bot. Mag. (Tokyo) 29: 311 (1915)
Pyrus insueta Koidz. Bot. Mag. (Tokyo) 33: 123 (1919)
Pyrus obovoidea Koidz. Bot. Mag. (Tokyo) 33: 123 (1919)
Pyrus longipedunculata Koidz. Bot. Mag. (Tokyo) 33: 126 (1919)
Pyrus tremulans Koidz. Bot. Mag. (Tokyo) 33: 126 (1919)
Pyrus insulsa Koidz. Bot. Mag. (Tokyo) 33: 127 (1919)
Pyrus iwatensis Koidz. Bot. Mag. (Tokyo) 33: 127 (1919)
Pyrus wayamana Koidz. Bot. Mag. (Tokyo) 33: 127 (1919)
Pyrus jocunda Koidz. Bot. Mag. (Tokyo) 33: 128 (1919)
Pyrus nambuana Koidz. Bot. Mag. (Tokyo) 33: 128 (1919)
Pyrus squarrosa Koidz. Bot. Mag. (Tokyo) 38: 89 (1924)
Pyrus zenskeana Koidz. Bot. Mag. (Tokyo) 38: 88 (1924)
Pyrus mikado Koidz. Bot. Mag. (Tokyo) 38: 89 (1924)
Pyrus inutilis Koidz. Bot. Mag. (Tokyo) 39: 16 (1925)
Pyrus insularis Koidz. Bot. Mag. (Tokyo) 43: 385 (1929)
Pyrus hakunensis Nakai Bot. Mag. (Tokyo) 49: 346 (1935)
Pyrus nankaiensis Nakai Bot. Mag. (Tokyo) 49: 346 (1935)
Pyrus seoulensis Nakai Bot. Mag. (Tokyo) 49: 348 (1935)
Pyrus amoena Poit. & Turpin Pomol. Franç. 3: Poirier n.º 6 (1846)
Pyrus aromatica Kikuchi & Nakai Bot. Mag. (Tokyo) 32: 33 (1918)
Pyrus crassipes Kikuchi & Nakai Bot. Mag. (Tokyo) 32: 35 (1918)
Pyrus mayebarana Koidz. Fl. Austro-Higo. : 26 (1931)
Pyrus leiostachya Koidz. Fl. Bitchuensis : 28 (1929)
Pyrus insula Koidz. Bot. Mag. (Tokyo) 33: 127 (1919)
Pyrus viris Nakai Fl. Sylv. Kor. 6: 51 (1916)
Pyrus ovoidea Rehder Proc. Amer. Acad. Arts 50: 228 (1915)
Pyrus acidula Nakai Bot. Mag. (Tokyo) 30: 27 (1916)
Pyrus vilis Nakai Fl. Sylv. Kor. 6: 51 (1916)
Pyrus macrostipes Nakai Bot. Mag. (Tokyo) 30: 28 (1916)
Pyrus sinensis var. asiae-mediae Popov
Pyrus ussuriensis var. heterophylla Gladkova Novosti Sist. Vyssh. Rast. 25: 102 (1988)
Pyrus ussuriensis var. typica Skvortsov Izv. Glavn. Bot. Sada R.S.F.S.R. 24: 149 (1925)
Pyrus communis var. ussurensis (Maxim.) Koidz. J. Coll. Sci. Imp. Univ. Tokyo 34(2): 53 (1913)

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
Pyrus ussuriensis var. hondoensis (Nakai & Kikuchi) Rehder J. Arnold Arbor. 2: 59. 1920 (1920)
Pyrus ussuriensis var. ussuriensis

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-0001131706
CMAUP NPO21358

Genomes (via NCBI) Top

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Scientific Literature Top

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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
> Alkaloids and derivatives
[(1S,3R,13S,14S,17S,18R,19R,20R,21S,22S,23R,24R,25S)-18,19,21,24-tetraacetyloxy-20-(acetyloxymethyl)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-22-yl] benzoate 70684079 Click to see 867.80 unknown via CMAUP database
[(1S,3R,13S,14S,17S,18R,19R,20R,21S,22S,23R,24R,25S)-19,21,24-triacetyloxy-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-20-yl]methyl acetate 102317474 Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)O)OC(=O)C)COC(=O)C)OC(=O)C)O)C 721.70 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see 418.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Epifriedelanol 119242 Click to see 428.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Pristimerin 159516 Click to see 464.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Tingenone 101520 Click to see 420.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10724415 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O)O 902.80 unknown via CMAUP database
Alcesefoliside 11828754 Click to see 756.70 unknown via CMAUP database
kaempferol 3-O-alpha-rhamnopyranosyl-(1-2)-beta-galactopyranoside 5487339 Click to see 594.50 unknown via CMAUP database
Mauritianin 10919701 Click to see 740.70 unknown via CMAUP database

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