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Sorbus cuspidata

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
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Details Top

Internal ID UUID6440406701027908688683
Scientific name Sorbus cuspidata
Authority Hedl.
First published in Kongl. Svenska Vetensk. Acad. Handl. , n.s., 35(1): 89 (1901)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pyrus vestita Wall. ex Hook.f. The flora of British India (Rosaceae) ; 1878 375 1878
Pyrus crenata Lindl. Edwards's Bot. Reg. 20: t. 1655. 1834 [1835 publ. 1834]
Pyrus vestita Wall. Numer. List [Wallich] n. 679. 1829

Common names Top

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Language Common/alternative name
Chinese 白叶花楸

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001016328
Tropicos 27808315
KEW urn:lsid:ipni.org:names:741689-1
The Plant List rjp-6957
Open Tree Of Life 3903537
NCBI Taxonomy 1770154
IPNI 741689-1
iNaturalist 484171
GBIF 3013052
EPPO SOUCU
EOL 636872
USDA GRIN 35014

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
A comparison of traditional plant knowledge between Daman people and Tibetans in Gyirong River Valley, Tibet, China Guo CA, Ding X, Hu H, Zhang Y, Bianba C, Bian B, Wang Y J Ethnobiol Ethnomed 05-May-2023
PMCID:PMC10163752
doi:10.1186/s13002-023-00583-7
PMID:37147662
Seasonal resource selection of an arboreal habitat specialist in a human-dominated landscape: A case study using red panda Bista D, Baxter GS, Hudson NJ, Murray PJ Curr Zool 26-Feb-2022
PMCID:PMC10039176
doi:10.1093/cz/zoac014
PMID:36974152
Collection calendar: the diversity and local knowledge of wild edible plants used by Chenthang Sherpa people to treat seasonal food shortages in Tibet, China Ding XY, Zhang Y, Wang L, Zhuang HF, Chen WY, Wang YH J Ethnobiol Ethnomed 10-Jun-2021
PMCID:PMC8190990
doi:10.1186/s13002-021-00464-x
PMID:34112198
Improved Trapping and Handling of an Arboreal, Montane Mammal: Red Panda Ailurus fulgens Bista D, Lama ST, Weerman J, Sherpa AP, Pandey P, Thapa MK, Acharya H, Hudson NJ, Baxter GS, Murray PJ Animals (Basel) 24-Mar-2021
PMCID:PMC8064068
doi:10.3390/ani11040921
PMID:33805041
Seasonal population density and winter survival strategies of endangered Kashmir gray langur (Semnopithecus ajax) in Dachigam National Park, Kashmir, India Mir ZR, Noor A, Habib B, Veeraswami GG Springerplus 29-Sep-2015
PMCID:PMC4627992
doi:10.1186/s40064-015-1366-z
PMID:26543697
Ecological status and traditional knowledge of medicinal plants in Kedarnath Wildlife Sanctuary of Garhwal Himalaya, India Bhat JA, Kumar M, Bussmann RW J Ethnobiol Ethnomed 02-Jan-2013
PMCID:PMC3560114
doi:10.1186/1746-4269-9-1
PMID:23281594
Neurocytoprotective effects of the bioactive constituents of Pueraria thomsonii in 6-hydroxydopamine (6-OHDA)-treated nerve growth factor (NGF)-differentiated PC12 cells. Lin CM, Lin RD, Chen ST, Lin YP, Chiu WT, Lin JW, Hsu FL, Lee MH Phytochemistry 01-Dec-2010
doi:10.1016/J.PHYTOCHEM.2010.08.015
PMID:20832831
Simultaneous analysis of isoflavones and saponins in Pueraria flowers using HPLC coupled to an evaporative light scattering detector and isolation of a new isoflavone diglucoside. Niiho Y, Nakajima Y, Yamazaki T, Okamoto M, Tsuchihashi R, Kodera M, Kinjo J, Nohara T J Nat Med 01-Jul-2010
doi:10.1007/S11418-010-0411-Z
PMID:20354803
Inhibitors for expression of IgE receptor on human mast cell from Puerariae Flos. Tamura S, Yoshihira K, Tokumaru M, Zisheng X, Murakami N Bioorg Med Chem Lett 01-Jul-2010
doi:10.1016/J.BMCL.2010.05.038
PMID:20627560
Optimal foraging on the roof of the world: Himalayan langurs and the classical prey model Sayers K, Norconk MA, Conklin-Brittain NL Am J Phys Anthropol 01-Mar-2010
PMCID:PMC2818116
doi:10.1002/ajpa.21149
PMID:19844998
Diterpenoids from Calceolaria hypericina M.C. Chamy, M. Piovano, J.A. Garbarino, A. Chaparro Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00299-M
Oleanene-type triterpene glycosides from puerariae radix. III. Three new saponins from Pueraria thomsonii. Arao T, Idzu T, Kinjo J, Nohara T, Isobe R Chem Pharm Bull (Tokyo) 01-Oct-1996
doi:10.1248/CPB.44.1970
PMID:8904828

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
(9-Acetyloxy-2,6,6,13-tetramethyl-12-tetracyclo[11.2.1.01,10.02,7]hexadecanyl) 3-methylbutanoate 162972708 Click to see CC(C)CC(=O)OC1CC2C(CC3C(CCCC3(C24CCC1(C4)C)C)(C)C)OC(=O)C 432.60 unknown https://doi.org/10.1016/0031-9422(95)00299-M
[(1S,2S,7S,9S,10S,12R,13S)-9-acetyloxy-2,6,6,13-tetramethyl-12-tetracyclo[11.2.1.01,10.02,7]hexadecanyl] 3-methylbutanoate 162972709 Click to see CC(C)CC(=O)OC1CC2C(CC3C(CCCC3(C24CCC1(C4)C)C)(C)C)OC(=O)C 432.60 unknown https://doi.org/10.1016/0031-9422(95)00299-M
3-oxo-3-[[(1S,2S,7S,9S,10S,12R,13S)-2,6,6,13-tetramethyl-12-(3-methylbutanoyloxy)-9-tetracyclo[11.2.1.01,10.02,7]hexadecanyl]oxy]propanoic acid 162893537 Click to see CC(C)CC(=O)OC1CC2C(CC3C(CCCC3(C24CCC1(C4)C)C)(C)C)OC(=O)CC(=O)O 476.60 unknown https://doi.org/10.1016/0031-9422(95)00299-M
3-Oxo-3-[[2,6,6,13-tetramethyl-12-(3-methylbutanoyloxy)-9-tetracyclo[11.2.1.01,10.02,7]hexadecanyl]oxy]propanoic acid 162893536 Click to see CC(C)CC(=O)OC1CC2C(CC3C(CCCC3(C24CCC1(C4)C)C)(C)C)OC(=O)CC(=O)O 476.60 unknown https://doi.org/10.1016/0031-9422(95)00299-M
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Stemarane diterpenoids
[(1S,2S,4S,7S,10S,13S)-2,6,6-trimethyl-12-methylidene-4-tetracyclo[11.2.1.01,10.02,7]hexadecanyl] acetate 162930963 Click to see CC(=O)OC1CC(C2CCC3CC(=C)C4CCC3(C4)C2(C1)C)(C)C 330.50 unknown https://doi.org/10.1016/0031-9422(95)00299-M
1-O-methyl 3-O-(2,6,6-trimethyl-12-methylidene-9-tetracyclo[11.2.1.01,10.02,7]hexadecanyl) propanedioate 163063880 Click to see CC1(CCCC2(C1CC(C3C24CCC(C4)C(=C)C3)OC(=O)CC(=O)OC)C)C 388.50 unknown https://doi.org/10.1016/0031-9422(95)00299-M
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-acetyloxy-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]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 101997830 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)C)CCC6(C5CC=C7C6(CCC8(C7CC(CC8OC(=O)C)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 969.20 unknown https://doi.org/10.1248/CPB.44.1970
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9S,10R,11S,12aS,14aR,14bR)-9,10-dihydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-11-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 162936418 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(C(C8O)O)(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 1137.30 unknown https://doi.org/10.1248/CPB.44.1970
6-[(9-Acetyloxy-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)oxy]-5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 85238306 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)C)CCC6(C5CC=C7C6(CCC8(C7CC(CC8OC(=O)C)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 969.20 unknown https://doi.org/10.1248/CPB.44.1970
6-[[11-Carboxy-9,10-dihydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 85287208 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(C(C8O)O)(C)C(=O)O)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 989.10 unknown https://doi.org/10.1248/CPB.44.1970
6-[[9,10-Dihydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-11-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 162936417 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(C(C8O)O)(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 1137.30 unknown https://doi.org/10.1248/CPB.44.1970
CID 5087640 5087640 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown https://doi.org/10.1248/CPB.44.1970
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.015
https://doi.org/10.1016/J.BMCL.2010.05.038
Tectorigenin 5281811 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/J.BMCL.2010.05.038
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
7-Hydroxy-3-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5385074 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O 416.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.015
Puerarin 5281807 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O 416.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.015
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)- 4183640 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.015
5-Hydroxy-3-(4-hydroxyphenyl)-6,7-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-4-one 137796330 Click to see C1=CC(=CC=C1C2=COC3=CC(=C(C(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1007/S11418-010-0411-Z
5,6,7,40-Tetrahydroxyisoflavone-6,7-di-o-b-D-glucopyranoside 44207161 Click to see C1=CC(=CC=C1C2=COC3=CC(=C(C(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1007/S11418-010-0411-Z
CID 124222341 124222341 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/S11418-010-0411-Z
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.015
Genistoside 5284639 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.015
Glycitin 187808 Click to see COC1=C(C=C2C(=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1007/S11418-010-0411-Z
Shekkanin 6124513 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1007/S11418-010-0411-Z
Tectorigenin 7-O-xylosylglucoside 100968221 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/S11418-010-0411-Z

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