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Vauquelinia corymbosa

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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
Collections

Details Top

Internal ID UUID64404040e0b99034622408
Scientific name Vauquelinia corymbosa
Authority Bonpl.
First published in Pl. Aequinoct. 1: 140 (1807)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vauquelinia karwinskyi Maxim. Trudy Imp. S.-Peterburgsk. Bot. Sada 6: 236 (1879)
Vauquelinia heterodon I.M.Johnst. J. Arnold Arbor. 21: 258 (1940)
Vauquelinia latifolia Rydb. ex Standl. Contr. U.S. Natl. Herb. 23: 323 (1922)

Common names Top

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Language Common/alternative name
English slimleaf rosewood

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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No germination or propagation data was added yet.

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-0001015639
USDA Plants VACO4
Tropicos 50004405
KEW urn:lsid:ipni.org:names:30131406-2
The Plant List rjp-6251
Open Tree Of Life 1085086
NCBI Taxonomy 32250
Nature Serve 2.151810
IUCN Red List 126611034
IPNI 30131406-2
iNaturalist 170137
GBIF 3001748
EOL 627224
USDA GRIN 454727

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
Phylogeny of genera in Maleae (Rosaceae) based on chloroplast genome analysis Sun J, Zhao D, Qiao P, Wang Y, Wu P, Wang K, Guo L, Huang L, Zhou S Front Plant Sci 26-Mar-2024
PMCID:PMC11002139
doi:10.3389/fpls.2024.1367645
PMID:38595768
Anti-Diabetic Potential of Polyphenol-Rich Fruits from the Maleae Tribe—A Review of In Vitro and In Vivo Animal and Human Trials Rutkowska M, Olszewska MA Nutrients 28-Aug-2023
PMCID:PMC10489674
doi:10.3390/nu15173756
PMID:37686786
Biocatalysis in the Chemistry of Lupane Triterpenoids Bachořík J, Urban M Molecules 14-Apr-2021
PMCID:PMC8070785
doi:10.3390/molecules26082271
PMID:33919839
Phylogeny of Maleae (Rosaceae) Based on Multiple Chloroplast Regions: Implications to Genera Circumscription Sun J, Shi S, Li J, Yu J, Wang L, Yang X, Guo L, Zhou S Biomed Res Int 19-Mar-2018
PMCID:PMC5884435
doi:10.1155/2018/7627191
PMID:29750171
Agrimoniin, an Active Ellagitannin from Comarum palustre Herb with Anti-α-Glucosidase and Antidiabetic Potential in Streptozotocin-Induced Diabetic Rats Kashchenko NI, Chirikova NK, Olennikov DN Molecules 02-Jan-2017
PMCID:PMC6155588
doi:10.3390/molecules22010073
PMID:28045450
Preventive effects of betulinic acid on streptozotocinnicotinamide induced diabetic nephropathy in male mouse Ahangarpour A, Oroojan AA, Khorsandi L, Shabani R, Mojaddami S J Nephropathol 03-Aug-2016
PMCID:PMC5125059
doi:10.15171/jnp.2016.24
PMID:27921024
α-Glucosidase Inhibitors from Vauquelinia corymbosa. Flores-Bocanegra L, Pérez-Vásquez A, Torres-Piedra M, Bye R, Linares E, Mata R Molecules 21-Aug-2015
PMCID:PMC6332183
doi:10.3390/MOLECULES200815330
PMID:26307962
α-Glucosidase Inhibitors from Vauquelinia corymbosa Flores-Bocanegra L, Pérez-Vásquez A, Torres-Piedra M, Bye R, Linares E, Mata R Molecules 21-Aug-2015
PMCID:PMC6332183
doi:10.3390/molecules200815330
PMID:26307962
Suppression of STAT3 and HIF-1 Alpha Mediates Anti-Angiogenic Activity of Betulinic Acid in Hypoxic PC-3 Prostate Cancer Cells Shin J, Lee HJ, Jung DB, Jung JH, Lee HJ, Lee EO, Lee SG, Shim BS, Choi SH, Ko SG, Ahn KS, Jeong SJ, Kim SH PLoS One 24-Jun-2011
PMCID:PMC3123343
doi:10.1371/journal.pone.0021492
PMID:21731766

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332183/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Methylarbutin 80131 Click to see COC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332183/
Picein 92123 Click to see CC(=O)C1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 298.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332183/
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin 182232 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332183/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl benzoate 11563181 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O 568.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332183/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332183/
Isoquercetin 5280804 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332183/
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332183/

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