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Polylepis incana

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 UUID64403ef4eca4e207891211
Scientific name Polylepis incana
Authority Kunth
First published in Nov. Gen. Sp. 6: 227 (1824)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Polylepis incana subsp. villosistyla Bitter Bot. Jahrb. Syst. 45: 642 (1911)

Common names Top

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Language Common/alternative name
Quechua uqi qiwuña

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-0000989076
Tropicos 27800829
KEW urn:lsid:ipni.org:names:727526-1
The Plant List rjp-17172
Open Tree Of Life 141740
NCBI Taxonomy 281893
IUCN Red List 32990
IPNI 727526-1
iNaturalist 442364
GBIF 5370633
Freebase /m/02xcb1h
EOL 300986
USDA GRIN 29286
Wikipedia Polylepis_incana

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
Phenolic Characterization of a Purple Maize (Zea mays cv. “Moragro”) by HPLC–QTOF-MS and Study of Its Bioaccessibility Using a Simulated In Vitro Digestion/Caco-2 Culture Model Rodriguez MD, Monsierra L, Mansilla PS, Pérez GT, de Pascual-Teresa S J Agric Food Chem 14-Mar-2024
PMCID:PMC10979446
doi:10.1021/acs.jafc.3c08960
PMID:38484116
The Unexpected Identity of Tympanis vagabunda Quijada L, Baral HO, Pfister DH Life (Basel) 28-Feb-2023
PMCID:PMC10058965
doi:10.3390/life13030661
PMID:36983817
A Phytosociological Study on Andean Rainforests of Peru, and a Comparison with the Surrounding Countries Galán-de-Mera A, Campos-de-la-Cruz J, Linares-Perea E, Montoya-Quino J, Torres-Marquina I, Vicente-Orellana JA Plants (Basel) 26-Nov-2020
PMCID:PMC7761437
doi:10.3390/plants9121654
PMID:33256180
Opposite latitudinal patterns for bird and arthropod predation revealed in experiments with differently colored artificial prey Zvereva EL, Castagneyrol B, Cornelissen T, Forsman A, Hernández‐Agüero JA, Klemola T, Paolucci L, Polo V, Salinas N, Theron KJ, Xu G, Zverev V, Kozlov MV Ecol Evol 25-Nov-2019
PMCID:PMC6953658
doi:10.1002/ece3.5862
PMID:31938518
Preserving Traditional Botanical Knowledge: The Importance of Phytogeographic and Ethnobotanical Inventory of Peruvian Dye Plants Mostacero León J, López Medina SE, Yabar H, De La Cruz Castillo J Plants (Basel) 18-Dec-2017
PMCID:PMC5750639
doi:10.3390/plants6040063
PMID:29258279
An ecological paradox: high species diversity and low position of the upper forest line in the Andean Depression Peters T, Braeuning A, Muenchow J, Richter M Ecol Evol 30-Apr-2014
PMCID:PMC4201428
doi:10.1002/ece3.1078
PMID:25360255
Genetic structuring of remnant forest patches in an endangered medicinal tree in North-western Ethiopia Yineger H, Schmidt DJ, Hughes JM BMC Genet 06-Mar-2014
PMCID:PMC4021171
doi:10.1186/1471-2156-15-31
PMID:24602239
Kaempferol 3-O-β-d-(6″-feruloylglucoside) fromPolylepis incana S. Catalano, A.R. Bilia, M. Martinozzi, I. Morelli Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89614-4
Chemical investigation of Polylepis incana (Rosaceae) S. Catalano, P.L. Cioni, M. Martinozzi, V. De Feo, I. Morelli Elsevier BV 25-Jul-2002
doi:10.1016/0305-1978(95)93663-N

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
19Alpha-Hydroxyasiatic Acid 490367 Click to see 504.70 unknown https://doi.org/10.1016/0305-1978(95)93663-N
Corosolic Acid 6918774 Click to see 472.70 unknown https://doi.org/10.1016/0305-1978(95)93663-N
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/10.1016/0305-1978(95)93663-N
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/0305-1978(95)93663-N
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/0305-1978(95)93663-N
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0305-1978(95)93663-N
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/0305-1978(95)93663-N
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/0305-1978(95)93663-N
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 74038837 Click to see COC1=C(C=CC(=C1)C=CC(=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 624.50 unknown https://doi.org/10.1016/S0031-9422(00)89614-4
kaempferol 3-O-(6"-O-feruloyl)-glucoside 23265189 Click to see 624.50 unknown https://doi.org/10.1016/S0031-9422(00)89614-4
Tiliroside 5320686 Click to see 594.50 unknown https://doi.org/10.1016/0305-1978(95)93663-N
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/0305-1978(95)93663-N
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 5317364 Click to see 436.40 unknown https://doi.org/10.1016/0305-1978(95)93663-N
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 44259215 Click to see 434.30 unknown https://doi.org/10.1016/0305-1978(95)93663-N
Guaijaverin 5481224 Click to see 434.30 unknown https://doi.org/10.1016/0305-1978(95)93663-N
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://doi.org/10.1016/0305-1978(95)93663-N

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