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Polyalthia evecta

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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 UUID643ff7b5496dd907666544
Scientific name Polyalthia evecta
Authority Finet & Gagnep.
First published in Mém. Soc. Bot. France 4: 91 (1906)

Description Top

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Synonyms Top

Scientific name Authority First published in
Miliusa concinna Ridl. J. Fed. Malay States Mus. 10: 127 (1920)
Unona evecta Pierre Fl. Forest. Cochinch. : t. 31 (1881)

Common names Top

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Language Common/alternative name
Khmer បាតផ្តិល

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000393686
KEW urn:lsid:ipni.org:names:74568-1
The Plant List kew-2406912
Open Tree Of Life 3868378
NCBI Taxonomy 1310103
IPNI 74568-1
GBIF 3156335
Elurikkus 367283
CMAUP NPO6522

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
Drug discovery inspired by bioactive small molecules from nature Kim S, Lim SW, Choi J Anim Cells Syst (Seoul) 21-Dec-2022
PMCID:PMC9809404
doi:10.1080/19768354.2022.2157480
PMID:36605590
Machine Learning and In Vitro Chemical Screening of Potential α-Amylase and α-Glucosidase Inhibitors from Thai Indigenous Plants Srisongkram T, Waithong S, Thitimetharoch T, Weerapreeyakul N Nutrients 09-Jan-2022
PMCID:PMC8781461
doi:10.3390/nu14020267
PMID:35057448
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Modulation of expression of heat shock proteins and apoptosis by Flueggea leucopyrus (Willd) decoction in three breast cancer phenotypes Mendis AS, Thabrew I, Samarakoon SR, Tennekoon KH BMC Complement Altern Med 09-Nov-2015
PMCID:PMC4640413
doi:10.1186/s12906-015-0927-6
PMID:26553005
An Investigation of the Growth Inhibitory Capacity of Several Medicinal Plants From Iran on Tumor Cell Lines Esmaeilbeig M, Kouhpayeh SA, Amirghofran Z Iran J Cancer Prev 27-Oct-2015
PMCID:PMC4667231
doi:10.17795/ijcp-4032
PMID:26634114
Antiproliferative and Apoptosis Inducing Effects of Non-Polar Fractions from Lawsonia inermis L. in Cervical (HeLa) Cancer Cells Kumar M, Kaur P, Kumar S, Kaur S Physiol Mol Biol Plants 19-Mar-2015
PMCID:PMC4411381
doi:10.1007/s12298-015-0285-3
PMID:25931778
Synergistic anticancer effect of the extracts from Polyalthia evecta caused apoptosis in human hepatoma (HepG2) cells Machana S, Weerapreeyakul N, Barusrux S, Thumanu K, Tanthanuch W Asian Pac J Trop Biomed 01-Aug-2012
PMCID:PMC3609358
doi:10.1016/S2221-1691(12)60103-8
PMID:23569977
Anticancer effect of the extracts from Polyalthia evecta against human hepatoma cell line (HepG2) Machana S, Weerapreeyakul N, Barusrux S Asian Pac J Trop Biomed 01-May-2012
PMCID:PMC3609308
doi:10.1016/S2221-1691(12)60058-6
PMID:23569932
Ethnobotanical investigation of 'wild' food plants used by rice farmers in Kalasin, Northeast Thailand Cruz-Garcia GS, Price LL J Ethnobiol Ethnomed 08-Nov-2011
PMCID:PMC3233498
doi:10.1186/1746-4269-7-33
PMID:22067578
Biological evaluation of plants of Laos used in the treatment of tuberculosis in Lao traditional medicine Elkington BG, Southavong B, Sydara K, Souliya O, Vanthanouvong M, Nettavong K, Thammachack B, Pak DH, Riley MC, Franzblau SG, Soejarto DD Pharm Biol 01-Jan-2009
PMCID:PMC3071617
doi:10.1080/13880200802398002
PMID:21479105
Biosynthesis and Function of Polyacetylenes and Allied Natural Products Minto RE, Blacklock BJ Prog Lipid Res 13-Mar-2008
PMCID:PMC2515280
doi:10.1016/j.plipres.2008.02.002
PMID:18387369
Children's traditional ecological knowledge of wild food resources: a case study in a rural village in Northeast Thailand Setalaphruk C, Price LL J Ethnobiol Ethnomed 15-Oct-2007
PMCID:PMC2100045
doi:10.1186/1746-4269-3-33
PMID:17937791
2-substituted furans from the roots of Polyalthia evecta. Kanokmedhakul S, Kanokmedhakul K, Kantikeaw I, Phonkerd N J Nat Prod 01-Jan-2006
doi:10.1021/NP0503202
PMID:16441071
A diynoic acid from Polyalthia evecta S. Kanokmedhakul, K. Kanokmedhakul, Ikuko I. Ohtani, M. Isobe Elsevier BV 23-Apr-2003
doi:10.1016/S0031-9422(97)00487-1

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl 19-(furan-2-yl)nonadec-5-ynoate 11566977 Click to see COC(=O)CCCC#CCCCCCCCCCCCCCC1=CC=CO1 374.60 unknown https://doi.org/10.1021/NP0503202
Methyl 19-(furan-2-yl)nonadeca-5,7-diynoate 11516228 Click to see COC(=O)CCCC#CC#CCCCCCCCCCCCC1=CC=CO1 370.50 unknown https://doi.org/10.1021/NP0503202
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
19-(2-Furyl)Nonadeca-5-Ynoic Acid 11566680 Click to see C1=COC(=C1)CCCCCCCCCCCCCC#CCCCC(=O)O 360.50 unknown https://doi.org/10.1021/NP0503202
19-(2-Furyl)nonadeca-5,7-diynoic acid 11494158 Click to see C1=COC(=C1)CCCCCCCCCCCC#CC#CCCCC(=O)O 356.50 unknown https://doi.org/10.1021/NP0503202
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
21-(2-Furyl)henicosa-5,7-diynoic acid 489938 Click to see C1=COC(=C1)CCCCCCCCCCCCCC#CC#CCCCC(=O)O 384.60 unknown https://doi.org/10.1016/S0031-9422(97)00487-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
21-(Furan-2-yl)henicosa-14,16-diynyl 19-(furan-2-yl)nonadeca-5,7-diynoate 11614600 Click to see C1=COC(=C1)CCCCCCCCCCCC#CC#CCCCC(=O)OCCCCCCCCCCCCCC#CC#CCCCCC2=CC=CO2 709.00 unknown https://doi.org/10.1021/NP0503202
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
21-(Furan-2-yl)henicosa-14,16-diyn-1-ol 11639293 Click to see C1=COC(=C1)CCCCC#CC#CCCCCCCCCCCCCCO 370.60 unknown https://doi.org/10.1021/NP0503202
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentacosa-7,9-diynylfuran 11611266 Click to see CCCCCCCCCCCCCCCC#CC#CCCCCCCC1=CC=CO1 410.70 unknown https://doi.org/10.1021/NP0503202
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1S,2R,3R,9R,10R,17S)-3-(3,5-dihydroxyphenyl)-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 101103994 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O 680.70 unknown via CMAUP database
(1S,2R,3R,9S,10S,17S)-3-[(2S,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydro-1-benzofuran-4-yl]-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 21606280 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=C8C(C(OC8=CC(=C7)OC9C(C(C(C(O9)CO)O)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)C(=C6)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 1069.10 unknown via CMAUP database
(1S,4R,5R,11R,12R,15R,16R,22S)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.9.1.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol 101053432 Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C6=C(C=C5O)OC(C6C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O)C9=C(C=C4O)OC(C9C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown via CMAUP database
(1S,4R,5R,11R,12R,15R,16S,22S)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.9.1.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol 101103995 Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C6=C(C=C5O)OC(C6C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O)C9=C(C=C4O)OC(C9C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown via CMAUP database
(2R,9S,10S,11S,12S)-12-(3,5-dihydroxyphenyl)-2-[(R)-[(1S,2R,3R,9S,10S,17S)-3-(3,5-dihydroxyphenyl)-5,13,15-trihydroxy-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaen-6-yl]-(4-hydroxyphenyl)methyl]-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.03,8.013,17]heptadeca-1(16),3(8),4,6,13(17),14-hexaene-5,7,14,16-tetrol 16149368 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6C(C8C9=C(C(C1C(C(C2=C1C8=C(C=C2O)O)C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)C(=CC(=C9)O)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 1361.40 unknown via CMAUP database
(2R,9S,10S,11S,12S)-12-(3,5-dihydroxyphenyl)-2-[(R)-[(1S,2R,3R,9S,10S,17S)-3-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-5,13,15-trihydroxy-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaen-6-yl]-(4-hydroxyphenyl)methyl]-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.03,8.013,17]heptadeca-1(16),3(8),4,6,13(17),14-hexaene-5,7,14,16-tetrol 16151489 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C(C5=C(C=C(C(=C35)C2C6=CC(=CC(=C6)O)O)O)O)C(C7=CC=C(C=C7)O)C8=C(C9=C1C(C(C9C2=C3C(C(OC3=CC(=C2)O)C2=CC=C(C=C2)O)C2=CC(=CC(=C2)O)O)C2=CC=C(C=C2)O)C(C2=C(C=C(C=C2O)O)C2C1=C8OC2C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)O 1587.60 unknown via CMAUP database
1beta,11alpha-Bis(4-hydroxyphenyl)-2alpha-[2alpha-(4-hydroxyphenyl)-3beta-[3-(beta-D-glucopyranosyloxy)-5-hydroxyphenyl]-6-hydroxy-2,3-dihydrobenzofuran-4-yl]-3-hydroxy-5,6beta-[(S)-2-(4-hydroxyphenyl)-1-oxaethane-1,2-diyl]-1,2,11,11abeta-tetrahydro-6H-dibenzo[cd,g]azulene-8,10-diol 21606279 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=C8C(C(OC8=CC(=C7)O)C9=CC=C(C=C9)O)C1=CC(=CC(=C1)OC1C(C(C(C(O1)CO)O)O)O)O)C(=C6)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 1069.10 unknown via CMAUP database
5-[(2R,3S)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 5315234 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown via CMAUP database
Epsilon-viniferin 5281728 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown via CMAUP database
Vaticanol A 44566412 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O 680.70 unknown via CMAUP database
Vaticanol B 10010985 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=C8C(C(OC8=CC(=C7)O)C9=CC=C(C=C9)O)C1=CC(=CC(=C1)O)O)C(=C6)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown via CMAUP database
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73642 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown via CMAUP database
Polydatin 5281718 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown via CMAUP database

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