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Polyalthia debilis

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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 UUID643ff7b47892d201084619
Scientific name Polyalthia debilis
Authority Finet & Gagnep.
First published in Mém. Soc. Bot. France 4: 96 (1906)

Description Top

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Synonyms Top

Scientific name Authority First published in
Popowia cambodica Finet & Gagnep. Mém. Soc. Bot. France 4: 108 (1906)
Unona dubia Craib Bull. Misc. Inform. Kew 1911: 10 (1911)
Unona debilis Pierre Fl. Forest. Cochinch. : t. 29 (1881)
Desmos cambodicus (Finet & Gagnep.) Ast Fl. Indo-Chine , Suppl. 1: 68 (1938)
Desmos dubius Craib Fl. Siam. 1: 38 (1925)
Popowia cambodica var. canaensis Bân Fl. Vietnam 1: 166 (2000)

Common names Top

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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-0000393656
KEW urn:lsid:ipni.org:names:74551-1
The Plant List kew-2406878
Open Tree Of Life 204171
NCBI Taxonomy 235800
IPNI 74551-1
GBIF 3156284

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
In-vitro antimalarial activity of methanolic leaf- and stem-derived extracts from four Annonaceae plants Lithanatudom P, Chawansuntati K, Saenjum C, Chaowasku T, Rattanathammethee K, Wungsintaweekul B, Osathanunkul M, Wipasa J BMC Res Notes 22-Dec-2023
PMCID:PMC10740295
doi:10.1186/s13104-023-06664-w
PMID:38135870
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
An Updated Review on the Synthesis and Antibacterial Activity of Molecular Hybrids and Conjugates Bearing Imidazole Moiety Rossi R, Ciofalo M Molecules 04-Nov-2020
PMCID:PMC7663458
doi:10.3390/molecules25215133
PMID:33158247
Azafluorene derivatives as inhibitors of SARS CoV-2 RdRp: Synthesis, physicochemical, quantum chemical, modeling and molecular docking analysis Venkateshan M, Muthu M, Suresh J, Ranjith Kumar R J Mol Struct 23-Jun-2020
PMCID:PMC7309803
doi:10.1016/j.molstruc.2020.128741
PMID:32834110
Southeast Asian Medicinal Plants as a Potential Source of Antituberculosis Agent Sanusi SB, Abu Bakar MF, Mohamed M, Sabran SF, Mainasara MM Evid Based Complement Alternat Med 03-Jul-2017
PMCID:PMC5610802
doi:10.1155/2017/7185649
PMID:29081822
Potent Antiproliferative Effect on Liver Cancer of Medicinal Plants Selected from the Thai/Lanna Medicinal Plant Recipe Database “MANOSROI III” Manosroi A, Akazawa H, Kitdamrongtham W, Akihisa T, Manosroi W, Manosroi J Evid Based Complement Alternat Med 07-Jun-2015
PMCID:PMC4475558
doi:10.1155/2015/397181
PMID:26136809
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
Analysis of additivity and synergism in the anti-plasmodial effect of purified compounds from plant extracts Deharo E, Ginsburg H Malar J 15-Mar-2011
PMCID:PMC3059463
doi:10.1186/1475-2875-10-S1-S5
PMID:21411016
Polyacetylenes from the roots of Polyalthia debilis. Panthama N, Kanokmedhakul S, Kanokmedhakul K J Nat Prod 27-Aug-2010
doi:10.1021/NP1001913
PMID:20795741
Bioactive Azafluorenone Alkaloids from Polyalthia debilis (Pierre) Finet & Gagnep Prachayasittikul S, Manam P, Chinworrungsee M, Isarankura-Na-Ayudhya C, Ruchirawat S, Prachayasittikul V Molecules 03-Nov-2009
PMCID:PMC6255371
doi:10.3390/molecules14114414
PMID:19924075
New antimalarial bis-dehydroaporphine alkaloids from Polyalthia debilis. Kanokmedhakul S, Kanokmedhakul K, Yodbuddee D, Phonkerd N J Nat Prod 01-May-2003
doi:10.1021/NP020498D
PMID:12762793

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
> Benzenoids / Phenol ethers / Anisoles
7-Methoxy-4-methylindeno[1,2-b]pyridin-5-one 23242544 Click to see CC1=C2C(=NC=C1)C3=C(C2=O)C=C(C=C3)OC 225.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255371/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
3-(15-Hydroxyicosa-11,13-diynyl)-5-(hydroxymethyl)oxolan-2-one 75254553 Click to see CCCCCC(C#CC#CCCCCCCCCCCC1CC(OC1=O)CO)O 404.60 unknown https://doi.org/10.1021/NP1001913
Debilisone B 46919581 Click to see CCCCCC(C#CC#CCCCCCCCCCCC1CC(OC1=O)CO)O 404.60 unknown https://doi.org/10.1021/NP1001913
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(4R,5S)-4-[(Z)-docos-17-en-13,15-diynyl]-5-(hydroxymethyl)oxolan-2-one 163068550 Click to see CCCCC=CC#CC#CCCCCCCCCCCCCC1CC(=O)OC1CO 414.60 unknown https://doi.org/10.1021/NP1001913
4-Docos-17-en-13,15-diynyl-5-(hydroxymethyl)oxolan-2-one 163068549 Click to see CCCCC=CC#CC#CCCCCCCCCCCCCC1CC(=O)OC1CO 414.60 unknown https://doi.org/10.1021/NP1001913
5-(Hydroxymethyl)-3-icos-15-en-11,13-diynyloxolan-2-one 75254554 Click to see CCCCC=CC#CC#CCCCCCCCCCCC1CC(OC1=O)CO 386.60 unknown https://doi.org/10.1021/NP1001913
5-(Hydroxymethyl)-3-icosa-11,13-diynyloxolan-2-one 75254552 Click to see CCCCCCC#CC#CCCCCCCCCCCC1CC(OC1=O)CO 388.60 unknown https://doi.org/10.1021/NP1001913
5-(Hydroxymethyl)-3-icosa-15,19-dien-11,13-diynyloxolan-2-one 75254555 Click to see C=CCCC=CC#CC#CCCCCCCCCCCC1CC(OC1=O)CO 384.60 unknown https://doi.org/10.1021/NP1001913
Debilisone A 46919580 Click to see CCCCCCC#CC#CCCCCCCCCCCC1CC(OC1=O)CO 388.60 unknown https://doi.org/10.1021/NP1001913
Debilisone C 46919582 Click to see CCCCC=CC#CC#CCCCCCCCCCCC1CC(OC1=O)CO 386.60 unknown https://doi.org/10.1021/NP1001913
Debilisone D 46919583 Click to see C=CCCC=CC#CC#CCCCCCCCCCCC1CC(OC1=O)CO 384.60 unknown https://doi.org/10.1021/NP1001913
Debilisone E 46919678 Click to see C=CCCC=CC#CC#CCCCCCCCCCCC1CC(OC1=O)CO 384.60 unknown https://doi.org/10.1021/NP1001913
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines / Naphthylquinolines
13-(3,5-Dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,12,14,16,18-heptaen-13-yl)-15-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,12,14(19),15,17-heptaene 10918691 Click to see COC1=CC=CC2=C1C(=C3C4=C2C5=C(C=C4CCN3)OCO5)C6=C7C8=C(C9=CC=CC=C96)C1=C(C=C8CCN7)OCO1 554.60 unknown https://doi.org/10.1021/NP020498D
Bidebiline C 10031219 Click to see COC1=CC=CC2=C1C(=C3C4=C2C5=C(C=C4CCN3)OCO5)C6=C7C8=C(C9=C6C(=CC=C9)OC)C1=C(C=C8CCN7)OCO1 584.60 unknown https://doi.org/10.1021/NP020498D
Bidebiline D 10054040 Click to see COC1=CC2=C(C=C1)C(=C3C4=C2C5=C(C=C4CCN3)OCO5)C6=C7C8=C(C9=C6C=CC(=C9)OC)C1=C(C=C8CCN7)OCO1 584.60 unknown https://doi.org/10.1021/NP020498D
Unonopsine 183531 Click to see C1CNC2=C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)C6=C7C8=C(C9=CC=CC=C96)C1=C(C=C8CCN7)OCO1 524.60 unknown https://doi.org/10.1021/NP020498D

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