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Polyalthia suberosa

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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 UUID644046b620cdd231027575
Scientific name Polyalthia suberosa
Authority (Roxb.) Thwaites
First published in Enum. Pl. Zeyl. : 398 (1864)

Description Top

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Synonyms Top

Scientific name Authority First published in
Guatteria suberosa (Roxb.) Dunal Monogr. Anonac. : 128 (1817)
Uvaria suberosa Roxb. Pl. Coromandel 1: 31 (1795)

Common names Top

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Language Common/alternative name
English corky debbar tree
Bengali মুড়মুড়ি
Thai กลึงกล่อม
Chinese 暗罗
Chinese 黑皮根
Chinese 山观音
Chinese 眉尾木
Chinese 老人皮
Chinese 鸡爪树
Chinese 暗羅

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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No forms added yet.

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya
      • Philippines

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001066143
Florida Plant Atlas 4191
USDA Plants POSU8
Tropicos 1601561
KEW urn:lsid:ipni.org:names:74734-1
The Plant List tro-1601561
Open Tree Of Life 1018738
NCBI Taxonomy 105757
IPNI 74734-1
iNaturalist 550980
GBIF 3156325
EOL 1054138
USDA GRIN 29201

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
Heterocyclic Iminoquinones and Quinones from the National Cancer Institute (NCI, USA) COMPARE Analysis Haji N, Faizi M, Koutentis PA, Carty MP, Aldabbagh F Molecules 04-Jul-2023
PMCID:PMC10343902
doi:10.3390/molecules28135202
PMID:37446864
Cytotoxic activity of essential oil from Leaves of Myrcia splendens against A549 Lung Cancer cells Montalvão MM, Felix FB, Propheta dos Santos EW, Santos JF, de Lucca Júnior W, Farias AS, de Souza Ribeiro A, Cavaleiro C, Machado SM, Scher R, Corrêa CB BMC Complement Med Ther 02-May-2023
PMCID:PMC10152754
doi:10.1186/s12906-023-03969-y
PMID:37131150
Complete plastome sequence of Monoon laui (Merr.) B. Xue and R.M.K. Saunders, 2012: an endemic species in Hainan Xiu H, Sun Y, Quan Y, Fu T, Sun Q Mitochondrial DNA B Resour 07-Sep-2022
PMCID:PMC9467546
doi:10.1080/23802359.2022.2116953
PMID:36106198
Ethnopharmacological-Based Validation of Polyalthia suberosa Leaf Extract in Neurological, Hyperalgesic, and Hyperactive Gut Disorders Using Animal Models Amin R, Quispe C, Herrera-Bravo J, Rahman MM, Novakovic R, Daştan SD, Kabra A, Sharifi-Rad J Evid Based Complement Alternat Med 17-Feb-2022
PMCID:PMC8872661
doi:10.1155/2022/1345006
PMID:35222665
Natural Bioactive Cinnamoyltyramine Alkylamides and Co-Metabolites Evidente A, Masi M Biomolecules 25-Nov-2021
PMCID:PMC8698393
doi:10.3390/biom11121765
PMID:34944409
Sterols and Triterpenes: Antiviral     Potential Supported by In-Silico Analysis Hisham Shady N, Youssif KA, Sayed AM, Belbahri L, Oszako T, Hassan HM, Abdelmohsen UR Plants (Basel) 26-Dec-2020
PMCID:PMC7823815
doi:10.3390/plants10010041
PMID:33375282
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A Sci Total Environ 07-Nov-2020
PMCID:PMC7833357
doi:10.1016/j.scitotenv.2020.143539
PMID:33234268
Bioactive Natural Antivirals: An Updated Review of the Available Plants and Isolated Molecules Mohan S, Elhassan Taha MM, Makeen HA, Alhazmi HA, Al Bratty M, Sultana S, Ahsan W, Najmi A, Khalid A Molecules 22-Oct-2020
PMCID:PMC7659943
doi:10.3390/molecules25214878
PMID:33105694
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D Molecules 29-Apr-2020
PMCID:PMC7249135
doi:10.3390/molecules25092070
PMID:32365518
Neuroprotection of SAK3 on scopolamine-induced cholinergic dysfunction in human neuroblastoma SH-SY5Y cells Suthprasertporn N, Mingchinda N, Fukunaga K, Thangnipon W Cytotechnology 14-Jan-2020
PMCID:PMC7002707
doi:10.1007/s10616-019-00366-7
PMID:31933104
One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones Yuan J, He Q, Song S, Zhang X, Miao Z, Yang C Molecules 20-Aug-2019
PMCID:PMC6720541
doi:10.3390/molecules24163017
PMID:31434258
The potential of plant systems to break the HIV‐TB link Habibi P, Daniell H, Soccol CR, Grossi‐de‐Sa MF Plant Biotechnol J 18-Jul-2019
PMCID:PMC6737023
doi:10.1111/pbi.13110
PMID:30908823
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Analgesic and Anti-Inflammatory Activities of Diethyl Ether and n-Hexane Extract of Polyalthia suberosa Leaves Yasmen N, Aziz MA, Tajmim A, Akter MI, Hazra AK, Rahman SM Evid Based Complement Alternat Med 23-Jan-2018
PMCID:PMC5827878
doi:10.1155/2018/5617234
PMID:29599807
The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates Salomo K, Smith JF, Feild TS, Samain MS, Bond L, Davidson C, Zimmers J, Neinhuis C, Wanke S Syst Bot 18-Dec-2017
PMCID:PMC5792071
doi:10.1600/036364417X696438
PMID:29398773

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 / Phenols / Methoxyphenols
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1016/S0031-9422(99)00535-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
23-(Furan-2-yl)tricosa-5,7-diynoic acid 10476795 Click to see C1=COC(=C1)CCCCCCCCCCCCCCCC#CC#CCCCC(=O)O 412.60 unknown https://doi.org/10.1055/S-2001-16469
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Suberosol 21592340 Click to see CC(C)C(=C)CCC(C)C1CC(C2(C1(CC=C3C2=CCC4C3(CCC(C4(C)C)O)C)C)C)O 454.70 unknown https://doi.org/10.1021/NP50097A017
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.3109/13880208509069005
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.3109/13880208509069005
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.3109/13880208509069005
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentacosa-16,18-diynylfuran 91432207 Click to see CCCCCCC#CC#CCCCCCCCCCCCCCCCC1=CC=CO1 410.70 unknown https://doi.org/10.1055/S-2001-16469
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines
5,10-Dimethoxy-4-methyl-1H-benzo[g]quinolin-2-one 489939 Click to see CC1=CC(=O)NC2=C(C3=CC=CC=C3C(=C12)OC)OC 269.29 unknown https://doi.org/10.1016/S0031-9422(99)00535-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-feruloyltyramine; Moupinamide 125213 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1016/S0031-9422(99)00535-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Cinnamamide, p-hydroxy-N-(p-hydroxyphenethyl)- 89322 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1016/S0031-9422(99)00535-X
Paprazine 5372945 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1016/S0031-9422(99)00535-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.3109/13880208509069005

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