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Glochidion lanceolarium

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 UUID68f8f758578dd487549120
Scientific name Glochidion lanceolarium
Authority (Roxb.) Voigt
First published in Hort. Suburb. Calcutt. : 153 (1845)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Phyllanthus fraxinifolius G.Lodd. Bot. Cab. 9: t. 839 (1824)
Bradleia lanceolaria Roxb. Fl. Ind. ed. 1832 , 3: 697 (1832)
Diasperus benthamianus Kuntze Revis. Gen. Pl. 2: 598 (1891)
Diasperus lanceolarius (Roxb.) Kuntze Revis. Gen. Pl. 2: 599 (1891)
Glochidion cantoniense Hance Ann. Sci. Nat., Bot. , sér. 5, 5: 241 (1866)
Glochidion macrophyllum Benth. London J. Bot. 1: 491 (1842)
Glochidion subsessile var. birmanicum Chakrab. & M.Gangop. J. Econ. Taxon. Bot. 13: 716 (1989)
Glochisandra acuminata Wight Icon. Pl. Ind. Orient. 5(2): 28 (1852)
Phyllanthus lanceolarius (Roxb.) Müll.Arg. Flora 48: 371 (1865)
Phyllanthus benthamianus Müll.Arg. Flora 48: 371 1865

Common names Top

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Language Common/alternative name
Chinese 艾胶树
Chinese 艾胶算盘子
Chinese 大叶算盘子

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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
Tropicos 50056982
KEW urn:lsid:ipni.org:names:354123-1
IUCN Red List 136143523
IPNI 354123-1
GBIF 5383103
World Flora Online wfo-0000973333
Tropicos 50056980
KEW urn:lsid:ipni.org:names:349452-1
The Plant List kew-90539
Open Tree Of Life 708048
NCBI Taxonomy 1036588
IPNI 349452-1
iNaturalist 630852
GBIF 3080126
EOL 1143246

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
Electrospun nanofibers synthesized from polymers incorporated with bioactive compounds for wound healing Palani N, Vijayakumar P, Monisha P, Ayyadurai S, Rajadesingu S J Nanobiotechnology 27-Apr-2024
PMCID:PMC11056076
doi:10.1186/s12951-024-02491-8
PMID:38678271
Plant-mediated synthesis of silver nanoparticles: unlocking their pharmacological potential–a comprehensive review Dhir R, Chauhan S, Subham P, Kumar S, Sharma P, Shidiki A, Kumar G Front Bioeng Biotechnol 09-Jan-2024
PMCID:PMC10803431
doi:10.3389/fbioe.2023.1324805
PMID:38264582
Recent advance on nanoparticles or nanomaterials with anti-multidrug resistant bacteria and anti-bacterial biofilm properties: A systematic review Moradi F, Ghaedi A, Fooladfar Z, Bazrgar A Heliyon 10-Nov-2023
PMCID:PMC10685370
doi:10.1016/j.heliyon.2023.e22105
PMID:38034786
Saponin-Derived Silver Nanoparticles from Phoenix dactylifera (Ajwa Dates) Exhibit Broad-Spectrum Bioactivities Combating Bacterial Infections Adnan M, Siddiqui AJ, Ashraf SA, Ashraf MS, Alomrani SO, Alreshidi M, Tepe B, Sachidanandan M, Danciu C, Patel M Antibiotics (Basel) 07-Sep-2023
PMCID:PMC10525761
doi:10.3390/antibiotics12091415
PMID:37760712
Virulence factors and quorum sensing as targets of new therapeutic options by plant-derived compounds against bacterial infections caused by human and animal pathogens Kitpipit W, Scholfield CN, Sangkanu S, Nissapatorn V, Pereira MD, Paul AK, Mitsuwan W Vet World 14-Jun-2023
PMCID:PMC10421536
doi:10.14202/vetworld.2023.1346-1355
PMID:37577190
Beyond the Risk of Biofilms: An Up-and-Coming Battleground of Bacterial Life and Potential Antibiofilm Agents Zeineldin M, Esmael A, Al-Hindi RR, Alharbi MG, Ashenafi Bekele D, Teklemariam AD Life (Basel) 11-Feb-2023
PMCID:PMC9959329
doi:10.3390/life13020503
PMID:36836860
Natural Strategies as Potential Weapons against Bacterial Biofilms Asma ST, Imre K, Morar A, Imre M, Acaroz U, Shah SR, Hussain SZ, Arslan-Acaroz D, Istanbullugil FR, Madani K, Athanassiou C, Atanasoff A, Morar D, Herman V, Zhu K Life (Basel) 17-Oct-2022
PMCID:PMC9604817
doi:10.3390/life12101618
PMID:36295053
Sustainable phyto-fabrication of silver nanoparticles using Gmelina arborea exhibit antimicrobial and biofilm inhibition activity Chandrasekharan S, Chinnasamy G, Bhatnagar S Sci Rep 07-Jan-2022
PMCID:PMC8742086
doi:10.1038/s41598-021-04025-w
PMID:34997051
Editorial: Insights Into New Strategies to Combat Biofilms Panda SK, Buroni S, Tiwari V, Nascimento da Silva LC Front Microbiol 23-Sep-2021
PMCID:PMC8495408
doi:10.3389/fmicb.2021.742647
PMID:34630368
Diversity and species-specificity of brood pollination of leafflower trees (Phyllanthaceae: Glochidion) by leafflower moths (Lepidoptera: Epicephala) in tropical Southeast Asia (Cambodia) Chheang P, Hembry DH, Yao G, Luo SX Plant Divers 16-Jul-2021
PMCID:PMC9043405
doi:10.1016/j.pld.2021.07.001
PMID:35505992
Anti-biofilm and Antibacterial Activities of Silver Nanoparticles Synthesized by the Reducing Activity of Phytoconstituents Present in the Indian Medicinal Plants Mohanta YK, Biswas K, Jena SK, Hashem A, Abd_Allah EF, Mohanta TK Front Microbiol 23-Jun-2020
PMCID:PMC7324531
doi:10.3389/fmicb.2020.01143
PMID:32655511
Non-structural carbohydrates regulated by season and species in the subtropical monsoon broad-leaved evergreen forest of Yunnan Province, China Liu W, Su J, Li S, Lang X, Huang X Sci Rep 18-Jan-2018
PMCID:PMC5773538
doi:10.1038/s41598-018-19271-8
PMID:29348653
The relationship between species richness and aboveground biomass in a primary Pinus kesiya forest of Yunnan, southwestern China Li S, Lang X, Liu W, Ou G, Xu H, Su J PLoS One 11-Jan-2018
PMCID:PMC5764369
doi:10.1371/journal.pone.0191140
PMID:29324901
A Novel, Enigmatic Basal Leafflower Moth Lineage Pollinating a Derived Leafflower Host Illustrates the Dynamics of Host Shifts, Partner Replacement, and Apparent Coadaptation in Intimate Mutualisms Luo SX, Yao G, Wang Z, Zhang D, Hembry DH Am Nat 12-Jan-2017
PMCID:PMC6103454
doi:10.1086/690623
PMID:28350503
Rainforests north of the Tropic of Cancer: Physiognomy, floristics and diversity in ‘lowland rainforests’ of Meghalaya, India Shankar U, Tripathi AK Plant Divers 21-Oct-2016
PMCID:PMC6112274
doi:10.1016/j.pld.2016.10.003
PMID:30159488

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
(11-Acetyloxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) acetate 73805709 Click to see 526.80 unknown https://doi.org/10.1016/S0031-9422(00)85232-2
(1R,3aR,5aR,5bR,7aS,9S,11S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,11-diol 101281305 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)89705-8
(4R,4aR,6aS,6aS,6bS,8aS,12aR,14aR,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 162968765 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85232-2
20(29)-Lupene-3,23-diol 21672675 Click to see 442.70 unknown https://doi.org/10.1039/J39710001004
3-Epiglochidiol diacetate 21582884 Click to see 526.80 unknown https://doi.org/10.1016/S0031-9422(00)85232-2
Epifriedelanol 119242 Click to see 428.70 unknown https://doi.org/10.1016/S0031-9422(00)85232-2
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85232-2
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(00)85232-2
Lup-20(29)-Ene-3bate,23-Diol 14167263 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)C 442.70 unknown https://doi.org/10.1039/J39710001004

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