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Phyllanthus taxodiifolius

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 UUID643fe79f76594675434814
Scientific name Phyllanthus taxodiifolius
Authority Beille
First published in Fl. Indo-Chine 5: 605 (1927)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Thai ไคร้หางนาค
Chinese 落羽杉叶下珠
Chinese 滇橄榄
Chinese 落羽松叶下珠

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-0000272204
Tropicos 50056859
KEW urn:lsid:ipni.org:names:354753-1
The Plant List kew-155005
Open Tree Of Life 772623
NCBI Taxonomy 296045
IPNI 354753-1
GBIF 5381133
EOL 1152531

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
ECDD-S16 targets vacuolar ATPase: A potential inhibitor compound for pyroptosis-induced inflammation Ekchariyawat P, Saengfak R, Sanongkiet S, Charoenwongpaiboon T, Khongpraphan S, Mala S, Luangjindarat C, Munyoo B, Chabang N, Charoensutthivarakul S, Borwornpinyo S, Tuchinda P, Ponpuak M, Pudla M, Utaisincharoen P PLoS One 27-Nov-2023
PMCID:PMC10681236
doi:10.1371/journal.pone.0292340
PMID:38011122
Phyllanthus taxodiifolius Beille Disrupted N-cadherin, Vimentin, Paxillin and Actin Stress Fibers in Glioblastoma Sunrat C, Kwanthongdee J, Uppakara K, Chabang N, Munyoo B, Tuchinda P, Saengsawang W Asian Pac J Cancer Prev 01-Jul-2022
PMCID:PMC9727360
doi:10.31557/APJCP.2022.23.7.2379
PMID:35901345
Lignans: a versatile source of anticancer drugs Mukhija M, Joshi BC, Bairy PS, Bhargava A, Sah AN Beni Suef Univ J Basic Appl Sci 04-Jun-2022
PMCID:PMC9166195
doi:10.1186/s43088-022-00256-6
PMID:35694188
Plant-Derived Natural Products as Lead Agents against Common Respiratory Diseases Oriola AO, Oyedeji AO Molecules 10-May-2022
PMCID:PMC9144277
doi:10.3390/molecules27103054
PMID:35630531
Preparation and Characterization of MUC-30-Loaded Polymeric Micelles against MCF-7 Cell Lines Using Molecular Docking Methods and In Vitro Study Nasongkla N, Tuchinda P, Munyoo B, Eawsakul K Evid Based Complement Alternat Med 28-May-2021
PMCID:PMC8179782
doi:10.1155/2021/5597681
PMID:34135981
Anti-COVID-19 drug candidates: A review on potential biological activities of natural products in the management of new coronavirus infection Prasansuklab A, Theerasri A, Rangsinth P, Sillapachaiyaporn C, Chuchawankul S, Tencomnao T J Tradit Complement Med 29-Dec-2020
PMCID:PMC7833040
doi:10.1016/j.jtcme.2020.12.001
PMID:33520683
A novel potent autophagy inhibitor ECDD-S27 targets vacuolar ATPase and inhibits cancer cell survival Paha J, Kanjanasirirat P, Munyoo B, Tuchinda P, Suvannang N, Nantasenamat C, Boonyarattanakalin K, Kittakoop P, Srikor S, Kongklad G, Rangkasenee N, Hongeng S, Utaisincharoen P, Borwornpinyo S, Ponpuak M Sci Rep 24-Jun-2019
PMCID:PMC6591302
doi:10.1038/s41598-019-45641-x
PMID:31235856
M3, a natural lignan xyloside, exhibits potent anticancer activity in HCT116 cells Shen W, Zhao Y, Chen H, Zhang T, Wu S, Liu P Oncol Lett 12-Dec-2018
PMCID:PMC6341843
doi:10.3892/ol.2018.9823
PMID:30675278
Identification of natural inhibitors against angiotensin I converting enzyme for cardiac safety using induced fit docking and MM-GBSA studies Vijayakumar B, Parasuraman S, Raveendran R, Velmurugan D Pharmacogn Mag 01-Aug-2014
PMCID:PMC4189283
doi:10.4103/0973-1296.139809
PMID:25298685
Biodistribution properties of cleistanthin A and cleistanthin B using magnetic resonance imaging in a normal and tumoric animal model Parasuraman S, Raveendran R, Ardestani MS, Ananthakrishnan R, Jabbari-Arabzadeh A, Alavidjeh MS, Aghasadeghi MR, Elangovan S, Dhanapathi H Pharmacogn Mag 01-Apr-2012
PMCID:PMC3371434
doi:10.4103/0973-1296.96559
PMID:22701286
Cytotoxic arylnaphthalide lignan glycosides from the aerial parts of Phyllanthus taxodiifolius. Tuchinda P, Kumkao A, Pohmakotr M, Sophasan S, Santisuk T, Reutrakul V Planta Med 01-Jan-2006
doi:10.1055/S-2005-873141
PMID:16450297

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
> Lignans, neolignans and related compounds / Lignan glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R)-2-[[9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-1-oxo-3H-benzo[f][2]benzofuran-4-yl]oxy]-4,5-dimethoxyoxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 163031428 Click to see 744.70 unknown https://doi.org/10.1055/S-2005-873141
[6-[2-[[9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-1-oxo-3H-benzo[f][2]benzofuran-4-yl]oxy]-4,5-dimethoxyoxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 73066508 Click to see 744.70 unknown https://doi.org/10.1055/S-2005-873141
9-(1,3-benzodioxol-5-yl)-4-[4,5-dimethoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one 78178231 Click to see 702.70 unknown https://doi.org/10.1055/S-2005-873141
9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-4-(3,4,5-trimethoxyoxan-2-yl)oxy-3H-benzo[f][2]benzofuran-1-one 72681024 Click to see 554.50 unknown https://doi.org/10.1055/S-2005-873141
9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-4-[(2S,3R,4S,5R)-3,4,5-trimethoxyoxan-2-yl]oxy-3H-benzo[f][2]benzofuran-1-one 60200398 Click to see 554.50 unknown https://doi.org/10.1055/S-2005-873141
Cleistanthin 44563408 Click to see 540.50 unknown https://doi.org/10.1055/S-2005-873141
Cleistanthin A 4485134 Click to see 540.50 unknown https://doi.org/10.1055/S-2005-873141
Cleistanthoside A 158941 Click to see COC1COC(C(C1OC)OC2C(C(C(C(O2)CO)O)O)O)OC3=C4COC(=O)C4=C(C5=CC(=C(C=C53)OC)OC)C6=CC7=C(C=C6)OCO7 702.70 unknown https://doi.org/10.1055/S-2005-873141
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,11b,12,13,13a,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one 4106989 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C=CC(=O)C5(C)C)C)C)C 422.70 unknown https://doi.org/10.1055/S-2005-873141
Npc156081 13942832 Click to see 422.70 unknown https://doi.org/10.1055/S-2005-873141

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