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Phyllanthus watsonii

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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 UUID643fe7a724dba397383132
Scientific name Phyllanthus watsonii
Authority Airy Shaw
First published in Kew Bull. 25: 493 (1971)

Description Top

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Synonyms Top

No known synonyms.

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-0000272364
Tropicos 50261467
KEW urn:lsid:ipni.org:names:354861-1
The Plant List kew-155155
Open Tree Of Life 3909274
NCBI Taxonomy 2708513
IUCN Red List 31489
IPNI 354861-1
iNaturalist 442051
GBIF 5381637
Freebase /m/02xc5_j
EOL 1152466
Wikipedia Phyllanthus_watsonii

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
Progress of Plant Medicine Derived Extracts and Alkaloids on Modulating Viral Infections and Inflammation Ti H, Zhuang Z, Yu Q, Wang S Drug Des Devel Ther 31-Mar-2021
PMCID:PMC8020337
doi:10.2147/DDDT.S299120
PMID:33833499
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082
Plants Metabolites: Possibility of Natural Therapeutics Against the COVID-19 Pandemic Bhuiyan FR, Howlader S, Raihan T, Hasan M Front Med (Lausanne) 07-Aug-2020
PMCID:PMC7427128
doi:10.3389/fmed.2020.00444
PMID:32850918
Antidiabetic Potential of Medicinal Plants and Their Active Components Salehi B, Ata A, V. Anil Kumar N, Sharopov F, Ramírez-Alarcón K, Ruiz-Ortega A, Abdulmajid Ayatollahi S, Valere Tsouh Fokou P, Kobarfard F, Amiruddin Zakaria Z, Iriti M, Taheri Y, Martorell M, Sureda A, N. Setzer W, Durazzo A, Lucarini M, Santini A, Capasso R, Adrian Ostrander E, -ur-Rahman A, Iqbal Choudhary M, C. Cho W, Sharifi-Rad J Biomolecules 30-Sep-2019
PMCID:PMC6843349
doi:10.3390/biom9100551
PMID:31575072
Phytochemicals in Prostate Cancer: From Bioactive Molecules to Upcoming Therapeutic Agents Salehi B, Fokou PV, Yamthe LR, Tali BT, Adetunji CO, Rahavian A, Mudau FN, Martorell M, Setzer WN, Rodrigues CF, Martins N, Cho WC, Sharifi-Rad J Nutrients 29-Jun-2019
PMCID:PMC6683070
doi:10.3390/nu11071483
PMID:31261861
ANTI-VIRAL EFFECTS OF MEDICINAL PLANTS IN THE MANAGEMENT OF DENGUE: A SYSTEMATIC REVIEW Frederico ÉH, Cardoso AL, Moreira-Marconi E, de Sá-Caputo DD, Guimarães CA, Dionello CD, Morel DS, Paineiras-Domingos LL, de Souza PL, Brandão-Sobrinho-Neto S, Carvalho-Lima RP, Guedes-Aguiar ED, Costa-Cavalcanti RG, Kutter CR, Bernardo-Filho M Afr J Tradit Complement Altern Med 07-Jul-2017
PMCID:PMC5514443
doi:10.21010/ajtcam.v14i4S.5
PMID:28740942
Suppression of ERK1/2 and hypoxia pathways by four Phyllanthus species inhibits metastasis of human breast cancer cells Lee SH, Jaganath IB, Atiya N, Manikam R, Sekaran SD J Food Drug Anal 02-Jun-2016
PMCID:PMC9337293
doi:10.1016/j.jfda.2016.03.010
PMID:28911625
Ellagitannins in Cancer Chemoprevention and Therapy Ismail T, Calcabrini C, Diaz AR, Fimognari C, Turrini E, Catanzaro E, Akhtar S, Sestili P Toxins (Basel) 13-May-2016
PMCID:PMC4885066
doi:10.3390/toxins8050151
PMID:27187472
Phytoconstituents as apoptosis inducing agents: strategy to combat cancer Kumar M, Kaur V, Kumar S, Kaur S Cytotechnology 04-Aug-2015
PMCID:PMC4960184
doi:10.1007/s10616-015-9897-2
PMID:26239338
Panepoxydone Targets NF-kB and FOXM1 to Inhibit Proliferation, Induce Apoptosis and Reverse Epithelial to Mesenchymal Transition in Breast Cancer Arora R, Yates C, Gary BD, McClellan S, Tan M, Xi Y, Reed E, Piazza GA, Owen LB, Dean-Colomb W PLoS One 04-Jun-2014
PMCID:PMC4045585
doi:10.1371/journal.pone.0098370
PMID:24896091
Growth Inhibition of Human Gynecologic and Colon Cancer Cells by Phyllanthus watsonii through Apoptosis Induction Ramasamy S, Abdul Wahab N, Zainal Abidin N, Manickam S, Zakaria Z PLoS One 20-Apr-2012
PMCID:PMC3335034
doi:10.1371/journal.pone.0034793
PMID:22536331
26-Nor-D:A-friedooleanane triterpenes from Phyllanthus watsonii Shunyo Matsunaga, Reiko Tanaka, Yoshikazu Takaoka, Yasuko In, Toshimasa Ishida, Mawardi Rahmani, Hazar Bebe M. Ismail Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80125-X

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 / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(3S,4R,4aS,6aS,6aS,8aR,12aR,14aS,14bS)-4,4a,6a,8a,11,11,14a-heptamethyl-2,3,4,5,6,6a,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-ol 162916952 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C)O 412.70 unknown https://doi.org/10.1016/0031-9422(92)80125-X
(4R,4aS,6aS,6aS,8aR,12aR,14aS,14bS)-4,4a,6a,8a,11,11,14a-heptamethyl-1,2,4,5,6,6a,8,9,10,12,12a,13,14,14b-tetradecahydropicen-3-one 162990618 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(92)80125-X
4,4a,6a,8a,11,11,14a-Heptamethyl-1,2,4,5,6,6a,8,9,10,12,12a,13,14,14b-tetradecahydropicen-3-one 162990616 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(92)80125-X
4,4a,6a,8a,11,11,14a-heptamethyl-2,3,4,5,6,6a,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-ol 162916951 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C)O 412.70 unknown https://doi.org/10.1016/0031-9422(92)80125-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Epifriedelanol 119242 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/10.1016/0031-9422(92)80125-X
Friedelin 91472 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/10.1016/0031-9422(92)80125-X
Glochidone 13942832 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/10.1016/0031-9422(92)80125-X
Glochidonol 14167335 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(=O)C5(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(92)80125-X
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(92)80125-X
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(92)80125-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(92)80125-X
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/10.1016/0031-9422(92)80125-X
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(92)80125-X
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/10.1016/0031-9422(92)80125-X
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/10.1016/0031-9422(92)80125-X

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