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Internal ID UUID643fe762f059c783230637
Scientific name Phyllanthus engleri
Authority Pax
First published in Pflanzenw. Ost-Afrikas , C: 236 (1895)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Tanzania
    • South Tropical Africa
      • Mozambique
      • Zambia
      • Zimbabwe
    • West-central Tropical Africa
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000270936
Tropicos 12806004
KEW urn:lsid:ipni.org:names:353842-1
The Plant List kew-153794
Open Tree Of Life 3908831
NCBI Taxonomy 1899179
IUCN Red List 168474065
IPNI 353842-1
GBIF 5381589
EOL 1153039
USDA GRIN 411728

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
Gilman reagent toward the synthesis of natural products Munir R, Zahoor AF, Nazeer U, Saeed MA, Mansha A, Irfan A, Tariq MU RSC Adv 04-Dec-2023
PMCID:PMC10694855
doi:10.1039/d3ra07359a
PMID:38053693
An Overview of Renal Cell Carcinoma Hallmarks, Drug Resistance, and Adjuvant Therapies DA SILVA PRADE J, DE SOUZA RS, DA SILVA D’ΑVILA CM, DA SILVA TC, LIVINALLI IC, BERTONCELLI AC, SACCOL FK, DE OLIVEIRA MENDES T, WENNING LG, DA ROSA SALLES T, RHODEN CR, CADONA FC Cancer Diagn Progn 03-Nov-2023
PMCID:PMC10619564
doi:10.21873/cdp.10264
PMID:37927802
Sharpless Asymmetric Dihydroxylation: An Impressive Gadget for the Synthesis of Natural Products: A Review Mushtaq A, Zahoor AF, Bilal M, Hussain SM, Irfan M, Akhtar R, Irfan A, Kotwica-Mojzych K, Mojzych M Molecules 17-Mar-2023
PMCID:PMC10051988
doi:10.3390/molecules28062722
PMID:36985698
Herbal remedies used by traditional healers to treat haemorrhoids in Tabora region, Tanzania Kacholi DS, Mvungi Amir H Pharm Biol 28-Oct-2022
PMCID:PMC9629089
doi:10.1080/13880209.2022.2136204
PMID:36307997
Biological Effects of Modifications of the Englerin A Glycolate Seenadera SP, Long SA, Akee R, Bermudez G, Parsonage G, Strope J, Peer C, Figg WD, Parker KA, Beech DJ, Beutler JA ACS Med Chem Lett 22-Aug-2022
PMCID:PMC9465829
doi:10.1021/acsmedchemlett.2c00258
PMID:36105325
The key role of sphingolipid metabolism in cancer: New therapeutic targets, diagnostic and prognostic values, and anti-tumor immunotherapy resistance Li RZ, Wang XR, Wang J, Xie C, Wang XX, Pan HD, Meng WY, Liang TL, Li JX, Yan PY, Wu QB, Liu L, Yao XJ, Leung EL Front Oncol 27-Jul-2022
PMCID:PMC9364366
doi:10.3389/fonc.2022.941643
PMID:35965565
Therapeutic Potential of Natural Products in the Treatment of Renal Cell Carcinoma: A Review Feng C, Lyu Y, Gong L, Wang J Nutrients 28-May-2022
PMCID:PMC9182762
doi:10.3390/nu14112274
PMID:35684073
Alterations in the Ca2+ toolkit in oesophageal adenocarcinoma Cutliffe AL, McKenna SL, Chandrashekar DS, Ng A, Devonshire G, Fitzgerald RC, O’Donovan TR, Mackrill JJ Explor Target Antitumor Ther 31-Dec-2021
PMCID:PMC9400700
doi:10.37349/etat.2021.00063
PMID:36046118
(-)-Englerin-A Has Analgesic and Anti-Inflammatory Effects Independent of TRPC4 and 5 de Sousa Valente J, Alawi KM, Bharde S, Zarban AA, Kodji X, Thapa D, Argunhan F, Barrett B, Nagy I, Brain SD Int J Mol Sci 15-Jun-2021
PMCID:PMC8232259
doi:10.3390/ijms22126380
PMID:34203675
Canonical transient receptor potential channels and their modulators: biology, pharmacology and therapeutic potentials Gao YY, Tian W, Zhang HN, Sun Y, Meng JR, Cao W, Li XQ Arch Pharm Res 24-Mar-2021
PMCID:PMC7989688
doi:10.1007/s12272-021-01319-5
PMID:33763843
Structural basis for human TRPC5 channel inhibition by two distinct inhibitors Song K, Wei M, Guo W, Quan L, Kang Y, Wu JX, Chen L eLife 08-Mar-2021
PMCID:PMC7987348
doi:10.7554/eLife.63429
PMID:33683200
Contribution of TRPC Channels in Neuronal Excitotoxicity Associated With Neurodegenerative Disease and Ischemic Stroke Jeon J, Bu F, Sun G, Tian JB, Ting SM, Li J, Aronowski J, Birnbaumer L, Freichel M, Zhu MX Front Cell Dev Biol 08-Jan-2021
PMCID:PMC7820370
doi:10.3389/fcell.2020.618663
PMID:33490083
Complex natural product production methods and options Park D, Swayambhu G, Lyga T, Pfeifer BA Synth Syst Biotechnol 05-Jan-2021
PMCID:PMC7803631
doi:10.1016/j.synbio.2020.12.001
PMID:33474503
Bridgehead Modifications of Englerin A Reduce TRPC4 Activity and Intravenous Toxicity but not Cell Growth Inhibition Wu Z, Suppo JS, Tumova S, Strope J, Bravo F, Moy M, Weinstein ES, Peer CJ, Figg WD, Chain WJ, Echavarren AM, Beech DJ, Beutler JA ACS Med Chem Lett 03-Aug-2020
PMCID:PMC7488277
doi:10.1021/acsmedchemlett.0c00186
PMID:32944138
Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes Lautié E, Russo O, Ducrot P, Boutin JA Front Pharmacol 07-Apr-2020
PMCID:PMC7154113
doi:10.3389/fphar.2020.00397
PMID:32317969

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 / Sesquiterpenoids
(10-Hydroxy-1,5-dimethyl-8-propan-2-yl-11-oxatricyclo[6.2.1.02,6]undecan-7-yl) 3-phenylprop-2-enoate 74405694 Click to see CC1CCC2C1C(C3(CC(C2(O3)C)O)C(C)C)OC(=O)C=CC4=CC=CC=C4 384.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2651161/
[(1R,2S,5S,6S,7R,8S,10S)-10-(2-hydroxyacetyl)oxy-1,5-dimethyl-8-propan-2-yl-11-oxatricyclo[6.2.1.02,6]undecan-7-yl] (E)-3-phenylprop-2-enoate 25194882 Click to see CC1CCC2C1C(C3(CC(C2(O3)C)OC(=O)CO)C(C)C)OC(=O)C=CC4=CC=CC=C4 442.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2651161/
Cinnamic acid (3abeta,8aalpha)-decahydro-1beta,4-dimethyl-5beta-hydroxy-7-(1-methylethyl)-4beta,7beta-epoxyazulene-8alpha-yl ester 25194883 Click to see CC1CCC2C1C(C3(CC(C2(O3)C)O)C(C)C)OC(=O)C=CC4=CC=CC=C4 384.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2651161/
Englerin-A 74405693 Click to see CC1CCC2C1C(C3(CC(C2(O3)C)OC(=O)CO)C(C)C)OC(=O)C=CC4=CC=CC=C4 442.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2651161/
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5R,7S,10R,11R,14R,15R,16S,17R,20R)-2,6,6,10,16,17,20-heptamethylhexacyclo[12.8.1.01,14.02,11.05,10.015,20]tricosan-7-ol 101600095 Click to see CC1CCC2(CCC34CC3(C2C1C)CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1039/JR9510002296
6a,14a-Methanopicene, perhydro-1,2,4a,6b,9,9,12a-heptamethyl-10-hydroxy- 634650 Click to see CC1CCC2(CCC34CC3(C2C1C)CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1039/JR9510002296

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