Erythroxylum laurifolium - Unknown
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Internal ID UUID64401b91e9c3f760287117
Scientific name Erythroxylum laurifolium
Authority Lam.
First published in Encycl. 2: 394 (1786)

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Erythroxylum laurifolium is a species of plant belonging to the genus Erythroxylum. It was originally identified and named by Jean-Baptiste de Lamarck. This plant is found exclusively in the islands of Reunion and Mauritius, making it endemic to these regions.

Synonyms Top

Scientific name Authority First published in
Roelana laurifolia Comm. ex DC. Prodr. 1: 575 (1824)

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Germination/Propagation Top

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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-0000679924
Tropicos 100334889
INPN 706263
KEW urn:lsid:ipni.org:names:544078-1
The Plant List kew-2801483
Open Tree Of Life 6100298
Observations.org 440943
NCBI Taxonomy 2589479
IPNI 544078-1
iNaturalist 926875
GBIF 3694277
EPPO EYTLA
Elurikkus 397010
USDA GRIN 15796
Wikipedia Erythroxylum_laurifolium

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)!
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Title Authors Publication Released IDs
A survey on the potential contribution of Reunion Island dye plant species diversity to the market demand for bioactive plant-based dyes and pigments Andriamanantena M, Pithon S, Dijoux M, Hoareau M, Fontaine C, Ferrard J, Lavergne C, Petit T, Caro Y J Ethnobiol Ethnomed 25-Mar-2023
PMCID:PMC10039506
doi:10.1186/s13002-023-00580-w
PMID:36964580
Extracts of select endemic plants from the Republic of Mauritius exhibiting anti-cancer and immunomodulatory properties Kauroo S, Govinden-Soulange J, Ranghoo-Sanmukhiya VM, Miranda K, Cotham WE, Walla MD, Nagarkatti M, Nagarkatti P Sci Rep 19-Feb-2021
PMCID:PMC7895923
doi:10.1038/s41598-021-83461-0
PMID:33608608
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
Erythroxylum in Focus: An Interdisciplinary Review of an Overlooked Genus Restrepo DA, Saenz E, Jara-Muñoz OA, Calixto-Botía IF, Rodríguez-Suárez S, Zuleta P, Chavez BG, Sanchez JA, D’Auria JC Molecules 21-Oct-2019
PMCID:PMC6833119
doi:10.3390/molecules24203788
PMID:31640255
Ethnopharmacology, Phytochemistry, and Global Distribution of Mangroves―A Comprehensive Review Nabeelah Bibi S, Fawzi MM, Gokhan Z, Rajesh J, Nadeem N, R.R. RK, R.D.D.G. A, Pandian SK Mar Drugs 18-Apr-2019
PMCID:PMC6520788
doi:10.3390/md17040231
PMID:31003533
Is heterostyly rare on oceanic islands? Watanabe K, Sugawara T AoB Plants 21-Jul-2015
PMCID:PMC4570599
doi:10.1093/aobpla/plv087
PMID:26199401
Inhibitory Potential of Five Traditionally Used Native Antidiabetic Medicinal Plants on α-Amylase, α-Glucosidase, Glucose Entrapment, and Amylolysis Kinetics In Vitro Picot CM, Subratty AH, Mahomoodally MF Adv Pharmacol Sci 02-Mar-2014
PMCID:PMC3958646
doi:10.1155/2014/739834
PMID:24723945
Underestimating the Toxicological Challenges Associated with the Use of Herbal Medicinal Products in Developing Countries Neergheen-Bhujun VS Biomed Res Int 19-Sep-2013
PMCID:PMC3791562
doi:10.1155/2013/804086
PMID:24163821
Angiotensin converting enzyme (ACE) inhibitory flavonoids from Erythroxylum laurifolium. Hansen K, Adsersen A, Smitt UW, Nyman U, Christensen SB, Schwartner C, Wagner H Phytomedicine 01-Mar-1996
doi:10.1016/S0944-7113(96)80075-4
PMID:23194768

Phytochemical Profile Top

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Name PubChem ID Canonical SMILES MW Found in Proof
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0944-7113(96)80075-4
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0944-7113(96)80075-4

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