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Brachylaena elliptica

Brachylaena elliptica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd2b6ba16d030147222
Scientific name Brachylaena elliptica
Authority Less.
First published in Syn. Gen. Compos. : 208 (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tarchonanthus ellipticus Thunb. Prodr. Pl. Cap. 2: 145 (1800)
Tarchonanthus camphoratus Houtt. ex DC. Prodr. 5: 430 (1836)
Brachylaena elliptica var. salicina (DC.) Harv.
Brachylaena dentata var. salicina DC.

Common names Top

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Language Common/alternative name
Afrikaans bitterblaar

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  • Africa
    • Northeast Tropical Africa
      • Djibouti
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000126043
Tropicos 2718820
KEW urn:lsid:ipni.org:names:186091-1
The Plant List gcc-87095
Open Tree Of Life 17910
NCBI Taxonomy 459735
IUCN Red List 149512937
IPNI 186091-1
iNaturalist 581261
GBIF 3140994

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
Potential use of the Asteraceae family as a cure for diabetes: A review of ethnopharmacology to modern day drug and nutraceuticals developments Mohanta YK, Mishra AK, Nongbet A, Chakrabartty I, Mahanta S, Sarma B, Panda J, Panda SK Front Pharmacol 03-Aug-2023
PMCID:PMC10441548
doi:10.3389/fphar.2023.1153600
PMID:37608892
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
Dipeptidyl peptidase-IV inhibitory action of Calebin A: An in silico and in vitro analysis Chalichem NS, Jupudi S, Yasam VR, Basavan D J Ayurveda Integr Med 29-Oct-2021
PMCID:PMC8642699
doi:10.1016/j.jaim.2021.08.008
PMID:34756798
Cytotoxic, Cellular Antioxidant, and Antiglucuronidase Properties of the Ethanol Leaf Extract from Bulbine asphodeloides Otang-Mbeng W, Sagbo IJ ScientificWorldJournal 14-Apr-2021
PMCID:PMC8060099
doi:10.1155/2021/6622318
PMID:33935597
Potential Synergistic Action of Bioactive Compounds from Plant Extracts against Skin Infecting Microorganisms Sitarek P, Merecz-Sadowska A, Kowalczyk T, Wieczfinska J, Zajdel R, Śliwiński T Int J Mol Sci 19-Jul-2020
PMCID:PMC7403983
doi:10.3390/ijms21145105
PMID:32707732
Inhibition of HIV-1 Protease by Carpobrotus edulis (L.) Omoruyi BE, Ighodaro DI, Afolayan AJ, Bradley G Evid Based Complement Alternat Med 07-Jun-2020
PMCID:PMC7298281
doi:10.1155/2020/9648056
PMID:32595755
Extraction of Phenolic Compounds from Tabernaemontana catharinensis Leaves and Their Effect on Oxidative Stress Markers in Diabetic Rats Sari R, Conterno P, da Silva LD, de Lima VA, Oldoni TL, Thomé GR, Carpes ST Molecules 21-May-2020
PMCID:PMC7288081
doi:10.3390/molecules25102391
PMID:32455579
Aqueous extract from Mangifera indica Linn. (Anacardiaceae) leaves exerts long-term hypoglycemic effect, increases insulin sensitivity and plasma insulin levels on diabetic Wistar rats Villas Boas GR, Rodrigues Lemos JM, de Oliveira MW, dos Santos RC, Stefanello da Silveira AP, Barbieri Bacha F, Ito CN, Bortolotte Cornelius E, Brioli Lima F, Sachilarid Rodrigues AM, Belmal Costa N, Francisco Bittencourt F, Freitas de Lima F, Meirelles Paes M, Gubert P, Oesterreich SA PLoS One 08-Jan-2020
PMCID:PMC6948748
doi:10.1371/journal.pone.0227105
PMID:31914140
Understanding glycaemic control and current approaches for screening antidiabetic natural products from evidence-based medicinal plants Lankatillake C, Huynh T, Dias DA Plant Methods 07-Sep-2019
PMCID:PMC6731622
doi:10.1186/s13007-019-0487-8
PMID:31516543
Medicinal Plants Used for the Traditional Management of Diabetes in the Eastern Cape, South Africa: Pharmacology and Toxicology Odeyemi S, Bradley G Molecules 25-Oct-2018
PMCID:PMC6278280
doi:10.3390/molecules23112759
PMID:30366359
In Vitro Antidiabetic Activity and Mechanism of Action of Brachylaena elliptica (Thunb.) DC Sagbo IJ, van de Venter M, Koekemoer T, Bradley G Evid Based Complement Alternat Med 04-Jul-2018
PMCID:PMC6077518
doi:10.1155/2018/4170372
PMID:30108655
Ethnopharmacological Survey of Plants Used in the Traditional Treatment of Gastrointestinal Pain, Inflammation and Diarrhea in Africa: Future Perspectives for Integration into Modern Medicine Stark TD, Mtui DJ, Balemba OB Animals (Basel) 04-Mar-2013
PMCID:PMC4495512
doi:10.3390/ani3010158
PMID:26487315
In vivo Studies on Antidiabetic Plants Used in South African Herbal Medicine J. Afolayan A, O. Sunmonu T J Clin Biochem Nutr 23-Jun-2010
PMCID:PMC2935160
doi:10.3164/jcbn.09-126R
PMID:20838564
Sesquiterpene lactones from the Genus brachylaena C. Zdero, F. Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83886-8

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 / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(6,10-Dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2-(hydroxymethyl)prop-2-enoate 162953910 Click to see CC1=CC2C(C(CC(=CCC1)C)OC(=O)C(=C)CO)C(=C)C(=O)O2 332.40 unknown https://doi.org/10.1016/S0031-9422(00)83886-8
[(3aR,4S,6E,10E,11aR)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 163195174 Click to see CC1=CC2C(C(CC(=CCC1)C)OC(=O)C(=C)CO)C(=C)C(=O)O2 332.40 unknown https://doi.org/10.1016/S0031-9422(00)83886-8
[(3aR,4S,6E,10Z,11aS)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 163039290 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=C)CO)C(=C)C(=O)O2)CO 348.40 unknown https://doi.org/10.1016/S0031-9422(00)83886-8

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