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Barleria trispinosa

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 UUID64400c5897a7f085995313
Scientific name Barleria trispinosa
Authority Vahl
First published in Symb. Bot. 1: 46 (1790)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Barleria diacantha Nees Prodr. [A. P. de Candolle] 11: 238, partim. 1847 [25 Nov 1847]
Barleria marghilomanae Volkens & Schweinf. Pays des Somalis : 216 (1898)
Justicia trispinosa Forssk. Fl. Aegypt.-Arab. : 6 (1775)

Common names Top

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Language Common/alternative name
Arabic الشخت
Arabic حميحماء
Arabic الحميحمان

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Barleria trispinosa subsp. glandulosissima I.Darbysh. Fl. Trop. E. Africa , Acanth.(2): 425 (2010)
Barleria trispinosa subsp. trispinosa Unknown

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Uganda
    • Northeast Tropical Africa
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000560612
Tropicos 103545
KEW urn:lsid:ipni.org:names:46256-1
The Plant List kew-2670255
Open Tree Of Life 5810728
NCBI Taxonomy 1532733
IPNI 46256-1
iNaturalist 1030633
GBIF 3770299

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
Bio-Guided Isolation of SARS-CoV-2 Main Protease Inhibitors from Medicinal Plants: In Vitro Assay and Molecular Dynamics Abdallah HM, El-Halawany AM, Darwish KM, Algandaby MM, Mohamed GA, Ibrahim SR, Koshak AE, Elhady SS, Fadil SA, Alqarni AA, Abdel-Naim AB, Elfaky MA Plants (Basel) 24-Jul-2022
PMCID:PMC9332707
doi:10.3390/plants11151914
PMID:35893619
Floristic composition of Jandaf Mountain as biodiversity hotspot area in southwestern Saudi Arabia Al-Namazi AA, Algarni SM, Wan JS, Al Mosallam MS, Alotaibi F Saudi J Biol Sci 05-Mar-2022
PMCID:PMC9280213
doi:10.1016/j.sjbs.2022.03.003
PMID:35844416
Defence emergence during early ontogeny reveals important differences between spines, thorns and prickles Coverdale TC Ann Bot 06-Jan-2020
PMCID:PMC6943688
doi:10.1093/aob/mcz189
PMID:31904092
Evaluation of the In Vitro Antiplasmodial, Antileishmanial, and Antitrypanosomal Activity of Medicinal Plants Used in Saudi and Yemeni Traditional Medicine Mothana RA, Al-Musayeib NM, Al-Ajmi MF, Cos P, Maes L Evid Based Complement Alternat Med 21-May-2014
PMCID:PMC4055400
doi:10.1155/2014/905639
PMID:24963330
Iridoid glycosides from Barleria trispinosa. Harraz FM, El-Halawany AM, El Gayed SH, Abdel-Sattar E Nat Prod Res 01-Jan-2009
doi:10.1080/14786410802278350
PMID:19521903

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 / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
methyl (1S,3R,3aS,7R,7aR)-1-acetyloxy-1-methyl-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,3a,6,7,7a-hexahydroindene-4-carboxylate 162855620 Click to see 592.60 unknown https://doi.org/10.1080/14786410802278350
methyl (1S,3R,3aS,7R,7aR)-1-acetyloxy-3-hydroxy-1-methyl-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,3a,6,7,7a-hexahydroindene-4-carboxylate 163025403 Click to see CC(=O)OC1(CC(C2C1C(CC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)C 446.40 unknown https://doi.org/10.1080/14786410802278350
methyl (1S,3R,3aS,7R,7aR)-1,3-diacetyloxy-1-methyl-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,3a,6,7,7a-hexahydroindene-4-carboxylate 162994736 Click to see 488.50 unknown https://doi.org/10.1080/14786410802278350
methyl (1S,3R,3aS,7R,7aR)-1,3-dihydroxy-1-methyl-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,3a,6,7,7a-hexahydroindene-4-carboxylate 163036926 Click to see 404.40 unknown https://doi.org/10.1080/14786410802278350
Methyl 1-acetyloxy-1-methyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2,3,3a,6,7,7a-hexahydroindene-4-carboxylate 162855619 Click to see CC1C(C(C(C(O1)OC2CC(C3C2C(=CCC3OC4C(C(C(C(O4)CO)O)O)O)C(=O)OC)(C)OC(=O)C)O)O)O 592.60 unknown https://doi.org/10.1080/14786410802278350
Methyl 1-acetyloxy-3-hydroxy-1-methyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,3a,6,7,7a-hexahydroindene-4-carboxylate 163025402 Click to see 446.40 unknown https://doi.org/10.1080/14786410802278350
Methyl 1,3-diacetyloxy-1-methyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,3a,6,7,7a-hexahydroindene-4-carboxylate 162994735 Click to see 488.50 unknown https://doi.org/10.1080/14786410802278350
Methyl 1,3-dihydroxy-1-methyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,3a,6,7,7a-hexahydroindene-4-carboxylate 163036925 Click to see 404.40 unknown https://doi.org/10.1080/14786410802278350

Gallery Top

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Collections Top

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