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Terminalia buceras

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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 UUID64405b8feb697380895204
Scientific name Terminalia buceras
Authority (L.) C.Wright
First published in Anales Acad. Ci. Méd. Habana 5: 409 (1869)

Description Top

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Synonyms Top

Scientific name Authority First published in
Buceras bucida Crantz Inst. Rei Herb. 1: 133 (1766)
Bucida buceras L. Syst. Nat. ed. 10 , 2: 1025 (1759)
Bucida ophiticola Bisse Feddes Repert. 85: 605 (1974)
Bucida palustris Borhidi & O.Muñiz Acta Bot. Acad. Sci. Hung. 21: 224 (1975 publ. 1976)
Bucida subinermis Bisse Feddes Repert. 85: 605 (1974)
Myrobalanus buceras Kuntze Revis. Gen. Pl. 1: 237 (1891)

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Southern America
    • Caribbean
      • Bahamas
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Turks-caicos Islands
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Western South America
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001296365
Florida Plant Atlas 2793
INPN 636975
KEW urn:lsid:ipni.org:names:171012-1
Open Tree Of Life 662525
NCBI Taxonomy 578533
Nature Serve 2.132363
IPNI 171012-1
iNaturalist 867073
GBIF 3698958
EOL 582721
USDA GRIN 462580
Wikipedia Terminalia_buceras

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
Bioprospecting of Helichrysum Species: Chemical Profile, Phytochemical Properties, and Antifungal Efficacy against Botrytis cinerea Matrose NA, Belay ZA, Obikeze K, Mokwena L, Caleb OJ Plants (Basel) 22-Dec-2022
PMCID:PMC9824591
doi:10.3390/plants12010058
PMID:36616185
Present scenarios and future prospects of herbal nanomedicine for antifungal therapy Yadav R, Pradhan M, Yadav K, Mahalvar A, Yadav H J Drug Deliv Sci Technol 13-May-2022
PMCID:PMC9101776
doi:10.1016/j.jddst.2022.103430
PMID:35582019
Lactiplantibacillus plantarum-Derived Biosurfactant Attenuates Quorum Sensing-Mediated Virulence and Biofilm Formation in Pseudomonas aeruginosa and Chromobacterium violaceum Patel M, Siddiqui AJ, Ashraf SA, Surti M, Awadelkareem AM, Snoussi M, Hamadou WS, Bardakci F, Jamal A, Jahan S, Sachidanandan M, Adnan M Microorganisms 13-May-2022
PMCID:PMC9145448
doi:10.3390/microorganisms10051026
PMID:35630468
Discovering the Potential of Natural Antioxidants in Age-Related Macular Degeneration: A Review Wong KH, Nam HY, Lew SY, Naidu M, David P, Kamalden TA, Hadie SN, Lim LW Pharmaceuticals (Basel) 14-Jan-2022
PMCID:PMC8777838
doi:10.3390/ph15010101
PMID:35056157
Comparison of Phytochemical Contents, Antioxidant and Antibacterial Activities of Various Solvent Extracts Obtained from ‘Maluma’ Avocado Pulp Powder Nguyen TV, Nguyen QD, Nguyen NN, Nguyen TT Molecules 20-Dec-2021
PMCID:PMC8709390
doi:10.3390/molecules26247693
PMID:34946774
Pest categorisation of Retithrips syriacus Bragard C, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Gregoire J, Malumphy C, Czwienczek E, Kertesz V, Maiorano A, MacLeod A EFSA J 08-Nov-2021
PMCID:PMC8573539
doi:10.2903/j.efsa.2021.6888
PMID:34765032
Natural Products from Medicinal Plants against Phytopathogenic Fusarium Species: Current Research Endeavours, Challenges and Prospects Seepe HA, Nxumalo W, Amoo SO Molecules 29-Oct-2021
PMCID:PMC8587185
doi:10.3390/molecules26216539
PMID:34770948
A Review on Antifungal Efficiency of Plant Extracts Entrenched Polysaccharide-Based Nanohydrogels Kaur N, Bains A, Kaushik R, Dhull SB, Melinda F, Chawla P Nutrients 15-Jun-2021
PMCID:PMC8232670
doi:10.3390/nu13062055
PMID:34203999
The Structure and Composition of Puerto Rico’s Urban Mangroves Branoff BL, Martinuzzi S Forests 21-Oct-2020
PMCID:PMC7751619
doi:10.3390/f11101119
PMID:33365113
Structured Pointcloud Segmentation for Individual Mangrove Tree Modeling Silván-Cárdenas JL, Gallardo-Cruz JA, Hernández-Huerta LM Pattern Recognition 29-Apr-2020
PMCID:PMC7297589
doi:10.1007/978-3-030-49076-8_17
Polyphenols from Salix tetrasperma Impair Virulence and Inhibit Quorum Sensing of Pseudomonas aeruginosa Mostafa I, Abbas HA, Ashour ML, Yasri A, El-Shazly AM, Wink M, Sobeh M Molecules 16-Mar-2020
PMCID:PMC7146421
doi:10.3390/molecules25061341
PMID:32187997
Raman Spectroscopy and Chemometric Modeling to Predict Physical-Chemical Honey Properties from Campeche, Mexico Anguebes-Franseschi F, Abatal M, Pat L, Flores A, Córdova Quiroz AV, Ramírez-Elias MA, San Pedro L, May Tzuc O, Bassam A Molecules 13-Nov-2019
PMCID:PMC6891675
doi:10.3390/molecules24224091
PMID:31766131
Leveraging phytochemicals: the plant phylogeny predicts sources of novel antibacterial compounds Prasad MA, Zolnik CP, Molina J Future Sci OA 25-Jul-2019
PMCID:PMC6695524
doi:10.2144/fsoa-2018-0124
PMID:31428453
Perceptions of the local beekeepers on the diversity and flowering phenology of the melliferous flora in the community of Xmabén, Hopelchén, Campeche, Mexico Coh-Martínez ME, Cetzal-Ix W, Martínez-Puc JF, Basu SK, Noguera-Savelli E, Cuevas MJ J Ethnobiol Ethnomed 08-Mar-2019
PMCID:PMC6408807
doi:10.1186/s13002-019-0296-1
PMID:30849998
Antifungal, anti-oxidant activity and cytotoxicity of South African medicinal plants against mycotoxigenic fungi Mongalo NI, Dikhoba PM, Soyingbe SO, Makhafola TJ Heliyon 29-Nov-2018
PMCID:PMC6275167
doi:10.1016/j.heliyon.2018.e00973
PMID:30761368

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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(7S,8S)-5,7-dihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-8-phenyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163033566 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=CC=C4)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1021/NP0203483
3-Methoxyminimiflorin 10433154 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)OC)C4=CC=CC=C4O)O)C=CC(O2)(C)C)C 436.50 unknown https://doi.org/10.1021/NP0203483
5-Hydroxy-8-(2-hydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 21721830 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=CC=C4O)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1021/NP0203483
5-Hydroxy-8-(2-hydroxyphenyl)-7-methoxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 85141570 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)OC)C4=CC=CC=C4O)O)C=CC(O2)(C)C)C 436.50 unknown https://doi.org/10.1021/NP0203483
5,7-Dihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-8-phenyl-7,8-dihydropyrano[3,2-g]chromen-6-one 53484196 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=CC=C4)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1021/NP0203483
5,7-Dihydroxy-8-(2-hydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 22297582 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=CC=C4O)O)C=CC(O2)(C)C)C 422.50 unknown https://doi.org/10.1021/NP0203483
Jayacanol 637111 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=CC=C4O)O)C=CC(O2)(C)C)C 422.50 unknown https://doi.org/10.1021/NP0203483
Minimiflorin 180733 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=CC=C4O)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1021/NP0203483
Mundulinol 10363971 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=CC=C4)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1021/NP0203483
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(7R,8R)-5-hydroxy-8-(2-hydroxyphenyl)-7-methoxy-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 11089909 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3=O)OC)C4=CC=CC=C4O)O)C 368.40 unknown https://doi.org/10.1021/NP0203483
5-Hydroxy-8-(2-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 10936669 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(CC3=O)C4=CC=CC=C4O)O)C 338.40 unknown https://doi.org/10.1021/NP0203483
5-Hydroxy-8-(2-hydroxyphenyl)-7-methoxy-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 85394946 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3=O)OC)C4=CC=CC=C4O)O)C 368.40 unknown https://doi.org/10.1021/NP0203483
Buceracidin B 44584124 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(CC3=O)C4=CC=CC=C4O)O)C 338.40 unknown https://doi.org/10.1021/NP0203483

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Collections Top

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