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Terminalia glabrescens

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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 UUID643ff9340c89a821866033
Scientific name Terminalia glabrescens
Authority Mart.
First published in Flora 20(2 Beibl.): 124 (1837)

Description Top

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Synonyms Top

Scientific name Authority First published in
Myrobalanus glabrescens Kuntze Revis. Gen. Pl. 1: 237 (1891)
Myrobalanus cambessedesii Kuntze Revis. Gen. Pl. 1: 237 (1891)
Chuncoa brasiliensis Cambess. Fl. Bras. Merid. 2: 244 (1830)
Chuncoa brasiliensis Cambess. ex A.St.-Hil. Fl. Bras. Merid. (quarto ed.) 2: 176

Common names Top

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Language Common/alternative name
Arabic هليلج أجرد

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000408734
Tropicos 8200089
KEW urn:lsid:ipni.org:names:171135-1
The Plant List kew-2434287
Open Tree Of Life 6120048
Observations.org 288821
NCBI Taxonomy 1924228
IPNI 171135-1
iNaturalist 784372
GBIF 3699114
EOL 5426290
Elurikkus 397962

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
Bark production of generalist and specialist species across savannas and forests in the Cerrado Chiminazzo MA, Bombo AB, Charles-Dominique T, Fidelis A Ann Bot 18-Jan-2023
PMCID:PMC10147323
doi:10.1093/aob/mcad014
PMID:36651635
Role of CCL2/CCR2 axis in the pathogenesis of COVID-19 and possible Treatments: All options on the Table Ranjbar M, Rahimi A, Baghernejadan Z, Ghorbani A, Khorramdelazad H Int Immunopharmacol 14-Oct-2022
PMCID:PMC9561120
doi:10.1016/j.intimp.2022.109325
PMID:36252475
Tree Species and Morphology of Holes Caused by Black-Tufted Marmosets to Obtain Exudates: Some Implications for the Exudativory Lamoglia JM, Boere V, Picoli EA, de Oliveira JA, Silva Neto CD, Silva ID Animals (Basel) 27-Sep-2022
PMCID:PMC9559504
doi:10.3390/ani12192578
PMID:36230319
Brazilian medicinal plants with corroborated anti-inflammatory activities: a review Ribeiro VP, Arruda C, Abd El-Salam M, Bastos JK Pharm Biol 12-Apr-2018
PMCID:PMC6130656
doi:10.1080/13880209.2018.1454480
PMID:29648503
In Vitro TNF-α Inhibitory Activity of Brazilian Plants and Anti-Inflammatory Effect of Stryphnodendron adstringens in an Acute Arthritis Model Henriques BO, Corrêa O, Azevedo EP, Pádua RM, de Oliveira VL, Oliveira TH, Boff D, Dias AC, de Souza DG, Amaral FA, Teixeira MM, Castilho RO, Braga FC Evid Based Complement Alternat Med 27-Oct-2016
PMCID:PMC5102725
doi:10.1155/2016/9872598
PMID:27867403
Tree Diversity and Dynamics of the Forest of Seu Nico, Viçosa, Minas Gerais, Brazil Gastauer M, Leyh W, Meira-Neto JA Biodivers Data J 31-Jul-2015
PMCID:PMC4549651
doi:10.3897/BDJ.3.e5425
PMID:26312053
Evaluation of the Effects of Some Brazilian Medicinal Plants on the Production of TNF-α and CCL2 by THP-1 Cells Gusman GS, Campana PR, Castro LC, Castilho RO, Teixeira MM, Braga FC Evid Based Complement Alternat Med 23-Mar-2015
PMCID:PMC4386292
doi:10.1155/2015/497123
PMID:25878716
Lup-20(29)-en-28-ol-3-one (betulone) Boryczka S, Michalik E, Kusz J, Nowak M, Chrobak E Acta Crystallogr Sect E Struct Rep Online 27-Apr-2013
PMCID:PMC3648317
doi:10.1107/S1600536813011008
PMID:23723937
Chemical constituents from Terminalia glabrescens Fernanda R. Garcez, Walmir S. Garcez, Daniel L. S. Miguel, Alessandro A. T. Serea, Fabiana C. Prado FapUNIFESP (SciELO) 25-Apr-2005
doi:10.1590/S0103-50532003000300021

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 / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1590/S0103-50532003000300021
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1590/S0103-50532003000300021
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1590/S0103-50532003000300021
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6bR,8S,10S,12aR)-8,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 86574170 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1590/S0103-50532003000300021
(4aS,6bR,8R,10S,12aR)-8,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5321562 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Arjunglucoside I 14658050 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 666.80 unknown https://doi.org/10.1590/S0103-50532003000300021
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Asiatic Acid 119034 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Betulone 10411004 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)CO 440.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1590/S0103-50532003000300021
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1590/S0103-50532003000300021
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1590/S0103-50532003000300021
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1590/S0103-50532003000300021
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1590/S0103-50532003000300021
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1590/S0103-50532003000300021

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