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Trichilia elegans

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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 UUID643ffea9c16f5998136466
Scientific name Trichilia elegans
Authority A.Juss.
First published in Fl. Bras. Merid. 2: 79 (1829)

Description Top

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Synonyms Top

Scientific name Authority First published in
Trichilia graciliflora Harms Nat. Pflanzenfam. [Engler & Prantl] 3, Abt. 4: 304, fig. 164. 1896 Engl. Bot. Jahrb. 30, Beibl. 67: 33. 1901. Argentina
Trichilia hirsuta C.DC. Fl. Bras. 11(1): 221 (1878)
Trichilia hassleri C.DC. Bull. Herb. Boissier , sér. 2, 3: 410 (1903)
Trichilia warmingii C.DC. Fl. Bras. 11(1): 220 (1878)
Trichilia warmingii var. macrophylla C.DC. Fl. Bras. 11(1): 221 (1878)
Trichilia elegans var. latifoliola C.DC. Monogr. Phan. 1: 680 (1878)
Heynichia malleoides Kunth Index Seminum (B, Berolinensis) 1844: 8 (1844)
Trichilia alba C.DC. Bull. Herb. Boissier , sér. 2, 3: 411 (1903)
Trichilia guayaquilensis C.DC. Monogr. Phan. 1: 682 (1878)
Trichilia subarborescens C.DC. Repert. Spec. Nov. Regni Veg. 7: 58 (1909)
Trichilia validinervia Harms in Pilg. Notizbl. Bot. Gart. Berlin-Dahlem 11: 785 (1933)
Moschoxylum viride Rusby Mem. Torrey Bot. Club 6: 18 (1896)
Trichilia weberbaueri C.DC. Repert. Spec. Nov. Regni Veg. 19: 55. 1923
Moschoxylum elegans A.Juss. Mém. Mus. Hist. Nat. 19: 239 (1830 publ. 1831)
Odontandra elegans Triana & Planch. Ann. Sci. Nat., Bot. , sér. 5, 15: 376 (1872)
Trichilia guayaquilensis var. candollei Kuntze Revis. Gen. Pl. 3(2): 36 (1898)
Odontosiphon elegans M.Roem. Fam. Nat. Syn. Monogr. 1: 106 (1846)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Trichilia elegans subsp. richardiana (A.Juss.) T.D.Penn. Fl. Neotrop. Monogr. 28: 88 (1981)

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Northern South America
      • Guyana
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000455435
Tropicos 20400600
KEW urn:lsid:ipni.org:names:579413-1
The Plant List kew-2514938
Open Tree Of Life 5747803
NCBI Taxonomy 879919
IUCN Red List 122658361
IPNI 579413-1
iNaturalist 809219
GBIF 7271353
USDA GRIN 40067

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
Essential Oils of Aromatic Plant Species from the Atlantic Rainforest Exhibit Extensive Chemical Diversity and Antimicrobial Activity Perigo CV, Haber LL, Facanali R, Vieira MA, Torres RB, Bernacci LC, Guimarães EF, Baitello JB, Sobral ME, Quecini V, Marques MO Antibiotics (Basel) 19-Dec-2022
PMCID:PMC9774909
doi:10.3390/antibiotics11121844
PMID:36551501
Insecticidal Activities and GC-MS Analysis of the Selected Family Members of Meliaceae Used Traditionally as Insecticides Shilaluke KC, Moteetee AN Plants (Basel) 10-Nov-2022
PMCID:PMC9698003
doi:10.3390/plants11223046
PMID:36432774
Diversity and antibacterial activity of endophytic bacteria associated with medicinal plant, Scrophularia striata Tavarideh F, Pourahmad F, Nemati M Vet Res Forum 15-Sep-2022
PMCID:PMC9548236
doi:10.30466/vrf.2021.529714.3174
PMID:36320307
Endophytic Diaporthe Associated with Morinda officinalis in China Luo M, Guo W, Zhao M, Manawasinghe IS, Guarnaccia V, Liu J, Hyde KD, Dong Z, You C J Fungi (Basel) 29-Jul-2022
PMCID:PMC9410054
doi:10.3390/jof8080806
PMID:36012794
Prototyping a Knowledge-Based System to Identify Botanical Extracts for Plant Health in Sub-Saharan Africa Silvie PJ, Martin P, Huchard M, Keip P, Gutierrez A, Sarter S Plants (Basel) 29-Apr-2021
PMCID:PMC8146496
doi:10.3390/plants10050896
PMID:33946682
Fungal Endophytes as Efficient Sources of Plant-Derived Bioactive Compounds and Their Prospective Applications in Natural Product Drug Discovery: Insights, Avenues, and Challenges Singh A, Singh DK, Kharwar RN, White JF, Gond SK Microorganisms 19-Jan-2021
PMCID:PMC7833388
doi:10.3390/microorganisms9010197
PMID:33477910
Diverging functional strategies but high sensitivity to an extreme drought in tropical dry forests González‐M. R, Posada JM, Carmona CP, Garzón F, Salinas V, Idárraga‐Piedrahita Á, Pizano C, Avella A, López‐Camacho R, Norden N, Nieto J, Medina SP, Rodríguez‐M. GM, Franke‐Ante R, Torres AM, Jurado R, Cuadros H, Castaño‐Naranjo A, García H, Salgado‐Negret B Ecol Lett 14-Dec-2020
PMCID:PMC9292319
doi:10.1111/ele.13659
PMID:33316132
Comparison of specific endophytic bacterial communities in different developmental stages of Passiflora incarnata using culture‐dependent and culture‐independent analysis Goulart MC, Cueva‐Yesquén LG, Hidalgo Martinez KJ, Attili‐Angelis D, Fantinatti‐Garboggini F Microbiologyopen 27-Aug-2019
PMCID:PMC6813437
doi:10.1002/mbo3.896
PMID:31454177
Diversity of endophytic mycobiota of tropical tree Tectona grandis Linn.f.: Spatiotemporal and tissue type effects Singh DK, Sharma VK, Kumar J, Mishra A, Verma SK, Sieber TN, Kharwar RN Sci Rep 16-Jun-2017
PMCID:PMC5473821
doi:10.1038/s41598-017-03933-0
PMID:28623306
Endophytic Actinobacteria and the Interaction of Micromonospora and Nitrogen Fixing Plants Trujillo ME, Riesco R, Benito P, Carro L Front Microbiol 01-Dec-2015
PMCID:PMC4664631
doi:10.3389/fmicb.2015.01341
PMID:26648923
Effects of growth stage and fulvic acid on the diversity and dynamics of endophytic bacterial community in Stevia rebaudiana Bertoni leaves Yu X, Yang J, Wang E, Li B, Yuan H Front Microbiol 25-Aug-2015
PMCID:PMC4548236
doi:10.3389/fmicb.2015.00867
PMID:26379644
To move or to evolve: contrasting patterns of intercontinental connectivity and climatic niche evolution in “Terebinthaceae” (Anacardiaceae and Burseraceae) Weeks A, Zapata F, Pell SK, Daly DC, Mitchell JD, Fine PV Front Genet 28-Nov-2014
PMCID:PMC4247111
doi:10.3389/fgene.2014.00409
PMID:25506354
Complement Activation and Inhibition in Wound Healing Cazander G, Jukema GN, Nibbering PH Clin Dev Immunol 30-Dec-2012
PMCID:PMC3546472
doi:10.1155/2012/534291
PMID:23346185
Checklist of vascular plants of the Department of Ñeembucú, Paraguay Egea JD, Peña-Chocarro M, Espada C, Knapp S PhytoKeys 30-Jan-2012
PMCID:PMC3281576
doi:10.3897/phytokeys.9.2279
PMID:22371688
Constituintes químicos e atividade inseticida dos extratos de frutos de Trichilia elegans E T. catigua (Meliaceae) Andréia Pereira Matos, Liliane Nebo, Paulo Cezar Vieira, João Batista Fernandes, Maria Fátima das Graças Fernandes d Silva, Ricardo Ribeiro Rodrigues FapUNIFESP (SciELO) 24-Sep-2009
doi:10.1590/S0100-40422009000600037

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 / Sesquiterpenoids
methyl (3S)-3-[(3S,3aS,5aR,6S,7S,9R,9aR)-9-acetyloxy-3-[(3S,5R,6S)-5-hydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-3a,6,9a-trimethyl-7-prop-1-en-2-yl-2,3,4,5,5a,7,8,9-octahydrocyclopenta[a]naphthalen-6-yl]-3-acetyloxypropanoate 162904005 Click to see CC(=C)C1CC(C2(C(C1(C)C(CC(=O)OC)OC(=O)C)CCC3(C2=CCC3C4CC(C(OC4)C(C)(C)O)O)C)C)OC(=O)C 618.80 unknown https://doi.org/10.1016/0031-9422(96)00141-0
methyl (3S)-3-[(3S,3aS,5aR,6S,7S,9R,9aR)-9-acetyloxy-3-[(3S,5R,6S)-5,6-dihydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-3a,6,9a-trimethyl-7-prop-1-en-2-yl-2,3,4,5,5a,7,8,9-octahydrocyclopenta[a]naphthalen-6-yl]-3-acetyloxypropanoate 163051427 Click to see CC(=C)C1CC(C2(C(C1(C)C(CC(=O)OC)OC(=O)C)CCC3(C2=CCC3C4CC(C(OC4)(C(C)(C)O)O)O)C)C)OC(=O)C 634.80 unknown https://doi.org/10.1016/0031-9422(96)00141-0
methyl (3S)-3-[(3S,3aS,5aR,6S,7S,9R,9aR)-9-acetyloxy-3-[(3S,5R,6S)-5,6-dihydroxy-7,7-dimethyloxepan-3-yl]-3a,6,9a-trimethyl-7-prop-1-en-2-yl-2,3,4,5,5a,7,8,9-octahydrocyclopenta[a]naphthalen-6-yl]-3-acetyloxypropanoate 162911179 Click to see CC(=C)C1CC(C2(C(C1(C)C(CC(=O)OC)OC(=O)C)CCC3(C2=CCC3C4CC(C(C(OC4)(C)C)O)O)C)C)OC(=O)C 618.80 unknown https://doi.org/10.1016/0031-9422(96)00141-0
Methyl 3-acetyloxy-3-[9-acetyloxy-3-(5,6-dihydroxy-7,7-dimethyloxepan-3-yl)-3a,6,9a-trimethyl-7-prop-1-en-2-yl-2,3,4,5,5a,7,8,9-octahydrocyclopenta[a]naphthalen-6-yl]propanoate 162911178 Click to see CC(=C)C1CC(C2(C(C1(C)C(CC(=O)OC)OC(=O)C)CCC3(C2=CCC3C4CC(C(C(OC4)(C)C)O)O)C)C)OC(=O)C 618.80 unknown https://doi.org/10.1016/0031-9422(96)00141-0
Methyl 3-acetyloxy-3-[9-acetyloxy-3-[5-hydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-3a,6,9a-trimethyl-7-prop-1-en-2-yl-2,3,4,5,5a,7,8,9-octahydrocyclopenta[a]naphthalen-6-yl]propanoate 162904004 Click to see CC(=C)C1CC(C2(C(C1(C)C(CC(=O)OC)OC(=O)C)CCC3(C2=CCC3C4CC(C(OC4)C(C)(C)O)O)C)C)OC(=O)C 618.80 unknown https://doi.org/10.1016/0031-9422(96)00141-0
Methyl 3-acetyloxy-3-[9-acetyloxy-3-[5,6-dihydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-3a,6,9a-trimethyl-7-prop-1-en-2-yl-2,3,4,5,5a,7,8,9-octahydrocyclopenta[a]naphthalen-6-yl]propanoate 163051426 Click to see CC(=C)C1CC(C2(C(C1(C)C(CC(=O)OC)OC(=O)C)CCC3(C2=CCC3C4CC(C(OC4)(C(C)(C)O)O)O)C)C)OC(=O)C 634.80 unknown https://doi.org/10.1016/0031-9422(96)00141-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1R,2R,4S,7S,8S,10S,12R)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,15,20-trioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-10-yl] acetate 163029377 Click to see CC(=O)OC1CC2(C(OC(=O)C3C2(O3)C4(C1C5(C=CC(=O)OC(C5CC4=O)(C)C)C)C)C6=COC=C6)C 512.50 unknown https://doi.org/10.1590/S0100-40422009000600037
[(1S,2R,4S,7R,8S,11R,12R,18R,20S)-7-[(2R)-2-acetyloxy-5-oxo-2H-furan-3-yl]-1,8,12,17,17-pentamethyl-5,15-dioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-20-yl] acetate 101716795 Click to see CC(=O)OC1CC2C(OC(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=CC(=O)OC6OC(=O)C)C)C)(C)C 572.60 unknown https://doi.org/10.1016/S0031-9422(00)00287-9
[(1S,2R,4S,7R,8S,11R,12R,18R,20S)-7-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-1,8,12,17,17-pentamethyl-5,15-dioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-20-yl] acetate 637835 Click to see CC(=O)OC1CC2C(OC(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=CC(=O)OC6O)C)C)(C)C 530.60 unknown https://doi.org/10.1016/S0031-9422(00)00287-9
[(1S,2R,4S,7R,8S,11R,12R,18R,20S)-7-[(2R)-2-hydroxy-5-oxo-2H-furan-4-yl]-1,8,12,17,17-pentamethyl-5,15-dioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-20-yl] acetate 162948147 Click to see CC(=O)OC1CC2C(OC(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=CC(OC6=O)O)C)C)(C)C 530.60 unknown https://doi.org/10.1016/S0031-9422(00)00287-9
[(1S,2R,4S,7R,8S,11R,12R,18R,20S)-7-[(2S)-2-acetyloxy-5-oxo-2H-furan-3-yl]-1,8,12,17,17-pentamethyl-5,15-dioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-20-yl] acetate 101716794 Click to see CC(=O)OC1CC2C(OC(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=CC(=O)OC6OC(=O)C)C)C)(C)C 572.60 unknown https://doi.org/10.1016/S0031-9422(00)00287-9
[(1S,2R,4S,7R,8S,11R,12R,18R,20S)-7-[(2S)-2-acetyloxy-5-oxo-2H-furan-4-yl]-1,8,12,17,17-pentamethyl-5,15-dioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-20-yl] acetate 163186761 Click to see CC(=O)OC1CC2C(OC(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=CC(OC6=O)OC(=O)C)C)C)(C)C 572.60 unknown https://doi.org/10.1016/S0031-9422(00)00287-9
[7-(2-acetyloxy-5-oxo-2H-furan-3-yl)-1,8,12,17,17-pentamethyl-5,15-dioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-20-yl] acetate 162954919 Click to see CC(=O)OC1CC2C(OC(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=CC(=O)OC6OC(=O)C)C)C)(C)C 572.60 unknown https://doi.org/10.1016/S0031-9422(00)00287-9
[7-(2-acetyloxy-5-oxo-2H-furan-4-yl)-1,8,12,17,17-pentamethyl-5,15-dioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-20-yl] acetate 162991687 Click to see CC(=O)OC1CC2C(OC(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=CC(OC6=O)OC(=O)C)C)C)(C)C 572.60 unknown https://doi.org/10.1016/S0031-9422(00)00287-9
[7-(2-hydroxy-5-oxo-2H-furan-3-yl)-1,8,12,17,17-pentamethyl-5,15-dioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-20-yl] acetate 78200767 Click to see CC(=O)OC1CC2C(OC(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=CC(=O)OC6O)C)C)(C)C 530.60 unknown https://doi.org/10.1016/S0031-9422(00)00287-9
[7-(2-hydroxy-5-oxo-2H-furan-4-yl)-1,8,12,17,17-pentamethyl-5,15-dioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-20-yl] acetate 162948145 Click to see CC(=O)OC1CC2C(OC(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=CC(OC6=O)O)C)C)(C)C 530.60 unknown https://doi.org/10.1016/S0031-9422(00)00287-9
[7-(Furan-3-yl)-1,8,12,17,17-pentamethyl-5,15,20-trioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-en-10-yl] acetate 163029376 Click to see CC(=O)OC1CC2(C(OC(=O)C3C2(O3)C4(C1C5(C=CC(=O)OC(C5CC4=O)(C)C)C)C)C6=COC=C6)C 512.50 unknown https://doi.org/10.1590/S0100-40422009000600037
Kihadanin A 180311 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=CC(=O)OC6O)C)C)C 486.50 unknown https://doi.org/10.1016/S0031-9422(96)00737-6
Kihadanin B 156766 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=CC(OC6=O)O)C)C)C 486.50 unknown https://doi.org/10.1016/S0031-9422(96)00737-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/S0031-9422(96)00737-6
Sitogluside 5742590 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/10.1016/S0031-9422(96)00737-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
methyl 2-[(3R,4R)-4-[(1aS,4R,4aS,6S,7R,8aS)-6-acetyloxy-4-(2-hydroxy-5-oxo-2H-furan-3-yl)-4a-methyl-8-methylidene-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromen-7-yl]-2,2,4-trimethyl-7-oxo-3H-oxepin-3-yl]acetate 101701625 Click to see CC(=O)OC1CC2(C(OC(=O)C3C2(O3)C(=C)C1C4(C=CC(=O)OC(C4CC(=O)OC)(C)C)C)C5=CC(=O)OC5O)C 574.60 unknown https://doi.org/10.1016/S0031-9422(96)00737-6
methyl 2-[(3R,4R)-4-[(1aS,4R,4aS,6S,7R,8aS)-6-acetyloxy-4-(2-hydroxy-5-oxo-2H-furan-4-yl)-4a-methyl-8-methylidene-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromen-7-yl]-2,2,4-trimethyl-7-oxo-3H-oxepin-3-yl]acetate 101701624 Click to see CC(=O)OC1CC2(C(OC(=O)C3C2(O3)C(=C)C1C4(C=CC(=O)OC(C4CC(=O)OC)(C)C)C)C5=CC(OC5=O)O)C 574.60 unknown https://doi.org/10.1016/S0031-9422(96)00737-6

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