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Simarouba versicolor

Simarouba versicolor - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Simarouba versicolor - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Simarouba versicolor - 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 UUID6440569c9e1cc535380947
Scientific name Simarouba versicolor
Authority A.St.-Hil.
First published in Pl. Usuel. Bras. : t. 5 (1824)

Description Top

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Synonyms Top

Scientific name Authority First published in
Simarouba antisyphilitica Mart. ex Engl. Fl. Bras. 12(2): 225 (1874)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001251841
Tropicos 50162808
KEW urn:lsid:ipni.org:names:814137-1
The Plant List tro-50162808
Open Tree Of Life 1010320
NCBI Taxonomy 459157
IUCN Red List 158178840
IPNI 814137-1
iNaturalist 884622
GBIF 7329580

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
Carbon Storage in Different Compartments in Eucalyptus Stands and Native Cerrado Vegetation Ribeiro FP, Gatto A, de Oliveira AD, Pulrolnik K, Valadão MB, Araújo JB, de Carvalho AM, Ferreira EA Plants (Basel) 24-Jul-2023
PMCID:PMC10386474
doi:10.3390/plants12142751
PMID:37514365
Anatomical traits related to leaf and branch hydraulic functioning on Amazonian savanna plants Simioni PF, Emilio T, Giles AL, Viana de Freitas G, Silva Oliveira R, Setime L, Pierre Vitoria A, Pireda S, Vieira da Silva I, Da Cunha M AoB Plants 24-Apr-2023
PMCID:PMC10198777
doi:10.1093/aobpla/plad018
PMID:37214224
Plants causing poisoning outbreaks of livestock in South America: A review Riet-Correa F, Machado M, Micheloud JF Toxicon X 21-Jan-2023
PMCID:PMC9898795
doi:10.1016/j.toxcx.2023.100150
PMID:36747993
Kaempferol: Antimicrobial Properties, Sources, Clinical, and Traditional Applications Periferakis A, Periferakis K, Badarau IA, Petran EM, Popa DC, Caruntu A, Costache RS, Scheau C, Caruntu C, Costache DO Int J Mol Sci 30-Nov-2022
PMCID:PMC9740324
doi:10.3390/ijms232315054
PMID:36499380
Toxic Potential of Cerrado Plants on Different Organisms Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF Int J Mol Sci 22-Mar-2022
PMCID:PMC8998518
doi:10.3390/ijms23073413
PMID:35408775
A Molecular Networking Strategy: High-Throughput Screening and Chemical Analysis of Brazilian Cerrado Plant Extracts against Cancer Cells Cortelo PC, Demarque DP, Dusi RG, Albernaz LC, Braz-Filho R, Goncharova EI, Bokesch HR, Gustafson KR, Beutler JA, Espindola LS Cells 20-Mar-2021
PMCID:PMC8004027
doi:10.3390/cells10030691
PMID:33804755
Archaea diversity in vegetation gradients from the Brazilian Cerrado Araujo AS, Mendes LW, Bezerra WM, Nunes LA, Lyra MD, Figueiredo MD, Melo VM Braz J Microbiol 11-Feb-2018
PMCID:PMC6066726
doi:10.1016/j.bjm.2017.08.010
PMID:29459210
Antimicrobial activity of some medicinal plants from the cerrado of the centralwestern region of Brazil Violante IM, Hamerski L, Garcez WS, Batista AL, Chang MR, Pott VJ, Garcez FR Braz J Microbiol 01-Jun-2012
PMCID:PMC3769025
doi:10.1590/S1517-83822012000400009
PMID:24031956
Ethnopharmacology of Medicinal Plants of the Pantanal Region (Mato Grosso, Brazil) Bieski IG, Rios Santos F, de Oliveira RM, Espinosa MM, Macedo M, Albuquerque UP, de Oliveira Martins DT Evid Based Complement Alternat Med 26-Feb-2012
PMCID:PMC3303862
doi:10.1155/2012/272749
PMID:22474496
Chemical constituents of Simarouba versicolor. Arriaga AC, de Mesquita AC, Pouliquen YB, de Lima RA, Cavalcante SH, de Carvalho MG, de Siqueira JA, Alegrio LV, Braz-Filho R An Acad Bras Cienc 01-Sep-2002
doi:10.1590/S0001-37652002000300004
PMID:12378309

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[2-(1,2-Dihydroxyethyl)-5-hydroxy-4-(3,4,5-trihydroxybenzoyl)oxyoxolan-3-yl] 3,4,5-trihydroxybenzoate;[2,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate;[4,5,6-trihydroxy-1-oxo-3-(3,4,5-trihydroxybenzoyl)oxyhexan-2-yl] 3,4,5-trihydroxybenzoate 163192237 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)CO)O.C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC2C(CO)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O.C1=C(C=C(C(=C1O)O)O)C(=O)OC(C=O)C(C(C(CO)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O 1453.10 unknown https://doi.org/10.1590/S0001-37652002000300004
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(8R,9R,10R,14S,17S)-17-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 91884737 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown https://doi.org/10.1590/S0001-37652002000300004
Ocotillone 12313665 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown https://doi.org/10.1590/S0001-37652002000300004
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
[(1S,4R,5R,6R,7S,8R,11R,13S,16S,17S,18S,19R)-4,5,16,17-tetrahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] (2S)-2-acetyloxy-2-methylbutanoate 49866282 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(C=C5C)O)O)C)OC1=O)O)O)C)OC(=O)C 538.60 unknown https://doi.org/10.1590/S0001-37652002000300004
[(1S,4R,5R,6R,7S,8R,11R,13S,17S,18S,19R)-4,5,17-Trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] 2-hydroxy-2-methylbutanoate 12310232 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)O 494.50 unknown https://doi.org/10.1590/S0001-37652002000300004
[(1S,4S,5R,6R,7S,8R,11R,13S,16S,17S,18S,19R)-4,5,16,17-tetrahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] (2S)-2-hydroxy-2-methylbutanoate 90469735 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(C=C5C)O)O)C)OC1=O)O)O)C)O 496.50 unknown https://doi.org/10.1590/S0001-37652002000300004
Amarolide 11-acetate 460540 Click to see CC1CC(C(=O)C2(C1CC3C4(C2C(C(=O)C(C4CC(=O)O3)C)OC(=O)C)C)C)O 406.50 unknown https://doi.org/10.1590/S0001-37652002000300004
Glaucarubinone 441796 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(=O)C=C5C)O)C)OC1=O)O)O)C)O 494.50 unknown https://doi.org/10.1590/S0001-37652002000300004
Simarubaceae 441794 Click to see CCC(C)(C(=O)OC1C2C(C(C3(C4C2(CO3)C(CC5C4(C(C(C=C5C)O)O)C)OC1=O)O)O)C)O 496.50 unknown https://doi.org/10.1590/S0001-37652002000300004
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(5R,9S,10R,13S,14S,17R)-17-[(3S)-5-hydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 129316918 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C5CC(C(OC5)C(C)(C)O)O)C)C)C 472.70 unknown https://doi.org/10.1590/S0001-37652002000300004
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Monohydroxy bile acids, alcohols and derivatives
(3S,6R)-6-[(8R,9S,10S,13R,14S,17R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2,3-dimethylheptan-1-ol 66699452 Click to see CC(CCC(C)C(C)CO)C1CCC2C1(CCC3C2CCC4C3(CCCC4)C)C 402.70 unknown https://doi.org/10.1590/S0001-37652002000300004
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergostanol 5283641 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C 402.70 unknown https://doi.org/10.1590/S0001-37652002000300004
> 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/S0001-37652002000300004
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/S0001-37652002000300004

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