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Ouratea semiserrata

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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 UUID644049b73b378300087660
Scientific name Ouratea semiserrata
Authority Engl.
First published in Fl. Bras. 12(2): 323 (1876)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ochna semiserrata Kuntze Revis. Gen. Pl. 1: 106 (1891)
Trichouratea caulipila Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 16: 234 (1902)
Camptouratea persistens Tiegh. Bull. Mus. Hist. Nat. (Paris) 8: 375 (1902)
Camptouratea semiserrata Tiegh. J. Bot. (Morot) 16: 192 (1902)
Gomphia persistens A.St.-Hil. Fl. Bras. Merid. 1: 62 (1825)
Gomphia semiserrata Mart. & Nees Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 12: 41 (1824)
Ouratea semiserrata var. persistens (A.St.-Hil.) Engl. in Mart.

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001087021
Tropicos 22800145
KEW urn:lsid:ipni.org:names:607204-1
The Plant List tro-22800145
Open Tree Of Life 5750828
NCBI Taxonomy 2699671
IUCN Red List 148752804
IPNI 607204-1
GBIF 7326844

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
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 Review on the Phytochemistry, Pharmacology, and Pharmacokinetics of Amentoflavone, a Naturally-Occurring Biflavonoid Yu S, Yan H, Zhang L, Shan M, Chen P, Ding A, Li SF Molecules 16-Feb-2017
PMCID:PMC6155574
doi:10.3390/molecules22020299
PMID:28212342
Anti-Inflammatory Activity of Natural Products Azab A, Nassar A, Azab AN Molecules 01-Oct-2016
PMCID:PMC6274146
doi:10.3390/molecules21101321
PMID:27706084
Novel Trichloro-and Tetrachloroisoflavone Isolated from Ouratea Semiserrta Javier R. Velandia, Mario G. De Carvalho, Raimundo Braz-filho Informa UK Limited 07-Jul-2007
doi:10.1080/10575639808048290
Biflavonoids and a glucopyranoside derivative from Ouratea semiserrata. Velandia JR, de Carvalho MG, Braz-Filho R, Werle AA Phytochem Anal 01-Sep-2002
doi:10.1002/PCA.656
PMID:12918874
DNA topoisomerase inhibitors: biflavonoids from Ouratea species. Grynberg NF, Carvalho MG, Velandia JR, Oliveira MC, Moreira IC, Braz-Filho R, Echevarria A Braz J Med Biol Res 01-Jul-2002
doi:10.1590/S0100-879X2002000700009
PMID:12131922

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
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Epieudesmin 7299790 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1002/PCA.656
(3aS,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 137795855 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1002/PCA.656
Eudesmin 234823 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1002/PCA.656
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(5R,9S,13S)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 49775756 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1002/PCA.656
Kaurenoic acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1002/PCA.656
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.1002/PCA.656
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/10.1002/PCA.656
> 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/10.1002/PCA.656
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/10.1002/PCA.656
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/10.1002/PCA.656
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/10.1002/PCA.656
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1002/PCA.656
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
beta-D-glucose 64689 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1002/PCA.656
Grape sugar 79025 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1002/PCA.656
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1590/S0100-879X2002000700009
https://doi.org/10.1002/PCA.656
> Phenylpropanoids and polyketides / Flavonoids / Flavones
8-[4-(4-Oxo-5,7-dihydroxy-4H-1-benzopyran-2-yl)phenoxy]-5,7,4'-trihydroxyflavone 11272651 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 538.50 unknown https://doi.org/10.1002/PCA.656
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1002/PCA.656
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,7-Dihydroxy-8-[4-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]-2-(4-hydroxyphenyl)chromen-4-one 163104549 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)OC4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O 552.50 unknown https://doi.org/10.1002/PCA.656
5,7-Dihydroxy-8-[4-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]-2-(4-methoxyphenyl)chromen-4-one 162861760 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O 566.50 unknown https://doi.org/10.1002/PCA.656
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
6,8-Dichloro-3-(3-chloro-4-hydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one 100927216 Click to see COC1=C(C(=C2C(=C1Cl)OC=C(C2=O)C3=CC(=C(C=C3)O)Cl)O)Cl 387.60 unknown https://doi.org/10.1080/10575639808048290
6,8-Dichloro-3-(3,5-dichloro-4-hydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one 100927217 Click to see COC1=C(C(=C2C(=C1Cl)OC=C(C2=O)C3=CC(=C(C(=C3)Cl)O)Cl)O)Cl 422.00 unknown https://doi.org/10.1080/10575639808048290

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