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Styrax camporum

Styrax camporum - 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 UUID64408279244a0370936423
Scientific name Styrax camporum
Authority Pohl
First published in Pl. Bras. Icon. Descr. 2: 53 (1830)

Description Top

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Synonyms Top

Scientific name Authority First published in
Styrax varians Seub. Fl. Bras. 7: 189 (1868)
Styrax gardnerianus A.DC. Prodr. 8: 263 (1844)
Styrax obliquinervius A.DC. Prodr. 8: 263 (1844)
Strigilia gardneriana Miers Ann. Mag. Nat. Hist. , ser. 3, 3: 282 (1859)
Strigilia obliquinervia Miers Ann. Mag. Nat. Hist. , ser. 3, 3: 282 (1859)
Strigilia chrysastera Miers Ann. Mag. Nat. Hist. , ser. 3, 3: 282 (1859)
Strigilia camporum Miers Ann. Mag. Nat. Hist. , ser. 3, 3: 282 (1859)
Strigilia subcordata Miers Ann. Mag. Nat. Hist. , ser. 3, 3: 282 (1859)
Styrax subcordatus Moric. Pl. Nouv. Amér. : 117 (1844)
Styrax candollei Seub. Fl. Bras. 7: 189 (1868)
Styrax gardnerianus var. ovatifolius Chodat & Hassl. Bull. Herb. Boissier , sér. 2, 3: 913 (1903)
Styrax gardnerianus var. pallidior Chodat & Hassl. Bull. Herb. Boissier , sér. 2, 3: 913 (1903)
Styrax floridus var. communis A.DC. Prodr. 8: 263 (1844)
Styrax camporum f. aureovelutinus Perkins Pflanzenr. (Engler) 4, Fam. 241: 49. 1907
Styrax camporum f. gardnerianus (A.DC.) Perkins Pflanzenr. , IV, 241: 49 (1907)
Styrax camporum f. lanceolatus Perkins Pflanzenr. (Engler) 4, Fam. 241: 49. 1907
Styrax chrysasterus Pohl Pl. Bras. Icon. Descr. 2: 59 (1830)
Styrax chrysasterus var. sellowianus A.DC. Prodr. 8: 264 (1844)

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000492242
Tropicos 30800001
KEW urn:lsid:ipni.org:names:826745-1
The Plant List kew-2580611
Open Tree Of Life 676749
Observations.org 512770
NCBI Taxonomy 153526
IUCN Red List 143270388
IPNI 826745-1
GBIF 7319990
EPPO STXCA
EOL 5240115
Elurikkus 588122
USDA GRIN 101821

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
Chemical Constituents and Their Biological Activities from Genus Styrax Xia DD, Han XY, Zhang Y, Zhang N Pharmaceuticals (Basel) 22-Jul-2023
PMCID:PMC10385552
doi:10.3390/ph16071043
PMID:37513954
Near-Zero Temperatures Arrest Movement of the Diaheliotropic Malva sylvestris Arvaniti E, Levizou E, Kyparissis A Plants (Basel) 29-Jun-2023
PMCID:PMC10346532
doi:10.3390/plants12132484
PMID:37447045
Successful identification of the species of the semipetrified amber medicinal resin benzoin using molecular diagnostic technology Feng J, He Q, Xie A, Liu Y Sci Rep 20-Feb-2023
PMCID:PMC9941088
doi:10.1038/s41598-023-30034-y
PMID:36808137
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
Isolation and acetylcholinesterase inhibitory activity of asterric acid derivatives produced by Talaromyces aurantiacus FL15, an endophytic fungus from Huperzia serrata Xiao Y, Liang W, Liu D, Zhang Z, Chang J, Zhu D 3 Biotech 05-Feb-2022
PMCID:PMC8817963
doi:10.1007/s13205-022-03125-2
PMID:35186657
Saccharification of acid–alkali pretreated sugarcane bagasse using immobilized enzymes from Phomopsis stipata de Almeida SG, de Mello GF, do Santos MG, da Silva DD, Giese EC, Hassanpour M, Zhang Z, Dussán KJ 3 Biotech 06-Jan-2022
PMCID:PMC8738833
doi:10.1007/s13205-021-03101-2
PMID:35070629
Antiparasitic Effects of Selected Isoflavones on Flatworms Faixová D, Hrčková G, Mačák Kubašková T, Mudroňová D Helminthologia 10-Feb-2021
PMCID:PMC7912234
doi:10.2478/helm-2021-0004
PMID:33664614
Nor-Lignans: Occurrence in Plants and Biological Activities—A Review Frezza C, Venditti A, Toniolo C, De Vita D, Franceschin M, Ventrone A, Tomassini L, Foddai S, Guiso M, Nicoletti M, Serafini M, Bianco A Molecules 03-Jan-2020
PMCID:PMC6983269
doi:10.3390/molecules25010197
PMID:31947789
Study of the cytotoxic activity of Styrax camporum extract and its chemical markers, egonol and homoegonol de Oliveira PF, Damasceno JL, Bertanha CS, Araújo AR, Pauletti PM, Tavares DC Cytotechnology 21-Mar-2015
PMCID:PMC4960157
doi:10.1007/s10616-015-9864-y
PMID:25795470
Natural Products as Leads in Schistosome Drug Discovery Neves BJ, Andrade CH, Cravo PV Molecules 23-Jan-2015
PMCID:PMC6272663
doi:10.3390/molecules20021872
PMID:25625682
Endophytic fungi producing of esterases: Evaluation in vitro of the enzymatic activity using pH indicator Lisboa HC, Biasetto CR, de Medeiros JB, Araújo ÂR, Silva DH, Teles HL, Trevisan HC Braz J Microbiol 10-Jan-2014
PMCID:PMC3910213
doi:10.1590/s1517-83822013005000067
PMID:24516461
Anti-Mycobacterium tuberculosis activity of fungus Phomopsis stipata de Prince KA, Sordi R, Pavan FR, Barreto Santos AC, Araujo AR, Leite SR, Leite CQ Braz J Microbiol 01-Jun-2012
PMCID:PMC3769001
doi:10.1590/S1517-838220120001000024
PMID:24031821
Cytotoxic lignans from the stems of Styrax camporum (Styracaceae). Teles HL, Hemerly JP, Paulettit PM, Pandolfi JR, Araujot AR, Valentini SR, Young MC, Bolzani VS, Silva DH Nat Prod Res 01-Jun-2005
doi:10.1080/14786410412331271979
PMID:15938136
Triterpenos de Styrax camporum (styracaceae) Patrícia Mendonça Pauletti, Angela Regina Araújo, Vanderlan da Silva Bolzani, Maria Claudia Marx Young FapUNIFESP (SciELO) 26-Apr-2005
doi:10.1590/S0100-40422002000300002
nor-Lignans from the leaves of Styrax ferrugineus (Styracaceae) with antibacterial and antifungal activity. Pauletti PM, Araújo AR, Young MC, Giesbrecht AM, Bolzani VD Phytochemistry 01-Nov-2000
doi:10.1016/S0031-9422(00)00225-9
PMID:11130670

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
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,6S)-6-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenol 59871518 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1080/14786410412331271979
Syringaresinol 100067 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1080/14786410412331271979
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol 332427 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1590/S0100-40422002000300002
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 15917996 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/S0100-40422002000300002
(1S,2R,4aS,6aS,6bR,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 5316084 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/S0100-40422002000300002
(1S,2R,4aS,6aS,6bR,10S,11S,12aR)-11-hydroxy-10-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 163015347 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O 618.80 unknown https://doi.org/10.1590/S0100-40422002000300002
(1S,2R,6aR,6aS,6bR,8aR,10R,11S,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 163186506 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/S0100-40422002000300002
(1S,2R,6aS,6bR,10S,11S,12aR)-11-hydroxy-10-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 163185121 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O 618.80 unknown https://doi.org/10.1590/S0100-40422002000300002
(4aS,6aS,6bR,10S,11S,12aR)-11-hydroxy-10-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-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 162960051 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1)C)C(=O)O)C 618.80 unknown https://doi.org/10.1590/S0100-40422002000300002
11-hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 72730089 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O 618.80 unknown https://doi.org/10.1590/S0100-40422002000300002
11-Hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-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 75110902 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1)C)C(=O)O)C 618.80 unknown https://doi.org/10.1590/S0100-40422002000300002
2beta-Hydroxyursolic acid 24721200 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/S0100-40422002000300002
Erythrodiol 101761 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1590/S0100-40422002000300002
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/S0100-40422002000300002
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Egonol 485186 Click to see COC1=CC(=CC2=C1OC(=C2)C3=CC4=C(C=C3)OCO4)CCCO 326.30 unknown https://doi.org/10.1016/S0031-9422(00)00225-9
https://doi.org/10.1080/14786410412331271979
Homoegonol 176929 Click to see COC1=C(C=C(C=C1)C2=CC3=C(O2)C(=CC(=C3)CCCO)OC)OC 342.40 unknown https://doi.org/10.1080/14786410412331271979

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