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Eremanthus goyazensis

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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 UUID643fd354a9317746131817
Scientific name Eremanthus goyazensis
Authority Sch.Bip.
First published in Jahresber. Pollichia 18-19: 165 (1861)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eremanthus weddellii Sch.Bip. Jahresber. Pollichia 18-19: 165 (1861)
Albertinia goyazensis Gardner London J. Bot. 6: 425 (1847)
Laxopetalum albidum Pohl Fl. Bras. 6(2): 163 (1873)

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000131042
Tropicos 2705515
KEW urn:lsid:ipni.org:names:203377-1
The Plant List gcc-91921
Open Tree Of Life 5794938
NCBI Taxonomy 1569398
IUCN Red List 189627686
IPNI 203377-1
GBIF 3133665

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
Therapeutic Interventions for Countering Leishmaniasis and Chagas’s Disease: From Traditional Sources to Nanotechnological Systems Souto EB, Dias-Ferreira J, Craveiro SA, Severino P, Sanchez-Lopez E, Garcia ML, Silva AM, Souto SB, Mahant S Pathogens 01-Aug-2019
PMCID:PMC6789685
doi:10.3390/pathogens8030119
PMID:31374930
Potential Anticancer Agents Characterized from Selected Tropical Plants Ren Y, Carcache de Blanco EJ, Fuchs JR, Soejarto DD, Burdette JE, Swanson SM, Kinghorn AD J Nat Prod 04-Mar-2019
PMCID:PMC6441492
doi:10.1021/acs.jnatprod.9b00018
PMID:30830783
Computer-Aided Drug Design Using Sesquiterpene Lactones as Sources of New Structures with Potential Activity against Infectious Neglected Diseases Herrera Acevedo C, Scotti L, Feitosa Alves M, Formiga Melo Diniz MD, Scotti MT Molecules 03-Jan-2017
PMCID:PMC6155652
doi:10.3390/molecules22010079
PMID:28054952
The Role of Natural Products in Drug Discovery and Development against Neglected Tropical Diseases Cheuka PM, Mayoka G, Mutai P, Chibale K Molecules 31-Dec-2016
PMCID:PMC6155950
doi:10.3390/molecules22010058
PMID:28042865
Development of Anticancer Agents from Plant-derived Sesquiterpene Lactones Ren Y, Yu J, Kinghorn AD Curr Med Chem 01-Jan-2016
PMCID:PMC5012922
doi:10.2174/0929867323666160510123255
PMID:27160533
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
In Silico Prediction and Experimental Evaluation of Furanoheliangolide Sesquiterpene Lactones as Potent Agents against Trypanosoma brucei rhodesiense Schmidt TJ, Da Costa FB, Lopes NP, Kaiser M, Brun R Antimicrob Agents Chemother 01-Jan-2014
PMCID:PMC3910805
doi:10.1128/AAC.01263-13
PMID:24165182
Goyazensolide Induces Apoptosis in Cancer Cells in vitro and in vivo. Acuña UM, Shen Q, Ren Y, Lantvit DD, Wittwer JA, Kinghorn AD, Swanson SM, de Blanco EJ Int J Cancer Res 01-Jan-2013
PMCID:PMC4303185
doi:10.3923/ijcr.2013.36.53
PMID:25621077
Eregoyazin and eregoyazidin, two new guaianolides from Eremanthus goyazensis Walter Vichnewski, F. Welbaneide, L. Machado, Jaime A. Rabi, Ramaswamy Murari, Werner Herz American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/JO00444A025
Sesquiterpene lactones and other constituents from Eremanthus seidelii, E. Goyazensis and Vanillosmopsis erythropappa Walter Vichnewski, Angela Mayumi Takahashi, Ana Maria Tucciturco Nasi, Dionéia Camilo Rodrigues, Gomes Goncalves, Diones Aparecida Dias, José Norberto Callegari Lopes, Virgil L. Goedken, Alicia B. Gutiérrez, Werner Herz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97763-X
Goyazensolide, a schistosomicidal heliangolide from Eremanthus goyazensis Walter Vichnewski, Silvio José Sarti, Benjamin Gilbert, Werner Herz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89082-2

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 / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(1R,3R,7R,8S,9Z)-10-(hydroxymethyl)-1-methyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl] 2-methylprop-2-enoate 162951406 Click to see CC(=C)C(=O)OC1C=C(C2=CC(=O)C(O2)(CC3C1C(=C)C(=O)O3)C)CO 360.40 unknown https://doi.org/10.1016/S0031-9422(00)89082-2
[10-(Hydroxymethyl)-1-methyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl] 2-methylprop-2-enoate 3478762 Click to see CC(=C)C(=O)OC1C=C(C2=CC(=O)C(O2)(CC3C1C(=C)C(=O)O3)C)CO 360.40 unknown https://doi.org/10.1016/S0031-9422(00)97763-X
https://doi.org/10.1016/S0031-9422(00)89082-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aS,6aR,9S,9aR,9bR)-6,9-dimethyl-3-methylidene-4,6a,7,9,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-2,8-dione 21587530 Click to see CC1C2C(CC1=O)C(=CCC3C2OC(=O)C3=C)C 246.30 unknown https://doi.org/10.1021/JO00444A025
(3S,3aS,6aR,9S,9aR,9bS)-3,6,9-trimethyl-3,3a,4,6a,7,9,9a,9b-octahydroazuleno[4,5-b]furan-2,8-dione 21587531 Click to see CC1C2CC=C(C3CC(=O)C(C3C2OC1=O)C)C 248.32 unknown https://doi.org/10.1021/JO00444A025
> Organoheterocyclic compounds / Furofurans
(1S,3R,7Z,12S,13R,15R)-13-hydroxy-3,7,12-trimethyl-13-prop-1-en-2-yl-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadeca-5,7-diene-4,11-dione 163187440 Click to see CC1=CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(=C)C)O 346.40 unknown https://doi.org/10.1021/JO00444A025
(1S,3R,7Z,9S,12S,13R,15R)-13-hydroxy-3,7,12-trimethyl-13-prop-1-en-2-yl-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadeca-5,7-diene-4,11-dione 163003287 Click to see CC1=CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(=C)C)O 346.40 unknown https://doi.org/10.1021/JO00444A025
(7Z)-13-hydroxy-3,7,12-trimethyl-13-prop-1-en-2-yl-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadeca-5,7-diene-4,11-dione 5841029 Click to see CC1=CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(=C)C)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)97763-X
https://doi.org/10.1021/JO00444A025
Eremantholide C 20835084 Click to see CC1=CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(=C)C)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)97763-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(00)97763-X

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