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Eremanthus erythropappus

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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
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Details Top

Internal ID UUID643fc603f257d555147199
Scientific name Eremanthus erythropappus
Authority (DC.) MacLeish
First published in Ann. Missouri Bot. Gard. 74(2): 284 (1987): (1987)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vanillosmopsis glomerata Sch.Bip. Jahresber. Pollichia 18-19: 167 (1861)
Vanillosmopsis lanceolata (Vell.) Kuntze Revis. Gen. Pl. 3[3]: 183 (1898)
Albertinia erythropappa DC. Prodr. 5: 82 (1836)
Albertinia incanescens Mart. ex Baker Fl. Bras. (Martius) 6(2): 15. 1873 [1 Jun 1873]
Albertinia claussenii Sch.Bip. ex Baker Fl. Bras. 6(2): 15 (1873)
Vernonia glomerata Sch.Bip. Bot. Zeitung (Berlin) iii. 155 (1845)
Albertinia candolleana Gardner London J. Bot. 5: 235 (1846)
Vanillosmopsis candolleana Sch.Bip. Jahresber. Pollichia 18-19: 168 (1861)
Albertinia incanescens Mart. ex Colla Herb. Pedem. 3: 290 (1834)
Chresta lanceolata Vell. t. 151
Vanillosmopsis erythropappa Sch.Bip. Jahresber. Pollichia 18-19: 167 (1861)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000001796
Tropicos 50159239
KEW urn:lsid:ipni.org:names:944719-1
The Plant List gcc-101735
Open Tree Of Life 1079714
NCBI Taxonomy 434655
IUCN Red List 149213853
IPNI 1127956-2
iNaturalist 627131
GBIF 3133616

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
Antibacterial effects of chitosan-based hydrogels containing Trachyspermum ammi essential oil on pathogens isolated from dogs with otitis externa Niaraki NJ, Jamshidi S, Fasaei BN, Joghataei SM BMC Vet Res 01-Apr-2024
PMCID:PMC10985873
doi:10.1186/s12917-024-03971-7
PMID:38561827
Lipid nanoparticles based on natural matrices with activity against multidrug resistant bacterial species da Silva EF, Bastos LM, Fonseca BB, Ribas RM, Sommerfeld S, Pires HM, dos Santos FA, Ribeiro LN Front Cell Infect Microbiol 09-Jan-2024
PMCID:PMC10803469
doi:10.3389/fcimb.2023.1328519
PMID:38264725
In Vitro Evaluation of Potentially Edible Brazilian Trees and Shrubs in Ruminant Nutrition de Morais JP, Campana M, Gregorini P, Garcia TM, Minussi JF, Pereira SN, Pereira FC, Del Valle TA Animals (Basel) 29-Nov-2023
PMCID:PMC10705355
doi:10.3390/ani13233703
PMID:38067053
Evaluation of the hydroalcoholic extract of Clarisia racemosa as an antiparasitic agent: an in vitro approach da Cruz Filho IJ, Duarte DM, Marques DS, da Rocha JV, Diniz EG, Brayner FA, Alves LC, de Azevedo Albuquerque MC, de Lima Aires A, Nogueira F, de Lima MD 3 Biotech 09-Nov-2023
PMCID:PMC10635994
doi:10.1007/s13205-023-03799-2
PMID:37953832
Chemical Characterization and Chemotaxonomic Significance of Essential Oil Constituents of Matricaria aurea Grown in Two Different Agro-Climatic Conditions Khan M, Khan M, Alshareef E, Alaqeel SI, Alkhathlan HZ Plants (Basel) 12-Oct-2023
PMCID:PMC10610148
doi:10.3390/plants12203553
PMID:37896017
α-Bisabolol, a Dietary Sesquiterpene, Attenuates Doxorubicin-Induced Acute Cardiotoxicity in Rats by Inhibiting Cellular Signaling Pathways, Nrf2/Keap-1/HO-1, Akt/mTOR/GSK-3β, NF-κB/p38/MAPK, and NLRP3 Inflammasomes Regulating Oxidative Stress and Inflammatory Cascades Nagoor Meeran MF, Arunachalam S, Azimullah S, Saraswathiamma D, Albawardi A, Almarzooqi S, Jha NK, Subramanya S, Beiram R, Ojha S Int J Mol Sci 13-Sep-2023
PMCID:PMC10530367
doi:10.3390/ijms241814013
PMID:37762315
A Comprehensive Review on Bioactive Compounds Found in Caesalpinia sappan Vij T, Anil PP, Shams R, Dash KK, Kalsi R, Pandey VK, Harsányi E, Kovács B, Shaikh AM Molecules 25-Aug-2023
PMCID:PMC10488625
doi:10.3390/molecules28176247
PMID:37687076
Engineering Saccharomyces cerevisiae for enhanced (–)-α-bisabolol production Jiang Y, Xia L, Gao S, Li N, Yu S, Zhou J Synth Syst Biotechnol 20-Jan-2023
PMCID:PMC9941373
doi:10.1016/j.synbio.2023.01.004
PMID:36824492
Volatile Oils Discrepancy between Male and Female Ochradenus arabicus and Their Allelopathic Activity on Dactyloctenium aegyptium Abd-ElGawad AM, Assaeed AM, El Gendy AE, Dar BA, Elshamy AI Plants (Basel) 26-Dec-2022
PMCID:PMC9824887
doi:10.3390/plants12010110
PMID:36616238
Can Essential Oils Be a Natural Alternative for the Control of Spodoptera frugiperda? A Review of Toxicity Methods and Their Modes of Action Usseglio VL, Dambolena JS, Zunino MP Plants (Basel) 20-Dec-2022
PMCID:PMC9823514
doi:10.3390/plants12010003
PMID:36616132
Overview on Adjunct Ingredients Used in Hydroxyapatite-Based Oral Care Products Enax J, Amaechi BT, Schulze zur Wiesche E, Meyer F Biomimetics (Basel) 19-Dec-2022
PMCID:PMC9775056
doi:10.3390/biomimetics7040250
PMID:36546950
α-Bisabolol Attenuates NF-κB/MAPK Signaling Activation and ER-Stress-Mediated Apoptosis by Invoking Nrf2-Mediated Antioxidant Defense Systems against Doxorubicin-Induced Testicular Toxicity in Rats Arunachalam S, Nagoor Meeran MF, Azimullah S, Kumar Jha N, Saraswathiamma D, Albawardi A, Beiram R, Ojha S Nutrients 03-Nov-2022
PMCID:PMC9657294
doi:10.3390/nu14214648
PMID:36364909
Phytochemical Profile, Preliminary Toxicity, and Antioxidant Capacity of the Essential Oils of Myrciaria floribunda (H. West ex Willd.) O. Berg. and Myrcia sylvatica (G. Mey) DC. (Myrtaceae) de Moraes ÂA, Ferreira OO, da Costa LS, Almeida LQ, Varela EL, Cascaes MM, de Jesus Pereira Franco C, Percário S, do Nascimento LD, de Oliveira MS, Andrade EH Antioxidants (Basel) 21-Oct-2022
PMCID:PMC9658195
doi:10.3390/antiox11102076
PMID:36290799
Towards an Eco-Friendly Coffee Rust Control: Compilation of Natural Alternatives from a Nutritional and Antifungal Perspective Castillo NE, Acosta YA, Parra-Arroyo L, Martínez-Prado MA, Rivas-Galindo VM, Iqbal HM, Bonaccorso AD, Melchor-Martínez EM, Parra-Saldívar R Plants (Basel) 17-Oct-2022
PMCID:PMC9609732
doi:10.3390/plants11202745
PMID:36297767
Chemical Composition and Antimicrobial Potential of Essential Oil of Acritopappus confertus (Gardner) R.M.King & H.Rob. (Asteraceae) da Cruz RP, Castro JW, Leite DO, de Carvalho NK, Almeida-Bezerra JW, Pereira RL, Rodrigues FF, Bezerra JJ, Costa AR, Mori E, de Farias PA, Coutinho HD, Morais-Braga MF, Iriti M, da Costa JG, Rodrigues FF Pharmaceuticals (Basel) 17-Oct-2022
PMCID:PMC9611346
doi:10.3390/ph15101275
PMID:36297389

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
(2S)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6097621 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97763-X
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1071/CH9892041
https://doi.org/10.1016/S0031-9422(00)97763-X
Levomenol 442343 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1071/CH9892041
https://doi.org/10.1016/0031-9422(91)83029-K
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(2Z)-2,11-dimethyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradeca-1(13),2-dien-9-yl] (E)-2-methylbut-2-enoate 6371779 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)C)C 358.40 unknown https://doi.org/10.1016/S0031-9422(00)97763-X
15-Deoxygoyazensolide 14314508 Click to see CC1=CC2C(C(CC3(C(=O)C=C1O3)C)OC(=O)C(=C)C)C(=C)C(=O)O2 344.40 unknown https://doi.org/10.1016/S0031-9422(00)97763-X
Lychnopholide 49767028 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)C)C 358.40 unknown https://doi.org/10.1016/S0031-9422(00)97763-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
alpha-Cyclocostunolide 442191 Click to see CC1=CCCC2(C1C3C(CC2)C(=C)C(=O)O3)C 232.32 unknown https://doi.org/10.1021/NP50042A020
Arbusculin A 160153 Click to see CC12CCCC(C1C3C(CC2)C(=C)C(=O)O3)(C)O 250.33 unknown https://doi.org/10.1021/NP50042A020
Magnolialide 636954 Click to see CC1=C2C3C(CCC2(C(CC1)O)C)C(=C)C(=O)O3 248.32 unknown https://doi.org/10.1021/NP50042A020
Reynosin 482788 Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C 248.32 unknown https://doi.org/10.1021/NP50042A020
Santamarine 188297 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1021/NP50042A020
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1,10-Dimethyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl) 2-methylprop-2-enoate 163045855 Click to see CC1=CC(C2C(CC3(C(=O)C=C1O3)C)OC(=O)C2=C)OC(=O)C(=C)C 344.40 unknown https://doi.org/10.1016/S0031-9422(00)97481-8
(10-Methyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl) 2-methylprop-2-enoate 163024448 Click to see CC1=CC(C2C(CC3C(=O)C=C1O3)OC(=O)C2=C)OC(=O)C(=C)C 330.30 unknown https://doi.org/10.1016/S0031-9422(00)97481-8
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 133640194 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/S0031-9422(00)97763-X
https://doi.org/10.1021/NP50042A020
[(1R,3S,7S,8R,9Z)-1,10-dimethyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl] 2-methylprop-2-enoate 163045857 Click to see CC1=CC(C2C(CC3(C(=O)C=C1O3)C)OC(=O)C2=C)OC(=O)C(=C)C 344.40 unknown https://doi.org/10.1016/S0031-9422(00)97481-8
https://doi.org/10.1016/S0031-9422(00)89082-2
[(1S,3S,7S,8R,9Z)-10-methyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl] 2-methylprop-2-enoate 163024449 Click to see CC1=CC(C2C(CC3C(=O)C=C1O3)OC(=O)C2=C)OC(=O)C(=C)C 330.30 unknown https://doi.org/10.1016/S0031-9422(00)97481-8
Costunolide 5281437 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/S0031-9422(00)97763-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aS,6R,6aS,9aR,9bS)-6-hydroxy-6-methyl-3,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 101967028 Click to see CC1(CCC2C(C3C1CCC3=C)OC(=O)C2=C)O 248.32 unknown https://doi.org/10.1021/NP50042A020
(6aR,9S,9bR)-9-methyl-3,6-dimethylidene-3a,4,5,6a,7,9,9a,9b-octahydroazuleno[4,5-b]furan-2,8-dione 101238032 Click to see CC1C2C(CC1=O)C(=C)CCC3C2OC(=O)C3=C 246.30 unknown https://doi.org/10.1021/NP50042A020
Dehydrocostus lactone, (-)- 73174 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1021/NP50042A020
Eremanthin 100572 Click to see CC1=CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1021/NP50042A020
https://doi.org/10.1016/S0031-9422(00)91233-0
https://doi.org/10.1016/S0031-9422(00)97763-X
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
Stolonoxide A methyl ester 10387437 Click to see COC(=O)CC1CCC(OO1)C2CCC(O2)CCCCCCC=CC=CCCC=C 420.60 unknown https://doi.org/10.1016/S0031-9422(00)97481-8

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