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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
Collections

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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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
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
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
α-Bisabolol Attenuates Doxorubicin Induced Renal Toxicity by Modulating NF-κB/MAPK Signaling and Caspase-Dependent Apoptosis in Rats Arunachalam S, Nagoor Meeran MF, Azimullah S, Jha NK, Saraswathiamma D, Subramanya S, Albawardi A, Ojha S Int J Mol Sci 10-Sep-2022
PMCID:PMC9502245
doi:10.3390/ijms231810528
PMID:36142441
Multidrug-Resistant Bacteria: Their Mechanism of Action and Prophylaxis Bharadwaj A, Rastogi A, Pandey S, Gupta S, Sohal JS Biomed Res Int 05-Sep-2022
PMCID:PMC9467707
doi:10.1155/2022/5419874
PMID:36105930
Multifactor assessments to determine the overall performance of supercritical fluid extraction from Gynura procumbens essential oil Idris SA, Markom M, Abd. Rahman N, Mohd Ali J Sci Rep 22-Aug-2022
PMCID:PMC9395385
doi:10.1038/s41598-022-16773-4
PMID:35995970
Anti-Inflammatory and Analgesic Properties of the Cannabis Terpene Myrcene in Rat Adjuvant Monoarthritis McDougall JJ, McKenna MK Int J Mol Sci 17-Jul-2022
PMCID:PMC9319952
doi:10.3390/ijms23147891
PMID:35887239
The Antifungal Activity of Cinnamon-Litsea Combined Essential Oil against Dominant Fungal Strains of Moldy Peanut Kernels Liu Y, Wang R, Zhao L, Huo S, Liu S, Zhang H, Tani A, Lv H Foods 28-May-2022
PMCID:PMC9180872
doi:10.3390/foods11111586
PMID:35681336
Bioactivity study and metabolic profiling of Colletotrichum alatae LCS1, an endophyte of club moss Lycopodium clavatum L. Santra HK, Banerjee D PLoS One 28-Apr-2022
PMCID:PMC9049576
doi:10.1371/journal.pone.0267302
PMID:35482744
Health Benefits, Pharmacological Effects, Molecular Mechanisms, and Therapeutic Potential of α-Bisabolol Eddin LB, Jha NK, Goyal SN, Agrawal YO, Subramanya SB, Bastaki SM, Ojha S Nutrients 25-Mar-2022
PMCID:PMC9002489
doi:10.3390/nu14071370
PMID:35405982

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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