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Heliopsis buphthalmoides

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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 UUID643fd16130417957645383
Scientific name Heliopsis buphthalmoides
Authority Dunal
First published in Mém. Mus. Hist. Nat. 5: 57 (1819)

Description Top

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Synonyms Top

Scientific name Authority First published in
Kallias ovata Cass. Dict. Sci. Nat., ed. 2. 24: 327 (1822)
Anthemis buphthalmoides Jacq. Pl. Hort. Schoenbr. 2: 13 (1797)
Anthemis ovatifolia Ortega Hort. Matr. 73.
Anthemis oppositifolia Lam. Encycl. 1: 576 (1785)
Andrieuxia mexicana DC. Prodr. 5: 559 (1836)
Acmella buphthalmoides (Jacq.) Rich. Syn. Pl. 2: 473. 1807.
Verbesina ovata Hort.Par. ex Poir. Encycl. 8: 454 (1808)
Spilanthes oppositifolia (Lam.) D'Arcy Ann. Missouri Bot. Gard. 62: 1142 (1976)
Acmella buphthalmoides Pers. Syn. Pl. 2(2): 473 (1807)
Heliopsis dubia Dunal Mém. Mus. Hist. Nat. 5: 58 (1819)
Heliopsis pulchra T.R.Fisher Ohio J. Sci. 61: 178, fig. 1 (1961)

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Southeast
    • Caribbean
      • Cuba
    • Central America
      • Costa Rica
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000114757
Tropicos 2700871
KEW urn:lsid:ipni.org:names:213524-1
The Plant List gcc-7624
Open Tree Of Life 7605122
NCBI Taxonomy 2912032
IPNI 213524-1
iNaturalist 291430
GBIF 5396481
EOL 6198080
Wikipedia Heliopsis_buphthalmoides

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
Effect of Light and Dark on the Phenolic Compound Accumulation in Tartary Buckwheat Hairy Roots Overexpressing ZmLC Park CH, Park YE, Yeo HJ, Park NI, Park SU Int J Mol Sci 29-Apr-2021
PMCID:PMC8125369
doi:10.3390/ijms22094702
PMID:33946760
Functions of dopamine in plants: a review Liu Q, Gao T, Liu W, Liu Y, Zhao Y, Liu Y, Li W, Ding K, Ma F, Li C Plant Signal Behav 11-Oct-2020
PMCID:PMC7671028
doi:10.1080/15592324.2020.1827782
PMID:33040671
Chemistry and Pharmacology of Alkylamides from Natural Origin Elufioye TO, Habtemariam S, Adejare A Rev Bras Farmacogn 09-Oct-2020
PMCID:PMC7546144
doi:10.1007/s43450-020-00095-5
PMID:33071385
Expression of the Tyrosine Hydroxylase Gene from Rat Leads to Oxidative Stress in Potato Plants Kostyn K, Boba A, Kostyn A, Kozak B, Starzycki M, Kulma A, Szopa J Antioxidants (Basel) 07-Aug-2020
PMCID:PMC7465045
doi:10.3390/antiox9080717
PMID:32784799
Metabolomic homeostasis shifts after callus formation and shoot regeneration in tomato Kumari A, Ray K, Sadhna S, Pandey AK, Sreelakshmi Y, Sharma R PLoS One 08-May-2017
PMCID:PMC5421760
doi:10.1371/journal.pone.0176978
PMID:28481937
ChemInform Abstract: POLYACETYLENIC COMPOUNDS. 269. NEW N‐ISOBUTYLAMIDES FROM HELIOPSIS SPECIES F. BOHLMANN, T. GERKE, M. AHMED, R. M. KING, H. ROBINSON Wiley 05-May-2016
doi:10.1002/CHIN.198349152
The effects of dopamine on root growth and enzyme activity in soybean seedlings Guidotti BB, Gomes BR, Siqueira-Soares RD, Soares AR, Ferrarese-Filho O Plant Signal Behav 24-Jun-2013
PMCID:PMC4002588
doi:10.4161/psb.25477
PMID:23838960
Indoleamines and calcium channels influence morphogenesis in in vitro cultures of Mimosa pudica L. Ramakrishna A, Giridhar P, Ravishankar GA Plant Signal Behav 01-Dec-2009
PMCID:PMC2819438
doi:10.4161/psb.4.12.10101
PMID:20514228
Molecular phylogenetic analyses of nuclear and plastid DNA sequences support dysploid and polyploid chromosome number changes and reticulate evolution in the diversification of Melampodium (Millerieae, Asteraceae) Blöch C, Weiss-Schneeweiss H, Schneeweiss GM, Barfuss MH, Rebernig CA, Villaseñor JL, Stuessy TF Mol Phylogenet Evol 09-Mar-2009
PMCID:PMC4268500
doi:10.1016/j.ympev.2009.02.021
PMID:19272456
Biosynthesis and Function of Polyacetylenes and Allied Natural Products Minto RE, Blacklock BJ Prog Lipid Res 13-Mar-2008
PMCID:PMC2515280
doi:10.1016/j.plipres.2008.02.002
PMID:18387369
Polyacetylenverbindungen, 269 Neue <i>NS</i>‐Isobutylamide aus <i>Heliopsis</i>‐Arten Ferdinand Bohlmann, Thomas Gerke, Maniruddin Ahmed, Robert M. King, Harold Robinson Wiley 19-Jul-2007
doi:10.1002/JLAC.198319830713
New Lignans and Isobutylamides from<i>Heliopsis buphthalmoides</i> J. Jakupovic, A. Schuster, F. Bohlmann, R. King, H. Robinson Georg Thieme Verlag KG 07-Mar-2007
doi:10.1055/S-2007-969055
Green Roots: Photosynthesis and Photoautotrophy in an Underground Plant Organ. Flores HE, Dai Y, Cuello JL, Maldonado-Mendoza IE, Loyola-Vargas VM Plant Physiol 01-Feb-1993
PMCID:PMC160580
doi:10.1104/pp.101.2.363
PMID:12231691
Growth Stimulation by Catecholamines in Plant Tissue/Organ Cultures Protacio CM, Dai YR, Lewis EF, Flores HE Plant Physiol 01-Jan-1992
PMCID:PMC1080153
doi:10.1104/pp.98.1.89
PMID:16668653

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 / Dibenzylbutane lignans
Dimethyl 2,3-bis(1,3-benzodioxol-5-ylmethyl)butanedioate 75229604 Click to see COC(=O)C(CC1=CC2=C(C=C1)OCO2)C(CC3=CC4=C(C=C3)OCO4)C(=O)OC 414.40 unknown https://doi.org/10.1055/S-2007-969055
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4R)-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 15560140 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O 358.40 unknown https://doi.org/10.1002/JLAC.198319830713
3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 345761 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O 358.40 unknown https://doi.org/10.1002/JLAC.198319830713
Matairesinol 119205 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O 358.40 unknown https://doi.org/10.1002/CHIN.198349152
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Tetradeca-2,4,10-triene-8-ynoic acid isobutylamide 86110935 Click to see CCCC=CC#CCCC=CC=CC(=O)NCC(C)C 273.40 unknown https://doi.org/10.1002/JLAC.198319830713
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9-Hydroxy-10,12-octadecadienoic acid 5282945 Click to see CCCCCC=CC=CC(CCCCCCCC(=O)O)O 296.40 unknown https://doi.org/10.1002/JLAC.198319830713
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1055/S-2007-969055
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1055/S-2007-969055
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1055/S-2007-969055
beta Farnesene 15228937 Click to see CCC(=C)CCC=C(C)CCC=C(C)C 206.37 unknown https://doi.org/10.1055/S-2007-969055
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969055
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969055
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969055
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969055
> Organic acids and derivatives / Carboximidic acids and derivatives / Carboximidic acids
(2E,4E,8E,10Z)-N-(2-methylpropyl)octadeca-2,4,8,10-tetraen-12-ynamide 13846796 Click to see CCCCCC#CC=CC=CCCC=CC=CC(=O)NCC(C)C 327.50 unknown https://doi.org/10.1002/JLAC.198319830713
N-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynamide 162857989 Click to see CCCC=CC#CC=CC=CCCC=CC=CC(=O)NCC(C)C 325.50 unknown https://doi.org/10.1002/JLAC.198319830713
> Organoheterocyclic compounds / Benzodioxoles
3-[2-(1,3-Benzodioxol-5-ylmethyl)-7-methoxy-1-benzofuran-5-yl]prop-2-en-1-ol 162956433 Click to see COC1=CC(=CC2=C1OC(=C2)CC3=CC4=C(C=C3)OCO4)C=CCO 338.40 unknown https://doi.org/10.1002/JLAC.198319830713
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
Hamaudol 164722 Click to see CC1=CC(=O)C2=C(C3=C(C=C2O1)OC(C(C3)O)(C)C)O 276.28 unknown https://doi.org/10.1002/JLAC.198319830713
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
methyl 4,7a-dihydroxy-2,9-dimethoxy-6a-methyl-5-oxo-8,10a-dihydro-7H-[1]benzofuro[5,6-c]isochromene-9-carboxylate 163065586 Click to see CC12CC3(CC(OC3C=C1C4=C(C(=CC(=C4)OC)O)C(=O)O2)(C(=O)OC)OC)O 406.40 unknown https://doi.org/10.1002/JLAC.198319830713
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[2-[4,5-Dihydroxy-2-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] acetate 74977553 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)OC(=O)C)O 796.70 unknown https://doi.org/10.1002/JLAC.198319830713

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