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Heliopsis longipes

Heliopsis longipes - 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 UUID643fce93043cd241789250
Scientific name Heliopsis longipes
Authority S.F.Blake
First published in Contr. U.S. Natl. Herb. 22: 608 (1924)

Description Top

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Synonyms Top

Scientific name Authority First published in
Philactis longipes A.Gray Proc. Amer. Acad. Arts xv. (1880) 35.

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

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Database ID/link to page
World Flora Online wfo-0000082614
UNII HJN24W2G8F
Tropicos 50180045
KEW urn:lsid:ipni.org:names:119693-2
The Plant List gcc-39118
Open Tree Of Life 243052
NCBI Taxonomy 185653
IPNI 119693-2
iNaturalist 289042
GBIF 5396489
Wikipedia Heliopsis_longipes

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
Pharmacological Characteristics of the Hydroethanolic Extract of Acmella oleracea (L) R. K. Jansen Flowers: ADME/Tox In Silico and In Vivo Antihypertensive and Chronic Toxicity Evaluation Rodrigues ET, Peretti P, Bezerra RM, Biancardi MF, Sousa FF, Mendes EP, Dutra JB, Silveira CC, Castro CH, Cruz JN, Santos CB, Santos FC, Pinheiro MT Evid Based Complement Alternat Med 29-Apr-2023
PMCID:PMC10163967
doi:10.1155/2023/1278720
PMID:37159592
De novo transcriptome assembly of Conium maculatum L. to identify candidate genes for coniine biosynthesis Peddinti G, Hotti H, Teeri TH, Rischer H Sci Rep 20-Oct-2022
PMCID:PMC9584964
doi:10.1038/s41598-022-21728-w
PMID:36266299
Proangiogenic Effect of Affinin and an Ethanolic Extract from Heliopsis longipes Roots: Ex Vivo and In Vivo Evidence García-Badillo PE, Avalos-Soriano A, López-Martínez J, García-Gasca T, Castro-Ruiz JE Molecules 18-Dec-2021
PMCID:PMC8706137
doi:10.3390/molecules26247670
PMID:34946751
Mexican Plants and Derivates Compounds as Alternative for Inflammatory and Neuropathic Pain Treatment—A Review Quiñonez-Bastidas GN, Navarrete A Plants (Basel) 25-Apr-2021
PMCID:PMC8145628
doi:10.3390/plants10050865
PMID:33923101
Solanum lycopersicum Seedlings. Metabolic Responses Induced by the Alkamide Affinin Campos-García T, Molina-Torres J Metabolites 27-Feb-2021
PMCID:PMC7997251
doi:10.3390/metabo11030143
PMID:33673570
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
Global gene expression analyses of the alkamide-producing plant Heliopsis longipes supports a polyketide synthase-mediated biosynthesis pathway Buitimea-Cantúa GV, Marsch-Martinez N, Ríos-Chavez P, Méndez-Bravo A, Molina-Torres J PeerJ 25-Sep-2020
PMCID:PMC7521342
doi:10.7717/peerj.10074
PMID:33033663
Chemical composition and broad-spectrum anthelmintic activity of a cultivar of toothache plant, Acmella oleracea, from Mizoram, India Lalthanpuii PB, Lalchhandama K Pharm Biol 13-May-2020
PMCID:PMC7269084
doi:10.1080/13880209.2020.1760316
PMID:32401104
A Review of Endothelium-Dependent and -Independent Vasodilation Induced by Phytochemicals in Isolated Rat Aorta Knox M, Vinet R, Fuentes L, Morales B, Martínez JL Animals (Basel) 29-Aug-2019
PMCID:PMC6769919
doi:10.3390/ani9090623
PMID:31470540
Insecticidal and Nematicidal Contributions of Mexican Flora in the Search for Safer Biopesticides Hernández-Carlos B, Gamboa-Angulo M Molecules 04-Mar-2019
PMCID:PMC6429201
doi:10.3390/molecules24050897
PMID:30836688
Medicinal Plants from North and Central America and the Caribbean Considered Toxic for Humans: The Other Side of the Coin Alonso-Castro AJ, Domínguez F, Ruiz-Padilla AJ, Campos-Xolalpa N, Zapata-Morales JR, Carranza-Alvarez C, Maldonado-Miranda JJ Evid Based Complement Alternat Med 02-Nov-2017
PMCID:PMC5688365
doi:10.1155/2017/9439868
PMID:29234446
Anti-inflammatory, Antinociceptive, and Antioxidant Activities of Methanol and Aqueous Extracts of Anacyclus pyrethrum Roots Manouze H, Bouchatta O, Gadhi AC, Bennis M, Sokar Z, Ba-M’hamed S Front Pharmacol 05-Sep-2017
PMCID:PMC5591861
doi:10.3389/fphar.2017.00598
PMID:28928658
Use of traditional herbal medicine as an alternative in dental treatment in Mexican dentistry: a review Cruz Martínez C, Diaz Gómez M, Oh MS Pharm Biol 25-Jul-2017
PMCID:PMC6130662
doi:10.1080/13880209.2017.1347188
PMID:28738710
Chemical composition and biological activities of Helicteres vegae and Heliopsis sinaloensis Olivas-Quintero S, López-Angulo G, Montes-Avila J, Díaz-Camacho SP, Vega-Aviña R, López-Valenzuela JÁ, Salazar-Salas NY, Delgado-Vargas F Pharm Biol 28-Mar-2017
PMCID:PMC6130667
doi:10.1080/13880209.2017.1306712
PMID:28347185
Affinin (Spilanthol), Isolated from Heliopsis longipes, Induces Vasodilation via Activation of Gasotransmitters and Prostacyclin Signaling Pathways Castro-Ruiz JE, Rojas-Molina A, Luna-Vázquez FJ, Rivero-Cruz F, García-Gasca T, Ibarra-Alvarado C Int J Mol Sci 22-Jan-2017
PMCID:PMC5297847
doi:10.3390/ijms18010218
PMID:28117739

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 / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,8E)-N-butan-2-yldeca-2,4,8-trienamide 6433895 Click to see CCC(C)NC(=O)C=CC=CCCC=CC 221.34 unknown https://doi.org/10.1016/S0378-8741(98)00134-2
(8R,9R)-8,9-dihydroxy-N-(2-methylpropyl)deca-2,6-dienamide 162902773 Click to see CC(C)CNC(=O)C=CCCC=CC(C(C)O)O 255.35 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
(E)-N-Isobutyldec-2-enamide 11031534 Click to see CCCCCCCC=CC(=O)NCC(C)C 225.37 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
N-(2-Methylbutyl)-(2E,6Z,8E)-decatrienamide 5352999 Click to see CCC(C)CNC(=O)C=CCCC=CC=CC 235.36 unknown https://doi.org/10.1016/S0031-9422(00)83490-1
N-(2-Methylpropyl)dec-2-enamide 71404146 Click to see CCCCCCCC=CC(=O)NCC(C)C 225.37 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
N-(2-methylpropyl)deca-2,6,8-trienamide 530394 Click to see CC=CC=CCCC=CC(=O)NCC(C)C 221.34 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
N-(2-methylpropyl)undec-3-en-8,10-diynamide 162965383 Click to see CC(C)CNC(=O)CC=CCCCC#CC#C 231.33 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
Spilanthol 5353001 Click to see CC=CC=CCCC=CC(=O)NCC(C)C 221.34 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
https://doi.org/10.1016/0305-1978(95)00099-2
https://doi.org/10.1016/S0378-8741(98)00134-2
https://doi.org/10.1016/J.JPBA.2010.02.010
https://doi.org/10.1002/PS.2274
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids
(1S,3R,8R,10S)-6-(3-hydroxy-3-methylbutyl)-3-(2-hydroxypropan-2-yl)-9,9-dimethyl-10-(3-methylbut-2-enyl)-8-(2-methylpropanoyl)-4-oxatricyclo[6.3.1.01,5]dodec-5-ene-7,12-dione 101336990 Click to see CC(C)C(=O)C12C(=O)C(=C3C(C1=O)(CC(C2(C)C)CC=C(C)C)CC(O3)C(C)(C)O)CCC(C)(C)O 502.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(1S,2S,4S)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] (2E,6Z,8E)-deca-2,6,8-trienoate 163191052 Click to see CC=CC=CCCC=CC(=O)OC1CC2CCC1(C2(C)C)C 302.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
[(1S,2S,4S)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] deca-2,6,8-trienoate 162866706 Click to see CC=CC=CCCC=CC(=O)OC1CC2CCC1(C2(C)C)C 302.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
1,7,7-Trimethylbicyclo[2.2.1]heptane-2,5-diol 182459 Click to see CC1(C2CC(C1(CC2O)C)O)C 170.25 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
Bicyclo[2.2.1]heptane-2,5-diol, 1,7,7-trimethyl-, (2-endo,5-exo)- 535224 Click to see CC1(C2CC(C1(CC2O)C)O)C 170.25 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(6-Acetyloxy-5-hydroxy-4a-methyl-8-methylidene-2-propan-2-yl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl) benzoate 162927595 Click to see CC(C)C1CCC2(C(C1OC(=O)C3=CC=CC=C3)C(=C)CC(C2O)OC(=O)C)C 400.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
> Organic acids and derivatives / Carboximidic acids and derivatives / Carboximidic acids
N-isobutyl-2,6-decadienamide 129834243 Click to see CCCC=CCCC=CC(=O)NCC(C)C 223.35 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Polyols / 1,2-diols
(2E,6Z,8R,9R)-8,9-dihydroxy-N-(2-methylpropyl)deca-2,6-dienamide 163188577 Click to see CC(C)CNC(=O)C=CCCC=CC(C(C)O)O 255.35 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(6R,9R)-6,9-dihydroxy-N-(2-methylpropyl)deca-2,7-dienamide 162932494 Click to see CC(C)CNC(=O)C=CCCC(C=CC(C)O)O 255.35 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014
> Organoheterocyclic compounds / Lactones
10-[(E)-2-[(2R,3R)-3-[(E)-pent-2-enyl]oxiran-2-yl]ethenyl]oxecan-2-one 101936988 Click to see CCC=CCC1C(O1)C=CC2CCCCCCCC(=O)O2 292.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.014

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