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Helianthus grosseserratus

Helianthus grosseserratus - 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 UUID643fc89336c4f628665618
Scientific name Helianthus grosseserratus
Authority M.Martens
First published in Index Seminum [Louvain] 1839: [4], adnot. [1839] ; later publ.: Linnaea 14(Litt.): 133. 1840.

Description Top

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Synonyms Top

Scientific name Authority First published in
Helianthus instabilis E.Watson Pap. Michigan Acad. Sci. 9: 423, pl. 65 (1929)
Helianthus grosseserratus var. hypoleucus A.Gray Syn. Fl. N. Amer. 1(2): 276 (1884)
Helianthus grosseserratus subsp. maximus R.W.Long Rhodora 56: 199 (1954)

Common names Top

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Language Common/alternative name
English sawtooth sunflower

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000023601
Flora of Alabama 795
Canadensys 3194
USDA Plants HEGR4
Tropicos 2724758
The Plant List gcc-122800
Open Tree Of Life 718849
NCBI Taxonomy 73291
Nature Serve 2.157634
IUCN Red List 20694301
IPNI 329259-2
iNaturalist 163617
GBIF 3119189
Freebase /m/04f070j
WisFlora 3815
EPPO HELGR
EOL 591753
Elurikkus 210956
USDA GRIN 27928
Wikipedia Helianthus_grosseserratus

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
The complete mitochondrial genome of Cuminum cyminum (Apiales: Apiaceae) and phylogenetic analysis Chen G, Kang R, Wang Z, Jiang Y, Zhou H, Abuduaini A, Suo F, Huang L Mitochondrial DNA B Resour 27-Jul-2023
PMCID:PMC10375935
doi:10.1080/23802359.2023.2238357
PMID:37521907
Authentication of milk thistle commercial products using UHPLC-QTOF-ESI + MS metabolomics and DNA metabarcoding Raclariu-Manolică AC, Mauvisseau Q, Paranaiba R, De Boer HJ, Socaciu C BMC Complement Med Ther 21-Jul-2023
PMCID:PMC10360273
doi:10.1186/s12906-023-04091-9
PMID:37480124
Comparative analysis of the plastid and mitochondrial genomes of Artemisia giraldii Pamp. Yue J, Lu Q, Ni Y, Chen P, Liu C Sci Rep 17-Aug-2022
PMCID:PMC9385723
doi:10.1038/s41598-022-18387-2
PMID:35978085
Reinventory of the vascular plants of Mormon Island Crane Meadows after forty years of restoration, invasion, and climate change Caven AJ, Wiese JD Heliyon 03-Jun-2022
PMCID:PMC9192816
doi:10.1016/j.heliyon.2022.e09640
PMID:35711997
Genetic basis and dual adaptive role of floral pigmentation in sunflowers Todesco M, Bercovich N, Kim A, Imerovski I, Owens GL, Dorado Ruiz Ó, Holalu SV, Madilao LL, Jahani M, Légaré JS, Blackman BK, Rieseberg LH eLife 18-Jan-2022
PMCID:PMC8765750
doi:10.7554/eLife.72072
PMID:35040432
Examining the utility of DNA barcodes for the identification of tallgrass prairie flora Herzog SA, Latvis M Appl Plant Sci 24-Jan-2021
PMCID:PMC7845766
doi:10.1002/aps3.11405
PMID:33552747
Foliar fungal endophyte community structure is independent of phylogenetic relatedness in an Asteraceae common garden Whitaker BK, Christian N, Chai Q, Clay K Ecol Evol 26-Nov-2020
PMCID:PMC7771118
doi:10.1002/ece3.6983
PMID:33391689
Evaluating Native Bee Communities and Nutrition in Managed Grasslands Stein DS, Debinski DM, Pleasants JM, Toth AL Environ Entomol 26-Mar-2020
PMCID:PMC7293027
doi:10.1093/ee/nvaa009
PMID:32215621
Multi-locus phylogeny and taxonomy of an unresolved, heterogeneous species complex within the genus Golovinomyces (Ascomycota, Erysiphales), including G. ambrosiae, G. circumfusus and G. spadiceus Qiu PL, Liu SY, Bradshaw M, Rooney-Latham S, Takamatsu S, Bulgakov TS, Tang SR, Feng J, Jin DN, Aroge T, Li Y, Wang LL, Braun U BMC Microbiol 05-Mar-2020
PMCID:PMC7059721
doi:10.1186/s12866-020-01731-9
PMID:32138640
Neo-Domestication of an Interspecific Tetraploid Helianthus annuus × Helianthus tuberous Population That Segregates for Perennial Habit Kantar MB, Hüber S, Herman A, Bock DG, Baute G, Betts K, Ott M, Brandvain Y, Wyse D, Stupar RM, Rieseberg LH Genes (Basel) 21-Aug-2018
PMCID:PMC6162802
doi:10.3390/genes9090422
PMID:30134600
Plastid primers for angiosperm phylogenetics and phylogeography Prince LM Appl Plant Sci 09-Jun-2015
PMCID:PMC4467757
doi:10.3732/apps.1400085
PMID:26082876
RNA-Seq Analysis and De Novo Transcriptome Assembly of Jerusalem Artichoke (Helianthus tuberosus Linne) Jung WY, Lee SS, Kim CW, Kim HS, Min SR, Moon JS, Kwon SY, Jeon JH, Cho HS PLoS One 06-Nov-2014
PMCID:PMC4222968
doi:10.1371/journal.pone.0111982
PMID:25375764
Sesquiterpene lactones from Helianthus grosseserratus Werner Herz, Narendra Kumar Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)85225-9

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 acid esters
(3-Hydroxy-11-methyl-2,7-dimethylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-1(13)-en-9-yl) 3-methylbutanoate 163090847 Click to see CC(C)CC(=O)OC1CC2(C(=O)C=C(O2)C(=C)C(C3C1C(=C)C(=O)O3)O)C 376.40 unknown https://doi.org/10.1016/0031-9422(81)85225-9
[(3R,4S,8R,9R,11R)-3-hydroxy-11-methyl-2,7-dimethylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-1(13)-en-9-yl] 3-methylbutanoate 163090848 Click to see CC(C)CC(=O)OC1CC2(C(=O)C=C(O2)C(=C)C(C3C1C(=C)C(=O)O3)O)C 376.40 unknown https://doi.org/10.1016/0031-9422(81)85225-9
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2R,4S,5R,9R,10S,11S,12R,13S,14S)-2-hydroxy-5,9,11,13-tetramethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-5-carboxylic acid 163025284 Click to see CC1C2C3C2(CC4(C3)C1C5(CCCC(C5CC4O)(C)C(=O)O)C)C 332.50 unknown https://doi.org/10.1016/0031-9422(81)85225-9
(1R,4S,5R,9S,10S,13R,15S)-15-acetyloxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 46233536 Click to see CC(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 360.50 unknown https://doi.org/10.1016/0031-9422(81)85225-9
(1R,4S,5R,9S,10S,13R,15S)-15-Hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 159930 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(81)85225-9
(1S,4S,5R,9S,10S,13R)-14-(acetyloxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-5-carboxylic acid 162933081 Click to see CC(=O)OCC1=CC23CCC4C(C2CCC1C3)(CCCC4(C)C(=O)O)C 360.50 unknown https://doi.org/10.1016/0031-9422(81)85225-9
(1S,4S,5R,9S,10S,13R)-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-5-carboxylic acid 71722009 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C4)CO)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(81)85225-9
14-(Acetyloxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-5-carboxylic acid 162933080 Click to see CC(=O)OCC1=CC23CCC4C(C2CCC1C3)(CCCC4(C)C(=O)O)C 360.50 unknown https://doi.org/10.1016/0031-9422(81)85225-9
2-Hydroxy-5,9,11,13-tetramethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-5-carboxylic acid 163025283 Click to see CC1C2C3C2(CC4(C3)C1C5(CCCC(C5CC4O)(C)C(=O)O)C)C 332.50 unknown https://doi.org/10.1016/0031-9422(81)85225-9
ent-17-Hydroxykaur-15-en-19-oic acid 13890715 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C4)CO)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(81)85225-9
Grandifloric acid 433554 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(81)85225-9
Xylopic acid 494328 Click to see CC(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 360.50 unknown https://doi.org/10.1016/0031-9422(81)85225-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(2Z,4R,8R,9R,11R)-2-(hydroxymethyl)-11-methyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradeca-1(13),2-dien-9-yl] 3-methylbutanoate 101607208 Click to see CC(C)CC(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)CO)C 376.40 unknown https://doi.org/10.1016/0031-9422(81)85225-9
[2-(Hydroxymethyl)-11-methyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradeca-1(13),2-dien-9-yl] 3-methylbutanoate 162903614 Click to see CC(C)CC(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)CO)C 376.40 unknown https://doi.org/10.1016/0031-9422(81)85225-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,4aS,8R,8aR,9aS)-8-hydroxy-5,8a-dimethyl-3-methylidene-3a,4,4a,8,9,9a-hexahydrobenzo[f][1]benzofuran-2,7-dione 163005093 Click to see CC1=CC(=O)C(C2(C1CC3C(C2)OC(=O)C3=C)C)O 262.30 unknown https://doi.org/10.1016/0031-9422(81)85225-9
(3aS,4aS,7R,8R,8aR,9aS)-7,8-dihydroxy-5,8a-dimethyl-3-methylidene-4,4a,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one 163016531 Click to see CC1=CC(C(C2(C1CC3C(C2)OC(=O)C3=C)C)O)O 264.32 unknown https://doi.org/10.1016/0031-9422(81)85225-9
(7-hydroxy-5,8a-dimethyl-3-methylidene-2-oxo-4,4a,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-8-yl) acetate 57509360 Click to see CC1=CC(C(C2(C1CC3C(C2)OC(=O)C3=C)C)OC(=O)C)O 306.40 unknown https://doi.org/10.1016/0031-9422(81)85225-9
[(3aS,4aS,7R,8R,8aR,9aS)-7-hydroxy-5,8a-dimethyl-3-methylidene-2-oxo-4,4a,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-8-yl] acetate 162943885 Click to see CC1=CC(C(C2(C1CC3C(C2)OC(=O)C3=C)C)OC(=O)C)O 306.40 unknown https://doi.org/10.1016/0031-9422(81)85225-9
7,8-dihydroxy-5,8a-dimethyl-3-methylidene-4,4a,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one 14779616 Click to see CC1=CC(C(C2(C1CC3C(C2)OC(=O)C3=C)C)O)O 264.32 unknown https://doi.org/10.1016/0031-9422(81)85225-9
8-Hydroxy-5,8a-dimethyl-3-methylidene-3a,4,4a,8,9,9a-hexahydrobenzo[f][1]benzofuran-2,7-dione 14021268 Click to see CC1=CC(=O)C(C2(C1CC3C(C2)OC(=O)C3=C)C)O 262.30 unknown https://doi.org/10.1016/0031-9422(81)85225-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
4-Hydroxy-6-(hydroxymethyl)-10-methyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 72656715 Click to see CC1=CC2C(C(CC(=CCC1)CO)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/0031-9422(81)85225-9
Deacetylovatifolin 11108215 Click to see CC1=CC2C(C(CC(=CCC1)CO)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/0031-9422(81)85225-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(81)85225-9
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1016/0031-9422(81)85225-9

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