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Internal ID UUID643fd31f3f0ab447514386
Scientific name Helianthus niveus
Authority (Benth.) Brandegee
First published in Proc. Calif. Acad. Sci. , ser. 2, 2: 173 (1889)

Description Top

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Synonyms Top

Scientific name Authority First published in
Helianthus niveus var. niveus (Benth.) Brandegee 1889

Common names Top

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Language Common/alternative name
English showy sunflower
Arabic دوار الشمس الثلجي

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Helianthus niveus subsp. tephrodes (A.Gray) Heiser Mem. Torrey Bot. Club 22(3): 43 (1969)

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 Northeast
      • Mexico Northwest
    • Southwestern U.S.A.
      • Arizona
      • California

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000129321
USDA Plants HENI3
Tropicos 2710403
KEW urn:lsid:ipni.org:names:298407-2
The Plant List gcc-90258
Open Tree Of Life 417272
NCBI Taxonomy 73301
Nature Serve 2.140488
IUCN Red List 20694323
IPNI 298407-2
iNaturalist 77358
GBIF 3093621
Freebase /m/03ylm51
EPPO HELNI
EOL 468058
Calflora (Californian flora) 4049
USDA GRIN 104312
Wikipedia Helianthus_niveus
CMAUP NPO19166

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 genomics of linkage drag in inbred lines of sunflower Huang K, Jahani M, Gouzy J, Legendre A, Carrere S, Lázaro-Guevara JM, González Segovia EG, Todesco M, Mayjonade B, Rodde N, Cauet S, Dufau I, Staton SE, Pouilly N, Boniface MC, Tapy C, Mangin B, Duhnen A, Gautier V, Poncet C, Donnadieu C, Mandel T, Hübner S, Burke JM, Vautrin S, Bellec A, Owens GL, Langlade N, Muños S, Rieseberg LH Proc Natl Acad Sci U S A 27-Mar-2023
PMCID:PMC10083583
doi:10.1073/pnas.2205783119
PMID:36972449
Re-evaluating Homoploid Reticulate Evolution in Helianthus Sunflowers Owens GL, Huang K, Todesco M, Rieseberg LH Mol Biol Evol 17-Jan-2023
PMCID:PMC9907532
doi:10.1093/molbev/msad013
PMID:36648104
HeliantHOME, a public and centralized database of phenotypic sunflower data Bercovich N, Genze N, Todesco M, Owens GL, Légaré JS, Huang K, Rieseberg LH, Grimm DG Sci Data 30-Nov-2022
PMCID:PMC9712528
doi:10.1038/s41597-022-01842-0
PMID:36450875
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
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
Genetic Diversity and Conservation Status of Helianthus verticillatus, an Endangered Sunflower of the Southern United States Edwards TP, Trigiano RN, Ownley BH, Windham AS, Wyman CR, Wadl PA, Hadziabdic D Front Genet 15-May-2020
PMCID:PMC7243268
doi:10.3389/fgene.2020.00410
PMID:32499812
Ancestral Reconstruction of Karyotypes Reveals an Exceptional Rate of Nonrandom Chromosomal Evolution in Sunflower Ostevik KL, Samuk K, Rieseberg LH Genetics 07-Feb-2020
PMCID:PMC7153943
doi:10.1534/genetics.120.303026
PMID:32033968
Characterization of a Novel Ourmia-Like Mycovirus Infecting Magnaporthe oryzae and Implications for Viral Diversity and Evolution Li CX, Zhu JZ, Gao BD, Zhu HJ, Zhou Q, Zhong J Viruses 05-Mar-2019
PMCID:PMC6465991
doi:10.3390/v11030223
PMID:30841545
RNA-seq data of control and powdery mildew pathogen (Golovinomyces orontii) treated transcriptomes of Helianthus niveus Sujatha M, Ulaganathan K, Bhanu BD, Soni PK Data Brief 04-Jan-2018
PMCID:PMC5988023
doi:10.1016/j.dib.2017.12.051
PMID:29876388
Chemosystematic Investigation of the Annual Species of Helianthus (Asteraceae) Otmar Spring, Edward E. Schilling Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(89)90094-X
Sesquiterpene lactones from Helianthus niveus subsp. niveus Alan Whittemore, Jonathan Gershenzon, Tom J. Mabry Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84894-3
Sesquiterpene lactones and diterpene carboxylic acids in Helianthus niveus subspecies Canescens Nobuo Ohno, Tom J. Mabry Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)87025-7

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 / Diterpenoids / Kaurane diterpenoids
(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(80)87025-7
5,9-Dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 433869 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(80)87025-7
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(80)87025-7
Kaurenoic acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(80)87025-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1,12-Dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl) 2-methylpropanoate 3487853 Click to see CC1=CC2C(C(CC3(C(CC1(O3)O)O)C)OC(=O)C(C)C)C(=C)C(=O)O2 366.40 unknown https://doi.org/10.1016/S0031-9422(00)84894-3
[(1R,2Z,4R,8R,9R,11R,12S)-1,12-dihydroxy-2-(hydroxymethyl)-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] (Z)-2-methylbut-2-enoate 90475906 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(=CC3C1C(=C)C(=O)O3)CO)O)O)C 394.40 unknown https://doi.org/10.1016/0031-9422(80)87025-7
[(1R,2Z,4S,8R,9R,11R,12S)-1,12-dihydroxy-2-(hydroxymethyl)-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] (Z)-2-methylbut-2-enoate 162893280 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(=CC3C1C(=C)C(=O)O3)CO)O)O)C 394.40 unknown https://doi.org/10.1016/0031-9422(80)87025-7
[(1R,2Z,4S,8R,9R,11S)-1-hydroxy-2-(hydroxymethyl)-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] (Z)-2-methylbut-2-enoate 44583816 Click to see CC=C(C)C(=O)OC1CC2(CCC(O2)(C(=CC3C1C(=C)C(=O)O3)CO)O)C 378.40 unknown https://doi.org/10.1016/0031-9422(80)87025-7
[(1S,2Z,4R,8R,9R,11S,12R)-1,12-dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] (Z)-2-methylbut-2-enoate 10667367 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(=CC3C1C(=C)C(=O)O3)C)O)O)C 378.40 unknown via CMAUP database
[(1S,2Z,4S,8R,9R,11R,12S)-1,12-dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] (Z)-2-methylbut-2-enoate 163099939 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(=CC3C1C(=C)C(=O)O3)C)O)O)C 378.40 unknown https://doi.org/10.1016/0031-9422(80)87025-7
[(1S,2Z,4S,8R,9R,11S)-1-hydroxy-2-(hydroxymethyl)-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] (Z)-2-methylbut-2-enoate 162944444 Click to see CC=C(C)C(=O)OC1CC2(CCC(O2)(C(=CC3C1C(=C)C(=O)O3)CO)O)C 378.40 unknown https://doi.org/10.1016/0031-9422(80)87025-7
[1-Hydroxy-2-(hydroxymethyl)-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] 2-methylbut-2-enoate 71440355 Click to see CC=C(C)C(=O)OC1CC2(CCC(O2)(C(=CC3C1C(=C)C(=O)O3)CO)O)C 378.40 unknown https://doi.org/10.1016/0031-9422(80)87025-7
[1,12-Dihydroxy-2-(hydroxymethyl)-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] 2-methylbut-2-enoate 433470 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(=CC3C1C(=C)C(=O)O3)CO)O)O)C 394.40 unknown https://doi.org/10.1016/0031-9422(80)87025-7
Annuithrin 3487849 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(=CC3C1C(=C)C(=O)O3)C)O)O)C 378.40 unknown https://doi.org/10.1016/0031-9422(80)87025-7
Orizabin 5281491 Click to see CC1=CC2C(C(CC3(C(CC1(O3)O)O)C)OC(=O)C(C)C)C(=C)C(=O)O2 366.40 unknown https://doi.org/10.1016/0305-1978(89)90094-X
https://doi.org/10.1016/S0031-9422(00)84894-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(4-Hydroxy-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl)methyl 2-methylpropanoate 162863403 Click to see CC1=CC2C(C(CC(=CCC1)COC(=O)C(C)C)O)C(=C)C(=O)O2 334.40 unknown https://doi.org/10.1016/S0031-9422(00)84894-3
(6-Hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,10,11,11a-hexahydrocyclodeca[b]furan-4-yl) 2-methylpropanoate 162994237 Click to see CC1CC2C(C(CC(C=CC1=O)(C)O)OC(=O)C(C)C)C(=C)C(=O)O2 350.40 unknown https://doi.org/10.1016/S0031-9422(00)84894-3
[(2S,4R,8S,9R,12R)-1,12-dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradecan-9-yl] 2-methylpropanoate 102004628 Click to see CC1CC2C(C(CC3(C(CC1(O3)O)O)C)OC(=O)C(C)C)C(=C)C(=O)O2 368.40 unknown https://doi.org/10.1016/0305-1978(89)90094-X
https://doi.org/10.1016/S0031-9422(00)84894-3
[(3aR,4R,6Z,10E,11aR)-4-hydroxy-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl]methyl 2-methylpropanoate 162863404 Click to see CC1=CC2C(C(CC(=CCC1)COC(=O)C(C)C)O)C(=C)C(=O)O2 334.40 unknown https://doi.org/10.1016/S0031-9422(00)84894-3
[(3aS,4R,6R,7Z,10S,11aR)-6-hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,10,11,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate 162994238 Click to see CC1CC2C(C(CC(C=CC1=O)(C)O)OC(=O)C(C)C)C(=C)C(=O)O2 350.40 unknown https://doi.org/10.1016/S0031-9422(00)84894-3
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/S0031-9422(00)84894-3
CID 13855920 13855920 Click to see CC1CC2C(C(CC3(C(CC1(O3)O)O)C)OC(=O)C(C)C)C(=C)C(=O)O2 368.40 unknown https://doi.org/10.1016/S0031-9422(00)84894-3
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/S0031-9422(00)84894-3
tagitinin A 181254 Click to see CC1CC2C(C(CC3(C(CC1(O3)O)O)C)OC(=O)C(C)C)C(=C)C(=O)O2 368.40 unknown https://doi.org/10.1016/S0031-9422(00)84894-3
Tirotundin 9975297 Click to see CC1CC2C(C(CC3(CCC1(O3)O)C)OC(=O)C(C)C)C(=C)C(=O)O2 352.40 unknown https://doi.org/10.1016/S0031-9422(00)84894-3
https://doi.org/10.1016/0305-1978(89)90094-X
Titrotundine 324884 Click to see CC1CC2C(C(CC3(CCC1(O3)O)C)OC(=O)C(C)C)C(=C)C(=O)O2 352.40 unknown https://doi.org/10.1016/S0031-9422(00)84894-3
https://doi.org/10.1016/0305-1978(89)90094-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7R,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 99641980 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown via CMAUP database
Limonin 179651 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Isobauerenol 3084367 Click to see CC1CCC2(CCC3(C4=C(CCC3(C2C1C)C)C5(CCC(C(C5CC4)(C)C)O)C)C)C 426.70 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database
Isodictamnine 442913 Click to see CN1C2=CC=CC=C2C(=O)C3=C1OC=C3 199.20 unknown via CMAUP database
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
Maculine 68232 Click to see COC1=C2C=COC2=NC3=CC4=C(C=C31)OCO4 243.21 unknown via CMAUP database
Maculosidine 68222 Click to see COC1=CC2=C(C(=C1)OC)N=C3C(=C2OC)C=CO3 259.26 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Alpha-methyldeoxybenzoin flavonoids
Angolensin 3584988 Click to see CC(C1=CC=C(C=C1)OC)C(=O)C2=C(C=C(C=C2)O)O 272.29 unknown https://doi.org/10.1016/0031-9422(80)87025-7
> Phenylpropanoids and polyketides / Coumarins and derivatives
Rutacultin 182049 Click to see CC(C)(C=C)C1=CC2=CC(=C(C=C2OC1=O)OC)OC 274.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(R)-6-(1,1-Dimethyl-allyl)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydro-furo[3,2-g]chromen-7-one 17753871 Click to see CC(C)(C=C)C1=CC2=CC3=C(C=C2OC1=O)OC(C3)C(C)(C)O 314.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
3-(1,1-Dimethylallyl)-7beta-hydroxy-8,8-dimethyl-7,8-dihydro-2H,6H-benzo[1,2-b:5,4-b']dipyran-2-one 92470573 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C=C)O)C 314.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Naringin 442428 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database

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