Dimorphotheca sinuata - Unknown
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Internal ID UUID643fcaa5abd83950636610
Scientific name Dimorphotheca sinuata
Authority DC.
First published in Prodr. 6: 72 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Acanthotheca integrifolia DC. Prodr. 6: 74 (1838)
Calendula tragus Curtis Bot. Mag. 12: t. 408. 1798
Dimorphotheca pseud-aurantiaca Schinz & Thell. Verz. Sam. Fruchte Bot. Gart. Zurich 1922: 31 (1923)
Dimorphotheca dentata Harv. Fl. Cap. 3: 423 (1865)
Acanthotheca dentata DC. Prodr. 6: 74 (1838)
Dimorphotheca integrifolia (DC.) Harv. Fl. Cap. 3: 424 (1865)
Dimorphotheca calendulacea Harv. Fl. Cap. 3: 423 (1865)

Common names Top

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Language Common/alternative name
English glandular cape marigold
Spanish calendula tragus
Spanish dimorphotheca dentata
Spanish dimorphotheca calendulacea
Spanish dimorphotheca aurantiaca
Spanish dimorphotheca integrifolia
Spanish dimorphotheca pseudo aurantiaca
Spanish dimorphotheca pseudo-aurantiaca
Afrikaans namakwalandse madeliefie
German buschige kapringelblume
German kapringelblume
German kap-ringelblume
Estonian oranž kuldlill
Persian آصفالسلطنه
Finnish keltasääkukka
Armenian Դիմորֆոտեկա նարնջագույն
Japanese アフリカキンセンカ
Polish dimorfoteka zatokowa
Polish dimorphotheca aurantiaca
Chinese 異果菊
Chinese 异果菊
Chinese 齿状异果菊
Chinese 齿状二形菊

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Western Australia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000040105
Canadensys 3051
USDA Plants DISI4
Tropicos 2709935
INPN 95022
KEW urn:lsid:ipni.org:names:201489-1
The Plant List gcc-138788
Open Tree Of Life 888564
NCBI Taxonomy 112408
NBN Atlas NBNSYS0200002027
Nature Serve 2.795526
IPNI 201489-1
iNaturalist 76662
GBIF 5402350
Freebase /m/02q9qt2
EPPO DMPSI
EOL 492273
Elurikkus 211007
Calflora (Californian flora) 2733
USDA GRIN 14151
Wikipedia Dimorphotheca_sinuata
CMAUP NPO6893

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
Unexpected Effects of Sulfate and Sodium Chloride Application on Yield Qualitative Characteristics and Symmetry Indicators of Hard and Soft Wheat Kernels Aniskina TS, Baranova EN, Lebedev SV, Reger NS, Besaliev IN, Panfilov AA, Kryuchkova VA, Gulevich AA Plants (Basel) 21-Feb-2023
PMCID:PMC10004740
doi:10.3390/plants12050980
PMID:36903841
Life Histories and Host-Range Evaluation of Two Chrysomelid Beetles (Zygogramma spp.) Released against Tithonia rotundifolia in South Africa Mawela KV, Simelane DO, Olckers T Insects 08-Mar-2022
PMCID:PMC8954993
doi:10.3390/insects13030267
PMID:35323565
Geographic Mosaics of Fly Pollinators With Divergent Color Preferences Drive Landscape-Scale Structuring of Flower Color in Daisy Communities Ellis AG, Anderson B, Kemp JE Front Plant Sci 01-Feb-2021
PMCID:PMC7882612
doi:10.3389/fpls.2021.617761
PMID:33597961
Magnetic Nanoparticles Coated with (R)-9-Acetoxystearic Acid for Biomedical Applications Micheletti G, Boga C, Telese D, Cassani MC, Boanini E, Nitti P, Ballarin B, Ghirri A, Barucca G, Rinaldi D ACS Omega 29-May-2020
PMCID:PMC7288358
doi:10.1021/acsomega.0c00163
PMID:32548454
Synthesis of 9-Hydroxystearic Acid Derivatives and Their Antiproliferative Activity on HT 29 Cancer Cells Calonghi N, Boga C, Telese D, Bordoni S, Sartor G, Torsello C, Micheletti G Molecules 15-Oct-2019
PMCID:PMC6832665
doi:10.3390/molecules24203714
PMID:31619025
Plant–pollinator interactions along the pathway to paternity Minnaar C, Anderson B, de Jager ML, Karron JD Ann Bot 07-Dec-2018
PMCID:PMC6344347
doi:10.1093/aob/mcy167
PMID:30535041
(9R)-9-Hydroxystearate-Functionalized Anticancer Ceramics Promote Loading of Silver Nanoparticles Boanini E, Cassani MC, Rubini K, Boga C, Bigi A Nanomaterials (Basel) 31-May-2018
PMCID:PMC6027231
doi:10.3390/nano8060390
PMID:29857541
Effects of germination season on life history traits and on transgenerational plasticity in seed dormancy in a cold desert annual Lu JJ, Tan DY, Baskin CC, Baskin JM Sci Rep 27-Apr-2016
PMCID:PMC4846867
doi:10.1038/srep25076
PMID:27117090
Germination Season and Watering Regime, but Not Seed Morph, Affect Life History Traits in a Cold Desert Diaspore-Heteromorphic Annual Lu JJ, Tan DY, Baskin JM, Baskin CC PLoS One 11-Jul-2014
PMCID:PMC4094427
doi:10.1371/journal.pone.0102018
PMID:25013967
Seed dimorphism, nutrients and salinity differentially affect seed traits of the desert halophyte Suaeda aralocaspica via multiple maternal effects Wang L, Baskin JM, Baskin CC, Cornelissen JH, Dong M, Huang Z BMC Plant Biol 25-Sep-2012
PMCID:PMC3515402
doi:10.1186/1471-2229-12-170
PMID:23006315
A Technique for Measuring Petal Gloss, with Examples from the Namaqualand Flora Whitney HM, Rands SA, Elton NJ, Ellis AG PLoS One 10-Jan-2012
PMCID:PMC3254604
doi:10.1371/journal.pone.0029476
PMID:22253729
Mining the bitter melon (momordica charantia l.) seed transcriptome by 454 analysis of non-normalized and normalized cDNA populations for conjugated fatty acid metabolism-related genes Yang P, Li X, Shipp MJ, Shockey JM, Cahoon EB BMC Plant Biol 16-Nov-2010
PMCID:PMC3012625
doi:10.1186/1471-2229-10-250
PMID:21080948
Functional Diversity in Fungal Fatty Acid Synthesis: THE FIRST ACETYLENASE FROM THE PACIFIC GOLDEN CHANTERELLE, CANTHARELLUS FORMOSUS Blacklock BJ, Scheffler BE, Shepard MR, Jayasuriya N, Minto RE J Biol Chem 06-Jul-2010
PMCID:PMC2937869
doi:10.1074/jbc.M110.151498
PMID:20606235
Molecular Analysis of a Bifunctional Fatty Acid Conjugase/Desaturase from Tung. Implications for the Evolution of Plant Fatty Acid Diversity Dyer JM, Chapital DC, Kuan JC, Mullen RT, Turner C, McKeon TA, Pepperman AB Plant Physiol 01-Dec-2002
PMCID:PMC166714
doi:10.1104/pp.102.010835
PMID:12481086

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
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Hydroxytyrosol 82755 Click to see C1=CC(=C(C=C1CCO)O)O 154.16 unknown via CMAUP database
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
4'-Demethyldehydropodophyllotoxin 15232507 Click to see COC1=CC(=CC(=C1O)OC)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)O)COC3=O 396.30 unknown via CMAUP database
Tetradehydropodophyllotoxin 5316463 Click to see COC1=CC(=CC(=C1OC)OC)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)O)COC3=O 410.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6R,6aR)-6-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13991182 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC6C(C(C(C(O6)CO)O)O)O 682.70 unknown via CMAUP database
(5R)-5beta-(3,4,5-Trimethoxyphenyl)-7alpha-(hydroxymethyl)-8alpha-(6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyloxy)-5,6,7,8-tetrahydronaphtho[2,3-d]-1,3-dioxole-6beta-carboxylic acid methyl ester 10887221 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(C(C3=CC4=C(C=C23)OCO4)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)CO)C(=O)OC 770.70 unknown via CMAUP database
Podorhizol beta-D-glucoside 443015 Click to see COC1=CC(=CC(=C1OC)OC)C(C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC5C(C(C(C(O5)CO)O)O)O 578.60 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
(3aR,4R,9R,9aR)-4,6,7-trihydroxy-9-(3,4,5-trimethoxyphenyl)-3a,4,9,9a-tetrahydro-3H-benzo[f]isobenzofuran-1-one 3010625 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC(=C(C=C24)O)O)O 402.40 unknown via CMAUP database
alpha-Peltatin 92129 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O 400.40 unknown via CMAUP database
Deoxypodophyllotoxin 345501 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown via CMAUP database
Isopicropodophyllone 11189106 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5 412.40 unknown via CMAUP database
Naphtho(2,3-c)furan-1(3H)-one, 3a,4,9,9a-tetrahydro-4,6,7-trihydroxy-9-(4-hydroxy-3,5-dimethoxyphenyl)-, (3aR,4R,9R,9aR)- 468863 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC(=C(C=C24)O)O)O 388.40 unknown via CMAUP database
Picropodopyllotoxone 3083574 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5 412.40 unknown via CMAUP database
Podophyllotoxone 443014 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(=O)C4=CC5=C(C=C24)OCO5 412.40 unknown via CMAUP database
Sikkimotoxin 3010626 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC(=C(C=C24)OC)OC)O 430.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
(5R,5aR,8aS,9R)-5-hydroxy-9-(4-hydroxy-3,5-dimethoxy-phenyl)-5a,6,8a,9-tetrahydro-5H-isobenzofuro[6,5-f][1,3]benzodioxol-8-one 456051 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 400.40 unknown via CMAUP database
(5R)-5beta-(3,4,5-Trimethoxyphenyl)-9alpha-(6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyloxy)-5,5abeta,6,8,8aalpha,9-hexahydrofuro[3',4':6,7]naphtho[2,3-d]-1,3-dioxole-6-one 10533021 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O 738.70 unknown via CMAUP database
(5R)-5beta-(3,4,5-Trimethoxyphenyl)-9beta-(beta-D-glucopyranosyloxy)-5,5abeta,6,8,8abeta,9-hexahydrofuro[3',4':6,7]naphtho[2,3-d]-1,3-dioxole-6-one 10918890 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O 576.50 unknown via CMAUP database
(5R)-9beta-(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyloxy)-5beta-(3,4,5-trimethoxyphenyl)-5,5abeta,6,8,8abeta,9-hexahydrofuro[3',4':6,7]naphtho[2,3-d]-1,3-dioxole-6-one 10919696 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O 738.70 unknown via CMAUP database
[(5aalpha,8abeta)-5beta-(3,4-Dihydroxy-5-methoxyphenyl)-5,5a,6,8,8a,9-hexahydro-6-oxofuro[3',4':6,7]naphtho[2,3-d]-1,3-dioxole-9beta-yl]beta-D-glucopyranoside 101242502 Click to see COC1=CC(=CC(=C1O)O)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O 548.50 unknown via CMAUP database
[4-[(5R,5aR,8aR,9R)-5-hydroxy-8-oxo-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-9-yl]-2,6-dimethoxyphenyl] acetate 53359026 Click to see CC(=O)OC1=C(C=C(C=C1OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O)OC 442.40 unknown via CMAUP database
4'-Demethylpodophyllotoxin 122667 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 400.40 unknown via CMAUP database
4'-Demthylpodophyllotoxin beta-D-glucoside 170385 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O 562.50 unknown via CMAUP database
6I1J8IM5I7 10844308 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O 562.50 unknown via CMAUP database
Lignan P 159949 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O 562.50 unknown via CMAUP database
Picropodophyllin 72435 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown via CMAUP database
Podofilox 10607 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown via CMAUP database
Podophyllotoxin glucoside 161177 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O 576.50 unknown via CMAUP database
sinolignan A 54581698 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C3COC(=O)C3C(C4=CC5=C(C=C24)OCO5)C6=CC(=C(C(=C6)OC)OC)OC)O)O)O 618.60 unknown via CMAUP database
sinolignan B 54581699 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O 724.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-[[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[4-(2-hydroxyethyl)phenoxy]oxane-3,4,5-triol 10961007 Click to see C1=CC(=CC=C1CCO)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database

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