Sandersonia aurantiaca - Unknown
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Internal ID UUID6440222b0b4ab132999284
Scientific name Sandersonia aurantiaca
Authority Hook.
First published in Bot. Mag. 79: t. 4716 (1853)

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Synonyms Top

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Common names Top

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Language Common/alternative name
English christmas bells
Afrikaans geelklokkies
Hebrew סנדרסוניה
Croatian sandersonija
Japanese サンダーソニア
Chinese 宮燈百合
Chinese 提灯花
Chinese 灯笼百合

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000735471
Tropicos 18400727
KEW urn:lsid:ipni.org:names:540483-1
The Plant List kew-287108
Open Tree Of Life 350155
Observations.org 432180
NCBI Taxonomy 61864
IPNI 540483-1
iNaturalist 553435
GBIF 2740395
Freebase /m/03d3w9g
EPPO ZNDAU
EOL 1082166
Elurikkus 294080
USDA GRIN 33011
Wikipedia Sandersonia

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
Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ Foods 08-Nov-2023
PMCID:PMC10671036
doi:10.3390/foods12224066
PMID:38002124
Embryo Rescue in Plant Breeding Rogo U, Fambrini M, Pugliesi C Plants (Basel) 29-Aug-2023
PMCID:PMC10489947
doi:10.3390/plants12173106
PMID:37687352
Dynamic changes occur in the cell wall composition and related enzyme activities during flower development in Rosa damascena Önder S, Tonguç M, Önder D, Erbaş S, Mutlucan M Front Plant Sci 31-Jul-2023
PMCID:PMC10425964
doi:10.3389/fpls.2023.1120098
PMID:37588417
Transcriptome Dynamics during Spike Differentiation of Wheat Reveal Amazing Changes in Cell Wall Metabolic Regulators Han J, Liu Y, Shen Y, Zhang D, Li W Int J Mol Sci 19-Jul-2023
PMCID:PMC10380499
doi:10.3390/ijms241411666
PMID:37511426
Lutein Isomers: Preparation, Separation, Structure Elucidation, and Occurrence in 20 Medicinal Plants Nagy V, Agócs A, Balázs VL, Purger D, Filep R, Sándor V, Turcsi E, Gulyás-Fekete G, Deli J Molecules 25-Jan-2023
PMCID:PMC9921531
doi:10.3390/molecules28031187
PMID:36770852
Flowering Mechanisms and Environmental Stimuli for Flower Transition: Bases for Production Scheduling in Greenhouse Floriculture Proietti S, Scariot V, De Pascale S, Paradiso R Plants (Basel) 05-Feb-2022
PMCID:PMC8839403
doi:10.3390/plants11030432
PMID:35161415
Building a Flower: The Influence of Cell Wall Composition on Flower Development and Reproduction Cruz-Valderrama JE, Bernal-Gallardo JJ, Herrera-Ubaldo H, de Folter S Genes (Basel) 26-Jun-2021
PMCID:PMC8304806
doi:10.3390/genes12070978
PMID:34206830
Proteome and Ubiquitome Changes during Rose Petal Senescence Lu J, Xu Y, Fan Y, Wang Y, Zhang G, Liang Y, Jiang C, Hong B, Gao J, Ma C Int J Mol Sci 04-Dec-2019
PMCID:PMC6940906
doi:10.3390/ijms20246108
PMID:31817087
Asparagine Synthesis during Tobacco Leaf Curing Bovet L, Cheval C, Hilfiker A, Battey J, Langlet D, Broye H, Schwaar J, Ozelley P, Lang G, Bakaher N, Laparra H, Goepfert S Plants (Basel) 11-Nov-2019
PMCID:PMC6918383
doi:10.3390/plants8110492
PMID:31718005
Differences in flavonoid pathway metabolites and transcripts affect yellow petal colouration in the aquatic plant Nelumbo nucifera Zhu HH, Yang JX, Xiao CH, Mao TY, Zhang J, Zhang HY BMC Plant Biol 24-Jun-2019
PMCID:PMC6592004
doi:10.1186/s12870-019-1886-8
PMID:31234776
Comparative Proteomic Analysis during the Involvement of Nitric Oxide in Hydrogen Gas-Improved Postharvest Freshness in Cut Lilies Huo J, Huang D, Zhang J, Fang H, Wang B, Wang C, Ma Z, Liao W Int J Mol Sci 09-Dec-2018
PMCID:PMC6320913
doi:10.3390/ijms19123955
PMID:30544843
Morphological and Molecular Variation Between Fusarium avenaceum, Fusarium arthrosporioides and Fusarium anguioides Strains Yli-Mattila T, Hussien T, Gavrilova O, Gagkaeva T Pathogens 29-Nov-2018
PMCID:PMC6313738
doi:10.3390/pathogens7040094
PMID:30501049
Extraction, development and validation of HPLC-UV method for rapid and sensitive determination of colchicine from Colchicum autumnale L. Bulbs Çankaya N, Bulduk İ, Çolak AM Saudi J Biol Sci 03-Oct-2018
PMCID:PMC6717106
doi:10.1016/j.sjbs.2018.10.003
PMID:31485175
Identification and comparative profiling of miRNAs in herbaceous peony (Paeonia lactiflora Pall.) with red/yellow bicoloured flowers Zhao D, Wei M, Shi M, Hao Z, Tao J Sci Rep 20-Mar-2017
PMCID:PMC5357961
doi:10.1038/srep44926
PMID:28317945
Proteomes and Ubiquitylomes Analysis Reveals the Involvement of Ubiquitination in Protein Degradation in Petunias Guo J, Liu J, Wei Q, Wang R, Yang W, Ma Y, Chen G, Yu Y Plant Physiol 03-Nov-2016
PMCID:PMC5210702
doi:10.1104/pp.16.00795
PMID:27810942

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
> Hydrocarbon derivatives / Tropones
1,2,3,10-tetramethoxy-7-(methylamino)-6,7-dihydro-5H-benzo[a]heptalen-9-one 2832 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 371.40 unknown https://doi.org/10.3987/COM-11-12260
2-Demethylcolchicine 23757 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)O)OC 385.40 unknown https://doi.org/10.3987/COM-11-12260
2-Demthyldemecolcine 146030 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)O)OC 357.40 unknown https://doi.org/10.3987/COM-11-12260
2-hydroxy-1,3,10-trimethoxy-7-(methylamino)-6,7-dihydro-5H-benzo[a]heptalen-9-one 14413735 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)O)OC 357.40 unknown https://doi.org/10.3987/COM-11-12260
2-hydroxy-N-(3-hydroxy-1,2,10-trimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl)acetamide 162938291 Click to see COC1=CC=C2C(=CC1=O)C(CCC3=CC(=C(C(=C32)OC)OC)O)NC(=O)CO 401.40 unknown https://doi.org/10.3987/COM-11-12260
2-hydroxy-N-[(7S)-3-hydroxy-1,2,10-trimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide 162938292 Click to see COC1=CC=C2C(=CC1=O)C(CCC3=CC(=C(C(=C32)OC)OC)O)NC(=O)CO 401.40 unknown https://doi.org/10.3987/COM-11-12260
3-Desmethylcolchicine 299664 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)O 385.40 unknown https://doi.org/10.3987/COM-11-12260
Colchicine 6167 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 399.40 unknown https://doi.org/10.3987/COM-11-12260
Demecolcine 220401 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 371.40 unknown https://doi.org/10.3987/COM-11-12260
N-(1,2,3,10-Tetramethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl)acetamide 2833 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 399.40 unknown https://doi.org/10.3987/COM-11-12260
N-(3-hydroxy-1,2,10-trimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl)acetamide 494161 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)O 385.40 unknown https://doi.org/10.3987/COM-11-12260
N-[(7S)-10-(hydroxymethyl)-1,2,3-trimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide 101798699 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)CO)OC)OC)OC 399.40 unknown https://doi.org/10.3987/COM-11-12260
O(sup 2)-Demethylcolchicine 541033 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)O)OC 385.40 unknown https://doi.org/10.3987/COM-11-12260
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1016/S0304-4238(97)00124-6
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Cryptoxanthin 5281235 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 552.90 unknown https://doi.org/10.1016/S0304-4238(97)00124-6
Lutein 5281243 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C 568.90 unknown https://doi.org/10.1016/S0304-4238(97)00124-6
Zeaxanthin 5280899 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 568.90 unknown https://doi.org/10.1016/S0304-4238(97)00124-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0304-4238(97)00124-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0304-4238(97)00124-6

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