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Felicia amelloides

Felicia amelloides - Unknown
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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 UUID643fd336a0c17670157001
Scientific name Felicia amelloides
Authority (L.) Voss
First published in Vilm. Blumengärtn. ed. 3 1: 472 (1894)

Description Top

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Synonyms Top

Scientific name Authority First published in
Agathaea coelestis Cass. Bull. Sci. Soc. Philom. Paris 1817: 183 (1817)
Felicia amelloides O.Hoffm. ex Zahlbr. Ann. Naturhist. Hofmus. xx. (1905) 53
Cineraria amoena Salisb. Prodr. Stirp. Chap. Allerton : 200 (1796)
Aster capensis var. rotundifolius (Thunb.) Harv.
Aster capensis Less. Syn. Gen. Compos. : 168 (1832)
Aster rotundifolius Thunb. Prodr. Pl. Cap. 2: 160 (1800)
Agathaea amelloides (L.) DC. Prodr. 5: 225 (1836)
Agathaea rotundifolia Nees Gen. Sp. Aster. : 258 (1832)
Felicia rotundifolia (Thunb.) H.P.Riley & Levyns J. S. African Bot. 29: 35 (1963)
Cineraria amelloides L. Sp. Pl. ed. 2 2: 1245 (1763)
Cineraria oppositifolia Moench Methodus : 588 (1794)

Common names Top

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Language Common/alternative name
English blue daisy
English blue daisy bush
English blue felicia
Arabic نبات الفيليسيا
Arabic قراف أزرق
German kapaster
French pâquerette bleue
Polish felicja gawędkowa
Chinese 蓝菊

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow at 4°C for 3 weeks, then increase to 20°C.

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-0000130071
USDA Plants FEAM6
Tropicos 2700771
INPN 706285
KEW urn:lsid:ipni.org:names:207656-1
The Plant List gcc-9098
Missouri Botanical Garden 277192
Open Tree Of Life 48047
Observations.org 298948
NCBI Taxonomy 696374
NBN Atlas NBNSYS0200002184
IPNI 207656-1
iNaturalist 146915
GBIF 5401151
Freebase /m/03wc4_r
EPPO FELAM
EOL 6269608
Elurikkus 730726
USDA GRIN 401673
Wikipedia Felicia_amelloides
CMAUP NPO21101

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
Risk assessment of Retithrips syriacus for the EU Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, van der Werf W, Yuen J, Zappalà L, Bezerra Lima ÉF, Makowski D, Crotta M, Gobbi A, Golic D, Maiorano A, Mosbach‐Schulz O, Rossi E, Terzidou A, Vicent Civera A EFSA J 29-Apr-2024
PMCID:PMC11056851
doi:10.2903/j.efsa.2024.8741
PMID:38686341
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
Effects of knocking out three anthocyanin modification genes on the blue pigmentation of gentian flowers Tasaki K, Higuchi A, Watanabe A, Sasaki N, Nishihara M Sci Rep 01-Nov-2019
PMCID:PMC6825144
doi:10.1038/s41598-019-51808-3
PMID:31676875
Effects of chloroplast dysfunction on mitochondria: white sectors in variegated leaves have higher mitochondrial DNA levels and lower dark respiration rates than green sectors Toshoji H, Katsumata T, Takusagawa M, Yusa Y, Sakai A Protoplasma 08-Oct-2011
PMCID:PMC3382374
doi:10.1007/s00709-011-0325-y
PMID:21984314

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Catalpic acid 5385589 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols / 1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols
[(2S)-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (Z)-octadec-9-enoate 10509461 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC 781.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4bR,6R,7R,8aS)-2-ethenyl-1,6,7-trihydroxy-2,4b,8,8-tetramethyl-1,5,6,7,8a,9-hexahydrophenanthren-3-one 56954823 Click to see CC1(C2CC=C3C(C(C(=O)C=C3C2(CC(C1O)O)C)(C)C=C)O)C 332.40 unknown via CMAUP database
(1R,4S,6S,9S,10S,13S)-6-hydroxy-5,5,9,13-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-7,12-dione 5352023 Click to see CC1(C2CCC34CC(C=C3)(C(=O)CC4C2(CC(=O)C1O)C)C)C 316.40 unknown via CMAUP database
(5beta,10alpha,13R)-3alpha-Hydroxypimara-8(14),15-diene-12-one 101448906 Click to see CC1(C2CCC3=CC(C(=O)CC3C2(CCC1O)C)(C)C=C)C 302.50 unknown via CMAUP database
17-Norkaur-15-ene-3,12-dione, 13-methyl-, (8I(2),13I(2))- 100926172 Click to see CC1(C2CCC34CC(C=C3)(C(=O)CC4C2(CCC1=O)C)C)C 300.40 unknown via CMAUP database
Beyerene 107412 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C=C4)C)C)C 272.50 unknown via CMAUP database
Ent-pimara-8(14),15-diene 12314280 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C 272.50 unknown via CMAUP database
yucalexin B-22 44448252 Click to see CC1(C2CCC34CC(C=C3)(C(=O)CC4C2(CC(C1O)O)C)C)C 318.40 unknown via CMAUP database
yucalexin P-15 44448251 Click to see CC1(C2CC=C3C(C(C(=O)C=C3C2(CC(=O)C1O)C)(C)C=C)O)C 330.40 unknown via CMAUP database
yucalexin P-17 44448241 Click to see CC1(C2CCC3=CC(C(CC3C2(CC(=O)C1O)C)O)(C)C=C)C 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
ent-Kaurene 11966109 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C 272.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(16S)-16-Hydroxy-13,16-secotrachyloba-13-ene-3-one 100926173 Click to see CC1(C2CCC34CC(C(CC3C2(CCC1=O)C)C=C4)(C)O)C 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(2R,4aR,6aR,6bR,8aR,12aR,14aS,14bR)-2,4a,6b,9,9,12a,14a-heptamethyl-10-oxo-3,4,5,6a,7,8,8a,11,12,13,14,14b-dodecahydro-1H-picene-2-carboxylic acid 102134163 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4(C3=CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 454.70 unknown via CMAUP database
Isotaraxerol 12443227 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown via CMAUP database
> 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 via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 38359273 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown via CMAUP database
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14R,17R)-17-[(E,1R,4S)-4-ethyl-1,5-dimethyl-hex-2-enyl]-8,10,13-trimethyl-1,2,3,4,7,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 23246947 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2(CC=C4C3(CCC(C4)O)C)C)C)C(C)C 426.70 unknown via CMAUP database
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 12943207 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C)C(C)C 410.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Epilotaustralin 185818 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown via CMAUP database
Linamarin 11128 Click to see CC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 247.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-((6-O-(beta-D-apiofuranosyl)beta-D-glucopyranosyl)oxy)propane 10316099 Click to see CC(C)OC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O 354.35 unknown via CMAUP database
ethyl beta-D-glucopyranoside 121667 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

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