PlantaeDB Logo
Login Sign-up

Ledebouria floribunda

We don't have an image yet. Upload an image!

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 UUID64401c324831a455321037
Scientific name Ledebouria floribunda
Authority (Baker) Jessop
First published in J. S. African Bot. 36: 251 (1970)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Scilla lauta N.E.Br. Bull. Misc. Inform. Kew 1921: 299 (1921)
Scilla floribunda Baker Refug. Bot. 3: t. 188 (1870)
Scilla tricolor Baker Gard. Chron. , n.s., 14: 230 (1880)
Scilla subsecunda Baker Gard. Chron. , n.s., 16: 38 (1881)
Scilla princeps Baker Refug. Bot. 3: t. 189 (1870)
Scilla pendula Baker Refug. Bot. 3(App.): 14 (1870)
Scilla polyantha Baker Gard. Chron. , n.s., 9: 104 (1878)
Drimia pendula Burch. ex Baker J. Linn. Soc., Bot. 13: 254 (1873)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 多花油点花

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000686569
Tropicos 18403063
KEW urn:lsid:ipni.org:names:537312-1
The Plant List kew-280843
Open Tree Of Life 1095472
NCBI Taxonomy 208127
IPNI 537312-1
iNaturalist 569174
GBIF 2773770
Freebase /m/011q7vy8
EOL 1003002
USDA GRIN 412305
Wikipedia Ledebouria_floribunda
CMAUP NPO11546

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
Environmental pressures on stomatal size may drive plant genome size evolution: evidence from a natural experiment with Cape geophytes Veselý P, Šmarda P, Bureš P, Stirton C, Muasya AM, Mucina L, Horová L, Veselá K, Šilerová A, Šmerda J, Knápek O Ann Bot 31-May-2020
PMCID:PMC7380457
doi:10.1093/aob/mcaa095
PMID:32474609
HM-Chromanone Isolated from Portulaca Oleracea L. Protects INS-1 Pancreatic β Cells against Glucotoxicity-Induced Apoptosis Park JE, Seo Y, Han JS Nutrients 14-Feb-2019
PMCID:PMC6412778
doi:10.3390/nu11020404
PMID:30769910
Inferences of biogeographical histories within subfamily Hyacinthoideae using S-DIVA and Bayesian binary MCMC analysis implemented in RASP (Reconstruct Ancestral State in Phylogenies) Ali SS, Yu Y, Pfosser M, Wetschnig W Ann Bot 27-Oct-2011
PMCID:PMC3241591
doi:10.1093/aob/mcr274
PMID:22039008
Three new homoisoflavanones from the bulbs of Ledebouria floribunda. Calvo MI Fitoterapia 01-Oct-2009
doi:10.1016/J.FITOTE.2009.05.010
PMID:19446611
Homoisoflavanones from Ledebouria floribunda. Calvo MI Fitoterapia 01-Mar-2009
doi:10.1016/J.FITOTE.2008.10.006
PMID:19027834

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-glucuronide 5319484 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Linarin 5317025 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 592.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(-)-5,7-Dihydroxy-3-(4-hydroxybenzyl)-4-chromanone 9971218 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)CC3=CC=C(C=C3)O 286.28 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
(3R)-7-(3,7-dimethylocta-2,6-dienyl)-5,6-dihydroxy-3-[(4-hydroxyphenyl)methyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162869903 Click to see CC(=CCCC(=CCC1=C(C2=C(C(=O)C(CO2)CC3=CC=C(C=C3)O)C(=C1O)O)CC=C(C)C)C)C 490.60 unknown https://doi.org/10.1016/J.FITOTE.2009.05.010
(3R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,6-dihydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 163190901 Click to see CC(=CCCC(=CCC1=CC2=C(C(=O)C(CO2)CC3=CC=C(C=C3)O)C(=C1O)O)C)C 422.50 unknown https://doi.org/10.1016/J.FITOTE.2009.05.010
(3R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,6-dihydroxy-3-[(4-hydroxyphenyl)methyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 163195469 Click to see CC(=CCCC(=CCC1=C(C2=C(C(=O)C(CO2)CC3=CC=C(C=C3)O)C(=C1O)O)CC=C(C)C)C)C 490.60 unknown https://doi.org/10.1016/J.FITOTE.2009.05.010
(3S)-5-hydroxy-3-[(4-hydroxyphenyl)methyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162944564 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OCC(C4=O)CC5=CC=C(C=C5)O)O)O)O)O)O)O)O 594.60 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
(3S)-5-hydroxy-3-[(4-methoxyphenyl)methyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 163055697 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OCC(C4=O)CC5=CC=C(C=C5)OC)O)O)O)O)O)O)O 608.60 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
(3S)-5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 92446292 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)CC3=CC=C(C=C3)O 286.28 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
(3S)-5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-6-methoxy-2,3-dihydrochromen-4-one 92155498 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)CC3=CC=C(C=C3)O)O 316.30 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
(3S)-5,7-dihydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 51520425 Click to see COC1=CC=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)O 300.30 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
(3S)-5,7-dihydroxy-6-methoxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 162992637 Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C(=C(C(=C3)O)OC)O 330.30 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
(3S)-7-hydroxy-3-[(4-hydroxyphenyl)methyl]-5-methoxy-2,3-dihydrochromen-4-one 92446294 Click to see COC1=CC(=CC2=C1C(=O)C(CO2)CC3=CC=C(C=C3)O)O 300.30 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
(7R)-5-hydroxy-7-[(4-methoxyphenyl)methyl]-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163041141 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OCC(C3=O)CC4=CC=C(C=C4)OC)O)C 366.40 unknown https://doi.org/10.1016/J.FITOTE.2009.05.010
3-(4-Hydroxybenzyl)-5,7-dihydroxy-6-methoxychroman-4-one 404572 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)CC3=CC=C(C=C3)O)O 316.30 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
3,9-Dihydroeucomin 11415348 Click to see COC1=CC=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)O 300.30 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
5-Hydroxy-3-[(4-hydroxyphenyl)methyl]-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162944563 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OCC(C4=O)CC5=CC=C(C=C5)O)O)O)O)O)O)O)O 594.60 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
5-Hydroxy-3-[(4-methoxyphenyl)methyl]-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 163055696 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OCC(C4=O)CC5=CC=C(C=C5)OC)O)O)O)O)O)O)O 608.60 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
5-Hydroxy-7-[(4-methoxyphenyl)methyl]-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163041140 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OCC(C3=O)CC4=CC=C(C=C4)OC)O)C 366.40 unknown https://doi.org/10.1016/J.FITOTE.2009.05.010
5,7-Dihydroxy-6-methoxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 10687851 Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C(=C(C(=C3)O)OC)O 330.30 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006
7-(3,7-Dimethylocta-2,6-dienyl)-5,6-dihydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 162936266 Click to see CC(=CCCC(=CCC1=CC2=C(C(=O)C(CO2)CC3=CC=C(C=C3)O)C(=C1O)O)C)C 422.50 unknown https://doi.org/10.1016/J.FITOTE.2009.05.010
7-Hydroxy-3-[(4-hydroxyphenyl)methyl]-5-methoxy-2,3-dihydrochromen-4-one 71436570 Click to see COC1=CC(=CC2=C1C(=O)C(CO2)CC3=CC=C(C=C3)O)O 300.30 unknown https://doi.org/10.1016/J.FITOTE.2008.10.006

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.