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Aeonium lindleyi

Aeonium lindleyi - Unknown
Part: Unknown
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 UUID6440079555814797188457
Scientific name Aeonium lindleyi
Authority Webb & Berthel.
First published in Hist. Nat. Iles Canaries 3(2; 1): 189 (1840)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Spanish bejequillo gomereta
Spanish sempervivum lindleyi
Chinese 登天乐

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Aeonium lindleyi subsp. viscatum (Bolle) Bañares Willdenowia 38: 481 (2008)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000521676
Tropicos 8902629
KEW urn:lsid:ipni.org:names:272240-1
The Plant List kew-2623603
Open Tree Of Life 604641
Observations.org 132076
NCBI Taxonomy 111153
IPNI 272240-1
iNaturalist 558334
GBIF 7334043
EOL 5550015
Elurikkus 590063

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
Inter- and intra-island speciation and their morphological and ecological correlates in Aeonium (Crassulaceae), a species-rich Macaronesian radiation Messerschmid TF, Abrahamczyk S, Bañares-Baudet Á, Brilhante MA, Eggli U, Hühn P, Kadereit JW, dos Santos P, de Vos JM, Kadereit G Ann Bot 23-Feb-2023
PMCID:PMC10147336
doi:10.1093/aob/mcad033
PMID:36821492
Scientists’ warning – The outstanding biodiversity of islands is in peril Fernández-Palacios JM, Kreft H, Irl SD, Norder S, Ah-Peng C, Borges PA, Burns KC, de Nascimento L, Meyer JY, Montes E, Drake DR Glob Ecol Conserv 01-Nov-2021
PMCID:PMC8556160
doi:10.1016/j.gecco.2021.e01847
PMID:34761079
Are thick leaves, large mesophyll cells and small intercellular air spaces requisites for CAM? Herrera A Ann Bot 23-Jan-2020
PMCID:PMC7218806
doi:10.1093/aob/mcaa008
PMID:31970387
Leishmanicidal and reversal multidrug resistance constituents from Aeonium lindleyi. Kennedy ML, Cortés F, Piñero JE, Castanys S, López-Arencibia A, Gamarro F, Bazzocchi IL, Jiménez IA Planta Med 01-Jan-2011
doi:10.1055/S-0030-1250144
PMID:20665372
A gas-liquid chromatographic and spectrometric identification of 2-methyldotriacontane G. Eglinton, R.J. Hamilton, W.B. Kelly, R.I. Reed Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86136-1

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methyldotriacontane 74399 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(C)C 464.90 unknown https://doi.org/10.1016/S0031-9422(00)86136-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4aS,8aS)-1-[(3R)-5-hydroxy-3-methylpentyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 93501015 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCO 310.50 unknown https://doi.org/10.1055/S-0030-1250144
(2S,4aR,5S,8aR)-5-[(3R)-5-hydroxy-3-methylpentyl]-1,1,4a-trimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol 15818304 Click to see CC(CCC1C(=C)CCC2C1(CCC(C2(C)C)O)C)CCO 308.50 unknown https://doi.org/10.1055/S-0030-1250144
(4aS,8aS)-4-[(3R)-5-hydroxy-3-methylpentyl]-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-1H-naphthalen-2-one 162936246 Click to see CC1=C(C2(CCCC(C2CC1=O)(C)C)C)CCC(C)CCO 306.50 unknown https://doi.org/10.1055/S-0030-1250144
[(3R)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentyl] acetate 162919545 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCOC(=O)C 352.60 unknown https://doi.org/10.1055/S-0030-1250144
1-(5-hydroxy-3-methylpentyl)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 14239431 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCO 310.50 unknown https://doi.org/10.1055/S-0030-1250144
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1055/S-0030-1250144
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1055/S-0030-1250144
> 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 https://doi.org/10.1055/S-0030-1250144
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Artemexitin 44259710 Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 346.30 unknown https://doi.org/10.1055/S-0030-1250144
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4H-1-Benzopyran-4-one, 5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxy- 5748580 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)OC)O)O 374.30 unknown https://doi.org/10.1055/S-0030-1250144
Combretol 12303802 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)OC)OC)O 388.40 unknown https://doi.org/10.1055/S-0030-1250144
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown https://doi.org/10.1055/S-0030-1250144
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown https://doi.org/10.1055/S-0030-1250144
Myricetin 3,7,3',5'-tetramethyl ether 44259713 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)O)OC)O 374.30 unknown https://doi.org/10.1055/S-0030-1250144
Pachypodol 5281677 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O 344.30 unknown https://doi.org/10.1055/S-0030-1250144
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown https://doi.org/10.1055/S-0030-1250144

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