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Aeonium cuneatum

Aeonium cuneatum - 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 UUID64400792d3d73434232635
Scientific name Aeonium cuneatum
Authority Webb & Berthel.
First published in Hist. Nat. Iles Canaries 3(2; 1): 184 (1840)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sempervivum cuneatum Webb & Berthel. Hist. Nat. Iles Canaries 3(2; 1): 197 (1841)

Common names Top

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Language Common/alternative name
Welsh aeoniwm
Chinese 熏染香

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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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-0000521638
Tropicos 8902618
INPN 610758
KEW urn:lsid:ipni.org:names:272212-1
The Plant List kew-2623568
Open Tree Of Life 82926
Observations.org 113987
NCBI Taxonomy 111147
NBN Atlas NHMSYS0000455623
IPNI 272212-1
iNaturalist 129063
GBIF 4198315
Freebase /m/05zvg_n
EPPO AEJCU
EOL 5549990
USDA GRIN 1572
Wikipedia Aeonium_cuneatum
CMAUP NPO11678

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
Benzophenones-natural metabolites with great Hopes in drug discovery: structures, occurrence, bioactivities, and biosynthesis Ibrahim SR, Fahad ALsiyud D, Alfaeq AY, Mohamed SG, Mohamed GA RSC Adv 04-Aug-2023
PMCID:PMC10402873
doi:10.1039/d3ra02788k
PMID:37546221
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
Biogeography of Mediterranean Hotspot Biodiversity: Re-Evaluating the 'Tertiary Relict' Hypothesis of Macaronesian Laurel Forests Kondraskov P, Schütz N, Schüßler C, de Sequeira MM, Guerra AS, Caujapé-Castells J, Jaén-Molina R, Marrero-Rodríguez Á, Koch MA, Linder P, Kovar-Eder J, Thiv M PLoS One 14-Jul-2015
PMCID:PMC4501571
doi:10.1371/journal.pone.0132091
PMID:26173113
Timing and Tempo of Early and Successive Adaptive Radiations in Macaronesia Kim SC, McGowen MR, Lubinsky P, Barber JC, Mort ME, Santos-Guerra A PLoS One 14-May-2008
PMCID:PMC2367450
doi:10.1371/journal.pone.0002139
PMID:18478126

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 / Anthracenes / Anthraquinones
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aS,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 7092625 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 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
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 5491386 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 410.70 unknown via CMAUP database
5alpha-Stigmasta-22-en-3-one 91617412 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown via CMAUP database
5alpha-Stigmastan-3-one 5491512 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(=O)C4)C)C)C(C)C 414.70 unknown via CMAUP database
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown via CMAUP database
6beta-Hydroxystigmast-4,22-dien-3-one 91034535 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 426.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
2,6-Dimethoxy-1-acetonylquinol 241783 Click to see CC(=O)CC1(C(=CC(=O)C=C1OC)OC)O 226.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(4-Hydroxy-3-methoxyphenyl)propan-1-one 15782 Click to see CCC(=O)C1=CC(=C(C=C1)O)OC 180.20 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(3R)-3-hydroxy-2,2-dimethyl-3,4-dihydrobenzo[g]chromene-5,10-dione 44245542 Click to see CC1(C(CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)O)C 258.27 unknown via CMAUP database
[(3R)-2,2-dimethyl-5,10-dioxo-3,4-dihydrobenzo[g]chromen-3-yl] (2E,6E)-2,6-dimethylocta-2,6-dienoate 101857710 Click to see CC=C(C)CCC=C(C)C(=O)OC1CC2=C(C(=O)C3=CC=CC=C3C2=O)OC1(C)C 408.50 unknown via CMAUP database
[(3R)-2,2-dimethyl-5,10-dioxo-3,4-dihydrobenzo[g]chromen-3-yl] (E)-5-[(2R,3R)-2,3-dimethyloxiran-2-yl]-2-methylpent-2-enoate 10693614 Click to see CC1C(O1)(C)CCC=C(C)C(=O)OC2CC3=C(C(=O)C4=CC=CC=C4C3=O)OC2(C)C 424.50 unknown via CMAUP database
3,4-Dihydro-3,3-dimethyl-2H-naphtho(2,3-b)pyran-5,10-dione 178515 Click to see CC1(CC2=C(C(=O)C3=CC=CC=C3C2=O)OC1)C 242.27 unknown via CMAUP database
ent-Rhinacanthin A 102098593 Click to see CC1(C(CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)O)C 258.27 unknown via CMAUP database
ent-Rhinacanthin B 102098594 Click to see CC=C(C)CCC=C(C)C(=O)OC1CC2=C(C(=O)C3=CC=CC=C3C2=O)OC1(C)C 408.50 unknown via CMAUP database
Rhinacanthone 196964 Click to see CC1(CC2=C(C3=CC=CC=C3C(=O)C2=O)OC1)C 242.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database

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