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Thymelaea lythroides

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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 UUID64405a1c419a8213405021
Scientific name Thymelaea lythroides
Authority Barratte & Murb.
First published in Acta Univ. Lund., 2 , 2(1): 69 (1905)

Description Top

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Synonyms Top

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Common names Top

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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-0001282372
Tropicos 50317133
KEW urn:lsid:ipni.org:names:832999-1
The Plant List tro-50317133
Open Tree Of Life 664733
NCBI Taxonomy 224054
IUCN Red List 163382540
IPNI 832999-1
GBIF 5523592
EOL 5468645

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
Tick infestation in spur-thighed tortoise population: a pilot study for unraveling epidemiological patterns and demographic consequences Segura A, Rafael M, Vaz-Rodrigues R, Rodríguez O, Gortázar C, de la Fuente J Exp Appl Acarol 16-Nov-2023
PMCID:PMC10689538
doi:10.1007/s10493-023-00863-7
PMID:37973690
Differences in Reproductive Success in Young and Old Females of a Long-Lived Species Segura A, Rodriguez-Caro RC, Graciá E, Acevedo P Animals (Basel) 10-Feb-2021
PMCID:PMC7916336
doi:10.3390/ani11020467
PMID:33578640
Predation of young tortoises by ravens: the effect of habitat structure on tortoise detectability and abundance Segura A, Jimenez J, Acevedo P Sci Rep 05-Feb-2020
PMCID:PMC7002411
doi:10.1038/s41598-020-58851-5
PMID:32024887
Botanicals as modulators of depression and mechanisms involved Zhang Z, Deng T, Wu M, Zhu A, Zhu G Chin Med 15-Jul-2019
PMCID:PMC6628492
doi:10.1186/s13020-019-0246-9
PMID:31338119
The Chemistry and Biological Activities of Natural Products from Northern African Plant Families: From Taccaceae to Zygophyllaceae Ntie-Kang F, Njume LE, Malange YI, Günther S, Sippl W, Yong JN Nat Prod Bioprospect 01-Mar-2016
PMCID:PMC4805656
doi:10.1007/s13659-016-0091-9
PMID:26931529
Bioactive Metabolites from Chaetomium aureum: Structure Elucidation and Inhibition of the Hsp90 Machine Chaperoning Activity Kabbaj FZ, Lu S, Faouzi ME, Meddah B, Proksch P, Cherrah Y, Altenbach HJ, Aly AH, Chadli A, Debbab A Bioorg Med Chem 20-Nov-2014
PMCID:PMC4274242
doi:10.1016/j.bmc.2014.11.021
PMID:25482429
Chemical constituents from aerial parts of Thymelaea lythroides Fatima Zahra Kabbaj, Daowan Lai, Bouchra Meddah, Hans-Josef Altenbach, Yahia Cherrah, Peter Proksch, My El Abbes Faouzi, Abdessamad Debbab Elsevier BV 17-Sep-2013
doi:10.1016/J.BSE.2013.08.013

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 / Benzoyl derivatives
Daphnenone 57338679 Click to see C1=CC=C(C=C1)CCC=CC(=O)C2=CC=C(C=C2)O 252.31 unknown https://doi.org/10.1016/J.BSE.2013.08.013
> Lignans, neolignans and related compounds / Furanoid lignans
5-[(3S,3aR,6S,6aR)-3-(1,3-benzodioxol-5-yl)-3a,6a-dimethyl-1,3,4,6-tetrahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 162854057 Click to see CC12COC(C1(COC2C3=CC4=C(C=C3)OCO4)C)C5=CC6=C(C=C5)OCO6 382.40 unknown https://doi.org/10.1016/J.BSE.2013.08.013
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Wikstromol 99938 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown https://doi.org/10.1016/J.BSE.2013.08.013
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
Bassiatin 10038289 Click to see CC(C)C1C(=O)N(C(C(=O)O1)CC2=CC=CC=C2)C 261.32 unknown https://doi.org/10.1016/J.BSE.2013.08.013
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Daphneolone 5316300 Click to see C1=CC=C(C=C1)CCC(CC(=O)C2=CC=C(C=C2)O)O 270.32 unknown https://doi.org/10.1016/J.BSE.2013.08.013
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
3-hydroxy-3-methyl-5-oxo-5-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[6-methoxy-2-oxo-3-(2-oxochromen-7-yl)oxychromen-7-yl]oxyoxan-2-yl]methoxy]pentanoic acid 14463052 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C3C=C(C(=O)OC3=C2)OC4=CC5=C(C=C4)C=CC(=O)O5)OC)O)O)O)O 658.60 unknown https://doi.org/10.1016/J.BSE.2013.08.013

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