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Periploca laevigata

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff77f522ac054364995
Scientific name Periploca laevigata
Authority Aiton
First published in Hort. Kew. 1: 301 (1789)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Periploca oleifolia Salisb. Prodr. Stirp. Chap. Allerton : 148 (1796)
Periploca punicifolia Cav. Icon. 3: 9 (1795)
Periploca laevigata f. anomalis G.Kunkel Cuad. Bot. Canaria 16: 44. 1972
Periploca laevigata f. obovata G.Kunkel Cuad. Bot. Canaria 28: 61. 1977 [1976 publ. 1977]
Periploca laevigata f. undulata G.Kunkel Cuad. Bot. Canaria 28: 61. 1977 [1976 publ. 1977]

Common names Top

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Language Common/alternative name
German glatte baumschlinge

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-0000392086
Tropicos 2604025
KEW urn:lsid:ipni.org:names:100468-1
The Plant List kew-2404061
Open Tree Of Life 270064
Observations.org 131139
NCBI Taxonomy 413294
IPNI 100468-1
iNaturalist 343441
iNaturalist 343439
iNaturalist 343440
iNaturalist 343438
GBIF 6022574
EPPO PRLLA
EOL 5332071
USDA GRIN 27369
Wikipedia Periploca_laevigata
PaleoBotany 72222

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
Evidence for Reductions in Physical and Chemical Plant Defense Traits in Island Flora Freedman MG, Long RW, Ramírez SR, Strauss SY Plants (Basel) 03-Apr-2024
PMCID:PMC11013342
doi:10.3390/plants13071026
PMID:38611555
Biochemical Composition, Antioxidant Capacity and Protective Effects of Three Fermented Plants Beverages on Hepatotoxicity and Nephrotoxicity Induced by Carbon Tetrachloride in Mice Gadhoumi H, Dhouafli Z, Yeddes W, serairi beji R, Miled K, Trifi M, Chirchi A, Saidani Tounsi M, Hayouni EA Indian J Microbiol 26-Dec-2023
PMCID:PMC10924858
doi:10.1007/s12088-023-01172-8
PMID:38468731
Quorum sensing gene regulation in Staphylococcus epidermidis reduces the attraction of Aedes aegypti (L.) (Diptera: Culicidae) Kim D, Crippen TL, Jordan HR, Tomberlin JK Front Microbiol 22-Jun-2023
PMCID:PMC10324375
doi:10.3389/fmicb.2023.1208241
PMID:37426032
Feeding Ecology of the Cuvier’s Gazelle (Gazella cuvieri, Ogilby, 1841) in the Sahara Desert Herrera-Sánchez FJ, López O, Rodríguez-Siles J, Díaz-Portero MÁ, Arredondo Á, Sáez JM, Álvarez B, Cancio I, de Lucas J, Pérez J, Valenzuela G, Martínez-Valderrama J, Sánchez-Cerdá M, Qninba A, Virgós E, Calleja JA, Bartolomé J, Albanell E, Serrano E, Abáigar T, Gil-Sánchez JM Animals (Basel) 06-Feb-2023
PMCID:PMC9951649
doi:10.3390/ani13040567
PMID:36830354
A New Lavender (Lavandula multifida L.) Ecotype from Arid Tunisia, with Differential Essential Oil Composition and Higher Antimicrobial Potential Tofah ML, Mseddi K, Al-Abbasi OK, Ben Yazid A, Khechine A, Gdoura R, Khannous L Life (Basel) 30-Dec-2022
PMCID:PMC9866874
doi:10.3390/life13010103
PMID:36676052
Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview Motti R, Paura B, Cozzolino A, de Falco B Plants (Basel) 28-Nov-2022
PMCID:PMC9736219
doi:10.3390/plants11233272
PMID:36501312
Isolation of a New Polysaccharide from Dandelion Leaves and Evaluation of Its Antioxidant, Antibacterial, and Anticancer Activities Li M, Zhang H, Hu X, Liu Y, Liu Y, Song M, Wu R, Wu J Molecules 07-Nov-2022
PMCID:PMC9658512
doi:10.3390/molecules27217641
PMID:36364468
Two Novel Polysaccharides From Clitocybe squamulosa: Their Isolation, Structures, and Bioactivities Guo D, Lei J, Xu L, Cheng Y, Feng C, Meng J, Chang M, Geng X Front Nutr 30-Jun-2022
PMCID:PMC9280651
doi:10.3389/fnut.2022.934769
PMID:35845786
Determination of Anti-Alzheimer’s Disease Activity of Selected Plant Ingredients Tuzimski T, Petruczynik A Molecules 18-May-2022
PMCID:PMC9147832
doi:10.3390/molecules27103222
PMID:35630702
Antimalarial Activity of Solvent Fractions of the Stem Bark of Periploca linearifolia Quart.-Dill. & A.Rich. (Asclepiadaceae) Against Plasmodium berghei in Mice Belay WY, Gurmu AE, Wubneh ZB J Exp Pharmacol 11-Jan-2022
PMCID:PMC8761000
doi:10.2147/JEP.S328954
PMID:35046734
Characterization and phytochemical constituents of Periploca hydaspidis Falc crude extract and its anticancer activities Ali S, Khan MR, Batool R, Shah SA, Iqbal J, Abbasi BA, Yaseen T, Zahra N, Aldhahrani A, Althobaiti F Saudi J Biol Sci 12-Aug-2021
PMCID:PMC8459161
doi:10.1016/j.sjbs.2021.08.020
PMID:34588860
Phytochemicals of Periploca aphylla Dcne. ameliorated streptozotocin-induced diabetes in rat Rashid U, Khan MR Environ Health Prev Med 22-Mar-2021
PMCID:PMC7986563
doi:10.1186/s12199-021-00962-0
PMID:33752586
Recent Advances in the Chemistry of Bioactive Compounds from Plants and Soil Microbes: a Review Haruna A, Yahaya SM 08-Feb-2021
PMCID:PMC7869076
doi:10.1007/s42250-020-00213-9
Identification of phytochemicals from North African plants for treating Alzheimer’s diseases and of their molecular targets by in silico network pharmacology approach Raafat K J Tradit Complement Med 12-Aug-2020
PMCID:PMC8116716
doi:10.1016/j.jtcme.2020.08.002
PMID:34012873
Identifying priority conservation areas in a Saharan environment by highlighting the endangered Cuvier’s Gazelle as a flagship species Herrera-Sánchez FJ, Gil-Sánchez JM, Álvarez B, Cancio I, de Lucas J, Arredondo Á, Díaz-Portero MÁ, Rodríguez-Siles J, Sáez JM, Pérez J, McCain E, Qninba A, Abáigar T Sci Rep 19-May-2020
PMCID:PMC7237411
doi:10.1038/s41598-020-65188-6
PMID:32427930

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S,2S,3S,5S)-2-ethenyl-2-(hydroxymethyl)-3,5-bis(prop-1-en-2-yl)cyclohexan-1-ol 14488238 Click to see CC(=C)C1CC(C(C(C1)O)(CO)C=C)C(=C)C 236.35 unknown https://doi.org/10.1021/NP50064A021
(2S,3S,5S)-2-ethenyl-2-(hydroxymethyl)-3,5-bis(prop-1-en-2-yl)cyclohexan-1-ol 162950132 Click to see 236.35 unknown https://doi.org/10.1021/NP50064A021
Periplocadiol 183691 Click to see 236.35 unknown https://doi.org/10.1021/NP50064A021
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aS,5bR,9S,11aR,13aR)-3a,5a,5b,8,8,11a,13a-heptamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-ol 163067287 Click to see 440.70 unknown https://doi.org/10.1016/J.ARABJC.2013.10.026
[(1R,3aR,5aS,5bR,9S,11aR,13aR)-3a,5a,5b,8,8,11a,13a-heptamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-yl] 3-hydroxydocosanoate 162817535 Click to see 779.30 unknown https://doi.org/10.1016/J.ARABJC.2013.10.026
[(1R,3aR,5aS,5bR,9S,11aR,13aR)-3a,5a,5b,8,8,11a,13a-heptamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-yl] 3-hydroxyhexadecanoate 162817542 Click to see 695.20 unknown https://doi.org/10.1016/J.ARABJC.2013.10.026
[(1R,3aR,5aS,5bR,9S,11aR,13aR)-3a,5a,5b,8,8,11a,13a-heptamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-yl] 3-hydroxyicosanoate 162817537 Click to see 751.30 unknown https://doi.org/10.1016/J.ARABJC.2013.10.026
[(1R,3aR,5aS,5bR,9S,11aR,13aR)-3a,5a,5b,8,8,11a,13a-heptamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-yl] 3-hydroxyoctadecanoate 162817539 Click to see CCCCCCCCCCCCCCCC(CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3(CCC5(C4C(CC5)C(=C)C)C)C)C)C)C)O 723.20 unknown https://doi.org/10.1016/J.ARABJC.2013.10.026
[(1R,3aR,5aS,5bR,9S,11aR,13aR)-3a,5a,5b,8,8,11a,13a-heptamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-yl] acetate 162873413 Click to see 482.80 unknown https://doi.org/10.1016/J.ARABJC.2013.10.026
[(1R,3aR,5aS,5bR,9S,11aR,13aR)-3a,5a,5b,8,8,11a,13a-heptamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12,13,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-yl] icosanoate 162817544 Click to see 735.30 unknown https://doi.org/10.1016/J.ARABJC.2013.10.026
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1021/NP50064A021
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 https://doi.org/10.1021/NP50064A021
Beta-Amyrin Acetate 92156 Click to see 468.80 unknown https://doi.org/10.1021/NP50064A021
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP50064A021
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP50064A021
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1021/NP50064A021

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