Thymelaea hirsuta - Unknown
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Internal ID UUID643ffee82ba86663508895
Scientific name Thymelaea hirsuta
Authority Endl.
First published in Gen. Pl. , Suppl. 4(2): 65 (1848)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lachnaea hirsuta Crantz Inst. Rei Herb. 1: 129 (1766)
Passerina hirsuta L. Sp. Pl. : 559 (1753)
Piptochlamys hirsuta C.A.Mey. Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 1: 358 (1843)
Passerina telonensis Gand. Dec. Pl. Nov. 1: 6 (1875)
Stellera hirsuta (L.) Oken Allg. Naturgesch. 3(3): 1492 (1841)
Sanamunda tomentosa Zumagl. Fl. Pedemont. 2: 156 (1864)
Giardia hirsuta (Endl.) C.Gerber Bull. Soc. Bot. France 46: cxii (1899)
Chlamydanthus hirsutus Griseb. Spic. Fl. Rumel. 2: 54 (1844)
Passerina metnan Forssk. Fl. Aegypt.-Arab. : 81 (1775)
Passerina polygalifolia Lapeyr. Hist. Pl. Pyrénées : 214 (1813)
Tartonia ovatifolia Raf. Autik. Bot. : 146 (1840)
Thymelaea hirsuta var. vulgaris Meisn. Prodr. 14(2): 557 1857
Thymelaea hirsuta var. rotundifolia Meisn. Prodr. 14(2): 557 1857
Thymelaea hirsuta var. angustifolia Meisn. Prodr. 14(2): 557 1857
Passerina hirsuta var. vestita Gren. & Godr. Fl. France 3(1): 63 1855
Thymelaea hirsuta var. polygalaefolia (Lapeyr.) Endl. Gen. Pl. Suppl. 4(2): 65 1848

Common names Top

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Language Common/alternative name
Spanish abolaga
Spanish sanamunda acipresada
Spanish pruebayernos
Spanish prueba yernos
Spanish passerina hirsuta var. linearis
Spanish passerina hirsuta var linearis
Spanish passerina hirsuta raza polygaliifolia
Spanish pala marina
Spanish bulaga
Spanish palmerina
Spanish boalaga
Spanish bofalaga
Spanish bohalaga
Spanish boja marina
Spanish bojalaga
Spanish bolago
Spanish bolaya
Spanish bora marina
Spanish borja marina
Spanish bufalaga marina
Spanish lechaina
Arabic مثنان أهلب
Catalan bufalaga hirsuta
Catalan pala marina
Catalan palmerina
German behaarte spatzenzunge
French passerine hirsute
French passerine hérissée
Hebrew מתנן שעיר
Kabyle aɣraz imsetɣen

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey
  • Europe
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000457608
Tropicos 32000164
INPN 126469
Flora of Italy 3152
KEW urn:lsid:ipni.org:names:832995-1
The Plant List kew-2518409
Open Tree Of Life 461201
Observations.org 128059
NCBI Taxonomy 69845
IPNI 832995-1
iNaturalist 333734
GBIF 5523602
EPPO THBHI
Elurikkus 537284
Wikipedia Thymelaea_hirsuta

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)!
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Title Authors Publication Released IDs
A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B J Ethnopharmacol 25-Mar-2024
PMCID:PMC7615571
doi:10.1016/j.jep.2023.117622
PMID:38128894
Antibacterial Metabolites Produced by Limonium lopadusanum, an Endemic Plant of Lampedusa Island Gargiulo E, Roscetto E, Galdiero U, Surico G, Catania MR, Evidente A, Taglialatela-Scafati O Biomolecules 22-Jan-2024
PMCID:PMC10813400
doi:10.3390/biom14010134
PMID:38275763
Exploring the anti-obesity bioactive compounds of Thymelaea hirsuta and Ziziphus spina-christi through integration of lipase inhibition screening and molecular docking analysis Abdallah RM, Hammoda HM, El-Gazzar NS, Ibrahim RS, Sallam SM RSC Adv 11-Sep-2023
PMCID:PMC10494966
doi:10.1039/d3ra05826c
PMID:37701277
Past, present and future trends in the remediation of heavy-metal contaminated soil - Remediation techniques applied in real soil-contamination events Sánchez-Castro I, Molina L, Prieto-Fernández MÁ, Segura A Heliyon 27-May-2023
PMCID:PMC10360604
doi:10.1016/j.heliyon.2023.e16692
PMID:37484356
Recent Developments in Polyphenol Applications on Human Health: A Review with Current Knowledge Rathod NB, Elabed N, Punia S, Ozogul F, Kim SK, Rocha JM Plants (Basel) 07-Mar-2023
PMCID:PMC10053535
doi:10.3390/plants12061217
PMID:36986905
A Review of Medicinal Plants with Renoprotective Activity in Diabetic Nephropathy Animal Models Putra IM, Fakhrudin N, Nurrochmad A, Wahyuono S Life (Basel) 16-Feb-2023
PMCID:PMC9963806
doi:10.3390/life13020560
PMID:36836916
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
Phytochemical Screening, Antifungal, and Anticancer Activities of Medicinal Plants Thymelaea Hirsuta, Urginea Maritima, and Plantago Albicans El-Bondkly EA, Al Shammari B, El-Gendy MM, Alsafari IA, El-Bondkly AA, El-Shenawy FS, El-Bondkly AM Biomed Res Int 30-Dec-2022
PMCID:PMC9822746
doi:10.1155/2022/9544915
PMID:36619300
Ethnopharmacobotany and Diversity of Mediterranean Endemic Plants in Marmilla Subregion, Sardinia, Italy Cocco E, Maccioni D, Sanjust E, Falconieri D, Farris E, Maxia A Plants (Basel) 18-Nov-2022
PMCID:PMC9695302
doi:10.3390/plants11223165
PMID:36432894
Molecular Analysis of the Melanogenesis Inhibitory Effect of Saponins-Rich Fraction of Argania spinosa Leaves Extract Villareal MO, Chaochaiphat T, Makbal R, Gadhi C, Isoda H Molecules 10-Oct-2022
PMCID:PMC9571574
doi:10.3390/molecules27196762
PMID:36235295
Identification of a Hydroxygallic Acid Derivative, Zingibroside R1 and a Sterol Lipid as Potential Active Ingredients of Cuscuta chinensis Extract That Has Neuroprotective and Antioxidant Effects in Aged Caenorhabditis elegans Sayed SM, Alseekh S, Siems K, Fernie AR, Luyten W, Schmitz-Linneweber C, Saul N Nutrients 09-Oct-2022
PMCID:PMC9570774
doi:10.3390/nu14194199
PMID:36235851
Aspergillus flavus YRB2 from Thymelaea hirsuta (L.) Endl., a non-aflatoxigenic endophyte with ability to overexpress defense-related genes against Fusarium root rot of maize Rashad YM, Abdalla SA, Shehata AS BMC Microbiol 30-Sep-2022
PMCID:PMC9524039
doi:10.1186/s12866-022-02651-6
PMID:36175855
Yuanhuacin and Related Anti-Inflammatory and Anticancer Daphnane Diterpenes from Genkwa Flos—An Overview Bailly C Biomolecules 23-Jan-2022
PMCID:PMC8961543
doi:10.3390/biom12020192
PMID:35204693
DNA Barcoding of Two Thymelaeaceae Species: Daphne mucronata Royle and Thymelaea hirsuta (L.) Endl Alkaraki AK, Aldmoor MA, Lahham JN, Awad M Plants (Basel) 16-Oct-2021
PMCID:PMC8537861
doi:10.3390/plants10102199
PMID:34686008
Characterizing Biomass Yield and Nutritional Value of Selected Indigenous Range Species from Arid Tunisia Louhaichi M, Gamoun M, Hassan S, Abdallah MA Plants (Basel) 27-Sep-2021
PMCID:PMC8539911
doi:10.3390/plants10102031
PMID:34685840

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 / Diterpenoids / Rhamnofolane and daphnane diterpenoids
[(1R,2R,6S,7R,8R,10S,11R,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-14-nonyl-5-oxo-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 162945571 Click to see CCCCCCCCCC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C=CC7=CC=C(C=C7)O)C)C=C(C6=O)C)O)O)CO 694.80 unknown https://doi.org/10.1021/NP800808H
[(1R,2R,6S,7S,8R,10S,11R,12R,14S,16S,17R,18R)-14-[(E)-hept-1-enyl]-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-3-phenylprop-2-enoate 162923405 Click to see CCCCCC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C=CC7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 648.70 unknown https://doi.org/10.1021/NP800808H
[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-14-[(E)-hept-1-enyl]-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-3-phenylprop-2-enoate 162923406 Click to see CCCCCC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C=CC7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 648.70 unknown https://doi.org/10.1021/NP800808H
[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-16-isopropenyl-4,18-dimethyl-5-oxo-14-phenyl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (2E,4E,6E)-deca-2,4,6-trienoate 101281330 Click to see CCCC=CC=CC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C 646.70 unknown https://doi.org/10.1016/0031-9422(90)83044-2
[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-but-2-enoate 163191332 Click to see CC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C 566.60 unknown https://doi.org/10.1016/0031-9422(90)83044-2
[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-heptadec-2-enoate 163069578 Click to see CCCCCCCCCCCCCCC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C 748.90 unknown https://doi.org/10.1016/0031-9422(90)83044-2
[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-pent-2-enoate 163012668 Click to see CCC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C 580.60 unknown https://doi.org/10.1016/0031-9422(90)83044-2
[(1R,2R,6S,7S,8R,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (2E,4E,6E)-deca-2,4,6-trienoate 118701514 Click to see CCCC=CC=CC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C 646.70 unknown https://doi.org/10.1016/0031-9422(90)83044-2
[(2R,6S,7S,8R,10S,11S,12R,16S,17R,18R)-14-[(E)-hept-1-enyl]-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-3-phenylprop-2-enoate 101477052 Click to see CCCCCC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C=CC7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 648.70 unknown https://doi.org/10.1021/NP800808H
[(2R,6S,7S,8R,10S,11S,12R,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-14-nonyl-5-oxo-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 101477053 Click to see CCCCCCCCCC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C=CC7=CC=C(C=C7)O)C)C=C(C6=O)C)O)O)CO 694.80 unknown https://doi.org/10.1021/NP800808H
[14-Hept-1-enyl-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] 3-phenylprop-2-enoate 74932761 Click to see CCCCCC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C=CC7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 648.70 unknown https://doi.org/10.1021/NP800808H
[6,7-Dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] 3-phenylprop-2-enoate 5462 Click to see CC1C(C2(C3C4C1(C5C=C(C(=O)C5(C(C6(C4O6)CO)O)O)C)OC(O3)(O2)C7=CC=CC=C7)C(=C)C)OC(=O)C=CC8=CC=CC=C8 628.70 unknown https://doi.org/10.1016/0031-9422(90)83044-2
[6,7-Dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] but-2-enoate 162861905 Click to see CC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C 566.60 unknown https://doi.org/10.1016/0031-9422(90)83044-2
[6,7-Dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] deca-2,4,6-trienoate 99839 Click to see CCCC=CC=CC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C 646.70 unknown https://doi.org/10.1016/0031-9422(90)83044-2
12-Benzoyldaphnetoxin 428494 Click to see CC1C(C2(C3C4C1(C5C=C(C(=O)C5(C(C6(C4O6)CO)O)O)C)OC(O3)(O2)C7=CC=CC=C7)C(=C)C)OC(=O)C8=CC=CC=C8 602.60 unknown https://doi.org/10.1016/0031-9422(90)83044-2
CID 5281366 5281366 Click to see CC1C(C2(C3C4C1(C5C=C(C(=O)C5(C(C6(C4O6)CO)O)O)C)OC(O3)(O2)C7=CC=CC=C7)C(=C)C)OC(=O)C=CC8=CC=CC=C8 628.70 unknown https://doi.org/10.1016/0031-9422(90)83044-2
Genkwadaphnin 73351913 Click to see CC1C(C2(C3C4C1(C5C=C(C(=O)C5(C(C6(C4O6)CO)O)O)C)OC(O3)(O2)C7=CC=CC=C7)C(=C)C)OC(=O)C8=CC=CC=C8 602.60 unknown https://doi.org/10.1016/0031-9422(90)83044-2
Gnidicin 70691946 Click to see CC1C(C2(C3C4C1(C5C=C(C(=O)C5(C(C6(C4O6)CO)O)O)C)OC(O3)(O2)C7=CC=CC=C7)C(=C)C)OC(=O)C=CC8=CC=CC=C8 628.70 unknown https://doi.org/10.1016/0031-9422(90)83044-2
> Nucleosides, nucleotides, and analogues / Purine nucleotides / Purine ribonucleotides / Purine ribonucleoside triphosphates
[[(2R,3R,4S,5S)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate 23638216 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N 507.18 unknown https://doi.org/10.1016/0031-9422(90)83044-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin 5281406 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)OC3=CC4=C(C=C3)C=CC(=O)O4)O 352.30 unknown https://doi.org/10.1002/(SICI)1099-1573(199806)12:4<282::AID-PTR225>3.0.CO;2-X

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