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Phlomis viscosa

Phlomis viscosa - 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 UUID643fe70e44c71479825333
Scientific name Phlomis viscosa
Authority Poir.
First published in Encycl. 5: 271 (1804)

Description Top

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Synonyms Top

Scientific name Authority First published in
Phlomis glandulosa Schenk Pl. Spec. Schubert : 20 (1840)
Phlomis major Clos Bull. Soc. Bot. France 15: 7 (1868)
Phlomis polymorpha Clos Bull. Soc. Bot. France 15: 7 (1868)
Phlomis virens DC. Cat. Pl. Horti Monsp. : 132 (1813)

Common names Top

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Language Common/alternative name
Arabic أذينة دبقة
Hebrew שלהבית דביקה
Polish Żeleźniak lepki

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-0000269566
Tropicos 100241627
KEW urn:lsid:ipni.org:names:454109-1
The Plant List kew-152486
Open Tree Of Life 499282
Observations.org 150126
NCBI Taxonomy 997746
IPNI 454109-1
iNaturalist 492964
GBIF 3900599
EPPO PLMVI
Elurikkus 436568

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
Flavonoids with Anti-Herpes Simplex Virus Properties: Deciphering Their Mechanisms in Disrupting the Viral Life Cycle Šudomová M, Hassan ST Viruses 29-Nov-2023
PMCID:PMC10748012
doi:10.3390/v15122340
PMID:38140581
Isolation of two triterpenoids from Phlomis purpurea, one of them with anti-oomycete activity against Phytophthora cinnamomi, and insights into its biosynthetic pathway Fernández-Calleja L, García-Domínguez M, Redondo BI, Martín JL, Villar CJ, Lombó F Front Plant Sci 25-Aug-2023
PMCID:PMC10485375
doi:10.3389/fpls.2023.1180808
PMID:37692445
Antimicrobial and Antiviral Compounds of Phlomis viscosa Poiret Yarmolinsky L, Nakonechny F, Budovsky A, Zeigerman H, Khalfin B, Sharon E, Yarmolinsky L, Ben-Shabat S, Nisnevitch M Biomedicines 02-Feb-2023
PMCID:PMC9953047
doi:10.3390/biomedicines11020441
PMID:36830977
Leucosceptosides A and B: Two Phenyl-Ethanoid Glycosides with Important Occurrence and Biological Activities Frezza C, De Vita D, Toniolo C, Sciubba F, Tomassini L, Venditti A, Bianco A, Serafini M, Foddai S Biomolecules 02-Dec-2022
PMCID:PMC9775335
doi:10.3390/biom12121807
PMID:36551235
Medicinal Properties of Anchusa strigosa and Its Active Compounds Yarmolinsky L, Budovsky A, Khalfin B, Yarmolinsky L, Ben-Shabat S Molecules 25-Nov-2022
PMCID:PMC9741094
doi:10.3390/molecules27238239
PMID:36500332
A Novel Herbal Hydrogel Formulation of Moringa oleifera for Wound Healing Ali A, Garg P, Goyal R, Kaur G, Li X, Negi P, Valis M, Kuca K, Kulshrestha S Plants (Basel) 24-Dec-2020
PMCID:PMC7824484
doi:10.3390/plants10010025
PMID:33374419
Plant-Derived Chemicals: A Source of Inspiration for New Drugs Seidel V Plants (Basel) 13-Nov-2020
PMCID:PMC7697361
doi:10.3390/plants9111562
PMID:33202730
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157
Effect of Bioactive Phytochemicals from Phlomis viscosa Poiret on Wound Healing Yarmolinsky L, Budovsky A, Yarmolinsky L, Khalfin B, Glukhman V, Ben-Shabat S Plants (Basel) 16-Dec-2019
PMCID:PMC6963389
doi:10.3390/plants8120609
PMID:31888128
Anti-angiogenic activity of Middle East medicinal plants of the Lamiaceae family Abdallah Q, Al-Deeb I, Bader A, Hamam F, Saleh K, Abdulmajid A Mol Med Rep 12-Jun-2018
PMCID:PMC6072233
doi:10.3892/mmr.2018.9155
PMID:29901194
Pollinator importance networks illustrate the crucial value of bees in a highly speciose plant community Ballantyne G, Baldock KC, Rendell L, Willmer PG Sci Rep 21-Aug-2017
PMCID:PMC5566368
doi:10.1038/s41598-017-08798-x
PMID:28827573
Uncovering the Geroprotective Potential of Medicinal Plants from the Judea Region of Israel Budovsky A, Shteinberg A, Maor H, Duman O, Yanai H, Wolfson M, Fraifeld VE Rejuvenation Res 01-Apr-2014
PMCID:PMC3995445
doi:10.1089/rej.2013.1509
PMID:24094064
Checklist of Hymenomycetes (Aphyllophorales s.l.) and Heterobasidiomycetes in Israel Ţura D, Zmitrovich IV, Wasser SP, Nevo E Mycobiology 31-Dec-2010
PMCID:PMC3741518
doi:10.4489/MYCO.2010.38.4.256
PMID:23956665
Two New Triterpene and a New Nortriterpene Glycosides from <i>Phlomis viscosa</i> İhsan Çalış, Hasan Kırmızıbekmez, Deniz Taşdemir, Peter Rüedi Wiley 25-Mar-2004
doi:10.1002/HLCA.200490059

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 / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,4aR,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101731586 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)COC6C(C(C(C(O6)CO)O)O)O 666.80 unknown https://doi.org/10.1002/HLCA.200490059
(2S,4aR,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162867074 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)COC6C(C(C(C(O6)CO)O)O)O 666.80 unknown https://doi.org/10.1002/HLCA.200490059
10,11-Dihydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-2-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162867071 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)COC6C(C(C(C(O6)CO)O)O)O 666.80 unknown https://doi.org/10.1002/HLCA.200490059
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 19-oxosteroids
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,3R,4aS,4bS,7R,8S,10aS,10bR,12aS)-3,7-dihydroxy-1-(hydroxymethyl)-1,1',1',10a,10b-pentamethyl-2,2'-dioxospiro[3,4,4b,5,7,9,10,11,12,12a-decahydrochrysene-8,3'-cyclopentane]-4a-carboxylate 162977165 Click to see CC1(CCC2(C1=O)CCC3(C(=CCC4C3(CCC5C4(CC(C(=O)C5(C)CO)O)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C)C2O)C)C 664.80 unknown https://doi.org/10.1002/HLCA.200490059
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,7-dihydroxy-1-(hydroxymethyl)-1,1',1',10a,10b-pentamethyl-2,2'-dioxospiro[3,4,4b,5,7,9,10,11,12,12a-decahydrochrysene-8,3'-cyclopentane]-4a-carboxylate 162977164 Click to see CC1(CCC2(C1=O)CCC3(C(=CCC4C3(CCC5C4(CC(C(=O)C5(C)CO)O)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C)C2O)C)C 664.80 unknown https://doi.org/10.1002/HLCA.200490059

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