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Phlomis floccosa

Phlomis floccosa - 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 UUID643fe70593562905536522
Scientific name Phlomis floccosa
Authority D.Don
First published in Edwards's Bot. Reg. 15: t. 1300 (1830)

Description Top

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Synonyms Top

Scientific name Authority First published in
Phlomis bicolor Benth. Labiat. Gen. Spec. 629. 1834 [Aug 1834]

Common names Top

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Language Common/alternative name
Arabic أذينة عهنية
Arabic زهيرة

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-0000269294
Tropicos 17604844
KEW urn:lsid:ipni.org:names:453893-1
The Plant List kew-152232
Open Tree Of Life 145274
Observations.org 125488
NCBI Taxonomy 572125
IPNI 453893-1
iNaturalist 966696
GBIF 3887961
EPPO PLMFL
Elurikkus 434001

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
Bio-Guided Isolation of SARS-CoV-2 Main Protease Inhibitors from Medicinal Plants: In Vitro Assay and Molecular Dynamics Abdallah HM, El-Halawany AM, Darwish KM, Algandaby MM, Mohamed GA, Ibrahim SR, Koshak AE, Elhady SS, Fadil SA, Alqarni AA, Abdel-Naim AB, Elfaky MA Plants (Basel) 24-Jul-2022
PMCID:PMC9332707
doi:10.3390/plants11151914
PMID:35893619
Anti-Candida Activity of Essential Oils from Lamiaceae Plants from the Mediterranean Area and the Middle East Potente G, Bonvicini F, Gentilomi GA, Antognoni F Antibiotics (Basel) 09-Jul-2020
PMCID:PMC7400371
doi:10.3390/antibiotics9070395
PMID:32660009
Iridoid glucosides from Phlomis rotata Cheng-Zhong Zhang, Chong Li, Shi-Ian Feng, Jian-Gong Shi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83486-5
Flavonoids of Phlomis aurea and P. floccosa Sabry I. El-Negoumy, Mohamed F. Abdalla, Nabiel A.M. Saleh Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(86)88052-9

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 / Iridoid O-glycosides
Durantoside II 6443018 Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)OC)O 582.50 unknown https://doi.org/10.1016/0031-9422(91)83486-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
trans-4-Methoxycinnamic acid 699414 Click to see COC1=CC=C(C=C1)C=CC(=O)O 178.18 unknown https://doi.org/10.1016/0031-9422(91)83486-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(2S)-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 163190331 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1016/0031-9422(86)88052-9
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 163191424 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O)O 608.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 21721979 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163185562 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(4S,5S)-3,4,5-trihydroxy-6-[[(2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163192941 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O)O 608.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
Echinacin 6439941 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9

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