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Phlomis grandiflora

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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 UUID643fe70625f69106855015
Scientific name Phlomis grandiflora
Authority H.S.Thomps.
First published in Ann. Bot. (Oxford) 19: 441 (1905)

Description Top

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Synonyms Top

Scientific name Authority First published in
Phlomis fimbrilligera Hub.-Mor. Bauhinia 1: 107 (1958)
Phlomis grandiflora var. fimbrilligera (Hub.-Mor.) Hub.-Mor. Fl. Turkey 7: 113 (1982)

Common names Top

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Language Common/alternative name
Arabic أذينة كبيرة الأزهار

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-0000269311
Tropicos 100241512
KEW urn:lsid:ipni.org:names:453905-1
The Plant List kew-152248
Open Tree Of Life 924597
NCBI Taxonomy 997719
IPNI 453905-1
iNaturalist 904294
GBIF 7307247
Wikipedia Phlomis_grandiflora

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
Phlomis fruticosa L. exerts in vitro antineurodegenerative and antioxidant activities and induces prooxidant effect in glioblastoma cell line Stojkovic D, Drakulic D, Dias MI, Zengin G, Barros L, Ivanov M, Gašic U, Rajcevic N, Stevanovic M, Ferreira IC, Sokovic M EXCLI J 14-Feb-2022
PMCID:PMC8971322
doi:10.17179/excli2021-4487
PMID:35368464
Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece Musarella CM, Brullo S, del Galdo GG Plants (Basel) 30-Nov-2020
PMCID:PMC7760968
doi:10.3390/plants9121678
PMID:33266088
The bear in Eurasian plant names: motivations and models Kolosova V, Svanberg I, Kalle R, Strecker L, Özkan AM, Pieroni A, Cianfaglione K, Molnár Z, Papp N, Łuczaj Ł, Dimitrova D, Šeškauskaitė D, Roper J, Hajdari A, Sõukand R J Ethnobiol Ethnomed 21-Feb-2017
PMCID:PMC5320662
doi:10.1186/s13002-016-0132-9
PMID:28222790
Naturally Occurring Cinnamic Acid Sugar Ester Derivatives Tian Y, Liu W, Lu Y, Wang Y, Chen X, Bai S, Zhao Y, He T, Lao F, Shang Y, Guo Y, She G Molecules 24-Oct-2016
PMCID:PMC6273327
doi:10.3390/molecules21101402
PMID:27783048
Germacrene D, A Common Sesquiterpene in the Genus Bursera (Burseraceae) Noge K, Becerra JX Molecules 15-Dec-2009
PMCID:PMC6255432
doi:10.3390/molecules14125289
PMID:20032892
Phlomisethanoside, a phenylethanoid glycoside from Phlomis grandiflora var. grandiflora Yoshio Takeda, Michiko Kinugawa, Toshiya Masuda, Gisho Honda, Hideaki Otsuka, Ekrem Sezik, Erdem Yesilada Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00734-1

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
CID 14312560 14312560 Click to see CC(=O)C=C=C1C(CC(CC1(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
8-Epiloganin 10548420 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
methyl (1S,4aR,6S,7S,7aR)-4a,6-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 21607798 Click to see CC1C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
methyl (1S,4aS,6S,7S,7aR)-6-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 35755834 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
methyl 4a,6-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 73800781 Click to see CC1C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 154496101 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
Acteoside;Kusaginin;TJC160 354009 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
> Phenylpropanoids and polyketides / Macrolides and analogues / Pectenotoxins and derivatives
14-(2,3-Dihydroxy-4-methyloxan-2-yl)-28-hydroxy-5,7,9,19,29-pentamethyl-18,31-dioxo-13,17,38,39,40,41,42,43-octaoxaoctacyclo[31.4.1.11,35.12,5.120,24.124,27.129,32.012,16]tritetraconta-8,10-diene-35-carbaldehyde 74051868 Click to see CC1CCOC(C1O)(C2CC3C(O2)C=CC(=CC(CC4(CCC(O4)C56CCC(O5)(CC(O6)C7C(=O)CC(O7)(C(C8CCC9(O8)CCCC(O9)C(C(=O)O3)C)O)C)C=O)C)C)C)O 873.00 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(3R,4S,5R)-5-[(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(4-hydroxyphenyl)ethoxy]oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 4-hydroxy-3-methoxybenzoate 163186477 Click to see COC1=C(C=CC(=C1)C(=O)OCC2(COC(C2O)OC3C(C(C(OC3OCCC4=CC=C(C=C4)O)CO)O)O)O)O 582.50 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
[5-[4,5-Dihydroxy-6-(hydroxymethyl)-2-[2-(4-hydroxyphenyl)ethoxy]oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 4-hydroxy-3-methoxybenzoate 163057513 Click to see COC1=C(C=CC(=C1)C(=O)OCC2(COC(C2O)OC3C(C(C(OC3OCCC4=CC=C(C=C4)O)CO)O)O)O)O 582.50 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
Hattushoside 398983 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OCC2(COC(C2O)OC3C(C(C(OC3OCCC4=CC=C(C=C4)O)CO)O)O)O 612.60 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
Hattushoside 11801891 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OCC2(COC(C2O)OC3C(C(C(OC3OCCC4=CC=C(C=C4)O)CO)O)O)O 612.60 unknown https://doi.org/10.1016/S0031-9422(98)00734-1
Phlomisethanoside 100978506 Click to see COC1=C(C=CC(=C1)C(=O)OCC2(COC(C2O)OC3C(C(C(OC3OCCC4=CC=C(C=C4)O)CO)O)O)O)O 582.50 unknown https://doi.org/10.1016/S0031-9422(98)00734-1

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