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Phlomis rigida

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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 UUID643fe70be013b235119057
Scientific name Phlomis rigida
Authority Labill.
First published in Icon. Pl. Syr. 3: 15 (1809)

Description Top

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Synonyms Top

Scientific name Authority First published in
Phlomis shepardii Post Fl. Syria : 658 (1896)
Anemitis rigida Raf. Fl. Tellur. 3: 87 (1837)

Common names Top

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Language Common/alternative name
Arabic أذينة خشنة

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-0000269477
Tropicos 100241592
KEW urn:lsid:ipni.org:names:454040-1
The Plant List kew-152400
Open Tree Of Life 873936
NCBI Taxonomy 997737
IPNI 454040-1
iNaturalist 966728
GBIF 3886577
USDA GRIN 28030

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
α-Amylase inhibitory activity of some traditionally used medicinal species of Labiatae Safamansouri H, Nikan M, Amin G, Sarkhail P, Gohari AR, Kurepaz-Mahmoodabadi M, Saeidnia S J Diabetes Metab Disord 02-Dec-2014
PMCID:PMC4262240
doi:10.1186/s40200-014-0114-1
PMID:25506585
Phlorigidosides A-C, iridoid glucosides from Phlomis rigida. Takeda Y, Matsumura H, Masuda T, Honda G, Otsuka H, Takaishi Y, Sezik E, Yesilada E Phytochemistry 01-Apr-2000
doi:10.1016/S0031-9422(99)00431-8
PMID:10820806

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
[(2S,3S,3aR,4S,5R,6S,6aS,7R,8R,10R,10aR,10bS)-7-benzoyloxy-3,3a,4,5,6,8,10a-heptahydroxy-2,10-dimethyl-8-prop-1-en-2-yl-1,2,3,4,6,6a,7,9,10,10b-decahydrobenzo[e]azulen-5-yl]methyl benzoate 162981352 Click to see CC1CC2C3(C(CC(C(C3C(C(C(C2(C1O)O)O)(COC(=O)C4=CC=CC=C4)O)O)OC(=O)C5=CC=CC=C5)(C(=C)C)O)C)O 626.70 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
5-Deoxypulchelloside I 11486568 Click to see CC1C2C(C(C1O)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
6beta-Hydroxyipolamiide 14137128 Click to see CC1(CC(C2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
8-O-Acetyl shanzhiside methyl ester 162823 Click to see CC(=O)OC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)C 448.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
Lamalbid 21637592 Click to see CC1(C2C(C(C1O)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC)O 422.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
methyl (1S,4aS,5R,7S,7aS)-5,7-dihydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 162968725 Click to see CC1(CC(C2C1C(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(99)00431-8
methyl (1S,4aS,5R,7S,7aS)-7-acetyloxy-5-hydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 163007873 Click to see CC(=O)OC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)C 448.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
methyl (1S,4aS,5S,6S,7R,7aS)-1-[(2S,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7-trihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 102237726 Click to see CC(=O)OC1C(C(C(OC1OC2C3C(C(C(C3(C)O)O)O)C(=CO2)C(=O)OC)CO)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
methyl (1S,4aS,5S,6S,7R,7aS)-5,6,7-trihydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 154496867 Click to see CC1(C2C(C(C1O)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC)O 422.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
methyl (1S,4aS,5S,6S,7R,7aS)-5,6,7-trihydroxy-7-methyl-1-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 49775357 Click to see CC1(C2C(C(C1O)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC)O 422.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
methyl (1S,4aS,5S,6S,7R,7aS)-7-acetyloxy-5,6-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 154497205 Click to see CC(=O)OC1(C2C(C(C1O)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC)C 464.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
methyl 1-[3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7-trihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 163024739 Click to see CC(=O)OC1C(C(C(OC1OC2C3C(C(C(C3(C)O)O)O)C(=CO2)C(=O)OC)CO)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
Methyl 4a,5,7-trihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 14137127 Click to see CC1(CC(C2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
methyl 5,6,7-trihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 73818239 Click to see CC1(C2C(C(C1O)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC)O 422.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
methyl 5,7-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 13892721 Click to see CC1(CC(C2C1C(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(99)00431-8
Methyl 7-acetyloxy-4a,5-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 124222270 Click to see CC(=O)OC1(CC(C2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O)C 464.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
methyl 7-acetyloxy-5-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 18759764 Click to see CC(=O)OC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)C 448.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
Phlorigidoside B 91885038 Click to see CC(=O)OC1(CC(C2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O)C 464.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
Shanzhiside methyl ester 13892722 Click to see CC1(CC(C2C1C(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(99)00431-8
Shanzhiside-methylester 3085296 Click to see CC1(CC(C2C1C(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(99)00431-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Methyl 5-hydroxy-2-methyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-ene-7-carboxylate 75034076 Click to see CC12C3C(C(C1O2)O)C(=COC3OC4C(C(C(C(O4)CO)O)O)O)C(=O)OC 404.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8
Phlorigidoside C 70686276 Click to see CC12C3C(C(C1O2)O)C(=COC3OC4C(C(C(C(O4)CO)O)O)O)C(=O)OC 404.40 unknown https://doi.org/10.1016/S0031-9422(99)00431-8

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