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Phlomis linearis

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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
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Details Top

Internal ID UUID643fe7081f004935890569
Scientific name Phlomis linearis
Authority Boiss. & Balansa
First published in Diagn. Pl. Orient. , ser. 2, 4: 46 (1859)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Arabic أذينة خطية

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000269363
Tropicos 100241543
KEW urn:lsid:ipni.org:names:453949-1
The Plant List kew-152296
Open Tree Of Life 349261
NCBI Taxonomy 997726
IPNI 453949-1
iNaturalist 966748
GBIF 3887429

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
Phytochemical characterisation of Phlomis linearis Boiss. & Bal and screening for anticholinesterase, antiamylase, antimicrobial, and cytotoxic properties GÖGER G, TÜRKYOLU Ü, GÜRŞEN EN, YUR S, KARADUMAN AB, GÖGER F, TEKİN M, ÖZEK G Turk J Chem 28-Apr-2021
PMCID:PMC8164195
doi:10.3906/kim-2009-59
PMID:34104051
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
Validating and Troubleshooting Ocular In Vitro Toxicology Tests Barile FA J Pharmacol Toxicol Methods 22-Jan-2010
PMCID:PMC2849866
doi:10.1016/j.vascn.2010.01.001
PMID:20096797
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
Phlinosides D and E, phenylpropanoid glycosides, and iridoids from Phlomis linearis. Caliş I, Başaran AA, Saracoglu I, Sticher O, Rüedi P Phytochemistry 01-Jan-1991
doi:10.1016/S0031-9422(00)98255-4
PMID:1367797
Phlinosides A, B and C, three phenylpropanoid glycosides from Phlomis linearis. Caliş I, Başaran AA, Saracoğlu I, Sticher O, Rüedi P Phytochemistry 01-Jan-1990
doi:10.1016/0031-9422(90)85436-J
PMID:1366427

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
Auroside 45027862 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(00)98255-4
https://doi.org/10.1016/0031-9422(91)83486-5
Ipolamiide 442425 Click to see CC1(CCC2(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(00)98255-4
https://doi.org/10.1016/0031-9422(91)83486-5
Lamiide 443327 Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 422.40 unknown https://doi.org/10.1016/0031-9422(91)83486-5
https://doi.org/10.1016/S0031-9422(00)98255-4
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(00)98255-4
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(00)98255-4
Methyl 4a,6,7-trihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 4204894 Click to see CC1(C(CC2(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(00)98255-4
Methyl 4a,7-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 3515874 Click to see CC1(CCC2(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(00)98255-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,6R,7R,8S,11R,12S,15S,16R,19S,20R,21R)-7,20-diethyl-19-hydroxy-3,7,11,16,20-pentamethyl-8-pentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-enyl] acetate 163191247 Click to see CCC1(C2CCC3(CC4=CCC5C(C4CCC3C2(CCC1OC(=O)C)C)(CCC(C5(C)CC)O)C)C)C 512.80 unknown https://doi.org/10.1016/0031-9422(90)85436-J
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Moniloside A 44575900 Click to see CC(C)C(CCC(C)C1CC(C2C1(CC=C3C2=CCC4C3(CCC(C4)OC5C(C(C(CO5)O)O)OC)C)C)O)O 562.80 unknown https://doi.org/10.1016/S0031-9422(00)98255-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163186218 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)O)O)CO)OCCC5=CC(=C(C=C5)O)O)O)C)O)O)O)O)O 770.70 unknown https://doi.org/10.1016/0031-9422(90)85436-J
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 101533037 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)O)O)CO)OCCC5=CC(=C(C=C5)O)O)O)C)O)O)O)O)O 770.70 unknown https://doi.org/10.1016/0031-9422(90)85436-J
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101609014 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)O)OC)CO)OCCC5=CC(=C(C=C5)O)O)O)C)O)O)O)O)O 784.80 unknown https://doi.org/10.1016/S0031-9422(00)98255-4
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 10327934 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 786.70 unknown https://doi.org/10.1016/0031-9422(90)85436-J
[4-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 195594 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)O)O)CO)OCCC5=CC(=C(C=C5)O)O)O)C)O)O)O)O)O 770.70 unknown https://doi.org/10.1016/0031-9422(90)85436-J
[4-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 3083271 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)O)OC)CO)OCCC5=CC(=C(C=C5)O)O)O)C)O)O)O)O)O 784.80 unknown https://doi.org/10.1016/S0031-9422(00)98255-4
[4-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 72726475 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)OC5C(C(C(CO5)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/0031-9422(90)85436-J
[4-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 73156275 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(CO5)O)O)O)O)O 770.70 unknown https://doi.org/10.1016/S0031-9422(00)98255-4
[4-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 3083112 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 786.70 unknown https://doi.org/10.1016/0031-9422(90)85436-J
Phlinoside B 6450096 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)OC5C(C(C(CO5)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/0031-9422(90)85436-J
Phlinoside C 6443993 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)O)O)CO)OCCC5=CC(=C(C=C5)O)O)O)C)O)O)O)O)O 770.70 unknown https://doi.org/10.1016/0031-9422(90)85436-J
Phlinoside D 6450124 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(CO5)O)O)O)O)O 770.70 unknown https://doi.org/10.1016/S0031-9422(00)98255-4

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