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Radula complanata

Radula complanata - 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 UUID6440502371d52053242350
Scientific name Radula complanata
Authority (L.) Dumort.
First published in Syll. Jungerm. Europ. 38 1831

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Czech struhatka zploštělá
Welsh cenoglys melynwyrdd
German abgeflachtes kratz-lebermoos
German gewöhnliches kratzmoos
Estonian korbasõõrik
Finnish haapasuomusammal
Hungarian lapított májmoha
Dutch gewoon schijfjesmos
Swedish plattsvepemossa
Ukrainian Радула сплющена
Chinese 扁萼苔

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001196711
Florida Plant Atlas 4815
USDA Plants RACO19
Tropicos 35185912
INPN 6657
The Plant List tro-35185912
Open Tree Of Life 692281
Observations.org 17779
NCBI Taxonomy 139838
NBN Atlas NHMSYS0000310549
Nature Serve 2.123325
iNaturalist 67842
GBIF 5286325
EPPO RDACO
EOL 604294
Elurikkus 6719

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
Recent Advances in the Phytochemistry of Bryophytes: Distribution, Structures and Biological Activity of Bibenzyl and Bisbibenzyl Compounds Sen K, Khan MI, Paul R, Ghoshal U, Asakawa Y Plants (Basel) 15-Dec-2023
PMCID:PMC10747515
doi:10.3390/plants12244173
PMID:38140499
Liverworts of Magadan: Life on the Edge of Beringia Bakalin VA, Klimova KG, Bakalin DA, Choi SS Plants (Basel) 22-Nov-2023
PMCID:PMC10708503
doi:10.3390/plants12233928
PMID:38068565
Diversity, Ecology and Phytogeography of Bryophytes across Temperate Forest Communities—Insight from Mt. Papuk (Croatia, SE Europe) Alegro A, Šegota V, Rimac A, Papp B Plants (Basel) 22-Sep-2023
PMCID:PMC10574398
doi:10.3390/plants12193346
PMID:37836086
The Bryophyte Flora of Vienna Zechmeister HG, Kropik M Plants (Basel) 20-Aug-2023
PMCID:PMC10458201
doi:10.3390/plants12163002
PMID:37631214
Impact of in vitro phytohormone treatments on the metabolome of the leafy liverwort Radula complanata (L.) Dumort Blatt-Janmaat K, Neumann S, Schmidt F, Ziegler J, Qu Y, Peters K Metabolomics 09-Mar-2023
PMCID:PMC9998581
doi:10.1007/s11306-023-01979-y
PMID:36892716
Host Tree and Geography Induce Metabolic Shifts in the Epiphytic Liverwort Radula complanata Blatt-Janmaat KL, Neumann S, Ziegler J, Peters K Plants (Basel) 27-Jan-2023
PMCID:PMC9919105
doi:10.3390/plants12030571
PMID:36771656
The Taxonomically Richest Liverwort Hemiboreal Flora in Eurasia Is in the South Kurils Bakalin VA, Klimova KG, Bakalin DA, Choi SS Plants (Basel) 25-Aug-2022
PMCID:PMC9460601
doi:10.3390/plants11172200
PMID:36079582
Tea plantations and their importance as host plants and hot spots for epiphytic cryptogams Wolski GJ, Piwowarczyk R, Plášek V, Kukwa M, Ruraż K Sci Rep 14-Sep-2021
PMCID:PMC8440766
doi:10.1038/s41598-021-97315-2
PMID:34521912
Liverwort flora of Ayan – a gained link between subarctic and hemiboreal floras in West Okhotiya (Pacific Russia) Bakalin V, Klimova K, Bakalin D, Choi SS Biodivers Data J 01-Apr-2021
PMCID:PMC8032650
doi:10.3897/BDJ.9.e65199
PMID:33841022
Bibenzyls and bisbybenzyls of bryophytic origin as promising source of novel therapeutics: pharmacology, synthesis and structure-activity Nandy S, Dey A Daru 15-Aug-2020
PMCID:PMC7429097
doi:10.1007/s40199-020-00341-0
PMID:32803687
Eukaryotic and Prokaryotic Phytochelatin Synthases Differ Less in Functional Terms Than Previously Thought: A Comparative Analysis of Marchantia polymorpha and Geitlerinema sp. PCC 7407 Bellini E, Varotto C, Borsò M, Rugnini L, Bruno L, Sanità di Toppi L Plants (Basel) 20-Jul-2020
PMCID:PMC7411734
doi:10.3390/plants9070914
PMID:32698350
Content Snapshot N/A Ann Bot 01-Jun-2020
PMCID:PMC7262462
doi:10.1093/aob/mcaa087
The distribution and evolution of fungal symbioses in ancient lineages of land plants Rimington WR, Duckett JG, Field KJ, Bidartondo MI, Pressel S Mycorrhiza 04-Mar-2020
PMCID:PMC7062687
doi:10.1007/s00572-020-00938-y
PMID:32130512
Different from tracheophytes, liverworts commonly have mixed 35S and 5S arrays Sousa A, Bechteler J, Temsch EM, Renner SS Ann Bot 17-Feb-2020
PMCID:PMC7262461
doi:10.1093/aob/mcaa027
PMID:32064492
Bryophyte Species Richness on Retention Aspens Recovers in Time but Community Structure Does Not Oldén A, Ovaskainen O, Kotiaho JS, Laaka-Lindberg S, Halme P PLoS One 07-Apr-2014
PMCID:PMC3978069
doi:10.1371/journal.pone.0093786
PMID:24710329

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 / Acyclic diterpenoids
(E)-(7R,11R)-3,7,11,15-tetramethylhexadec-2-ene-1-ol 145386 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/0031-9422(82)85245-X
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/0031-9422(82)85245-X
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
Zeorin 159931 Click to see CC1(CCCC2(C1C(CC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)O)C)C 444.70 unknown https://doi.org/10.4268/CJCMM20111518
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,5aS,9bS)-5a,9-dimethyl-3-methylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one 12305186 Click to see CC1=C2C3C(CCC2(CCC1)C)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.1016/0031-9422(82)85245-X
5a,9-dimethyl-3-methylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one 3478505 Click to see CC1=C2C3C(CCC2(CCC1)C)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.1016/0031-9422(82)85245-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.4268/CJCMM20111518
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.4268/CJCMM20111518
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(82)85245-X
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(82)85245-X
> Organoheterocyclic compounds / Benzoxepines
(9R)-9-benzyl-6-hydroxy-3-methyl-5,9-dihydro-2H-furo[3,4-h][1]benzoxepin-7-one 162851245 Click to see CC1=CCC2=C(C=C3C(OC(=O)C3=C2O)CC4=CC=CC=C4)OC1 322.40 unknown https://doi.org/10.1016/0031-9422(82)85245-X
9-benzyl-6-hydroxy-3-methyl-5,9-dihydro-2H-furo[3,4-h][1]benzoxepin-7-one 162851243 Click to see CC1=CCC2=C(C=C3C(OC(=O)C3=C2O)CC4=CC=CC=C4)OC1 322.40 unknown https://doi.org/10.1016/0031-9422(82)85245-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 133562575 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(84)83098-8
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 138454316 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(84)83098-8
Neoschaftoside 442619 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(84)83098-8
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(84)83098-8
> Phenylpropanoids and polyketides / Stilbenes
(3S,5R)-12-hydroxy-5-methyl-10-(2-phenylethyl)-4,7-dioxatricyclo[6.4.0.03,5]dodeca-1(8),9,11-triene-11-carboxylic acid 163071364 Click to see CC12COC3=C(CC1O2)C(=C(C(=C3)CCC4=CC=CC=C4)C(=O)O)O 340.40 unknown https://doi.org/10.1016/S0031-9422(00)89292-4
1-Methoxy-3-[2-(4-methoxyphenyl)ethyl]benzene 14926725 Click to see COC1=CC=C(C=C1)CCC2=CC(=CC=C2)OC 242.31 unknown https://doi.org/10.1016/0031-9422(82)85245-X
2-[(3,3-Dimethyloxiran-2-yl)methyl]-5-(2-phenylethyl)benzene-1,3-diol 129709890 Click to see CC1(C(O1)CC2=C(C=C(C=C2O)CCC3=CC=CC=C3)O)C 298.40 unknown https://doi.org/10.1016/0031-9422(82)85245-X
2-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-5-(2-phenylethyl)benzene-1,3-diol 163031437 Click to see CC1(C(O1)CC2=C(C=C(C=C2O)CCC3=CC=CC=C3)O)C 298.40 unknown https://doi.org/10.1016/0031-9422(82)85245-X
2-Carboxy-3,5-dihydroxy-4-(3-methyl-2-butenyl)bibenzyl 9945203 Click to see CC(=CCC1=C(C=C(C(=C1O)C(=O)O)CCC2=CC=CC=C2)O)C 326.40 unknown https://doi.org/10.1016/S0031-9422(00)89292-4
https://doi.org/10.1016/0031-9422(82)85245-X
3-Methoxy-5-(2-phenylethyl)-2-prenylphenol 14805915 Click to see CC(=CCC1=C(C=C(C=C1OC)CCC2=CC=CC=C2)O)C 296.40 unknown https://doi.org/10.1016/S0031-9422(00)89292-4
3-Methoxybibenzyl 12465095 Click to see COC1=CC=CC(=C1)CCC2=CC=CC=C2 212.29 unknown https://doi.org/10.1016/0031-9422(82)85245-X
https://doi.org/10.1016/S0031-9422(00)89292-4
3,5-Dihydroxy-4-(3,7-dimethyl-2,6-octadienyl) bibenzyl 69713304 Click to see CC(=CCCC(=CCC1=C(C=C(C=C1O)CCC2=CC=CC=C2)O)C)C 350.50 unknown https://doi.org/10.1016/0031-9422(82)85245-X
3,5-Dihydroxy-4-geranylbibenzyl 14060723 Click to see CC(=CCCC(=CCC1=C(C=C(C=C1O)CCC2=CC=CC=C2)O)C)C 350.50 unknown https://doi.org/10.1016/0031-9422(82)85245-X
4-(3-Methyl-2-butenyl)-5-phenethylbenzene-1,3-diol 14805893 Click to see CC(=CCC1=C(C=C(C=C1O)O)CCC2=CC=CC=C2)C 282.40 unknown https://doi.org/10.1016/0031-9422(91)84130-K
4-Prenyldihydropinosylvin 442715 Click to see CC(=CCC1=C(C=C(C=C1O)CCC2=CC=CC=C2)O)C 282.40 unknown https://doi.org/10.1016/0031-9422(82)85245-X
https://doi.org/10.1016/S0031-9422(00)89292-4
6-Hydroxy-3-methyl-8-(2-phenylethyl)-2,5-dihydro-1-benzoxepine-7-carboxylic acid 14805959 Click to see CC1=CCC2=C(C=C(C(=C2O)C(=O)O)CCC3=CC=CC=C3)OC1 324.40 unknown https://doi.org/10.1016/0031-9422(82)85245-X
https://doi.org/10.1016/0031-9422(91)84130-K
Radulannin A 9970905 Click to see CC1=CCC2=C(C=C(C=C2OC1)CCC3=CC=CC=C3)O 280.40 unknown https://doi.org/10.1016/0031-9422(91)84130-K
Radulannin L 14805961 Click to see CC1=CCC2=C(C=C(C=C2OC1)CCC3=CC=CC=C3O)O 296.40 unknown https://doi.org/10.1016/0031-9422(91)84147-K
https://doi.org/10.1016/0031-9422(91)84130-K

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