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Radula perrottetii

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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 UUID6440522a66f62898210130
Scientific name Radula perrottetii
Authority Gottsche ex Stephani
First published in Hedwigia 23: 154 1884

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Japanese オオケビラゴケ
Chinese 直瓣扁萼蘚
Chinese 直瓣扁萼苔

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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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

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Database ID/link to page
World Flora Online wfo-0001208458
Tropicos 35209461
INPN 779851
The Plant List tro-35209461
Open Tree Of Life 896868
NCBI Taxonomy 280841
iNaturalist 1233478
GBIF 8707240
EOL 6075411
Wikipedia Cladoradula_perrottetii

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
Cannabinoid and Opioid Receptor Affinity and Modulation of Cancer-Related Signaling Pathways of Machaeriols and Machaeridiols from Machaerium Pers. Muhammad I, Ibrahim MA, Kumarihamy M, Lambert JA, Zhang J, Mohammad MH, Khan SI, Pasco DS, Balachandran P Molecules 18-May-2023
PMCID:PMC10361207
doi:10.3390/molecules28104162
PMID:37241903
Biosynthesis of Phytocannabinoids and Structural Insights: A Review Govindarajan RK, Mishra AK, Cho KH, Kim KH, Yoon KM, Baek KH Metabolites 17-Mar-2023
PMCID:PMC10051821
doi:10.3390/metabo13030442
PMID:36984882
Synthesis and Inhibitory Activity of Machaeridiol-Based Novel Anti-MRSA and Anti-VRE Compounds and Their Profiling for Cancer-Related Signaling Pathways Kumarihamy M, Tripathi S, Balachandran P, Avula B, Zhao J, Wang M, Bennett MM, Zhang J, Carr MA, Lovell KM, Wellington OI, Marquart ME, Nanayakkara NP, Muhammad I Molecules 05-Oct-2022
PMCID:PMC9570708
doi:10.3390/molecules27196604
PMID:36235141
Antibacterial Effects of Phytocannabinoids Scott C, Neira Agonh D, Lehmann C Life (Basel) 07-Sep-2022
PMCID:PMC9505641
doi:10.3390/life12091394
PMID:36143430
Harnessing ortho-Quinone Methides in Natural Product Biosynthesis and Biocatalysis Purdy TN, Moore BS, Lukowski AL J Nat Prod 02-Feb-2022
PMCID:PMC9006567
doi:10.1021/acs.jnatprod.1c01026
PMID:35108487
Endocannabinoid System as a Promising Therapeutic Target in Inflammatory Bowel Disease – A Systematic Review Hryhorowicz S, Kaczmarek-Ryś M, Zielińska A, Scott RJ, Słomski R, Pławski A Front Immunol 22-Dec-2021
PMCID:PMC8727741
doi:10.3389/fimmu.2021.790803
PMID:35003109
Total Synthesis of Oxepin and Dihydrooxepin Containing Natural Products Sokol KR, Magauer T Synthesis (Stuttg) 24-Jun-2021
PMCID:PMC7612190
doi:10.1055/s-0037-1610776
PMID:35001983
Biosynthesis and Synthetic Biology of Psychoactive Natural Products Jamieson CS, Misa J, Tang Y, Billingsley JM Chem Soc Rev 21-Jun-2021
PMCID:PMC8217322
doi:10.1039/d1cs00065a
PMID:33908526
Bis-Bibenzyls from the Liverwort Pellia endiviifolia and Their Biological Activity Ivković I, Novaković M, Veljić M, Mojsin M, Stevanović M, Marin PD, Bukvički D Plants (Basel) 26-May-2021
PMCID:PMC8227020
doi:10.3390/plants10061063
PMID:34073157
Bryo-Activities: A Review on How Bryophytes Are Contributing to the Arsenal of Natural Bioactive Compounds against Fungi Commisso M, Guarino F, Marchi L, Muto A, Piro A, Degola F Plants (Basel) 21-Jan-2021
PMCID:PMC7911284
doi:10.3390/plants10020203
PMID:33494524
Antimicrobial Constituents from Machaerium Pers.: Inhibitory Activities and Synergism of Machaeriols and Machaeridiols against Methicillin-Resistant Staphylococcus aureus, Vancomycin-Resistant Enterococcus faecium, and Permeabilized Gram-Negative Pathogens Muhammad I, Jacob MR, Ibrahim MA, Raman V, Kumarihamy M, Wang M, Al-Adhami T, Hind C, Clifford M, Martin B, Zhao J, Sutton JM, Rahman KM Molecules 18-Dec-2020
PMCID:PMC7765828
doi:10.3390/molecules25246000
PMID:33352963
A closer look at cannabimimetic terpenes, polyphenols, and flavonoids: a promising road forward Cavalli J, Dutra RC Neural Regen Res 12-Dec-2020
PMCID:PMC8284286
doi:10.4103/1673-5374.301011
PMID:33318442
Germacrene A–A Central Intermediate in Sesquiterpene Biosynthesis Xu H, Dickschat JS Chemistry 30-Sep-2020
PMCID:PMC7821278
doi:10.1002/chem.202002163
PMID:32442350
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

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
> Benzenoids / Benzene and substituted derivatives / Toluenes
1-[(1R)-1,4-dimethylcyclohex-3-en-1-yl]-4-methylbenzene 163067853 Click to see CC1=CCC(CC1)(C)C2=CC=C(C=C2)C 200.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.003
> Lignans, neolignans and related compounds
4-[2-(3-Hydroxyphenyl)ethyl]-2-[4-[2-(3-hydroxyphenyl)ethyl]phenoxy]phenol 10646095 Click to see C1=CC(=CC(=C1)O)CCC2=CC=C(C=C2)OC3=C(C=CC(=C3)CCC4=CC(=CC=C4)O)O 426.50 unknown https://doi.org/10.1016/S0031-9422(00)90371-6
https://doi.org/10.1002/CHIN.198615367
https://doi.org/10.1016/0031-9422(91)84130-K
5-[2-(3-Hydroxyphenyl)ethyl]-3-[4-[2-(3-hydroxyphenyl)ethyl]phenoxy]-2-methoxyphenol 14332032 Click to see COC1=C(C=C(C=C1OC2=CC=C(C=C2)CCC3=CC(=CC=C3)O)CCC4=CC(=CC=C4)O)O 456.50 unknown https://doi.org/10.1016/0031-9422(91)84130-K
https://doi.org/10.1016/S0031-9422(00)90371-6
https://doi.org/10.1002/CHIN.198615367
Marchantin A 442710 Click to see C1CC2=C(C(=CC=C2)O)OC3=CC=CC(=C3)CCC4=CC(=C(C(=C4)OC5=CC=C1C=C5)O)O 440.50 unknown https://doi.org/10.1016/0031-9422(91)84130-K
Perrotettin F 11953464 Click to see C1=CC(=CC(=C1)O)CCC2=CC=C(C=C2)OC3=CC(=CC(=C3O)O)CCC4=CC(=CC=C4)O 442.50 unknown https://doi.org/10.1002/CHIN.198615367
https://doi.org/10.1016/S0031-9422(00)90371-6
https://doi.org/10.1016/0031-9422(91)84130-K
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(00)90371-6
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(00)90371-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(91)84130-K
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Delta-Tocopherol 92094 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown https://doi.org/10.1016/S0031-9422(00)90371-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene 519346 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown https://doi.org/10.1016/0031-9422(91)84130-K
3-methyl-6-[(1S)-1,2,2-trimethylcyclopentyl]benzene-1,2-diol 14109425 Click to see CC1=C(C(=C(C=C1)C2(CCCC2(C)C)C)O)O 234.33 unknown https://doi.org/10.1016/0031-9422(82)85245-X
Cuparene 86895 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown https://doi.org/10.1016/0031-9422(91)84130-K
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(3S,4aS,8aR)-5,8a-dimethyl-3-prop-1-en-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene 12309809 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.003
beta-Helmiscapene 12309814 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.003
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)84130-K
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
2-[2-Hydroxy-5-[2-(3-hydroxyphenyl)ethyl]phenyl]-4-[2-(3-hydroxyphenyl)ethyl]phenol 86178955 Click to see C1=CC(=CC(=C1)O)CCC2=CC(=C(C=C2)O)C3=C(C=CC(=C3)CCC4=CC(=CC=C4)O)O 426.50 unknown https://doi.org/10.1016/S0031-9422(00)90371-6
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dihydroxy-6-carbomethoxy-2-(3-methyl-2-butenyl)bibenzyl 14805953 Click to see CC(=CCC1=C(C(=C(C=C1O)O)C(=O)OC)CCC2=CC=CC=C2)C 340.40 unknown https://doi.org/10.1016/0031-9422(91)84130-K
4-(3-Hydroxy-3-methylbutyl)-5-(2-phenylethyl)benzene-1,2,3-triol 101594595 Click to see CC(C)(CCC1=C(C(=C(C=C1CCC2=CC=CC=C2)O)O)O)O 316.40 unknown https://doi.org/10.1016/0031-9422(91)84130-K
4-(3-Methylbut-2-enyl)-5-(2-phenylethyl)benzene-1,2,3-triol 86056178 Click to see CC(=CCC1=C(C(=C(C=C1CCC2=CC=CC=C2)O)O)O)C 298.40 unknown https://doi.org/10.1016/0031-9422(91)84130-K
6-(2-Phenylethyl)-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-4,7-diol 162845458 Click to see CC(=C)C1CC2=C(C=C(C(=C2O1)O)CCC3=CC=CC=C3)O 296.40 unknown https://doi.org/10.1016/0031-9422(91)84130-K
https://doi.org/10.1016/S0031-9422(00)90371-6
Perrottetin B 163184504 Click to see CC(C)(C=CC1=C(C(=C(C=C1CCC2=CC=CC=C2)O)O)O)O 314.40 unknown https://doi.org/10.1016/0031-9422(91)84130-K
Perrottetinene 24766094 Click to see CC1=CC2C(CC1)C(OC3=CC(=CC(=C23)O)CCC4=CC=CC=C4)(C)C 348.50 unknown https://doi.org/10.1016/S0031-9422(00)90371-6

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