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Ricciocarpos natans

Ricciocarpos natans - 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
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Details Top

Internal ID UUID64405025ac935365819983
Scientific name Ricciocarpos natans
Authority (L.) Corda
First published in Naturalientausch 12: 651 1829

Description Top

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Synonyms Top

Scientific name Authority First published in
Riccia natans L. Syst. Nat. (ed. 10) 2: 1339 1759

Common names Top

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Language Common/alternative name
Czech nalžovka plovoucí
Welsh grisial-lys eddiog
German schwimmendes wasser-sternlebermoos
German wasser-sternlebermoos
German schwimmlebermoos
Finnish sorsansammal
Japanese イチョウウキゴケ属
Japanese イチョウウキゴケ
Korean 은행이끼
Dutch kroosmos
Swedish vattenstjärna
Ukrainian Річчієкарп плаваючий
Chinese 浮蘚
Chinese 浮苔

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-0001196734
Florida Plant Atlas 4834
USDA Plants RINA2
Tropicos 35185937
INPN 6237
The Plant List tro-35185937
Open Tree Of Life 108927
Observations.org 17796
NCBI Taxonomy 53035
NBN Atlas NHMSYS0000310456
Nature Serve 2.127700
iNaturalist 56422
GBIF 2688638
EPPO RCINA
EOL 600690

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
Why should we study plant sex chromosomes? Charlesworth D, Harkess A Plant Cell 02-Jan-2024
PMCID:PMC11062472
doi:10.1093/plcell/koad278
PMID:38163640
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
The monoicous secondarily aquatic liverwort Ricciocarpos natans as a model within the radiation of derived Marchantiopsida Singh S, Bowman JL Front Plant Sci 28-Nov-2023
PMCID:PMC10715061
doi:10.3389/fpls.2023.1260596
PMID:38089807
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
The Bryophyte Flora of Vienna Zechmeister HG, Kropik M Plants (Basel) 20-Aug-2023
PMCID:PMC10458201
doi:10.3390/plants12163002
PMID:37631214
The Liverwort and Hornwort Flora of Jeju Island, Republic of Korea: A Volcanic Island with a Unique Mixture of Subtropical, Temperate, Boreal, and Arctomontane Taxa Choi SS, Bakalin VA, Bum HM, Park SJ, Kim DS, Ahn US, Moon MO Plants (Basel) 20-Jun-2023
PMCID:PMC10301385
doi:10.3390/plants12122384
PMID:37376013
The renaissance and enlightenment of Marchantia as a model system Bowman JL, Arteaga-Vazquez M, Berger F, Briginshaw LN, Carella P, Aguilar-Cruz A, Davies KM, Dierschke T, Dolan L, Dorantes-Acosta AE, Fisher TJ, Flores-Sandoval E, Futagami K, Ishizaki K, Jibran R, Kanazawa T, Kato H, Kohchi T, Levins J, Lin SS, Nakagami H, Nishihama R, Romani F, Schornack S, Tanizawa Y, Tsuzuki M, Ueda T, Watanabe Y, Yamato KT, Zachgo S Plant Cell 17-Aug-2022
PMCID:PMC9516144
doi:10.1093/plcell/koac219
PMID:35976122
Stress, senescence, and specialized metabolites in bryophytes Kulshrestha S, Jibran R, van Klink JW, Zhou Y, Brummell DA, Albert NW, Schwinn KE, Chagné D, Landi M, Bowman JL, Davies KM J Exp Bot 08-Mar-2022
PMCID:PMC9291361
doi:10.1093/jxb/erac085
PMID:35259256
The Role of H2O2-Scavenging Enzymes (Ascorbate Peroxidase and Catalase) in the Tolerance of Lemna minor to Antibiotics: Implications for Phytoremediation Gomes MP, Kitamura RS, Marques RZ, Barbato ML, Zámocký M Antioxidants (Basel) 13-Jan-2022
PMCID:PMC8772849
doi:10.3390/antiox11010151
PMID:35052655
CO2 sequestration by propagation of the fast-growing Azolla spp. Hamdan HZ, Houri AF Environ Sci Pollut Res Int 16-Oct-2021
PMCID:PMC8520330
doi:10.1007/s11356-021-16986-6
PMID:34657254
Evolution of Flavylium-Based Color Systems in Plants: What Physical Chemistry Can Tell Us Pina F, Alejo-Armijo A, Clemente A, Mendoza J, Seco A, Basílio N, Parola AJ Int J Mol Sci 07-Apr-2021
PMCID:PMC8067881
doi:10.3390/ijms22083833
PMID:33917158
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
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
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
The Evolution of Flavonoid Biosynthesis: A Bryophyte Perspective Davies KM, Jibran R, Zhou Y, Albert NW, Brummell DA, Jordan BR, Bowman JL, Schwinn KE Front Plant Sci 04-Feb-2020
PMCID:PMC7010833
doi:10.3389/fpls.2020.00007
PMID:32117358

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 / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(4S)-4-hydroxy-3-[2-(4-hydroxyphenyl)ethyl]cyclohex-2-en-1-one 162932560 Click to see C1CC(=O)C=C(C1O)CCC2=CC=C(C=C2)O 232.27 unknown https://doi.org/10.1016/S0031-9422(00)89795-2
4-Hydroxy-3-[2-(4-hydroxyphenyl)ethyl]cyclohex-2-en-1-one 162932559 Click to see C1CC(=O)C=C(C1O)CCC2=CC=C(C=C2)O 232.27 unknown https://doi.org/10.1016/S0031-9422(00)89795-2
5-Hydroxy-3-[2-(4-hydroxyphenyl)ethyl]cyclohex-2-en-1-one 11207011 Click to see C1C(CC(=O)C=C1CCC2=CC=C(C=C2)O)O 232.27 unknown https://doi.org/10.1016/S0031-9422(00)89795-2
> Lignans, neolignans and related compounds
Pusilatin B 10033490 Click to see C1CC2=C(C=CC(=C2)O)C3=C(C=C(CCC4=CC(=C(C(=C4)OC5=CC=C1C=C5)O)C6=C(C7=CC(=C6)CCC8=CC(=C(C=C8)C9=C(CCC1=CC=C(O7)C=C1)C=C(C=C9)O)O)O)C=C3)O 847.00 unknown https://doi.org/10.1016/S0031-9422(00)89795-2
Riccardin C 10070992 Click to see C1CC2=C(C=CC(=C2)O)C3=C(C=C(CCC4=CC(=C(C=C4)O)OC5=CC=C1C=C5)C=C3)O 424.50 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
> 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/10.1016/0031-9422(90)85189-M
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/0031-9422(90)85189-M
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(90)85189-M
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1006/ABBI.1996.0352
> 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(90)85189-M
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(90)85189-M
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(3,4-dihydroxyphenyl)-ethyl-O-beta-D-glucopyranoside 5316821 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
2-(Hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol 4961358 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
2-[2-(3,4-Dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13845930 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
Salidroside 159278 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
> Organoheterocyclic compounds / Benzofurans
[(2S,3aS,7aR)-2-(furan-3-yl)-4,4-dimethyl-2,3,3a,5,6,7-hexahydro-1-benzofuran-7a-yl]methanol 14705526 Click to see CC1(CCCC2(C1CC(O2)C3=COC=C3)CO)C 250.33 unknown https://doi.org/10.1016/0031-9422(90)85189-M
> Organoheterocyclic compounds / Benzopyrans
(3R,4aS,8aR)-3-(Furan-3-yl)-5,5-dimethyloctahydro-1H-isochromen-1-one 10857827 Click to see CC1(CCCC2C1CC(OC2=O)C3=COC=C3)C 248.32 unknown https://doi.org/10.1006/ABBI.1998.0666
https://doi.org/10.1016/0031-9422(90)85189-M
Ricciocarpin B 11242514 Click to see CC1(CCCC2C1CC(OC2=O)C3=CC(=O)OC3)C 264.32 unknown https://doi.org/10.1016/0031-9422(90)85189-M
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(3aR,5aS,9aS,9bR)-3a-(hydroxymethyl)-7,9b-dimethyl-2,3,5a,8,9,9a-hexahydro-1H-cyclopenta[c]chromen-4-one 162965599 Click to see CC1=CC2C(CC1)C3(CCCC3(C(=O)O2)CO)C 250.33 unknown https://doi.org/10.1016/0031-9422(90)85189-M
(3aR,5aS,9aS,9bR)-3a,7,9b-trimethyl-2,3,5a,8,9,9a-hexahydro-1H-cyclopenta[c]chromen-4-one 162948854 Click to see CC1=CC2C(CC1)C3(CCCC3(C(=O)O2)C)C 234.33 unknown https://doi.org/10.1016/0031-9422(90)85189-M
(3aS,5aS,9aR,9bS)-3a-(hydroxymethyl)-7,9b-dimethyl-2,3,5a,8,9,9a-hexahydro-1H-cyclopenta[c]chromen-4-one 14705520 Click to see CC1=CC2C(CC1)C3(CCCC3(C(=O)O2)CO)C 250.33 unknown https://doi.org/10.1016/0031-9422(90)85189-M
(3aS,5aS,9aR,9bS)-3a,7,9b-trimethyl-2,3,5a,8,9,9a-hexahydro-1H-cyclopenta[c]chromen-4-one 14705518 Click to see CC1=CC2C(CC1)C3(CCCC3(C(=O)O2)C)C 234.33 unknown https://doi.org/10.1016/0031-9422(90)85189-M
(5aS,9aS,9bR)-3a-(hydroxymethyl)-7,9b-dimethyl-2,3,5a,8,9,9a-hexahydro-1H-cyclopenta[c]chromen-4-one 163188177 Click to see CC1=CC2C(CC1)C3(CCCC3(C(=O)O2)CO)C 250.33 unknown https://doi.org/10.1016/0031-9422(90)85189-M
> Phenylpropanoids and polyketides / Stilbenes
Lunularic acid 161413 Click to see C1=CC(=C(C(=C1)O)C(=O)O)CCC2=CC=C(C=C2)O 258.27 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
Lunularin 181511 Click to see C1=CC(=CC(=C1)O)CCC2=CC=C(C=C2)O 214.26 unknown https://doi.org/10.1016/0031-9422(90)85189-M
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2S,3R,4S,5S,6R)-2-[2-[2-(3,4-dihydroxyphenyl)ethyl]-4-hydroxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101635451 Click to see C1=CC(=C(C=C1CCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 408.40 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
(2S,3R,4S,5S,6R)-2-[4-hydroxy-2-[2-(4-hydroxyphenyl)ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101635450 Click to see C1=CC(=CC=C1CCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 392.40 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
(2S,3S,4S,5S,6R)-2-[2-[2-(3,4-dihydroxyphenyl)ethyl]-4-hydroxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162931517 Click to see C1=CC(=C(C=C1CCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 408.40 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
(2S,3S,4S,5S,6R)-2-[4-hydroxy-2-[2-(4-hydroxyphenyl)ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163003321 Click to see C1=CC(=CC=C1CCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 392.40 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
2-[2-[2-(3,4-Dihydroxyphenyl)ethyl]-4-hydroxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162931516 Click to see C1=CC(=C(C=C1CCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 408.40 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
2-[4-Hydroxy-2-[2-(4-hydroxyphenyl)ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163003320 Click to see C1=CC(=CC=C1CCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 392.40 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
2-hydroxy-6-[2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethyl]benzoic acid 101634590 Click to see C1=CC(=C(C(=C1)O)C(=O)O)CCC2=CC(=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 436.40 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
2-hydroxy-6-[2-[4-hydroxy-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethyl]benzoic acid 162972153 Click to see C1=CC(=C(C(=C1)O)C(=O)O)CCC2=CC(=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 436.40 unknown https://doi.org/10.1016/S0031-9422(00)97567-8
2-Hydroxy-6-[2-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethyl]benzoic acid 162972152 Click to see C1=CC(=C(C(=C1)O)C(=O)O)CCC2=CC(=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 436.40 unknown https://doi.org/10.1016/S0031-9422(00)97567-8

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