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Corsinia coriandrina

Corsinia coriandrina - 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 UUID64405003a565d889944433
Scientific name Corsinia coriandrina
Authority (Spreng.) Lindb.
First published in Hepaticol. Utveckl. 30 1877

Description Top

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Synonyms Top

Scientific name Authority First published in
Riccia coriandrina Spreng. Anleit. Kenntn. Gew. 3: 320 1804

Common names Top

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Language Common/alternative name
Chinese 花地钱

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-0001196280
USDA Plants COCO39
Tropicos 35185074
INPN 6194
The Plant List tro-35185074
Open Tree Of Life 386618
NCBI Taxonomy 63791
Nature Serve 2.125834
iNaturalist 160922
GBIF 2688608
EPPO QRSCO
EOL 604406

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
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
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
Synthesis of Benzo[b]furans by Intramolecular C–O Bond Formation Using Iron and Copper Catalysis Henry MC, Sutherland A Org Lett 18-Mar-2020
PMCID:PMC7146889
doi:10.1021/acs.orglett.0c00754
PMID:32186389
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
Does Calypogeia azurea (Calypogeiaceae, Marchantiophyta) occur outside Europe? Molecular and morphological evidence Buczkowska K, Bakalin V, Bączkiewicz A, Aguero B, Gonera P, Ślipiko M, Szczecińska M, Sawicki J PLoS One 10-Oct-2018
PMCID:PMC6179228
doi:10.1371/journal.pone.0204561
PMID:30304042
The evolution of the stomatal apparatus: intercellular spaces and sporophyte water relations in bryophytes—two ignored dimensions Duckett JG, Pressel S Philos Trans R Soc Lond B Biol Sci 18-Dec-2017
PMCID:PMC5745334
doi:10.1098/rstb.2016.0498
PMID:29254963
Modeling Species Distributions from Heterogeneous Data for the Biogeographic Regionalization of the European Bryophyte Flora Mateo RG, Vanderpoorten A, Muñoz J, Laenen B, Désamoré A PLoS One 11-Feb-2013
PMCID:PMC3569459
doi:10.1371/journal.pone.0055648
PMID:23409015
Olefinic Isothiocyanates and Iminodithiocarbonates from the Liverwort <i>Corsinia coriandrina</i> Stephan H. von Reuß, Wilfried A. König Wiley 17-Mar-2005
doi:10.1002/EJOC.200400586
Corsifurans A-C, 2-arylbenzofurans of presumed stilbenoid origin from Corsinia coriandrina (Hepaticae). von Reuss SH, König WA Phytochemistry 01-Dec-2004
doi:10.1016/J.PHYTOCHEM.2004.10.002
PMID:15541739

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 / Phenol ethers / Anisoles
1-(2-Isothiocyanatoethenyl)-4-methoxybenzene 72789643 Click to see COC1=CC=C(C=C1)C=CN=C=S 191.25 unknown https://doi.org/10.1002/EJOC.200400586
1-[(E)-2-isothiocyanatoethenyl]-4-methoxybenzene 11298450 Click to see COC1=CC=C(C=C1)C=CN=C=S 191.25 unknown https://doi.org/10.1002/EJOC.200400586
1-[(Z)-2-isothiocyanatoethenyl]-4-methoxybenzene 11194842 Click to see COC1=CC=C(C=C1)C=CN=C=S 191.25 unknown https://doi.org/10.1002/EJOC.200400586
N-[(E)-2-(4-methoxyphenyl)ethenyl]-1,1-bis(methylsulfanyl)methanimine 12159827 Click to see COC1=CC=C(C=C1)C=CN=C(SC)SC 253.40 unknown https://doi.org/10.1002/EJOC.200400586
N-[2-(4-methoxyphenyl)ethenyl]-1,1-bis(methylsulfanyl)methanimine 72978793 Click to see COC1=CC=C(C=C1)C=CN=C(SC)SC 253.40 unknown https://doi.org/10.1002/EJOC.200400586
Srbslxuypcrciy-hjwrwdbzsa- 11482188 Click to see COC1=CC=C(C=C1)C=CN=C(SC)SC 253.40 unknown https://doi.org/10.1002/EJOC.200400586
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-2-(4-methoxyphenyl)-2,3-dihydro-1-benzofuran-5-ol 162945298 Click to see COC1=CC=C(C=C1)C2CC3=C(O2)C=CC(=C3)O 242.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.002
(2R)-5-methoxy-2-(4-methoxyphenyl)-2,3-dihydro-1-benzofuran 15741494 Click to see COC1=CC=C(C=C1)C2CC3=C(O2)C=CC(=C3)OC 256.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.002
5-Benzofuranol, 2,3-dihydro-2-(4-methoxyphenyl)- 11160849 Click to see COC1=CC=C(C=C1)C2CC3=C(O2)C=CC(=C3)O 242.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.002
5-Methoxy-2-(4-methoxyphenyl)-2,3-dihydro-1-benzofuran 11253865 Click to see COC1=CC=C(C=C1)C2CC3=C(O2)C=CC(=C3)OC 256.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.002
5-Methoxy-2-(4-methoxyphenyl)benzofuran 11161125 Click to see COC1=CC=C(C=C1)C2=CC3=C(O2)C=CC(=C3)OC 254.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.002
> Phenylpropanoids and polyketides / Stilbenes
(E)-3,4'-Dimethoxystilbene 14954814 Click to see COC1=CC=C(C=C1)C=CC2=CC(=CC=C2)OC 240.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.002
1-Methoxy-3-[2-(4-methoxyphenyl)ethenyl]benzene 66772020 Click to see COC1=CC=C(C=C1)C=CC2=CC(=CC=C2)OC 240.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.002
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/J.PHYTOCHEM.2004.10.002
4Z-3,4'-dimethoxystilbene 44428189 Click to see COC1=CC=C(C=C1)C=CC2=CC(=CC=C2)OC 240.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.002
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/J.PHYTOCHEM.2004.10.002
Lunularin 181511 Click to see C1=CC(=CC(=C1)O)CCC2=CC=C(C=C2)O 214.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.10.002

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