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Marchantia paleacea

Marchantia paleacea - 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 UUID6440501812b81228568112
Scientific name Marchantia paleacea
Authority Bertol.
First published in Opusc. Sci. 1: 242 1817

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 粗裂地钱
Chinese 粗裂地錢

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Marchantia paleacea subsp. diptera (Nees & Mont.) Inoue J. Jap. Bot. 64: 194 1989

Varieties (abbr. var.) Top

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Name Authority First published in
Marchantia paleacea var. xerophila (Burgeff) J.J.Engel & B.C.Tan J. Hattori Bot. Lab. 60: 315 1986

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-0001196532
Florida Plant Atlas 4795
USDA Plants MAPA25
Tropicos 35185594
INPN 6181
The Plant List tro-35185594
Open Tree Of Life 565727
NCBI Taxonomy 56867
Nature Serve 2.1035645
iNaturalist 165153
GBIF 2688573
EOL 599449
Wikipedia Marchantia_paleacea

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_014180765.2 ASM1418076v2 Contig John Innes Centre 2021-05-25 64.0x 239.18 Mb

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
In Silico Analysis of Glutamate Receptors in Capsicum chinense: Structure, Evolution, and Molecular Interactions León-García F, García-Laynes F, Estrada-Tapia G, Monforte-González M, Martínez-Estevez M, Echevarría-Machado I Plants (Basel) 12-Mar-2024
PMCID:PMC10975470
doi:10.3390/plants13060812
PMID:38592787
Genome-wide identification, expression profiling, and protein interaction analysis of the CCoAOMT gene family in the tea plant (Camellia sinensis) Wang Y, Wang T, Qi S, Zhao J, Kong J, Xue Z, Sun W, Zeng W BMC Genomics 04-Mar-2024
PMCID:PMC10913456
doi:10.1186/s12864-024-09972-y
PMID:38438984
Characterization of the complete chloroplast genome of Barbella flagellifera (Cardot) Nog. 1938 (Bryidae, Meteoriaceae) Yuan ZY, Wang Q, Sulayman M Mitochondrial DNA B Resour 26-Feb-2024
PMCID:PMC10898263
doi:10.1080/23802359.2024.2318393
PMID:38414806
Cytochrome c oxidase subunit I gene in Thalassiosira nordenskioeldii strains inhabiting in cold and warm sea waters UCHIDA Y, UCHIDA H, SATO T, NISHIMOTO Y, TSUTSUMI K, OI T, TANIGUCHI M, INOUE K, SUZUKI Y Proc Jpn Acad Ser B Phys Biol Sci 09-Feb-2024
PMCID:PMC10978971
doi:10.2183/pjab.100.010
PMID:38346753
Telomere Length Variation in Model Bryophytes Valeeva LR, Sannikova AV, Shafigullina NR, Abdulkina LR, Sharipova MR, Shakirov EV Plants (Basel) 28-Jan-2024
PMCID:PMC10856949
doi:10.3390/plants13030387
PMID:38337920
Comparative analysis of SPL transcription factors from streptophyte algae and embryophytes reveals evolutionary trajectories of SPL family in streptophytes Alisha A, Szweykowska-Kulinska Z, Sierocka I Sci Rep 18-Jan-2024
PMCID:PMC10796333
doi:10.1038/s41598-024-51626-2
PMID:38238367
Molecular cloning and functional analysis of 4-coumarate: CoA ligases from Marchantia paleacea and their roles in lignin and flavanone biosynthesis Gao S, Liu XY, Ni R, Fu J, Tan H, Cheng AX, Lou HX PLoS One 08-Jan-2024
PMCID:PMC10773943
doi:10.1371/journal.pone.0296079
PMID:38190396
The complete chloroplast genome of Porella gracillima Mitt. (Porellaceae) and phylogenetic relationships to other bryophytes Lee JK, Park MJ, Park SJ, Park JS Mitochondrial DNA B Resour 21-Dec-2023
PMCID:PMC10763829
doi:10.1080/23802359.2023.2294898
PMID:38173922
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 first mitogenome of Lauraceae (Cinnamomum chekiangense) Bi C, Sun N, Han F, Xu K, Yang Y, Ferguson DK Plant Divers 18-Nov-2023
PMCID:PMC10851304
doi:10.1016/j.pld.2023.11.001
PMID:38343589
Plants acquired mitochondrial linear plasmids horizontally from fungi likely during the conquest of land Wei Y, Gong Z, Han GZ Mob DNA 17-Oct-2023
PMCID:PMC10583447
doi:10.1186/s13100-023-00304-7
PMID:37849012
Control of arbuscule development by a transcriptional negative feedback loop in Medicago Zhang Q, Wang S, Xie Q, Xia Y, Lu L, Wang M, Wang G, Long S, Cai Y, Xu L, Wang E, Jiang Y Nat Commun 16-Sep-2023
PMCID:PMC10505183
doi:10.1038/s41467-023-41493-2
PMID:37717076
Strigolactones and Shoot Branching: What Is the Real Hormone and How Does It Work? Dun EA, Brewer PB, Gillam EM, Beveridge CA Plant Cell Physiol 01-Aug-2023
PMCID:PMC10504579
doi:10.1093/pcp/pcad088
PMID:37526426
Activation of Strigolactone Biosynthesis by the DWARF14-LIKE/KARRIKIN-INSENSITIVE2 Pathway in Mycorrhizal Angiosperms, but Not in Arabidopsis, a Non-mycorrhizal Plant Mashiguchi K, Morita R, Tanaka K, Kodama K, Kameoka H, Kyozuka J, Seto Y, Yamaguchi S Plant Cell Physiol 26-Jul-2023
PMCID:PMC10504576
doi:10.1093/pcp/pcad079
PMID:37494415
KAI2 Can Do: Karrikin Receptor Function in Plant Development and Response to Abiotic and Biotic Factors Varshney K, Gutjahr C Plant Cell Physiol 19-Jul-2023
PMCID:PMC10504578
doi:10.1093/pcp/pcad077
PMID:37548562

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
> Lignans, neolignans and related compounds
2,15-Dioxapentacyclo[22.2.2.13,7.110,14.016,21]triaconta-1(26),3(30),4,6,10(29),11,13,16(21),17,19,24,27-dodecaene-4,5,8,17-tetrol 5319273 Click to see C1CC2=C(C(=CC=C2)O)OC3=CC=CC(=C3)CC(C4=CC(=C(C(=C4)OC5=CC=C1C=C5)O)O)O 456.50 unknown https://doi.org/10.1248/CPB.42.1376
5,13-Dihydroxy-3-methoxy-15-oxapentacyclo[20.2.2.216,19.110,14.02,7]nonacosa-1(24),2(7),3,5,10(29),11,13,16,18,22(26),27-undecaene-23,25-dione 163192404 Click to see COC1=CC(=CC2=C1C3=CC(=O)C(=CC3=O)CCC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC2)O)O 468.50 unknown https://doi.org/10.1080/10575630290004242
Isoriccardin C 13831041 Click to see C1CC2=CC(=C(C=C2)C3=C(CCC4=CC(=C(C=C4)O)OC5=CC=C1C=C5)C=CC=C3O)O 424.50 unknown https://doi.org/10.1080/10575630290004242
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/S0031-9422(97)00273-2
https://doi.org/10.1248/CPB.42.1376
Marchantin B 5319271 Click to see C1CC2=C(C(=C(C=C2)O)O)OC3=CC=CC(=C3)CCC4=CC(=C(C(=C4)OC5=CC=C1C=C5)O)O 456.50 unknown https://doi.org/10.1248/CPB.42.1376
Marchantin C 5319272 Click to see C1CC2=C(C(=CC=C2)O)OC3=CC=CC(=C3)CCC4=CC(=C(C=C4)O)OC5=CC=C1C=C5 424.50 unknown https://doi.org/10.1080/10575630290004242
https://doi.org/10.1248/CPB.42.1376
Marchantin E 5319274 Click to see COC1CC2=CC(=CC=C2)OC3=C(CCC4=CC=C(C=C4)OC5=CC1=CC(=C5O)O)C=CC=C3O 470.50 unknown https://doi.org/10.1248/CPB.42.1376
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13E)-labda-7,13-dien-15-ol 639636 Click to see CC1=CCC2C(CCCC2(C1CCC(=CCO)C)C)(C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(97)00273-2
5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-ol 72829262 Click to see CC1=CCC2C(CCCC2(C1CCC(=CCO)C)C)(C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(97)00273-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00273-2
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00273-2
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-[(8Z,11Z)-hexadeca-8,11-dienyl]-5-methylidenefuran-2-one 102427198 Click to see CCCCC=CCC=CCCCCCCCC1=CC(=C)OC1=O 316.50 unknown https://doi.org/10.1016/S0031-9422(97)00273-2
3-[(Z)-hexadec-8-enyl]-5-methylidenefuran-2-one 102427199 Click to see CCCCCCCC=CCCCCCCCC1=CC(=C)OC1=O 318.50 unknown https://doi.org/10.1016/S0031-9422(97)00273-2
3-Hexadec-8-enyl-5-methylidenefuran-2-one 163044420 Click to see CCCCCCCC=CCCCCCCCC1=CC(=C)OC1=O 318.50 unknown https://doi.org/10.1016/S0031-9422(97)00273-2
3-Hexadeca-8,11-dienyl-5-methylidenefuran-2-one 162904824 Click to see CCCCC=CCC=CCCCCCCCC1=CC(=C)OC1=O 316.50 unknown https://doi.org/10.1016/S0031-9422(97)00273-2
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate 5459387 Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C=C)C 871.20 unknown https://doi.org/10.1016/0922-338X(96)87735-X
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate 6433193 Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C=C)C 871.20 unknown https://doi.org/10.1016/0922-338X(96)87735-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(92)80270-O
> Phenylpropanoids and polyketides / Stilbenes
5-[(1R)-2-[3-[2-hydroxy-6-[2-(4-hydroxyphenyl)ethyl]phenoxy]phenyl]-1-methoxyethyl]-3-methoxybenzene-1,2-diol 154497151 Click to see COC1=CC(=CC(=C1O)O)C(CC2=CC(=CC=C2)OC3=C(C=CC=C3O)CCC4=CC=C(C=C4)O)OC 502.60 unknown https://doi.org/10.1248/CPB.42.1376
5-[2-[3-[2-Hydroxy-6-[2-(4-hydroxyphenyl)ethyl]phenoxy]phenyl]-1-methoxyethyl]-3-methoxybenzene-1,2-diol 10006248 Click to see COC1=CC(=CC(=C1O)O)C(CC2=CC(=CC=C2)OC3=C(C=CC=C3O)CCC4=CC=C(C=C4)O)OC 502.60 unknown https://doi.org/10.1248/CPB.42.1376
Paleatin A 10027781 Click to see COC1=CC(=CC(=C1O)O)CCC2=CC(=CC=C2)OC3=C(C=CC=C3O)CCC4=CC=C(C=C4)O 472.50 unknown https://doi.org/10.1248/CPB.42.1376

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