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Blasia pusilla

Blasia pusilla - 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 UUID64404ffa3a67b162169643
Scientific name Blasia pusilla
Authority L.
First published in Sp. Pl. 1138 1753

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Belarusian Блазія маленькая
Czech jamuška drobná
Welsh cenddeil-lys
Welsh cenddail-lys
German blasiusmoos
German flaschenmoos
Estonian savitalluk
Finnish röyhelösammal
Japanese ウスバゼニゴケ
Dutch flesjesmos
Russian Блазия маленькая
Russian Блазия крошечная
Swedish lerbålmossa
Chinese 壶苞苔

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-0001196148
USDA Plants BLPU2
Tropicos 35184837
INPN 6282
The Plant List tro-35184837
Open Tree Of Life 756399
Observations.org 17692
NCBI Taxonomy 122625
NBN Atlas NBNSYS0000036027
Nature Serve 2.124891
iNaturalist 56441
GBIF 2688661
Freebase /m/02wc8hp
EPPO BLSPU
EOL 604421
Elurikkus 3121
Wikipedia Blasia

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
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
Hormogonium Development and Motility in Filamentous Cyanobacteria Risser DD Appl Environ Microbiol 18-May-2023
PMCID:PMC10304961
doi:10.1128/aem.00392-23
PMID:37199640
Four new suomilides isolated from the cyanobacterium Nostoc sp. KVJ20 and proposal of their biosynthetic origin Schneider YK, Liaimer A, Isaksson J, Wilhelmsen OS, Andersen JH, Hansen KØ, Hansen EH Front Microbiol 20-Apr-2023
PMCID:PMC10157211
doi:10.3389/fmicb.2023.1130018
PMID:37152725
Tridepsides as potential bioactives: a review on their chemistry and the global distribution of their lichenic and non-lichenic natural sources Norouzi H, Sohrabi M, Yousefi M, Boustie J Front Fungal Biol 19-Apr-2023
PMCID:PMC10512237
doi:10.3389/ffunb.2023.1088966
PMID:37746133
Bioactive Compounds Produced by Endophytic Microorganisms Associated with Bryophytes—The “Bryendophytes” Stelmasiewicz M, Świątek Ł, Gibbons S, Ludwiczuk A Molecules 05-Apr-2023
PMCID:PMC10096483
doi:10.3390/molecules28073246
PMID:37050009
Autophagy regulates plastid reorganization during spermatogenesis in the liverwort Marchantia polymorpha Norizuki T, Minamino N, Sato M, Ueda T Front Plant Sci 09-Feb-2023
PMCID:PMC9947651
doi:10.3389/fpls.2023.1101983
PMID:36844055
Phylotranscriptomics of liverworts: revisiting the backbone phylogeny and ancestral gene duplications Dong S, Yu J, Zhang L, Goffinet B, Liu Y Ann Bot 08-Sep-2022
PMCID:PMC9851303
doi:10.1093/aob/mcac113
PMID:36075207
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
Evolutionary genomic insights into cyanobacterial symbioses in plants de Vries S, de Vries J Quant Plant Biol 08-Aug-2022
PMCID:PMC10095879
doi:10.1017/qpb.2022.3
PMID:37077989
Deciphering Chemical Mediators Regulating Specialized Metabolism in a Symbiotic Cyanobacterium Krumbholz J, Ishida K, Baunach M, Teikari JE, Rose MM, Sasso S, Hertweck C, Dittmann E Angew Chem Int Ed Engl 09-May-2022
PMCID:PMC9324945
doi:10.1002/anie.202204545
PMID:35403785
Natural Products Targeting Liver X Receptors or Farnesoid X Receptor She J, Gu T, Pang X, Liu Y, Tang L, Zhou X Front Pharmacol 05-Jan-2022
PMCID:PMC8766425
doi:10.3389/fphar.2021.772435
PMID:35069197
The RGF/GLV/CLEL Family of Short Peptides Evolved Through Lineage-Specific Losses and Diversification and Yet Conserves Its Signaling Role Between Vascular Plants and Bryophytes Furumizu C, Sawa S Front Plant Sci 20-Jul-2021
PMCID:PMC8329595
doi:10.3389/fpls.2021.703012
PMID:34354727
Comparative genomic insights into culturable symbiotic cyanobacteria from the water fern Azolla Pratte BS, Thiel T Microb Genom 28-Jun-2021
PMCID:PMC8461463
doi:10.1099/mgen.0.000595
PMID:34181515

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 / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
Sparassol 596344 Click to see CC1=CC(=CC(=C1C(=O)OC)O)OC 196.20 unknown https://doi.org/10.1016/0040-4020(96)00889-7
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methyl 2,4-dihydroxy-6-methylbenzoate 76658 Click to see CC1=CC(=CC(=C1C(=O)OC)O)O 182.17 unknown https://doi.org/10.1016/0040-4020(96)00889-7
> Benzenoids / Benzene and substituted derivatives / Styrenes
5-[2-(4-Hydroxyphenyl)ethenyl]cyclohexa-1,3-diene-1,3-diol 122177172 Click to see C1C(C=C(C=C1O)O)C=CC2=CC=C(C=C2)O 230.26 unknown https://doi.org/10.1016/0040-4020(96)00889-7
> Lignans, neolignans and related compounds
26-[(16,24-Dihydroxy-14-oxapentacyclo[20.2.2.210,13.115,19.02,7]nonacosa-1(24),2(7),3,5,10(29),11,13(28),15,17,19(27),22,25-dodecaen-5-yl)oxy]-14-oxapentacyclo[20.2.2.210,13.115,19.02,7]nonacosa-1(24),2(7),3,5,10(29),11,13(28),15,17,19(27),22,25-dodecaene-5,16,24-triol 163192715 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)OC6=CC7=C(C=C6)C8=C(C=C(CCC9=CC(=C(C=C9)O)OC1=CC=C(CC7)C=C1)C=C8)O)O 847.00 unknown https://doi.org/10.1016/S0040-4039(00)75996-X
https://doi.org/10.1016/0040-4020(96)00889-7
4-(5,16,24-Trihydroxy-14-oxapentacyclo[20.2.2.210,13.115,19.02,7]nonacosa-1(24),2,4,6,10(29),11,13(28),15,17,19(27),22,25-dodecaen-4-yl)-14-oxapentacyclo[20.2.2.210,13.115,19.02,7]nonacosa-1(24),2,4,6,10(29),11,13(28),15,17,19(27),22,25-dodecaene-5,16,24-triol 102363088 Click to see C1CC2=CC(=C(C=C2C3=C(C=C(CCC4=CC(=C(C=C4)O)OC5=CC=C1C=C5)C=C3)O)C6=C(C=C7CCC8=CC=C(C=C8)OC9=C(C=CC(=C9)CCC1=CC(=C(C7=C6)C=C1)O)O)O)O 847.00 unknown https://doi.org/10.1016/S0040-4039(00)75996-X
https://doi.org/10.1016/0040-4020(96)00889-7
4-(5,16,24-Trihydroxy-14-oxapentacyclo[20.2.2.210,13.115,19.02,7]nonacosa-1(24),2(7),3,5,10(29),11,13(28),15(27),16,18,22,25-dodecaen-17-yl)-14-oxapentacyclo[20.2.2.210,13.115,19.02,7]nonacosa-1(24),2,4,6,10(29),11,13(28),15,17,19(27),22,25-dodecaene-5,16,24-triol 10259971 Click to see C1CC2=CC(=C(C=C2C3=C(C=C(CCC4=CC(=C(C=C4)O)OC5=CC=C1C=C5)C=C3)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)O 847.00 unknown https://doi.org/10.1016/S0040-4039(00)75996-X
https://doi.org/10.1016/0040-4020(96)00889-7
4-[(5,24-Dihydroxy-14-oxapentacyclo[20.2.2.210,13.115,19.02,7]nonacosa-1(24),2(7),3,5,10(29),11,13(28),15,17,19(27),22,25-dodecaen-16-yl)oxy]-14-oxapentacyclo[20.2.2.210,13.115,19.02,7]nonacosa-1(24),2,4,6,10(29),11,13(28),15,17,19(27),22,25-dodecaene-5,16,24-triol 162931507 Click to see C1CC2=CC(=C(C=C2C3=C(C=C(CCC4=CC(=C(C=C4)O)OC5=CC=C1C=C5)C=C3)O)OC6=C7C=C(CCC8=CC(=C(C=C8)C9=C(CCC1=CC=C(O7)C=C1)C=C(C=C9)O)O)C=C6)O 847.00 unknown https://doi.org/10.1016/S0040-4039(00)75996-X
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/S0040-4039(00)75996-X
https://doi.org/10.1016/0040-4020(96)00889-7
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/10.1016/0040-4020(96)00889-7
https://doi.org/10.1016/S0040-4039(00)75996-X
Riccardin F 11510446 Click to see COC1=C2C=C(CCC3=CC(=C(C=C3)C4=C(CCC5=CC=C(O2)C=C5)C=C(C=C4)O)O)C=C1 438.50 unknown https://doi.org/10.1016/0040-4020(96)00889-7
https://doi.org/10.1016/S0040-4039(00)75996-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid 1094 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/0040-4020(96)00889-7
Epishikimic acid 11332752 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/0040-4020(96)00889-7
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/0040-4020(96)00889-7
> Phenylpropanoids and polyketides / Depsides and depsidones
Benzoic acid, 2-hydroxy-4-[(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-6-methyl-, methyl ester 597048 Click to see CC1=CC(=CC(=C1C(=O)OC2=CC(=C(C(=C2)C)C(=O)OC)O)O)OC 346.30 unknown https://doi.org/10.1016/0040-4020(96)00889-7
Tenuiorin 10391110 Click to see CC1=CC(=CC(=C1C(=O)OC2=CC(=C(C(=C2)C)C(=O)OC3=CC(=C(C(=C3)C)C(=O)OC)O)O)O)OC 496.50 unknown https://doi.org/10.1016/0040-4020(96)00889-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0040-4020(96)00889-7
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0040-4020(96)00889-7
> Phenylpropanoids and polyketides / Stilbenes
Dihydroresveratrol 185914 Click to see C1=CC(=CC=C1CCC2=CC(=CC(=C2)O)O)O 230.26 unknown https://doi.org/10.1016/0040-4020(96)00889-7
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/10.1016/0040-4020(96)00889-7
Lunularin 181511 Click to see C1=CC(=CC(=C1)O)CCC2=CC=C(C=C2)O 214.26 unknown https://doi.org/10.1016/0040-4020(96)00889-7

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