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Lycopodium deuterodensum

Lycopodium deuterodensum - 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 UUID6440780cd9691659149650
Scientific name Lycopodium deuterodensum
Authority Herter
First published in Index Lycopodiarum 1949

Description Top

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Synonyms Top

Scientific name Authority First published in
Pseudolycopodium densum (Rothm.) Holub Folia Geobot. Phytotax. 18(4): 442 (1983)
Lepidotis densa Rothm. Feddes Repertorium Specierum Novarum Regni Vegetabilis 54 1944

Common names Top

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Language Common/alternative name
English bushy clubmoss
mi puakarimu
Polish pseudolycopodium densum

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Tasmania
      • Victoria
    • New Zealand
      • Chatham Islands
      • New Zealand North

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001119817
Tropicos 26614978
INPN 671167
KEW urn:lsid:ipni.org:names:131665-3
PaleoBotany 30236
Open Tree Of Life 429343
NCBI Taxonomy 73627
IPNI 131665-3
iNaturalist 366753
GBIF 3991027

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
Simple and Divided Leaves in Ferns: Exploring the Genetic Basis for Leaf Morphology Differences in the Genus Elaphoglossum (Dryopteridaceae) Vasco A, Ambrose BA Int J Mol Sci 22-Jul-2020
PMCID:PMC7432805
doi:10.3390/ijms21155180
PMID:32707812
Evidence for Co-evolutionary History of Early Diverging Lycopodiaceae Plants With Fungi Benucci GM, Burnard D, Shepherd LD, Bonito G, Munkacsi AB Front Microbiol 15-Jan-2020
PMCID:PMC6974469
doi:10.3389/fmicb.2019.02944
PMID:32010072
Metagenome Profiling Identifies Potential Biocontrol Agents for Selaginella kraussiana in New Zealand Dang Z, McLenachan PA, Lockhart PJ, Waipara N, Er O, Reynolds C, Blanchon D Genes (Basel) 31-Jan-2019
PMCID:PMC6409722
doi:10.3390/genes10020106
PMID:30709012
A Phylogenetic Study of the ANT Family Points to a preANT Gene as the Ancestor of Basal and euANT Transcription Factors in Land Plants Dipp-Álvarez M, Cruz-Ramírez A Front Plant Sci 29-Jan-2019
PMCID:PMC6361745
doi:10.3389/fpls.2019.00017
PMID:30761165
The Huperzia selago Shoot Tip Transcriptome Sheds New Light on the Evolution of Leaves Evkaikina AI, Berke L, Romanova MA, Proux-Wéra E, Ivanova AN, Rydin C, Pawlowski K, Voitsekhovskaja OV Genome Biol Evol 29-Aug-2017
PMCID:PMC5622374
doi:10.1093/gbe/evx169
PMID:28957460
Insights into the Structure, Function, and Ion-Mediated Signaling Pathways Transduced by Plant Integrin-Linked Kinases Popescu SC, Brauer EK, Dimlioglu G, Popescu GV Front Plant Sci 03-Apr-2017
PMCID:PMC5376563
doi:10.3389/fpls.2017.00376
PMID:28421082
Two New Abietanes from Lycopodium deuterodensum Hiroyuki Fuchino, Hisanori Nakamura, Yuka Toyoshima, Takashi Hakamatsuka, Nobutoshi Tanaka, Richard C. Cambie, John E. Braggins CSIRO Publishing 05-Aug-2004
doi:10.1071/C97182
GC/MS Examination of four Lycopodium species for alkaloid content Robert V. Gerard, David B. MacLean Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81570-8

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,10S,13S,14S,15S)-14-hydroxy-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadecan-11-one 154496352 Click to see CC1CC23C4CCCN2CCCC3C(=O)CC4C1O 263.37 unknown https://doi.org/10.1016/S0031-9422(00)81570-8
12-Epilycopodine 605459 Click to see CC1CC2CC(=O)C3CCCN4C3(C1)C2CCC4 247.38 unknown https://doi.org/10.1071/C97182
Lycopodine 5462445 Click to see CC1CC2CC(=O)C3CCCN4C3(C1)C2CCC4 247.38 unknown https://doi.org/10.1071/C97182
N-[(1R,2R,13S,15R)-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadec-10-en-11-yl]acetamide 101289809 Click to see CC1CC2CC(=C3CCCN4C3(C1)C2CCC4)NC(=O)C 288.40 unknown https://doi.org/10.1016/S0031-9422(00)81570-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,6R,11R,12R,15R,16R,21R)-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene-8,19-diol 138113880 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown https://doi.org/10.1071/C97182
16-Oxoserratenediol 101280207 Click to see CC1(C2CCC3(CC4=CC(=O)C5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 456.70 unknown https://doi.org/10.1071/C97182
21-Episerratenediol 12309682 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown https://doi.org/10.1071/C97182
21-Episerratriol 72976421 Click to see CC1(C(CCC2(C1CC=C3C2CCC4C(C3)(CCC5C4(CCC(C5(C)CO)O)C)C)C)O)C 458.70 unknown https://doi.org/10.1071/C97182
5,5'-(Ethane-1,2-diyl)bis(1,1,4a-trimethyl-6-methylidenedecahydronaphthalen-2-ol) 5320292 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)CCC3C(=C)CCC4C3(CCC(C4(C)C)O)C)C 442.70 unknown https://doi.org/10.1071/C97182
8,19-Dihydroxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-5-one 73808018 Click to see CC1(C2CCC3(CC4=CC(=O)C5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 456.70 unknown https://doi.org/10.1071/C97182
alpha-Onocerin 11453544 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)CCC3C(=C)CCC4C3(CCC(C4(C)C)O)C)C 442.70 unknown https://doi.org/10.1071/C97182
CID 634946 634946 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown https://doi.org/10.1071/C97182
CID 91895438 91895438 Click to see CC1(C(CCC2(C1CC=C3C2CCC4C(C3)(CCC5C4(CCC(C5(C)CO)O)C)C)C)O)C 458.70 unknown https://doi.org/10.1071/C97182
Serratriol 91895439 Click to see CC1(C(CCC2(C1CC=C3C2CCC4C(C3)(CCC5C4(CCC(C5(C)CO)O)C)C)C)O)C 458.70 unknown https://doi.org/10.1071/C97182
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
Methicillin 6087 Click to see CC1(C(N2C(S1)C(C2=O)NC(=O)C3=C(C=CC=C3OC)OC)C(=O)O)C 380.40 unknown https://doi.org/10.1016/S0031-9422(00)81570-8
> Organoheterocyclic compounds / Azaspirodecane derivatives
Lycoflexine 442486 Click to see CC1CC2CC(=O)C34C2(CCCN(C3)CCC4)C(=O)C1 275.40 unknown https://doi.org/10.1016/S0031-9422(00)81570-8
> Organoheterocyclic compounds / Phenanthrolines
Lycodine 5462443 Click to see CC1CC2CC3=C(C=CC=N3)C4(C1)C2CCCN4 242.36 unknown https://doi.org/10.1016/S0031-9422(00)81570-8

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