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Selaginella moellendorffii

Selaginella moellendorffii - 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 UUID64404d05651c1544923695
Scientific name Selaginella moellendorffii
Authority Hieron.
First published in Nat. Pflanzenfam. 1(abt. 4, lief. 210): 680, no (1901)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lycopodioides moellendorffii (Hieron.) H.S.Kung Fl. Sichuanica 6: 75 (1988)

Common names Top

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Language Common/alternative name
Japanese イヌカタヒバ
Chinese 地柏枝
Chinese 细叶卷柏
Chinese 江南卷柏
Chinese 異葉卷柏

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001126409
Tropicos 26622966
KEW urn:lsid:ipni.org:names:60457176-2
The Plant List tro-26622966
Open Tree Of Life 799880
NCBI Taxonomy 88036
IPNI 60457176-2
iNaturalist 405935
GBIF 5836522
Freebase /m/02rv7wx
EPPO SELMO
Wikipedia Selaginella_moellendorffii

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCF_000143415.4 v1.0 Scaffold Selaginella Consortium 2010-07-06 7.0x 202.48 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
Origin, evolution, and diversification of inositol 1,4,5-trisphosphate 3-kinases in plants and animals Xiong T, Zhang Z, Fan T, Ye F, Ye Z BMC Genomics 08-Apr-2024
PMCID:PMC11000326
doi:10.1186/s12864-024-10257-7
PMID:38589807
Mechanism of action of microRNA166 on nitric oxide in alfalfa (Medicago sativa L.) under drought stress Wei B, Wang Y, Ruan Q, Zhu X, Wang X, Wang T, Zhao Y, Wei X BMC Genomics 28-Mar-2024
PMCID:PMC10976769
doi:10.1186/s12864-024-10095-7
PMID:38549050
Genome-wide characterization of heavy metal-associated isoprenylated plant protein gene family from Citrus sinensis in response to huanglongbing Huang G, Hu Y, Li F, Zuo X, Wang X, Li F, Li R Front Plant Sci 27-Mar-2024
PMCID:PMC11004388
doi:10.3389/fpls.2024.1369883
PMID:38601304
A fungal core effector exploits the OsPUX8B.2–OsCDC48-6 module to suppress plant immunity Shi X, Xie X, Guo Y, Zhang J, Gong Z, Zhang K, Mei J, Xia X, Xia H, Ning N, Xiao Y, Yang Q, Wang GL, Liu W Nat Commun 22-Mar-2024
PMCID:PMC10959940
doi:10.1038/s41467-024-46903-7
PMID:38519521
Subscaling of a cytosolic RNA binding protein governs cell size homeostasis in the multiple fission alga Chlamydomonas Liu D, Lopez-Paz C, Li Y, Zhuang X, Umen J PLoS Genet 18-Mar-2024
PMCID:PMC10977881
doi:10.1371/journal.pgen.1010503
PMID:38498520
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
Identification of two mutant JASON-RELATED genes associated with unreduced pollen production in potato Clot CR, Vexler L, de La O Leyva-Perez M, Bourke PM, Engelen CJ, Hutten RC, van de Belt J, Wijnker E, Milbourne D, Visser RG, Juranić M, van Eck HJ Theor Appl Genet 12-Mar-2024
PMCID:PMC10933213
doi:10.1007/s00122-024-04563-7
PMID:38472376
Evolutionary and Structural Analysis of PP16 in Viridiplantae Jiménez-López D, Xoconostle-Cázares B, Calderón-Pérez B, Vargas-Hernández BY, Núñez-Muñoz LA, Ramírez-Pool JA, Ruiz-Medrano R Int J Mol Sci 29-Feb-2024
PMCID:PMC10931576
doi:10.3390/ijms25052839
PMID:38474088
Genome-wide identification of the N6-methyladenosine regulatory genes reveals NtFIP37B increases drought resistance of tobacco (Nicotiana tabacum L.) Su H, Meng L, Qu Z, Zhang W, Liu N, Cao P, Jin J BMC Plant Biol 26-Feb-2024
PMCID:PMC10895791
doi:10.1186/s12870-024-04813-2
PMID:38403644
Recurrent evolutionary switches of mitochondrial cytochrome c maturation systems in Archaeplastida Li H, Akella S, Engstler C, Omini JJ, Rodriguez M, Obata T, Carrie C, Cerutti H, Mower JP Nat Commun 20-Feb-2024
PMCID:PMC10879542
doi:10.1038/s41467-024-45813-y
PMID:38378784
Helenus and Ajax, Two Groups of Non-Autonomous LTR Retrotransposons, Represent a New Type of Small RNA Gene-Derived Mobile Elements Kojima KK Biology (Basel) 13-Feb-2024
PMCID:PMC10886601
doi:10.3390/biology13020119
PMID:38392337
The Emerging Role of Non-Coding RNAs (ncRNAs) in Plant Growth, Development, and Stress Response Signaling Yadav A, Mathan J, Dubey AK, Singh A Noncoding RNA 07-Feb-2024
PMCID:PMC10893181
doi:10.3390/ncrna10010013
PMID:38392968
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
Cloned genes and genetic regulation of anthocyanin biosynthesis in maize, a comparative review Chachar Z, Lai R, Ahmed N, Lingling M, Chachar S, Paker NP, Qi Y Front Plant Sci 24-Jan-2024
PMCID:PMC10847539
doi:10.3389/fpls.2024.1310634
PMID:38328707
Unveiling the structure and interactions of SOG1, a NAC domain transcription factor: An in-silico perspective Mahapatra K J Genet Eng Biotechnol 23-Jan-2024
PMCID:PMC10980851
doi:10.1016/j.jgeb.2023.100333
PMID:38494249

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Acoradiene 90351 Click to see CC1CCC(C12CCC(=CC2)C)C(=C)C 204.35 unknown https://doi.org/10.1002/HLCA.201000116
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(2S)-3-hydroxy-2-[4-(3-hydroxypropyl)-2,6-dimethoxyphenoxy]propyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163031610 Click to see COC1=CC(=CC(=C1OC(CC2=CC(=C(C(=C2)OC)OC3C(C(C(C(O3)CO)O)O)O)OC)CO)OC)CCCO 584.60 unknown https://doi.org/10.1002/HLCA.201000116
2-[4-[3-Hydroxy-2-[4-(3-hydroxypropyl)-2,6-dimethoxyphenoxy]propyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163031609 Click to see COC1=CC(=CC(=C1OC(CC2=CC(=C(C(=C2)OC)OC3C(C(C(C(O3)CO)O)O)O)OC)CO)OC)CCCO 584.60 unknown https://doi.org/10.1002/HLCA.201000116
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(E)-N-(4-aminobutyl)-3-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enamide 50918049 Click to see C1=CC(=C(C=C1C=CC(=O)NCCCCN)OC2C(C(C(C(O2)CO)O)O)O)O 412.40 unknown https://doi.org/10.1002/HLCA.201000116
N-(4-aminobutyl)-3-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enamide 75581962 Click to see C1=CC(=C(C=C1C=CC(=O)NCCCCN)OC2C(C(C(C(O2)CO)O)O)O)O 412.40 unknown https://doi.org/10.1002/HLCA.201000116
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines / Tetrodotoxins
3-Amino-14-(hydroxymethyl)-8,10-dioxa-2,4-diazatetracyclo[7.3.1.17,11.01,6]tetradec-3-ene-5,9,12,13,14-pentol 4490623 Click to see C(C1(C2C3C(N=C(NC34C(C1OC(C4O)(O2)O)O)N)O)O)O 319.27 unknown https://doi.org/10.1002/HLCA.201000116
> Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines
Neoselaginellic acid 44179585 Click to see CC(=CCC1(CCN(C1=O)C)C2=CC=CC=C2N(C)C)C(=O)O 316.40 unknown https://doi.org/10.1021/NP9001515
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3R,4S,5S,6R)-2-[[(2S,3S)-2-(4-hydroxy-3,5-dimethoxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162952603 Click to see COC1=CC(=CC2=C1OC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C(=C4)OC)O)OC)CCCO 552.60 unknown https://doi.org/10.1002/HLCA.201000116
(2R,3R,4S,5S,6R)-2-[[2-(4-hydroxy-3,5-dimethoxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-1-benzofuran-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 102262568 Click to see COC1=CC(=CC2=C1OC(=C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C(=C4)OC)O)OC)CCCO 550.60 unknown https://doi.org/10.1002/HLCA.201000116
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(2R,3S)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 162906337 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 552.60 unknown https://doi.org/10.1002/HLCA.201000116
(2S,3R)-3-(hydroxymethyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-carboxylic acid 102262565 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=CC(=C3)C(=O)O)CO)O 286.28 unknown https://doi.org/10.1002/HLCA.201000116
(2S,3S,10R,11R,18S,19R,21S,25S)-3,11,19-tris(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.12,5.110,13.021,25.09,27.017,26]heptacosa-1(24),5,7,9(27),13,15,17(26),22-octaene-7,15,23-triol 163059668 Click to see C1=CC(=CC=C1C2C3C4C(O2)C=C(C=C4C5C(OC6=CC(=CC(=C56)C7C(OC8=CC(=CC3=C78)O)C9=CC=C(C=C9)O)O)C1=CC=C(C=C1)O)O)O 680.70 unknown https://doi.org/10.1002/HLCA.201000116
(E)-3-[(2S,3R)-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoic acid 102262563 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)C=CC(=O)O 402.40 unknown https://doi.org/10.1002/HLCA.201000116
2-(Hydroxymethyl)-6-[4-[3-(hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 162906336 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 552.60 unknown https://doi.org/10.1002/HLCA.201000116
2-[[2-(4-Hydroxy-3,5-dimethoxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-1-benzofuran-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162876197 Click to see COC1=CC(=CC2=C1OC(=C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C(=C4)OC)O)OC)CCCO 550.60 unknown https://doi.org/10.1002/HLCA.201000116
2-[[2-(4-Hydroxy-3,5-dimethoxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162952602 Click to see COC1=CC(=CC2=C1OC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C(=C4)OC)O)OC)CCCO 552.60 unknown https://doi.org/10.1002/HLCA.201000116
3-(Hydroxymethyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-carboxylic acid 162870078 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=CC(=C3)C(=O)O)CO)O 286.28 unknown https://doi.org/10.1002/HLCA.201000116
3-[2-(4-Hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoic acid 162953889 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)C=CC(=O)O 402.40 unknown https://doi.org/10.1002/HLCA.201000116
4-[3-(Hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2,6-dimethoxyphenol 56849116 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)CCCO 390.40 unknown https://doi.org/10.1002/HLCA.201000116
5-Methoxy-trans-dihydrodehydrodiconiferyl alcohol 56838440 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)CCCO 390.40 unknown https://doi.org/10.1002/HLCA.201000116
methyl 3-[(2S,3R)-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propanoate 102262569 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)CCC(=O)OC 418.40 unknown https://doi.org/10.1002/HLCA.201000116
Methyl 3-[2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propanoate 163069357 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)CCC(=O)OC 418.40 unknown https://doi.org/10.1002/HLCA.201000116
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-(4-aminobutyl)-3-(3,4-dihydroxyphenyl)prop-2-enamide 439877 Click to see C1=CC(=C(C=C1C=CC(=O)NCCCCN)O)O 250.29 unknown https://doi.org/10.1002/HLCA.201000116
N-Caffeoylputrescine 5280559 Click to see C1=CC(=C(C=C1C=CC(=O)NCCCCN)O)O 250.29 unknown https://doi.org/10.1002/HLCA.201000116
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(2,3,4,5,6-Pentahydroxycyclohexyl) 3-(3,4-dihydroxyphenyl)prop-2-enoate 69876098 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(C(C2O)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1002/HLCA.201000116
cis-p-Coumaroylagmatine 10826328 Click to see C1=CC(=CC=C1C=CC(=O)NCCCCN=C(N)N)O 276.33 unknown https://doi.org/10.1002/HLCA.201000116
p-Cumaroylagmatin 440362 Click to see C1=CC(=CC=C1C=CC(=O)NCCCCN=C(N)N)O 276.33 unknown https://doi.org/10.1002/HLCA.201000116
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1248/BPB.24.311
https://doi.org/10.1016/J.JEP.2015.01.031
https://doi.org/10.1021/NP960608E
Ginkgetin 5271805 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 566.50 unknown https://doi.org/10.1021/NP960608E
Podocarpusflavone A 5320644 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 552.50 unknown https://doi.org/10.1021/NP960608E
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Ethyl 2-[7-hydroxy-2-(4-hydroxyphenyl)-4-oxo-chromen-5-yl]acetate 49776865 Click to see CCOC(=O)CC1=C2C(=CC(=C1)O)OC(=CC2=O)C3=CC=C(C=C3)O 340.30 unknown https://doi.org/10.1016/J.FITOTE.2009.09.007

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