Selaginella sinensis - Unknown
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Internal ID UUID64404d09ad7c6332359615
Scientific name Selaginella sinensis
Authority (Desv.) Spring
First published in Bull. Acad. Roy. Sci. Bruxelles 10(1): 137 (1843)

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Synonyms Top

Scientific name Authority First published in
Selaginella mongholica Rupr. Beitr. Pflanzenk. Russ. Reiches 3: 32 (1845)
Lycopodium sinense Desv. Mém. Soc. Linn. Paris 6(2): 189 (1827)
Lycopodioides sinensis (Desv.) Satou Hikobia 12(3): 269 (1997)

Common names Top

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Language Common/alternative name
Chinese 黑顶卷柏
Chinese 中华卷柏

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Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Hainan
      • Inner Mongolia
      • Manchuria
    • Mongolia
      • Mongolia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001127258
Tropicos 26623998
KEW urn:lsid:ipni.org:names:60467467-2
The Plant List tro-26623998
Open Tree Of Life 1058263
NCBI Taxonomy 137174
IPNI 60467467-2
iNaturalist 601655
GBIF 7867535
EOL 11829787

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
Sea Buckthorn Flavonoid Extracted by High Hydrostatic Pressure Inhibited IgE-Stimulated Mast Cell Activation through the Mitogen-Activated Protein Kinase Signaling Pathway Yan Z, Feng X, Li X, Gao Z, Wang Z, Ren G, Long F Foods 12-Feb-2024
PMCID:PMC10887968
doi:10.3390/foods13040560
PMID:38397537
A systematic review on antimicrobial activities of green synthesised Selaginella silver nanoparticles Wadhwa K, Kaur H, Kapoor N, Ghorai SM, Gupta R, Sahgal A Expert Rev Mol Med 03-Aug-2023
PMCID:PMC10752228
doi:10.1017/erm.2023.21
PMID:37534437
Phylogeny, character evolution, and classification of Selaginellaceae (lycophytes) Zhou XM, Zhang LB Plant Divers 20-Jul-2023
PMCID:PMC10772194
doi:10.1016/j.pld.2023.07.003
PMID:38197007
Neuroprotective Potential of Biflavone Ginkgetin: A Review Tatlı Çankaya İİ, Devkota HP, Zengin G, Šamec D Life (Basel) 16-Feb-2023
PMCID:PMC9964866
doi:10.3390/life13020562
PMID:36836918
Sinensiols H–J, three new lignan derivatives from Selaginella sinensis (Desv.) Spring Zhu Q, Gao B, Chen Q, Luo T, Xu G, Liao S Beilstein J Org Chem 07-Oct-2022
PMCID:PMC9551277
doi:10.3762/bjoc.18.146
PMID:36262670
Origins of the seed: The “golden-trio hypothesis” Bai SN, Rao GY, Yang J Front Plant Sci 29-Aug-2022
PMCID:PMC9465013
doi:10.3389/fpls.2022.965000
PMID:36105705
Medicinal Plants and Fungi Traditionally Used by Dulong People in Northwest Yunnan, China Cheng Z, Hu X, Lu X, Fang Q, Meng Y, Long C Front Pharmacol 09-May-2022
PMCID:PMC9124798
doi:10.3389/fphar.2022.895129
PMID:35614945
Inhibition of the main protease of SARS-CoV-2 (Mpro) by repurposing/designing drug-like substances and utilizing nature’s toolbox of bioactive compounds Antonopoulou I, Sapountzaki E, Rova U, Christakopoulos P Comput Struct Biotechnol J 14-Mar-2022
PMCID:PMC8920478
doi:10.1016/j.csbj.2022.03.009
PMID:35308802
Coronavirus Infection-Associated Cell Death Signaling and Potential Therapeutic Targets Yapasert R, Khaw-on P, Banjerdpongchai R Molecules 09-Dec-2021
PMCID:PMC8706825
doi:10.3390/molecules26247459
PMID:34946543
Correction to Ultrasonic-Assisted Ionic Liquid Extraction of Two Biflavonoids from Selaginella tamariscina Jiang Y, Wang S, Yu M, wu D, Lei J, Li W, He Y, Gang W ACS Omega 07-Apr-2021
PMCID:PMC8153778
doi:10.1021/acsomega.1c01480
PMID:34056204
Exploration of natural compounds with anti-SARS-CoV-2 activity via inhibition of SARS-CoV-2 Mpro Bharadwaj S, Dubey A, Yadava U, Mishra SK, Kang SG, Dwivedi VD Brief Bioinform 07-Jan-2021
PMCID:PMC7929395
doi:10.1093/bib/bbaa382
PMID:33406222
Comparison of Chemical Composition and Biological Activities of Eight Selaginella Species Křížkovská B, Kumar R, Řehořová K, Sýkora D, Dobiasová S, Kučerová D, Tan MC, Linis V, Oyong G, Ruml T, Lipov J, Viktorová J Pharmaceuticals (Basel) 26-Dec-2020
PMCID:PMC7823444
doi:10.3390/ph14010016
PMID:33375355
Biflavonoid as potential 3-chymotrypsin-like protease (3CLpro) inhibitor of SARS-Coronavirus Hartini Y, Saputra B, Wahono B, Auw Z, Indayani F, Adelya L, Namba G, Hariono M Results Chem 25-Dec-2020
PMCID:PMC7832947
doi:10.1016/j.rechem.2020.100087
PMID:33520632
Challenges and future directions of potential natural products leads against 2019-nCoV outbreak Ospanov M, León F, Jenis J, Khan IA, Ibrahim MA Curr Plant Biol 08-Oct-2020
PMCID:PMC7543902
doi:10.1016/j.cpb.2020.100180
PMID:33052305
Hinokiflavone induces apoptosis via activating mitochondrial ROS/JNK/caspase pathway and inhibiting NF‐κB activity in hepatocellular carcinoma Mu W, Cheng X, Zhang X, Liu Y, Lv Q, Liu G, Zhang J, Li X J Cell Mol Med 09-Jun-2020
PMCID:PMC7348176
doi:10.1111/jcmm.15474
PMID:32519392

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 / Naphthalenes / Naphthols and derivatives
1-Naphthol 7005 Click to see C1=CC=C2C(=C1)C=CC=C2O 144.17 unknown https://doi.org/10.1007/S10600-012-0230-4
> Lignans, neolignans and related compounds / Lignan glycosides
Pinoresinol diglucoside 174003 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC6C(C(C(C(O6)CO)O)O)O 682.70 unknown https://doi.org/10.1007/S10600-012-0230-4
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
6-[5-(5,7-Dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenyl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 10392851 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 552.50 unknown https://doi.org/10.1248/BPB.24.311
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/10.1007/S10600-012-0230-4
Robustaflavone 5281694 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O)O 538.50 unknown https://doi.org/10.1248/BPB.24.311
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-012-0230-4

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