Weigela subsessilis - Unknown
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Internal ID UUID643ffb9a2ac66181730541
Scientific name Weigela subsessilis
Authority L.H.Bailey
First published in Gentes Herbarum 2: 51 (1929)

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Synonyms Top

Scientific name Authority First published in
Diervilla subsessilis Nakai Bot. Mag. (Tokyo) 32: 229 (1918)

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Language Common/alternative name
English korean weigela
Korean 병꽃나무
Chinese 短梗锦带花

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Varieties (abbr. var.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000428031
Tropicos 50256572
KEW urn:lsid:ipni.org:names:150060-1
Open Tree Of Life 82213
NCBI Taxonomy 79620
IUCN Red List 97530634
IPNI 150060-1
iNaturalist 568858
GBIF 3856121
USDA GRIN 42007
Wikipedia Weigela_subsessilis

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
Dietary Polyphenols Remodel DNA Methylation Patterns of NRF2 in Chronic Disease Divyajanani S, Harithpriya K, Ganesan K, Ramkumar KM Nutrients 27-Jul-2023
PMCID:PMC10420661
doi:10.3390/nu15153347
PMID:37571283
The Modulation of Melanogenesis in B16 Cells Upon Treatment with Plant Extracts and Isolated Plant Compounds Merecz-Sadowska A, Sitarek P, Kowalczyk T, Zajdel K, Kucharska E, Zajdel R Molecules 07-Jul-2022
PMCID:PMC9324663
doi:10.3390/molecules27144360
PMID:35889231
A New Lichenized Fungus, Psoroglaena humidosilvae, from a Forested Wetland of Korea, with a Taxonomic Key to the Species of Psoroglaena Lee BG, Hur JS J Fungi (Basel) 12-Apr-2022
PMCID:PMC9028879
doi:10.3390/jof8040392
PMID:35448623
Anti-Diabetic Potential of Plant-Based Pentacyclic Triterpene Derivatives: Progress Made to Improve Efficacy and Bioavailability Oboh M, Govender L, Siwela M, Mkhwanazi BN Molecules 29-Nov-2021
PMCID:PMC8659003
doi:10.3390/molecules26237243
PMID:34885816
The species range‐size patterns for vascular plants of Seorak Mountain (Korea): Relationship between group of life forms and phytogeography affinity along the elevational gradient Lee M, Song JH, Byeon SY, Lee JE, Kim HJ, Chae S, Yun CW, Kim J Ecol Evol 24-Aug-2021
PMCID:PMC8462172
doi:10.1002/ece3.8033
PMID:34594545
Anti-Inflammatory Effects of Weigela subsessilis Callus Extract via Suppression of MAPK and NF-κB Signaling Lim HJ, Jie EY, Park IS, Kim SJ, Ahn WS, Jeong SI, Kim SW, Jung CH Plants (Basel) 09-Aug-2021
PMCID:PMC8400516
doi:10.3390/plants10081635
PMID:34451680
NRF2-Related Epigenetic Modifications in Cardiac and Vascular Complications of Diabetes Mellitus Wang J, Xiao M, Wang J, Wang S, Zhang J, Guo Y, Tang Y, Gu J Front Endocrinol (Lausanne) 25-Jun-2021
PMCID:PMC8269153
doi:10.3389/fendo.2021.598005
PMID:34248833
Diagnostic Evaluation and Preparation of the Reference Information for River Restoration in South Korea Lim CH, Pi JH, Kim AR, Cho HJ, Lee KS, You YH, Lee KH, Kim KD, Moon JS, Lee CS Int J Environ Res Public Health 10-Feb-2021
PMCID:PMC7916817
doi:10.3390/ijerph18041724
PMID:33578983
Biological effects of corosolic acid as an anti-inflammatory, anti-metabolic syndrome and anti-neoplasic natural compound Zhao J, Zhou H, An Y, Shen K, Yu L Oncol Lett 02-Dec-2020
PMCID:PMC7723172
doi:10.3892/ol.2020.12345
PMID:33363621
Triterpenoid corosolic acid modulates global CpG methylation and transcriptome of tumor promotor TPA induced mouse epidermal JB6 P+ cells Hudlikar RR, Sargsyan D, Wu R, Su S, Zheng M, Kong AN Chem Biol Interact 03-Mar-2020
PMCID:PMC7238714
doi:10.1016/j.cbi.2020.109025
PMID:32135139
Osteoarthritis Is a Low-Grade Inflammatory Disease: Obesity's Involvement and Herbal Treatment Zeddou M Evid Based Complement Alternat Med 04-Nov-2019
PMCID:PMC6874989
doi:10.1155/2019/2037484
PMID:31781260
Extraction of Kaempferol and Its Glycosides Using Supercritical Fluids from Plant Sources: A Review Cid-Ortega S, Monroy-Rivera JA Food Technol Biotechnol 01-Dec-2018
PMCID:PMC6399721
doi:10.17113/ftb.56.04.18.5870
PMID:30923445
The Role of Natural Products in Targeting Cardiovascular Diseases via Nrf2 Pathway: Novel Molecular Mechanisms and Therapeutic Approaches Ooi BK, Chan KG, Goh BH, Yap WH Front Pharmacol 15-Nov-2018
PMCID:PMC6249275
doi:10.3389/fphar.2018.01308
PMID:30498447
Pharmacological Properties, Molecular Mechanisms, and Pharmaceutical Development of Asiatic Acid: A Pentacyclic Triterpenoid of Therapeutic Promise Nagoor Meeran MF, Goyal SN, Suchal K, Sharma C, Patil CR, Ojha SK Front Pharmacol 04-Sep-2018
PMCID:PMC6131672
doi:10.3389/fphar.2018.00892
PMID:30233358
Corosolic acid reduces 5-FU chemoresistance in human gastric cancer cells by activating AMPK Park JB, Lee JS, Lee MS, Cha EY, Kim S, Sul JY Mol Med Rep 03-Jul-2018
PMCID:PMC6102703
doi:10.3892/mmr.2018.9244
PMID:30015846

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 / Coumarinolignans
3-(4-Hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 100151 Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O 386.40 unknown https://doi.org/10.1248/BPB.28.1095
CID 335652 335652 Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O 386.40 unknown https://doi.org/10.1248/BPB.28.1095
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1248/BPB.29.830
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-Methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 346340 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1248/BPB.28.1095
7-hydroxy-6-methoxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)(2H-3,4,5,6-tetrahydr opyran-2-yl)oxy]chromen-2-one 5909448 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 370.31 unknown https://doi.org/10.1248/BPB.28.1095
Fraxin 5273568 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 370.31 unknown https://doi.org/10.1248/BPB.28.1095
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1248/BPB.28.1095
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1248/BPB.28.1095

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