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Syringa pubescens subsp. patula

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Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64402b241dd92021889122
Scientific name Syringa pubescens subsp. patula
Authority (Palib.) M.C.Chang & X.L.Chen
First published in Invest. Stud. Nat. 10: 34 (1990)

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Common names Top

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Language Common/alternative name
Korean 털개회나무
Chinese 关东丁香
Chinese 关东巧玲花

Varieties (abbr. var.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000818657
USDA Plants SYPUP2
Tropicos 23000718
KEW urn:lsid:ipni.org:names:956631-1
The Plant List kew-356452
Open Tree Of Life 129925
NCBI Taxonomy 150407
IPNI 956631-1
iNaturalist 349197
GBIF 5549619
USDA GRIN 405015

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
Disruptive Effects of Two Curcuminoids (Demethoxycurcumin and Bisdemethoxycurcumin) on the Larval Development of Drosophila melanogaster Jeon JH, Jeong SA, Park DS, Park HH, Shin SW, Oh HW Insects 18-Dec-2023
PMCID:PMC10744261
doi:10.3390/insects14120959
PMID:38132632
In Ovo and In Silico Evaluation of the Anti-Angiogenic Potential of Syringin Aventurado CA, Billones JB, Vasquez RD, Castillo AL Drug Des Devel Ther 25-Nov-2020
PMCID:PMC7701684
doi:10.2147/DDDT.S271952
PMID:33268982
Regulation of Anti-Oxidative, Anti-Inflammatory, and Anti-Apoptotic Activity of Advanced Cooling Composition (ACC) in UVB-Irradiated Human HaCaT Keratinocytes Park J, Woo YK, Cho HJ Int J Mol Sci 07-Sep-2020
PMCID:PMC7555985
doi:10.3390/ijms21186527
PMID:32906658
Rhamnus davurica leaf extract inhibits Fyn activation by antigen in mast cells for anti-allergic activity Kim JH, Kim AR, Kim HS, Kim HW, Park YH, You JS, Park YM, Her E, Kim HS, Kim YM, Choi WS BMC Complement Altern Med 25-Mar-2015
PMCID:PMC4379541
doi:10.1186/s12906-015-0607-6
PMID:25887889
Responses to shading of naturalized and non-naturalized exotic woody species Feng Y, van Kleunen M Ann Bot 13-Aug-2014
PMCID:PMC4171072
doi:10.1093/aob/mcu163
PMID:25122655
Leaf Phenological Characters of Main Tree Species in Urban Forest of Shenyang Xu S, Xu W, Chen W, He X, Huang Y, Wen H PLoS One 25-Jun-2014
PMCID:PMC4070915
doi:10.1371/journal.pone.0099277
PMID:24963625
Two new neolignans from Syringa velutina Kom. Feng XS, Qu Y, Xu L, Wang DC, Wu LJ, Meng FH, Liu YR Molecules 27-Feb-2009
PMCID:PMC6253940
doi:10.3390/MOLECULES14030953
PMID:19255553
Two New Neolignans from Syringa velutina Kom Feng XS, Qu Y, Xu L, Wang DC, Wu LJ, Meng FH, Liu YR Molecules 27-Feb-2009
PMCID:PMC6253940
doi:10.3390/molecules14030953
PMID:19255553
Studies on constituents with cytotoxic activity from the stem bark of Syringa velutina. Park HJ, Lee MS, Lee KT, Sohn IC, Han YN, Miyamoto K Chem Pharm Bull (Tokyo) 01-Jul-1999
doi:10.1248/CPB.47.1029
PMID:10434406

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 / Lignan glycosides
(2R,3R,4S,5S,6R)-2-[(E)-3-[4-[(1S,2R)-1,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 122203703 Click to see 598.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253940/
2-[3-[4-[1,3-Dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162968813 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C(=C2)OC)O)OC)O)OC)C=CCOC3C(C(C(C(O3)CO)O)O)O 598.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253940/
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(Z)-methyl 4-(2-(3,4-dihydroxyphenethoxy)-2-oxoethyl)-3-ethylidene-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-3,4-dihydro-2H-pyran-5-carboxylate 134688908 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown https://doi.org/10.1248/CPB.47.1029
Ligstroside 14136859 Click to see 524.50 unknown https://doi.org/10.1248/CPB.47.1029
methyl (5Z)-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 14136858 Click to see 524.50 unknown https://doi.org/10.1248/CPB.47.1029
Oleuropein 5281544 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown https://doi.org/10.1248/CPB.47.1029
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-[2-(3,4-Dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13845930 Click to see 316.30 unknown https://doi.org/10.1248/CPB.47.1029
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3S,4R,5S,6S)-2-methyl-6-[[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[2-hydroxy-5-(2-hydroxyethyl)phenoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol 15939776 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=CC(=C3)CCO)O)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.47.1029
2-Methyl-6-[[3,4,5-trihydroxy-6-[2-hydroxy-5-(2-hydroxyethyl)phenoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol 5326345 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=CC(=C3)CCO)O)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.47.1029
Syringin 5316860 Click to see 372.40 unknown https://doi.org/10.1248/CPB.47.1029

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