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Syringa reticulata subsp. amurensis

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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 UUID64402b244f14b179622079
Scientific name Syringa reticulata subsp. amurensis
Authority (Rupr.) P.S.Green & M.C.Chang
First published in Novon 5: 329 (1995)

Description Top

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Common names Top

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Language Common/alternative name
English amur lilac
Belarusian траскун амурскі
Chinese 暴马丁香
Chinese 暴马子
Chinese 荷花丁香

Varieties (abbr. var.) Top

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No variety added yet.

Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Manchuria
    • Eastern Asia
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000818668
USDA Plants SYREA
Tropicos 50045322
KEW urn:lsid:ipni.org:names:986407-1
The Plant List kew-356462
Missouri Botanical Garden 291371
Open Tree Of Life 994741
NCBI Taxonomy 149021
IPNI 986407-1
iNaturalist 68830
GBIF 5549615
USDA GRIN 405013

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
Species diversity of pathogenic wood-rotting fungi (Agaricomycetes, Basidiomycota) in China Yuan Y, Bian LS, Wu YD, Chen JJ, Wu F, Liu HG, Zeng GY, Dai YC Mycology 08-Aug-2023
PMCID:PMC10424591
doi:10.1080/21501203.2023.2238779
PMID:37583455
Genome-Wide Analysis and Expression of the GRAS Transcription Factor Family in Avena sativa Ling L, Li M, Chen N, Ren G, Qu L, Yue H, Wu X, Zhao J Genes (Basel) 06-Jan-2023
PMCID:PMC9858933
doi:10.3390/genes14010164
PMID:36672905
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
Macro-Nutritional Adaptive Strategies of Moose (Alces alces) Related to Population Density Ma Y, Bao H, Bencini R, Raubenheimer D, Dou H, Liu H, Wang S, Jiang G Animals (Basel) 31-Dec-2019
PMCID:PMC7022907
doi:10.3390/ani10010073
PMID:31906149
Hydnoporia, an older name for Pseudochaete and Hymenochaetopsis, and typification of the genus Hymenochaete (Hymenochaetales, Basidiomycota) Miettinen O, Larsson KH, Spirin V Fungal Syst Evol 04-Jun-2019
PMCID:PMC7241676
doi:10.3114/fuse.2019.04.07
PMID:32467908
Aboveground-belowground biodiversity linkages differ in early and late successional temperate forests Li H, Wang X, Liang C, Hao Z, Zhou L, Ma S, Li X, Yang S, Yao F, Jiang Y Sci Rep 17-Jul-2015
PMCID:PMC4505317
doi:10.1038/srep12234
PMID:26184121
Synopsis of Phyllosticta in China Zhang K, Shivas RG, Cai L Mycology 17-Apr-2015
PMCID:PMC4409051
doi:10.1080/21501203.2015.1027507
PMID:26000199
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
Influence of Long-Term Thinning on the Biomass Carbon and Soil Respiration in a Larch (Larix gmelinii) Forest in Northeastern China Wang H, Liu W, Wang W, Zu Y ScientificWorldJournal 04-Apr-2013
PMCID:PMC3654284
doi:10.1155/2013/865645
PMID:23710153
Phenolic compounds of the bark of Syringa amurensis V. A. Kurkin, R. I. Evstratova, G. G. Zapesochnaya, M. E. Pimenova Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630670

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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
5-(4-Hydroxy-3-methoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-4-(hydroxymethyl)oxolan-3-ol 586733 Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O 376.40 unknown https://doi.org/10.1007/BF00630670
Lariciresinol, (+)- 134203 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1007/BF00630670
> Lignans, neolignans and related compounds / Lignan glycosides
2-[[2-(4-Hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 24150655 Click to see COC1=C(C=CC(=C1)CC2COC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1007/BF00630670
Lariciresinol 9-O-|A-D-glucopyranoside 145709428 Click to see COC1=C(C=CC(=C1)CC2COC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1007/BF00630670
> 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/10.1007/BF00630670
2H-Pyran-4-acetic acid, 3-ethylidene-2-(beta-D-glucopyranosyloxy)-3,4-dihydro-5-(methoxycarbonyl)-, 2-(4-hydroxyphenyl)ethyl ester, [2S-(2alpha,3E,4beta)]-; Ligstroside 72727933 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 524.50 unknown https://doi.org/10.1007/BF00630670
Ligstroside 14136859 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 524.50 unknown https://doi.org/10.1007/BF00630670
methyl (4S,5E,6R)-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 75492723 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 524.50 unknown https://doi.org/10.1007/BF00630670
methyl 4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 3789874 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/10.1007/BF00630670
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/10.1007/BF00630670
> Lipids and lipid-like molecules / Saccharolipids
methyl 5-ethylidene-4-[2-oxo-2-[[3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]ethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 72987608 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O 686.70 unknown https://doi.org/10.1007/BF00630670
Nuezhenide 6440999 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O 686.70 unknown https://doi.org/10.1007/BF00630670
Specnuezhenide 91895359 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O 686.70 unknown https://doi.org/10.1007/BF00630670
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]oxane-3,4,5-triol 3496897 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1007/BF00630670
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1007/BF00630670
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1007/BF00630670
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1007/BF00630670
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1007/BF00630670
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1007/BF00630670

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