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Fraxinus chinensis subsp. rhynchophylla

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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 UUID64402ccd1f887544629573
Scientific name Fraxinus chinensis subsp. rhynchophylla
Authority (Hance) A.E.Murray
First published in Kalmia 13: 6 (1983)

Description Top

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Common names Top

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Language Common/alternative name
English korean ash
English fraxinus chinensis ssp. rhynchophylla
Chinese 秦皮
Chinese 花曲柳
Chinese 花曲柳（苦枥白错树、尖叶白赌树）
Chinese 大叶白蜡树

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
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000832401
UNII 35IN6UV38J
Tropicos 23000675
KEW urn:lsid:ipni.org:names:922141-1
The Plant List kew-369615
Open Tree Of Life 663317
NCBI Taxonomy 126596
IPNI 922141-1
iNaturalist 601637
GBIF 3684429
USDA GRIN 411386

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
Fraxetin Targeting to Sortase A Decreases the Pathogenicity of Streptococcus agalactiae to Nile Tilapia Dong J, Zhang Y, Yang Q, Liu Y, Zhou S, Ai X Animals (Basel) 29-Apr-2024
PMCID:PMC11083127
doi:10.3390/ani14091337
PMID:38731341
Microencapsulation of Tecoma stans Extracts: Bioactive Properties Preservation and Physical Characterization Analysis García-Jiménez JR, Luna-Guevara ML, Luna-Guevara JJ, Conde-Hernández LA, Ramos-Cassellis ME, Hernández-Cocoletzi H Foods 25-Mar-2024
PMCID:PMC11011495
doi:10.3390/foods13071001
PMID:38611307
Scopoletin: a review of its pharmacology, pharmacokinetics, and toxicity Gao XY, Li XY, Zhang CY, Bai CY Front Pharmacol 23-Feb-2024
PMCID:PMC10923241
doi:10.3389/fphar.2024.1268464
PMID:38464713
The dual effect of endoplasmic reticulum stress in digestive system tumors and intervention of Chinese botanical drug extracts: a review Zhang J, Chen Y, Chen B, Sun D, Sun Z, Liang J, Liang J, Xiong X, Yan H Front Pharmacol 21-Feb-2024
PMCID:PMC10917068
doi:10.3389/fphar.2024.1339146
PMID:38449811
Effect of herbal extracts in animal nutrition as feed additives Alem WT Heliyon 26-Jan-2024
PMCID:PMC10845724
doi:10.1016/j.heliyon.2024.e24973
PMID:38322944
Exploring Chinese herbal medicine for ischemic stroke: insights into microglia and signaling pathways Zhang W, Xu H, Li C, Han B, Zhang Y Front Pharmacol 22-Jan-2024
PMCID:PMC10838993
doi:10.3389/fphar.2024.1333006
PMID:38318134
Esculetin Alleviates IL-1β-Evoked Nucleus Pulposus Cell Death, Extracellular Matrix Remodeling, and Inflammation by Activating Nrf2/HO-1/NF-kb Huang C, Zou K, Wang Y, Tang K, Wu Y ACS Omega 18-Dec-2023
PMCID:PMC10785627
doi:10.1021/acsomega.3c06771
PMID:38222570
Esculetin unveiled: Decoding its anti‐tumor potential through molecular mechanisms—A comprehensive review Rezoan Hossain M, Zahra Shova FT, Akter M, Shuvo S, Ahmed N, Akter A, Haque M, Salma U, Roman Mogal M, Saha HR, Sarkar BC, Sohel M Cancer Rep (Hoboken) 08-Dec-2023
PMCID:PMC10809201
doi:10.1002/cnr2.1948
PMID:38062981
Target Screen of Anti-Hyperuricemia Compounds from Cortex Fraxini In Vivo Based on ABCG2 and Bioaffinity Ultrafiltration Mass Spectrometry Huang X, Dong W, Luo X, Xu L, Wang Y Molecules 01-Dec-2023
PMCID:PMC10708028
doi:10.3390/molecules28237896
PMID:38067624
TCM and related active compounds in the treatment of gout: the regulation of signaling pathway and urate transporter Sun X, Yang L, Sun H, Sun Y, Wei S, Han Y, Wang W, Kong L, Wang X Front Pharmacol 29-Nov-2023
PMCID:PMC10716793
doi:10.3389/fphar.2023.1275974
PMID:38094893
Host cell-based screening assays for identification of molecules targeting Pseudomonas aeruginosa cyclic di-GMP signaling and biofilm formation Hu Y, Webb JS, An SQ Front Microbiol 15-Nov-2023
PMCID:PMC10684931
doi:10.3389/fmicb.2023.1279922
PMID:38033560
Network pharmacology and molecular docking reveal potential mechanism of esculetin in the treatment of ulcerative colitis Cai T, Cai B Medicine (Baltimore) 10-Nov-2023
PMCID:PMC10637478
doi:10.1097/MD.0000000000035852
PMID:37960728
Asymbiotic Seed Germination and In Vitro Seedling Development of the Endangered Orchid Species Cypripedium guttatum Park HB, An J, Bae KH, Hong SH, Park HJ, Kim S, Lee CW, Lee BD, Baek JH, Kim NY, Hwang JE Plants (Basel) 07-Nov-2023
PMCID:PMC10675115
doi:10.3390/plants12223788
PMID:38005685
Pharmacological activities of esculin and esculetin: A review Cai T, Cai B Medicine (Baltimore) 06-Oct-2023
PMCID:PMC10553009
doi:10.1097/MD.0000000000035306
PMID:37800835
Antibacterial Activity of a Phenylpropanoid from the Root Extract of Carduus leptacanthus Fresen Dagne A, Degu S, Abebe A, Bisrat D J Trop Med 06-Sep-2023
PMCID:PMC10499531
doi:10.1155/2023/4983608
PMID:37711213

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 / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1055/S-2006-960840
4-Hydroxy-3-methoxycinnamaldehyde 5280536 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1055/S-2006-960840
Homovanillyl alcohol 16928 Click to see COC1=C(C=CC(=C1)CCO)O 168.19 unknown https://doi.org/10.1248/CPB.29.2391
https://doi.org/10.1248/CPB.31.2262
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown https://doi.org/10.1248/CPB.31.2262
https://doi.org/10.1248/CPB.29.2391
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isoolivil 5316262 Click to see COC1=C(C=C2C(C(C(CC2=C1)(CO)O)CO)C3=CC(=C(C=C3)O)OC)O 376.40 unknown https://doi.org/10.1248/CPB.32.4482
> Lignans, neolignans and related compounds / Furanoid lignans
3,6-Bis(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-ol 13824420 Click to see COC1=C(C=CC(=C1)C2C3COC(C3(CO2)O)C4=CC(=C(C=C4)O)OC)O 374.40 unknown https://doi.org/10.1248/YAKUSHI1947.107.6_435
https://doi.org/10.1248/CPB.32.4482
Fraxiresinol 21632950 Click to see COC1=CC(=CC(=C1O)OC)C2C3(COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 404.40 unknown https://doi.org/10.1248/YAKUSHI1947.107.6_435
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1248/CPB.32.4482
> 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/10.1248/CPB.32.4482
> 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/BPB.31.2273
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/S10600-010-9498-4
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/S10600-010-9498-4
methyl (4S,5E,6R)-4-[2-[2-(3,4-diacetyloxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163190189 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)OC(=O)C)OC(=O)C 792.70 unknown https://doi.org/10.1016/0031-9422(75)85070-9
methyl 4-[2-[2-(3,4-diacetyloxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 541168 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)OC(=O)C)OC(=O)C 792.70 unknown https://doi.org/10.1016/0031-9422(75)85070-9
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/S10600-010-9498-4
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/S10600-010-9498-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown https://doi.org/10.1248/CPB.31.2262
https://doi.org/10.1248/CPB.29.2391
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
2H-1-Benzopyran-2-one, 6-(beta-D-glucopyranosyloxy)-7-hydroxy- 5351506 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1248/CPB.33.4069
https://doi.org/10.1248/CPB.31.2262
https://doi.org/10.1248/YAKUSHI1947.73.7_771
7-hydroxy-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 5420916 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1248/CPB.33.4069
7-hydroxy-6-methoxy-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 147277854 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/CPB.33.4069
7-hydroxy-6-methoxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 5281418 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/CPB.43.1385
https://doi.org/10.1248/CPB.33.4069
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/CPB.33.4069
https://doi.org/10.1620/TJEM.30.534
Cichoriin 442101 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown https://doi.org/10.1007/S10600-014-0850-Y
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1248/YAKUSHI1947.73.7_771
https://doi.org/10.1248/CPB.31.2262
https://doi.org/10.1007/S10600-014-0850-Y
https://doi.org/10.1248/CPB.33.4069
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/10.1620/TJEM.30.534
https://doi.org/10.1248/CPB.43.1385
https://doi.org/10.1007/S10600-014-0850-Y
https://doi.org/10.1248/CPB.33.4069
Mandshurin 11740722 Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)OC3C(C(C(C(O3)CO)O)O)O 384.30 unknown https://doi.org/10.1248/CPB.43.1385
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/10.1007/S10600-014-0850-Y
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxidin 3083616 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC 222.19 unknown https://doi.org/10.1055/S-2006-960840
https://doi.org/10.1248/YAKUSHI1947.107.6_435
Fraxinol 3047739 Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)O 222.19 unknown https://doi.org/10.1248/CPB.43.1385
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1248/CPB.31.2262
https://doi.org/10.1248/CPB.33.4069
https://doi.org/10.1248/YAKUSHI1947.107.6_435
https://doi.org/10.1248/CPB.29.2391
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Fraxetin 5273569 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O 208.17 unknown https://doi.org/10.1248/CPB.33.4069
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-6-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]chromen-2-one 162902404 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OCC3C(C(C(C(O3)O)O)O)O)O 340.28 unknown https://doi.org/10.1016/0031-9422(75)85070-9
7-hydroxy-6-[[(2R,3S,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methoxy]chromen-2-one 163187893 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OCC3C(C(C(C(O3)O)O)O)O)O 340.28 unknown https://doi.org/10.1016/0031-9422(75)85070-9
Isofraxidin 5318565 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O 222.19 unknown https://doi.org/10.1248/YAKUSHI1947.107.6_435
https://doi.org/10.1248/CPB.33.4069
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1248/YAKUSHI1947.107.6_435
https://doi.org/10.1055/S-2006-960840
https://doi.org/10.1248/CPB.33.4069

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