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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
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
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
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
Phytochemicals targeting glycolysis in colorectal cancer therapy: effects and mechanisms of action Zhan L, Su F, Li Q, Wen Y, Wei F, He Z, Chen X, Yin X, Wang J, Cai Y, Gong Y, Chen Y, Ma X, Zeng J Front Pharmacol 24-Aug-2023
PMCID:PMC10484417
doi:10.3389/fphar.2023.1257450
PMID:37693915
Two Species Delimitation of Pseudaulacaspis (Hemiptera: Diaspididae) Based on Morphology, Molecular Clustering, and Niche Differentiation Lu Y, Deng S, Niu M, Li H, Zhao Q, Zhang H, Wei J Insects 25-Jul-2023
PMCID:PMC10456064
doi:10.3390/insects14080666
PMID:37623377
A Transcriptome-Wide Analysis of Psoriasis: Identifying the Potential Causal Genes and Drug Candidates Jeong Y, Song J, Lee Y, Choi E, Won Y, Kim B, Jang W Int J Mol Sci 20-Jul-2023
PMCID:PMC10380797
doi:10.3390/ijms241411717
PMID:37511476
Manipulating Microbiota in Inflammatory Bowel Disease Treatment: Clinical and Natural Product Interventions Explored Zhu M, Song Y, Xu Y, Xu H Int J Mol Sci 02-Jul-2023
PMCID:PMC10342055
doi:10.3390/ijms241311004
PMID:37446182
Natural products as novel anti-obesity agents: insights into mechanisms of action and potential for therapeutic management Shaik Mohamed Sayed UF, Moshawih S, Goh HP, Kifli N, Gupta G, Singh SK, Chellappan DK, Dua K, Hermansyah A, Ser HL, Ming LC, Goh BH Front Pharmacol 20-Jun-2023
PMCID:PMC10318930
doi:10.3389/fphar.2023.1182937
PMID:37408757
Mitochondrial dysfunction-targeting therapeutics of natural products in Parkinson’s disease He T, Lin X, Su A, Zhang Y, Xing Z, Mi L, Wei T, Li Z, Wu W Front Pharmacol 10-May-2023
PMCID:PMC10206024
doi:10.3389/fphar.2023.1117337
PMID:37234707
Deciphering the pharmacological mechanisms of Fraxini Cortex for ulcerative colitis treatment based on network pharmacology and in vivo studies Wang T, Su X, Peng J, Tan X, Yang G, Zhang T, Chen F, Wang C, Ma K BMC Complement Med Ther 09-May-2023
PMCID:PMC10170718
doi:10.1186/s12906-023-03983-0
PMID:37161415
Synergy, Additivity and Antagonism between Esculetin and Six Commonly Used Chemotherapeutics in Various Malignant Melanoma Cell Lines—An Isobolographic Analysis Wróblewska-Łuczka P, Góralczyk A, Łuszczki JJ Molecules 05-May-2023
PMCID:PMC10180450
doi:10.3390/molecules28093889
PMID:37175299
Natural Coumarin Derivatives Activating Nrf2 Signaling Pathway as Lead Compounds for the Design and Synthesis of Intestinal Anti-Inflammatory Drugs Di Stasi LC Pharmaceuticals (Basel) 30-Mar-2023
PMCID:PMC10142712
doi:10.3390/ph16040511
PMID:37111267
The Related Mechanisms Predicted through Network-Based Pharmacological Analysis and the Anti-Inflammatory Effects of Fraxinus rhynchophylla Hance Bark on Contact Dermatitis in Mice Kim S, Lyu JH, Yang B, Kim S, Kim JH, Kim H, Cho S Int J Mol Sci 23-Mar-2023
PMCID:PMC10094049
doi:10.3390/ijms24076091
PMID:37047066
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831

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
> 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
Ligustroside 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 (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-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
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
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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