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Edgeworthia chrysantha

Edgeworthia chrysantha - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644018f671368427640071
Scientific name Edgeworthia chrysantha
Authority Lindl.
First published in J. Hort. Soc. London 1: 148 (1846)

Description Top

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Synonyms Top

Scientific name Authority First published in
Magnolia sericea Thunb. Pl. Jap. Nov. Sp. : 8 (1824)
Magnolia tomentosa Thunb. Trans. Linn. Soc. London 2: 336 (1794)
Yulania tomentosa (Thunb.) D.L.Fu J. Wuhan Bot. Res. 19(3): 198. 2001
Daphne papyracia hort. ex Koehne Deut. Dendrol. : 422 (1893)
Daphne papyrifera Siebold Verh. Batav. Genootsch. Kunsten 12: 22 (1830)
Edgeworthia papyrifera Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 199 (1846)
Edgeworthia tomentosa Nakai Bot. Mag. (Tokyo) 33: 206 (1919)

Common names Top

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Language Common/alternative name
English oriental paperbush
Czech micumata
German mitsumata
Persian میتسوماتا
Italian bastone di san giuseppe
Italian arbusto della carta
Japanese ミツマタ
Japanese 三椏
Korean 삼지닥나무
Chinese 雪花皮
Chinese 結香
Chinese 黄花结香
Chinese 黄瑞香
Chinese 蒙花
Chinese 金腰带
Chinese 打结花
Chinese 岩泽兰
Chinese 山棉皮
Chinese 三桠皮
Chinese 三叉树
Chinese 结香花
Chinese 结香
Chinese 梦花根
Chinese 梦花
Chinese 雪里开

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) 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 South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000663230
USDA Plants EDCH
Tropicos 50103978
KEW urn:lsid:ipni.org:names:831625-1
The Plant List kew-2784524
Missouri Botanical Garden 293415
PFAF Edgeworthia papyrifera
Open Tree Of Life 268293
NCBI Taxonomy 142181
IPNI 831625-1
iNaturalist 133126
GBIF 5420855
Freebase /m/09rt3_w
EPPO EDGPA
USDA GRIN 14884
Wikipedia Edgeworthia_chrysantha

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
Endophytic Aspergillii and Penicillii from medicinal plants: a focus on antimicrobial and multidrug resistant pathogens inhibitory activity Mamangkey J, Mendes LW, Mustopa AZ, Hartanto A BioTechnologia (Pozn) 29-Mar-2024
PMCID:PMC11020150
doi:10.5114/bta.2024.135644
PMID:38633888
Metabolome integrated with transcriptome reveals the mechanism of three different color formations in Taxus mairei arils Yan Y, Wen Y, Wang Y, Wu X, Li X, Wang C, Zhao Y Front Plant Sci 23-Jan-2024
PMCID:PMC10844565
doi:10.3389/fpls.2024.1330075
PMID:38322825
A study on the effect of natural products against the transmission of B.1.1.529 Omicron Alkafaas SS, Abdallah AM, Hussien AM, Bedair H, Abdo M, Ghosh S, Elkafas SS, Apollon W, Saki M, Loutfy SA, Onyeaka H, Hessien M Virol J 25-Aug-2023
PMCID:PMC10464336
doi:10.1186/s12985-023-02160-6
PMID:37626376
Benzophenones-natural metabolites with great Hopes in drug discovery: structures, occurrence, bioactivities, and biosynthesis Ibrahim SR, Fahad ALsiyud D, Alfaeq AY, Mohamed SG, Mohamed GA RSC Adv 04-Aug-2023
PMCID:PMC10402873
doi:10.1039/d3ra02788k
PMID:37546221
Spiro-Flavonoids in Nature: A Critical Review of Structural Diversity and Bioactivity Pecio Ł, Pecio S, Mroczek T, Oleszek W Molecules 14-Jul-2023
PMCID:PMC10385819
doi:10.3390/molecules28145420
PMID:37513292
Tigliane and daphnane diterpenoids from Thymelaeaceae family: chemistry, biological activity, and potential in drug discovery Otsuki K, Li W J Nat Med 09-Jun-2023
PMCID:PMC10465420
doi:10.1007/s11418-023-01713-x
PMID:37294498
Changes in homegardens in relocation villages, a case study in the Baiku Yao area in Southern China Hu R, Xu C, Nong Y, Luo B J Ethnobiol Ethnomed 27-Feb-2023
PMCID:PMC9972620
doi:10.1186/s13002-023-00578-4
PMID:36849896
Complete chloroplast genome of Daphne pseudomezereum var. koreana (Thymelaeaceae) Yoo SC, Park J, Oh SH Mitochondrial DNA B Resour 25-Feb-2023
PMCID:PMC9970196
doi:10.1080/23802359.2023.2179356
PMID:36860477
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
Overview of Bioactive Fungal Secondary Metabolites: Cytotoxic and Antimicrobial Compounds Conrado R, Gomes TC, Roque GS, De Souza AO Antibiotics (Basel) 11-Nov-2022
PMCID:PMC9687038
doi:10.3390/antibiotics11111604
PMID:36421247
The antimicrobial, antibiofilm, and wound healing properties of ethyl acetate crude extract of an endophytic fungus Paecilomyces sp. (AUMC 15510) in earthworm model Salem SH, El-Maraghy SS, Abdel-Mallek AY, Abdel-Rahman MA, Hassanein EH, Al-Bedak OA, El-Aziz FE Sci Rep 10-Nov-2022
PMCID:PMC9649741
doi:10.1038/s41598-022-23831-4
PMID:36357560
Araufuranone: A New Phytotoxic Tetrasubstituted Dihydrofuro[3,2-b]furan-2(5H)-One Isolated from Ascochyta araujiae Masi M, Boari A, Sautua F, Carmona MA, Vurro M, Evidente A Biomolecules 10-Sep-2022
PMCID:PMC9496196
doi:10.3390/biom12091274
PMID:36139113
Marine Compounds with Anti-Candida sp. Activity: A Promised “Land” for New Antifungals Alves AM, Cruz-Martins N, Rodrigues CF J Fungi (Basel) 25-Jun-2022
PMCID:PMC9320905
doi:10.3390/jof8070669
PMID:35887426
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
Fungal perylenequinones Khiralla A, Mohammed AO, Yagi S Mycol Prog 04-Apr-2022
PMCID:PMC8977438
doi:10.1007/s11557-022-01790-4
PMID:35401071

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
CID 10220146 10220146 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)O)(C)C 224.30 unknown https://doi.org/10.1016/S0031-9422(00)98226-8
CID 15431310 15431310 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC(=O)C)(C)C 266.33 unknown https://doi.org/10.1016/S0031-9422(00)98226-8
CID 73194627 73194627 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC(=O)C)(C)C 266.33 unknown https://doi.org/10.1016/S0031-9422(00)98226-8
Grasshopper ketone 13922639 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)O)(C)C 224.30 unknown https://doi.org/10.1016/S0031-9422(00)98226-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
[(2R,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (9Z,12Z,15Z)-octadeca-9,12,15-trienoate 101609199 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 837.30 unknown https://doi.org/10.1016/S0031-9422(00)98226-8
[(2R,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (9Z,12Z)-octadeca-9,12-dienoate 14101633 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 839.30 unknown https://doi.org/10.1016/S0031-9422(00)98226-8
[6-[[17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl octadeca-9,12-dienoate 75072327 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 839.30 unknown https://doi.org/10.1016/S0031-9422(00)98226-8
[6-[[17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl octadeca-9,12,15-trienoate 77916710 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 837.30 unknown https://doi.org/10.1016/S0031-9422(00)98226-8
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S10600-009-9230-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
8-[7-[(2S,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-2-oxochromen-8-yl]-7-hydroxy-3-(2-oxochromen-7-yl)oxychromen-2-one 14463048 Click to see C1C(C(C(O1)OC2=C(C3=C(C=C2)C=CC(=O)O3)C4=C(C=CC5=C4OC(=O)C(=C5)OC6=CC7=C(C=C6)C=CC(=O)O7)O)O)(CO)O 614.50 unknown https://doi.org/10.1016/0031-9422(89)85042-3
Edgeworoside B 101835681 Click to see C1C(C(C(O1)OC2=C(C3=C(C=C2)C=CC(=O)O3)C4=C(C=CC5=C4OC(=O)C(=C5)OC6=CC7=C(C=C6)C=CC(=O)O7)O)O)(CO)O 614.50 unknown https://doi.org/10.1016/0031-9422(90)89043-9
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,7-Dimethoxycoumarin 2775 Click to see COC1=CC2=C(C=CC(=O)O2)C(=C1)OC 206.19 unknown https://doi.org/10.1016/0031-9422(89)85042-3
6-Methoxy-2-oxo-3-(2-oxochromen-7-yloxy)chromen-7-yl acetate 1269245 Click to see CC(=O)OC1=C(C=C2C=C(C(=O)OC2=C1)OC3=CC4=C(C=C3)C=CC(=O)O4)OC 394.30 unknown https://doi.org/10.1016/S0031-9422(00)98226-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
(3S)-3-hydroxy-3-methyl-5-oxo-5-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[6-methoxy-2-oxo-3-(2-oxochromen-7-yl)oxychromen-7-yl]oxyoxan-2-yl]methoxy]pentanoic acid 163020588 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C3C=C(C(=O)OC3=C2)OC4=CC5=C(C=C4)C=CC(=O)O5)OC)O)O)O)O 658.60 unknown https://doi.org/10.1016/0031-9422(90)89043-9
7-hydroxy-3-(2-oxochromen-7-yl)oxy-8-[2-oxo-7-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-8-yl]chromen-2-one 162903475 Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C=CC(=O)O3)C4=C(C=CC5=C4OC(=O)C(=C5)OC6=CC7=C(C=C6)C=CC(=O)O7)O)O)O)O 628.50 unknown https://doi.org/10.1016/0031-9422(89)85042-3
7-Hydroxy-8-[2-oxo-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-8-yl]chromen-2-one 14463050 Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C=CC(=O)O3)C4=C(C=CC5=C4OC(=O)C=C5)O)O)O)O 468.40 unknown https://doi.org/10.1016/0031-9422(90)89043-9
7-hydroxy-8-[2-oxo-7-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-8-yl]chromen-2-one 162980786 Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C=CC(=O)O3)C4=C(C=CC5=C4OC(=O)C=C5)O)O)O)O 468.40 unknown https://doi.org/10.1016/0031-9422(90)89043-9
7-hydroxy-8-[2-oxo-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-8-yl]chromen-2-one 101835682 Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C=CC(=O)O3)C4=C(C=CC5=C4OC(=O)C=C5)O)O)O)O 468.40 unknown https://doi.org/10.1016/0031-9422(90)89043-9
https://doi.org/10.1248/BPB.31.1761
7-hydroxy-8-[2-oxo-7-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-8-yl]chromen-2-one 162980785 Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C=CC(=O)O3)C4=C(C=CC5=C4OC(=O)C=C5)O)O)O)O 468.40 unknown https://doi.org/10.1016/0031-9422(89)85042-3
Daphnorin 185819 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)OC3=CC4=C(C=C3)C=CC(=O)O4)OC5C(C(C(C(O5)CO)O)O)O 514.40 unknown https://doi.org/10.1016/0031-9422(89)85042-3
Edgeworoside A 45360264 Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C=CC(=O)O3)C4=C(C=CC5=C4OC(=O)C(=C5)OC6=CC7=C(C=C6)C=CC(=O)O7)O)O)O)O 628.50 unknown https://doi.org/10.1248/BPB.31.1761
https://doi.org/10.1016/0031-9422(89)85042-3
Edgeworside A 11958884 Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C=CC(=O)O3)C4=C(C=CC5=C4OC(=O)C(=C5)OC6=CC7=C(C=C6)C=CC(=O)O7)O)O)O)O 628.50 unknown https://doi.org/10.1016/0031-9422(89)85042-3
Rutarensin 11958880 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C3C=C(C(=O)OC3=C2)OC4=CC5=C(C=C4)C=CC(=O)O5)OC)O)O)O)O 658.60 unknown https://doi.org/10.1016/0031-9422(90)89043-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin 5281406 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)OC3=CC4=C(C=C3)C=CC(=O)O4)O 352.30 unknown https://doi.org/10.1007/S10600-009-9230-4
https://doi.org/10.1016/S0031-9422(00)98226-8
https://doi.org/10.1016/0031-9422(89)85042-3
Edgeworin 10925304 Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3=CC4=C(C=C(C=C4)O)OC3=O 322.30 unknown https://doi.org/10.1248/BPB.31.1761
https://doi.org/10.1016/0031-9422(89)85042-3
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/0031-9422(89)85042-3
https://doi.org/10.1007/S10600-009-9230-4

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