Edgeworthia gardneri

Details Top

Internal ID UUID644018f69aa83099074804
Scientific name Edgeworthia gardneri
Authority (Wall.) Meisn.
First published in Denkschr. Königl.-Baier. Bot. Ges. Regensburg 3: 280 (1841)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Traditional uses — non-medicinal — Among the Eastern Himalaya, communities have long used the inner bark and young twigs of Edgeworthia gardneri for paper-making and cordage. In Sikkim and West Bengal, the bast fibers are stripped, rinsed, and bruised to separate fibers that are laid and pressed into sheets, a craft described by J. McCann in 1959 and still practiced in the Darjeeling Hills and Sikkimese valleys today. Throughout Sikkim and Nepal, the same bast has been valued as a strong rope and twine for baskets and lashings (Long & Grierson, 1987). In Assam’s tea‑growing districts, the bast is processed into paper or mixed with other fibers for board and packing material, and small‑scale workshops near Jalukie still rely on this supply (Borthakur, 1993). Documented infusions, decoctions, tinctures, macerations, or poultices for Edgeworthia gardneri do not appear in the cited ethnobotanical monographs.

One practical recipe — paper sheets — For small‑batch paper: clean 200 g of fresh inner bark, remove excess wood, and soak in water 12–24 h; boil for 45–60 min in 2 L of water, stirring occasionally, to soften the fibers. Drain, rinse, and beat the bast in a large tray of fresh water until fibers separate, about 5–10 min with a hand swatter. Skim a thin mat of fiber onto a framed screen, drain, and press under light weight for 30–45 min; air‑dry flat. Watch for splintering of unseasoned fiber and maintain even fiber distribution for a uniform sheet.

Active constituents — The bast is rich in lignans and phenylpropanoids typical of Thymelaeaceae, with syringin, edgeworthin, and coumarins such as scopoletin, umbelliferone, and scoparone identified from Edgeworthia species (Hirano et al., 1991). Lignans contribute to fiber strength, and coumarins add antimicrobial properties that help protect stored bast and finished paper.

Modern relevance — Today, craft cooperatives in West Bengal and Sikkim continue the Edgeworthia gardneri bark craft to supply local bookbinders, while research on fiber composition and preservation continues to inform small‑scale production techniques (Mishra & Ghosh, 2022).

General Uses Top

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Common products:
- High-grade rag paper and specialty printing/writing papers based on bast fibers from the inner bark.

Industrial and craft applications:
- Long, flexible bast fibers used in traditional East Asian papermaking. The fibers are processed by retting, beating, and sheet formation to yield paper with high strength and fine texture.

Food and beverages (non-medicinal):
- No documented food or beverage uses.

Colorants and tanning:
- No documented dye, ink, or tannin applications.

Wood and fiber:
- Bast fiber bundles from the phloem; fiber morphology features high alpha-cellulose and lignin content and long fiber length, facilitating inter-fiber bonding and strength in handmade sheets. Xylem vessels are distinctly annular or helical, a feature used for species identification in fiber provenance studies. Short wood is unsuitable for timber; the species is cultivated for fiber.

Fragrance and cosmetics:
- No documented fragrance or cosmetic uses.

Properties relevant to use:
- Long, fine bast fibers enable formation of cohesive, strong paper. Annular or helical vessel elements in the xylem serve as diagnostic characters for species-level verification.

Standards and regulation:
- No species-specific standards identified.

Sustainability and sourcing:
- Harvest involves stripping and retting bark from stems, followed by cultivation for regeneration. Smallholder or semi-cultivated production is practiced within the native Himalayan range; quantitative sustainability assessments are not established in the available sources.

Synonyms Top

Scientific name Authority First published in
Daphne gardneri Wall. Asiat. Res. 13: 388 (1820)

Common names Top

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Language Common/alternative name
English argeli
English argelee
English indian papertree
English nepalese paperbush
Tamil எட்ச்வொர்தியா கார்த்னெரி
Chinese 滇结香
Chinese 长梗结香
Chinese 构皮树
Chinese 滇結香

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
    • Indo-China
      • Myanmar
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000663233
Tropicos 50177243
KEW urn:lsid:ipni.org:names:831626-1
The Plant List kew-2784521
PFAF Edgeworthia gardneri
Open Tree Of Life 6119385
NCBI Taxonomy 2203444
IUCN Red List 150283975
IPNI 831626-1
iNaturalist 243937
GBIF 5523712
Freebase /m/0n48y9y
EPPO EDGGA
EOL 487837
USDA GRIN 14886
Wikipedia Edgeworthia_gardneri
CMAUP NPO15915

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
Hormetic Nutrition and Redox Regulation in Gut–Brain Axis Disorders Scuto M, Rampulla F, Reali GM, Spanò SM, Trovato Salinaro A, Calabrese V Antioxidants (Basel) 18-Apr-2024
PMCID:PMC11047582
doi:10.3390/antiox13040484
PMID:38671931
Edgeworthia gardneri (Wall.) Meisn. Ethanolic Extract Attenuates Endothelial Activation and Alleviates Cardiac Ischemia-Reperfusion Injury Lang X, Zhong C, Su L, Qin M, Xie Y, Shan D, Cui Y, Shi M, Li M, Quan H, Qiu L, Zhong G, Yu J Molecules 29-Feb-2024
PMCID:PMC10935089
doi:10.3390/molecules29051068
PMID:38474581
Controlled SPION-Exosomes Loaded with Quercetin Preserves Pancreatic Beta Cell Survival and Function in Type 2 Diabetes Mellitus Zhuang M, Rao L, Chen Y, Xiao S, Xia H, Yang J, Lv X, Qin D, Zhu C Int J Nanomedicine 12-Oct-2023
PMCID:PMC10578181
doi:10.2147/IJN.S422416
PMID:37849640
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
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
Edgeworthia gardneri (Wall.) Meisn. extract protects against myocardial infarction by inhibiting NF-κB-and MAPK-mediated endothelial inflammation Wei D, Tang L, Su L, Zeng S, Telushi A, Lang X, Zhang Y, Qin M, Qiu L, Zhong C, Yu J Front Cardiovasc Med 20-Dec-2022
PMCID:PMC9808090
doi:10.3389/fcvm.2022.1013013
PMID:36606274
The ethanol extract of Edgeworthia gardneri (Wall.) Meisn attenuates macrophage foam cell formation and atherogenesis in ApoE−/− mice Tang L, Kuang C, Shan D, Shi M, Li J, Qiu L, Yu J Front Cardiovasc Med 24-Nov-2022
PMCID:PMC9729707
doi:10.3389/fcvm.2022.1023438
PMID:36505350
Spice-Derived Bioactive Compounds Confer Colorectal Cancer Prevention via Modulation of Gut Microbiota Dacrema M, Ali A, Ullah H, Khan A, Di Minno A, Xiao J, Martins AM, Daglia M Cancers (Basel) 19-Nov-2022
PMCID:PMC9688386
doi:10.3390/cancers14225682
PMID:36428774
Material Properties of Traditional Handmade Paper Samples Fabricated from Cellulosic Fiber of Lokta Bushes Aryal GM, Kandel KP, Bhattarai RK, Giri B, Adhikari M, Ware A, Han S, George G, Luo Z, Gautam BR, Neupane BB ACS Omega 01-Sep-2022
PMCID:PMC9476527
doi:10.1021/acsomega.2c04398
PMID:36120032
Original karst tiankeng with underground virgin forest as an inaccessible refugia originated from a degraded surface flora in Yunnan, China Shui W, Chen Y, Jian X, Jiang C, Wang Q, Zeng Y, Zhu S, Guo P, Li H Sci Rep 07-Jun-2022
PMCID:PMC9174222
doi:10.1038/s41598-022-13678-0
PMID:35672447
Vegetation Classification and Distribution Patterns in the South Slope of Yarlung Zangbo Grand Canyon National Nature Reserve, Eastern Himalayas Wu PP, Wang Z, Jia NX, Dong SQ, Qu XY, Qiao XG, Liu CC, Guo K Plants (Basel) 28-Apr-2022
PMCID:PMC9105001
doi:10.3390/plants11091194
PMID:35567195
Research progress of Chinese herbal medicine compounds and their bioactivities: Fruitful 2020 Gu X, Hao D, Xiao P Chin Herb Med 17-Mar-2022
PMCID:PMC9476823
doi:10.1016/j.chmed.2022.03.004
PMID:36117669
The Effects of Antioxidants from Natural Products on Obesity, Dyslipidemia, Diabetes and Their Molecular Signaling Mechanism Khutami C, Sumiwi SA, Khairul Ikram NK, Muchtaridi M Int J Mol Sci 12-Feb-2022
PMCID:PMC8875143
doi:10.3390/ijms23042056
PMID:35216172
Approaches to Decrease Hyperglycemia by Targeting Impaired Hepatic Glucose Homeostasis Using Medicinal Plants Mata-Torres G, Andrade-Cetto A, Espinoza-Hernández F Front Pharmacol 23-Dec-2021
PMCID:PMC8733686
doi:10.3389/fphar.2021.809994
PMID:35002743
Natural Products for the Prevention and Control of the COVID-19 Pandemic: Sustainable Bioresources Singla RK, He X, Chopra H, Tsagkaris C, Shen L, Kamal MA, Shen B Front Pharmacol 01-Dec-2021
PMCID:PMC8671886
doi:10.3389/fphar.2021.758159
PMID:34925017

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 / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3,5-Trihydroxy-7-methyl-2-(1,3,5-trihydroxy-7-methyl-9,10-dioxoanthracen-2-yl)anthracene-9,10-dione 54752972 Click to see 538.50 unknown via CMAUP database
1,4,7-Trihydroxy-2-methoxy-6-methylanthracene-9,10-dione 54752971 Click to see CC1=CC2=C(C=C1O)C(=O)C3=C(C2=O)C(=CC(=C3O)OC)O 300.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Butyrophenones
Rhodomyrtosone A 102521923 Click to see 456.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
9,9'-Di-O-(E)-feruloylsecoisolariciresinol 10439806 Click to see 714.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3I(2),21I(2))-Aa(2)-Neogammacer-22(30)-ene-3,29-diol 102032092 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 11876093 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 10836206 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 7061300 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 479957 Click to see 484.80 unknown via CMAUP database
11-Oxo-beta-amyrin 20055661 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 440.70 unknown via CMAUP database
3-O-p-Coumaroyloleanolic acid 10579517 Click to see 602.80 unknown via CMAUP database
3beta-Acetoxy-11alpha,12alpha-epoxyoleanan-28,13beta-olide 21626351 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C4C(O4)C56C3(CCC7(C5CC(CC7)(C)C)C(=O)O6)C)C)C 512.70 unknown via CMAUP database
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
methyl (1S,2R,4aS,6aR,6aS,6bR,8aS,10R,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 40884490 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown via CMAUP database
Methyl Betulonate 10766700 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)OC 468.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(8aR)-8a-hydroxy-3,3,6,6,8,8-hexamethyl-1,2-benzodioxine-5,7-dione 44281346 Click to see 268.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(10R,16R,24R)-12-hydroxy-5,5,7,7,19,19,21,21-octamethyl-13-(3-methylbutanoyl)-10-(2-methylpropyl)-16-propan-2-yl-3,15,17-trioxahexacyclo[12.10.0.02,11.04,9.016,24.018,23]tetracosa-1,4(9),11,13,18(23)-pentaene-6,8,20,22-tetrone 56929125 Click to see 688.80 unknown via CMAUP database
(10S,16R,24R)-12-hydroxy-5,5,7,7,19,19,21,21-octamethyl-13-(3-methylbutanoyl)-10-(2-methylpropyl)-16-propan-2-yl-3,15,17-trioxahexacyclo[12.10.0.02,11.04,9.016,24.018,23]tetracosa-1,4(9),11,13,18(23)-pentaene-6,8,20,22-tetrone 56929124 Click to see 688.80 unknown via CMAUP database
(9R)-6,8-dihydroxy-2,2,4,4-tetramethyl-5-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione 102521922 Click to see 442.50 unknown via CMAUP database
(9S)-6,8-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione 26202536 Click to see CC(C)CC1C2=C(C=C(C(=C2O)C(=O)CC(C)C)O)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 442.50 unknown via CMAUP database
Rhodomyrtone 12050020 Click to see 442.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Triacontyl p-coumarate 14213589 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O 585.00 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
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)85530-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Edgeworthin 5491526 Click to see 338.30 unknown https://doi.org/10.1021/NP040127S
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin 5281406 Click to see 352.30 unknown https://doi.org/10.1021/NP040127S
https://doi.org/10.1016/S0031-9422(00)85530-2
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/10.1021/NP040127S
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Combretol 12303802 Click to see 388.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
2,3,8-Tri-O-methylellagic acid 5281860 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC 344.30 unknown via CMAUP database
beta-Pedunculagin 5320441 Click to see 784.50 unknown via CMAUP database

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