Coscinium fenestratum

Details Top

Internal ID UUID644013c87cf0e521736349
Scientific name Coscinium fenestratum
Authority (Gaertn.) Colebr.
First published in Trans. Linn. Soc. London 13: 65 (1821)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Natural yellow dye obtained from the stem bark of Coscinium fenestratum, used in textile coloring.
- Small‑diameter woody stems fashioned into walking sticks, tool handles and other craft objects.

Industrial and craft applications:
- The dye is employed in artisanal and small‑scale textile dyeing of cotton, silk and wool, typically applied in acidic baths with mordants such as alum to improve colour fastness.
- The bark is a source of tannins used in the vegetable tanning of leather, converting raw hides to durable leather.

Colorants and tanning:
- Extraction of the bark with hot water or ethanol yields a bright yellow solution rich in alkaloids and phenolics; the colorant imparts a vivid yellow hue to protein fibres.
- The bark’s tannin content is suitable for leather tanning, allowing rapid extraction and producing a firm, light‑fast leather.

Wood and fiber:
- The dense wood of mature vines is strong and suitable for small utilitarian items such as handles, cane‑type implements and decorative objects.
- The outer bark provides a coarse bast fibre that can be spun into twine or used for low‑stress rope applications.

Properties relevant to use:
- The dye is water‑soluble under acidic conditions and imparts a characteristic yellow colour; with mordants, the colour shows acceptable lightfastness for textile use.
- The tannins are extractable with hot water and have high reactivity with collagen, enabling effective vegetable tanning.
- The wood is dense and dimensionally stable, making it suitable for precision craft work.

Standards and regulation:
- Textile applications of the natural dye are subject to the ISO 105 colour‑fastness test suite, and the dye falls under national colourant safety regulations (e.g., EU REACH for colourants in textiles).

Sustainability and sourcing:
- Coscinium fenestratum is listed as vulnerable on the IUCN Red List; commercial harvesting of bark for dye and stems for craft use contributes to its decline, highlighting the need for sustainable management and the development of cultivated sources.

Synonyms Top

Scientific name Authority First published in
Menispermum fenestratum Gaertn. Fruct. Sem. Pl. 1: 219 (1788)
Pereiria medica Lindl. Fl. Med. : 370 (1838)
Coscinium maingayi Pierre Fl. Forest. Cochinch. : t. 112 (1885)
Coscinium miosepalum Diels Pflanzenr. , IV, 94: 113 (1910)
Coscinium peltatum Merr. Univ. Calif. Publ. Bot. 15: 59 (1929)
Coscinium usitatum Pierre Fl. Forest. Cochinch. : t. 112 (1885)
Coscinium wallichianum Miers Contr. Bot. 3: 23 (1871)
Coscinium wightianum Miers & Diels Pflanzenr. , IV, 94: 112 (1910)
Coscinium fenestratum var. macrophyllum Yamam. J. Soc. Trop. Agric. 16: 39 (1944)
Coscinium fenestratum var. ovalifolium Yamam. J. Soc. Trop. Agric. 16: 39 (1944)

Common names Top

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Language Common/alternative name
Kannada ಬಳ್ಳಿ ಅರಿಶಿನ
Malayalam മരമഞ്ഞൾ

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000623526
Tropicos 50278913
KEW urn:lsid:ipni.org:names:580661-1
The Plant List kew-2739895
Open Tree Of Life 688896
NCBI Taxonomy 483232
IUCN Red List 50126585
IPNI 580661-1
iNaturalist 427389
GBIF 5592750
Freebase /m/0_qgxsg
USDA GRIN 406445
Wikipedia Coscinium_fenestratum

Genomes (via NCBI) Top

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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
Computational analysis and experimental verification of donor–acceptor behaviour of berberine, and its co-oligomers and co-polymers with ethylenedıoxythıophene Gamini Rajapakse RM, Horrocks BR, Gunarathna HM, Malikaramage AU, Egodawele MG, Herath WH, Sandakelum L, Bandara VM, Bowatta WV, Susanthi Jayasinghe JM, Seneviratne VN, Ranatunga U, Perera LL, Dassanayake SM, Udawatte CP Sci Rep 18-Nov-2023
PMCID:PMC10657409
doi:10.1038/s41598-023-47541-7
PMID:37980445
Addressing the preventive and therapeutic perspective of berberine against diabetes Shrivastava S, Sharma A, Saxena N, Bhamra R, Kumar S Heliyon 03-Nov-2023
PMCID:PMC10663750
doi:10.1016/j.heliyon.2023.e21233
PMID:38027723
Berberine influences multiple diseases by modifying gut microbiota Yang F, Gao R, Luo X, Liu R, Xiong D Front Nutr 03-Aug-2023
PMCID:PMC10435753
doi:10.3389/fnut.2023.1187718
PMID:37599699
Berberine isolation from Coscinium fenestratum: optical, electrochemical, and computational studies Rajapakse RM, Horrocks BR, Malikaramage AU, Gunarathna HM, Egodawele MG, Jayasinghe JM, Ranatunga U, Herath WH, Sandakelum L, Wylie S, Abewardana PG, Seneviratne VN, Perera LL, Velauthapillai D RSC Adv 07-Jun-2023
PMCID:PMC10245225
doi:10.1039/d3ra01769a
PMID:37293467
An overview on medicinal plants used for combating coronavirus: Current potentials and challenges Abou Baker DH, Hassan EM, El Gengaihi S J Agric Food Res 20-May-2023
PMCID:PMC10198795
doi:10.1016/j.jafr.2023.100632
PMID:37251276
A multivariate and quantitative assessment of medicinal plants used by the indigenous Malayali tribes in the Javadhu hills of Tiruvannamalai district, Tamil Nadu, India Silambarasan R, Sasidharan S, Nair J H, Kumar S N, R A, Nair AS, Selavinayagam KT Heliyon 18-Apr-2023
PMCID:PMC10256831
doi:10.1016/j.heliyon.2023.e15607
PMID:37305490
Plant ingredients in Thai food: a well-rounded diet for natural bioactive associated with medicinal properties Buathong R, Duangsrisai S PeerJ 01-Mar-2023
PMCID:PMC9985418
doi:10.7717/peerj.14568
PMID:36879911
Berberine Ameliorates Metabolic-Associated Fatty Liver Disease Mediated Metabolism Disorder and Redox Homeostasis by Upregulating Clock Genes: Clock and Bmal1 Expressions Ye C, Zhang Y, Lin S, Chen Y, Wang Z, Feng H, Fang G, Quan S Molecules 16-Feb-2023
PMCID:PMC9960773
doi:10.3390/molecules28041874
PMID:36838862
A Review of Fibraurea tinctoria and Its Component, Berberine, as an Antidiabetic and Antioxidant Purwaningsih I, Maksum IP, Sumiarsa D, Sriwidodo S Molecules 29-Jan-2023
PMCID:PMC9919506
doi:10.3390/molecules28031294
PMID:36770960
13-Butoxyberberine Bromide Inhibits Migration and Invasion in Skin Cancer A431 Cells Laomethakorn P, Tayeh M, Samosorn S, Tananyuthawongse C, Watanapokasin R Molecules 19-Jan-2023
PMCID:PMC9921070
doi:10.3390/molecules28030991
PMID:36770659
Potential Antimicrobe Producer of Endophytic Bacteria from Yellow Root Plant (Arcangelisia flava (L.)) Originated from Enggano Island Sipriyadi, Masrukhin, Wibowo RH, Darwis W, Yudha S, Purnaningsih I, Siboro R Int J Microbiol 16-Nov-2022
PMCID:PMC10270767
doi:10.1155/2022/6435202
PMID:37332491
Comparative Studies of Palmatine with Metformin and Glimepiride on the Modulation of Insulin Dependent Signaling Pathway In Vitro, In Vivo & Ex Vivo Nwabueze OP, Sharma M, Balachandran A, Gaurav A, Abdul Rani AN, Małgorzata J, Beata MM, Lavilla CA Jr, Billacura MP Pharmaceuticals (Basel) 25-Oct-2022
PMCID:PMC9695187
doi:10.3390/ph15111317
PMID:36355489
Advancements and future prospective of DNA barcodes in the herbal drug industry Mahima K, Sunil Kumar KN, Rakhesh KV, Rajeswaran PS, Sharma A, Sathishkumar R Front Pharmacol 21-Oct-2022
PMCID:PMC9635000
doi:10.3389/fphar.2022.947512
PMID:36339543
Retraction: Biosurfactant producing multifarious Streptomyces puniceus RHPR9 of Coscinium fenestratum rhizosphere promotes plant growth in chilli N/A PLoS One 31-Aug-2022
PMCID:PMC9432687
doi:10.1371/journal.pone.0273533
PMID:36044452
Role of ethno-phytomedicine knowledge in healthcare of COVID-19: advances in traditional phytomedicine perspective Nasir Ahmed M, Hughes K Beni Suef Univ J Basic Appl Sci 04-Aug-2022
PMCID:PMC9362587
doi:10.1186/s43088-022-00277-1
PMID:35966214

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
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(+-)-Tetrahydroberberine 34458 Click to see 339.40 unknown https://doi.org/10.1016/S0031-9422(00)97910-X
(S)-Canadine 21171 Click to see 339.40 unknown https://doi.org/10.1016/S0031-9422(00)97910-X
10-Hydroxy-9-methoxy-5,6,13,13a-tetrahydro-[1,3]dioxolo[4,5-g] isoquino[3,2-a]isoquinolin-8-one 100916731 Click to see 339.30 unknown https://doi.org/10.1016/0031-9422(92)80301-T
2-Hydroxy-3,9,10-trimethoxy-5,6,13,13a-tetrahydroisoquinolino[2,1-b]isoquinolin-8-one 162897730 Click to see 355.40 unknown https://doi.org/10.1016/0031-9422(92)80301-T
8-Oxocanadine 470418 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2=O)OCO5)C=C1)OC 353.40 unknown https://doi.org/10.1016/0031-9422(92)80301-T
https://doi.org/10.1016/S0031-9422(00)97910-X
8-Oxoisocorypalmine 162897731 Click to see 355.40 unknown https://doi.org/10.1016/0031-9422(92)80301-T
8-Oxotetrahydrothalifendine 470416 Click to see 339.30 unknown https://doi.org/10.1016/0031-9422(92)80301-T
Berberine 2353 Click to see 336.40 unknown https://doi.org/10.1016/0031-9422(92)80301-T
https://doi.org/10.1016/S0031-9422(00)97910-X
Gusanlung B 133161 Click to see 353.40 unknown https://doi.org/10.1016/0031-9422(92)80301-T
https://doi.org/10.1016/S0031-9422(00)97910-X
> Benzenoids / Phenol ethers / Anisoles
Oxoberberine 631722 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC(=C(C=C4C=CN3C2)OC)OC)OC 351.40 unknown https://doi.org/10.1016/S0031-9422(00)97910-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see 382.70 unknown https://doi.org/10.1002/ARDP.19302680505
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/S0031-9422(00)97910-X
https://doi.org/10.1016/0031-9422(92)80301-T
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(92)80301-T
https://doi.org/10.1016/S0031-9422(00)97910-X
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)97910-X
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
17,18-Dimethoxy-5,8-dioxa-14-azapentacyclo[12.8.0.02,11.04,9.016,21]docosa-1(22),2,4(9),10,16(21),17,19-heptaen-15-one 162895741 Click to see 365.40 unknown https://doi.org/10.1016/0031-9422(92)80301-T
8-Oxypalmatine 10926678 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC(=C(C=C4CCN3C2=O)OC)OC)OC 367.40 unknown https://doi.org/10.1016/0031-9422(92)80301-T
Oxyberberine 11066 Click to see 351.40 unknown https://doi.org/10.1016/0031-9422(92)80301-T
https://doi.org/10.1016/S0031-9422(00)97910-X

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