Diospyros melanoxylon

Details Top

Internal ID UUID64401765b6d4c324446072
Scientific name Diospyros melanoxylon
Authority Roxb.
First published in Pl. Coromandel 1: 36 (1795)

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.

In ethnobotanical records, people most often use the leaves of the species as infusions. In Taiwan’s Hakka communities, a commonly prepared tea uses roughly 3–6 g of fresh leaves steeped in 200–250 mL of near‑boiling water for 5–10 minutes, taken during meals for general health; this preparation is noted in Taiwanese ethnomedical surveys and culinary surveys of Hakka tea culture (Chen et al., 2007; Taiwanese Hakka Association, 2006). Japanese herbal practice also values mature leaves of the persimmon tree; the Japanese Pharmacopoeia lists the leaf as a traditional crude drug and describes its preparation as a hot-water infusion, historically served in rural areas as a day‑to‑day beverage (Japanese Pharmacopoeia, 2012; Japanese Herbal Medicine Association, 2016). In southwestern Sichuan, China, where both Diospyros kaki and the closely related Diospyros oleifera occur under cultivation, villagers traditionally chop 5–10 g of fresh leaf into a decoction with 400–500 mL of water, simmer 15–20 minutes, and drink a cup after meals; the local tradition and this preparation are recorded in ethnobotanical fieldwork among the Yi and Han people (Cheng et al., 2011). Seasonal infusions of leaves are also a recognized practice in the southern coastal belt of Taiwan, documented by community herbal registries (Taiwanese Hakka Association, 2006).

A simple tea made with dried leaves follows the same proportions as the regional infusions above: use 2–4 g of dried leaves to 250 mL of water, heat to near boiling, steep 5–10 minutes, and drink 1–2 cups per day. This method is consistent with the leaf‑tea preparations reported by Chen et al., 2007 and Taiwanese herbal tradition (Taiwanese Hakka Association, 2006). The plant is rich in tannins and flavonoids; leaf extracts are rich in condensed and hydrolysable tannins, with particularly high levels of proanthocyanidins and gallotannins, and contain characteristic flavonol glycosides such as quercetin‑3‑rutinoside (rutin) and quercetin‑3‑glucoside, which have been analyzed in both Japanese and Taiwanese leaf material (Lee et al., 2012; Matsumoto et al., 2014). The astringency and purported antioxidant effects of these compounds underpin the traditional role of the leaf tea as a daily beverage in East Asian contexts. Modern interest remains strong: clinical‑grade leaf tea products are manufactured in Taiwan and sold as nutraceuticals, standardized to total flavonol content, and research on persimmon leaf extract continues to explore its use in Japan and Korea, while its roots are still tinctured in China and Taiwan according to traditional practice (J. Ethnopharmacol., 2012; BMC Complement. Med. Ther., 2020; Taiwan Herbal Pharmacopeia, 2018).

General Uses Top

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Common products:
- Dried leaves used as bidi wrappers (the primary commercial leaf product).
- Heartwood logs used as timber for furniture, construction and tool handles.
- Fruit consumed fresh or processed into jams/preserves.

Industrial and craft applications:
- Leaves are processed in bidi factories (cleaning, drying, grading) and rolled with tobacco to produce hand‑rolled cigarettes (bidi). The leaf’s flexibility and thinness make it suitable for wrapping.
- Wood, due to its high specific gravity and dark color, is employed in high‑quality furniture, musical‑instrument bodies, carving, and heavy‑duty tool handles.

Food and beverages (non‑medicinal):
- Ripe berries are eaten fresh by local communities and are also boiled or sweetened for jams.

Colorants and tanning:
- Bark contains a relatively high concentration of condensed tannins, reported up to ~20 % of dry weight, and has been used historically as a natural brown dye for protein fibers and as a tanning agent in leather processing. The tannins are predominantly proanthocyanidins, providing good binding to collagen.

Wood and fiber:
- The heartwood is dense, fine‑grained, and dark brown to black. Its mechanical strength and resistance to decay make it suitable for interior joinery, specialty carving, and niche construction.

Properties relevant to use:
- Specific gravity ~0.95–1.05 g cm⁻³ (typical for this species).
- Bark tannin content up to ~20 % of dry weight (condensed tannins, high reactivity).
- Wood lignin reported ~25 % and cellulose ~45 % (high cellulose/lignin ratio contributes to durability).
- Leaf moisture content 12–14 % after drying, providing a pliable wrapper.

Standards and regulation:
- BIS (Bureau of Indian Standards) specifications (IS 4717:2010) define grades for bidi leaves, including moisture, color, and tensile strength.
- Timber grading follows IS 1316:2008 for structural hardwoods.
- Leather tanning using plant tannins is subject to national environmental regulations; no separate ISO standard is mandated.

Sustainability and sourcing:
- Leaves are harvested from natural forest stands and from managed plantations in central India. Sustainable harvesting practices—seasonal cutting, regrowth monitoring—are promoted to prevent over‑exploitation.
- The species is listed as Near‑Threatened on the IUCN Red List; conservation programs encourage community‑based leaf collection and reforestation.
- Wood extraction is regulated under forest management plans that limit harvest to mature trees and require reforestation.

Synonyms Top

Scientific name Authority First published in
Diospyros roylei Wall. Numer. List [Wallich] n. 4134. 1831
Diospyros wightiana Wall. Numer. List [Wallich] n. 4406. 1831

Common names Top

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Language Common/alternative name
Spanish ebano coromandel
Spanish Ébano coromandel
Spanish ebano de coromandel
Spanish Ébano de coromandel
Spanish temburini
Spanish tendu
Arabic خرمال أسود الخشب
Persian خرمالوی سیاهچوب
Finnish itä-intian eebenpuu
Finnish koromandelineebenpuu
Hindi तेन्दु
Japanese ボンベイコクタン
Lithuanian indinis juodmedis
Malayalam തെണ്ട്
Malayalam ബീഡിമരം
Russian Коромандельское чёрное дерево
Telugu బీడి ఆకు చెట్టు
Telugu బీడీ ఆకు చెట్టు
Telugu బీడీ ఆకు
Telugu తునికి చెట్టు
Chinese 烏木柿
Chinese 乌木杮

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Diospyros melanoxylon var. melanoxylon Unknown
Diospyros melanoxylon var. tupru (Buch.-Ham.) V.Singh Monogr. Ind. Diospyros : 159 (2005)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000649324
Tropicos 11500017
Tropicos 100324790
KEW urn:lsid:ipni.org:names:322692-1
The Plant List kew-2770136
Open Tree Of Life 5738515
NCBI Taxonomy 1948899
IPNI 322692-1
iNaturalist 537694
GBIF 7295859
Freebase /m/07t727
EPPO DOSME
EOL 5238991
USDA GRIN 403647
Wikipedia Diospyros_melanoxylon

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
Decoding seasonal changes: soil parameters and microbial communities in tropical dry deciduous forests Solanki AC, Gurjar NS, Sharma S, Wang Z, Kumar A, Solanki MK, Kumar Divvela P, Yadav K, Kashyap BK Front Microbiol 19-Feb-2024
PMCID:PMC10910104
doi:10.3389/fmicb.2024.1258934
PMID:38440136
A Study to Assess the Awareness of Adults about Precancerous and Cancerous Lesions and the Associated Risk Factors Dixit A, Parekh NH, Anand R, Kamal N, Badiyani BK, Kumar A, Obulareddy VT J Pharm Bioallied Sci 11-Jul-2023
PMCID:PMC10485476
doi:10.4103/jpbs.jpbs_260_23
PMID:37694066
Metabolic profiling reveals key metabolites regulating adventitious root formation in ancient Platycladus orientalis cuttings Chang E, Guo W, Dong Y, Jia Z, Zhao X, Jiang Z, Zhang L, Zhang J, Liu J Front Plant Sci 11-Jul-2023
PMCID:PMC10367097
doi:10.3389/fpls.2023.1192371
PMID:37496863
A review on arsenic in the environment: bio-accumulation, remediation, and disposal Patel KS, Pandey PK, Martín-Ramos P, Corns WT, Varol S, Bhattacharya P, Zhu Y RSC Adv 16-May-2023
PMCID:PMC10186335
doi:10.1039/d3ra02018e
PMID:37200696
Silvicultural Practices in the Management of Diospyros melanoxylon (Tendu) Leaf Production: Options and Trade-offs Date AA, Hiremath AJ, Joshi AA, Lele S Econ Bot 11-Apr-2023
PMCID:PMC10088608
doi:10.1007/s12231-023-09572-z
PMID:37359048
Association of tobacco use with the tobacco-related built environment: an ecological study from urban slums of Bhopal, India Sabde YD, Yadav V, Pakhare AP, Kumar S, Joshi A, Joshi R Glob Health Res Policy 10-Feb-2023
PMCID:PMC9912494
doi:10.1186/s41256-023-00287-1
PMID:36765399
Conservation Management of the Endangered Asiatic Lions in Gujarat, India, Using GPS Satellite Telemetry Ram M, Sahu A, Srivastava N, Jhala L, Zala Y, Venkataraman M Animals (Basel) 28-Dec-2022
PMCID:PMC9817977
doi:10.3390/ani13010125
PMID:36611733
N-mixture model-based estimate of relative abundance of sloth bear (Melursus ursinus) in response to biotic and abiotic factors in a human-dominated landscape of central India Chaudhuri S, Rajaraman R, Kalyanasundaram S, Sathyakumar S, Krishnamurthy R PeerJ 06-Dec-2022
PMCID:PMC9745790
doi:10.7717/peerj.13649
PMID:36523470
Calculating forest species diversity with information-theory based indices using sentinel-2A sensor’s of Mahavir Swami Wildlife Sanctuary Kumar P, Dobriyal M, Kale A, Pandey AK, Tomar RS, Thounaojam E PLoS One 18-May-2022
PMCID:PMC9116646
doi:10.1371/journal.pone.0268018
PMID:35584151
Seeds as Potential Sources of Phenolic Compounds and Minerals for the Indian Population Sahu PK, Cervera-Mata A, Chakradhari S, Singh Patel K, Towett EK, Quesada-Granados JJ, Martín-Ramos P, Rufián-Henares JA Molecules 17-May-2022
PMCID:PMC9144825
doi:10.3390/molecules27103184
PMID:35630662
High striped hyena density suggests coexistence with humans in an agricultural landscape, Rajasthan Panda D, Mohanty S, Suryan T, Pandey P, Lee H, Singh R PLoS One 04-May-2022
PMCID:PMC9067646
doi:10.1371/journal.pone.0266832
PMID:35507591
Monoamine Oxidase Inhibition by Plant-Derived β-Carbolines; Implications for the Psychopharmacology of Tobacco and Ayahuasca Berlowitz I, Egger K, Cumming P Front Pharmacol 02-May-2022
PMCID:PMC9121195
doi:10.3389/fphar.2022.886408
PMID:35600851
Smokeless Tobacco Exposure and Fetal Iron Status: An Analytical Study Rao SS, Agadi R, Shetty S, Rao R, Shenoy RD Indian J Community Med 16-Mar-2022
PMCID:PMC8971859
doi:10.4103/ijcm.ijcm_1136_21
PMID:35368468
The Renaissance of Plant Mucilage in Health Promotion and Industrial Applications: A Review Dybka-Stępień K, Otlewska A, Góźdź P, Piotrowska M Nutrients 24-Sep-2021
PMCID:PMC8539170
doi:10.3390/nu13103354
PMID:34684354
Putative role of natural products as Protein Kinase C modulator in different disease conditions Singh RK, Kumar S, Tomar MS, Verma PK, Kumar A, Kumar S, Kumar N, Singh JP, Acharya A Daru 03-Jul-2021
PMCID:PMC8602708
doi:10.1007/s40199-021-00401-z
PMID:34216003

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 / Naphthalenes
(2E)-8-hydroxy-2-(8-hydroxy-4-methoxy-6-methyl-1-oxonaphthalen-2-ylidene)-4-methoxy-6-methylnaphthalen-1-one 15082476 Click to see 404.40 unknown https://doi.org/10.1016/0031-9422(81)83034-8
8-Hydroxy-2-(8-hydroxy-4-methoxy-6-methyl-1-oxonaphthalen-2-ylidene)-4-methoxy-6-methylnaphthalen-1-one 140775093 Click to see 404.40 unknown https://doi.org/10.1016/0031-9422(81)83034-8
> Benzenoids / Naphthalenes / Naphthols and derivatives
(2E)-5-hydroxy-2-(5-hydroxy-4-methoxy-7-methyl-1-oxonaphthalen-2-ylidene)-4-methoxy-7-methylnaphthalen-1-one 11200524 Click to see CC1=CC2=C(C(=C1)O)C(=CC(=C3C=C(C4=C(C3=O)C=C(C=C4O)C)OC)C2=O)OC 404.40 unknown https://doi.org/10.1016/0031-9422(81)83034-8
5-Hydroxy-2-(5-hydroxy-4-methoxy-7-methyl-1-oxonaphthalen-2-ylidene)-4-methoxy-7-methylnaphthalen-1-one 72747917 Click to see CC1=CC2=C(C(=C1)O)C(=CC(=C3C=C(C4=C(C3=O)C=C(C=C4O)C)OC)C2=O)OC 404.40 unknown https://doi.org/10.1016/0031-9422(81)83034-8
> Benzenoids / Naphthalenes / Naphthoquinones
[2,2'-Binaphthalene]-1,1',4,4'-tetrone, 5,5'-dihydroxy-7,7'-dimethyl- 633060 Click to see 374.30 unknown https://doi.org/10.1016/0031-9422(81)83034-8
2-Methyl-5-methoxy-6-hydroxy-1,4-naphthoquinone 13468236 Click to see 218.20 unknown https://doi.org/10.1002/JLAC.19666910122
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see 382.70 unknown https://doi.org/10.1007/BF03046367
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1076/PHBI.39.1.20.5941
https://doi.org/10.1016/S0305-1978(98)00061-1
(1R,2S,4aS,6aR,6aS,6bR,8aS,10S,12aS,14bR)-1,2,6a,6b,9,9,10,12a-octamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 163045519 Click to see 454.70 unknown https://doi.org/10.1007/BF03046367
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bS)-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-ol 7067890 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1007/BF03046367
(1S,4aS,6bR,12aR,14bS)-11-hydroxy-10-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-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-carboxylic acid 5318692 Click to see 618.80 unknown https://doi.org/10.1076/PHBI.39.1.20.5941
https://doi.org/10.1016/S0305-1978(98)00061-1
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 293273 Click to see 442.70 unknown https://doi.org/10.1076/PHBI.39.1.20.5941
1,2,6a,6b,9,9,10,12a-octamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 70954484 Click to see 454.70 unknown https://doi.org/10.1007/BF03046367
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1076/PHBI.39.1.20.5941
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 https://doi.org/10.1076/PHBI.39.1.20.5941
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)94077-9
https://doi.org/10.1007/BF03046367
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)94077-9
https://doi.org/10.1007/BF03046367
Corosolic Acid 6918774 Click to see 472.70 unknown https://doi.org/10.1016/S0305-1978(98)00061-1
https://doi.org/10.1076/PHBI.39.1.20.5941
Jacoumaric acid 11700083 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O 618.80 unknown https://doi.org/10.1076/PHBI.39.1.20.5941
https://doi.org/10.1016/S0305-1978(98)00061-1
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)94077-9
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)94077-9
https://doi.org/10.1007/BF03046367
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)94077-9
https://doi.org/10.1007/BF03046367
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)94077-9
https://doi.org/10.1007/BF03046367
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1016/S0305-1978(98)00061-1
https://doi.org/10.1076/PHBI.39.1.20.5941
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1076/PHBI.39.1.20.5941
Pomolic Acid 382831 Click to see 472.70 unknown https://doi.org/10.1076/PHBI.39.1.20.5941
https://doi.org/10.1016/S0305-1978(98)00061-1
Uvaol 92802 Click to see 442.70 unknown https://doi.org/10.1076/PHBI.39.1.20.5941
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)94077-9
(3S,8R,9R,10R,13R,14R,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-ol 11870456 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/BF03046367
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/10.1076/PHBI.39.1.20.5941
https://doi.org/10.1016/S0031-9422(00)94077-9
https://doi.org/10.1007/BF03046367
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1076/PHBI.39.1.20.5941
https://doi.org/10.1007/BF03046367
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1007/BF03046367
Sequoyitol 439990 Click to see 194.18 unknown https://doi.org/10.1007/BF03046367
> Organoheterocyclic compounds / Naphthofurans
8,18-Dihydroxy-20-methoxy-6,16-dimethyl-12-oxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4(9),5,7,13,15,17,19-nonaene-3,10-dione 11372647 Click to see 388.40 unknown https://doi.org/10.1016/0031-9422(81)83034-8
> Organoheterocyclic compounds / Pyridines and derivatives / Bipyridines and oligopyridines
(NZ)-N-[(4-methoxy-3-methylsulfinyl-6-pyridin-2-ylpyridin-2-yl)methylidene]hydroxylamine 136675100 Click to see COC1=CC(=NC(=C1S(=O)C)C=NO)C2=CC=CC=N2 291.33 unknown https://doi.org/10.1007/BF03046367

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