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
Suggest a correction!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
Add a new one! Suggest a correction!| 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 |
Varieties (abbr. var.) Top
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Diospyros melanoxylon var. melanoxylon | Unknown | |
| Diospyros melanoxylon var. tupru | (Buch.-Ham.) V.Singh | Monogr. Ind. Diospyros : 159 (2005) |
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 click to expand
-
Indian Subcontinent
- Bangladesh
- India
- Sri Lanka
-
Indian Subcontinent
Links to other databases Top
Suggest others/fix!| 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)!
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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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |