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Diospyros celebica

Diospyros celebica - 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 UUID64401743af0ac932280758
Scientific name Diospyros celebica
Authority Bakh.
First published in Gard. Bull. Straits Settlem. 7: 166 (1933)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English sulawesi ebony
English indonesian ebony
English macassar ebony
Arabic خرمال سولاوسي
Indonesian eboni bergaris
Indonesian kayu-hitam sulawesi
Indonesian kayu hitam sulawesi
Norwegian Bokmål makassaribenholt
Chinese 西里伯斯柿
Chinese 蘇拉威西烏木
Chinese 苏拉威西乌木

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000648666
Tropicos 100324435
KEW urn:lsid:ipni.org:names:322219-1
The Plant List kew-2769521
PFAF Diospyros celebica
Open Tree Of Life 1256
NCBI Taxonomy 413731
IUCN Red List 33203
IPNI 322219-1
iNaturalist 191525
GBIF 4071419
Freebase /m/07s8b_9
EPPO DOSCE
EOL 5238518
USDA GRIN 452733
Wikipedia Diospyros_celebica

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
Use and sustainability of wood in acoustic guitars: An overview based on the global market Calvano S, Negro F, Ruffinatto F, Zanuttini-Frank D, Zanuttini R Heliyon 14-Apr-2023
PMCID:PMC10147972
doi:10.1016/j.heliyon.2023.e15218
PMID:37128325
Collecting wood core samples from Macassar ebony (Diospyros celebica Bakh.) for multi-purpose analysis using pickering punch Siregar IZ, Majiidu M, Dwiyanti FG, Harnelly E, Damayanti R, Karlinasari L, Rafi M, Septaningsih DA, Parker-Forney M MethodsX 14-May-2022
PMCID:PMC9168166
doi:10.1016/j.mex.2022.101728
PMID:35677845
Generating long-read sequences using Oxford Nanopore Technology from Diospyros celebica genomic DNA Siregar IZ, Dwiyanti FG, Pratama R, Matra DD, Majiidu M BMC Res Notes 27-Feb-2021
PMCID:PMC7913452
doi:10.1186/s13104-021-05484-0
PMID:33640010
Leveraging biodiversity knowledge for potential phyto-therapeutic applications Sharma V, Sarkar IN J Am Med Inform Assoc 21-Mar-2013
PMCID:PMC3721164
doi:10.1136/amiajnl-2012-001445
PMID:23518859
Ebenaceae extractives. Part 10. Macassaric acid, an o-methoxycarbonylcinnamic acid from macassar ebony Bhim C. Maiti, Oliver C. Musgrave Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19900000307
Ebenaceae extractives. Part 9. New naphthoquinones and binaphthylquinones from macassar ebony Bhim C. Maiti, Oliver C. Musgrave Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19860000675
Pharmacology and chemotaxonomy of Diospyros. Mallavadhani UV, Panda AK, Rao YR Phytochemistry 01-Oct-1998
doi:10.1016/S0031-9422(97)01020-0
PMID:9788142

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
1,2,8-Trimethoxy-6-methylnaphthalene 13661033 Click to see CC1=CC2=C(C(=C1)OC)C(=C(C=C2)OC)OC 232.27 unknown https://doi.org/10.1039/P19860000675
> 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/10.1039/P19860000675
https://doi.org/10.1016/S0031-9422(97)01020-0
1,8-Dimethoxy-6-methylnaphthalen-2-ol 90470793 Click to see CC1=CC2=C(C(=C1)OC)C(=C(C=C2)O)OC 218.25 unknown https://doi.org/10.1039/P19860000675
> Benzenoids / Naphthalenes / Naphthoquinones
2-(1,5-Dihydroxy-4-methoxy-7-methylnaphthalen-2-yl)-5-hydroxy-7-methylnaphthalene-1,4-dione 162875597 Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=CC(=C4C(=CC(=CC4=C3O)C)O)OC 390.40 unknown https://doi.org/10.1039/P19860000675
https://doi.org/10.1016/S0031-9422(97)01020-0
2-(4,6-Dihydroxy-5-methoxy-2-methylnaphthalen-1-yl)-5-hydroxy-7-methylnaphthalene-1,4-dione 162955086 Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=C4C=CC(=C(C4=C(C=C3C)O)OC)O 390.40 unknown https://doi.org/10.1039/P19860000675
https://doi.org/10.1016/S0031-9422(97)01020-0
2-Methyl-5-methoxy-6-hydroxy-1,4-naphthoquinone 13468236 Click to see CC1=CC(=O)C2=C(C1=O)C=CC(=C2OC)O 218.20 unknown https://doi.org/10.1039/P19860000675
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1039/P19860000675
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(Z)-3-(3-methoxy-2-methoxycarbonyl-5-methylphenyl)prop-2-enoic acid 14539515 Click to see CC1=CC(=C(C(=C1)OC)C(=O)OC)C=CC(=O)O 250.25 unknown https://doi.org/10.1039/P19900000307

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