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Diospyros batocana

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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 UUID6440173d6ce9d575044847
Scientific name Diospyros batocana
Authority Hiern
First published in Trans. Cambridge Philos. Soc. 12: 174 (1873)

Description Top

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Synonyms Top

Scientific name Authority First published in
Diospyros odorata Hiern ex De Wild. Pl. Bequaert. iii. 550 (1926), nomen; Hiern ex Greves in Journ. Bot. 1929,lxvii. Suppl. 2, 78, descr.
Diospyros xanthocarpa Gürke Kunene-Sambesi Exped. : 328 (1903)
Diospyros odorata var. rhodesiana Rendle J. Bot. 70: 93. 1932

Common names Top

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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
  • Africa
    • South Tropical Africa
      • Angola
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
    • West-central Tropical Africa
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000648555
Tropicos 11500250
KEW urn:lsid:ipni.org:names:322123-1
The Plant List kew-2769419
Open Tree Of Life 447972
NCBI Taxonomy 570478
IPNI 322123-1
iNaturalist 583881
GBIF 4070760

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
The use of medicinal plants in common ophthalmic disorders: A systematic review with meta-analysis Alghamdi AH, Ahmed AA, Bashir M, Abdalgadir H, Khalid A, Gul S Heliyon 11-Apr-2023
PMCID:PMC10161615
doi:10.1016/j.heliyon.2023.e15340
PMID:37151714
Use of Multi-Date and Multi-Spectral UAS Imagery to Classify Dominant Tree Species in the Wet Miombo Woodlands of Zambia Shamaoma H, Chirwa PW, Zekeng JC, Ramoelo A, Hudak AT, Handavu F, Syampungani S Sensors (Basel) 16-Feb-2023
PMCID:PMC9960281
doi:10.3390/s23042241
PMID:36850838
Data for developing allometric models and evaluating carbon stocks of the Zambezi Teak Forests in Zambia Ngoma J, Moors E, Kruijt B, Speer JH, Vinya R, Chidumayo EN, Leemans R Data Brief 28-Feb-2018
PMCID:PMC5854870
doi:10.1016/j.dib.2018.02.057
PMID:29556519
Identification of methylnaphthazarin in Diospyros species Margarida A. Ferreira, M.Áurea Cruz Costa, A. Correia Alves Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)88412-5
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
Naphthaquinones of Diospyros batocana. Alves AC, Costa MA, Paul MI Planta Med 01-Feb-1983
doi:10.1055/S-2007-969969
PMID:17405105

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 / Naphthoquinones
(1aR,7aS)-3-hydroxy-4-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-5-methyl-1a,7a-dihydronaphtho[2,3-b]oxirene-2,7-dione 163045795 Click to see CC1=CC2=C(C(=O)C3C(C2=O)O3)C(=C1C4=C5C(=O)C=CC(=O)C5=C(C=C4C)O)O 390.30 unknown https://doi.org/10.1016/S0031-9422(00)88412-5
(1aS,7aR)-3-hydroxy-4-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-5-methyl-1a,7a-dihydronaphtho[2,3-b]oxirene-2,7-dione 163045796 Click to see CC1=CC2=C(C(=O)C3C(C2=O)O3)C(=C1C4=C5C(=O)C=CC(=O)C5=C(C=C4C)O)O 390.30 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
[2,2'-Binaphthalene]-1,1',4,4'-tetrone, 5,5'-dihydroxy-7,7'-dimethyl- 633060 Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=CC(=O)C4=C(C3=O)C=C(C=C4O)C 374.30 unknown https://doi.org/10.1055/S-2007-969969
3-Hydroxy-4-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-5-methyl-1a,7a-dihydronaphtho[2,3-b]oxirene-2,7-dione 14101672 Click to see CC1=CC2=C(C(=O)C3C(C2=O)O3)C(=C1C4=C5C(=O)C=CC(=O)C5=C(C=C4C)O)O 390.30 unknown https://doi.org/10.1016/S0031-9422(00)88412-5
https://doi.org/10.1055/S-2007-969969
7-Methyljuglone 26905 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1)O 188.18 unknown https://doi.org/10.1055/S-2007-969969
8-Hydroxy-2-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-6-methylnaphthalene-1,4-dione 12173109 Click to see CC1=CC2=C(C(=C1)O)C(=O)C(=CC2=O)C3=CC(=O)C4=C(C3=O)C=C(C=C4O)C 374.30 unknown https://doi.org/10.1055/S-2007-969969
8-Hydroxy-2-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-6-methylnaphthalene-1,4-dione 167673 Click to see CC1=CC2=C(C(=C1)O)C(=O)C(=CC2=O)C3=CC(=O)C4=C(C3=O)C(=CC(=C4)C)O 374.30 unknown https://doi.org/10.1055/S-2007-969969
Diospyrin 308140 Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=C(C4=C(C=C3C)C(=O)C=CC4=O)O 374.30 unknown https://doi.org/10.1055/S-2007-969969
Diosquinone 122720 Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=C(C4=C(C=C3C)C(=O)C5C(C4=O)O5)O 390.30 unknown https://doi.org/10.1055/S-2007-969969
Isodiospyrin 99298 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1C3=C4C(=O)C=CC(=O)C4=C(C=C3C)O)O 374.30 unknown https://doi.org/10.1055/S-2007-969969
Methylnaphthazarin 271296 Click to see CC1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 204.18 unknown https://doi.org/10.1055/S-2007-969969

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