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Diospyros mannii

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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 UUID64401764209fd313311680
Scientific name Diospyros mannii
Authority Hiern
First published in Trans. Cambridge Philos. Soc. 12: 255 (1873)

Description Top

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Synonyms Top

Scientific name Authority First published in
Diospyros aggregata Gürke Bot. Jahrb. Syst. 43: 204 (1909)
Diospyros ivorensis Aubrév. & Pellegr. Bull. Soc. Bot. France 83: 621 (1936 publ. 1937)
Diospyros pseudaggregata Mildbr. & Mildbr. Notizbl. Bot. Gart. Berlin-Dahlem 9: 1047 (1926)
Diospyros talbotii Wernham Cat. Pl. Oban : 57 (1913)
Ebenus mannii (Hiern) Kuntze Revis. Gen. Pl. 2: 408. 1891 [5 Nov 1891]

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • West Tropical Africa
      • Ghana
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000649299
Tropicos 11500365
KEW urn:lsid:ipni.org:names:322669-1
The Plant List kew-2770112
Open Tree Of Life 1049032
NCBI Taxonomy 413757
IUCN Red List 173651
IPNI 322669-1
iNaturalist 467372
GBIF 4069801

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
Food-Associated Calling in Gorillas (Gorilla g. gorilla) in the Wild Luef EM, Breuer T, Pika S PLoS One 24-Feb-2016
PMCID:PMC4766192
doi:10.1371/journal.pone.0144197
PMID:26909518
Comparative Phylogeography in Rainforest Trees from Lower Guinea, Africa Heuertz M, Duminil J, Dauby G, Savolainen V, Hardy OJ PLoS One 08-Jan-2014
PMCID:PMC3885573
doi:10.1371/journal.pone.0084307
PMID:24416215
3′-methoxydiospyrin, a 7-methyljuglone dimer from diospyros mannii J.A.D. Jeffreys, Muhamad Bin Zakaria, Peter G. Waterman Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80286-1

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
5-Hydroxy-6-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-2-methoxy-7-methylnaphthalene-1,4-dione 162939160 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)OC)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80286-1
7-Methyljuglone 26905 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1)O 188.18 unknown https://doi.org/10.1016/S0031-9422(00)80286-1
8-Hydroxy-7-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-2-methoxy-6-methylnaphthalene-1,4-dione 163072521 Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=C(C4=C(C=C3C)C(=O)C=C(C4=O)OC)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)80286-1
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/10.1016/S0031-9422(00)80286-1
Isoplumbagin 375105 Click to see CC1=CC(=O)C2=C(C1=O)C(=CC=C2)O 188.18 unknown https://doi.org/10.1016/S0031-9422(00)80286-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9R,11aR,11bS,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-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 162996343 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)80286-1
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-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]chrysene-3a-carboxylic acid 12358880 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/10.1016/S0031-9422(00)80286-1
(1R,3aS,5aR,5bR,7aR,9S,11aS,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 162952647 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)80286-1
9-Hydroxy-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]chrysene-3a-carboxylic acid 2371 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/10.1016/S0031-9422(00)80286-1
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)80286-1
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/10.1016/S0031-9422(00)80286-1
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)80286-1
Lup-20(29)-ene-3beta,28-diol 221023 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)80286-1
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)80286-1

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