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Anthocleista djalonensis

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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 UUID644009acda1f1731441116
Scientific name Anthocleista djalonensis
Authority A.Chev.
First published in Mém. Soc. Bot. France 8: 47 (1908)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anthocleista kerstingii Gilg ex Volkens Notizbl. Bot. Gart. Berlin-Dahlem 22: 33 (1909)

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
    • Northeast Tropical Africa
      • Chad
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000538471
Tropicos 19000663
KEW urn:lsid:ipni.org:names:545605-1
The Plant List kew-2641618
Open Tree Of Life 6069510
IUCN Red List 156093304
IPNI 545605-1
iNaturalist 507281
GBIF 4019367
EOL 5345620
Wikipedia Anthocleista_djalonensis

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)!
Title Authors Publication Released IDs
Isolation, Structure Elucidation, and Synthesis of Irlbacholine, 1,22-Bis[[[2-(trimethylammonium)ethoxy]phosphinyl]oxy]docosane: A Novel Antifungal Plant Metabolite from Irlbachia alata and Anthocleista djalonensis Donald E. Bierer, R. Eric Gerber, Shivanand D. Jolad, Rosa P. Ubillas, Joaquin Randle, Ewa Nauka, John Latour, Jeffrey M. Dener, Diana M. Fort American Chemical Society (ACS) 18-Mar-2005
doi:10.1021/JO00126A066
Monoterpene diol, iridoid glucoside and dibenzo-α-pyrone from Anthocleista djalonensis Patricia A. Onocha, Dominic A. Okorie, Joseph D. Connolly, David S. Roycroft Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00121-M
A new phthalide and xanthones from Anthocleista djalonensis and Anthocleista vogelli Dominic A. Okorie Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97499-5

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
methyl 5,7-dimethoxy-6-methyl-1-oxo-3H-2-benzofuran-4-carboxylate 101316749 Click to see CC1=C(C2=C(COC2=O)C(=C1OC)C(=O)OC)OC 266.25 unknown https://doi.org/10.1016/S0031-9422(00)97499-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6aS,6bR,12aS)-2,2,6a,6b,9,9,12a-heptamethyl-10,13-dioxo-1,3,4,5,6,6a,7,8,8a,11,12,14b-dodecahydropicene-4a-carboxylic acid 163187259 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 468.70 unknown https://doi.org/10.1016/0031-9422(95)00121-M
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(95)00121-M
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(95)00121-M
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(95)00121-M
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/10.1016/0031-9422(95)00121-M
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(95)00121-M
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(95)00121-M
Stigmast-4-en-3-one, (24S)- 579897 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(95)00121-M
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(95)00121-M
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines / Phosphocholines
Irlbacholine 177983 Click to see C[N+](C)(C)CCOP(=O)([O-])OCCCCCCCCCCCCCCCCCCCCCCOP(=O)([O-])OCC[N+](C)(C)C 672.90 unknown https://doi.org/10.1021/JO00126A066
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
1D-1-O-Methyl-myo-inositol 440078 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1016/0031-9422(95)00121-M
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/10.1016/0031-9422(95)00121-M
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 354447 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/0031-9422(95)00121-M
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 581257 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/0031-9422(95)00121-M
Sweroside 161036 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/0031-9422(95)00121-M
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Lichexanthone 5358904 Click to see CC1=CC(=CC2=C1C(=O)C3=C(C=C(C=C3O2)OC)O)OC 286.28 unknown https://doi.org/10.1016/S0031-9422(00)97499-5
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(3R,4S)-4-[(2R)-1-hydroxybut-3-en-2-yl]-3-(hydroxymethyl)oxan-2-one 101414288 Click to see C=CC(CO)C1CCOC(=O)C1CO 200.23 unknown https://doi.org/10.1016/0031-9422(95)00121-M
4-(1-Hydroxybut-3-en-2-yl)-3-(hydroxymethyl)oxan-2-one 15241181 Click to see C=CC(CO)C1CCOC(=O)C1CO 200.23 unknown https://doi.org/10.1016/0031-9422(95)00121-M
> Phenylpropanoids and polyketides / Coumarins and derivatives
Alternariol monomethyl ether 5360741 Click to see CC1=CC(=CC2=C1C3=C(C(=CC(=C3)OC)O)C(=O)O2)O 272.25 unknown https://doi.org/10.1016/0031-9422(95)00121-M

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