Alstonia congensis - Unknown
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Internal ID UUID644039b43e70b616653774
Scientific name Alstonia congensis
Authority Engl.
First published in Bot. Jahrb. Syst. 8: 64 (1886)

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Synonyms Top

Scientific name Authority First published in
Alstonia congensis var. glabrata Hutch. & Dalziel Fl. W. Trop. Afr. 2: 42. 1931
Alstonia gilletii De Wild. Miss. Ém. Laurent 1: 537 (1907)
Alstonia pedicellata Pierre ex A.Chev. Vég. Ut. Afr. Trop. Franç. 9: 273 (1917)

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Language Common/alternative name
Chinese 图案木

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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
    • West Tropical Africa
      • Benin
      • Burkina
      • Guinea-Bissau
      • Liberia
      • Nigeria
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000952011
Tropicos 1805167
KEW urn:lsid:ipni.org:names:76517-1
The Plant List kew-7014
Open Tree Of Life 6067602
IUCN Red List 60760828
IPNI 76517-1
GBIF 5535748
USDA GRIN 463437
Wikipedia Alstonia_congensis

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
391. Echitamine in Alstonia barks John A. Goodson Royal Society of Chemistry (RSC) 21-Apr-2004
doi:10.1039/JR9320002626
Alkaloids from Alstonia congensis Catherine Caron, Alain Graftieaux, Georges Massiot, Louisette Le Men-Olivier, Clement Delaude Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80218-3

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
> Alkaloids and derivatives / Macroline alkaloids
19-(Z)-Akuammidine 138113962 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC 352.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
> Alkaloids and derivatives / Strychnos alkaloids
Akuammicine 10314057 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC 322.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
Curan-17-oic acid, 2,16-didehydro-19-hydroxy-, methyl ester, (20xi)- 541842 Click to see CC(C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)O 340.40 unknown https://doi.org/10.1039/JR9320002626
Dihydrocondylocarpine 100004 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
Echitamidin 190982 Click to see CC(C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)O 340.40 unknown https://doi.org/10.1039/JR9320002626
Echitamidine 10991442 Click to see CC(C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)O 340.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
methyl (1S,11S,17R,18S)-18-ethyl-6-methoxy-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2(7),3,5,9-tetraene-10-carboxylate 14286084 Click to see CCC1C2CCN3C1C4(CC3)C5=C(C(=CC=C5)OC)NC4=C2C(=O)OC 354.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
Methyl 12-(1-hydroxypropan-2-yl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate 5317005 Click to see CC(CO)C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC 354.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
https://doi.org/10.1039/JR9320002626
Methyl 18-ethyl-6-methoxy-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2(7),3,5,9-tetraene-10-carboxylate 14286083 Click to see CCC1C2CCN3C1C4(CC3)C5=C(C(=CC=C5)OC)NC4=C2C(=O)OC 354.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
Tubotaiwin 78358510 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
> Alkaloids and derivatives / Vallesaman alkaloids
angustilobine B, (rac)- 13891905 Click to see COC(=O)C12COCC=C3C1CCN(C3)CC4=C2NC5=CC=CC=C45 338.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
Methyl 15-ethenyl-14-oxa-1,10-diazapentacyclo[13.3.1.03,11.04,9.012,16]nonadeca-3(11),4,6,8-tetraene-12-carboxylate 13891901 Click to see COC(=O)C12COC3(C1CCN(C3)CC4=C2NC5=CC=CC=C45)C=C 338.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
Desoxycortone 6166 Click to see CC12CCC3C(C1CCC2C(=O)CO)CCC4=CC(=O)CCC34C 330.50 unknown https://doi.org/10.1016/0031-9422(89)80218-3
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
CID 11953926 11953926 Click to see CC=C1C[N+]2(CCC34C2(C(CC1C3(CO)C(=O)OC)O)NC5=CC=CC=C45)C 385.50 unknown https://doi.org/10.1016/0031-9422(89)80218-3
https://doi.org/10.1039/JR9320002626
methyl (1S,9R,10S,12S,13E,15S,18S)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-15-methyl-8-aza-15-azoniapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate 124841318 Click to see CC=C1C[N+]2(CCC34C2(C(CC1C3(CO)C(=O)OC)O)NC5=CC=CC=C45)C 385.50 unknown https://doi.org/10.1039/JR9320002626
methyl (1S,9R,12R,18R)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-15-methyl-8-aza-15-azoniapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate 137795385 Click to see CC=C1C[N+]2(CCC34C2(C(CC1C3(CO)C(=O)OC)O)NC5=CC=CC=C45)C 385.50 unknown https://doi.org/10.1016/0031-9422(89)80218-3
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
methyl (3S,3aR,7aS)-7a-ethenyl-3-(1H-indol-2-yl)-6-methyl-3a,4,5,7-tetrahydro-2H-furo[2,3-c]pyridine-3-carboxylate 14286086 Click to see CN1CCC2C(C1)(OCC2(C3=CC4=CC=CC=C4N3)C(=O)OC)C=C 340.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3
methyl 7a-ethenyl-3-(1H-indol-2-yl)-6-methyl-3a,4,5,7-tetrahydro-2H-furo[2,3-c]pyridine-3-carboxylate 14286085 Click to see CN1CCC2C(C1)(OCC2(C3=CC4=CC=CC=C4N3)C(=O)OC)C=C 340.40 unknown https://doi.org/10.1016/0031-9422(89)80218-3

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