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Hunteria congolana

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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 UUID643fdf47c8881099497886
Scientific name Hunteria congolana
Authority Pichon
First published in Bol. Soc. Brot. , sér. 2, 27: 101 (1953)

Description Top

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Synonyms Top

No known synonyms.

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
    • East Tropical Africa
      • Kenya
    • West-central Tropical Africa
      • Congo
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000215655
Tropicos 100204440
KEW urn:lsid:ipni.org:names:79342-1
The Plant List kew-100795
Open Tree Of Life 6067834
NCBI Taxonomy 2708856
IPNI 79342-1
GBIF 5536561
Freebase /m/0wfw8ds
Wikipedia Hunteria_congolana

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
Enantiomeric Natural Products: Occurrence and Biogenesis Finefield JM, Sherman DH, Kreitman M, Williams RM Angew Chem Int Ed Engl 03-May-2012
PMCID:PMC3498912
doi:10.1002/anie.201107204
PMID:22555867
Alkaloids of Hunteria zeylanica C. Lavaud, G. Massiot, J. Vercauteren, L. Le Men-olivier Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)95285-3

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 / Aspidospermatan-type alkaloids
(+)-Vincadifformine 811594 Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
Methyl 2,3-didehydroaspidospermidine-3-carboxylate 579873 Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
> Alkaloids and derivatives / Eburnan-type alkaloids
(15R,17S,19S)-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-ol 10469866 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine, 13a-ethyl-2,3,5,6,13a,13b-hexahydro- 610470 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C=C2 278.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
Eburnamenin-14-ol, 14,15-dihydro-, (14alpha)- 442066 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
Eburnamenin-14-ol, 14,15-dihydro-, (14beta)- 619344 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
Eburnamenin-14(15H)-one 92112 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(=O)C2 294.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
Eburnamenine 6857502 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C=C2 278.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
Eburnamonine 3195 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(=O)C2 294.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
> Alkaloids and derivatives / Pleiocarpaman alkaloids
methyl (1R,4S,7S,14R,20R,21S,24E,25S,26S,38S,39S)-24-ethylidene-39-methyl-3,11,22,27-tetrazadodecacyclo[20.11.2.13,15.14,7.17,11.121,25.01,20.04,14.020,27.028,33.014,38.019,37]nonatriaconta-15(37),16,18,28,30,32-hexaene-26-carboxylate 163189030 Click to see CC=C1CN2CCC34CN5C6=C(C=CC=C6C37C2CC1C(N7C8=CC=CC=C48)C(=O)OC)C91C52CCC3(C2C)C9N(CCC3)CC1 614.80 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
methyl (8R,13E,14S,16S,17S,18S)-13-ethylidene-1,11-diazapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6-triene-18-carboxylate 11088635 Click to see CC=C1CN2CCC3C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC 324.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
Pleiocarpamine 5385014 Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC 322.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
> Alkaloids and derivatives / Strychnos alkaloids
(12-Ethylidene-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraen-10-yl) acetate 162992577 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)OC(=O)C 322.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
[(1R,11S,12E,17S)-12-ethylidene-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraen-10-yl] acetate 163186406 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)OC(=O)C 322.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
benzylcarbonyl-DL-Abu-DL-xiThr(1)-DL-Phe-DL-Pro-DL-Val-DL-Val-DL-Val-(1) 78136536 Click to see CCC(C(=O)NC1C(OC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C2CCCN2C(=O)C(NC1=O)CC3=CC=CC=C3)C(C)C)C(C)C)C(C)C)C)NC(=O)CC4=CC=CC=C4 846.00 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1S,2S,3R,6E,7S,9R,10S)-6-ethylidene-3-hydroxy-11-methyl-4,21-dioxa-11,20-diazahexacyclo[8.7.3.22,9.01,10.02,7.012,17]docosa-12,14,16-trien-22-one 163185764 Click to see CC=C1COC(C23C1CC(C45C2(CCN4)C6=CC=CC=C6N5C)OC3=O)O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
6-Ethylidene-3-hydroxy-11-methyl-4,21-dioxa-11,20-diazahexacyclo[8.7.3.22,9.01,10.02,7.012,17]docosa-12,14,16-trien-22-one 163016120 Click to see CC=C1COC(C23C1CC(C45C2(CCN4)C6=CC=CC=C6N5C)OC3=O)O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
methyl (E)-2-[(1S,9S,10R,13S,17S)-13-formyl-8-methyl-12-oxo-11-oxa-8,16-diazapentacyclo[7.4.3.210,13.01,9.02,7]octadeca-2,4,6-trien-17-yl]but-2-enoate 163190352 Click to see CC=C(C1CC2C34C(C1(C(=O)O2)C=O)(CCN3)C5=CC=CC=C5N4C)C(=O)OC 396.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
methyl (E)-2-[(1S,9S,10R,13S,17S)-13-formyl-8,16-dimethyl-12-oxo-11-oxa-8,16-diazapentacyclo[7.4.3.210,13.01,9.02,7]octadeca-2,4,6-trien-17-yl]but-2-enoate 163189048 Click to see CC=C(C1CC2C34C(C1(C(=O)O2)C=O)(CCN3C)C5=CC=CC=C5N4C)C(=O)OC 410.50 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
Methyl 2-(13-formyl-8-methyl-12-oxo-11-oxa-8,16-diazapentacyclo[7.4.3.210,13.01,9.02,7]octadeca-2,4,6-trien-17-yl)but-2-enoate 436035 Click to see CC=C(C1CC2C34C(C1(C(=O)O2)C=O)(CCN3)C5=CC=CC=C5N4C)C(=O)OC 396.40 unknown https://doi.org/10.1016/S0031-9422(00)95285-3
Methyl 2-(13-formyl-8,16-dimethyl-12-oxo-11-oxa-8,16-diazapentacyclo[7.4.3.210,13.01,9.02,7]octadeca-2,4,6-trien-17-yl)but-2-enoate 162911703 Click to see CC=C(C1CC2C34C(C1(C(=O)O2)C=O)(CCN3C)C5=CC=CC=C5N4C)C(=O)OC 410.50 unknown https://doi.org/10.1016/S0031-9422(00)95285-3

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