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Ancistrocladus barteri

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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 UUID64403c910d187648741037
Scientific name Ancistrocladus barteri
Authority Scott Elliot
First published in J. Linn. Soc., Bot. 30: 73 (1894)

Description Top

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Synonyms Top

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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
    • West Tropical Africa
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Senegal
      • Sierra Leone

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000970228
KEW urn:lsid:ipni.org:names:320527-1
The Plant List kew-8754
Open Tree Of Life 389770
NCBI Taxonomy 714094
IPNI 320527-1
iNaturalist 183308
GBIF 3658996
EOL 6874696

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
Ancistrobrevine C: A “Mixed” Ancistrocladaceae/Dioncophyllaceae-Type Naphthylisoquinoline Alkaloid from<i>Ancistrocladus abbreviatus</i> G. Bringmann, F. Pokorny, M. Stäblein, L. Assi Georg Thieme Verlag KG 16-Jan-2007
doi:10.1055/S-2006-960378
Activity of extracts and naphthylisoquinoline alkaloids from Triphyophyllum peltatum, Ancistrocladus abbreviatus and A. Barteri against Plasmodium falciparum in vitro☆ Guido François, Gerhard Bringmann, J.David Phillipson, Laurent Aké Assi, Carine Dochez, Martin Rübenacker, Christoph Schneider, Marc Wéry, David C. Warhurst, Geoffrey C. Kirby Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86875-2
Molluscicidal activity of naphthylisoquinoline alkaloids from Triphyophyllum and Ancistrocladus species. Bringmann G, Holenz J, Assi LA, Zhao C, Hostettmann K Planta Med 01-Dec-1996
doi:10.1055/S-2006-957970
PMID:17252498
Activities of extracts and naphthylisoquinoline alkaloids from Triphyophyllum peltatum, Ancistrocladus abbreviatus and Ancistrocladus barteri against Plasmodium berghei (Anka strain) in vitro. François G, Bringmann G, Dochez C, Schneider C, Timperman G, Aké Assi L J Ethnopharmacol 01-May-1995
doi:10.1016/0378-8741(95)01240-E
PMID:7650949

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 / Tetralins
Isoshinanolone 443777 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1055/S-2006-960378
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
[(1R,2S,3S,4S,5S,8R,9S,10R,11R,14R,16S,17R,18R,19R)-2,19-diacetyloxy-3-hydroxy-5-methyl-12-methylidene-4-(2-methylpropanoyloxy)-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-10-yl] benzoate 163104266 Click to see CC(C)C(=O)OC1C(C(C23C4C1(CN5C4CC67C2C(C(C(C6C35)OC(=O)C8=CC=CC=C8)C(=C)C7)OC(=O)C)C)OC(=O)C)O 619.70 unknown https://doi.org/10.1016/0378-8741(95)01240-E
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1S,2S,6R,7S,8R,12R,14S,15S,19S,20R)-7,10-dihydroxy-17-methoxy-7,15,19,20-tetramethyl-3,5,11-trioxapentacyclo[10.7.1.02,6.08,20.014,19]icos-16-en-18-one 101921953 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C5C(C(C4CC(O3)O)(C)O)OCO5)C)C)OC 408.50 unknown https://doi.org/10.1016/S0031-9422(00)86875-2
https://doi.org/10.1016/0378-8741(95)01240-E
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(1R,3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-8-ol 14844756 Click to see CC1CC2=C(C(N1C)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 391.50 unknown https://doi.org/10.1016/0378-8741(95)01240-E
(1R,3S)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-6-methoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-8-ol 101664024 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)OC 421.50 unknown https://doi.org/10.1016/0378-8741(95)01240-E
(3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 375943 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 377.50 unknown https://doi.org/10.1016/0378-8741(95)01240-E
(3R)-7-[5-hydroxy-2-(hydroxymethyl)-4-methoxynaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 375947 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)O)O 379.40 unknown https://doi.org/10.1016/0378-8741(95)01240-E
Ancistrocladine 161741 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 407.50 unknown https://doi.org/10.1016/0378-8741(95)01240-E
Dioncopeltine A 185971 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)O)O 379.40 unknown https://doi.org/10.1016/0378-8741(95)01240-E
Dioncophyllin A 3095 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 377.50 unknown https://doi.org/10.1055/S-2006-957970
Dioncophylline A 443773 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 377.50 unknown https://doi.org/10.1016/0378-8741(95)01240-E
Dioncophylline B 178558 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C(C4=C(C=C3)C=C(C=C4OC)C)O)O 363.40 unknown https://doi.org/10.1016/0378-8741(95)01240-E

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