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Internal ID UUID64403c8fa1343416394640
Scientific name Ancistrocladus abbreviatus
Authority Airy Shaw
First published in Kew Bull. 4: 67 (1949)

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Name Authority First published in
Ancistrocladus abbreviatus subsp. lateralis Gereau Ann. Missouri Bot. Gard. 92: 373 (2005)

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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
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Cameroon

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000970207
Tropicos 1400005
KEW urn:lsid:ipni.org:names:71934-1
The Plant List kew-8752
Open Tree Of Life 992165
NCBI Taxonomy 122295
IPNI 71934-1
iNaturalist 183307
GBIF 7321386
EOL 6874693

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
Naphthylisoquinoline alkaloids: novel agents against the causative pathogens of eumycetoma and actinomycetoma—en route to broad-spectrum antimycetomal drugs Khalid SA, Abd Algaffar S, Tajuddeen N, Lombe BK, Bringmann G Antimicrob Agents Chemother 11-Apr-2024
PMCID:PMC11064494
doi:10.1128/aac.01612-23
PMID:38602413
Correction: Naphthylisoindolinone alkaloids: the first ring-contracted naphthylisoquinolines, from the tropical liana Ancistrocladus abbreviatus, with cytotoxic activity Fayez S, Bruhn T, Feineis D, Assi LA, Kushwaha PP, Kumar S, Bringmann G RSC Adv 24-Oct-2022
PMCID:PMC9589400
doi:10.1039/d2ra90105f
PMID:36337954
Naphthylisoindolinone alkaloids: the first ring-contracted naphthylisoquinolines, from the tropical liana Ancistrocladus abbreviatus, with cytotoxic activity Fayez S, Bruhn T, Feineis D, Assi LA, Kushwaha PP, Kumar S, Bringmann G RSC Adv 12-Oct-2022
PMCID:PMC9555057
doi:10.1039/d2ra05758a
PMID:36320727
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
Multiple Myeloma Inhibitory Activity of Plant Natural Products Jöhrer K, Ҫiҫek SS Cancers (Basel) 29-May-2021
PMCID:PMC8198565
doi:10.3390/cancers13112678
PMID:34072312
Ancistrobreveines A–D and related dehydrogenated naphthylisoquinoline alkaloids with antiproliferative activities against leukemia cells, from the West African liana Ancistrocladus abbreviatus Fayez S, Feineis D, Assi LA, Seo EJ, Efferth T, Bringmann G RSC Adv 20-May-2019
PMCID:PMC9064271
doi:10.1039/c9ra03105g
PMID:35521375
The Challenge of Reproducibility and Accuracy in Nutrition Research: Resources and Pitfalls Sorkin BC, Kuszak AJ, Williamson JS, Hopp DC, Betz JM Adv Nutr 09-Mar-2016
PMCID:PMC4785474
doi:10.3945/an.115.010595
PMID:26980822
Ethnomedicinal Plants Used by Traditional Healers to Treat Oral Health Problems in Cameroon Ashu Agbor M, Naidoo S Evid Based Complement Alternat Med 01-Oct-2015
PMCID:PMC4606091
doi:10.1155/2015/649832
PMID:26495020
Why vouchers matter in botanical research Culley TM Appl Plant Sci 29-Oct-2013
PMCID:PMC4103463
doi:10.3732/apps.1300076
PMID:25202501
High Throughput Extraction of Plant, Marine and Fungal Specimens for Preservation of Biologically Active Molecules McCloud TG Molecules 24-Jun-2010
PMCID:PMC6257593
doi:10.3390/molecules15074526
PMID:20657375
Dioncoline A and its Atropisomer: “Inverse Hybrid Type” Ancistrocladaceae/Dioncophyllaceae Alkaloids from<i>Ancistrocladus abbreviatus</i> G. Bringmann, R. Zagst, D. Lisch, L. Assi Georg Thieme Verlag KG 07-Nov-2008
doi:10.1055/S-2006-961727
Antitumoral and antileishmanial dioncoquinones and ancistroquinones from cell cultures of Triphyophyllum peltatum (Dioncophyllaceae) and Ancistrocladus abbreviatus (Ancistrocladaceae). Bringmann G, Rüdenauer S, Irmer A, Bruhn T, Brun R, Heimberger T, Stühmer T, Bargou R, Chatterjee M Phytochemistry 01-Oct-2008
doi:10.1016/J.PHYTOCHEM.2008.06.019
PMID:18723197
ancistrobrevine B, the first naphthylisoquinoline alkaloid with A 5,8′-coupling site, and related compounds from Ancistrocladus abbreviatus Gerhard Bringmann, Rainer Zagst, Helmut Reuscher, Laurent Aké Assi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97574-5
Ancistrobrevine C from Ancistrocladus abbreviatus: The first mixed ‘ancistrocladaceae/dioncophyllaceae-type’ naphthylisoquinoline alkaloid Gerhard Bringmann, Frank Pokorny, Michaela Stäblein, Manuela Schäffer, Laurent Aké Assi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85123-9
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

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
Droserone 442739 Click to see CC1=C(C2=C(C(=CC=C2)O)C(=O)C1=O)O 204.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
Malvone A 135542082 Click to see CC1=C(C(=O)C2=C(C1=O)C=CC(=C2O)O)OC 234.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
Plumbagin 10205 Click to see CC1=CC(=O)C2=C(C1=O)C=CC=C2O 188.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
[(1S,4S,5R)-4-acetyloxy-6-methylidene-5-prop-1-en-2-ylcyclohex-2-en-1-yl] 2-methylbut-2-enoate 162869391 Click to see CC=C(C)C(=O)OC1C=CC(C(C1=C)C(=C)C)OC(=O)C 290.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Xylarenolide 139586528 Click to see CC1(CCC2(C(=CC3C4C2(CCCC4(C(=O)O3)C)C)C1)O)CC(=O)O 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,8aS,9aS)-5,8a-dimethyl-3-methylidene-3a,4,9,9a-tetrahydrobenzo[f][1]benzofuran-2,6-dione 162925596 Click to see CC1=C2CC3C(CC2(C=CC1=O)C)OC(=O)C3=C 244.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 76141271 Click to see CC1(CCC2(CCC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O)C 454.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid amides / Tertiary carboxylic acid amides
1-[7-Hydroxy-5-(1-hydroxyethyl)-2,3,7,7a-tetrahydrocyclopenta[b]pyridin-1-yl]ethanone 163081842 Click to see CC(C1=CC(C2C1=CCCN2C(=O)C)O)O 223.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1R,2S,4aR,6R,8aS)-1-[2-[(1R,2S,4aR,6S,8aS)-2,6-dihydroxy-5,5,8a-trimethyl-1,2,3,4,4a,6,7,8-octahydronaphthalen-1-yl]ethyl]-5,5,8a-trimethyl-1,2,3,4,4a,6,7,8-octahydronaphthalene-2,6-diol 12137296 Click to see CC1(C2CCC(C(C2(CCC1O)C)CCC3C(CCC4C3(CCC(C4(C)C)O)C)O)O)C 450.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(1R,3R)-5-[3-[4-[(1S,3S)-6,8-dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl]-1-hydroxy-8-methoxy-6-methylnaphthalen-2-yl]-4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol 44592719 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O 756.90 unknown https://doi.org/10.1006/ABBI.1997.0494
(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/S0031-9422(00)86875-2
https://doi.org/10.1016/S0031-9422(00)95222-1
(1R,3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-6-methoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-8-ol 162914748 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/10.1055/S-2006-961727
(1R,3S)-5-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol 12306781 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/S0031-9422(00)97574-5
(1R,3S)-5-(4,5-dimethoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol 162977286 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C 407.50 unknown https://doi.org/10.1016/S0031-9422(00)97574-5
(1R,3S)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 162889281 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/S0031-9422(00)97574-5
(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/S0031-9422(00)86875-2
(1S,3S)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-8-ol 163019169 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/S0031-9422(00)95222-1
(1S)-1,2,3,4-Tetrahydro-8-methoxy-1alpha,3beta-dimethyl-5-[(aR)-4,5-dimethoxy-2-methyl-1-naphthalenyl]isoquinoline-6-ol 4332940 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/S0031-9422(00)97574-5
(3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-6-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-8-ol 136900226 Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)OC 405.50 unknown https://doi.org/10.1016/0031-9422(93)85123-9
5-(4,5-Dimethoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol 85367289 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C 407.50 unknown https://doi.org/10.1016/S0031-9422(00)97574-5
5-(5-Hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 3956689 Click to see CC1CC2=C(C=CC(=C2C(N1)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)O 363.40 unknown https://doi.org/10.1055/S-2006-957970
5-[3-[4-(6,8-Dihydroxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-5-yl)-1-hydroxy-8-methoxy-6-methylnaphthalen-2-yl]-4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol 4185 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O 756.90 unknown https://doi.org/10.1006/ABBI.1997.0494
7-(4,5-Dimethoxy-2-methylnaphthalen-1-yl)-6-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-8-ol 162903981 Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)OC 405.50 unknown https://doi.org/10.1016/0031-9422(93)85123-9
8-Methoxy-5-(8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)-6-methylnaphthalen-1-ol 21362782 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)O)OC 377.50 unknown https://doi.org/10.1055/S-2006-957970
8-methoxy-5-[(1R,3R)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl]-6-methylnaphthalen-1-ol 59095071 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)O)OC 377.50 unknown https://doi.org/10.1055/S-2006-957970
Ancistrobrevine B 11015040 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C 407.50 unknown https://doi.org/10.1016/S0031-9422(00)97574-5
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/S0031-9422(00)86875-2
Dioncophylline C 443774 Click to see CC1CC2=C(C=CC(=C2C(N1)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)O 363.40 unknown https://doi.org/10.1055/S-2006-957970
Michellamine A 454909 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O 756.90 unknown https://doi.org/10.1006/ABBI.1997.0494
Michellamine A 453654 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=CC(=C(C4=C3C=C(C=C4OC)C)O)C5=C(C6=C(C=C(C=C6OC)C)C(=C5)C7=C8CC(NC(C8=C(C=C7O)O)C)C)O 756.90 unknown https://doi.org/10.1021/JM00116A011
N-Methyldioncophyllin a 633164 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/S0031-9422(00)95222-1
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(15S)-11,19,20-trihydroxy-7,7-dimethyl-15-(2-methylprop-1-enyl)-2,8,16-trioxapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),3(12),4(9),5,10,17,19,21-octaen-13-one 162987165 Click to see CC(=CC1C2=C(C3=CC(=C(C=C3O1)O)O)OC4=C(C2=O)C(=CC5=C4C=CC(O5)(C)C)O)C 434.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019
> Phenylpropanoids and polyketides / Macrolides and analogues
Michaolide E 16723567 Click to see CC1=CCC(C2(C(O2)C3C(C(CC(=CCC1)C)OC(=O)C)C(=C)C(=O)O3)C)OC(=O)C 432.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.019

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