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Ancistrocladus congolensis

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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 UUID64403c9310a89790849859
Scientific name Ancistrocladus congolensis
Authority J.Léonard
First published in Bull. Soc. Roy. Bot. Belgique 82: 33 (1949)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000970266
Tropicos 1400015
KEW urn:lsid:ipni.org:names:71937-1
The Plant List kew-8758
Open Tree Of Life 389772
NCBI Taxonomy 714097
IPNI 71937-1
iNaturalist 946364
GBIF 3658983

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
Ethnopharmacological Potential of Phytochemicals and Phytogenic Products against Human RNA Viral Diseases as Preventive Therapeutics Paul A, Chakraborty N, Sarkar A, Acharya K, Ranjan A, Chauhan A, Srivastava S, Singh AK, Rai AK, Mubeen I, Prasad R Biomed Res Int 20-Feb-2023
PMCID:PMC9970710
doi:10.1155/2023/1977602
PMID:36860811
Bioactivity and In Silico Studies of Isoquinoline and Related Alkaloids as Promising Antiviral Agents: An Insight Sharma D, Sharma N, Manchanda N, Prasad SK, Sharma PC, Thakur VK, Rahman MM, Dhobi M Biomolecules 21-Dec-2022
PMCID:PMC9856122
doi:10.3390/biom13010017
PMID:36671402
African and Asian Medicinal Plants as a Repository for Prospective Antiviral Metabolites Against HIV-1 and SARS CoV-2: A Mini Review Anywar G, Akram M, Chishti MA Front Pharmacol 25-Aug-2021
PMCID:PMC8424073
doi:10.3389/fphar.2021.703837
PMID:34512337
Computational study to discover potent phytochemical inhibitors against drug target, squalene synthase from Leishmania donovani Wadanambi PM, Mannapperuma U Heliyon 31-May-2021
PMCID:PMC8188062
doi:10.1016/j.heliyon.2021.e07178
PMID:34141935
Antimicrobial Importance of Medicinal Plants in Nigeria Ugboko HU, Nwinyi OC, Oranusi SU, Fatoki TH, Omonhinmin CA ScientificWorldJournal 22-Sep-2020
PMCID:PMC7528132
doi:10.1155/2020/7059323
PMID:33029108
Biologically Active Isoquinoline Alkaloids covering 2014-2018 Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH Med Res Rev 29-Jul-2020
PMCID:PMC7554109
doi:10.1002/med.21703
PMID:32729169
Compounds from African Medicinal Plants with Activities Against Selected Parasitic Diseases: Schistosomiasis, Trypanosomiasis and Leishmaniasis Simoben CV, Ntie-Kang F, Akone SH, Sippl W Nat Prod Bioprospect 09-May-2018
PMCID:PMC5971035
doi:10.1007/s13659-018-0165-y
PMID:29744736
Six naphthylisoquinoline alkaloids and a related benzopyranone from a Congolese Ancistrocladus species related to Ancistrocladus congolensis. Bringmann G, Spuziak J, Faber JH, Gulder T, Kajahn I, Dreyer M, Heubl G, Brun R, Mudogo V Phytochemistry 01-Feb-2008
doi:10.1016/J.PHYTOCHEM.2007.10.027
PMID:18054973
Ancistrocongolines A-D, new naphthylisoquinoline alkaloids from ancistrocladus congolensis. Bringmann G, Messer K, Brun R, Mudogo V J Nat Prod 01-Aug-2002
doi:10.1021/NP010622D
PMID:12193010
Ancistrine, ancistine, ancistrocladeine trois alcaloides isoles de L'ancistrocladus ealaensis J.P. Foucher, J.L. Pousset, A. Cavé Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(75)85253-8

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
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(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/J.PHYTOCHEM.2007.10.027
(1S,3R)-5-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-6,8-dimethoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline 162900583 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 421.50 unknown https://doi.org/10.1016/0031-9422(75)85253-8
(1S,3R)-5-(4,5-dimethoxy-7-methylnaphthalen-1-yl)-6-methoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-8-ol 162904112 Click to see CC1CC2=C(C(N1C)C)C(=CC(=C2C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C)OC)O 421.50 unknown https://doi.org/10.1021/NP010622D
(1S,3S)-5-(4-hydroxy-5-methoxy-7-methylnaphthalen-1-yl)-1,2,3-trimethyl-3,4-dihydro-1H-isoquinoline-6,8-diol 162877740 Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C 393.50 unknown https://doi.org/10.1021/NP010622D
(3S)-5-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-6-ol 136676242 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 405.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.10.027
5-(4-Methoxy-2-methylnaphthalen-1-yl)-3-methyl-1,2-dihydroisoquinoline-6,8-diol 162889620 Click to see CC1=CC2=C(CN1)C(=CC(=C2C3=C(C=C(C4=CC=CC=C43)OC)C)O)O 347.40 unknown https://doi.org/10.1016/0031-9422(75)85253-8
5-(4,5-Dimethoxy-2-methylnaphthalen-1-yl)-8-methoxy-3-methyl-1,2-dihydroisoquinolin-6-ol 162859472 Click to see CC1=CC(=C2C(=C1C3=C4C=C(NCC4=C(C=C3O)OC)C)C=CC=C2OC)OC 391.50 unknown https://doi.org/10.1016/0031-9422(75)85253-8
Ancistrobertsonine A 15840195 Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C 421.50 unknown https://doi.org/10.1021/NP010622D
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/10.1021/NP010622D
https://doi.org/10.1016/J.PHYTOCHEM.2007.10.027
Ancistrocongoline A 392424 Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C 393.50 unknown https://doi.org/10.1021/NP010622D
Ancistrocongoline B 11742933 Click to see CC1CC2=C(C(N1C)C)C(=CC(=C2C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C)OC)O 421.50 unknown https://doi.org/10.1021/NP010622D
Ancistrocongoline C 636651 Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C 421.50 unknown https://doi.org/10.1021/NP010622D
Ancistrocongoline D 10409129 Click to see CC1CC2=CC(=C(C(=C2C(N1)C)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 407.50 unknown https://doi.org/10.1021/NP010622D
ancistrotanzanine B 10002166 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C 419.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.10.027
Korupensamine A 392421 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)O)OC)C 379.40 unknown https://doi.org/10.1021/NP010622D
O-Methylancistrocladinine 11212280 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 419.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.10.027

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