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Ancistrocladus likoko

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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 UUID64403c9a5da90411423190
Scientific name Ancistrocladus likoko
Authority J.Léonard
First published in Bull. Soc. Roy. Bot. Belgique 82: 34 (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-0000970396
Tropicos 50042021
KEW urn:lsid:ipni.org:names:71946-1
The Plant List kew-8770
Open Tree Of Life 784348
NCBI Taxonomy 714102
IPNI 71946-1
iNaturalist 946359
GBIF 3659015
EOL 6874712

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
Jozimine A2, a Dimeric Naphthylisoquinoline (NIQ) Alkaloid, Shows In Vitro Cytotoxic Effects against Leukemia Cells through NF-κB Inhibition Damiescu R, Yücer R, Klauck SM, Bringmann G, Efferth T, Dawood M Int J Mol Sci 07-Mar-2024
PMCID:PMC10970593
doi:10.3390/ijms25063087
PMID:38542061
Chemical Constituents of Callistemon subulatus and Their Anti-Pancreatic Cancer Activity against Human PANC-1 Cell Line Maneenet J, Tawila AM, Omar AM, Phan ND, Ojima C, Kuroda M, Sato M, Mizoguchi M, Takahashi I, Awale S Plants (Basel) 21-Sep-2022
PMCID:PMC9570665
doi:10.3390/plants11192466
PMID:36235333
Tumor microenvironment: a prospective target of natural alkaloids for cancer treatment Luo Y, Yin S, Lu J, Zhou S, Shao Y, Bao X, Wang T, Qiu Y, Yu H Cancer Cell Int 20-Jul-2021
PMCID:PMC8290600
doi:10.1186/s12935-021-02085-6
PMID:34284780
Mitochondrial Targeting in an Anti-Austerity Approach Involving Bioactive Metabolites Isolated from the Marine-Derived Fungus Aspergillus sp. Abdel-Naime WA, Kimishima A, Setiawan A, Fahim JR, Fouad MA, Kamel MS, Arai M Mar Drugs 07-Nov-2020
PMCID:PMC7694948
doi:10.3390/md18110555
PMID:33171814
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
Michellamines A6 and A7, and further mono- and dimeric naphthylisoquinoline alkaloids from a Congolese Ancistrocladus liana and their antiausterity activities against pancreatic cancer cells Lombe BK, Feineis D, Mudogo V, Brun R, Awale S, Bringmann G RSC Adv 31-Jan-2018
PMCID:PMC9078195
doi:10.1039/c8ra00363g
PMID:35542436
Plant-derived compounds in treatment of leishmaniasis Oryan A Iran J Vet Res 01-Jan-2015
PMCID:PMC4789233
PMID:27175144
Antileishmanial Activity of Parthenolide, a Sesquiterpene Lactone Isolated from Tanacetum parthenium Tiuman TS, Ueda-Nakamura T, Garcia Cortez DA, Dias Filho BP, Morgado-Díaz JA, de Souza W, Nakamura CV Antimicrob Agents Chemother 01-Jan-2005
PMCID:PMC538891
doi:10.1128/AAC.49.11.176-182.2005
PMID:15616293
Ancistrolikokine D, a 5,8'-coupled naphthylisoquinoline alkaloid, and related natural products from Ancistrocladus likoko. Bringmann G, Saeb W, Rückert M, Mies J, Michel M, Mudogo V, Brun R Phytochemistry 01-Feb-2003
doi:10.1016/S0031-9422(02)00570-8
PMID:12560038
Ancistrolikokines A-C: new 5,8'-coupled naphthylisoquinoline alkaloids from Ancistrocladus likoko. Bringmann G, Günther C, Saeb W, Mies J, Wickramasinghe A, Mudogo V, Brun R J Nat Prod 01-Oct-2000
doi:10.1021/NP000199T
PMID:11076547

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
(1S,3R)-5-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-6-ol 162878049 Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C 407.50 unknown https://doi.org/10.1021/NP000199T
(3R)-5-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-6-ol 163000264 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C 391.50 unknown https://doi.org/10.1016/S0031-9422(02)00570-8
(3S)-5-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-3,4-dihydro-2H-isoquinolin-6-one 5324374 Click to see CC1CC2=C(C(=O)C=C(C2=C(N1)C)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C 391.50 unknown https://doi.org/10.1016/S0031-9422(02)00570-8
Ancistrolikokine A 10476499 Click to see CC1CC2=C(C(N1C)C)C(=CC(=C2C3=C4C=C(C=C(C4=C(C=C3)O)OC)C)OC)O 407.50 unknown https://doi.org/10.1021/NP000199T
Ancistrolikokine B 10000664 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C 393.50 unknown https://doi.org/10.1021/NP000199T
Ancistrolikokine C 10024375 Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C 407.50 unknown https://doi.org/10.1021/NP000199T
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/10.1016/S0031-9422(02)00570-8
https://doi.org/10.1021/NP000199T
Korupensamine E 392425 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C 393.50 unknown https://doi.org/10.1021/NP000199T

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