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Duguetia hadrantha

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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 UUID644018977b3c6205004994
Scientific name Duguetia hadrantha
Authority R.E.Fr.
First published in Acta Horti Berg. 12: 65. 1934

Description Top

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Synonyms Top

Scientific name Authority First published in
Aberemoa hadrantha Diels ex Pilg. Verh. Bot. Vereins Prov. Brandenburg 47: 128 (1905)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000657849
Tropicos 1600744
KEW urn:lsid:ipni.org:names:72868-1
The Plant List kew-2779101
Open Tree Of Life 126765
NCBI Taxonomy 294152
IUCN Red List 145660430
IPNI 85704-2
GBIF 3157624
EOL 1054720

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
Duguetia pycnastera Sandwith (Annonaceae) Leaf Essential Oil Inhibits HepG2 Cell Growth In Vitro and In Vivo Costa EV, de Souza CA, Galvão AF, Silva VR, Santos LD, Dias RB, Rocha CA, Soares MB, da Silva FM, Koolen HH, Bezerra DP Molecules 02-Sep-2022
PMCID:PMC9458038
doi:10.3390/molecules27175664
PMID:36080430
Biological Activity of Naturally Derived Naphthyridines Chabowska G, Barg E, Wójcicka A Molecules 16-Jul-2021
PMCID:PMC8306249
doi:10.3390/molecules26144324
PMID:34299599
Ecological quality of a forest in a state of succession based on structural parameters: A case study in an evergreen Amazonian-Andean forest, Ecuador García-Quintana Y, Arteaga-Crespo Y, Torres-Navarrete B, Robles-Morillo M, Bravo-Medina C, Sarmiento-Rosero A Heliyon 30-Jul-2020
PMCID:PMC7394865
doi:10.1016/j.heliyon.2020.e04592
PMID:32775736
Oxoisoaporphines and Aporphines: Versatile Molecules with Anticancer Effects Rodríguez-Arce E, Cancino P, Arias-Calderón M, Silva-Matus P, Saldías M Molecules 27-Dec-2019
PMCID:PMC6983244
doi:10.3390/molecules25010108
PMID:31892146
Protocol for Identifying Natural Agents That Selectively Affect Adhesion, Thickness, Architecture, Cellular Phenotypes, Extracellular Matrix, and Human White Blood Cell Impenetrability of Candida albicans Biofilms Park YN, Srikantha T, Daniels KJ, Jacob MR, Agarwal AK, Li XC, Soll DR Antimicrob Agents Chemother 24-Oct-2017
PMCID:PMC5655110
doi:10.1128/AAC.01319-17
PMID:28893778
Azaphenanthrene Alkaloids with Antitumoral Activity from Anaxagorea dolichocarpa Sprague & Sandwith (Annonaceae) Lúcio AS, da Silva Almeida JR, Barbosa-Filho JM, Pita JC, Branco MV, de Fátima Formiga Melo Diniz M, de Fátima Agra M, da-Cunha EV, da Silva MS, Tavares JF Molecules 22-Aug-2011
PMCID:PMC6264400
doi:10.3390/molecules16087125
PMID:21860364
Role of Heme in the Antifungal Activity of the Azaoxoaporphine Alkaloid Sampangine Agarwal AK, Xu T, Jacob MR, Feng Q, Lorenz MC, Walker LA, Clark AM Eukaryot Cell 21-Dec-2007
PMCID:PMC2238161
doi:10.1128/EC.00323-07
PMID:18156292
Antimalarial, cytotoxic, and antifungal alkaloids from Duguetia hadrantha. Muhammad I, Dunbar DC, Takamatsu S, Walker LA, Clark AM J Nat Prod 01-May-2001
doi:10.1021/NP000436S
PMID:11374943

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 / 1-azaoxoaporphines
3-Methoxysampangine 122683 Click to see COC1=CN=C2C3=CC=CC=C3C(=O)C4=NC=CC1=C24 262.26 unknown https://doi.org/10.1021/NP000436S
Sampangine 387195 Click to see C1=CC=C2C(=C1)C3=NC=CC4=C3C(=NC=C4)C2=O 232.24 unknown https://doi.org/10.1021/NP000436S
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines
Hadranthine A 5276612 Click to see CN1C2=C(C3=C(C=C(C=C3)OC)C4=NC=CC(=C24)C(=O)C1=O)OC 322.30 unknown https://doi.org/10.1021/NP000436S
Hadranthine B 10401313 Click to see COC1=C2C3=C(C=CN=C3C4=CC=CC=C41)C(=O)C(=O)N2 278.26 unknown https://doi.org/10.1021/NP000436S
Imbiline-1 5276613 Click to see CN1C2=C(C3=CC=CC=C3C4=NC=CC(=C24)C(=O)C1=O)OC 292.29 unknown https://doi.org/10.1021/NP000436S

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