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New Antimalarial Bis-dehydroaporphine Alkaloids from Polyalthia debilis

https://doi.org/10.1021/np020498d
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-1-4612-2908-7openalex-snapshot
Alkaloids: Chemical and Biological Perspectives
inferredcites →https://doi.org/10.1016/0031-9422(96)00219-1openalex-snapshot
Two 7,7′-bisdehydroaporphine alkaloids from Polyalthia bullata
inferredcites →https://doi.org/10.1016/s0031-9422(00)82394-8openalex-snapshot
Three bis-dehydroaporphines from Oxandra cf. major
inferredcites →https://doi.org/10.1016/s0031-9422(97)00487-1openalex-snapshot
A diynoic acid from Polyalthia evecta
inferredcites →https://doi.org/10.1016/s0031-9422(99)00535-xopenalex-snapshot
An azaanthracene alkaloid from Polyalthia suberosa
inferredcites →https://doi.org/10.1016/s0040-4039(00)85782-2openalex-snapshot
Un nouveau type d'alcaloïdes isoquinoleiques, les bisaporphines
inferredcites →https://doi.org/10.1016/s0040-4039(01)92418-9openalex-snapshot
La polyveoline, nouvel indolosesquiterpene isole du polyalthia suaveolens, annonacees
inferredcites →https://doi.org/10.1021/np50033a018openalex-snapshot
Alcaloïdes des Annonacees, L: Alcaloïdes De Polyalthia cauliflora
inferredcites →https://doi.org/10.1021/np960578fopenalex-snapshot
Cerasodine and Cerasonine: New Oxoprotoberberine Alkaloids from Polyalthia cerasoides
inferredcites →https://doi.org/10.1039/p19800002812openalex-snapshot
Synthesis of potentially basic hydrocarbons by sulphur extrusion and/or bis-Wittig reactions. Two syntheses of benz[5,6]indeno[2,1-a]phenalene and a new synthesis of dibenzo[de,mn]naphthacene (zethrene)
inferredcites →https://doi.org/10.1055/s-2001-16469openalex-snapshot
2-Substituted Furans from Polyalthia suberosa
inferredcites →https://doi.org/10.1055/s-2001-16470openalex-snapshot
New Naphthoquinones from Arnebia hispidissima Roots
inferredcites →https://doi.org/10.1126/science.948741openalex-snapshot
Neurons Selective for Orientation and Binocular Disparity in the Visual Wulst of the Barn Owl ( Tyto alba )
inferredcites →https://doi.org/10.1128/aac.16.6.710openalex-snapshot
Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113586zenodo-depositor-declared
Dimeric aporphine alkaloids from the twigs of Trivalvaria costata (Hook.f. & Thomson) I.M.Turner
inferred← citeshttps://doi.org/10.1002/chem.200400220openalex-snapshot
Synthesis of Phenanthrenes and Polycyclic Heteroarenes by Transition‐Metal Catalyzed Cycloisomerization Reactions
inferred← citeshttps://doi.org/10.1002/hlca.200790080openalex-snapshot
Chemical Constituents of Polyalthia nemoralis
inferred← citeshttps://doi.org/10.1002/hlca.201300231openalex-snapshot
A Chiron Approach for the Total Synthesis of Crassalactone A
inferred← citeshttps://doi.org/10.1002/hlca.201400237openalex-snapshot
Stereoselective Total Synthesis of Crassalactone A, a Natural Cytotoxic Styryl Lactone
inferred← citeshttps://doi.org/10.1002/slct.202302821openalex-snapshot
Total Synthesis of Aporphine Alkaloids via Benzyne Chemistry: Progress Towards a Late‐Stage Enantioselective Hydrogenation and Neuroprotective Activity Evaluations
inferred← citeshttps://doi.org/10.1007/s11101-026-10257-3openalex-snapshot
Phytochemical diversity and therapeutic potential of the Polyalthia genus: a comprehensive review
inferred← citeshttps://doi.org/10.1016/bs.alkal.2014.09.002openalex-snapshot
Alkaloids of the Annonaceae: Occurrence and a Compilation of Their Biological Activities
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.12.005openalex-snapshot
Aspergilones A and B, two benzylazaphilones with an unprecedented carbon skeleton from the gorgonian-derived fungus Aspergillus sp.
inferred← citeshttps://doi.org/10.1016/j.bse.2022.104550openalex-snapshot
New (4 → 2)-abeo-clerodane diterpenoids from the Polyalthia laui and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.fitote.2008.06.007openalex-snapshot
Cytotoxic activity screening of some indigenous Thai plants
inferred← citeshttps://doi.org/10.1016/j.fitote.2010.11.025openalex-snapshot
A new dimeric aporphine from the roots of Artabotrys spinosus
inferred← citeshttps://doi.org/10.1016/j.jep.2015.04.014openalex-snapshot
Clerodane diterpenes from Polyalthia longifolia (Sonn) Thw. var. pendula: Potential antimalarial agents for drug resistant Plasmodium falciparum infection
inferred← citeshttps://doi.org/10.1016/j.jep.2018.10.001openalex-snapshot
The medicinal uses, toxicities and anti-inflammatory activity of Polyalthia species (Annonaceae)
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2007.03.016openalex-snapshot
In search of cyclooxygenase inhibitors, anti-Mycobacterium tuberculosis and anti-malarial drugs from Thai flora and microbes
inferred← citeshttps://doi.org/10.1016/j.phymed.2009.09.005openalex-snapshot
Antiproliferative, apoptotic and antimutagenic activity of isolated compounds from Polyalthia cerasoides seeds
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114941openalex-snapshot
Anti-lipotoxic alkaloids from the roots of Polyalthia cerasoides
inferred← citeshttps://doi.org/10.1016/j.phytol.2020.06.009openalex-snapshot
Dimeric dehydroaporphinoids with antiplasmodial properties from the liana of Artabotrys aurantiacus (Annonaceae)
inferred← citeshttps://doi.org/10.1016/j.sajb.2023.02.015openalex-snapshot
Plants from Annonaceae family as antimalarials: An ethnopharmacology and phytochemistry review to identify potential lead molecules
inferred← citeshttps://doi.org/10.1016/j.tet.2015.05.040openalex-snapshot
Divergent total synthesis of crassalactones B and C and evaluation of their antiproliferative activity
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.04.114openalex-snapshot
Divergent synthesis of cytotoxic styryl lactones isolated from Polyalthia crassa. The first total synthesis of crassalactone B
inferred← citeshttps://doi.org/10.1016/s0079-6468(05)43006-4openalex-snapshot
Recent Advances in the Search for Newer Antimalarial Agents
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00759openalex-snapshot
Mitrephorines A–E and Other Cytotoxic Aporphinoids from the Bark of Mitrephora tomentosa
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00243openalex-snapshot
3,4-seco-Norclerodane Diterpenoids from the Roots of Polyalthia laui
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00247openalex-snapshot
Copper-Catalyzed Asymmetric Ring-Opening Reaction of Cyclic Diaryliodonium Salts with Imides
inferred← citeshttps://doi.org/10.1021/np0503202openalex-snapshot
2-Substituted Furans from the Roots of Polyalthia evecta
inferred← citeshttps://doi.org/10.1021/np060323uopenalex-snapshot
Cytotoxic Styryl-Lactones from the Leaves and Twigs of Polyalthia crassa
inferred← citeshttps://doi.org/10.1021/np070293aopenalex-snapshot
Bioactive Constituents of the Roots of Polyalthia cerasoides
inferred← citeshttps://doi.org/10.1021/np1001913openalex-snapshot
Polyacetylenes from the Roots of Polyalthia debilis
inferred← citeshttps://doi.org/10.1039/b306880copenalex-snapshot
Concise total synthesis of the aporphine alkaloid 7,7′-bisdehydro-O-methylisopiline by an InCl 3 mediated cycloisomerization reaction
inferred← citeshttps://doi.org/10.1039/b316108kopenalex-snapshot
β-Phenylethylamines and the isoquinoline alkaloids
inferred← citeshttps://doi.org/10.1039/d5np00032gopenalex-snapshot
Natural tricyclic and hyper-polycyclic aromatic hydrocarbons: structure, biosynthesis, bioactivity, and synthesis
inferred← citeshttps://doi.org/10.1080/10286020802242281openalex-snapshot
Four new alkaloids fromPolyalthia nemoralis(Annonaceae)
inferred← citeshttps://doi.org/10.1080/13880200701501300openalex-snapshot
Constituents ofPolyalthia jucunda. and Their Cytotoxic Effect on Human Cancer Cell Lines
inferred← citeshttps://doi.org/10.1080/14786419.2017.1295236openalex-snapshot
A new norsesquiterpene from the roots of Polyalthia laui
inferred← citeshttps://doi.org/10.11606/t.60.2012.tde-28062012-113118openalex-snapshot
Otimização das condições de cultivo de Beauveria bassiana e Mycoleptodiscus indicus visando à produção de metabólitos com atividades antimicrobiana, antiparasitária e antitumoral
inferred← citeshttps://doi.org/10.1177/1934578x1000501005openalex-snapshot
An Unusual Bisnor-clerodane Diterpenoid from Polyalthia Simiarum
inferred← citeshttps://doi.org/10.1177/1934578x1801301011openalex-snapshot
Bioactive Aporphine Alkaloids from the Roots of Artabotrys spinosus : Cholinesterase Inhibitory Activity and Molecular Docking Studies
inferred← citeshttps://doi.org/10.1186/1475-2875-10-s1-s5openalex-snapshot
Analysis of additivity and synergism in the anti-plasmodial effect of purified compounds from plant extracts
inferred← citeshttps://doi.org/10.14456/ijps.2008.18openalex-snapshot
Antioxidative Activity and Antimutagenicity of Three Plants in Annonaceae in Plant Genetics Conservation at Khok Phutaka, Amphur Phuwiang, Khon Kaen
inferred← citeshttps://doi.org/10.2174/1386207326666230329090413openalex-snapshot
Complex Oligomers and their Bioactivity of Annonaceae Family
inferred← citeshttps://doi.org/10.2174/1570163819666220511154837openalex-snapshot
Anti-proliferative Activity of Labdane Diterpenes Isolated from Polyalthia cerasoides and their Molecular Interaction Studies
inferred← citeshttps://doi.org/10.3390/molecules14114414openalex-snapshot
Bioactive Azafluorenone Alkaloids from Polyalthia debilis (Pierre) Finet & Gagnep.
inferred← citeshttps://doi.org/10.3390/ph15101218openalex-snapshot
Novel Aporphine- and Proaporphine–Clerodane Hybrids Identified from the Barks of Taiwanese Polyalthia longifolia (Sonn.) Thwaites var. pendula with Strong Anti-DENV2 Activity
inferred← citeshttps://doi.org/10.4103/jcrt.jcrt_1170_19openalex-snapshot
Antiproliferative, apoptotic, and antimutagenic properties of stem bark and seed fractions of Polyalthia cerasoides (Roxb.)
inferred← citeshttps://doi.org/10.7324/japs.2015.50303openalex-snapshot
Antimicrobial and cytotoxic acetogenin from Polyalthia debilis
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