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A QSAR Study of the Antimalarial Activity of Some Synthetic 1,2,4-Trioxanes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hlca.19930760804openalex-snapshot
Synthesis, Structure, and Antimalarial Activity of Tricyclic 1,2,4‐Trioxanes Related to Artemisinin
inferredcites →https://doi.org/10.1002/jcc.540040211openalex-snapshot
CHARMM : A program for macromolecular energy, minimization, and dynamics calculations
inferredcites →https://doi.org/10.1016/0006-2952(92)90713-sopenalex-snapshot
Hemin-catalyzed decomposition of artemisinin (qinghaosu)
inferredcites →https://doi.org/10.1016/0169-4758(96)80661-2openalex-snapshot
Transmission dynamics of Plasmodium falciparum: Reply
inferredcites →https://doi.org/10.1016/0263-7855(94)80094-4openalex-snapshot
Perspectives in medicinal chemistry
inferredcites →https://doi.org/10.1017/cbo9780511693632.005openalex-snapshot
Department of Biochemistry
inferredcites →https://doi.org/10.1021/ci00022a012openalex-snapshot
Chemical Function Queries for 3D Database Search
inferredcites →https://doi.org/10.1126/science.3887571openalex-snapshot
Qinghaosu (Artemisinin): an Antimalarial Drug from China
inferredcites →https://doi.org/10.1126/science.3992245openalex-snapshot
Model Structure for the Inflammatory Protein C5a
inferredcites →https://doi.org/10.4269/ajtmh.1972.21.493openalex-snapshot
Chemotherapy and Drug Resistance in Malaria
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/chin.199719258openalex-snapshot
ChemInform Abstract: A QSAR Study of the Antimalarial Activity of Some Synthetic 1,2,4‐ Trioxanes
inferred← citeshttps://doi.org/10.1002/jcc.26519openalex-snapshot
ClassicalGSG : Prediction of log P using classical molecular force fields and geometric scattering for graphs
inferred← citeshttps://doi.org/10.1002/jps.20106openalex-snapshot
Nuclear magnetic resonance and molecular modeling analysis of the interaction of the antimalarial drugs artelinic acid and artesunic acid with β‐cyclodextrin
inferred← citeshttps://doi.org/10.1002/med.21979openalex-snapshot
An overview on the antimalarial activity of 1,2,4‐trioxanes, 1,2,4‐trioxolanes and 1,2,4,5‐tetraoxanes
inferred← citeshttps://doi.org/10.1002/qsar.200330829openalex-snapshot
Artemisinin Derivatives with Antimalarial Activity against Plasmodium falciparum Designed with the Aid of Quantum Chemical and Partial Least Squares Methods
inferred← citeshttps://doi.org/10.1006/eesa.1999.1784openalex-snapshot
Applicability of CATALYST in Ecotoxicology, a New Promising Tool for 3D-QSAR: Study of Chlorophenols
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Drug discovery: Past, present and future
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Molecular modeling study on chemically diverse series of cyclooxygenase-2 selective inhibitors: generation of predictive pharmacophore model using Catalyst
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Six-Membered Rings With 1,2,4-Oxygen or Sulfur Atoms
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00811-7openalex-snapshot
Six-membered Rings with 1,2,4-Oxygen or Sulfur Atoms
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.107043openalex-snapshot
Recent advances in the synthesis and antimalarial activity of 1,2,4-trioxanes
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.11.015openalex-snapshot
Antimalarial activity: A QSAR modeling using CODESSA PRO software
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.04.001openalex-snapshot
3D-QSAR studies of 2,2-diphenylpropionates to aid discovery of novel potent muscarinic antagonists
inferred← citeshttps://doi.org/10.1016/j.jmgm.2004.06.003openalex-snapshot
The use of a pharmacophore model for identification of novel ligands for the benzodiazepine binding site of the GABAA receptor
inferred← citeshttps://doi.org/10.1016/s0022-3565(24)34917-1openalex-snapshot
Three- and Four-Dimensional Quantitative Structure Activity Relationship Analyses of Cytochrome P-450 3A4 Inhibitors
inferred← citeshttps://doi.org/10.1016/s0065-2490(97)80016-0openalex-snapshot
Peroxidic Antimalarials
inferred← citeshttps://doi.org/10.1016/s0223-5234(00)01202-2openalex-snapshot
A feature based pharmacophore for Candida albicans MyristoylCoA: protein N-myristoyltransferase inhibitors
inferred← citeshttps://doi.org/10.1016/s0960-894x(01)00361-4openalex-snapshot
CoMFA of Artemisinin derivatives: effect of location and size of lattice
inferred← citeshttps://doi.org/10.1016/s1074-5521(02)00117-5openalex-snapshot
Heme-Artemisinin Adducts Are Crucial Mediators of the Ability of Artemisinin to Inhibit Heme Polymerization
inferred← citeshttps://doi.org/10.1021/ci0004558openalex-snapshot
Modeling Antimalarial Activity: Application of Kinetic Energy Density Quantum Similarity Measures as Descriptors in QSAR
inferred← citeshttps://doi.org/10.1021/ci020368aopenalex-snapshot
Use of Catalyst Pharmacophore Models for Screening of Large Combinatorial Libraries
inferred← citeshttps://doi.org/10.1021/ci050257mopenalex-snapshot
Ligand-Based Molecular Modeling Study on a Chemically Diverse Series of Cholecystokinin-B/Gastrin Receptor Antagonists: Generation of Predictive Model
inferred← citeshttps://doi.org/10.1021/ci100180eopenalex-snapshot
Pharmacophore Modeling of Substituted 1,2,4-Trioxanes for Quantitative Prediction of their Antimalarial Activity
inferred← citeshttps://doi.org/10.1021/ci980093sopenalex-snapshot
Four-Dimensional Quantitative Structure−Activity Relationship Analysis of a Series of Interphenylene 7-Oxabicycloheptane Oxazole Thromboxane A2 Receptor Antagonists
inferred← citeshttps://doi.org/10.1021/ci990276uopenalex-snapshot
Correlating the Molecular Electrostatic Potentials of Some Organic Peroxides with Their Antimalarial Activities
inferred← citeshttps://doi.org/10.1021/jm010360copenalex-snapshot
Pharmacophore Mapping of a Series of 2,4-Diamino-5-deazapteridine Inhibitors of Mycobacterium avium Complex Dihydrofolate Reductase
inferred← citeshttps://doi.org/10.1021/jm040108fopenalex-snapshot
A Three-Dimensional in Silico Pharmacophore Model for Inhibition of Plasmodium falciparum Cyclin-Dependent Kinases and Discovery of Different Classes of Novel Pfmrk Specific Inhibitors
inferred← citeshttps://doi.org/10.1021/jm970711gopenalex-snapshot
Design, Synthesis, Derivatization, and Structure−Activity Relationships of Simplified, Tricyclic, 1,2,4-Trioxane Alcohol Analogues of the Antimalarial Artemisinin
inferred← citeshttps://doi.org/10.1021/jm980146xopenalex-snapshot
Structure−Activity Relationships for Antiplasmodial Activity among 7-Substituted 4-Aminoquinolines
inferred← citeshttps://doi.org/10.1021/jm990530+openalex-snapshot
Methyl-Substituted Dispiro-1,2,4,5-tetraoxanes: Correlations of Structural Studies with Antimalarial Activity
inferred← citeshttps://doi.org/10.1023/a:1011945119287openalex-snapshot
Evaluation of designed ligands by a multiple screening method: Application to glycogen phosphorylase inhibitors constructed with a variety of approaches
inferred← citeshttps://doi.org/10.1023/a:1015917510236openalex-snapshot
Antimalarial activity of synthetic 1,2,4-trioxanes and cyclic peroxy ketals, a quantum similarity study
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Safety assessment of peroxide antimalarials: clinical and chemical perspectives
inferred← citeshttps://doi.org/10.1074/jbc.274.27.19383openalex-snapshot
Artemisinin, an Endoperoxide Antimalarial, Disrupts the Hemoglobin Catabolism and Heme Detoxification Systems in Malarial Parasite
inferred← citeshttps://doi.org/10.1128/aac.48.7.2624-2632.2004openalex-snapshot
The Antimalarial Potential of 4-Quinolinecarbinolamines May Be Limited due to Neurotoxicity and Cross-Resistance in Mefloquine-ResistantPlasmodium falciparumStrains
inferred← citeshttps://doi.org/10.1201/b17407-6openalex-snapshot
In Silico Models for Development of Insect Repellents
inferred← citeshttps://doi.org/10.1517/17460441.2010.497812openalex-snapshot
Advances in quantitative structure–activity relationship models of antimalarials
inferred← citeshttps://doi.org/10.3390/molecules26061756openalex-snapshot
Six New Phenylpropanoid Derivatives from Chemically Converted Extract of Alpinia galanga (L.) and Their Antiparasitic Activities
inferred← citeshttps://doi.org/10.3987/com-99-s146openalex-snapshot
The Structure and Antimalarial Activity of Some 1,2,4-Trioxanes, 1,2,4,5-Tetroxanes, an Bicyclic Endoperoxides. Implications for the Mode of Action
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Estudo teorico de alguns intermediarios radicalares e neutros da artemisinina e da interação existente entre o heme e a artemisinina
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