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Structure−Activity Relationships for the Antileishmanial and Antitrypanosomal Activities of 1‘-Substituted 9-Anilinoacridines

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

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DNA-directed alkylating agents. 3. Structure-activity relationships for acridine-linked aniline mustards: consequences of varying the length of the linker chain
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Potential antitumor agents. 36. Quantitative relationships between experimental antitumor activity, toxicity, and structure for the general class of 9-anilinoacridine antitumor agents
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Quantitative structure-inhibitory activity relationships of phenols and fatty acids for Bacillus subtilis spore germination
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9-Substituted 3,6-Bis(dimethylamino)acridines
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The Mesylation of Kojic Acid and Other 3-(or 5)-Hydroxy-4H-pyran-4-ones. Displacement of a Mesyloxy Group under Acidic Conditions1,2
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High-Density Functional Gastrin Releasing Peptide Receptors on Primate Cells
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Structure-activity relationships and modes of action of 9-anilinoacridines against chloroquine-resistant Plasmodium falciparum in vitro
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9-Anilinoacridines as potential antileishmanial agents
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Trypanosoma cruzi: Selective Isolation of Pure Trypomastigotes from Cultured Muscle Cells
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Continuous Cultivation of Trypanosoma brucei Blood Stream Forms in a Medium Containing a Low Concentration of Serum Protein without Feeder Cell Layers
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What points at this work

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

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ChemInform Abstract: Structure‐Activity Relationships for the Antileishmanial and Antitrypanosomal Activities of 1′‐Substituted 9‐Anilinoacridines.
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Dyes, trypanosomiasis and DNA: a historical and critical review
inferred← citeshttps://doi.org/10.3184/146867816x14720534560565openalex-snapshot
Theoretical Investigation on the Kinetics and Mechanism of the Synthesis of Fluorescent 3,8-Disubstituted-3H-Imidazo [4,5-a] Acridine-11-Carbonitriles
inferred← citeshttps://doi.org/10.31857/s268695352370019xopenalex-snapshot
AMINO DERIVATIVES OF ACRIDINE: SYNTHESIS, STUDY OF ANTICHOLINESTERASE AND ANTIOXIDANT ACTIVITIES
inferred← citeshttps://doi.org/10.3389/fphar.2023.1219980openalex-snapshot
Derivatives of 9-phosphorylated acridine as butyrylcholinesterase inhibitors with antioxidant activity and the ability to inhibit β-amyloid self-aggregation: potential therapeutic agents for Alzheimer’s disease
inferred← citeshttps://doi.org/10.3390/microorganisms13061297openalex-snapshot
Synthesis, Biological Evaluation, Molecular Dynamics, and QM-MM Calculation of Spiro-Acridine Derivatives Against Leishmaniasis
inferred← citeshttps://doi.org/10.3390/molecules16021593openalex-snapshot
Synthesis and Anti-Intestinal Nematode Activity of Variously Substituted Benzonaphthyridine Derivatives
inferred← citeshttps://doi.org/10.3390/ph15020148openalex-snapshot
Evolution of Acridines and Xanthenes as a Core Structure for the Development of Antileishmanial Agents
inferred← citeshttps://doi.org/10.38212/2224-6614.2546openalex-snapshot
Pharmacokinetics of a new antitumor agent, 1-[3-(Furo[3,2-C]quinolin-4-ylamino)phenyl]-ethanoe-O-methyl-oxime, in rat using a high performance liquid chromatography method
inferred← citeshttps://doi.org/10.4172/pharmaceutical-sciences.1000439openalex-snapshot
Synthesis, Characterization and Antitumour Activity of Some Novel Oxazine Substituted 9-Anilinoacridines and their 3D-QSAR Studies
inferred← citeshttps://doi.org/10.5530/ijper.51.1.15openalex-snapshot
Molecular Docking studies and in-silico ADMET Screening of Some novel Oxazine substituted 9-Anilinoacridines as Topoisomerase II Inhibitors
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