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Topological Descriptors in Modeling the Antimalarial Activity of 4-(3‘,5‘-Disubstituted anilino)quinolines

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What this work says

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

inferredcites →https://doi.org/10.1001/jama.1971.03190050031006openalex-snapshot

Determination of the Drug Sensitivity of Plasmodium falciparum

inferredcites →https://doi.org/10.1002/qsar.19940130306openalex-snapshot

Variable Selection in QSAR Studies. I. An Evolutionary Algorithm

inferredcites →https://doi.org/10.1002/qsar.19940130403openalex-snapshot

Variable Selection in QSAR Studies. II. A Highly Efficient Combination of Systematic Search and Evolution

inferredcites →https://doi.org/10.1002/qsar.200330814openalex-snapshot

A Combinatorial Approach to the Variable Selection in Multiple Linear Regression: Analysis of Selwood et al. Data Set – A Case Study

inferredcites →https://doi.org/10.1002/qsar.200330854openalex-snapshot

CP‐MLR/PLS Directed Structure‐Activity Modeling of the HIV‐1 RT Inhibitory Activity of 2,3‐Diaryl‐1,3‐thiazolidin‐4‐ones

inferredcites →https://doi.org/10.1006/bbrc.1993.2060openalex-snapshot

Control of Heme Polymerase by Chloroquine and Other Quinoline Derivatives

inferredcites →https://doi.org/10.1016/0006-2952(88)90733-2openalex-snapshot

Drug-protein conjugates—XIV

inferredcites →https://doi.org/10.1016/0006-2952(92)90198-ropenalex-snapshot

The mechanism of bioactivation and antigen formation of amodiaquine in the rat

inferredcites →https://doi.org/10.1016/0163-7258(93)90056-jopenalex-snapshot

Chloroquine: Mechanism of drug action and resistance in plasmodium falciparum

inferredcites →https://doi.org/10.1016/0223-5234(94)90206-2openalex-snapshot

Conformational and structural features determining in vitro antimalarial activity in some indolo[3,2-c]quinolines, anilinoquinolines and tetrahydroindolo[3,2-d]benzazepines

inferredcites →https://doi.org/10.1016/j.bmc.2004.10.025openalex-snapshot

CP-MLR directed QSAR studies on the antimycobacterial activity of functionalized alkenols—topological descriptors in modeling the activity

inferredcites →https://doi.org/10.1016/s0140-6736(86)92371-8openalex-snapshot

FREQUENCY OF SEVERE NEUTROPENIA ASSOCIATED WITH AMODIAQUINE PROPHYLAXIS AGAINST MALARIA

inferredcites →https://doi.org/10.1016/s0163-7258(97)00084-3openalex-snapshot

4-Aminoquinolines—Past, present, and future; A chemical perspective

inferredcites →https://doi.org/10.1021/ci00020a020openalex-snapshot

Application of Genetic Function Approximation to Quantitative Structure-Activity Relationships and Quantitative Structure-Property Relationships

inferredcites →https://doi.org/10.1021/ci9501047openalex-snapshot

Use of Structure−Activity Data To Compare Structure-Based Clustering Methods and Descriptors for Use in Compound Selection

inferredcites →https://doi.org/10.1021/jm00156a009openalex-snapshot

Antimalarial drugs. 60. Synthesis, antimalarial activity, and quantitative structure-activity relationships of tebuquine and a series of related 5-[(7-chloro-4-quinolinyl)amino]-3-[(alkylamino)methyl][1,1'-biphenyl]-2-ols and N.omega.-oxides

inferredcites →https://doi.org/10.1021/jm00156a010openalex-snapshot

Syntheses and in vitro evaluation of 4-(2-aminoethyl)-2(3H)-indolones and related compounds as peripheral prejunctional dopamine receptor agonists

inferredcites →https://doi.org/10.1021/jm010842oopenalex-snapshot

Synthesis and in Vitro and in Vivo Antimalarial Activity of New 4-Anilinoquinolines

inferredcites →https://doi.org/10.1021/jm960370ropenalex-snapshot

Synthesis, Antimalarial Activity, and Molecular Modeling of Tebuquine Analogues

inferredcites →https://doi.org/10.1021/jm970487vopenalex-snapshot

Three-Dimensional Quantitative Structure−Activity Relationships from Molecular Similarity Matrices and Genetic Neural Networks. 1. Method and Validations

inferredcites →https://doi.org/10.1021/jm980146xopenalex-snapshot

Structure−Activity Relationships for Antiplasmodial Activity among 7-Substituted 4-Aminoquinolines

inferredcites →https://doi.org/10.1023/b:jcam.0000017373.50020.41openalex-snapshot

TOPS-MODE versus DRAGON descriptors to predict permeability coefficients through low-density polyethylene

inferredcites →https://doi.org/10.1128/aac.42.3.682openalex-snapshot

Relationship between Antimalarial Drug Activity, Accumulation, and Inhibition of Heme Polymerization in Plasmodium falciparum In Vitro

inferredcites →https://doi.org/10.1136/bmj.292.6522.721openalex-snapshot

Amodiaquine induced agranulocytosis and liver damage.

inferredcites →https://doi.org/10.2174/1389557013407188openalex-snapshot

Structure-Function Relationships in Chloroquine and Related 4-Aminoquinoline Antimalarials

What points at this work

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

inferred← citeshttps://doi.org/10.1002/9783527628766.biblioopenalex-snapshot

Bibliography

inferred← citeshttps://doi.org/10.1002/ardp.201000029openalex-snapshot

NMR QSAR Model for the Analysis of 4‐(5‐Arylamino‐1,3,4‐thiadiazol‐2‐yl)benzene‐1,3‐diols

inferred← citeshttps://doi.org/10.1002/bit.21214openalex-snapshot

MODEL—molecular descriptor lab: A web‐based server for computing structural and physicochemical features of compounds

inferred← citeshttps://doi.org/10.1002/chin.200616219openalex-snapshot

Topological Descriptors in Modeling the Antimalarial Activity of 4‐(3′,5′‐Disubstituted anilino)quinolines.

inferred← citeshttps://doi.org/10.1002/minf.201800021openalex-snapshot

AntiMalarial Mode of Action (AMMA) Database: Data Selection, Verification and Chemical Space Analysis

inferred← citeshttps://doi.org/10.1007/s00044-012-0344-zopenalex-snapshot

CP-MLR/PLS-directed QSAR studies on the antimalarial activity and cytotoxicity of substituted 4-aminoquinolines

inferred← citeshttps://doi.org/10.1007/s00044-012-0348-8openalex-snapshot

Modeling of antitubercular activity of biphenyl analogs of 2-nitroimidazo[2,1-b][1,3]oxazine to rationalize their activity profile

inferred← citeshttps://doi.org/10.1007/s10822-017-0019-4openalex-snapshot

QSAR modeling and chemical space analysis of antimalarial compounds

inferred← citeshttps://doi.org/10.1007/s10847-013-0337-7openalex-snapshot

Application of self organizing maps and GA-MLR for the estimation of stability constant of 18-crown-6 ether derivatives with sodium cation

inferred← citeshttps://doi.org/10.1007/s11030-016-9705-8openalex-snapshot

QSAR models of antiproliferative activity of imidazo[2,1-b][1,3,4]thiadiazoles in various cancer cell lines

inferred← citeshttps://doi.org/10.1016/j.arabjc.2014.11.047openalex-snapshot

QSAR study on 4-alkynyldihydrocinnamic acid analogs as free fatty acid receptor 1 agonists and antidiabetic agents: Rationales to improve activity

inferred← citeshttps://doi.org/10.1016/j.bmc.2008.11.040openalex-snapshot

Convenient QSAR model for predicting the complexation of structurally diverse compounds with β-cyclodextrins

inferred← citeshttps://doi.org/10.1016/j.chemolab.2011.08.007openalex-snapshot

Comparative QSARs for antimalarial endochins: Importance of descriptor-thinning and noise reduction prior to feature selection

inferred← citeshttps://doi.org/10.1016/j.ejmech.2007.06.018openalex-snapshot

QSAR studies on benzoylaminobenzoic acid derivatives as inhibitors of β-ketoacyl-acyl carrier protein synthase III

inferred← citeshttps://doi.org/10.1016/j.ejmech.2008.01.020openalex-snapshot

QSAR study about ATP-sensitive potassium channel activation of cromakalim analogues using CP-MLR approach

inferred← citeshttps://doi.org/10.1016/j.ejmech.2008.01.025openalex-snapshot

QSAR study on tetrahydroquinoline analogues as plasmodium protein farnesyltransferase inhibitors: A comparison of rationales of malarial and mammalian enzyme inhibitory activities for selectivity

inferred← citeshttps://doi.org/10.1016/j.ejmech.2008.09.022openalex-snapshot

Topological descriptors in modeling the agonistic activity of human A3 adenosine receptor ligands: The derivatives of 2-chloro-N6-substituted-4′-thioadenosine-5′-uronamide

inferred← citeshttps://doi.org/10.1021/jm070110hopenalex-snapshot

C-3 Alkyl/Arylalkyl-2,3-dideoxy Hex-2-enopyranosides as Antitubercular Agents: Synthesis, Biological Evaluation, and QSAR Study

inferred← citeshttps://doi.org/10.1039/c6ra00846aopenalex-snapshot

N-(7-Chloroquinolinyl-4-aminoalkyl)arylsulfonamides as antimalarial agents: rationale for the activity with reference to inhibition of hemozoin formation

inferred← citeshttps://doi.org/10.1080/00268970903078559openalex-snapshot

Feature selection method based on fuzzy entropy for regression in QSAR studies

inferred← citeshttps://doi.org/10.1080/14756360801915336openalex-snapshot

Topological descriptors in modeling malonyl coenzyme A decarboxylase inhibitory activity: N-Alkyl-N-(1,1,1,3,3,3-hexafluoro-2-hydroxypropylphenyl)amide derivatives

inferred← citeshttps://doi.org/10.1080/14756360801915351openalex-snapshot

Modeling of vascular endothelial growth factor receptor 2 (VEGFR2) kinase inhibitory activity of 2-anilino-5-aryloxazoles using chemometric tools

inferred← citeshttps://doi.org/10.1080/14756360801915377openalex-snapshot

Topological descriptors in modelling antimalarial activity: N1-(7-chloro-4-quinolyl)-1,4-bis(3-aminopropyl)piperazine as prototype

inferred← citeshttps://doi.org/10.1080/14756360802318878openalex-snapshot

Modeling of cyclooxygenase-2 and 5-lipooxygenase inhibitory activity of apoptosis-inducing agents potentially useful in prostate cancer chemotherapy: Derivatives of diarylpyrazole

inferred← citeshttps://doi.org/10.1080/14756360802608054openalex-snapshot

Modeling of the growth hormone secretagogue receptor antagonistic activity using chemometric tools

inferred← citeshttps://doi.org/10.1155/2013/154629openalex-snapshot

Topological Features in Profiling the Antimalarial Activity Landscape of Anilinoquinolines: A Multipronged QSAR Study

inferred← citeshttps://doi.org/10.1186/s40064-015-1593-3openalex-snapshot

In-silico combinatorial design and pharmacophore modeling of potent antimalarial 4-anilinoquinolines utilizing QSAR and computed descriptors

inferred← citeshttps://doi.org/10.1201/b19853-2openalex-snapshot

Overview and Recent Advances in QSAR Studies

inferred← citeshttps://doi.org/10.1201/b19853-7openalex-snapshot

Overview and Recent Advances in QSAR Studies

inferred← citeshttps://doi.org/10.1371/journal.pone.0040654openalex-snapshot

Systems Biological Approach of Molecular Descriptors Connectivity: Optimal Descriptors for Oral Bioavailability Prediction

inferred← citeshttps://doi.org/10.1517/17460441.2010.497812openalex-snapshot

Advances in quantitative structure–activity relationship models of antimalarials

inferred← citeshttps://doi.org/10.3109/14756366.2011.587414openalex-snapshot

QSAR of 2-(4-methylsulphonylphenyl)pyrimidine derivatives as cyclooxygenase-2 inhibitors: simple structural fragments as potential modulators of activity

inferred← citeshttps://doi.org/10.3109/14756366.2011.654111openalex-snapshot

CP-MLR/PLS directed QSAR study on the glutaminyl cyclase inhibitory activity of imidazoles: rationales to advance the understanding of activity profile

inferred← citeshttps://doi.org/10.70675/bc3c6c45z38f7z43b9zb1b6z82b1e1107978openalex-snapshot

Analysis of the chemical space of antimalarial compounds by generative topographie mapping

inferred← citeshttps://doi.org/10.9734/bjpr/2015/19615openalex-snapshot

Synthesis, Characterization and Evaluation of Biological Properties of Pyrazolo- and Oxazolo-pyridocarbazoles and Pyridoazacarbazoles as Potent Anti-microbial Agents

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