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A Comparative Molecular Field Analysis (CoMFA) and Comparative Molecular Similarity Indices Analysis (CoMSIA) of Anthranilamide Derivatives That Are Multidrug Resistance Modulators

https://doi.org/10.1021/jm060239b
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What this work says

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

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A novel hypothesis for the mechanism of action of P-glycoprotein as a multidrug transporter
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Bootstrapping principal component regression models
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Crossvalidation, Bootstrapping, and Partial Least Squares Compared with Multiple Regression in Conventional QSAR Studies
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The Use of Composite Crystal-field Environments in Molecular Recognition and the de Novo Design of Protein Ligands
inferredcites →https://doi.org/10.1007/0-306-46858-1_6openalex-snapshot
Comparative Molecular Similarity Indices Analysis: CoMSIA
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Drug Resistance in Cancer Therapy
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Drug resistance: The clinical problem
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Molecular and Cellular Biology of Multidrug Resistance in Tumor Cells
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Characteristics of Multidrug Resistance in Human Tumor Cells
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Molecular and Clinical Advances in Anticancer Drug Resistance
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Modulators of P-glycoprotein-associated multidrug resistance
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A fast new approach to pharmacophore mapping and its application to dopaminergic and benzodiazepine agonists
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Reversal of multidrug resistance by phenothiazines and structurally related compounds
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Reversal of typical multidrug resistance by cyclosporin and its non-immunosuppressive analogue SDZ PSC 833 in Chinese hamster ovary cells expressing themdr1 phenotype
inferredcites →https://doi.org/10.1007/bf01757351openalex-snapshot
Clinical importance of P-glycoprotein-related resistance in leukemia and myelodysplastic syndromes — first experience with their reversal
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A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants
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Structural characteristics of compounds that modulate P-glycoprotein-associated multidrug resistance
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Structure–activity relationships of a series of tariquidar analogs as multidrug resistance modulators
inferredcites →https://doi.org/10.1016/s0006-2952(99)00229-4openalex-snapshot
Structure–activity relationship studies of propafenone analogs based on P-glycoprotein ATPase activity measurements
inferredcites →https://doi.org/10.1016/s0026-895x(24)12542-4openalex-snapshot
The Importance of a Nitrogen Atom in Modulators of Multidrug Resistance
inferredcites →https://doi.org/10.1016/s0026-895x(25)09013-3openalex-snapshot
Structural requirements for activity of propafenone-type modulators in P-glycoprotein-mediated multidrug resistance.
inferredcites →https://doi.org/10.1016/s0026-895x(25)10091-6openalex-snapshot
Structural features determining activity of phenothiazines and related drugs for inhibition of cell growth and reversal of multidrug resistance.
inferredcites →https://doi.org/10.1016/s0960-894x(99)00030-xopenalex-snapshot
Reversal of P-glycoprotein mediated multidrug resistance by novel anthranilamide derivatives
inferredcites →https://doi.org/10.1016/s1093-3263(01)00123-1openalex-snapshot
Beware of q2!
inferredcites →https://doi.org/10.1021/bi00165a003openalex-snapshot
Analysis of the steady-state and initial rate of doxorubicin efflux from a series of multidrug resistant cells expressing different levels of P-glycoprotein
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Atomic physicochemical parameters for three dimensional structure directed quantitative structure-activity relationships. 4. Additional parameters for hydrophobic and dispersive interactions and their application for an automated superposition of certain naturally occurring nucleoside antibiotics
inferredcites →https://doi.org/10.1021/ci00063a007openalex-snapshot
Review of ring perception algorithms for chemical graphs
inferredcites →https://doi.org/10.1021/ci0203702openalex-snapshot
On the Use of Neural Network Ensembles in QSAR and QSPR
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Compass: Predicting Biological Activities from Molecular Surface Properties. Performance Comparisons on a Steroid Benchmark
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Structure−Function Relationships of Multidrug Resistance P-Glycoprotein
inferredcites →https://doi.org/10.1021/jm970732aopenalex-snapshot
Three-Dimensional Quantitative Similarity−Activity Relationships (3D QSiAR) from SEAL Similarity Matrices
inferredcites →https://doi.org/10.1021/jm970786kopenalex-snapshot
Molecular Modeling of Phenothiazines and Related Drugs As Multidrug Resistance Modifiers: A Comparative Molecular Field Analysis Study
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Resistance to Antineoplastic Drugs
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The molecular interaction of the high affinity reversal agent XR9576 with P‐glycoprotein
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Multidrug resistance in oncology: diagnostic and therapeutic approaches
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Essential features of the P-glycoprotein pharmacophore as defined by a series of reserpine analogs that modulate multidrug resistance.
inferredcites →https://doi.org/10.1073/pnas.90.1.312openalex-snapshot
The multidrug resistance (mdr1) gene product functions as an ATP channel.
inferredcites →https://doi.org/10.1093/jnci/84.23.1811openalex-snapshot
High-Dose Oral Tamoxifen, a Potential Multidrug-Resistance-Reversal Agent: Phase I Trial in Combination With Vinblastine
inferredcites →https://doi.org/10.1093/jnci/84.23.1816openalex-snapshot
Activity of Topotecan, a New Topoisomerase I Inhibitor, Against Human Tumor Colony-Forming Units In Vitro
inferredcites →https://doi.org/10.1146/annurev.bi.58.070189.001033openalex-snapshot
THE BIOCHEMISTRY OF P-GLYCOPROTEIN-MEDIATED MULTIDRUG RESISTANCE
inferredcites →https://doi.org/10.1146/annurev.bi.62.070193.002125openalex-snapshot
BIOCHEMISTRY OF MULTIDRUG RESISTANCE MEDIATED BY THE MULTIDRUG TRANSPORTER
inferredcites →https://doi.org/10.1146/annurev.biophys.28.1.269openalex-snapshot
STRUCTURE AND CONFORMATION OF COMPLEX CARBOHYDRATES OF GLYCOPROTEINS, GLYCOLIPIDS, AND BACTERIAL POLYSACCHARIDES
inferredcites →https://doi.org/10.1172/jci112450openalex-snapshot
Cyclosporin A reverses vincristine and daunorubicin resistance in acute lymphatic leukemia in vitro.
inferredcites →https://doi.org/10.1182/blood.v80.6.1528.1528openalex-snapshot
Immunosuppressants FK506 and rapamycin function as reversal agents of the multidrug resistance phenotype
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P-glycoprotein expression in malignant lymphoma and reversal of clinical drug resistance with chemotherapy plus high-dose verapamil.
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Phase I/pharmacokinetic study of high-dose progesterone and doxorubicin.
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Phase I trial of doxorubicin with cyclosporine as a modulator of multidrug resistance.
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Comparative Molecular Field Analysis (CoMFA) and Comparative Molecular Similarity Index Analysis (CoMSIA) Study of Mutagen X

What points at this work

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

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Structure–Activity Relationships of Tariquidar Analogs as Multidrug Resistance Modulators
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Recent Studies of QSAR on Inhibitors of Estrogen Receptor and Human Eosinophil Phosphodiesterase
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