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Comparative molecular field analysis of non-steroidal aromatase inhibitors related to fadrozole

https://doi.org/10.1007/bf00124467
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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/jcc.540100804openalex-snapshot
Validation of the general purpose tripos 5.2 force field
inferredcites →https://doi.org/10.1002/qsar.2660110403openalex-snapshot
Study of Benzodiazepines Receptor Sites Using a Combined QSAR‐CoMFA Approach
inferredcites →https://doi.org/10.1016/0040-4020(80)80168-2openalex-snapshot
Iterative partial equalization of orbital electronegativity—a rapid access to atomic charges
inferredcites →https://doi.org/10.1016/0960-0760(93)90243-popenalex-snapshot
A detailed molecular model for human aromatase
inferredcites →https://doi.org/10.1016/0960-0760(93)90245-ropenalex-snapshot
Structure-activity relationships and binding model of novel aromatase inhibitors
inferredcites →https://doi.org/10.1016/s0021-9258(17)32197-xopenalex-snapshot
Mutagenesis study at a postulated hydrophobic region near the active site of aromatase cytochrome P450.
inferredcites →https://doi.org/10.1016/s0021-9258(18)99048-4openalex-snapshot
Structure-function relationships of human aromatase cytochrome P-450 using molecular modeling and site-directed mutagenesis
inferredcites →https://doi.org/10.1021/ci00021a029openalex-snapshot
Molecular Shape and QSAR Analyses of a Family of Substituted Dichlorodiphenyl Aromatase Inhibitors
inferredcites →https://doi.org/10.1021/ja00226a005openalex-snapshot
Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins
inferredcites →https://doi.org/10.1021/ja00244a051openalex-snapshot
Stochastic exploration of molecular mechanics energy surfaces. Hunting for the global minimum
inferredcites →https://doi.org/10.1021/ja00299a024openalex-snapshot
Development and use of quantum mechanical molecular models. 76. AM1: a new general purpose quantum mechanical molecular model
inferredcites →https://doi.org/10.1021/jm00062a012openalex-snapshot
Aromatase inhibitors: synthesis, biological activity, and binding mode of azole-type compounds
inferredcites →https://doi.org/10.1021/jm00106a038openalex-snapshot
Fadrozole hydrochloride: a potent, selective, nonsteroidal inhibitor of aromatase for the treatment of estrogen-dependent disease
inferredcites →https://doi.org/10.1021/jm00173a001openalex-snapshot
Mechanism and inhibition of cytochrome P-450 aromatase
inferredcites →https://doi.org/10.3109/14756369109069065openalex-snapshot
Structure-Activity Studies of Non-Steroidal Aromatase Inhibitors: The Crystal and Molecular Structures of CGS 16949A and CGS 18320B

What points at this work

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

inferred← citeshttps://doi.org/10.1002/cem.2524openalex-snapshot
Genetic algorithm for CoMFA setting optimization: 3D‐QSAR study on α‐aminosuberic acid derivatives as anti‐cancer compounds
inferred← citeshttps://doi.org/10.1002/jcc.21528openalex-snapshot
Modeling of diarylalkyl‐imidazole and diarylalkyl‐triazole derivatives as potent aromatase inhibitors for treatment of hormone‐dependent cancer
inferred← citeshttps://doi.org/10.1002/jccs.201200459openalex-snapshot
Virtual Screening: Using Molecular Docking and 3D‐QSAR Analysis of Matrix Metalloproteinase Inhibitors
inferred← citeshttps://doi.org/10.1002/med.10010openalex-snapshot
Nonsteroidal aromatase inhibitors: Recent advances
inferred← citeshttps://doi.org/10.1007/0-306-46858-1_15openalex-snapshot
Building a Bridge between G-Protein-Coupled Receptor Modelling, Protein Crystallography and 3D QSAR Studies for Ligand Design
inferred← citeshttps://doi.org/10.1007/s00216-010-3959-2openalex-snapshot
Circular dichroism in drug discovery and development: an abridged review
inferred← citeshttps://doi.org/10.1016/j.ejmech.2009.12.063openalex-snapshot
A comparison of different electrostatic potentials on prediction accuracy in CoMFA and CoMSIA studies
inferred← citeshttps://doi.org/10.1016/j.ejmech.2010.06.033openalex-snapshot
Exploring benzcyclo derivatives as potent aromatase inhibitors using ligand-based modeling studies
inferred← citeshttps://doi.org/10.1016/s0169-409x(02)00009-1openalex-snapshot
Pharmacophore modeling of cytochromes P450
inferred← citeshttps://doi.org/10.1016/s0303-7207(01)00433-6openalex-snapshot
Aromatase inhibitors: past, present and future
inferred← citeshttps://doi.org/10.1016/s0968-0896(00)00203-0openalex-snapshot
Linking CoMFA and protein homology models of enzyme–inhibitor interactions: an application to non-steroidal aromatase inhibitors
inferred← citeshttps://doi.org/10.1016/s0968-0896(97)10053-0openalex-snapshot
Comparative molecular field analysis of non-steroidal aromatase inhibitors: an extended model for two different structural classes
inferred← citeshttps://doi.org/10.1021/ci049612jopenalex-snapshot
Improved CoMFA Modeling by Optimization of Settings
inferred← citeshttps://doi.org/10.1021/ci800390mopenalex-snapshot
Partial Charge Calculation Method Affects CoMFA QSAR Prediction Accuracy
inferred← citeshttps://doi.org/10.1021/jm000955sopenalex-snapshot
A New Class of Nonsteroidal Aromatase Inhibitors: Design and Synthesis of Chromone and Xanthone Derivatives and Inhibition of the P450 Enzymes Aromatase and 17α-Hydroxylase/C17,20-Lyase
inferred← citeshttps://doi.org/10.1021/jm0510676openalex-snapshot
Synthesis and Biological Activity of 7-Phenyl-6,9-dihydro-3H-pyrrolo[3,2-f]quinolin-9-ones: A New Class of Antimitotic Agents Devoid of Aromatase Activity
inferred← citeshttps://doi.org/10.1021/jm058042ropenalex-snapshot
Enantioselective Nonsteroidal Aromatase Inhibitors Identified through a Multidisciplinary Medicinal Chemistry Approach
inferred← citeshttps://doi.org/10.1021/jm060186yopenalex-snapshot
Lead Optimization Providing a Series of Flavone Derivatives as Potent Nonsteroidal Inhibitors of the Cytochrome P450 Aromatase Enzyme
inferred← citeshttps://doi.org/10.1023/a:1007919704457openalex-snapshot
Molecular modeling of the intestinal bile acid carrier: a comparative molecular field analysis study.
inferred← citeshttps://doi.org/10.1023/a:1017015028419openalex-snapshot
List of CoMFA references, 1993-1996
inferred← citeshttps://doi.org/10.1023/a:1017058710672openalex-snapshot
Building a bridge between G-protein-coupled receptor modelling, protein crystallography and 3D QSAR studies for ligand design
inferred← citeshttps://doi.org/10.1080/10629360903438347openalex-snapshot
Mechanism-based categorization of aromatase inhibitors: a potential discovery and screening tool
inferred← citeshttps://doi.org/10.1080/17460441.2019.1646245openalex-snapshot
Recent advances in computational design of potent aromatase inhibitors: open-eye on endocrine-resistant breast cancers
inferred← citeshttps://doi.org/10.1517/17460441.2013.768983openalex-snapshot
Computational methods for the design of potent aromatase inhibitors
inferred← citeshttps://doi.org/10.15272/ajbps.v3i27.421openalex-snapshot
Molecular Modelling Studies on Chemometric Properties of Protein Tyrosine Kinase Inhibitors for Indolinone Derivatives
inferred← citeshttps://doi.org/10.17179/excli2018-1417openalex-snapshot
Towards understanding aromatase inhibitory activity via QSAR modeling
inferred← citeshttps://doi.org/10.1897/01-171openalex-snapshot
Quantitative structure-activity relationship methods: Perspectives on drug discovery and toxicology
inferred← citeshttps://doi.org/10.4018/978-1-4666-8136-1.ch011openalex-snapshot
Ligand- and Structure-Based Drug Design of Non-Steroidal Aromatase Inhibitors (NSAIs) in Breast Cancer
inferred← citeshttps://doi.org/10.4018/978-1-5225-0549-5.ch004openalex-snapshot
Ligand- and Structure-Based Drug Design of Non-Steroidal Aromatase Inhibitors (NSAIs) in Breast Cancer
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