Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Molecular Models02:00

Molecular Models

44.2K
Physical models representing molecular architectures of chemical compounds play essential roles in understanding chemistry. The use of molecular models makes it easier to visualize the structures and shapes of atoms and molecules.
44.2K
Structure-Activity Relationships and Drug Design01:28

Structure-Activity Relationships and Drug Design

1.9K
Drug design is a dynamic field that involves discovering and developing new medications based on specific biological targets. This process heavily relies on structure-activity relationships (SAR) and quantitative structure-activity relationships (QSAR) to guide the design and optimization of efficient drugs.
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence...
1.9K
Molecular Shapes01:18

Molecular Shapes

62.9K
Molecules have characteristic shapes that are crucial for their function. The arrangement of various electron groups around the central atom dictates their molecular geometry. Electron pairs in the valence shell of a central atom will adopt an arrangement that minimizes repulsions between the electron pairs by maximizing the distance between them. The valence electrons form either bonding pairs, located primarily between bonded atoms, or lone pairs.
Two regions of electron density in a diatomic...
62.9K
Predicting Molecular Geometry02:27

Predicting Molecular Geometry

46.4K
VSEPR Theory for Determination of Electron Pair Geometries
46.4K
Resonance and Hybrid Structures02:16

Resonance and Hybrid Structures

27.9K
According to the theory of resonance, if two or more Lewis structures with the same arrangement of atoms can be written for a molecule, ion, or radical, the actual distribution of electrons is an average of that shown by the various Lewis structures.
Resonance Structures and Resonance Hybrids
The Lewis structure of a nitrite anion (NO2−) may actually be drawn in two different ways, distinguished by the locations of the N–O and N=O bonds.
27.9K
Quantitative Aspects of Drug-Receptor Interaction01:30

Quantitative Aspects of Drug-Receptor Interaction

2.0K
The receptor occupancy theory connects a drug's response to the number of occupied receptors. With higher drug concentrations, more receptors are occupied, leading to increased responses. The formation of drug-receptor complexes involves association and dissociation rates, which reach equilibrium when the forward and backward reactions are equal. The equilibrium association constant (Ka) and its inverse, the equilibrium dissociation constant (Kd), indicate drug affinity. Higher Ka and lower...
2.0K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Identification of TAK-756, A Potent TAK1 Inhibitor for the Treatment of Osteoarthritis through Intra-Articular Administration.

Journal of medicinal chemistry·2024
Same author

Nonclassical Zwitterions as a Design Principle to Reduce Lipophilicity without Impacting Permeability.

Journal of medicinal chemistry·2024
Same author

Reactivities of acrylamide warheads toward cysteine targets: a QM/ML approach to covalent inhibitor design.

Journal of computer-aided molecular design·2024
Same author

Quantitative and functional characterisation of extracellular vesicles after passive loading with hydrophobic or cholesterol-tagged small molecules.

Journal of controlled release : official journal of the Controlled Release Society·2023
Same author

Avoid missing pK<sub>a</sub>s: High-throughput workflow using solution pH-metric in tandem with UV-metric measurements.

Journal of pharmaceutical and biomedical analysis·2023
Same author

Lessons for Oral Bioavailability: How Conformationally Flexible Cyclic Peptides Enter and Cross Lipid Membranes.

Journal of medicinal chemistry·2023
Same journal

PACEff Builder: An Efficient Platform for Constructing PACE Hybrid-Resolution Models for Molecular Dynamics Simulations of Aqueous Protein, Peptide Assembly, and Membrane Protein Systems.

Journal of chemical information and modeling·2026
Same journal

TransKla: A Local-Global Cross-Attention Based Transformer Approach for Prediction of Lysine Lactylation Sites.

Journal of chemical information and modeling·2026
Same journal

CondenSimAdapter: A Versatile Builder for Multiscale Simulations of Protein Condensates with Broad Force-Field Compatibility and Robust Dense-Phase Relaxation.

Journal of chemical information and modeling·2026
Same journal

Simulation Guided Design of a Potentially Hyperactive Ice Nucleating Protein.

Journal of chemical information and modeling·2026
Same journal

Setting the Bases of the Photogenotoxicity of <i>p</i>-Aminobenzoic Acid.

Journal of chemical information and modeling·2026
Same journal

Probing Charge-Controlled Inter-Domain Flexibility: Integrating Experimental and Coarse-Grained Approaches.

Journal of chemical information and modeling·2026
See all related articles

Related Experiment Video

Updated: Feb 26, 2026

Curation of Computational Chemical Libraries Demonstrated with Alpha-Amino Acids
08:21

Curation of Computational Chemical Libraries Demonstrated with Alpha-Amino Acids

Published on: April 13, 2022

3.1K

Developing Collaborative QSAR Models Without Sharing Structures.

Peter Gedeck1, Suzanne Skolnik2, Stephane Rodde3

  • 1Peter Gedeck LLC , 2309 Grove Avenue, Falls Church, Virginia 22046, United States.

Journal of Chemical Information and Modeling
|July 21, 2017
PubMed
Summary
This summary is machine-generated.

Collaborative quantitative structure-activity relationship (QSAR) model development is enhanced by sharing aggregated data, not individual chemical structures. This method expands model applicability domains while protecting proprietary information.

More Related Videos

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors
10:29

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors

Published on: May 9, 2025

2.5K
In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox
05:47

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox

Published on: August 28, 2019

14.7K

Related Experiment Videos

Last Updated: Feb 26, 2026

Curation of Computational Chemical Libraries Demonstrated with Alpha-Amino Acids
08:21

Curation of Computational Chemical Libraries Demonstrated with Alpha-Amino Acids

Published on: April 13, 2022

3.1K
Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors
10:29

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors

Published on: May 9, 2025

2.5K
In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox
05:47

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox

Published on: August 28, 2019

14.7K

Area of Science:

  • cheminformatics
  • computational chemistry
  • drug discovery

Background:

  • Quantitative Structure-Activity Relationship (QSAR) models improve with more data, but predictive performance degrades when chemical structures diverge from the training set.
  • Expanding the applicability domain of QSAR models requires increasing the diversity of training data, often by combining diverse data sources.
  • Integrating proprietary data into QSAR model development is challenging due to intellectual property concerns and the need to protect confidential structural information.

Purpose of the Study:

  • To present a novel method for collaborative development of linear regression QSAR models.
  • To address the challenge of incorporating diverse datasets, including proprietary data, into QSAR model development.
  • To enable the creation of QSAR models with expanded applicability domains without compromising data confidentiality.

Main Methods:

  • Development of a collaborative linear regression modeling approach.
  • Utilizing aggregated data sharing to prevent disclosure of individual data points and confidential structural information.
  • Comparing models developed through collaborative aggregated data sharing with those built using combined datasets.

Main Results:

  • The proposed method allows for the collaborative development of QSAR models using aggregated data.
  • Confidential structural information is protected by not sharing individual data points.
  • The final QSAR models developed through this collaborative approach are equivalent in performance to models built with directly combined datasets.

Conclusions:

  • Collaborative QSAR model development can be effectively achieved by sharing data in an aggregated form.
  • This approach successfully expands the applicability domain of QSAR models while safeguarding proprietary information.
  • The method offers a viable solution for integrating diverse data sources in a privacy-preserving manner for improved QSAR modeling.