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

43.5K
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.
43.5K
Predicting Molecular Geometry02:27

Predicting Molecular Geometry

44.7K
VSEPR Theory for Determination of Electron Pair Geometries
44.7K
Mechanistic Models: Compartment Models in Algorithms for Numerical Problem Solving01:29

Mechanistic Models: Compartment Models in Algorithms for Numerical Problem Solving

282
Mechanistic models play a crucial role in algorithms for numerical problem-solving, particularly in nonlinear mixed effects modeling (NMEM). These models aim to minimize specific objective functions by evaluating various parameter estimates, leading to the development of systematic algorithms. In some cases, linearization techniques approximate the model using linear equations.
In individual population analyses, different algorithms are employed, such as Cauchy's method, which uses a...
282
Model Approaches for Pharmacokinetic Data: Distributed Parameter Models01:06

Model Approaches for Pharmacokinetic Data: Distributed Parameter Models

238
Pharmacokinetic models are mathematical constructs that represent and predict the time course of drug concentrations in the body, providing meaningful pharmacokinetic parameters. These models are categorized into compartment, physiological, and distributed parameter models.
The distributed parameter models are specifically designed to account for variations and differences in some drug classes. This model is particularly useful for assessing regional concentrations of anticancer or...
238
Molecules with Multiple Chiral Centers02:25

Molecules with Multiple Chiral Centers

14.8K
Molecules that possess multiple chiral centers can afford a large number of stereoisomers. For instance, while some molecules like 2-butanol have one chiral center, defined as a tetrahedral carbon atom with four different substituents attached, several molecules like butane-2,3-diol have multiple chiral centers. A simple formula to predict the number of stereoisomers possible for a molecule with n chiral centers is 2n. However, there can be a lower number where some of the stereoisomers are...
14.8K
Multicompartment Models: Overview01:14

Multicompartment Models: Overview

497
Multicompartment models are mathematical constructs that depict how drugs are distributed and eliminated within the body. They segment the body into several compartments, symbolizing various physiological or anatomical areas connected through drug transfer processes such as absorption, metabolism, distribution, and elimination.
These models offer a more comprehensive representation of drug behavior in the body than one-compartment models. They accommodate the complexity of drug distribution,...
497

You might also read

Related Articles

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

Sort by
Same author

Unveiling the neurotoxic mechanism of amino-functionalized graphene quantum dots: Mitophagy-driven ferroptosis underlies progressive anxiety-like behaviors.

Journal of hazardous materials·2026
Same author

Microlipophagy-mediated lipid remodeling contributes to radioresistant phenotypes in small cell lung cancer.

Archives of biochemistry and biophysics·2026
Same author

Cu(OH)<sub>2</sub> nanopesticide triggered heart failure-like pathogenesis in mice by potentially targeting mmu-miRNA-590-3p and mmu-miRNA-338-5p in Wnt/β-catenin signaling.

Particle and fibre toxicology·2026
Same author

Flexible Multimodal Neuroimaging Fusion for Alzheimer's Disease Progression Prediction.

Applications of medical artificial intelligence. AMAI (Workshop) (4th : 2024 : Taejon-si, Korea)·2026
Same author

Cu(OH)<sub>2</sub> nanopesticide induced adolescent social behavior deficits via long noncoding RNA-mediated synaptic network dysfunction.

Journal of hazardous materials·2026
Same author

Phytotoxicity of flufenoxuron in barley: Disrupted crosstalk between auxin signaling and carbon metabolism.

Ecotoxicology and environmental safety·2026
Same journal

Visual Self-Refinement for Autoregressive Models.

Findings of ACL. EMNLP. Conference on Empirical Methods in Natural Language Processing·2026
Same journal

README: Bridging Medical Jargon and Lay Understanding for Patient Education through Data-Centric NLP.

Findings of ACL. EMNLP. Conference on Empirical Methods in Natural Language Processing·2026
Same journal

MedCOD: Enhancing English-to-Spanish Medical Translation of Large Language Models Using Enriched Chain-of-Dictionary Framework.

Findings of ACL. EMNLP. Conference on Empirical Methods in Natural Language Processing·2026
Same journal

Large Language Models are In-context Teachers for Knowledge Reasoning.

Findings of ACL. EMNLP. Conference on Empirical Methods in Natural Language Processing·2026
Same journal

Using tournaments to calculate AUROC for zero-shot classification with LLMs.

Findings of ACL. EMNLP. Conference on Empirical Methods in Natural Language Processing·2026
Same journal

Multi-label Sequential Sentence Classification via Large Language Model.

Findings of ACL. EMNLP. Conference on Empirical Methods in Natural Language Processing·2026
See all related articles

Related Experiment Video

Updated: Jan 13, 2026

Interactive Molecular Model Assembly with 3D Printing
06:15

Interactive Molecular Model Assembly with 3D Printing

Published on: August 13, 2020

10.8K

Large Language Models for Controllable Multi-property Multi-objective Molecule Optimization.

Vishal Dey1, Xiao Hu1, Xia Ning1,2,3,4

  • 1Department of Computer Science and Engineering, The Ohio State University, USA.

Findings of ACL. EMNLP. Conference on Empirical Methods in Natural Language Processing
|January 6, 2026
PubMed
Summary
This summary is machine-generated.

Researchers developed GeLLM4O-Cs, a new AI model for drug design, that excels at optimizing multiple molecular properties simultaneously. This advancement addresses limitations in current methods, enabling more effective molecule optimization for pharmaceutical development.

More Related Videos

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

3.0K
Pharmacophore Modeling for Targets with Extensive Ligand Libraries: A Case Study on SARS-CoV-2 Mpro
05:50

Pharmacophore Modeling for Targets with Extensive Ligand Libraries: A Case Study on SARS-CoV-2 Mpro

Published on: September 26, 2025

1.4K

Related Experiment Videos

Last Updated: Jan 13, 2026

Interactive Molecular Model Assembly with 3D Printing
06:15

Interactive Molecular Model Assembly with 3D Printing

Published on: August 13, 2020

10.8K
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

3.0K
Pharmacophore Modeling for Targets with Extensive Ligand Libraries: A Case Study on SARS-CoV-2 Mpro
05:50

Pharmacophore Modeling for Targets with Extensive Ligand Libraries: A Case Study on SARS-CoV-2 Mpro

Published on: September 26, 2025

1.4K

Area of Science:

  • Computational chemistry
  • Artificial intelligence in drug discovery
  • Machine learning for molecular optimization

Background:

  • Real-world drug design necessitates optimizing multiple molecular properties to meet pharmaceutical standards.
  • Existing computational methods and instruction-tuned Large Language Models (LLMs) struggle with nuanced, property-specific optimization objectives.
  • This limitation hinders the practical application of AI in complex drug development scenarios.

Purpose of the Study:

  • To introduce C-MuMOInstruct, the first dataset for instruction tuning focused on multi-property optimization with explicit, property-specific goals.
  • To develop GeLLM4O-Cs, a series of instruction-tuned LLMs capable of targeted, property-specific molecular optimization.
  • To enhance the practical applicability of AI in realistic drug design workflows.

Main Methods:

  • Creation of the C-MuMOInstruct dataset, featuring property-specific objectives for multi-property optimization.
  • Development of GeLLM4O-Cs, LLMs fine-tuned using the C-MuMOInstruct dataset.
  • Experimental evaluation across 5 in-distribution and 5 out-of-distribution tasks to assess performance against baselines.

Main Results:

  • GeLLM4O-Cs demonstrated superior performance compared to strong baselines, achieving up to a 126% higher success rate in molecular optimization tasks.
  • The models exhibited strong 0-shot generalization capabilities, successfully handling novel optimization tasks and unseen instructions.
  • Consistent outperformance across diverse in-distribution and out-of-distribution test cases.

Conclusions:

  • GeLLM4O-Cs represent a significant advancement in AI-driven molecular optimization for drug design.
  • The developed models effectively address the challenge of property-specific multi-objective optimization.
  • This work paves the way for foundational LLMs capable of supporting diverse and realistic optimization objectives in pharmaceutical research.