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

Sampling Plans01:23

Sampling Plans

244
Sampling is a crucial step in analytical chemistry, allowing researchers to collect representative data from a large population. Common sampling methods include random, judgmental, systematic, stratified, and cluster sampling.
Random sampling is a method where each member of the population has an equal chance of being selected for the sample. It involves selecting individuals randomly, often using random number generators or lottery-type methods. For example, when analyzing the properties of a...
244
Structure-Activity Relationships and Drug Design01:28

Structure-Activity Relationships and Drug Design

993
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...
993
Drug Discovery: Overview01:26

Drug Discovery: Overview

8.5K
Drug discovery is a multifaceted process involving extensive screening, testing, and optimization of lead compounds to identify potential new drugs for therapeutic use. It combines several approaches, including screening large numbers of natural products, chemical modification of known active molecules, identification of new drug targets, and rational design based on biological mechanisms and drug-receptor structure. These approaches are carried out in both academic research laboratories and...
8.5K

You might also read

Related Articles

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

Sort by
Same author

Highlights from the Windy City: Early Career Medicinal Chemists Experiences at Medicinal Chemistry Frontiers 2025.

Journal of medicinal chemistry·2026
Same author

Highlights from the Lowlands: Early Career Researchers Shine at Medicinal Chemistry Frontiers 2024.

ChemMedChem·2024
Same author

Empowering Voices: Inspiring Women in Medicinal Chemistry.

ACS medicinal chemistry letters·2024
Same author

Empowering Voices: Inspiring Women in Medicinal Chemistry.

Journal of medicinal chemistry·2024
Same author

Discovery and SAR Study of Boronic Acid-Based Selective PDE3B Inhibitors from a Novel DNA-Encoded Library.

Journal of medicinal chemistry·2024
Same author

YMCC and YSN: An Opportunity for Scientific and Cultural Exchange.

ACS medicinal chemistry letters·2023

Related Experiment Video

Updated: Aug 29, 2025

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis
09:56

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis

Published on: September 6, 2019

6.9K

Library Synthesis: Building Block Selection, Handling, and Tracking.

Katelyn J Billings1, Melissa C Grenier-Davies2

  • 1Relay Therapeutics, Cambridge, MA, USA. kbillings@relaytx.com.

Methods in Molecular Biology (Clifton, N.J.)
|September 9, 2022
PubMed
Summary
This summary is machine-generated.

Selecting and handling small molecule building blocks is key for successful DNA-encoded libraries. Proper strategies ensure high-quality hits and accurate synthesis for drug discovery.

Keywords:
2D barcoded tubesBuilding blocksDNA-encoded libraryDiversity selectionLibrary optimizationProperty filtersReactivitySmall molecules

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

2.7K
Automated Robotic Liquid Handling Assembly of Modular DNA Devices
11:22

Automated Robotic Liquid Handling Assembly of Modular DNA Devices

Published on: December 1, 2017

12.5K

Related Experiment Videos

Last Updated: Aug 29, 2025

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis
09:56

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis

Published on: September 6, 2019

6.9K
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

2.7K
Automated Robotic Liquid Handling Assembly of Modular DNA Devices
11:22

Automated Robotic Liquid Handling Assembly of Modular DNA Devices

Published on: December 1, 2017

12.5K

Area of Science:

  • Medicinal Chemistry
  • Synthetic Chemistry
  • Drug Discovery

Background:

  • DNA-encoded libraries (DELs) are powerful tools for identifying drug leads.
  • The quality of small molecule building blocks directly influences DEL screening efficiency.
  • Effective sample management is essential for subsequent synthesis and validation.

Purpose of the Study:

  • To outline strategies for selecting optimal small molecule building blocks for DELs.
  • To provide best practices for handling and tracking samples used in DEL synthesis and validation.

Main Methods:

  • Review of building block selection methodologies in DEL construction.
  • Discussion of sample handling and tracking protocols for library synthesis.
  • Guidance on ensuring synthetic map accuracy for follow-up studies.

Main Results:

  • Identification of key factors influencing building block selection for DELs.
  • Establishment of best practices for sample management in DEL workflows.
  • Emphasis on the link between building block choice, assay quality, and synthetic success.

Conclusions:

  • Strategic building block selection is paramount for high-quality DEL screening.
  • Robust sample handling and tracking are critical for efficient validation and synthesis.
  • Implementing these practices enhances the overall success rate of DNA-encoded library campaigns.