Ic50 Value

An IC50 value is the concentration of a compound required to inhibit a biological or biochemical activity by 50%, providing a quantitative measure of potency. It is determined by exposing a target system to a range of concentrations, measuring the resulting response, and fitting the data to a concentration-response curve to identify the midpoint of inhibition. In chemistry and drug discovery, IC50 values help compare inhibitors, characterize enzyme or receptor interactions, and guide compound optimization. Because the value depends on assay conditions, including substrate concentration, incubation time, and experimental system, meaningful comparisons require standardized methods and careful interpretation.

Ic50 Value - Related Videos

Research

JoVE Journal - Immunology and Infection
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Fluorescence-based Neuraminidase Inhibition Assay to Assess the Susceptibility of Influenza Viruses to The Neuraminidase Inhibitor Class of Antivirals

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Cited by 53 •

2017

We describe the use of a phenotypic fluorescence-based neuraminidase inhibition assay to assess the susceptibility of influenza A and B viruses to the neuraminidase inhibitor class of antivirals.

Research

JoVE Journal - Cancer Research

Establishing Dual Resistance to EGFR-TKI and MET-TKI in Lung Adenocarcinoma Cells In Vitro with a 2-step Dose-escalation Procedure

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Cited by 5 •

2017

An in vitro method for establishing dual resistance to an EGFR-TKI and a MET-TKI in cancer cells is described. This method is useful for developing treatments for patients with EGFR-mutations, who exhibit disease progression despite EGFR-TKI treatment with MET-amplification. It can also be modified for inhibitors targeting other molecules.

Research

JoVE Journal - Biochemistry

Studies of Chaperone-Cochaperone Interactions using Homogenous Bead-Based Assay

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Cited by 4 •

2021

This protocol presents a technique for probing protein-protein interactions using glutathione-linked donor beads with GST-fused TPR-motif co-chaperones and acceptor beads coupled with an Hsp90-derived peptide. We have used this technique to screen small molecules to disrupt Hsp90-FKBP51 or Hsp90-FKBP52 interactions and identified potent and selective Hsp90-FKBP51 interaction inhibitors.

In Vitro Drug Screening Against All Life Cycle Stages of Trypanosoma cruzi Using Parasites Expressing β-galactosidase

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Cited by 7 •

2021

We describe a high-throughput colorimetric assay measuring β-galactosidase activity in three life cycle stages of Trypanosoma cruzi, the causative agent of Chagas disease. This assay can be used to identify trypanocidal compounds in an easy, fast, and reproducible manner.

Ookluc: A Plasmodium berghei Line for Identifying Transmission-blocking Compounds

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2025

Plasmodium sexual development occurs in the mosquito midgut. Targeting the parasite's sexual stages is a promising strategy to block transmission. We developed Ookluc, a transgenic P. berghei expressing nanoluciferase after zygote formation, enabling high-throughput screening of transmission-blocking compounds. This article details the methods for screening using Ookluc.

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