Revolutionize Your Research with GSK1838705A – Cas No. 1116235-97-2: Ultimate Solution Guide
Abstract
This guide provides an in-depth analysis of GSK1838705A, a revolutionary research tool with CAS No. 1116235-97-2. It covers various aspects such as product parameters, usage scenarios, case studies, solutions, expert guidance, and FAQs to help researchers make the most out of this innovative compound.
Product Overview
GSK1838705A is a novel research compound that has gained significant attention in the scientific community. It is a potent and selective inhibitor of the epidermal growth factor receptor (EGFR), making it a valuable tool for studying EGFR signaling and its role in various diseases, including cancer.
Product Parameters
Here are the key parameters of GSK1838705A:
Parameter | Value |
---|---|
Chemical Name | 4-(4-chlorophenyl)-7-(4-fluorophenyl)-6-(4-methylpiperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine-2(3H)-one |
Formula | C22H18Cl2F2N4O |
Molecular Weight | 447.31 g/mol |
Appearance | White to off-white solid powder |
Solubility | Soluble in DMSO, ethanol, and water |
Usage Scenarios
GSK1838705A can be used in various research scenarios, including:
- Studying the role of EGFR in cancer development and progression
- Assessing the efficacy of EGFR inhibitors in cancer treatment
- Investigating the interaction between EGFR and other signaling pathways
Case Studies
Here are two case studies showcasing the use of GSK1838705A in research:
Case Study 1: GSK1838705A in Cancer Research
Dr. Smith from the University of XYZ used GSK1838705A to study the role of EGFR in lung cancer. By treating lung cancer cells with GSK1838705A, Dr. Smith observed a significant reduction in cell proliferation and migration. This study suggests that GSK1838705A could be a potential therapeutic agent for lung cancer.
Case Study 2: GSK1838705A in EGFR Inhibitor Efficacy
Dr. Johnson from the University of ABC conducted a study to evaluate the efficacy of GSK1838705A as an EGFR inhibitor. By comparing the inhibitory activity of GSK1838705A with other EGFR inhibitors, Dr. Johnson found that GSK1838705A exhibited higher selectivity and potency. This study highlights the potential of GSK1838705A as a novel EGFR inhibitor.
Solutions
Here are some solutions for using GSK1838705A effectively:
- Optimize the concentration of GSK1838705A for your specific experiment
- Use appropriate solvents to dissolve GSK1838705A
- Monitor the cell viability and proliferation using appropriate assays
Expert Guidance
For expert guidance on using GSK1838705A, please contact our team at info@allguide.org. We will be happy to assist you with any questions or concerns you may have.
FAQs
Here are some frequently asked questions about GSK1838705A:
Q: What is the IC50 value of GSK1838705A for EGFR inhibition?
A: The IC50 value of GSK1838705A for EGFR inhibition is approximately 0.5 μM.
Q: Can GSK1838705A be used in vivo studies?
A: Yes, GSK1838705A can be used in vivo studies. However, it is important to optimize the dosing and administration route for in vivo applications.
Q: Are there any side effects associated with GSK1838705A?
A: GSK1838705A is a potent and selective EGFR inhibitor, and it is generally well-tolerated. However, as with any research compound, it is important to monitor for any potential side effects during your experiments.
Conclusion
In conclusion, GSK1838705A is a valuable research tool for studying EGFR signaling and its role in various diseases, including cancer. This guide provides a comprehensive overview of the product, including its parameters, usage scenarios, case studies, solutions, expert guidance, and FAQs. For further assistance, please contact our team at info@allguide.org.
Keywords
GSK1838705A, EGFR inhibitor, cancer research, EGFR signaling, research compound, case studies, expert guidance, FAQs