Date published: 2026-6-4

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AG 1387

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Application:
AG 1387 is An AG 555 analog with anticancer and antiviral properties
Purity:
≥98%
Molecular Weight:
448.3
Molecular Formula:
C19H17IN2O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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AG 1387 is a tyrosine kinase inhibitor that has been extensively used in scientific research to study the signaling pathways involving the epidermal growth factor receptor (EGFR). This compound is particularly notable for its selective inhibition of the EGFR tyrosine kinase, making it a powerful tool for dissecting the role of this receptor in various cellular processes. In research contexts, AG 1387 helps in elucidating the mechanism by which EGFR transduces signals into the cell. By inhibiting the tyrosine kinase activity of EGFR, AG 1387 prevents the receptor from phosphorylating downstream signaling proteins, thereby blocking the cascade of signals that lead to cell proliferation, migration, and survival. This has allowed researchers to explore the specific contributions of EGFR-mediated signaling to processes such as cell cycle progression, apoptosis, and angiogenesis in a controlled manner. Additionally, AG 1387 has been used in studies investigating the development of resistance to EGFR inhibitors. By applying this compound in various experimental models, scientists can observe how cells adapt to the blockade of EGFR signaling, which has implications for understanding the mechanisms underlying resistance in cancer cells. Furthermore, AG 1387 has been instrumental in the study of receptor dimerization and cross-talk between different receptor tyrosine kinases. Its ability to specifically target EGFR enables researchers to dissect the interactions between EGFR and other receptors, such as HER2 or MET, providing insights into how these interactions affect cellular responses.


AG 1387 References

  1. Inhibitors of tyrosine kinases in the treatment of psoriasis.  |  Ben-Bassat, H. and Klein, BY. 2000. Curr Pharm Des. 6: 933-42. PMID: 10828317
  2. Inhibitors of tyrosine kinases in the treatment of psoriasis.  |  Ben-Bassat, H. and Levitzki, A. 2000. Isr Med Assoc J. 2 Suppl: 69-73. PMID: 10909421
  3. Inhibition of murine AIDS (MAIDS) development in C57BL/6J mice by tyrphostin AG-1387.  |  Sklan, EH., et al. 2000. Virology. 278: 95-102. PMID: 11112485
  4. Revealing the mode of action of DNA topoisomerase I and its inhibitors by atomic force microscopy.  |  Argaman, M., et al. 2003. Biochem Biophys Res Commun. 301: 789-97. PMID: 12565850
  5. DNA topoisomerase I as one of the cellular targets of certain tyrphostin derivatives.  |  Bendetz-Nezer, S., et al. 2004. Mol Pharmacol. 66: 627-34. PMID: 15322255
  6. Tyrphostins. 2. Heterocyclic and alpha-substituted benzylidenemalononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2/neu tyrosine kinases.  |  Gazit, A., et al. 1991. J Med Chem. 34: 1896-907. PMID: 1676428
  7. IAP Proteins Antagonist: An Introduction and Chemistry of Smac Mimetics under Clinical Development.  |  Ali, R., et al. 2018. Curr Med Chem. 25: 3768-3795. PMID: 29532750
  8. The Immuno-Modulatory Effects of Inhibitor of Apoptosis Protein Antagonists in Cancer Immunotherapy.  |  Michie, J., et al. 2020. Cells. 9: PMID: 31947615
  9. Inhibition of topoisomerase I activity by tyrphostin derivatives, protein tyrosine kinase blockers: mechanism of action.  |  Aflalo, E., et al. 1994. Cancer Res. 54: 5138-42. PMID: 7923131
  10. The Effects of Combinations of a Green Tea Extract and an Active Ingredient Thereof, with Standard Antiretroviral Drugs on sc-1 Cells Infected with the LP-BM5 Virus.  |  Dias, Andreia Sofia Pires. 2009. University of Pretoria (South Africa).

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

AG 1387, 5 mg

sc-221219
5 mg
$120.00

AG 1387, 25 mg

sc-221219A
25 mg
$480.00