neratinib

Neratinib (HKI-272) (HKI-272) is an orally available, irreversible tyrosine kinase inhibitor for HER2 and EGFR (IC50: 59/92 nM), respectively.

Neratinib pyridine N-oxide is an irreversible inhibitor of the HER-2 receptor tyrosine kinase with potential antineoplastic activity.

Neratinib dimethylamine N-oxide is an irreversible inhibitor of the HER-2 receptor tyrosine kinase with potential antineoplastic activity.

Neratinib maleate monohydrate is an irreversible inhibitor of the HER-2 receptor tyrosine kinase with potential antineoplastic activity.

Neratinib impurity 13 is an impurity of Neratinib.

Neratinib Impurity 11 is a byproduct of the compound Neratinib.

Neratinib maleate (HKI-272 maleate) is an irreversible, orally active and highly selective inhibitor of HER2 and EGFR with IC50 values of 59 nM and 92 nM, respectively.Neratinib maleate has antitumor activity and can be used to treat gastrointestinal, respiratory, genitourinary, and cutaneous and musculoskeletal diseases, and can be used to study breast and prostate cancer. used in the study of breast and prostate cancer.

Neratinib-D6 is the deuterated form of Neratinib. Neratinib (T2325) (HKI-272) is an orally active, irreversible tyrosine kinase inhibitor that suppresses the activity of HER2 and EGFR, with IC50 values of 59 nM and 92 nM, respectively.

Neratinib-D6 (Standard) is a reference standard of Neratinib-D6 intended for quantitative analysis, quality control, and related biochemical research applications. Neratinib-d6 is the deuterated form of Neratinib. Neratinib (HKI-272) is an orally active, irreversible tyrosine kinase inhibitor that suppresses the activity of HER2 and EGFR, with IC50 values of 59 nM and 92 nM, respectively.

MDL-102234 is an adenosine A1 receptor antagonist.

HBY-793 is an HIV-1 proteinase inhibitor.

p53 Activator 14 (Compound 7A) is a derivative of Neratinib that can induce DNA damage and activate p53, thereby inhibiting the proliferation of various cancer cells, with an IC50 of 7.21 μM for HCT116 cells. This compound hinders adhesion, migration, and invasion of HCT116 cells, disrupts the cell cycle, and triggers apoptosis. In addition, p53 Activator 14 exhibits anti-tumor properties and inhibits angiogenesis in the chick embryo chorioallantoic membrane (CAM) model.