Molecular Formula | C31H33N5O4.C2H6O3S |
Molar Mass | 649.75706 |
Melting Point | >233°C (dec.) |
Solubility | DMSO (Slightly), Methanol (Slightly) |
Appearance | Form Yellow solid, color Light Yellow to Yellow |
Color | Light Yellow to Yellow |
Storage Condition | -20°C Freezer |
Use | Uses Nidanib Ethylate is the salt form of Nidanib. It is a vascular kinase inhibitor for the treatment of idiopathic pulmonary fibrosis. It can also inhibit the process of angiogenesis that can be used to assist cancer treatment. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 1.539 ml | 7.695 ml | 15.39 ml |
5 mM | 0.308 ml | 1.539 ml | 3.078 ml |
10 mM | 0.154 ml | 0.77 ml | 1.539 ml |
5 mM | 0.031 ml | 0.154 ml | 0.308 ml |
overview | nidanib ethyl sulfonate is a small molecule inhibitor of multi-receptor tyrosine kinase and non-receptor tyrosine kinase. It was first approved by the U.S. FDA in 2014 and was first developed and sold by Boehringer Ingelheim. It has been approved by the US Food and Drug Administration (FDA), the European Medicines Agency (EMA) and the Agency for Medicines and Medical Devices (PMDA) for the treatment of idiopathic pulmonary fibrosis and approved by EMA for non-small cell lung cancer. |
application | nidanib ethyl sulfonate is a tyrosine kinase inhibitor that can be used as an API for the treatment of idiopathic pulmonary fibrosis (IPF). |
Use | Nidanib Ethyl Sulfonate is the salt form of Nidanib. It is a vascular kinase inhibitor for the treatment of idiopathic pulmonary fibrosis. It can also inhibit the process of angiogenesis that can be used to assist cancer treatment. |
target | TargetValue VEGFR2 (Cell-Free Assay) 13 nM VEGFR3 (Cell-Free Assay) 13 nM VEGFR1 (Cell-Free Assay) 34 nM FGFR2 (Cell-Free Assay) 37 nM PDGFRα (Cell-Free Assay) 59 nM |
Target | Value |
VEGFR2 (Cell-free assay) | 13 nM |
VEGFR3 (Cell-free assay) | 13 nM |
VEGFR1 (Cell-free assay) | 34 nM |
FGFR2 (Cell-free assay) | 37 nM |
PDGFRα (Cell-free assay) | 59 nM |
Solubility | DMSO (Slightly), Methanol (Slightly) |