PF06463922 |PF-06463922 |Provide by DC CHEM
DC Chemicals provides PF06463922, other names: PF06463922,PF-06463922,PF 06463922, cas: 1454846-35-5. In stock.
Contact: website: www.dcchemicals.com,
sales@dcchemicals.com,order@dcchemicals.com,info@dcchemicals.com,
Tel: +86-21-58447131;Fax:+86-21-61643354；
PF06463922 is an orally available, ATP-competitive inhibitor of the receptor tyrosine kinases, anaplastic lymphoma kinase (ALK) and C-ros oncogene 1 (Ros1), with potential antineoplastic activity.
PF06463922, other names: PF06463922,PF-06463922,PF 06463922, cas: 1454846-35-5, Molecule formular: C21H19FN6O2, Molecule Weight: 406.1, Chemical name: (10R)-7-Amino-12-fluoro-2,10,16-trimethyl-15-oxo-10,15,16,17-tetrahydro-2H-8,4-(metheno)pyrazolo[4,3-h][2,5,11]-benzoxadiazacyclotetradecine-3-carbonitrile.
PF06463922 is an orally available, ATP-competitive inhibitor of the receptor tyrosine kinases, anaplastic lymphoma kinase (ALK) and C-ros oncogene 1 (Ros1), with potential antineoplastic activity. Upon administration, ALK/ROS1 inhibitor PF-06463922 binds to and inhibits both ALK and ROS1 kinases. The kinase inhibition leads to disruption of ALK- and ROS1-mediated signaling and eventually inhibits tumor cell growth in ALK- and ROS1-overexpressing tumor cells. In addition, PF-06463922 is able to cross the blood brain barrier. ALK belongs to the insulin receptor superfamily and plays an important role in nervous system development; ALK dysregulation and gene rearrangements are associated with a series of tumors. ROS1, overexpressed in certain cancer cells, plays a key role in cell growth and survival of cancer cells. For the detailed information of PF06463922, the solubility of PF06463922 in water, the solubility of PF06463922 in DMSO, the solubility of PF06463922 in PBS buffer, the animal experiment (test) of PF06463922, the cell expriment (test) of PF06463922, the in vivo, in vitro and clinical trial test of PF06463922, the EC50, IC50,and affinity,of PF06463922, Please contact DC Chemicals.
没有评论:
发表评论