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Skip Navigation LinksHome > Kinase Inhibitors > c-Met > Altiratinib (DCC-2701)
Altiratinib (DCC-2701)
Abstract (Ref 1): Altiratinib (DCC-2701) was designed based on the rationale of engineering a single therapeutic agent able to address multiple hallmarks of cancer. Specifically, Altiratinib inhibits not only mechanisms of tumor initiation and progression, but also drug resistance mechanisms in the tumor and microenvironment through balanced inhibition of MET, TIE2 (TEK), and VEGFR2 (KDR) kinases. This profile was achieved by optimizing binding into the switch control pocket of all three kinases, inducing type II inactive conformations. Altiratinib durably inhibits MET, both wild-type and mutated forms, in vitro and in vivo. Through its balanced inhibitory potency versus MET, TIE2, and VEGFR2, Altiratinib provides an agent that inhibits three major evasive (re)vascularization and resistance pathways (HGF, ANG, and VEGF) and blocks tumor invasion and metastasis. Altiratinib exhibits properties amenable to oral administration and exhibits substantial blood-brain barrier penetration, an attribute of significance for eventual treatment of brain cancers and brain metastases.
Catalog NO: CT-D2701
Synonym: DCC-2701
CAS NO: 1345847-93-9
Mol. Formula: C₂₆H₂₁F₃N₄O₄
MW: 510.5 (or refer to Certificate, batch-specific)
** in vivo Quality material. 99% Pure by HPLC (Attached). Hydrate, validated by a spot-on Elemental Analysis. Bulk stock. Same day shipping.