Description
An inhibitor of PI3Kδ (IC50 = 0.011 µM); selective for PI3Kδ over PI3Kα, PI3Kβ, and PI3Kγ (IC50s = 0.244, 0.424, and 2.23 µM, respectively); inhibits phosphorylation of Akt in Rat-1 fibroblasts expressing P13K p110δ (IC50 = 0.056 µM); inhibits the MLR in isolated human PBMCs and isolated mouse splenocytes (IC50s = 0.079 and 0.033 µM, respectively); reduces the production of rat anti-rat collagen antibodies, as well as reduces paw swelling and joint erosion in a rat model of collagen-induced arthritis at 3 and 10 mg/kg
Formal name: 1-[(3S)-3-[[5,6,7,8-tetrahydro-6-[6-methoxy-5-(trifluoromethyl)-3-pyridinyl]pyrido[4,3-d]pyrimidin-4-yl]amino]-1-pyrrolidinyl]-1-propanone
Synonyms: CDZ 173
Molecular weight: 450.5
CAS: 1354690-24-6
Purity: ≥98% (mixture of rotamers)
Formulation: A crystalline solid
Product Type|Biochemicals|Kinase Inhibitors|PI3K||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Research Area|Immunology & Inflammation|Adaptive Immunity||Research Area|Immunology & Inflammation|Autoimmunity|Rheumatoid Arthritis||Research Area|Immunology & Inflammation|Innate Immunity