FIELD: chemistry.
SUBSTANCE: present invention relates to a novel deuterated quinazolinone compound of formula (I) or a pharmaceutically acceptable salt thereof having the properties of a PI3K inhibitor. Compounds can be used to treat or prevent diseases such as cancer, cell proliferation disorders, inflammation, infections, autoimmune diseases. In formula (I)
R1 and R2 are independently hydrogen or halogen; R3 is selected from hydrogen, deuterium, CH3, CH2D, CHD2, CD3, CH2CH3, CD2CH3, CH2CD3 and CD2CD3; each of R4, R11, R12 and R13 independently represents hydrogen or deuterium; each of R5, R6, R7, R8, R9 and R10 independently represents hydrogen; provided that at least one of the R3, R4, R11, R12 or R13 is deuterated or is deuterium.
EFFECT: deuterated compounds of the present invention have increased activity as compared to non-deuterated or compounds deuterated to other positions.
10 cl, 1 tbl, 17 ex
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