3 research outputs found
Discovery of Mammalian Target of Rapamycin (mTOR) Kinase Inhibitor CC-223
We report here the synthesis and
structure–activity relationship
(SAR) of a novel series of mammalian target of rapamycin (mTOR) kinase
inhibitors. A series of 4,6- or 1,7-disubstituted-3,4-dihydropyrazino[2,3-<i>b</i>]pyrazine-2(1<i>H</i>)-ones were optimized for
in vivo efficacy. These efforts resulted in the identification of
compounds with excellent mTOR kinase inhibitory potency, with exquisite
kinase selectivity over the related lipid kinase PI3K. The improved
PK properties of this series allowed for exploration of in vivo efficacy
and ultimately the selection of CC-223 for clinical development
Discovery of Mammalian Target of Rapamycin (mTOR) Kinase Inhibitor CC-223
We report here the synthesis and
structure–activity relationship
(SAR) of a novel series of mammalian target of rapamycin (mTOR) kinase
inhibitors. A series of 4,6- or 1,7-disubstituted-3,4-dihydropyrazino[2,3-<i>b</i>]pyrazine-2(1<i>H</i>)-ones were optimized for
in vivo efficacy. These efforts resulted in the identification of
compounds with excellent mTOR kinase inhibitory potency, with exquisite
kinase selectivity over the related lipid kinase PI3K. The improved
PK properties of this series allowed for exploration of in vivo efficacy
and ultimately the selection of CC-223 for clinical development
Optimization of a Series of Triazole Containing Mammalian Target of Rapamycin (mTOR) Kinase Inhibitors and the Discovery of CC-115
We report here the
synthesis and structure–activity relationship
(SAR) of a novel series of triazole containing mammalian target of
rapamycin (mTOR) kinase inhibitors. SAR studies examining the potency,
selectivity, and PK parameters for a series of triazole containing
4,6- or 1,7-disubstituted-3,4-dihydropyrazino[2,3-<i>b</i>]pyrazine-2(1H)-ones resulted in the identification of triazole containing
mTOR kinase inhibitors with improved PK properties. Potent compounds
from this series were found to block both mTORC1(pS6) and mTORC2(pAktS473)
signaling in PC-3 cancer cells, in vitro and in vivo. When assessed
in efficacy models, analogs exhibited dose-dependent efficacy in tumor
xenograft models. This work resulted in the selection of CC-115 for
clinical development