JP2015534981A5 - - Google Patents
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- JP2015534981A5 JP2015534981A5 JP2015537809A JP2015537809A JP2015534981A5 JP 2015534981 A5 JP2015534981 A5 JP 2015534981A5 JP 2015537809 A JP2015537809 A JP 2015537809A JP 2015537809 A JP2015537809 A JP 2015537809A JP 2015534981 A5 JP2015534981 A5 JP 2015534981A5
- Authority
- JP
- Japan
- Prior art keywords
- dihydropyrazino
- pyrazin
- methyl
- pyridin
- triazol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- -1 5-fluoro-2-methyl-4- (1H-1,2,4-triazol-3-yl) phenyl Chemical group 0.000 claims 31
- 102000013530 TOR Serine-Threonine Kinases Human genes 0.000 claims 27
- 108010065917 TOR Serine-Threonine Kinases Proteins 0.000 claims 27
- 206010060862 Prostate cancer Diseases 0.000 claims 23
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 23
- 238000000034 method Methods 0.000 claims 22
- 229940043355 kinase inhibitor Drugs 0.000 claims 19
- 239000003757 phosphotransferase inhibitor Substances 0.000 claims 19
- HUTNOYOBQPAKIA-UHFFFAOYSA-N 1h-pyrazin-2-one Chemical compound OC1=CN=CC=N1 HUTNOYOBQPAKIA-UHFFFAOYSA-N 0.000 claims 14
- 230000037361 pathway Effects 0.000 claims 12
- 102000038030 PI3Ks Human genes 0.000 claims 11
- 108091007960 PI3Ks Proteins 0.000 claims 11
- 102000005768 DNA-Activated Protein Kinase Human genes 0.000 claims 7
- 108010006124 DNA-Activated Protein Kinase Proteins 0.000 claims 7
- 239000012472 biological sample Substances 0.000 claims 7
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- 102100022466 Eukaryotic translation initiation factor 4E-binding protein 1 Human genes 0.000 claims 6
- 108050000946 Eukaryotic translation initiation factor 4E-binding protein 1 Proteins 0.000 claims 6
- 102000014160 PTEN Phosphohydrolase Human genes 0.000 claims 6
- 108010011536 PTEN Phosphohydrolase Proteins 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 6
- 102000052116 epidermal growth factor receptor activity proteins Human genes 0.000 claims 6
- 108700015053 epidermal growth factor receptor activity proteins Proteins 0.000 claims 6
- 230000035772 mutation Effects 0.000 claims 6
- YOHYSYJDKVYCJI-UHFFFAOYSA-N n-[3-[[6-[3-(trifluoromethyl)anilino]pyrimidin-4-yl]amino]phenyl]cyclopropanecarboxamide Chemical compound FC(F)(F)C1=CC=CC(NC=2N=CN=C(NC=3C=C(NC(=O)C4CC4)C=CC=3)C=2)=C1 YOHYSYJDKVYCJI-UHFFFAOYSA-N 0.000 claims 6
- 230000002018 overexpression Effects 0.000 claims 6
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 5
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 5
- 239000000651 prodrug Substances 0.000 claims 4
- 229940002612 prodrug Drugs 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 239000012453 solvate Substances 0.000 claims 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 3
- 230000005764 inhibitory process Effects 0.000 claims 3
- 230000027405 negative regulation of phosphorylation Effects 0.000 claims 3
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- ZRGPQVFLCQCXGM-CQSZACIVSA-N (2r)-6-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-2-methyl-4-[2-(oxan-4-yl)ethyl]-1,2-dihydropyrazino[2,3-b]pyrazin-3-one Chemical compound N([C@@H](C1=O)C)C2=NC=C(C=3C=NC(=CC=3)C(C)(C)O)N=C2N1CCC1CCOCC1 ZRGPQVFLCQCXGM-CQSZACIVSA-N 0.000 claims 1
- ZRGPQVFLCQCXGM-AWEZNQCLSA-N (2s)-6-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-2-methyl-4-[2-(oxan-4-yl)ethyl]-1,2-dihydropyrazino[2,3-b]pyrazin-3-one Chemical compound N([C@H](C1=O)C)C2=NC=C(C=3C=NC(=CC=3)C(C)(C)O)N=C2N1CCC1CCOCC1 ZRGPQVFLCQCXGM-AWEZNQCLSA-N 0.000 claims 1
- JGVQLNHQPVSEMZ-UHFFFAOYSA-N 2-(1h-imidazo[4,5-b]pyridin-6-yl)-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C12=NC(C=3C=C4NC=NC4=NC=3)=CN=C2NC(=O)CN1CCC1CCOCC1 JGVQLNHQPVSEMZ-UHFFFAOYSA-N 0.000 claims 1
- ZWGFWBUSBXEMAU-UHFFFAOYSA-N 2-(1h-indazol-5-yl)-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C12=NC(C=3C=C4C=NNC4=CC=3)=CN=C2NC(=O)CN1CCC1CCOCC1 ZWGFWBUSBXEMAU-UHFFFAOYSA-N 0.000 claims 1
- GPRUOGSZNIVNIG-UHFFFAOYSA-N 2-(1h-indazol-6-yl)-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C12=NC(C=3C=C4NN=CC4=CC=3)=CN=C2NC(=O)CN1CCC1CCOCC1 GPRUOGSZNIVNIG-UHFFFAOYSA-N 0.000 claims 1
- FLGMERISMNGPIM-UHFFFAOYSA-N 2-(1h-indol-5-yl)-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C12=NC(C=3C=C4C=CNC4=CC=3)=CN=C2NC(=O)CN1CCC1CCOCC1 FLGMERISMNGPIM-UHFFFAOYSA-N 0.000 claims 1
- UCNUXNCLAQVMMR-UHFFFAOYSA-N 2-(1h-indol-6-yl)-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C12=NC(C=3C=C4NC=CC4=CC=3)=CN=C2NC(=O)CN1CCC1CCOCC1 UCNUXNCLAQVMMR-UHFFFAOYSA-N 0.000 claims 1
- OVPLJWRLASUHJY-UHFFFAOYSA-N 2-(2-amino-7-methyl-3h-benzimidazol-5-yl)-8-[[3-(trifluoromethyl)phenyl]methyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C=1C=2N=C(N)NC=2C(C)=CC=1C(N=C12)=CN=C1NC(=O)CN2CC1=CC=CC(C(F)(F)F)=C1 OVPLJWRLASUHJY-UHFFFAOYSA-N 0.000 claims 1
- JWGOSMIWSZNTEA-UHFFFAOYSA-N 2-(7-methyl-3h-benzimidazol-5-yl)-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C=1C=2NC=NC=2C(C)=CC=1C(N=C12)=CN=C1NC(=O)CN2CCC1CCOCC1 JWGOSMIWSZNTEA-UHFFFAOYSA-N 0.000 claims 1
- UZUWXKYUGWKVFP-UHFFFAOYSA-N 2-[2-methyl-4-(1h-1,2,4-triazol-5-yl)phenyl]-7,8-dihydro-5h-pyrazino[2,3-b]pyrazin-6-one Chemical compound C=1C=C(C=2N=C3NCC(=O)NC3=NC=2)C(C)=CC=1C1=NN=CN1 UZUWXKYUGWKVFP-UHFFFAOYSA-N 0.000 claims 1
- MQKOPINQZVDCFE-UHFFFAOYSA-N 2-[2-methyl-4-(1h-1,2,4-triazol-5-yl)phenyl]-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound CC1=CC(C=2NC=NN=2)=CC=C1C(N=C12)=CN=C1NC(=O)CN2CCC1CCOCC1 MQKOPINQZVDCFE-UHFFFAOYSA-N 0.000 claims 1
- MLEUAHJZHFABNI-UHFFFAOYSA-N 2-[2-methyl-6-(1h-1,2,4-triazol-5-yl)pyridin-3-yl]-8-(oxan-4-ylmethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound CC1=NC(C=2NC=NN=2)=CC=C1C(N=C12)=CN=C1NC(=O)CN2CC1CCOCC1 MLEUAHJZHFABNI-UHFFFAOYSA-N 0.000 claims 1
- RBLRRVZXUXIHNG-UHFFFAOYSA-N 2-[2-methyl-6-(1h-1,2,4-triazol-5-yl)pyridin-3-yl]-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound CC1=NC(C=2NC=NN=2)=CC=C1C(N=C12)=CN=C1NC(=O)CN2CCC1CCOCC1 RBLRRVZXUXIHNG-UHFFFAOYSA-N 0.000 claims 1
- QSTJXBOEOLUXBG-UHFFFAOYSA-N 2-[3-fluoro-2-methyl-4-(1h-1,2,4-triazol-5-yl)phenyl]-8-(2-methoxyethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound N1=C2N(CCOC)CC(=O)NC2=NC=C1C(C(=C1F)C)=CC=C1C1=NN=CN1 QSTJXBOEOLUXBG-UHFFFAOYSA-N 0.000 claims 1
- RPFKJQXAUBYMLL-UHFFFAOYSA-N 2-[3-fluoro-2-methyl-4-(1h-1,2,4-triazol-5-yl)phenyl]-8-(oxan-4-yl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound CC1=C(F)C(C2=NNC=N2)=CC=C1C(N=C12)=CN=C1NC(=O)CN2C1CCOCC1 RPFKJQXAUBYMLL-UHFFFAOYSA-N 0.000 claims 1
- KDNANMZVIXBBHI-UHFFFAOYSA-N 2-[3-fluoro-2-methyl-4-(1h-1,2,4-triazol-5-yl)phenyl]-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound CC1=C(F)C(C=2NC=NN=2)=CC=C1C(N=C12)=CN=C1NC(=O)CN2CCC1CCOCC1 KDNANMZVIXBBHI-UHFFFAOYSA-N 0.000 claims 1
- XCAKYWRPAFRUKL-UHFFFAOYSA-N 2-[3-fluoro-4-(1h-1,2,4-triazol-5-yl)phenyl]-8-(2-methoxyethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound N1=C2N(CCOC)CC(=O)NC2=NC=C1C(C=C1F)=CC=C1C1=NN=CN1 XCAKYWRPAFRUKL-UHFFFAOYSA-N 0.000 claims 1
- VQOJDNXHKRRVKG-UHFFFAOYSA-N 2-[3-fluoro-4-(1h-1,2,4-triazol-5-yl)phenyl]-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound FC1=CC(C=2N=C3N(CCC4CCOCC4)CC(=O)NC3=NC=2)=CC=C1C1=NN=CN1 VQOJDNXHKRRVKG-UHFFFAOYSA-N 0.000 claims 1
- OSCZBKPQIHRLCX-UHFFFAOYSA-N 2-[4-(1h-1,2,4-triazol-5-yl)phenyl]-8-[[3-(trifluoromethyl)phenyl]methyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound FC(F)(F)C1=CC=CC(CN2C3=NC(=CN=C3NC(=O)C2)C=2C=CC(=CC=2)C=2NC=NN=2)=C1 OSCZBKPQIHRLCX-UHFFFAOYSA-N 0.000 claims 1
- BPXGEUALTFPZOM-UHFFFAOYSA-N 2-[4-(2-hydroxypropan-2-yl)phenyl]-8-(oxan-4-ylmethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=CC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2CC3CCOCC3)C2=N1 BPXGEUALTFPZOM-UHFFFAOYSA-N 0.000 claims 1
- NJXKFIOLXCRUCQ-UHFFFAOYSA-N 2-[4-(2-hydroxypropan-2-yl)phenyl]-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=CC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2CCC3CCOCC3)C2=N1 NJXKFIOLXCRUCQ-UHFFFAOYSA-N 0.000 claims 1
- BDYYRVQPWCHOGW-UHFFFAOYSA-N 2-[4-methyl-6-(1h-1,2,4-triazol-5-yl)pyridin-3-yl]-8-(oxan-4-ylmethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound CC1=CC(C2=NNC=N2)=NC=C1C(N=C12)=CN=C1NC(=O)CN2CC1CCOCC1 BDYYRVQPWCHOGW-UHFFFAOYSA-N 0.000 claims 1
- CKRKNYZYXVCPMX-UHFFFAOYSA-N 2-[5-fluoro-2-methyl-4-(1H-1,2,4-triazol-5-yl)phenyl]-4-propan-2-yl-1,2-dihydropyrazino[2,3-b]pyrazin-3-one Chemical compound FC=1C(=CC(=C(C1)C1NC=2C(=NC=CN2)N(C1=O)C(C)C)C)C1=NNC=N1 CKRKNYZYXVCPMX-UHFFFAOYSA-N 0.000 claims 1
- QXCHUWFFMQNYIJ-UHFFFAOYSA-N 2-[5-fluoro-2-methyl-4-(1h-1,2,4-triazol-5-yl)phenyl]-8-(2-methoxyethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound N1=C2N(CCOC)CC(=O)NC2=NC=C1C(C(=C1)C)=CC(F)=C1C=1N=CNN=1 QXCHUWFFMQNYIJ-UHFFFAOYSA-N 0.000 claims 1
- MGLOYVHEYOOETR-UHFFFAOYSA-N 2-[5-fluoro-2-methyl-4-(1h-1,2,4-triazol-5-yl)phenyl]-8-(oxan-4-yl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound FC=1C=C(C=2N=C3N(C4CCOCC4)CC(=O)NC3=NC=2)C(C)=CC=1C=1N=CNN=1 MGLOYVHEYOOETR-UHFFFAOYSA-N 0.000 claims 1
- HLKYWXBABQWMDJ-UHFFFAOYSA-N 2-[5-fluoro-2-methyl-4-(1h-1,2,4-triazol-5-yl)phenyl]-8-propan-2-yl-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound N1=C2N(C(C)C)CC(=O)NC2=NC=C1C(C(=C1)C)=CC(F)=C1C=1N=CNN=1 HLKYWXBABQWMDJ-UHFFFAOYSA-N 0.000 claims 1
- KQVBDNFZBDBYCA-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)-2-methylpyridin-3-yl]-8-(oxan-4-ylmethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound CC1=NC(C(C)(C)O)=CC=C1C1=CN=C(NC(=O)CN2CC3CCOCC3)C2=N1 KQVBDNFZBDBYCA-UHFFFAOYSA-N 0.000 claims 1
- NJPJPESOUGQOMJ-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-(2-methoxyethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound N1=C2N(CCOC)CC(=O)NC2=NC=C1C1=CC=C(C(C)(C)O)N=C1 NJPJPESOUGQOMJ-UHFFFAOYSA-N 0.000 claims 1
- TYAMMNKVQSFFRX-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-(2-methylpropyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound N1=C2N(CC(C)C)CC(=O)NC2=NC=C1C1=CC=C(C(C)(C)O)N=C1 TYAMMNKVQSFFRX-UHFFFAOYSA-N 0.000 claims 1
- GXKVTFYWASGFEH-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-(2-morpholin-4-ylethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=NC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2CCN3CCOCC3)C2=N1 GXKVTFYWASGFEH-UHFFFAOYSA-N 0.000 claims 1
- BLYAPPOKCOQUMX-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-(2-phenylethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=NC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2CCC=3C=CC=CC=3)C2=N1 BLYAPPOKCOQUMX-UHFFFAOYSA-N 0.000 claims 1
- CBIIYNCVOYUQDQ-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-(3-methoxypropyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound N1=C2N(CCCOC)CC(=O)NC2=NC=C1C1=CC=C(C(C)(C)O)N=C1 CBIIYNCVOYUQDQ-UHFFFAOYSA-N 0.000 claims 1
- IBHHJGZOOHWZKC-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-(oxan-4-yl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=NC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2C3CCOCC3)C2=N1 IBHHJGZOOHWZKC-UHFFFAOYSA-N 0.000 claims 1
- UWUPKVZQISLSSA-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-(oxan-4-ylmethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=NC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2CC3CCOCC3)C2=N1 UWUPKVZQISLSSA-UHFFFAOYSA-N 0.000 claims 1
- RRSHKGLMZARSTK-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-(oxolan-3-ylmethyl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=NC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2CC3COCC3)C2=N1 RRSHKGLMZARSTK-UHFFFAOYSA-N 0.000 claims 1
- CXWODWYNTIZYON-ZIAGYGMSSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[(1r,3r)-3-methoxycyclopentyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1[C@H](OC)CC[C@H]1N1C2=NC(C=3C=NC(=CC=3)C(C)(C)O)=CN=C2NC(=O)C1 CXWODWYNTIZYON-ZIAGYGMSSA-N 0.000 claims 1
- CXWODWYNTIZYON-KGLIPLIRSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[(1r,3s)-3-methoxycyclopentyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1[C@@H](OC)CC[C@H]1N1C2=NC(C=3C=NC(=CC=3)C(C)(C)O)=CN=C2NC(=O)C1 CXWODWYNTIZYON-KGLIPLIRSA-N 0.000 claims 1
- CXWODWYNTIZYON-UONOGXRCSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[(1s,3r)-3-methoxycyclopentyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1[C@H](OC)CC[C@@H]1N1C2=NC(C=3C=NC(=CC=3)C(C)(C)O)=CN=C2NC(=O)C1 CXWODWYNTIZYON-UONOGXRCSA-N 0.000 claims 1
- CXWODWYNTIZYON-KBPBESRZSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[(1s,3s)-3-methoxycyclopentyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1[C@@H](OC)CC[C@@H]1N1C2=NC(C=3C=NC(=CC=3)C(C)(C)O)=CN=C2NC(=O)C1 CXWODWYNTIZYON-KBPBESRZSA-N 0.000 claims 1
- TUHJKXZTDPWLDV-GFCCVEGCSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[(3r)-oxolan-3-yl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=NC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2[C@H]3COCC3)C2=N1 TUHJKXZTDPWLDV-GFCCVEGCSA-N 0.000 claims 1
- TUHJKXZTDPWLDV-LBPRGKRZSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[(3s)-oxolan-3-yl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=NC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2[C@@H]3COCC3)C2=N1 TUHJKXZTDPWLDV-LBPRGKRZSA-N 0.000 claims 1
- LRCRCWGIMZXSLR-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[2-(oxan-3-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=NC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2CCC3COCCC3)C2=N1 LRCRCWGIMZXSLR-UHFFFAOYSA-N 0.000 claims 1
- UVDSVTKKZYTBOB-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[2-(oxan-4-yl)ethyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=NC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2CCC3CCOCC3)C2=N1 UVDSVTKKZYTBOB-UHFFFAOYSA-N 0.000 claims 1
- FEXBAHRJAIMNNR-UKRRQHHQSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[[(1r,3r)-3-methoxycyclopentyl]methyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1[C@H](OC)CC[C@H]1CN1C2=NC(C=3C=NC(=CC=3)C(C)(C)O)=CN=C2NC(=O)C1 FEXBAHRJAIMNNR-UKRRQHHQSA-N 0.000 claims 1
- FEXBAHRJAIMNNR-HIFRSBDPSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[[(1r,3s)-3-methoxycyclopentyl]methyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1[C@@H](OC)CC[C@H]1CN1C2=NC(C=3C=NC(=CC=3)C(C)(C)O)=CN=C2NC(=O)C1 FEXBAHRJAIMNNR-HIFRSBDPSA-N 0.000 claims 1
- FEXBAHRJAIMNNR-DZGCQCFKSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[[(1s,3r)-3-methoxycyclopentyl]methyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1[C@H](OC)CC[C@@H]1CN1C2=NC(C=3C=NC(=CC=3)C(C)(C)O)=CN=C2NC(=O)C1 FEXBAHRJAIMNNR-DZGCQCFKSA-N 0.000 claims 1
- VGYOLLKVSKNHQS-CYBMUJFWSA-N 2-[6-(2-hydroxypropan-2-yl)pyridin-3-yl]-8-[[(2r)-oxolan-2-yl]methyl]-5,7-dihydropyrazino[2,3-b]pyrazin-6-one Chemical compound C1=NC(C(C)(O)C)=CC=C1C1=CN=C(NC(=O)CN2C[C@@H]3OCCC3)C2=N1 VGYOLLKVSKNHQS-CYBMUJFWSA-N 0.000 claims 1
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| GB0509748D0 (en) | 2005-05-13 | 2005-06-22 | Univ Glasgow | Materials and methods relating to cell based therapies |
| US20070238745A1 (en) * | 2006-04-07 | 2007-10-11 | University Of South Florida | PI3K-Akt Pathway Inhibitors |
| CA2666624C (en) | 2006-10-19 | 2015-12-29 | Signal Pharmaceuticals, Llc | Heteroaryl compounds, compositions thereof, and use thereof as protein kinase inhibitors |
| MX337906B (es) * | 2006-10-19 | 2016-03-28 | Signal Pharm Llc | Compuestos de heteroarilo, composiciones de los mismos, y su uso como inhibidores de proteina cinasas. |
| EP2349984A1 (en) * | 2008-10-17 | 2011-08-03 | Merck & Co. | Combination therapy |
| US8110578B2 (en) * | 2008-10-27 | 2012-02-07 | Signal Pharmaceuticals, Llc | Pyrazino[2,3-b]pyrazine mTOR kinase inhibitors for oncology indications and diseases associated with the mTOR/PI3K/Akt pathway |
| SG10201500511TA (en) * | 2009-10-26 | 2015-03-30 | Signal Pharm Llc | Methods Of Synthesis And Purification Of Heteroaryl Compounds |
| US20120238562A1 (en) * | 2011-03-09 | 2012-09-20 | Cedars-Sinai Medical Center | Treatment of cancer by targeting molecules that influence mst1/stk4 signaling |
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- 2013-10-17 BR BR112015008834A patent/BR112015008834A2/pt not_active Application Discontinuation
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- 2013-10-17 US US14/055,985 patent/US20140113904A1/en not_active Abandoned
- 2013-10-17 MX MX2015004874A patent/MX368407B/es active IP Right Grant
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