TW202016102A - Erk抑制劑及其應用 - Google Patents
Erk抑制劑及其應用 Download PDFInfo
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- TW202016102A TW202016102A TW108119658A TW108119658A TW202016102A TW 202016102 A TW202016102 A TW 202016102A TW 108119658 A TW108119658 A TW 108119658A TW 108119658 A TW108119658 A TW 108119658A TW 202016102 A TW202016102 A TW 202016102A
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- Taiwan
- Prior art keywords
- hydroxymethyl
- benzyl
- fluoro
- pyridin
- pyrazine
- Prior art date
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
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- FZGAVPAHNQGDCT-JOCHJYFZSA-N (3R)-7-[5-chloro-2-(cyclopentylamino)pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1CCCC1)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 FZGAVPAHNQGDCT-JOCHJYFZSA-N 0.000 claims description 2
- KJDANSHIIORTDQ-HXUWFJFHSA-N (3R)-7-[5-chloro-2-(cyclopropylamino)pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1CC1)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 KJDANSHIIORTDQ-HXUWFJFHSA-N 0.000 claims description 2
- VMEQMKKLHWYOPQ-GOSISDBHSA-N (3R)-7-[5-chloro-2-(ethylamino)pyrimidin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=NC(=NC=1)NCC)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 VMEQMKKLHWYOPQ-GOSISDBHSA-N 0.000 claims description 2
- CCKFOKDZEUOBJZ-HXUWFJFHSA-N (3R)-7-[5-chloro-2-(oxetan-3-ylamino)pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1COC1)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 CCKFOKDZEUOBJZ-HXUWFJFHSA-N 0.000 claims description 2
- OAJFKSWENFVEPU-BPGUCPLFSA-N (3R)-7-[5-chloro-2-(oxolan-3-ylamino)pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1COCC1)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 OAJFKSWENFVEPU-BPGUCPLFSA-N 0.000 claims description 2
- JIOJEFNDCGLQEY-LJQANCHMSA-N (3R)-7-[5-chloro-2-(propan-2-ylamino)pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(hydroxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC(C)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)CO)C=1 JIOJEFNDCGLQEY-LJQANCHMSA-N 0.000 claims description 2
- PLAYZCWFHSPTTP-HXUWFJFHSA-N (3R)-7-[5-chloro-2-(propan-2-ylamino)pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC(C)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 PLAYZCWFHSPTTP-HXUWFJFHSA-N 0.000 claims description 2
- FXEAGPGQXCEWPE-OAQYLSRUSA-N (3R)-7-[5-chloro-2-[(1,3-dimethylpyrazol-4-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC=1C(=NN(C=1)C)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 FXEAGPGQXCEWPE-OAQYLSRUSA-N 0.000 claims description 2
- LICSMKNAGKPUHD-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[(1-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=NN(C=C1)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 LICSMKNAGKPUHD-HXUWFJFHSA-N 0.000 claims description 2
- UYWAAXHGANOEJC-OAQYLSRUSA-N (3R)-7-[5-chloro-2-[(1-methylpyrazol-4-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC=1C=NN(C=1)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 UYWAAXHGANOEJC-OAQYLSRUSA-N 0.000 claims description 2
- UYBPVAABZNWRLU-OZAIVSQSSA-N (3R)-7-[5-chloro-2-[(2,2-dimethyloxan-4-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1CC(OCC1)(C)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 UYBPVAABZNWRLU-OZAIVSQSSA-N 0.000 claims description 2
- HVCNUSNKWWXILG-OAQYLSRUSA-N (3R)-7-[5-chloro-2-[(2,4-dimethylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC1)NC1=C(C=NN1C)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C1 HVCNUSNKWWXILG-OAQYLSRUSA-N 0.000 claims description 2
- NCDUEFINTCOUKL-OAQYLSRUSA-N (3R)-7-[5-chloro-2-[(2,5-dimethylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC(=NN1C)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 NCDUEFINTCOUKL-OAQYLSRUSA-N 0.000 claims description 2
- SMRYIVDMPNLCRQ-OAQYLSRUSA-N (3R)-7-[5-chloro-2-[(2-ethylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1CC)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 SMRYIVDMPNLCRQ-OAQYLSRUSA-N 0.000 claims description 2
- FORVWEKAPJTVOU-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[(2-hydroxy-2-methylpropyl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NCC(C)(C)O)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 FORVWEKAPJTVOU-HXUWFJFHSA-N 0.000 claims description 2
- JCFHXZTXXXRBSS-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[2-(hydroxymethyl)-5-(trifluoromethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)C(F)(F)F)CO)COC)C=1 JCFHXZTXXXRBSS-HXUWFJFHSA-N 0.000 claims description 2
- PICKIPIGQNAXDK-GOSISDBHSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[2-(hydroxymethyl)pyridin-3-yl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC=2C(=NC=CC=2)CO)COC)C=1 PICKIPIGQNAXDK-GOSISDBHSA-N 0.000 claims description 2
- ZJEOAIMPOFYFBG-LJQANCHMSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[3-(hydroxymethyl)-6-methylpyridin-2-yl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC2=NC(=CC=C2CO)C)COC)C=1 ZJEOAIMPOFYFBG-LJQANCHMSA-N 0.000 claims description 2
- NLZURUQLYUCEPB-GOSISDBHSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[3-(hydroxymethyl)pyridin-2-yl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC2=NC=CC=C2CO)COC)C=1 NLZURUQLYUCEPB-GOSISDBHSA-N 0.000 claims description 2
- DOVMKYJLEUADLC-GOSISDBHSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[3-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C(=CC=C2)F)CO)COC)C=1 DOVMKYJLEUADLC-GOSISDBHSA-N 0.000 claims description 2
- ARBRYQCJXZIHRO-GOSISDBHSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[4,5-difluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=C(C(=C2)F)F)CO)COC)C=1 ARBRYQCJXZIHRO-GOSISDBHSA-N 0.000 claims description 2
- KNJQXNFYCBAEJL-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[4-(hydroxymethyl)-6-methylpyridin-3-yl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC=2C=NC(=CC=2CO)C)COC)C=1 KNJQXNFYCBAEJL-HXUWFJFHSA-N 0.000 claims description 2
- WQGAMTOOAXOVOE-LJQANCHMSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[4-(hydroxymethyl)pyridin-3-yl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC=2C=NC=CC=2CO)COC)C=1 WQGAMTOOAXOVOE-LJQANCHMSA-N 0.000 claims description 2
- GODHMEGEWDPFFA-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[4-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=C(C=C2)F)CO)COC)C=1 GODHMEGEWDPFFA-HXUWFJFHSA-N 0.000 claims description 2
- ABOVXFVSCYDMKL-OAQYLSRUSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COCOC)C1 ABOVXFVSCYDMKL-OAQYLSRUSA-N 0.000 claims description 2
- DKWOVXTXRBJLJJ-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 DKWOVXTXRBJLJJ-HXUWFJFHSA-N 0.000 claims description 2
- VZUOAYWGBQTYFZ-MRXNPFEDSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)amino]pyridin-4-yl]-3-(methoxymethyl)-2-[[3,4,5-trifluoro-2-(hydroxymethyl)phenyl]methyl]-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C(=C(C(=C2)F)F)F)CO)COC)C=1 VZUOAYWGBQTYFZ-MRXNPFEDSA-N 0.000 claims description 2
- HKGLQGJQNGKOPI-JOCHJYFZSA-N (3R)-7-[5-chloro-2-[(2-methylpyrazol-3-yl)methylamino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NCC1=CC=NN1C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 HKGLQGJQNGKOPI-JOCHJYFZSA-N 0.000 claims description 2
- LFSBDBPBQPEWBW-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[(3,3-difluorocyclobutyl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1CC(C1)(F)F)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 LFSBDBPBQPEWBW-HXUWFJFHSA-N 0.000 claims description 2
- MBNPXJLEXLEANP-OAQYLSRUSA-N (3R)-7-[5-chloro-2-[(3,5-dimethyl-1,2-oxazol-4-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC=1C(=NOC=1C)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 MBNPXJLEXLEANP-OAQYLSRUSA-N 0.000 claims description 2
- YSNRRYNTFFCTAB-OAQYLSRUSA-N (3R)-7-[5-chloro-2-[(4,5-dimethyl-1,3-thiazol-2-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC=1SC(=C(N=1)C)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 YSNRRYNTFFCTAB-OAQYLSRUSA-N 0.000 claims description 2
- GBOOQVVMDOMCCL-LJQANCHMSA-N (3R)-7-[5-chloro-2-[(4-fluoro-2-methylpyrazol-3-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound CN1C(=C(C=N1)F)NC2=NC=C(C(=C2)C3=CN4C[C@@H](N(C(=O)C4=C3)CC5=C(C=CC(=C5)F)CO)COC)Cl GBOOQVVMDOMCCL-LJQANCHMSA-N 0.000 claims description 2
- DBJCABXBSDNPGJ-NSQNTRMNSA-N (3R)-7-[5-chloro-2-[(4-methoxycyclohexyl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1CCC(CC1)OC)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 DBJCABXBSDNPGJ-NSQNTRMNSA-N 0.000 claims description 2
- RCWUJKAFOWTMLK-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[(4-methyl-1,3-thiazol-2-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC=1SC=C(N=1)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 RCWUJKAFOWTMLK-HXUWFJFHSA-N 0.000 claims description 2
- XJKDLBVYESNWKQ-JOCHJYFZSA-N (3R)-7-[5-chloro-2-[(4-methyloxan-4-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1(CCOCC1)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 XJKDLBVYESNWKQ-JOCHJYFZSA-N 0.000 claims description 2
- MERVJTLFHZKDNV-FOIFJWKZSA-N (3R)-7-[5-chloro-2-[(5,5-dimethyloxolan-3-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1COC(C1)(C)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 MERVJTLFHZKDNV-FOIFJWKZSA-N 0.000 claims description 2
- UWPKHWHCENPSOP-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[(5-methyl-1,3-thiazol-2-yl)amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC=1SC(=CN=1)C)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 UWPKHWHCENPSOP-HXUWFJFHSA-N 0.000 claims description 2
- IPPSDWAUNBGABK-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[[1-(2,2-difluoroethyl)pyrazol-3-yl]amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=NN(C=C1)CC(F)F)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 IPPSDWAUNBGABK-HXUWFJFHSA-N 0.000 claims description 2
- YVGMGYQGQHYGKN-HXUWFJFHSA-N (3R)-7-[5-chloro-2-[[2-(2,2-difluoroethyl)pyrazol-3-yl]amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC=1)NC1=CC=NN1CC(F)F)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 YVGMGYQGQHYGKN-HXUWFJFHSA-N 0.000 claims description 2
- OYPBURQKKKNBJC-LJQANCHMSA-N (3R)-7-[5-chloro-2-[[2-(difluoromethyl)pyrazol-3-yl]amino]pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=CC(=NC1)NC1=CC=NN1C(F)F)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C1 OYPBURQKKKNBJC-LJQANCHMSA-N 0.000 claims description 2
- FCXRXXZFYHPPQT-LJQANCHMSA-N (3R)-7-[5-chloro-3-fluoro-2-(propan-2-ylamino)pyridin-4-yl]-2-[[5-fluoro-2-(hydroxymethyl)phenyl]methyl]-3-(methoxymethyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1-one Chemical compound ClC=1C(=C(C(=NC=1)NC(C)C)F)C=1C=C2N(C[C@@H](N(C2=O)CC2=C(C=CC(=C2)F)CO)COC)C=1 FCXRXXZFYHPPQT-LJQANCHMSA-N 0.000 claims description 2
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- 230000001629 suppression Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
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- 235000012222 talc Nutrition 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- GAXAFYOXCGGDFH-UHFFFAOYSA-N tert-butyl 3,3-bis(hydroxymethyl)azetidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CC(CO)(CO)C1 GAXAFYOXCGGDFH-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
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- 150000003536 tetrazoles Chemical class 0.000 description 1
- 229960004559 theobromine Drugs 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 description 1
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 238000013271 transdermal drug delivery Methods 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 description 1
- 229960000281 trometamol Drugs 0.000 description 1
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- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/12—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains three hetero rings
- C07D493/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| WOPCT/CN2018/090385 | 2018-06-08 | ||
| CN2018090385 | 2018-06-08 | ||
| WOPCT/CN2018/120975 | 2018-12-13 | ||
| CN2018120975 | 2018-12-13 |
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| TW202016102A true TW202016102A (zh) | 2020-05-01 |
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| TW108119658A TW202016102A (zh) | 2018-06-08 | 2019-06-06 | Erk抑制劑及其應用 |
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| US (1) | US11466013B2 (https=) |
| EP (1) | EP3805217A4 (https=) |
| JP (1) | JP2021525783A (https=) |
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| IL (1) | IL279276A (https=) |
| SG (1) | SG11202012241RA (https=) |
| TW (1) | TW202016102A (https=) |
| WO (1) | WO2019233457A1 (https=) |
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| WO2021110169A1 (zh) * | 2019-12-06 | 2021-06-10 | 南京明德新药研发有限公司 | 作为erk抑制剂的噻唑并内酰胺类化合物及其应用 |
| WO2022253186A1 (zh) * | 2021-06-02 | 2022-12-08 | 南京明德新药研发有限公司 | 一种二甲基取代的噻唑并吡咯酮类化合物的晶型及其制备方法 |
| WO2022268065A1 (en) * | 2021-06-22 | 2022-12-29 | Fochon Biosciences, Ltd. | Compounds as erk inhibitors |
| US20240270743A1 (en) * | 2021-08-11 | 2024-08-15 | Landos Biopharma, Inc. | Tetrahydropyrazolopyridine-analog ligands of nlrx1 and uses thereof |
| WO2024218632A1 (en) * | 2023-04-17 | 2024-10-24 | Array Biopharma Inc. | Erk protein kinase inhibitors |
| AU2024265078A1 (en) | 2023-05-04 | 2025-12-11 | Revolution Medicines, Inc. | Combination therapy for a ras related disease or disorder |
| IL326136A (en) | 2023-08-07 | 2026-03-01 | Revolution Medicines Inc | RMC-6291 for use in the treatment of a disease or disorder associated with the RAS protein |
| CN117209485A (zh) * | 2023-08-31 | 2023-12-12 | 四川大学华西医院 | 一种具有抗肿瘤活性的嘧啶骨架类化合物及其制备方法和应用 |
| US20250154171A1 (en) | 2023-10-12 | 2025-05-15 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025240847A1 (en) | 2024-05-17 | 2025-11-20 | Revolution Medicines, Inc. | Ras inhibitors |
| US20250375445A1 (en) | 2024-06-07 | 2025-12-11 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| WO2025265060A1 (en) | 2024-06-21 | 2025-12-26 | Revolution Medicines, Inc. | Therapeutic compositions and methods for managing treatment-related effects |
| WO2026006747A1 (en) | 2024-06-28 | 2026-01-02 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2026015825A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Use of ras inhibitor for treating pancreatic cancer |
| WO2026015796A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015801A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015790A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026050446A1 (en) | 2024-08-29 | 2026-03-05 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2026072904A2 (en) | 2024-09-26 | 2026-04-02 | Revolution Medicines, Inc. | Compositions and methods for treating lung cancer |
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| HUP0202332A2 (en) * | 2000-02-05 | 2002-10-28 | Vertex Pharma | Pyrazole compositions useful as inhibitors of erk |
| GB0614070D0 (en) * | 2006-07-14 | 2006-08-23 | Glaxo Group Ltd | Compounds |
| JP2011511756A (ja) * | 2007-08-02 | 2011-04-14 | ナームローゼ・フエンノートチヤツプ・オルガノン | Trpv1モジュレータとしての5−フェニル−イソオキサゾール−3−カルボキサミド誘導体 |
| WO2016026078A1 (en) | 2014-08-19 | 2016-02-25 | Changzhou Jiekai Pharmatech Co., Ltd. | Heterocyclic compounds as erk inhibitors |
| WO2016205418A1 (en) | 2015-06-15 | 2016-12-22 | Asana Biosciences, Llc | Heterocyclic inhibitors of erk1 and erk2 and their use in the treatment of cancer |
| WO2017080980A1 (en) * | 2015-11-09 | 2017-05-18 | Astrazeneca Ab | Dihydropyrrolopyrazinone derivatives useful in the treatment of cancer |
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