HRP20250088T1 - Derivati piridazin-3(2h)-ona spojeni s azolom - Google Patents
Derivati piridazin-3(2h)-ona spojeni s azolom Download PDFInfo
- Publication number
- HRP20250088T1 HRP20250088T1 HRP20250088TT HRP20250088T HRP20250088T1 HR P20250088 T1 HRP20250088 T1 HR P20250088T1 HR P20250088T T HRP20250088T T HR P20250088TT HR P20250088 T HRP20250088 T HR P20250088T HR P20250088 T1 HRP20250088 T1 HR P20250088T1
- Authority
- HR
- Croatia
- Prior art keywords
- dihydro
- pyridazin
- acetamide
- oxo
- ethyl
- Prior art date
Links
- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical class OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 33
- 150000003839 salts Chemical class 0.000 claims 29
- 125000005843 halogen group Chemical group 0.000 claims 18
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 12
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 10
- 239000001257 hydrogen Substances 0.000 claims 10
- 125000001424 substituent group Chemical group 0.000 claims 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 7
- 229910052757 nitrogen Inorganic materials 0.000 claims 7
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 3
- -1 cyano, hydroxy Chemical group 0.000 claims 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- 208000011117 substance-related disease Diseases 0.000 claims 3
- YKUSWSIQEAESMZ-AWEZNQCLSA-N C(C)(C)N1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C Chemical compound C(C)(C)N1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C YKUSWSIQEAESMZ-AWEZNQCLSA-N 0.000 claims 2
- GIZXIFZVUQNKDE-NSHDSACASA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C GIZXIFZVUQNKDE-NSHDSACASA-N 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 208000035475 disorder Diseases 0.000 claims 2
- 206010013663 drug dependence Diseases 0.000 claims 2
- 125000004941 pyridazin-5-yl group Chemical group N1=NC=CC(=C1)* 0.000 claims 2
- 125000004942 pyridazin-6-yl group Chemical group N1=NC=CC=C1* 0.000 claims 2
- 125000006413 ring segment Chemical group 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 208000019901 Anxiety disease Diseases 0.000 claims 1
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims 1
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims 1
- 208000020925 Bipolar disease Diseases 0.000 claims 1
- PEAMVILVBHOPID-LBPRGKRZSA-N C(C)(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound C(C)(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C PEAMVILVBHOPID-LBPRGKRZSA-N 0.000 claims 1
- FNKKZQSNPGOFLW-AWEZNQCLSA-N C(C)(C)(C)N1N=CC2=C1C(N(N=C2C(C)C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O Chemical compound C(C)(C)(C)N1N=CC2=C1C(N(N=C2C(C)C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O FNKKZQSNPGOFLW-AWEZNQCLSA-N 0.000 claims 1
- QVPMMYUJZNBPJJ-INIZCTEOSA-N C(C)(C)(C)N1N=CC2=C1C(N(N=C2C(C)C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O Chemical compound C(C)(C)(C)N1N=CC2=C1C(N(N=C2C(C)C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O QVPMMYUJZNBPJJ-INIZCTEOSA-N 0.000 claims 1
- WEVOIXISTDAPEE-ZDUSSCGKSA-N C(C)(C)(C)N1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)=O Chemical compound C(C)(C)(C)N1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)=O WEVOIXISTDAPEE-ZDUSSCGKSA-N 0.000 claims 1
- XWFSLJIIGDGZDY-LBPRGKRZSA-N C(C)(C)(C)N1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O Chemical compound C(C)(C)(C)N1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O XWFSLJIIGDGZDY-LBPRGKRZSA-N 0.000 claims 1
- KMFQUVRHTYXUOO-AWEZNQCLSA-N C(C)(C)(C)N1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O Chemical compound C(C)(C)(C)N1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O KMFQUVRHTYXUOO-AWEZNQCLSA-N 0.000 claims 1
- YKWZDXKULGTLGO-LBPRGKRZSA-N C(C)(C)(C)N1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)=O Chemical compound C(C)(C)(C)N1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)=O YKWZDXKULGTLGO-LBPRGKRZSA-N 0.000 claims 1
- XZZJCAKXWZSOPJ-ZDUSSCGKSA-N C(C)(C)(C)N1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)=O Chemical compound C(C)(C)(C)N1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)=O XZZJCAKXWZSOPJ-ZDUSSCGKSA-N 0.000 claims 1
- QXKVTERQQUOSCN-LBPRGKRZSA-N C(C)(C)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C Chemical compound C(C)(C)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C QXKVTERQQUOSCN-LBPRGKRZSA-N 0.000 claims 1
- CWROVSOSGZUVLT-ZDUSSCGKSA-N C(C)(C)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C Chemical compound C(C)(C)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C CWROVSOSGZUVLT-ZDUSSCGKSA-N 0.000 claims 1
- MATQFDBFNWVSJD-SFHVURJKSA-N C(C)(C)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)N(N=C2)C1=CC=CC=C1 Chemical compound C(C)(C)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)N(N=C2)C1=CC=CC=C1 MATQFDBFNWVSJD-SFHVURJKSA-N 0.000 claims 1
- VPHUPUCHQKFJDO-INIZCTEOSA-N C(C)(C)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)=O)N(N=C2)C1=CC=CC=C1 Chemical compound C(C)(C)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)=O)N(N=C2)C1=CC=CC=C1 VPHUPUCHQKFJDO-INIZCTEOSA-N 0.000 claims 1
- LXMUDSPHXLJOSI-AWEZNQCLSA-N C(C)(C)N1N=C(C2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C)C Chemical compound C(C)(C)N1N=C(C2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C)C LXMUDSPHXLJOSI-AWEZNQCLSA-N 0.000 claims 1
- UFFGTOZNBKKDPN-LBPRGKRZSA-N C(C)(C)N1N=C(C2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C)C Chemical compound C(C)(C)N1N=C(C2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C)C UFFGTOZNBKKDPN-LBPRGKRZSA-N 0.000 claims 1
- NAYBTUDROONHAC-ZDUSSCGKSA-N C(C)(C)N1N=C(C2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C)C Chemical compound C(C)(C)N1N=C(C2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C)C NAYBTUDROONHAC-ZDUSSCGKSA-N 0.000 claims 1
- OEDZYAMUJPKHKA-AWEZNQCLSA-N C(C)(C)N1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C Chemical compound C(C)(C)N1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C OEDZYAMUJPKHKA-AWEZNQCLSA-N 0.000 claims 1
- KKGQQRCKZMJUQW-LBPRGKRZSA-N C(C)(C)N1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)=O)C Chemical compound C(C)(C)N1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)=O)C KKGQQRCKZMJUQW-LBPRGKRZSA-N 0.000 claims 1
- ZEKDWAVPDDSPGJ-AWEZNQCLSA-N C(C)(C)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C Chemical compound C(C)(C)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C ZEKDWAVPDDSPGJ-AWEZNQCLSA-N 0.000 claims 1
- WVDMMTGTMBDWAQ-NSHDSACASA-N C(C)(C)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)=O)C Chemical compound C(C)(C)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)=O)C WVDMMTGTMBDWAQ-NSHDSACASA-N 0.000 claims 1
- UTERAIBUAOYOOW-LBPRGKRZSA-N C(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound C(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C UTERAIBUAOYOOW-LBPRGKRZSA-N 0.000 claims 1
- JXAOUMRYCQSWGL-KKUKGAKGSA-N C(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C([2H])([2H])[2H])C Chemical compound C(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C([2H])([2H])[2H])C JXAOUMRYCQSWGL-KKUKGAKGSA-N 0.000 claims 1
- JXAOUMRYCQSWGL-AWEZNQCLSA-N C(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C Chemical compound C(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C JXAOUMRYCQSWGL-AWEZNQCLSA-N 0.000 claims 1
- FKOMTPZSAAECCH-LBPRGKRZSA-N C(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C Chemical compound C(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C FKOMTPZSAAECCH-LBPRGKRZSA-N 0.000 claims 1
- LMMZNDAFKZTCFU-ZDUSSCGKSA-N C(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C Chemical compound C(C)(C)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C LMMZNDAFKZTCFU-ZDUSSCGKSA-N 0.000 claims 1
- VNVKBVUVIPMEBG-LBPRGKRZSA-N C(C)(C)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound C(C)(C)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C VNVKBVUVIPMEBG-LBPRGKRZSA-N 0.000 claims 1
- SGOGQVHOKRCPKW-AWEZNQCLSA-N C(C)(C)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C Chemical compound C(C)(C)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C SGOGQVHOKRCPKW-AWEZNQCLSA-N 0.000 claims 1
- ZEMUEVLQTPKIBM-LBPRGKRZSA-N C(C)(C)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C Chemical compound C(C)(C)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C ZEMUEVLQTPKIBM-LBPRGKRZSA-N 0.000 claims 1
- BGNYMLQUHFELLP-LBPRGKRZSA-N C(C)(C)N1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F Chemical compound C(C)(C)N1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F BGNYMLQUHFELLP-LBPRGKRZSA-N 0.000 claims 1
- YKUSWSIQEAESMZ-KKUKGAKGSA-N C(C)(C)N1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C([2H])([2H])[2H] Chemical compound C(C)(C)N1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C([2H])([2H])[2H] YKUSWSIQEAESMZ-KKUKGAKGSA-N 0.000 claims 1
- CXCFXDQCXCWNTH-LBPRGKRZSA-N C(C)(C)N1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F Chemical compound C(C)(C)N1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F CXCFXDQCXCWNTH-LBPRGKRZSA-N 0.000 claims 1
- RRDVRKYTEJZAJB-LBPRGKRZSA-N C1(=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C)C)=O)C Chemical compound C1(=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C)C)=O)C RRDVRKYTEJZAJB-LBPRGKRZSA-N 0.000 claims 1
- HVKVCAGCSIVTQK-LBPRGKRZSA-N C1(=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2C)C)C)=O)C Chemical compound C1(=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2C)C)C)=O)C HVKVCAGCSIVTQK-LBPRGKRZSA-N 0.000 claims 1
- AFWBMVTXFXYQJC-LBPRGKRZSA-N C1(CC1)C1=CN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O)C Chemical compound C1(CC1)C1=CN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O)C AFWBMVTXFXYQJC-LBPRGKRZSA-N 0.000 claims 1
- YDCRGZYNZWNCNH-AWEZNQCLSA-N C1(CC1)C1=CN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C Chemical compound C1(CC1)C1=CN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C YDCRGZYNZWNCNH-AWEZNQCLSA-N 0.000 claims 1
- VYKXXAFQVFURGS-LBPRGKRZSA-N C1(CC1)C1=NN(C=2C(=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)C)C Chemical compound C1(CC1)C1=NN(C=2C(=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)C)C VYKXXAFQVFURGS-LBPRGKRZSA-N 0.000 claims 1
- RDDSCXFVYWPPEU-NSHDSACASA-N C1(CC1)C1=NN(C=2C(=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C)C Chemical compound C1(CC1)C1=NN(C=2C(=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C)C RDDSCXFVYWPPEU-NSHDSACASA-N 0.000 claims 1
- DZQNEBGKKRTQSI-ZDUSSCGKSA-N C1(CC1)C1=NN(C=2C(=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C)C Chemical compound C1(CC1)C1=NN(C=2C(=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C)C DZQNEBGKKRTQSI-ZDUSSCGKSA-N 0.000 claims 1
- FAGLRMBXUCERBW-NSHDSACASA-N C1(CC1)C1=NN(C=2C(=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C)C Chemical compound C1(CC1)C1=NN(C=2C(=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C)C FAGLRMBXUCERBW-NSHDSACASA-N 0.000 claims 1
- HEBATXROLZDIJW-LBPRGKRZSA-N C1(CC1)C1=NN(C=2C(=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C)C Chemical compound C1(CC1)C1=NN(C=2C(=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C)C HEBATXROLZDIJW-LBPRGKRZSA-N 0.000 claims 1
- GRNJKQCMUAOMOC-LBPRGKRZSA-N C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)=O)C Chemical compound C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)=O)C GRNJKQCMUAOMOC-LBPRGKRZSA-N 0.000 claims 1
- MCNCWFQHOBPECY-LBPRGKRZSA-N C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)C)F)=O)C Chemical compound C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)C)F)=O)C MCNCWFQHOBPECY-LBPRGKRZSA-N 0.000 claims 1
- YBEWMWNOAJBKSC-NSHDSACASA-N C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC(=CC=C1)F)=O)C Chemical compound C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC(=CC=C1)F)=O)C YBEWMWNOAJBKSC-NSHDSACASA-N 0.000 claims 1
- VVLUQUKYSUPZAA-NSHDSACASA-N C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O)C Chemical compound C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O)C VVLUQUKYSUPZAA-NSHDSACASA-N 0.000 claims 1
- ZRUBEAIURQFZTI-ZDUSSCGKSA-N C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C Chemical compound C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C ZRUBEAIURQFZTI-ZDUSSCGKSA-N 0.000 claims 1
- ZRBXDWKXOXSAIR-NSHDSACASA-N C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)=O)C Chemical compound C1(CC1)C1=NN(C=2C(N(N=CC=21)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)=O)C ZRBXDWKXOXSAIR-NSHDSACASA-N 0.000 claims 1
- PLTGWMWEGJGQER-LBPRGKRZSA-N C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)C Chemical compound C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)C PLTGWMWEGJGQER-LBPRGKRZSA-N 0.000 claims 1
- GGZXOJUHRCFMFN-AWEZNQCLSA-N C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)C(C)C Chemical compound C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)C(C)C GGZXOJUHRCFMFN-AWEZNQCLSA-N 0.000 claims 1
- IDCKKBZVGLUOJP-NSHDSACASA-N C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C IDCKKBZVGLUOJP-NSHDSACASA-N 0.000 claims 1
- HDZFKCCFIBDFFD-ZDUSSCGKSA-N C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C(C)C Chemical compound C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C(C)C HDZFKCCFIBDFFD-ZDUSSCGKSA-N 0.000 claims 1
- JCNHIYGITUJXFO-ZDUSSCGKSA-N C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C Chemical compound C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C JCNHIYGITUJXFO-ZDUSSCGKSA-N 0.000 claims 1
- BTIFLGXATIIXRY-HNNXBMFYSA-N C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C(C)C Chemical compound C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C(C)C BTIFLGXATIIXRY-HNNXBMFYSA-N 0.000 claims 1
- MPCMRWRNCNEJGT-NSHDSACASA-N C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C Chemical compound C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C MPCMRWRNCNEJGT-NSHDSACASA-N 0.000 claims 1
- OUHIHWCAEKQAHZ-ZDUSSCGKSA-N C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C(C)C Chemical compound C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C(C)C OUHIHWCAEKQAHZ-ZDUSSCGKSA-N 0.000 claims 1
- NRLXZWUOFCNWHA-LBPRGKRZSA-N C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C Chemical compound C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C NRLXZWUOFCNWHA-LBPRGKRZSA-N 0.000 claims 1
- LTKRJEYSSHZTTH-AWEZNQCLSA-N C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C(C)C Chemical compound C1(CC1)C1=NN(C=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C(C)C LTKRJEYSSHZTTH-AWEZNQCLSA-N 0.000 claims 1
- PKRLQENNNHKYDN-INIZCTEOSA-N C1(CC1)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)=O)N(N=C2)C1=CC=CC=C1 Chemical compound C1(CC1)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)=O)N(N=C2)C1=CC=CC=C1 PKRLQENNNHKYDN-INIZCTEOSA-N 0.000 claims 1
- SRZJNCCQXBHPHG-HNNXBMFYSA-N C1(CC1)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O)N(N=C2)C1=CC=CC=C1 Chemical compound C1(CC1)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O)N(N=C2)C1=CC=CC=C1 SRZJNCCQXBHPHG-HNNXBMFYSA-N 0.000 claims 1
- ZAGSSFDXQFRHIF-KRWDZBQOSA-N C1(CC1)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)N(N=C2)C1=CC=CC=C1 Chemical compound C1(CC1)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)N(N=C2)C1=CC=CC=C1 ZAGSSFDXQFRHIF-KRWDZBQOSA-N 0.000 claims 1
- NAMPUNFTRSVBPI-HNNXBMFYSA-N C1(CC1)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)=O)N(N=C2)C1=CC=CC=C1 Chemical compound C1(CC1)C=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)=O)N(N=C2)C1=CC=CC=C1 NAMPUNFTRSVBPI-HNNXBMFYSA-N 0.000 claims 1
- NMGCIWJCVWKMGI-INIZCTEOSA-N C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)C)C Chemical compound C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)C)C NMGCIWJCVWKMGI-INIZCTEOSA-N 0.000 claims 1
- HSHIIKAOUQKERT-KRWDZBQOSA-N C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1C)C)C)C Chemical compound C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1C)C)C)C HSHIIKAOUQKERT-KRWDZBQOSA-N 0.000 claims 1
- ZZDPMYRYSJKFMI-AWEZNQCLSA-N C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)C)F)C Chemical compound C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)C)F)C ZZDPMYRYSJKFMI-AWEZNQCLSA-N 0.000 claims 1
- YTHRAHHRIRITHV-ZDUSSCGKSA-N C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C YTHRAHHRIRITHV-ZDUSSCGKSA-N 0.000 claims 1
- VAURQKOUOBEEIN-HNNXBMFYSA-N C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C Chemical compound C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C VAURQKOUOBEEIN-HNNXBMFYSA-N 0.000 claims 1
- SHZNBVOVZHGGHD-AWEZNQCLSA-N C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C Chemical compound C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C SHZNBVOVZHGGHD-AWEZNQCLSA-N 0.000 claims 1
- OFLWFUCKEHMKOP-AWEZNQCLSA-N C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=CC=C1)C Chemical compound C1(CC1)N1C=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=CC=C1)C OFLWFUCKEHMKOP-AWEZNQCLSA-N 0.000 claims 1
- LNYULYOTELRUGE-ZDUSSCGKSA-N C1(CC1)N1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C Chemical compound C1(CC1)N1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C LNYULYOTELRUGE-ZDUSSCGKSA-N 0.000 claims 1
- XIYDWRPLPRUFLN-NSHDSACASA-N C1(CC1)N1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)=O)C Chemical compound C1(CC1)N1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)=O)C XIYDWRPLPRUFLN-NSHDSACASA-N 0.000 claims 1
- QVHHWXWPDPYYII-UHFFFAOYSA-N C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)NC(C)C1=CC2=C(OCCO2)C=C1)=O)C Chemical compound C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)NC(C)C1=CC2=C(OCCO2)C=C1)=O)C QVHHWXWPDPYYII-UHFFFAOYSA-N 0.000 claims 1
- DPOSXICMGKVELQ-LBPRGKRZSA-N C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)=O)C Chemical compound C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)=O)C DPOSXICMGKVELQ-LBPRGKRZSA-N 0.000 claims 1
- WAJTXNSYKCQFMK-HNNXBMFYSA-N C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=C(C=C(C=C1C)C)C)=O)C Chemical compound C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=C(C=C(C=C1C)C)C)=O)C WAJTXNSYKCQFMK-HNNXBMFYSA-N 0.000 claims 1
- YIQGTNLRZHBPGU-LBPRGKRZSA-N C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)C)F)=O)C Chemical compound C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)C)F)=O)C YIQGTNLRZHBPGU-LBPRGKRZSA-N 0.000 claims 1
- NOUSLWXFNJGJSO-ZDUSSCGKSA-N C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C Chemical compound C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C NOUSLWXFNJGJSO-ZDUSSCGKSA-N 0.000 claims 1
- YBCILDYBWDPHTJ-JTQLQIEISA-N C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)=O)C Chemical compound C1(CC1)N1N=C(C2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)=O)C YBCILDYBWDPHTJ-JTQLQIEISA-N 0.000 claims 1
- SRTSNNZTFOZQGV-JTQLQIEISA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C(=CC=C1)F)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C(=CC=C1)F)F)C SRTSNNZTFOZQGV-JTQLQIEISA-N 0.000 claims 1
- HLLHHMQUNQBRLQ-LBPRGKRZSA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)C HLLHHMQUNQBRLQ-LBPRGKRZSA-N 0.000 claims 1
- VBIFQYJUADXXAV-JTQLQIEISA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)F)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)F)F)C VBIFQYJUADXXAV-JTQLQIEISA-N 0.000 claims 1
- WTUUCUXAPZZHFO-NSHDSACASA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)OC)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)OC)F)C WTUUCUXAPZZHFO-NSHDSACASA-N 0.000 claims 1
- KWJGTZPLUKDOLM-VIFPVBQESA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1F)F)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1F)F)F)C KWJGTZPLUKDOLM-VIFPVBQESA-N 0.000 claims 1
- NSSVVOVDHPDRKI-AWEZNQCLSA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=CC(=C1)C)C)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=CC(=C1)C)C)C NSSVVOVDHPDRKI-AWEZNQCLSA-N 0.000 claims 1
- MNRLKETUOVHLKH-LBPRGKRZSA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)C)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)C)F)C MNRLKETUOVHLKH-LBPRGKRZSA-N 0.000 claims 1
- IITMOAUJNRTXEE-LBPRGKRZSA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)F)C)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)F)C)C IITMOAUJNRTXEE-LBPRGKRZSA-N 0.000 claims 1
- TXPHRVTZQCUBEQ-NSHDSACASA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)F)OC)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)F)OC)C TXPHRVTZQCUBEQ-NSHDSACASA-N 0.000 claims 1
- CEYBUBKEJBYINO-ZDUSSCGKSA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)OC)C)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)OC)C)C CEYBUBKEJBYINO-ZDUSSCGKSA-N 0.000 claims 1
- NPONLUBARIOQKK-NSHDSACASA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)OC)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=C(C=C1)OC)F)C NPONLUBARIOQKK-NSHDSACASA-N 0.000 claims 1
- NERDPZCELDMPPR-JTQLQIEISA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=CC(=C1)F)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=CC(=C1)F)F)C NERDPZCELDMPPR-JTQLQIEISA-N 0.000 claims 1
- JPRLDRUPJRLVLG-NSHDSACASA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=CC=C1)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC(=CC=C1)F)C JPRLDRUPJRLVLG-NSHDSACASA-N 0.000 claims 1
- QZFPZZHXFWOUSO-FUPFOCIHSA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C([2H])([2H])[2H])C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C([2H])([2H])[2H])C QZFPZZHXFWOUSO-FUPFOCIHSA-N 0.000 claims 1
- QZFPZZHXFWOUSO-ZDUSSCGKSA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C QZFPZZHXFWOUSO-ZDUSSCGKSA-N 0.000 claims 1
- DGHDXZFHCMKSGQ-NSHDSACASA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C DGHDXZFHCMKSGQ-NSHDSACASA-N 0.000 claims 1
- IUYZEUBENFERRB-LBPRGKRZSA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C IUYZEUBENFERRB-LBPRGKRZSA-N 0.000 claims 1
- MLDNJWDVWLAQRX-JTQLQIEISA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)C MLDNJWDVWLAQRX-JTQLQIEISA-N 0.000 claims 1
- GIZXIFZVUQNKDE-LLVKDONJSA-N C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound C1(CC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@H](C)C1=CC=C(C=C1)C(F)(F)F)C GIZXIFZVUQNKDE-LLVKDONJSA-N 0.000 claims 1
- GYMSRIILKXNOSQ-LBPRGKRZSA-N C1(CC1)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)C Chemical compound C1(CC1)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)C GYMSRIILKXNOSQ-LBPRGKRZSA-N 0.000 claims 1
- LNZPUPOONIPZFY-NSHDSACASA-N C1(CC1)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound C1(CC1)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C LNZPUPOONIPZFY-NSHDSACASA-N 0.000 claims 1
- CJXWBYSJCDORSC-ZDUSSCGKSA-N C1(CC1)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C Chemical compound C1(CC1)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C CJXWBYSJCDORSC-ZDUSSCGKSA-N 0.000 claims 1
- RDOVRMVSIGJIOU-NSHDSACASA-N C1(CC1)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C Chemical compound C1(CC1)N1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C RDOVRMVSIGJIOU-NSHDSACASA-N 0.000 claims 1
- LXNFWQWJGCBEOU-ZDUSSCGKSA-N C1(CC1)N1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C Chemical compound C1(CC1)N1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C LXNFWQWJGCBEOU-ZDUSSCGKSA-N 0.000 claims 1
- YZNKFJPNZWSPSX-HXUWFJFHSA-N C1(CC1)[C@H](NC(CN1N=CC2=C(C1=O)C(=NN2C1CC1)C)=O)C1=CC=CC=C1 Chemical compound C1(CC1)[C@H](NC(CN1N=CC2=C(C1=O)C(=NN2C1CC1)C)=O)C1=CC=CC=C1 YZNKFJPNZWSPSX-HXUWFJFHSA-N 0.000 claims 1
- YADGJLYQURQSDS-LBPRGKRZSA-N C1(CCC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound C1(CCC1)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C YADGJLYQURQSDS-LBPRGKRZSA-N 0.000 claims 1
- RYNAHDMMJUETPX-LTKVMPMFSA-N C12(CC(C1)C2)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound C12(CC(C1)C2)N1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C RYNAHDMMJUETPX-LTKVMPMFSA-N 0.000 claims 1
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 1
- IUISFZRYMCCQGY-INIZCTEOSA-N CC=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)N(N=C2)C1=CC=CC=C1 Chemical compound CC=1C2=C(C(N(N=1)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)N(N=C2)C1=CC=CC=C1 IUISFZRYMCCQGY-INIZCTEOSA-N 0.000 claims 1
- RAAMTAOIRFTICR-NSHDSACASA-N CN1C=CC2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O Chemical compound CN1C=CC2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O RAAMTAOIRFTICR-NSHDSACASA-N 0.000 claims 1
- VKHGYNPKRNTPQK-FUPFOCIHSA-N CN1C=CC2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C([2H])([2H])[2H])=O Chemical compound CN1C=CC2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C([2H])([2H])[2H])=O VKHGYNPKRNTPQK-FUPFOCIHSA-N 0.000 claims 1
- VKHGYNPKRNTPQK-ZDUSSCGKSA-N CN1C=CC2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O Chemical compound CN1C=CC2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O VKHGYNPKRNTPQK-ZDUSSCGKSA-N 0.000 claims 1
- DJDOFBSFMABAIC-LBPRGKRZSA-N CN1C=CC2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=CC=C1)=O Chemical compound CN1C=CC2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=CC=C1)=O DJDOFBSFMABAIC-LBPRGKRZSA-N 0.000 claims 1
- OSGVLSAPWLXRHV-LBPRGKRZSA-N CN1C=NC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C Chemical compound CN1C=NC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C OSGVLSAPWLXRHV-LBPRGKRZSA-N 0.000 claims 1
- HCGMEFUBIKSXJG-VIFPVBQESA-N CN1C=NC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)C Chemical compound CN1C=NC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)C HCGMEFUBIKSXJG-VIFPVBQESA-N 0.000 claims 1
- NJVPFCNIBQHVBO-JTQLQIEISA-N CN1C=NC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F Chemical compound CN1C=NC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F NJVPFCNIBQHVBO-JTQLQIEISA-N 0.000 claims 1
- HKENHDFFULBVIT-LBPRGKRZSA-N CN1C=NC=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C Chemical compound CN1C=NC=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C HKENHDFFULBVIT-LBPRGKRZSA-N 0.000 claims 1
- CMZPSMXCUDASDA-JTQLQIEISA-N CN1C=NC=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F Chemical compound CN1C=NC=2C=NN(C(C=21)=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F CMZPSMXCUDASDA-JTQLQIEISA-N 0.000 claims 1
- MLTFQBRQIVFAJR-LBPRGKRZSA-N CN1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C Chemical compound CN1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O)C MLTFQBRQIVFAJR-LBPRGKRZSA-N 0.000 claims 1
- ZIAASDUSXMENBW-JTQLQIEISA-N CN1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)=O)C Chemical compound CN1N=C(C2=C1C(N(N=C2)CC(=O)N[C@@H](C)C1=NC=C(C=C1)C(F)(F)F)=O)C ZIAASDUSXMENBW-JTQLQIEISA-N 0.000 claims 1
- GEDQZONDXQLXKF-JTQLQIEISA-N CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C GEDQZONDXQLXKF-JTQLQIEISA-N 0.000 claims 1
- PMXCZFCQTIQWPL-VIFPVBQESA-N CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C(F)(F)F Chemical compound CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C(F)(F)F PMXCZFCQTIQWPL-VIFPVBQESA-N 0.000 claims 1
- NTYHMLMOUUXQDL-LBPRGKRZSA-N CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C Chemical compound CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C NTYHMLMOUUXQDL-LBPRGKRZSA-N 0.000 claims 1
- QVPPCROMOXWFCT-NSHDSACASA-N CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C(F)(F)F Chemical compound CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C(F)(F)F QVPPCROMOXWFCT-NSHDSACASA-N 0.000 claims 1
- CMJBZBISKOUVAD-JTQLQIEISA-N CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C Chemical compound CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C CMJBZBISKOUVAD-JTQLQIEISA-N 0.000 claims 1
- ZMJCIXBQUYUGHI-NSHDSACASA-N CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C Chemical compound CN1N=C(C2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC)C ZMJCIXBQUYUGHI-NSHDSACASA-N 0.000 claims 1
- LRRAPPJVKQNWEG-JTQLQIEISA-N CN1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C Chemical compound CN1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)C LRRAPPJVKQNWEG-JTQLQIEISA-N 0.000 claims 1
- IAQRFFGCNNJZSO-LBPRGKRZSA-N CN1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C Chemical compound CN1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)C IAQRFFGCNNJZSO-LBPRGKRZSA-N 0.000 claims 1
- ZJVHPEVGANUBNM-JTQLQIEISA-N CN1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C Chemical compound CN1N=CC2=C1C(=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)OC(F)(F)F)C ZJVHPEVGANUBNM-JTQLQIEISA-N 0.000 claims 1
- GGPYBYDYANGWQX-NSHDSACASA-N CN1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)=O Chemical compound CN1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=C(C=C(C=C1)C)F)=O GGPYBYDYANGWQX-NSHDSACASA-N 0.000 claims 1
- HKTATIXCZZXSFM-JTQLQIEISA-N CN1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O Chemical compound CN1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F)=O HKTATIXCZZXSFM-JTQLQIEISA-N 0.000 claims 1
- MQCLGSBRUPINJS-LBPRGKRZSA-N CN1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O Chemical compound CN1N=CC2=C1C(N(N=C2C)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C)=O MQCLGSBRUPINJS-LBPRGKRZSA-N 0.000 claims 1
- GIWFRSSQAZJUTL-LBPRGKRZSA-N CN1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C Chemical compound CN1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C GIWFRSSQAZJUTL-LBPRGKRZSA-N 0.000 claims 1
- FEZNIPPKYLJFBK-JTQLQIEISA-N CN1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F Chemical compound CN1N=CC2=C1C=NN(C2=O)CC(=O)N[C@@H](C)C1=CC=C(C=C1)C(F)(F)F FEZNIPPKYLJFBK-JTQLQIEISA-N 0.000 claims 1
- HNMAJGHOIBUMGY-NSHDSACASA-N COC1=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C)C)=O Chemical compound COC1=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C)C)=O HNMAJGHOIBUMGY-NSHDSACASA-N 0.000 claims 1
- SSZOEADAEJRXFP-HNNXBMFYSA-N COC1=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2)C1=CC=CC=C1)C)=O Chemical compound COC1=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2)C1=CC=CC=C1)C)=O SSZOEADAEJRXFP-HNNXBMFYSA-N 0.000 claims 1
- MMZZPQLADFLCOI-LBPRGKRZSA-N COC1=CC=C(C=C1)[C@H](C)NC(CN1N=CC2=C(C1=O)N(C=C2)C)=O Chemical compound COC1=CC=C(C=C1)[C@H](C)NC(CN1N=CC2=C(C1=O)N(C=C2)C)=O MMZZPQLADFLCOI-LBPRGKRZSA-N 0.000 claims 1
- PWUFUCAZTSAOJN-JTQLQIEISA-N ClC1=C(C(=CC=C1)F)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C1CC1)C)=O Chemical compound ClC1=C(C(=CC=C1)F)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C1CC1)C)=O PWUFUCAZTSAOJN-JTQLQIEISA-N 0.000 claims 1
- DXTRENLMQCHCCH-JTQLQIEISA-N ClC1=C(C(=CC=C1)F)[C@H](C)NC(CN1N=CC2=C(C1=O)N(N=C2C1CC1)C)=O Chemical compound ClC1=C(C(=CC=C1)F)[C@H](C)NC(CN1N=CC2=C(C1=O)N(N=C2C1CC1)C)=O DXTRENLMQCHCCH-JTQLQIEISA-N 0.000 claims 1
- ZGEVWKVLWDWKRA-JTQLQIEISA-N ClC1=C(C=CC(=C1)F)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2C)C1CC1)C)=O Chemical compound ClC1=C(C=CC(=C1)F)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2C)C1CC1)C)=O ZGEVWKVLWDWKRA-JTQLQIEISA-N 0.000 claims 1
- YKOIATOHXOWPCS-LBPRGKRZSA-N ClC1=C(C=CC(=C1)F)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=CN2C1CC1)C)=O Chemical compound ClC1=C(C=CC(=C1)F)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=CN2C1CC1)C)=O YKOIATOHXOWPCS-LBPRGKRZSA-N 0.000 claims 1
- LGBUOJZQVQJJKH-JTQLQIEISA-N ClC1=C(C=CC(=C1)F)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C1CC1)C)=O Chemical compound ClC1=C(C=CC(=C1)F)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C1CC1)C)=O LGBUOJZQVQJJKH-JTQLQIEISA-N 0.000 claims 1
- DOPRKOTYQVDVEW-AWEZNQCLSA-N ClC1=CC(=C(C=C1)C[C@H](C)NC(CN1N=CC2=C(C1=O)C(=CN2C1CC1)C)=O)OC Chemical compound ClC1=CC(=C(C=C1)C[C@H](C)NC(CN1N=CC2=C(C1=O)C(=CN2C1CC1)C)=O)OC DOPRKOTYQVDVEW-AWEZNQCLSA-N 0.000 claims 1
- IOGQTHCTMFKTIK-AWEZNQCLSA-N ClC1=CC(=C(C=C1)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=CN2C1CC1)C)=O)C Chemical compound ClC1=CC(=C(C=C1)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=CN2C1CC1)C)=O)C IOGQTHCTMFKTIK-AWEZNQCLSA-N 0.000 claims 1
- MSAXPLPQHRMGOL-JTQLQIEISA-N ClC1=CC(=C(C=C1)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C1CC1)C)=O)F Chemical compound ClC1=CC(=C(C=C1)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C1CC1)C)=O)F MSAXPLPQHRMGOL-JTQLQIEISA-N 0.000 claims 1
- ZIELKUIITYJSCK-UHFFFAOYSA-N ClC1=CC=C(C=C1)C1N(CCC1)C(CN1N=CC2=C(C1=O)C(=NN2C)C1CC1)=O Chemical compound ClC1=CC=C(C=C1)C1N(CCC1)C(CN1N=CC2=C(C1=O)C(=NN2C)C1CC1)=O ZIELKUIITYJSCK-UHFFFAOYSA-N 0.000 claims 1
- AVBVFRRDISTSKD-UHFFFAOYSA-N ClC1=CC=C(C=C1)C1N(CCC1)C(CN1N=CC2=C(C1=O)N(N=C2C)C1CC1)=O Chemical compound ClC1=CC=C(C=C1)C1N(CCC1)C(CN1N=CC2=C(C1=O)N(N=C2C)C1CC1)=O AVBVFRRDISTSKD-UHFFFAOYSA-N 0.000 claims 1
- HEVIERYDZUVNCV-NSHDSACASA-N ClC1=CC=C(C=C1)[C@H](C)NC(CN1N=CC2=C(C1=O)N(C=C2)C)=O Chemical compound ClC1=CC=C(C=C1)[C@H](C)NC(CN1N=CC2=C(C1=O)N(C=C2)C)=O HEVIERYDZUVNCV-NSHDSACASA-N 0.000 claims 1
- 208000028698 Cognitive impairment Diseases 0.000 claims 1
- 208000030814 Eating disease Diseases 0.000 claims 1
- OKFANELEIDPKES-JTQLQIEISA-N FC(C1=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C)C)=O)(F)F Chemical compound FC(C1=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C)C)=O)(F)F OKFANELEIDPKES-JTQLQIEISA-N 0.000 claims 1
- SGAAFRLCTOEVRO-VIFPVBQESA-N FC(C=1C=CC(=NC=1)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2C)C)C)=O)(F)F Chemical compound FC(C=1C=CC(=NC=1)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2C)C)C)=O)(F)F SGAAFRLCTOEVRO-VIFPVBQESA-N 0.000 claims 1
- QQDWXGHOKPCZIO-JTQLQIEISA-N FC(OC1=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C)C)=O)(F)F Chemical compound FC(OC1=CC=C(C=C1)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C)C)=O)(F)F QQDWXGHOKPCZIO-JTQLQIEISA-N 0.000 claims 1
- CFRMAKXGDVFLFO-VIFPVBQESA-N FC1=C(C(=CC=C1)F)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C)C)=O Chemical compound FC1=C(C(=CC=C1)F)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C)C)=O CFRMAKXGDVFLFO-VIFPVBQESA-N 0.000 claims 1
- KAOAKUQXBVHVNM-ZDUSSCGKSA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C(C)C)C)C)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C(C)C)C)C)=O KAOAKUQXBVHVNM-ZDUSSCGKSA-N 0.000 claims 1
- VDJFPMMAKFBXJT-NSHDSACASA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C)C)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C)C)=O VDJFPMMAKFBXJT-NSHDSACASA-N 0.000 claims 1
- NWFRULDJBXUQFU-ZDUSSCGKSA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=C(C2=C(C1=O)C=NN2C(C)C)C)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=C(C2=C(C1=O)C=NN2C(C)C)C)=O NWFRULDJBXUQFU-ZDUSSCGKSA-N 0.000 claims 1
- HNTDFISTEDLAPM-KRWDZBQOSA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2)C1=CC=CC=C1)C(C)C)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2)C1=CC=CC=C1)C(C)C)=O HNTDFISTEDLAPM-KRWDZBQOSA-N 0.000 claims 1
- ZBKMCCQHDPDNFG-HNNXBMFYSA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2)C1=CC=CC=C1)C)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2)C1=CC=CC=C1)C)=O ZBKMCCQHDPDNFG-HNNXBMFYSA-N 0.000 claims 1
- MEZKQWMLEJLBFQ-ZDUSSCGKSA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C(C)C)C)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C(C)C)C)=O MEZKQWMLEJLBFQ-ZDUSSCGKSA-N 0.000 claims 1
- CCRZJGKXWNSDAP-ZDUSSCGKSA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C)C(C)C)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C)C(C)C)=O CCRZJGKXWNSDAP-ZDUSSCGKSA-N 0.000 claims 1
- AMBCPPFBLWDPEE-JTQLQIEISA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C)C(F)(F)F)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C)C(F)(F)F)=O AMBCPPFBLWDPEE-JTQLQIEISA-N 0.000 claims 1
- CSVPWLLZDMJQKL-ZDUSSCGKSA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)C=NN2C(C)C)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)C=NN2C(C)C)=O CSVPWLLZDMJQKL-ZDUSSCGKSA-N 0.000 claims 1
- XXTUPNSBGKDYPQ-NSHDSACASA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)C=NN2C)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)C=NN2C)=O XXTUPNSBGKDYPQ-NSHDSACASA-N 0.000 claims 1
- SMNFNGLWZTYWMT-LBPRGKRZSA-N FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)N(C=C2)C)=O Chemical compound FC1=C(C=CC(=C1)C)[C@H](C)NC(CN1N=CC2=C(C1=O)N(C=C2)C)=O SMNFNGLWZTYWMT-LBPRGKRZSA-N 0.000 claims 1
- STXAKGCHZJDWLJ-JTQLQIEISA-N FC=1C=C(C=CC=1)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2C)C)C)=O Chemical compound FC=1C=C(C=CC=1)[C@H](C)NC(CN1N=C(C2=C(C1=O)N(N=C2C)C)C)=O STXAKGCHZJDWLJ-JTQLQIEISA-N 0.000 claims 1
- XCNVYNUGYYGCBV-JTQLQIEISA-N FC=1C=C(C=CC=1C)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C)C(F)(F)F)=O Chemical compound FC=1C=C(C=CC=1C)[C@H](C)NC(CN1N=CC2=C(C1=O)C(=NN2C)C(F)(F)F)=O XCNVYNUGYYGCBV-JTQLQIEISA-N 0.000 claims 1
- LISAPNDPWWHHBH-LBPRGKRZSA-N FC=1C=C(C=CC=1OC)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C(C)C)C)=O Chemical compound FC=1C=C(C=CC=1OC)[C@H](C)NC(CN1N=C(C2=C(C1=O)C(=NN2C)C(C)C)C)=O LISAPNDPWWHHBH-LBPRGKRZSA-N 0.000 claims 1
- 208000019454 Feeding and Eating disease Diseases 0.000 claims 1
- 208000001640 Fibromyalgia Diseases 0.000 claims 1
- GFMYHVLDCTYZTM-UHFFFAOYSA-N O1CCCC2=CC(=CC=C12)C(C)NC(CN1N=C(C2=C(C1=O)N(N=C2C)C1CC1)C)=O Chemical compound O1CCCC2=CC(=CC=C12)C(C)NC(CN1N=C(C2=C(C1=O)N(N=C2C)C1CC1)C)=O GFMYHVLDCTYZTM-UHFFFAOYSA-N 0.000 claims 1
- UJEJUIYFVBCGIV-UHFFFAOYSA-N O1CCCC2=CC(=CC=C12)C(C)NC(CN1N=CC2=C(C1=O)C(=NN2C1CC1)C)=O Chemical compound O1CCCC2=CC(=CC=C12)C(C)NC(CN1N=CC2=C(C1=O)C(=NN2C1CC1)C)=O UJEJUIYFVBCGIV-UHFFFAOYSA-N 0.000 claims 1
- 208000021384 Obsessive-Compulsive disease Diseases 0.000 claims 1
- 208000002193 Pain Diseases 0.000 claims 1
- 208000018737 Parkinson disease Diseases 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims 1
- 208000029560 autism spectrum disease Diseases 0.000 claims 1
- 208000010877 cognitive disease Diseases 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 235000014632 disordered eating Nutrition 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 206010015037 epilepsy Diseases 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 208000028173 post-traumatic stress disease Diseases 0.000 claims 1
- 201000000980 schizophrenia Diseases 0.000 claims 1
- 208000019116 sleep disease Diseases 0.000 claims 1
- 208000020685 sleep-wake disease Diseases 0.000 claims 1
- 201000009032 substance abuse Diseases 0.000 claims 1
- 231100000736 substance abuse Toxicity 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 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
- A61K31/495—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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/05—Isotopically modified compounds, e.g. labelled
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962901052P | 2019-09-16 | 2019-09-16 | |
| PCT/US2020/050823 WO2021055326A1 (en) | 2019-09-16 | 2020-09-15 | Azole-fused pyridazin-3(2h)-one derivatives |
| EP20781670.3A EP4031552B1 (en) | 2019-09-16 | 2020-09-15 | Azole-fused pyridazin-3(2h)-one derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20250088T1 true HRP20250088T1 (hr) | 2025-03-28 |
Family
ID=72670806
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HRP20250088TT HRP20250088T1 (hr) | 2019-09-16 | 2020-09-15 | Derivati piridazin-3(2h)-ona spojeni s azolom |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US12370192B2 (https=) |
| EP (1) | EP4031552B1 (https=) |
| JP (1) | JP7566888B2 (https=) |
| KR (1) | KR102924294B1 (https=) |
| CN (1) | CN114728975A (https=) |
| AR (1) | AR119971A1 (https=) |
| AU (1) | AU2020348675B2 (https=) |
| BR (1) | BR112022004819A2 (https=) |
| CA (1) | CA3150508A1 (https=) |
| CO (1) | CO2022004684A2 (https=) |
| CR (1) | CR20220160A (https=) |
| DO (1) | DOP2022000057A (https=) |
| EC (1) | ECSP22020159A (https=) |
| ES (1) | ES2997267T3 (https=) |
| HR (1) | HRP20250088T1 (https=) |
| HU (1) | HUE069908T2 (https=) |
| IL (1) | IL291181B2 (https=) |
| JO (1) | JOP20220063A1 (https=) |
| MX (1) | MX2022003177A (https=) |
| PE (1) | PE20221341A1 (https=) |
| PH (1) | PH12022550597A1 (https=) |
| PL (1) | PL4031552T3 (https=) |
| RS (1) | RS66463B1 (https=) |
| TW (1) | TWI873185B (https=) |
| WO (1) | WO2021055326A1 (https=) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JO3115B1 (ar) | 2011-08-22 | 2017-09-20 | Takeda Pharmaceuticals Co | مركبات بيريدازينون واستخدامها كمثبطات daao |
| CR20220160A (es) | 2019-09-16 | 2022-06-16 | Takeda Pharmaceuticals Co | Derivados de piridazin-3(2h)-ona fusionados con azol |
| WO2021224680A1 (en) | 2020-05-08 | 2021-11-11 | Takeda Pharmaceutical Company Limited | Substituted benzotriazinone metabolites of a gpr139 agonist |
| GB202106872D0 (en) * | 2021-05-13 | 2021-06-30 | Addex Pharmaceuticals Sa | Novel compounds |
| CN114149371B (zh) * | 2021-11-26 | 2023-08-22 | 首都医科大学 | 四取代吡唑类化合物及其应用 |
| CN116693545A (zh) * | 2022-03-01 | 2023-09-05 | 上海科技大学 | 噻吩并含氮杂环类化合物、含其的药物组合物、其制备方法及其应用 |
| CN116693536A (zh) * | 2022-03-01 | 2023-09-05 | 上海科技大学 | 吡咯并三嗪酮类化合物、含其的药物组合物、其制备方法及其应用 |
| IT202200024948A1 (it) * | 2022-12-05 | 2024-06-05 | Angelini Pharma S P A | Composti attivatori dei canali potassio KV7.2/KV7.3 |
| CN116063179A (zh) * | 2023-02-20 | 2023-05-05 | 南京杰运医药科技有限公司 | 一种4-甲氧基乙酰乙酸甲酯的合成方法 |
| WO2025119351A1 (zh) * | 2023-12-08 | 2025-06-12 | 深圳湾实验室 | Gpr139激动剂 |
| WO2025124544A1 (zh) * | 2023-12-14 | 2025-06-19 | 华润医药研究院(深圳)有限公司 | 3,4-二氢-2H-苯并[b][1,4]二氧杂环庚烷类化合物及其制备方法和医药用途 |
| WO2025162441A1 (zh) * | 2024-02-02 | 2025-08-07 | 上海科技大学 | 稠杂环类化合物与其制备方法、药物组合物及应用 |
Family Cites Families (70)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3794726A (en) | 1972-08-21 | 1974-02-26 | Uniroyal Inc | Inhibiting aggressive behavior with 1,2,3-benzotriazin-(3h)-one |
| WO1987004928A1 (fr) | 1986-02-24 | 1987-08-27 | Mitsui Petrochemical Industries, Ltd. | Agents therapeutiques de la neuropathie |
| EP0315390B1 (en) | 1987-11-04 | 1994-07-20 | Beecham Group Plc | Novel 4-oxobenzotriazines and 4-oxoquinazolines |
| JPH0285851A (ja) | 1988-09-22 | 1990-03-27 | Konica Corp | 新規な写真用カプラー |
| US5376645A (en) | 1990-01-23 | 1994-12-27 | University Of Kansas | Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof |
| KR0166088B1 (ko) | 1990-01-23 | 1999-01-15 | . | 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도 |
| JP2874960B2 (ja) | 1990-06-03 | 1999-03-24 | コニカ株式会社 | 新規な染料を含有するハロゲン化銀写真感光材料 |
| JPH04119890A (ja) | 1990-09-11 | 1992-04-21 | Konica Corp | ピラゾロチアジアジン系色素 |
| JP3430375B2 (ja) | 1993-11-12 | 2003-07-28 | コニカ株式会社 | 感熱転写材料及び該材料に好適な色素 |
| DE4339868A1 (de) * | 1993-11-23 | 1995-05-24 | Merck Patent Gmbh | Imidazopyridazine |
| GB9518953D0 (en) | 1995-09-15 | 1995-11-15 | Pfizer Ltd | Pharmaceutical formulations |
| DE19704923A1 (de) | 1997-02-10 | 1998-08-13 | Hoechst Schering Agrevo Gmbh | Klebstoffhaltige Schädlingsbekämpfungsmittel |
| GB9711643D0 (en) | 1997-06-05 | 1997-07-30 | Janssen Pharmaceutica Nv | Glass thermoplastic systems |
| CN1293665A (zh) | 1998-02-18 | 2001-05-02 | 神经研究公司 | 新化合物及其用作阳性ampa受体调节剂 |
| AU1153601A (en) | 1999-10-29 | 2001-05-08 | Merck Sharp & Dohme Limited | Method to treat pain utilizing benzimidazole NMDA NR2B antagonists |
| JP2003526341A (ja) | 1999-11-04 | 2003-09-09 | コロラド ステート ユニバーシティー リサーチ ファウンデーション | 昆虫を誘引するための装置および方法 |
| FR2801587B1 (fr) | 1999-11-30 | 2002-01-11 | Adir | Nouveaux derives de benzothiadiazines, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| JP2002085851A (ja) | 2000-09-19 | 2002-03-26 | Totan Information Technology Kk | 経済指標予想ゲームシステム |
| MXPA04003297A (es) | 2001-10-10 | 2004-07-23 | Neurosearch As | Derivados novedosos de benzotiacina su preparacion y uso. |
| FR2833955B1 (fr) | 2001-12-21 | 2004-01-30 | Servier Lab | Nouveaux derives de benzothiazine et de benzothiadiazine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| AU2003235121A1 (en) | 2002-04-26 | 2003-11-10 | Takeda Pharmaceutical Company Limited | Novel thiol derivative, process for producing the same and use thereof |
| JP4079727B2 (ja) | 2002-09-06 | 2008-04-23 | セントラル硝子株式会社 | 光学活性1−(フルオロ、トリフルオロメチルまたはトリフルオロメトキシ置換フェニル)アルキルアミンn−モノアルキル誘導体とその製造方法 |
| JP3981316B2 (ja) | 2002-09-27 | 2007-09-26 | 京セラ株式会社 | 半導体素子収納用パッケージ |
| FR2854634B1 (fr) | 2003-05-05 | 2005-07-08 | Servier Lab | Nouveaux derives de thiadiazine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| CA2526506A1 (en) | 2003-06-09 | 2004-12-16 | Boehringer Ingelheim International Gmbh | Inhibitors of papilloma virus |
| AU2004261283B2 (en) | 2003-07-31 | 2008-05-01 | Irm, Llc | Bicyclic compounds and compositions as PDF inhibitors |
| FR2865474B1 (fr) | 2004-01-26 | 2008-06-13 | Servier Lab | Nouveaux derives de benzothiazines fluorees, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| FR2875805B1 (fr) | 2004-09-27 | 2006-12-29 | Genfit S A | Composes derives de n-(benzyl) phenylacetamide substitues, preparation et utilisations |
| FR2879201B1 (fr) | 2004-12-10 | 2007-02-16 | Servier Lab | Nouveaux derives de benzothiazine et benzothiadiazine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| JP4738988B2 (ja) | 2005-11-17 | 2011-08-03 | 花王株式会社 | 2連式吐出器 |
| TWI403320B (zh) | 2005-12-16 | 2013-08-01 | Infinity Discovery Inc | 用於抑制bcl蛋白和結合夥伴間之交互作用的化合物及方法 |
| TW200736227A (en) | 2005-12-23 | 2007-10-01 | Astrazeneca Ab | New compounds III |
| AU2007262661A1 (en) | 2006-06-23 | 2007-12-27 | Nufarm Australia Limited | Phenoxy alkanoate herbicidal composition and method of preparation and use |
| TWI433839B (zh) | 2006-08-11 | 2014-04-11 | Neomed Inst | 新穎的苯并咪唑衍生物290 |
| FR2909090B1 (fr) | 2006-11-23 | 2009-01-09 | Sanofi Aventis Sa | Derives de 2,5-dihydro-3h-pyrazolo[4,3-c]pyridazin-3-one substitues,leur preparation et leur application en therapeutique. |
| WO2008073789A1 (en) | 2006-12-11 | 2008-06-19 | Eli Lilly And Company | Ampa receptor potentiators |
| US20080167374A1 (en) | 2007-01-09 | 2008-07-10 | Loveland Products, Inc. | Pesticide composition and method of use |
| US8148367B2 (en) | 2007-01-12 | 2012-04-03 | Takeda Pharmaceutical Company Limited | Renin inhibitors |
| WO2008094556A2 (en) | 2007-01-30 | 2008-08-07 | Biogen Idec Ma Inc. | Imidazolone compounds as tgf-beta family type i receptors, alk5 and/or alk4 antagonists |
| WO2009004430A1 (en) | 2007-06-29 | 2009-01-08 | Pfizer Inc. | N-benzyl oxazolidinones and related heterocycleic compounds as potentiators of glutamate receptors |
| MX2010005028A (es) | 2007-11-05 | 2010-05-27 | Schering Corp | Moduladores de gamma secretasa. |
| JP2009119088A (ja) | 2007-11-16 | 2009-06-04 | Hoya Corp | 内視鏡用バイポーラ高周波処置具 |
| WO2009086303A2 (en) | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| WO2009097970A1 (de) | 2008-02-05 | 2009-08-13 | Sanofi-Aventis | Triazolopyridazine als par1-inhibitoren, ihre herstellung und verwendung als arzneimittel |
| WO2009119088A1 (ja) | 2008-03-25 | 2009-10-01 | 武田薬品工業株式会社 | 複素環化合物 |
| JP2009248543A (ja) | 2008-04-11 | 2009-10-29 | Fujifilm Corp | 光情報記録媒体および情報記録方法 |
| TW201012803A (en) | 2008-06-06 | 2010-04-01 | Organon Nv | Heterocyclic derivatives |
| FR2933698A1 (fr) | 2008-07-09 | 2010-01-15 | Servier Lab | Nouveaux derives de benzothiadiazines cycloalkylees, leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
| CN102149407A (zh) * | 2008-09-10 | 2011-08-10 | 贝林格尔.英格海姆国际有限公司 | 治疗糖尿病和相关病症的组合疗法 |
| AU2009313527A1 (en) | 2008-11-06 | 2010-05-14 | Merck Sharp & Dohme Corp. | Gamma secretase modulators |
| TW201030002A (en) | 2009-01-16 | 2010-08-16 | Bristol Myers Squibb Co | Bicyclic compounds for the reduction of beta-amyloid production |
| JP2012051806A (ja) | 2009-02-26 | 2012-03-15 | Eisai R & D Management Co Ltd | イミダゾリルピラジン誘導体 |
| FR2943342B1 (fr) | 2009-03-20 | 2011-03-04 | Servier Lab | Nouveaux derives de benzothiadiazepines,leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
| WO2010140339A1 (ja) | 2009-06-01 | 2010-12-09 | 武田薬品工業株式会社 | 複素環化合物 |
| WO2011007756A1 (ja) | 2009-07-13 | 2011-01-20 | 武田薬品工業株式会社 | 複素環化合物及びその用途 |
| WO2011036885A1 (ja) | 2009-09-25 | 2011-03-31 | 武田薬品工業株式会社 | 複素環化合物 |
| WO2011036889A1 (ja) | 2009-09-25 | 2011-03-31 | 武田薬品工業株式会社 | 複素環化合物 |
| WO2011138265A2 (en) | 2010-05-03 | 2011-11-10 | Evotec Ag | Indole and indazole derivatives as orexin receptor antagonists |
| US9150591B2 (en) | 2010-08-10 | 2015-10-06 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| WO2014152917A2 (en) | 2013-03-14 | 2014-09-25 | Janssen Pharmaceutica Nv | Physiological ligands for gpr139 |
| MD20170011A2 (ro) | 2014-08-06 | 2017-08-31 | Pfizer Inc. | Compuşi imidazopiridazinici |
| JO3719B1 (ar) | 2014-11-20 | 2021-01-31 | Takeda Pharmaceuticals Co | 4- أوكسو-4،3- داي هيدرو-3،2،1- بنزوترايازينات كمواد ضابطة لأجل gpr139 |
| WO2020081999A1 (en) | 2018-10-18 | 2020-04-23 | Essa Pharma, Inc. | Androgen receptor modulators and methods for their use |
| WO2020097609A1 (en) | 2018-11-09 | 2020-05-14 | Blackthorn Therapeutics, Inc. | Gpr139 receptor modulators |
| CA3134545A1 (en) | 2019-03-28 | 2020-10-01 | Essa Pharma, Inc. | Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof |
| JP2022547952A (ja) | 2019-09-16 | 2022-11-16 | ノバルティス アーゲー | Brd9二機能性分解誘導薬及びその使用方法 |
| CR20220160A (es) | 2019-09-16 | 2022-06-16 | Takeda Pharmaceuticals Co | Derivados de piridazin-3(2h)-ona fusionados con azol |
| JP2021080177A (ja) | 2019-11-14 | 2021-05-27 | 武田薬品工業株式会社 | 複素環化合物及びその用途 |
| WO2021224680A1 (en) | 2020-05-08 | 2021-11-11 | Takeda Pharmaceutical Company Limited | Substituted benzotriazinone metabolites of a gpr139 agonist |
| US20230310441A1 (en) | 2020-09-21 | 2023-10-05 | Takeda Pharmaceutical Company | Treatment for schizophrenia |
-
2020
- 2020-09-15 CR CR20220160A patent/CR20220160A/es unknown
- 2020-09-15 PH PH1/2022/550597A patent/PH12022550597A1/en unknown
- 2020-09-15 CN CN202080079367.0A patent/CN114728975A/zh active Pending
- 2020-09-15 JP JP2022516328A patent/JP7566888B2/ja active Active
- 2020-09-15 HR HRP20250088TT patent/HRP20250088T1/hr unknown
- 2020-09-15 US US17/753,803 patent/US12370192B2/en active Active
- 2020-09-15 IL IL291181A patent/IL291181B2/en unknown
- 2020-09-15 KR KR1020227012292A patent/KR102924294B1/ko active Active
- 2020-09-15 PL PL20781670.3T patent/PL4031552T3/pl unknown
- 2020-09-15 WO PCT/US2020/050823 patent/WO2021055326A1/en not_active Ceased
- 2020-09-15 ES ES20781670T patent/ES2997267T3/es active Active
- 2020-09-15 TW TW109131750A patent/TWI873185B/zh active
- 2020-09-15 JO JOP/2022/0063A patent/JOP20220063A1/ar unknown
- 2020-09-15 HU HUE20781670A patent/HUE069908T2/hu unknown
- 2020-09-15 EP EP20781670.3A patent/EP4031552B1/en active Active
- 2020-09-15 BR BR112022004819A patent/BR112022004819A2/pt unknown
- 2020-09-15 MX MX2022003177A patent/MX2022003177A/es unknown
- 2020-09-15 RS RS20250125A patent/RS66463B1/sr unknown
- 2020-09-15 CA CA3150508A patent/CA3150508A1/en active Pending
- 2020-09-15 AU AU2020348675A patent/AU2020348675B2/en active Active
- 2020-09-15 AR ARP200102558A patent/AR119971A1/es unknown
- 2020-09-15 PE PE2022000427A patent/PE20221341A1/es unknown
-
2022
- 2022-03-15 DO DO2022000057A patent/DOP2022000057A/es unknown
- 2022-03-16 EC ECSENADI202220159A patent/ECSP22020159A/es unknown
- 2022-04-12 CO CONC2022/0004684A patent/CO2022004684A2/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TWI873185B (zh) | 2025-02-21 |
| CR20220160A (es) | 2022-06-16 |
| IL291181A (en) | 2022-05-01 |
| WO2021055326A1 (en) | 2021-03-25 |
| CO2022004684A2 (es) | 2022-07-08 |
| EP4031552A1 (en) | 2022-07-27 |
| CN114728975A (zh) | 2022-07-08 |
| MX2022003177A (es) | 2022-04-06 |
| US12370192B2 (en) | 2025-07-29 |
| PH12022550597A1 (en) | 2024-03-04 |
| EP4031552C0 (en) | 2024-11-06 |
| CA3150508A1 (en) | 2021-03-25 |
| IL291181B1 (en) | 2025-05-01 |
| DOP2022000057A (es) | 2022-06-30 |
| AU2020348675B2 (en) | 2025-11-20 |
| BR112022004819A2 (pt) | 2022-06-07 |
| AR119971A1 (es) | 2022-01-26 |
| AU2020348675A1 (en) | 2022-04-14 |
| HUE069908T2 (hu) | 2025-04-28 |
| PL4031552T3 (pl) | 2025-03-17 |
| JOP20220063A1 (ar) | 2023-01-30 |
| RS66463B1 (sr) | 2025-02-28 |
| JP7566888B2 (ja) | 2024-10-15 |
| IL291181B2 (en) | 2025-09-01 |
| KR20220063228A (ko) | 2022-05-17 |
| US20230028114A1 (en) | 2023-01-26 |
| ECSP22020159A (es) | 2022-05-31 |
| EP4031552B1 (en) | 2024-11-06 |
| KR102924294B1 (ko) | 2026-02-09 |
| ES2997267T3 (en) | 2025-02-14 |
| JP2022548602A (ja) | 2022-11-21 |
| PE20221341A1 (es) | 2022-09-13 |
| TW202124386A (zh) | 2021-07-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HRP20250088T1 (hr) | Derivati piridazin-3(2h)-ona spojeni s azolom | |
| JP2022548602A5 (https=) | ||
| FI3932919T3 (fi) | Jak-inhibiittoriyhdiste ja sen käyttö | |
| RU2019115115A (ru) | Производные пиперидина в качестве ингибиторов убиквитин-специфической протеазы 7 | |
| JP2019535664A5 (https=) | ||
| JP2015514056A5 (https=) | ||
| JP2023525035A5 (https=) | ||
| JP2021503458A5 (https=) | ||
| JP2015527401A5 (https=) | ||
| JP2016537384A5 (https=) | ||
| RU2007126570A (ru) | Аминоимидазолоны, применяемые для ингибирования бета-секретазы | |
| ME02202B (me) | Jedinjenja pirolopirimidina kao inhibitori cdk4/6 | |
| JP2015508075A5 (https=) | ||
| NZ592809A (en) | SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINE COMPOUNDS AS TRK KINASE INHIBITORS | |
| HRP20110015T1 (hr) | DERIVATI IMIDAZO[1,2-a]PIRIDIN-2-KARBOKSAMIDA, NJIHOVO DOBIVANJE I NJIHOVA UPOTREBA U TERAPIJI | |
| HRP20180080T1 (hr) | Pirimidopirimidinoni korisni kao inhibitori wee-1 kinaze | |
| NZ594322A (en) | Poly (ADP-Ribose) Polymerase (PARP) Inhibitors | |
| HRP20191003T1 (hr) | Derivati 4-okso-3,4-dihidro-1,2,3-benzotriazina kao modulatori gpr139 | |
| JP2017511365A5 (https=) | ||
| RU2009140469A (ru) | Производные пирролопиримидин-7-она и их применение в качестве фармацевтических средств | |
| RU2010148534A (ru) | Производные имидазолидинона в качестве ингибиторов в 11b-hsd1 | |
| JP2013544893A5 (https=) | ||
| RU2017135520A (ru) | Бициклические производные хиназолинона | |
| NZ630467A (en) | Substituted pyrrolopyrimidine compounds, compositions thereof, and methods of treatment therewith | |
| RU2009113612A (ru) | Ацетамидные производные хиназолинона и изохинолинона |