CA2867210A1 - Carboxamide compounds and their use as calpain inhibitors v - Google Patents
Carboxamide compounds and their use as calpain inhibitors v Download PDFInfo
- Publication number
- CA2867210A1 CA2867210A1 CA 2867210 CA2867210A CA2867210A1 CA 2867210 A1 CA2867210 A1 CA 2867210A1 CA 2867210 CA2867210 CA 2867210 CA 2867210 A CA2867210 A CA 2867210A CA 2867210 A1 CA2867210 A1 CA 2867210A1
- Authority
- CA
- Canada
- Prior art keywords
- alkyl
- amino
- nicotinamide
- ch2ch2
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- -1 Carboxamide compounds Chemical class 0.000 title claims abstract description 903
- 108010079785 calpain inhibitors Proteins 0.000 title description 26
- 150000001875 compounds Chemical class 0.000 claims abstract description 238
- 108010032088 Calpain Proteins 0.000 claims abstract description 93
- 102000007590 Calpain Human genes 0.000 claims abstract description 93
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 72
- 150000002367 halogens Chemical class 0.000 claims abstract description 72
- 150000003839 salts Chemical class 0.000 claims abstract description 29
- 229940002612 prodrug Drugs 0.000 claims abstract description 27
- 239000000651 prodrug Substances 0.000 claims abstract description 27
- 230000000694 effects Effects 0.000 claims abstract description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 26
- 150000004677 hydrates Chemical class 0.000 claims abstract description 24
- 239000003814 drug Substances 0.000 claims abstract description 23
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 10
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims abstract description 4
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims description 423
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 371
- 235000005152 nicotinamide Nutrition 0.000 claims description 216
- 239000011570 nicotinamide Substances 0.000 claims description 215
- 229960003966 nicotinamide Drugs 0.000 claims description 215
- 150000003254 radicals Chemical class 0.000 claims description 193
- 125000001424 substituent group Chemical group 0.000 claims description 101
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 85
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 79
- 238000011282 treatment Methods 0.000 claims description 56
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 claims description 52
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 47
- 125000001072 heteroaryl group Chemical group 0.000 claims description 46
- 229910052739 hydrogen Inorganic materials 0.000 claims description 44
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 41
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 39
- 125000003118 aryl group Chemical group 0.000 claims description 36
- 125000004432 carbon atom Chemical group C* 0.000 claims description 36
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 35
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 34
- 239000001257 hydrogen Substances 0.000 claims description 34
- 238000000034 method Methods 0.000 claims description 28
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 26
- 208000035475 disorder Diseases 0.000 claims description 25
- 229910052757 nitrogen Inorganic materials 0.000 claims description 25
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims description 24
- 229910052731 fluorine Inorganic materials 0.000 claims description 22
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 22
- 125000005842 heteroatom Chemical group 0.000 claims description 21
- 230000006735 deficit Effects 0.000 claims description 20
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 20
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 19
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 19
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 19
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 19
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 229920006395 saturated elastomer Polymers 0.000 claims description 18
- 229910052717 sulfur Inorganic materials 0.000 claims description 18
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 17
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 17
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 15
- 229910052801 chlorine Inorganic materials 0.000 claims description 14
- 230000006378 damage Effects 0.000 claims description 14
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims description 13
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 11
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims description 9
- 201000010099 disease Diseases 0.000 claims description 9
- VUWZPRWSIVNGKG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH2] VUWZPRWSIVNGKG-UHFFFAOYSA-N 0.000 claims description 9
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 claims description 8
- 108010081348 HRT1 protein Hairy Proteins 0.000 claims description 8
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- 208000015122 neurodegenerative disease Diseases 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 7
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 7
- 210000003734 kidney Anatomy 0.000 claims description 7
- 201000004792 malaria Diseases 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 7
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 7
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical group C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims description 6
- 208000024827 Alzheimer disease Diseases 0.000 claims description 5
- 210000004556 brain Anatomy 0.000 claims description 5
- 210000002216 heart Anatomy 0.000 claims description 5
- 208000028867 ischemia Diseases 0.000 claims description 5
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 208000002177 Cataract Diseases 0.000 claims description 4
- 102000000589 Interleukin-1 Human genes 0.000 claims description 4
- 108010002352 Interleukin-1 Proteins 0.000 claims description 4
- 206010027476 Metastases Diseases 0.000 claims description 4
- 206010028980 Neoplasm Diseases 0.000 claims description 4
- 201000005485 Toxoplasmosis Diseases 0.000 claims description 4
- 206010015037 epilepsy Diseases 0.000 claims description 4
- 208000014674 injury Diseases 0.000 claims description 4
- 201000006417 multiple sclerosis Diseases 0.000 claims description 4
- 201000006938 muscular dystrophy Diseases 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 3
- 208000003890 Coronary Vasospasm Diseases 0.000 claims description 3
- 241000124008 Mammalia Species 0.000 claims description 3
- 208000029549 Muscle injury Diseases 0.000 claims description 3
- 208000018737 Parkinson disease Diseases 0.000 claims description 3
- 208000010362 Protozoan Infections Diseases 0.000 claims description 3
- 238000002399 angioplasty Methods 0.000 claims description 3
- 210000004204 blood vessel Anatomy 0.000 claims description 3
- 208000001286 intracranial vasospasm Diseases 0.000 claims description 3
- 208000002780 macular degeneration Diseases 0.000 claims description 3
- 208000031225 myocardial ischemia Diseases 0.000 claims description 3
- 125000004483 piperidin-3-yl group Chemical group N1CC(CCC1)* 0.000 claims description 3
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims description 3
- 230000035755 proliferation Effects 0.000 claims description 3
- 238000011321 prophylaxis Methods 0.000 claims description 3
- 208000037803 restenosis Diseases 0.000 claims description 3
- 210000002027 skeletal muscle Anatomy 0.000 claims description 3
- 210000000329 smooth muscle myocyte Anatomy 0.000 claims description 3
- 230000001225 therapeutic effect Effects 0.000 claims description 3
- 238000002560 therapeutic procedure Methods 0.000 claims description 3
- 125000004486 1-methylpiperidin-3-yl group Chemical group CN1CC(CCC1)* 0.000 claims description 2
- 125000004575 3-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 208000023105 Huntington disease Diseases 0.000 claims description 2
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims description 2
- 125000004567 azetidin-3-yl group Chemical group N1CC(C1)* 0.000 claims description 2
- 238000002512 chemotherapy Methods 0.000 claims description 2
- 230000001684 chronic effect Effects 0.000 claims description 2
- 208000020832 chronic kidney disease Diseases 0.000 claims description 2
- 208000017169 kidney disease Diseases 0.000 claims description 2
- 230000009401 metastasis Effects 0.000 claims description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 2
- 210000000653 nervous system Anatomy 0.000 claims description 2
- 230000008733 trauma Effects 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 6
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 5
- 229910020008 S(O) Inorganic materials 0.000 claims 3
- BNYTUBFUVIYKJH-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-(5-benzyl-6,7-dihydro-4h-pyrazolo[4,3-c]pyridin-2-yl)pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C3CCN(CC=4C=CC=CC=4)CC3=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 BNYTUBFUVIYKJH-UHFFFAOYSA-N 0.000 claims 2
- 125000004484 1-methylpiperidin-4-yl group Chemical group CN1CCC(CC1)* 0.000 claims 1
- 125000004562 2,3-dihydroindol-1-yl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 claims 1
- OWCDBTVHPCCDKH-UHFFFAOYSA-N 2-[3-(1,3,3a,4,6,6a-hexahydrofuro[3,4-c]pyrrol-5-ylmethyl)pyrazol-1-yl]-n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3CC4COCC4C3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 OWCDBTVHPCCDKH-UHFFFAOYSA-N 0.000 claims 1
- GVMFSSSFBUEBAE-UHFFFAOYSA-N 2-[3-(2,3,4a,5,6,7,8,8a-octahydrobenzo[b][1,4]oxazin-4-ylmethyl)pyrazol-1-yl]-n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3C4CCCCC4OCC3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 GVMFSSSFBUEBAE-UHFFFAOYSA-N 0.000 claims 1
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 1
- 125000005865 C2-C10alkynyl group Chemical group 0.000 claims 1
- WJIUQDVFQWUHSF-KJMDXERQSA-N NC(C(C(CC1=CC=CC=C1)NC(C1=C(N=CC=C1)N1N=C(C=C1)CN1C[C@@H](O[C@H](C1)C)C)=O)=O)=O Chemical compound NC(C(C(CC1=CC=CC=C1)NC(C1=C(N=CC=C1)N1N=C(C=C1)CN1C[C@@H](O[C@H](C1)C)C)=O)=O)=O WJIUQDVFQWUHSF-KJMDXERQSA-N 0.000 claims 1
- VUZKLWFBVBTEEM-UHFFFAOYSA-N n-(1-amino-1,2-dioxoheptan-3-yl)-2-[3-(1,3-dihydroisoindol-2-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound CCCCC(C(=O)C(N)=O)NC(=O)C1=CC=CN=C1N1N=C(CN2CC3=CC=CC=C3C2)C=C1 VUZKLWFBVBTEEM-UHFFFAOYSA-N 0.000 claims 1
- AUQFBJSWVVVMBB-UHFFFAOYSA-N n-(1-amino-1,2-dioxoheptan-3-yl)-2-[3-(piperidin-1-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound CCCCC(C(=O)C(N)=O)NC(=O)C1=CC=CN=C1N1N=C(CN2CCCCC2)C=C1 AUQFBJSWVVVMBB-UHFFFAOYSA-N 0.000 claims 1
- ATRGULGMEOVARJ-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-(4,5,6,7-tetrahydropyrazolo[3,4-c]pyridin-2-yl)pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C3CNCCC3=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 ATRGULGMEOVARJ-UHFFFAOYSA-N 0.000 claims 1
- MFWXXIYPGHHSKP-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-(4,5,6,7-tetrahydropyrazolo[4,3-b]pyridin-2-yl)pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C3CCCNC3=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 MFWXXIYPGHHSKP-UHFFFAOYSA-N 0.000 claims 1
- GKRVFYNZSLLCGN-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-(4,5,6,7-tetrahydropyrazolo[4,3-c]pyridin-2-yl)pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C3CCNCC3=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 GKRVFYNZSLLCGN-UHFFFAOYSA-N 0.000 claims 1
- USEUCNMOKUMNEV-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-(4-benzyl-6,7-dihydro-5h-pyrazolo[4,3-b]pyridin-2-yl)pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C3CCCN(CC=4C=CC=CC=4)C3=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 USEUCNMOKUMNEV-UHFFFAOYSA-N 0.000 claims 1
- JVSVUBOMHVJXFZ-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-(5,6-dihydro-4h-pyrrolo[3,4-c]pyrazol-2-yl)pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C3CNCC3=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 JVSVUBOMHVJXFZ-UHFFFAOYSA-N 0.000 claims 1
- KNYMNZCWZJCQQN-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-(6-ethyl-5,7-dihydro-4h-pyrazolo[3,4-c]pyridin-2-yl)pyridine-3-carboxamide Chemical compound N1=C2CN(CC)CCC2=CN1C1=NC=CC=C1C(=O)NC(C(=O)C(N)=O)CC1=CC=CC=C1 KNYMNZCWZJCQQN-UHFFFAOYSA-N 0.000 claims 1
- SUBXLLJHDNCMRC-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(1,3-dihydroisoindol-2-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3CC4=CC=CC=C4C3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 SUBXLLJHDNCMRC-UHFFFAOYSA-N 0.000 claims 1
- JYQRHBUMDNLJNV-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(1-methylpiperidin-4-yl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C1CN(C)CCC1C1=NN(C=2C(=CC=CN=2)C(=O)NC(CC=2C=CC=CC=2)C(=O)C(N)=O)C=C1 JYQRHBUMDNLJNV-UHFFFAOYSA-N 0.000 claims 1
- YDYBYGOVADVOLI-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(2,3-dihydro-1,4-benzoxazin-4-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3C4=CC=CC=C4OCC3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 YDYBYGOVADVOLI-UHFFFAOYSA-N 0.000 claims 1
- PQSWIYVNEDLAQK-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(2,3-dihydroindol-1-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3C4=CC=CC=C4CC3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 PQSWIYVNEDLAQK-UHFFFAOYSA-N 0.000 claims 1
- BYSYXXOVEBAZAT-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(2-oxa-7-azaspiro[3.5]nonan-7-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3CCC4(COC4)CC3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 BYSYXXOVEBAZAT-UHFFFAOYSA-N 0.000 claims 1
- RIXUBJZLQDRIIJ-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(3,4-dihydro-1h-isoquinolin-2-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3CC4=CC=CC=C4CC3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 RIXUBJZLQDRIIJ-UHFFFAOYSA-N 0.000 claims 1
- RMEKGIQNDPPYPY-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(anilinomethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CNC=3C=CC=CC=3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 RMEKGIQNDPPYPY-UHFFFAOYSA-N 0.000 claims 1
- GYPJJZXDLXQBSI-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(azetidin-1-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3CCC3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 GYPJJZXDLXQBSI-UHFFFAOYSA-N 0.000 claims 1
- QRJJITXLBSQEGP-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(diethylaminomethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound N1=C(CN(CC)CC)C=CN1C1=NC=CC=C1C(=O)NC(C(=O)C(N)=O)CC1=CC=CC=C1 QRJJITXLBSQEGP-UHFFFAOYSA-N 0.000 claims 1
- LNYKWHMNUSKRNS-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(morpholin-4-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3CCOCC3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 LNYKWHMNUSKRNS-UHFFFAOYSA-N 0.000 claims 1
- NUKLZJVEVJHYNI-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(piperidin-1-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3CCCCC3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 NUKLZJVEVJHYNI-UHFFFAOYSA-N 0.000 claims 1
- IBELZVWXCCEZLC-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-(pyrrolidin-1-ylmethyl)pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C=1C=CN=C(N2N=C(CN3CCCC3)C=C2)C=1C(=O)NC(C(=O)C(=O)N)CC1=CC=CC=C1 IBELZVWXCCEZLC-UHFFFAOYSA-N 0.000 claims 1
- WJIUQDVFQWUHSF-UHFFFAOYSA-N n-(4-amino-3,4-dioxo-1-phenylbutan-2-yl)-2-[3-[(2,6-dimethylmorpholin-4-yl)methyl]pyrazol-1-yl]pyridine-3-carboxamide Chemical compound C1C(C)OC(C)CN1CC1=NN(C=2C(=CC=CN=2)C(=O)NC(CC=2C=CC=CC=2)C(=O)C(N)=O)C=C1 WJIUQDVFQWUHSF-UHFFFAOYSA-N 0.000 claims 1
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- 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
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
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- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- 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
- 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
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-
- 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
- C07D491/02—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 two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- 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
- C07D491/02—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 two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
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- Neurosurgery (AREA)
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- Molecular Biology (AREA)
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- Psychiatry (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
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| US201261619590P | 2012-04-03 | 2012-04-03 | |
| US61/619,590 | 2012-04-03 | ||
| PCT/EP2013/055291 WO2013149800A1 (en) | 2012-04-03 | 2013-03-14 | Carboxamide compounds and their use as calpain inhibitors v |
Publications (1)
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| CA2867210A1 true CA2867210A1 (en) | 2013-10-10 |
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| US (1) | US9150545B2 (enExample) |
| EP (1) | EP2834230A1 (enExample) |
| JP (1) | JP2015512427A (enExample) |
| CN (1) | CN104364247A (enExample) |
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| SG (1) | SG11201406345XA (enExample) |
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| WO2017156071A1 (en) | 2016-03-09 | 2017-09-14 | Blade Therapeutics, Inc. | Cyclic keto-amide compounds as calpain modulators and methods of production and use thereof |
| AU2017292646A1 (en) | 2016-07-05 | 2019-02-07 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
| WO2018064119A1 (en) * | 2016-09-28 | 2018-04-05 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
| CA3093749A1 (en) * | 2018-03-28 | 2019-10-03 | Blade Therapeutics, Inc. | Method of treating fibrotic disease |
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| US4826835A (en) | 1985-10-23 | 1989-05-02 | Rorer Pharmaceutical Corporation | Pyridyl-pyridazinone and pyridyl-pyrazolinone compounds and their use in the treatment of congestive heart failure |
| US4743608A (en) | 1986-07-15 | 1988-05-10 | Rorer Pharmaceutical Corporation | Pyridone-pyridyl-imidazolyl and triazolyl compounds and their use as cardiotonic agents |
| DE19642591A1 (de) | 1996-10-15 | 1998-04-16 | Basf Ag | Neue Piperidin-Ketocarbonsäure-Derivate, deren Herstellung und Anwendung |
| DE19650975A1 (de) | 1996-12-09 | 1998-06-10 | Basf Ag | Neue heterocyclisch substituierte Benzamide und deren Anwendung |
| PL334059A1 (en) | 1996-12-11 | 2000-01-31 | Basf Ag | Ketone benzamides useful as calpain inhibitors |
| US6083944A (en) | 1997-10-07 | 2000-07-04 | Cephalon, Inc. | Quinoline-containing α-ketoamide cysteine and serine protease inhibitors |
| DE19817459A1 (de) | 1998-04-20 | 1999-10-21 | Basf Ag | Neue heterozyklische substituierte Amide, Herstellung und Anwendung |
| DE19817461A1 (de) | 1998-04-20 | 1999-10-21 | Basf Ag | Neue substituierte Benzamide, deren Herstellung und Anwendung |
| TR200003071T2 (tr) | 1998-04-20 | 2001-04-20 | Basf Aktiengesellschaft | Sistein-proteazı önleyici etkiye sahip yeni heterosiklik ikame edilmiş amidler |
| CN1306505A (zh) | 1998-04-20 | 2001-08-01 | Basf公司 | 新的取代酰胺、其制备以及应用 |
| PL343495A1 (en) | 1998-04-20 | 2001-08-27 | Basf Ag | Heterocyclically substituted amides used as calpain inhibitors |
| DE19818614A1 (de) | 1998-04-20 | 1999-10-21 | Basf Ag | Neue substituierte Amide, deren Herstellung und Anwendung |
| ATE524440T1 (de) | 1998-05-25 | 2011-09-15 | Abbott Gmbh & Co Kg | Heterocyclische substituierte amide, deren herstellung und anwendung |
| DE10114762A1 (de) | 2001-03-26 | 2002-10-02 | Knoll Gmbh | Verwendung von Cysteinprotease-Inhibitoren |
| RU2441020C2 (ru) | 2005-08-02 | 2012-01-27 | Вертекс Фармасьютикалз Инкорпорейтед | Ингибиторы серинпротеазы |
| PT2439205E (pt) * | 2006-12-29 | 2015-07-16 | Abbvie Deutschland | Compostos de carboxamida e seus usos como inibidores de calpaína |
| JP2010519339A (ja) | 2007-02-26 | 2010-06-03 | アキリオン ファーマシューティカルズ，インコーポレーテッド | Ｈｃｖ複製阻害剤として有用な三級アミン置換ペプチド |
| TWI453019B (zh) * | 2007-12-28 | 2014-09-21 | Abbvie Deutschland | 甲醯胺化合物 |
| TWI519530B (zh) * | 2009-02-20 | 2016-02-01 | 艾伯維德國有限及兩合公司 | 羰醯胺化合物及其作為鈣蛋白酶（ｃａｌｐａｉｎ）抑制劑之用途 |
| JP5577548B2 (ja) * | 2009-12-09 | 2014-08-27 | マーベル ワールド トレード リミテッド | 無線通信のフレームパディング |
| US8430139B2 (en) * | 2009-12-11 | 2013-04-30 | Agco Corporation | Automated refilling connection for a liquid material container of an applicator |
| US8598211B2 (en) | 2009-12-22 | 2013-12-03 | Abbvie Inc. | Carboxamide compounds and their use as calpain inhibitors IV |
| US9051304B2 (en) | 2009-12-22 | 2015-06-09 | AbbVie Deutschland GmbH & Co. KG | Carboxamide compounds and their use as calpain inhibitors V |
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2013
- 2013-03-14 EP EP13709139.3A patent/EP2834230A1/en not_active Withdrawn
- 2013-03-14 US US14/390,381 patent/US9150545B2/en not_active Expired - Fee Related
- 2013-03-14 MX MX2014011998A patent/MX2014011998A/es unknown
- 2013-03-14 JP JP2015503800A patent/JP2015512427A/ja active Pending
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- 2013-03-14 SG SG11201406345XA patent/SG11201406345XA/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US9150545B2 (en) | 2015-10-06 |
| EP2834230A1 (en) | 2015-02-11 |
| US20150065477A1 (en) | 2015-03-05 |
| CN104364247A (zh) | 2015-02-18 |
| RU2014144285A (ru) | 2016-05-27 |
| SG11201406345XA (en) | 2014-11-27 |
| WO2013149800A1 (en) | 2013-10-10 |
| MX2014011998A (es) | 2015-05-11 |
| JP2015512427A (ja) | 2015-04-27 |
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