CA2892931A1 - Cyclohexyl and quinuclidinyl carbamate derivatives having ss2 adrenergic agonist and m3 muscarinic antagonist activities - Google Patents
Cyclohexyl and quinuclidinyl carbamate derivatives having ss2 adrenergic agonist and m3 muscarinic antagonist activities Download PDFInfo
- Publication number
- CA2892931A1 CA2892931A1 CA2892931A CA2892931A CA2892931A1 CA 2892931 A1 CA2892931 A1 CA 2892931A1 CA 2892931 A CA2892931 A CA 2892931A CA 2892931 A CA2892931 A CA 2892931A CA 2892931 A1 CA2892931 A1 CA 2892931A1
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- CA
- Canada
- Prior art keywords
- group
- hydroxy
- oxo
- amino
- carbamate
- 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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- 229940121948 Muscarinic receptor antagonist Drugs 0.000 title claims abstract description 7
- 239000003149 muscarinic antagonist Substances 0.000 title claims abstract description 7
- 239000000048 adrenergic agonist Substances 0.000 title claims abstract description 6
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 title claims description 76
- 230000000694 effects Effects 0.000 title claims description 16
- LSUSEBREYXZDHC-UHFFFAOYSA-N 1-azabicyclo[2.2.2]octan-2-yl carbamate Chemical class C1CN2C(OC(=O)N)CC1CC2 LSUSEBREYXZDHC-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 193
- 238000000034 method Methods 0.000 claims abstract description 34
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 10
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 374
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 231
- -1 3-bromoisoxazol-5-yl Chemical group 0.000 claims description 154
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 106
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 97
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 78
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 70
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 46
- 125000001424 substituent group Chemical group 0.000 claims description 39
- 125000005843 halogen group Chemical group 0.000 claims description 37
- 229910052757 nitrogen Inorganic materials 0.000 claims description 33
- 125000003118 aryl group Chemical group 0.000 claims description 32
- 125000005842 heteroatom Chemical group 0.000 claims description 32
- 125000000217 alkyl group Chemical group 0.000 claims description 31
- 125000002950 monocyclic group Chemical group 0.000 claims description 31
- 229910052717 sulfur Inorganic materials 0.000 claims description 30
- 150000003839 salts Chemical class 0.000 claims description 28
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 27
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 26
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 25
- 125000002619 bicyclic group Chemical group 0.000 claims description 24
- 201000010099 disease Diseases 0.000 claims description 24
- 229920006395 saturated elastomer Polymers 0.000 claims description 24
- 238000011282 treatment Methods 0.000 claims description 24
- 125000004122 cyclic group Chemical group 0.000 claims description 22
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 22
- 125000003545 alkoxy group Chemical group 0.000 claims description 20
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims description 19
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 18
- 125000006269 biphenyl-2-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C(*)C([H])=C([H])C([H])=C1[H] 0.000 claims description 18
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 15
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 14
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- 125000002947 alkylene group Chemical group 0.000 claims description 13
- 208000006673 asthma Diseases 0.000 claims description 13
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 13
- 229910052801 chlorine Inorganic materials 0.000 claims description 12
- 125000001072 heteroaryl group Chemical group 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 125000004043 oxo group Chemical group O=* 0.000 claims description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 11
- 230000001575 pathological effect Effects 0.000 claims description 11
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 11
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims description 10
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 9
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 9
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 8
- 208000019693 Lung disease Diseases 0.000 claims description 8
- 208000020446 Cardiac disease Diseases 0.000 claims description 7
- 208000010412 Glaucoma Diseases 0.000 claims description 7
- 206010061218 Inflammation Diseases 0.000 claims description 7
- 208000012902 Nervous system disease Diseases 0.000 claims description 7
- 125000004450 alkenylene group Chemical group 0.000 claims description 7
- 125000004419 alkynylene group Chemical group 0.000 claims description 7
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 7
- 208000019622 heart disease Diseases 0.000 claims description 7
- 230000004054 inflammatory process Effects 0.000 claims description 7
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 7
- 208000018522 Gastrointestinal disease Diseases 0.000 claims description 6
- 241001465754 Metazoa Species 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 6
- 229940123932 Phosphodiesterase 4 inhibitor Drugs 0.000 claims description 5
- 239000003246 corticosteroid Substances 0.000 claims description 5
- 125000005647 linker group Chemical group 0.000 claims description 5
- 239000002587 phosphodiesterase IV inhibitor Substances 0.000 claims description 5
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 4
- 208000025966 Neurological disease Diseases 0.000 claims description 4
- 229910006074 SO2NH2 Inorganic materials 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 4
- 230000027455 binding Effects 0.000 claims description 4
- 238000002560 therapeutic procedure Methods 0.000 claims description 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 3
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 3
- 229940126157 adrenergic receptor agonist Drugs 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 3
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 239000013066 combination product Substances 0.000 claims description 2
- 229940127555 combination product Drugs 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 3
- JYNLMDLHXSODRK-HKBQPEDESA-N [5-[4-[2-chloro-4-[[[(2r)-2-hydroxy-2-(8-hydroxy-2-oxo-1h-quinolin-5-yl)ethyl]amino]methyl]-5-methoxyanilino]-4-oxobutyl]-2-phenylphenyl]carbamic acid Chemical compound ClC=1C=C(CNC[C@H](O)C=2C=3C=CC(=O)NC=3C(O)=CC=2)C(OC)=CC=1NC(=O)CCCC(C=C1NC(O)=O)=CC=C1C1=CC=CC=C1 JYNLMDLHXSODRK-HKBQPEDESA-N 0.000 claims 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 2
- IQUKEEOVVMYVLT-GRMGZNQSSA-N CC(Cc1ccc(NC(=O)CCCc2ccc(c(NC(=O)O[C@H]3CC[C@H](N)CC3)c2)-c2ccccc2)cc1)NC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 Chemical compound CC(Cc1ccc(NC(=O)CCCc2ccc(c(NC(=O)O[C@H]3CC[C@H](N)CC3)c2)-c2ccccc2)cc1)NC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 IQUKEEOVVMYVLT-GRMGZNQSSA-N 0.000 claims 1
- SXZMZLCFHSOOQR-APGGIDQDSA-N CN(CCCc1ccccc1)[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)Nc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 Chemical compound CN(CCCc1ccccc1)[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)Nc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 SXZMZLCFHSOOQR-APGGIDQDSA-N 0.000 claims 1
- NHIZQNQGNNNCEL-PJWSZRIZSA-N CN[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCn2nnc3cc(CNC[C@H](O)c4ccc(O)c5[nH]c(=O)ccc45)ccc23)ccc1-c1ccccc1 Chemical compound CN[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCn2nnc3cc(CNC[C@H](O)c4ccc(O)c5[nH]c(=O)ccc45)ccc23)ccc1-c1ccccc1 NHIZQNQGNNNCEL-PJWSZRIZSA-N 0.000 claims 1
- KXVCAMAYBLGJEE-LHEWISCISA-N COc1cc(C(=O)NCCCCc2ccc(c(NC(=O)OC34CCN(CC3)CC4)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 Chemical compound COc1cc(C(=O)NCCCCc2ccc(c(NC(=O)OC34CCN(CC3)CC4)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 KXVCAMAYBLGJEE-LHEWISCISA-N 0.000 claims 1
- DKEYIFSYCLTCFD-PBCNQIPESA-N COc1cc(C(=O)NCCCc2ccc(c(NC(=O)O[C@H]3CC[C@H](N)CC3)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 Chemical compound COc1cc(C(=O)NCCCc2ccc(c(NC(=O)O[C@H]3CC[C@H](N)CC3)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 DKEYIFSYCLTCFD-PBCNQIPESA-N 0.000 claims 1
- LKMNEVBGWPHKDS-PBCNQIPESA-N COc1cc(NC(=O)CCCc2ccc(c(NC(=O)O[C@H]3CC[C@H](N)CC3)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 Chemical compound COc1cc(NC(=O)CCCc2ccc(c(NC(=O)O[C@H]3CC[C@H](N)CC3)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 LKMNEVBGWPHKDS-PBCNQIPESA-N 0.000 claims 1
- UITHQOQPCHMHFI-BHVANESWSA-N COc1cc(NC(=O)CCc2ccc(c(NC(=O)OC34CCN(CC3)CC4)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 Chemical compound COc1cc(NC(=O)CCc2ccc(c(NC(=O)OC34CCN(CC3)CC4)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 UITHQOQPCHMHFI-BHVANESWSA-N 0.000 claims 1
- JNHRTMOVJFFXHF-PBCNQIPESA-N COc1cc(NC(=O)NCCCc2ccc(c(NC(=O)O[C@H]3CC[C@H](N)CC3)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 Chemical compound COc1cc(NC(=O)NCCCc2ccc(c(NC(=O)O[C@H]3CC[C@H](N)CC3)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 JNHRTMOVJFFXHF-PBCNQIPESA-N 0.000 claims 1
- MRXCJOAHPDUELM-HFAAXNRMSA-N COc1cc(NC(=O)OCCc2ccc(c(NC(=O)O[C@H]3CC[C@H](N)CC3)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 Chemical compound COc1cc(NC(=O)OCCc2ccc(c(NC(=O)O[C@H]3CC[C@H](N)CC3)c2)-c2ccccc2)c(Cl)cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 MRXCJOAHPDUELM-HFAAXNRMSA-N 0.000 claims 1
- PGVVJYCFVDQZTC-PEWNMUGKSA-N COc1cc2n(CCCCc3ccc(c(NC(=O)O[C@H]4CC[C@H](N)CC4)c3)-c3ccccc3)c(=O)oc2cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 Chemical compound COc1cc2n(CCCCc3ccc(c(NC(=O)O[C@H]4CC[C@H](N)CC4)c3)-c3ccccc3)c(=O)oc2cc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 PGVVJYCFVDQZTC-PEWNMUGKSA-N 0.000 claims 1
- IGNIMYXNZKWYQG-PEWNMUGKSA-N ClC1=C(OCC(=O)N(CCC2=CC(=C(C=C2)C2=CC=CC=C2)NC(O[C@@H]2CC[C@H](CC2)N)=O)C)C=C(C(=C1)CNC[C@@H](C1=C2C=CC(NC2=C(C=C1)O)=O)O)OC Chemical compound ClC1=C(OCC(=O)N(CCC2=CC(=C(C=C2)C2=CC=CC=C2)NC(O[C@@H]2CC[C@H](CC2)N)=O)C)C=C(C(=C1)CNC[C@@H](C1=C2C=CC(NC2=C(C=C1)O)=O)O)OC IGNIMYXNZKWYQG-PEWNMUGKSA-N 0.000 claims 1
- RHQBFVKSQMOCEJ-QNGWXLTQSA-N N12CCC(CC1)(CC2)OC(NC2=C(C=CC(=C2)CCCC(=O)NC2=C(C=C(C(=C2)OC)CNC[C@@H](C2=C1C=CC(NC1=C(C=C2)O)=O)O)Cl)C2=CC=CC=C2)=O Chemical compound N12CCC(CC1)(CC2)OC(NC2=C(C=CC(=C2)CCCC(=O)NC2=C(C=C(C(=C2)OC)CNC[C@@H](C2=C1C=CC(NC1=C(C=C2)O)=O)O)Cl)C2=CC=CC=C2)=O RHQBFVKSQMOCEJ-QNGWXLTQSA-N 0.000 claims 1
- SAZAIKWUSASFIF-QNGWXLTQSA-N N12CCC(CC1)(CC2)OC(NC2=C(C=CC(=C2)CCCC(=O)NC2=CC=C(C=C2)CNC[C@@H](C2=C1C=CC(NC1=C(C=C2)O)=O)O)C2=CC=CC=C2)=O Chemical compound N12CCC(CC1)(CC2)OC(NC2=C(C=CC(=C2)CCCC(=O)NC2=CC=C(C=C2)CNC[C@@H](C2=C1C=CC(NC1=C(C=C2)O)=O)O)C2=CC=CC=C2)=O SAZAIKWUSASFIF-QNGWXLTQSA-N 0.000 claims 1
- FFHSFEDGLGWGMK-VKVOJFMMSA-N N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCC(=O)Nc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 Chemical compound N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCC(=O)Nc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 FFHSFEDGLGWGMK-VKVOJFMMSA-N 0.000 claims 1
- GDWGZPIBBFIVLD-QXGWMLRCSA-N N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)NCc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 Chemical compound N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)NCc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 GDWGZPIBBFIVLD-QXGWMLRCSA-N 0.000 claims 1
- GSRXHJHFBWUICX-CTUFICKCSA-N N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)N[C@H]2C[C@H](CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)C2)ccc1-c1ccccc1 Chemical compound N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)N[C@H]2C[C@H](CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)C2)ccc1-c1ccccc1 GSRXHJHFBWUICX-CTUFICKCSA-N 0.000 claims 1
- JZDUYRDVGLDMRJ-CGPQEVDYSA-N N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)Nc2ccc(CCNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 Chemical compound N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)Nc2ccc(CCNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 JZDUYRDVGLDMRJ-CGPQEVDYSA-N 0.000 claims 1
- WVIXMPMZRSYLAJ-RLSUVSHZSA-N N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)Nc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cn2)ccc1-c1ccccc1 Chemical compound N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)Nc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cn2)ccc1-c1ccccc1 WVIXMPMZRSYLAJ-RLSUVSHZSA-N 0.000 claims 1
- MYPNIBUVUHVWKB-XEUOYXRDSA-N N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)Nc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)nc2)ccc1-c1ccccc1 Chemical compound N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCC(=O)Nc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)nc2)ccc1-c1ccccc1 MYPNIBUVUHVWKB-XEUOYXRDSA-N 0.000 claims 1
- XLHVQEYJYLFVSZ-CGPQEVDYSA-N N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCCC(=O)Nc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 Chemical compound N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCCC(=O)Nc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 XLHVQEYJYLFVSZ-CGPQEVDYSA-N 0.000 claims 1
- KMUJOTLFXSWFPB-ZJSPHFAPSA-N N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCCCn2c3ccc(CNC[C@H](O)c4ccc(O)c5[nH]c(=O)ccc45)cc3oc2=O)ccc1-c1ccccc1 Chemical compound N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCCCn2c3ccc(CNC[C@H](O)c4ccc(O)c5[nH]c(=O)ccc45)cc3oc2=O)ccc1-c1ccccc1 KMUJOTLFXSWFPB-ZJSPHFAPSA-N 0.000 claims 1
- QHTZQZDBZWADBV-GJKXJCFRSA-N N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCCOc2ccc(CCNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 Chemical compound N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCCOc2ccc(CCNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 QHTZQZDBZWADBV-GJKXJCFRSA-N 0.000 claims 1
- DFNACOSHHZKSBV-CGPQEVDYSA-N N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCCOc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 Chemical compound N[C@H]1CC[C@@H](CC1)OC(=O)Nc1cc(CCCCOc2ccc(CNC[C@H](O)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1-c1ccccc1 DFNACOSHHZKSBV-CGPQEVDYSA-N 0.000 claims 1
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- WASRJUXSLHUONH-UHFFFAOYSA-N ethyl 4-aminocyclohexane-1-carboxylate Chemical compound CCOC(=O)C1CCC(N)CC1 WASRJUXSLHUONH-UHFFFAOYSA-N 0.000 description 1
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- KEWHKYJURDBRMN-ZEODDXGYSA-M ipratropium bromide hydrate Chemical compound O.[Br-].O([C@H]1C[C@H]2CC[C@@H](C1)[N@@+]2(C)C(C)C)C(=O)C(CO)C1=CC=CC=C1 KEWHKYJURDBRMN-ZEODDXGYSA-M 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate Chemical compound [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
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- 238000002955 isolation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
- C07D453/04—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems having a quinolyl-4, a substituted quinolyl-4 or a alkylenedioxy-quinolyl-4 radical linked through only one carbon atom, attached in position 2, e.g. quinine
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- 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
- A61K31/439—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 the ring forming part of a bridged ring system, e.g. quinuclidine
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- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4704—2-Quinolinones, e.g. carbostyril
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- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- A61K31/47—Quinolines; Isoquinolines
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- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/55—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound the modifying agent being also a pharmacologically or therapeutically active agent, i.e. the entire conjugate being a codrug, i.e. a dimer, oligomer or polymer of pharmacologically or therapeutically active compounds
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| PCT/EP2013/076973 WO2014095920A1 (en) | 2012-12-18 | 2013-12-17 | New cyclohexyl and quinuclidinyl carbamate derivatives having beta2 adrenergic agonist and m3 muscarinic antagonist activity |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11175268B2 (en) | 2014-06-09 | 2021-11-16 | Biometry Inc. | Mini point of care gas chromatographic test strip and method to measure analytes |
| US11255840B2 (en) | 2016-07-19 | 2022-02-22 | Biometry Inc. | Methods of and systems for measuring analytes using batch calibratable test strips |
| US11435340B2 (en) | 2014-06-09 | 2022-09-06 | Biometry Inc. | Low cost test strip and method to measure analyte |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| EP2386555A1 (en) | 2010-05-13 | 2011-11-16 | Almirall, S.A. | New cyclohexylamine derivatives having beta2 adrenergic agonist and m3 muscarinic antagonist activities |
| ITRM20110083U1 (it) | 2010-05-13 | 2011-11-14 | De La Cruz Jose Antonio Freire | Piastra per la costruzione di carrelli per aeroplani |
| EP2592078A1 (en) | 2011-11-11 | 2013-05-15 | Almirall, S.A. | New cyclohexylamine derivatives having beta2 adrenergic agonist and M3 muscarinic antagonist activities |
| EA201500651A1 (ru) | 2012-12-18 | 2015-11-30 | Альмираль, С.А. | НОВЫЕ ПРОИЗВОДНЫЕ ЦИКЛОГЕКСИЛ- И ХИНУКЛИДИНИЛКАРБАМАТА, ОБЛАДАЮЩИЕ АГОНИСТИЧЕСКОЙ АКТИВНОСТЬЮ ПО ОТНОШЕНИЮ К β2 АДРЕНЕРГИЧЕСКОМУ РЕЦЕПТОРУ И АНТАГОНИСТИЧЕСКОЙ АКТИВНОСТЬЮ ПО ОТНОШЕНИЮ К МУСКАРИНОВОМУ РЕЦЕПТОРУ М3 |
| TWI643853B (zh) | 2013-02-27 | 2018-12-11 | 阿爾米雷爾有限公司 | 同時具有β2腎上腺素受體促效劑和M3毒蕈鹼受體拮抗劑活性之2-氨基-1-羥乙基-8-羥基喹啉-2(1H)-酮衍生物之鹽類 |
| TWI641373B (zh) | 2013-07-25 | 2018-11-21 | 阿爾米雷爾有限公司 | 具有蕈毒鹼受體拮抗劑和β2腎上腺素受體促效劑二者之活性的2-胺基-1-羥乙基-8-羥基喹啉-2(1H)-酮衍生物之鹽 |
| TW201517906A (zh) | 2013-07-25 | 2015-05-16 | Almirall Sa | 含有maba化合物和皮質類固醇之組合 |
| TW201617343A (zh) | 2014-09-26 | 2016-05-16 | 阿爾米雷爾有限公司 | 具有β2腎上腺素促效劑及M3蕈毒拮抗劑活性之新穎雙環衍生物 |
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