JP2009534420A5 - - Google Patents
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- JP2009534420A5 JP2009534420A5 JP2009506793A JP2009506793A JP2009534420A5 JP 2009534420 A5 JP2009534420 A5 JP 2009534420A5 JP 2009506793 A JP2009506793 A JP 2009506793A JP 2009506793 A JP2009506793 A JP 2009506793A JP 2009534420 A5 JP2009534420 A5 JP 2009534420A5
- Authority
- JP
- Japan
- Prior art keywords
- chloro
- urea
- hydroxyphenyl
- phenyl
- diazabicyclo
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- -1 phenyloxy Chemical group 0.000 claims 33
- 150000001875 compounds Chemical class 0.000 claims 26
- 125000000217 alkyl group Chemical group 0.000 claims 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 12
- 229910052736 halogen Inorganic materials 0.000 claims 8
- 150000002367 halogens Chemical group 0.000 claims 8
- 102000019034 Chemokines Human genes 0.000 claims 7
- 108010012236 Chemokines Proteins 0.000 claims 7
- 201000010099 disease Diseases 0.000 claims 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 7
- 125000006555 (C3-C5) cycloalkyl group Chemical group 0.000 claims 6
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 6
- 241000124008 Mammalia Species 0.000 claims 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 6
- 239000004202 carbamide Substances 0.000 claims 6
- 125000001424 substituent group Chemical group 0.000 claims 6
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 230000001404 mediated effect Effects 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- 150000003839 salts Chemical class 0.000 claims 5
- GZBLFQYBTDMOIN-MQVJKMGUSA-N 1-[3-[[(1s,5r)-3-(butylamino)-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]-4-chloro-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound N1([C@]2([H])CC[C@]1(CC(C2)NCCCC)[H])S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1Cl GZBLFQYBTDMOIN-MQVJKMGUSA-N 0.000 claims 4
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims 4
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 claims 4
- 208000011341 adult acute respiratory distress syndrome Diseases 0.000 claims 4
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims 4
- 208000006673 asthma Diseases 0.000 claims 4
- 125000004122 cyclic group Chemical group 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 4
- MJMBYVFAKNILJO-OKILXGFUSA-N 1-[4-chloro-2-hydroxy-3-[[(1r,5s)-3-hydroxyimino-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]phenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound N1([C@]2([H])CC[C@]1(CC(C2)=NO)[H])S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1C MJMBYVFAKNILJO-OKILXGFUSA-N 0.000 claims 3
- ZBDSJFYZOPFXIP-GOOCMWNKSA-N 1-[4-chloro-2-hydroxy-3-[[(1s,5r)-3-(methylamino)-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]phenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound N1([C@]2([H])CC[C@]1(CC(C2)NC)[H])S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1C ZBDSJFYZOPFXIP-GOOCMWNKSA-N 0.000 claims 3
- RNNBGAHBGNJAGE-UHFFFAOYSA-N 1-[4-chloro-3-(3,8-diazabicyclo[3.2.1]octan-3-ylsulfonyl)-2-hydroxyphenyl]-3-(2-phenoxyphenyl)urea Chemical compound C1=CC(Cl)=C(S(=O)(=O)N2CC3CCC(N3)C2)C(O)=C1NC(=O)NC1=CC=CC=C1OC1=CC=CC=C1 RNNBGAHBGNJAGE-UHFFFAOYSA-N 0.000 claims 3
- HONMASBTBAPAJJ-UHFFFAOYSA-N 1-[4-chloro-3-(3,8-diazabicyclo[3.2.1]octan-3-ylsulfonyl)-2-hydroxyphenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound CC1=C(F)C=CC=C1NC(=O)NC1=CC=C(Cl)C(S(=O)(=O)N2CC3CCC(N3)C2)=C1O HONMASBTBAPAJJ-UHFFFAOYSA-N 0.000 claims 3
- AUIYZBPIYFZKJY-GOOCMWNKSA-N 1-[4-chloro-3-[[(1r,5s)-3-(cyclopropylamino)-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C([C@]1(CC[C@@](C2)(N1S(=O)(=O)C=1C(=C(NC(=O)NC=3C(=C(F)C=CC=3)Cl)C=CC=1Cl)O)[H])[H])C2NC1CC1 AUIYZBPIYFZKJY-GOOCMWNKSA-N 0.000 claims 3
- UKEODWQYKLFNKV-AGUYFDCRSA-N 1-[4-chloro-3-[[(1r,5s)-3-(ethylamino)-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound N1([C@]2([H])CC[C@]1(CC(C2)NCC)[H])S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1Cl UKEODWQYKLFNKV-AGUYFDCRSA-N 0.000 claims 3
- WUMHAFGYRJQVAA-MQVJKMGUSA-N 1-[4-chloro-3-[[(1r,5s)-3-(ethylamino)-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]-2-hydroxyphenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound N1([C@]2([H])CC[C@]1(CC(C2)NCC)[H])S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1C WUMHAFGYRJQVAA-MQVJKMGUSA-N 0.000 claims 3
- XJPKPJLOCXRDSH-KBPBESRZSA-N 1-[4-chloro-3-[[(1s,4s)-5-(cyclopropylmethyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl]sulfonyl]-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C([C@]1(N(C[C@@]2(C1)[H])S(=O)(=O)C=1C(=CC=C(NC(=O)NC=3C(=C(F)C=CC=3)Cl)C=1O)Cl)[H])N2CC1CC1 XJPKPJLOCXRDSH-KBPBESRZSA-N 0.000 claims 3
- XGGAKJCYUCGHMZ-PHIMTYICSA-N 1-[4-chloro-3-[[(1s,5r)-3,8-diazabicyclo[3.2.1]octan-8-yl]sulfonyl]-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound N1([C@]2([H])CC[C@]1(CNC2)[H])S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1Cl XGGAKJCYUCGHMZ-PHIMTYICSA-N 0.000 claims 3
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims 3
- 206010040070 Septic Shock Diseases 0.000 claims 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 3
- GQHISURWNNDZTN-RYUDHWBXSA-N 1-(2-chloro-3-fluorophenyl)-3-[4-chloro-2-hydroxy-3-[[(1s,4s)-5-(2-hydroxyethyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl]sulfonyl]phenyl]urea Chemical compound C([C@]1(N(C[C@]2([H])C1)CCO)[H])N2S(=O)(=O)C(C=1O)=C(Cl)C=CC=1NC(=O)NC1=CC=CC(F)=C1Cl GQHISURWNNDZTN-RYUDHWBXSA-N 0.000 claims 2
- ZGFRYCRDXCTXBA-QWRGUYRKSA-N 1-(2-chloro-3-fluorophenyl)-3-[4-chloro-2-hydroxy-3-[[(1s,4s)-5-methyl-2,5-diazabicyclo[2.2.1]heptan-2-yl]sulfonyl]phenyl]urea Chemical compound C([C@]1(N(C[C@]2([H])C1)C)[H])N2S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1Cl ZGFRYCRDXCTXBA-QWRGUYRKSA-N 0.000 claims 2
- DAZVVDHMHGRJEE-OALUTQOASA-N 1-[4-chloro-2-hydroxy-3-[[(1s,4s)-5-methyl-2,5-diazabicyclo[2.2.1]heptan-2-yl]sulfonyl]phenyl]-3-(2-phenylmethoxyphenyl)urea Chemical compound C([C@]1(N(C[C@]2([H])C1)C)[H])N2S(=O)(=O)C(C=1O)=C(Cl)C=CC=1NC(=O)NC1=CC=CC=C1OCC1=CC=CC=C1 DAZVVDHMHGRJEE-OALUTQOASA-N 0.000 claims 2
- HSBKLRQSRFANNZ-UHFFFAOYSA-N 1-[4-chloro-3-(1,8-diazaspiro[4.5]decan-8-ylsulfonyl)-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C1=CC(Cl)=C(S(=O)(=O)N2CCC3(NCCC3)CC2)C(O)=C1NC(=O)NC1=CC=CC(F)=C1Cl HSBKLRQSRFANNZ-UHFFFAOYSA-N 0.000 claims 2
- DWMIADSRLTYJBG-UHFFFAOYSA-N 1-[4-chloro-3-(1,8-diazaspiro[4.5]decan-8-ylsulfonyl)-2-hydroxyphenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound CC1=C(F)C=CC=C1NC(=O)NC1=CC=C(Cl)C(S(=O)(=O)N2CCC3(NCCC3)CC2)=C1O DWMIADSRLTYJBG-UHFFFAOYSA-N 0.000 claims 2
- ACQFHYAQGLSNAC-UHFFFAOYSA-N 1-[4-chloro-3-(6,8-dihydro-5h-imidazo[1,2-a]pyrazin-7-ylsulfonyl)-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C1=CC(Cl)=C(S(=O)(=O)N2CC3=NC=CN3CC2)C(O)=C1NC(=O)NC1=CC=CC(F)=C1Cl ACQFHYAQGLSNAC-UHFFFAOYSA-N 0.000 claims 2
- DNOKBVYRPWLULP-ZJUUUORDSA-N 1-[4-chloro-3-[[(1s,4r)-2,5-diazabicyclo[2.2.1]heptan-2-yl]sulfonyl]-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C([C@@]1(NC[C@]2([H])C1)[H])N2S(=O)(=O)C(C=1O)=C(Cl)C=CC=1NC(=O)NC1=CC=CC(F)=C1Cl DNOKBVYRPWLULP-ZJUUUORDSA-N 0.000 claims 2
- DNOKBVYRPWLULP-UWVGGRQHSA-N 1-[4-chloro-3-[[(1s,4s)-2,5-diazabicyclo[2.2.1]heptan-2-yl]sulfonyl]-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C([C@]1(NC[C@]2([H])C1)[H])N2S(=O)(=O)C(C=1O)=C(Cl)C=CC=1NC(=O)NC1=CC=CC(F)=C1Cl DNOKBVYRPWLULP-UWVGGRQHSA-N 0.000 claims 2
- UNIWORFJYDXWQB-HOTGVXAUSA-N 1-[4-chloro-3-[[(1s,4s)-2,5-diazabicyclo[2.2.1]heptan-2-yl]sulfonyl]-2-hydroxyphenyl]-3-(2-phenoxyphenyl)urea Chemical compound C([C@]1(NC[C@]2([H])C1)[H])N2S(=O)(=O)C(C=1O)=C(Cl)C=CC=1NC(=O)NC1=CC=CC=C1OC1=CC=CC=C1 UNIWORFJYDXWQB-HOTGVXAUSA-N 0.000 claims 2
- QKZATTLECOGXEB-ROUUACIJSA-N 1-[4-chloro-3-[[(1s,4s)-2,5-diazabicyclo[2.2.1]heptan-2-yl]sulfonyl]-2-hydroxyphenyl]-3-(2-phenylmethoxyphenyl)urea Chemical compound C([C@]1(NC[C@]2([H])C1)[H])N2S(=O)(=O)C(C=1O)=C(Cl)C=CC=1NC(=O)NC1=CC=CC=C1OCC1=CC=CC=C1 QKZATTLECOGXEB-ROUUACIJSA-N 0.000 claims 2
- NBNZDLOYGFNKSX-PHIMTYICSA-N 1-[4-chloro-3-[[(1s,5r)-3,8-diazabicyclo[3.2.1]octan-3-yl]sulfonyl]-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C([C@]1(CC[C@@](C2)(N1)[H])[H])N2S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1Cl NBNZDLOYGFNKSX-PHIMTYICSA-N 0.000 claims 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims 2
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims 2
- 102000012740 beta Adrenergic Receptors Human genes 0.000 claims 2
- 108010079452 beta Adrenergic Receptors Proteins 0.000 claims 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 239000012948 isocyanate Substances 0.000 claims 2
- 150000002513 isocyanates Chemical class 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims 1
- GBVWZFOKWBOKSZ-PHIMTYICSA-N 1-(2-chloro-3-fluorophenyl)-3-[4-chloro-2-hydroxy-3-[[(1s,5r)-3-oxo-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]phenyl]urea Chemical compound N1([C@]2([H])CC[C@]1(CC(=O)C2)[H])S(=O)(=O)C(C=1O)=C(Cl)C=CC=1NC(=O)NC1=CC=CC(F)=C1Cl GBVWZFOKWBOKSZ-PHIMTYICSA-N 0.000 claims 1
- CHWTWYIXLKQNQB-UHFFFAOYSA-N 1-[3-(1,2,3,3a,4,6,7,7a-octahydropyrrolo[3,2-c]pyridin-5-ylsulfonyl)-4-chloro-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C1=CC(Cl)=C(S(=O)(=O)N2CC3CCNC3CC2)C(O)=C1NC(=O)NC1=CC=CC(F)=C1Cl CHWTWYIXLKQNQB-UHFFFAOYSA-N 0.000 claims 1
- SEGNSEUXIMDNPI-UHFFFAOYSA-N 1-[3-(1,2,3,3a,4,6,7,7a-octahydropyrrolo[3,2-c]pyridin-5-ylsulfonyl)-4-chloro-2-hydroxyphenyl]-3-(2-chloropyridin-3-yl)urea Chemical compound C1=CC(Cl)=C(S(=O)(=O)N2CC3CCNC3CC2)C(O)=C1NC(=O)NC1=CC=CN=C1Cl SEGNSEUXIMDNPI-UHFFFAOYSA-N 0.000 claims 1
- MSWCEQJQBLVFIL-UHFFFAOYSA-N 1-[3-(1,2,3,3a,4,6,7,7a-octahydropyrrolo[3,2-c]pyridin-5-ylsulfonyl)-4-chloro-2-hydroxyphenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound CC1=C(F)C=CC=C1NC(=O)NC1=CC=C(Cl)C(S(=O)(=O)N2CC3CCNC3CC2)=C1O MSWCEQJQBLVFIL-UHFFFAOYSA-N 0.000 claims 1
- QLMRDUBUVLKBGI-UHFFFAOYSA-N 1-[3-[(3-benzyl-3,8-diazabicyclo[3.2.1]octan-8-yl)sulfonyl]-4-chloro-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C1=CC(Cl)=C(S(=O)(=O)N2C3CCC2CN(CC=2C=CC=CC=2)C3)C(O)=C1NC(=O)NC1=CC=CC(F)=C1Cl QLMRDUBUVLKBGI-UHFFFAOYSA-N 0.000 claims 1
- MXUATWBPBVOFSG-WOJBJXKFSA-N 1-[3-[[(1r,5r)-8-benzyl-3,8-diazabicyclo[3.2.1]octan-3-yl]sulfonyl]-4-chloro-2-hydroxyphenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound C([C@]1(CC[C@](C2)(N1CC=1C=CC=CC=1)[H])[H])N2S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1C MXUATWBPBVOFSG-WOJBJXKFSA-N 0.000 claims 1
- VNXUBUYGDOEUNX-AYHJJNSGSA-N 1-[3-[[(1r,5s)-3-(butylamino)-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]-4-chloro-2-hydroxyphenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound N1([C@]2([H])CC[C@]1(CC(C2)NCCCC)[H])S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1C VNXUBUYGDOEUNX-AYHJJNSGSA-N 0.000 claims 1
- FSTBHAOLTGRZFJ-PBWFPOADSA-N 1-[3-[[(1r,5s)-8-azabicyclo[3.2.1]octan-3-yl]sulfamoyl]-4-chloro-2-hydroxyphenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound C([C@]1(CC[C@@](C2)(N1)[H])[H])C2NS(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1C FSTBHAOLTGRZFJ-PBWFPOADSA-N 0.000 claims 1
- JCPBTWNWWDTTTI-FOSCPWQOSA-N 1-[3-[[(1s,5r)-8-azabicyclo[3.2.1]octan-3-yl]sulfamoyl]-4-chloro-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C([C@]1(CC[C@@](C2)(N1)[H])[H])C2NS(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1Cl JCPBTWNWWDTTTI-FOSCPWQOSA-N 0.000 claims 1
- UHTDYTDNMSYVNS-MRXNPFEDSA-N 1-[3-[[(3s)-1-azabicyclo[2.2.2]octan-3-yl]sulfamoyl]-4-chloro-2-hydroxyphenyl]-3-(2-chloro-3-fluorophenyl)urea Chemical compound C1=CC(Cl)=C(S(=O)(=O)N[C@H]2C3CCN(CC3)C2)C(O)=C1NC(=O)NC1=CC=CC(F)=C1Cl UHTDYTDNMSYVNS-MRXNPFEDSA-N 0.000 claims 1
- HTNYBKNNYOEOFO-PHIMTYICSA-N 1-[4-chloro-2-hydroxy-3-[[(1r,5s)-3-oxo-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]phenyl]-3-(2,2-difluoro-1,3-benzodioxol-4-yl)urea Chemical compound N1([C@]2([H])CC[C@]1(CC(=O)C2)[H])S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC2=C1OC(F)(F)O2 HTNYBKNNYOEOFO-PHIMTYICSA-N 0.000 claims 1
- LWQJHWZPPFFHCA-ALOPSCKCSA-N 1-[4-chloro-2-hydroxy-3-[[(1s,5r)-3-(propylamino)-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]phenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound N1([C@]2([H])CC[C@]1(CC(C2)NCCC)[H])S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1C LWQJHWZPPFFHCA-ALOPSCKCSA-N 0.000 claims 1
- CBYWOYRIOIDQCQ-PHIMTYICSA-N 1-[4-chloro-2-hydroxy-3-[[(1s,5r)-3-oxo-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]phenyl]-3-(2-chloropyridin-3-yl)urea Chemical compound N1([C@]2([H])CC[C@]1(CC(=O)C2)[H])S(=O)(=O)C(C=1O)=C(Cl)C=CC=1NC(=O)NC1=CC=CN=C1Cl CBYWOYRIOIDQCQ-PHIMTYICSA-N 0.000 claims 1
- ASDFMPKGRQQQOW-BETUJISGSA-N 1-[4-chloro-2-hydroxy-3-[[(1s,5r)-3-oxo-8-azabicyclo[3.2.1]octan-8-yl]sulfonyl]phenyl]-3-(3-fluoro-2-methylphenyl)urea Chemical compound N1([C@]2([H])CC[C@]1(CC(=O)C2)[H])S(=O)(=O)C(C(=CC=1)Cl)=C(O)C=1NC(=O)NC1=CC=CC(F)=C1C ASDFMPKGRQQQOW-BETUJISGSA-N 0.000 claims 1
- ZDJFKZQIMPXIHG-UHFFFAOYSA-N 1-[4-chloro-3-(1,8-diazaspiro[4.5]decan-8-ylsulfonyl)-2-hydroxyphenyl]-3-(2-ethylphenyl)urea Chemical compound CCC1=CC=CC=C1NC(=O)NC1=CC=C(Cl)C(S(=O)(=O)N2CCC3(NCCC3)CC2)=C1O ZDJFKZQIMPXIHG-UHFFFAOYSA-N 0.000 claims 1
- RCYAOPOAKRDRPB-UHFFFAOYSA-N 1-[4-chloro-3-(1,8-diazaspiro[4.5]decan-8-ylsulfonyl)-2-hydroxyphenyl]-3-[2-(trifluoromethoxy)phenyl]urea Chemical compound C1=CC(Cl)=C(S(=O)(=O)N2CCC3(NCCC3)CC2)C(O)=C1NC(=O)NC1=CC=CC=C1OC(F)(F)F RCYAOPOAKRDRPB-UHFFFAOYSA-N 0.000 claims 1
- OZVJRQMLLBIHEU-UHFFFAOYSA-N 1-[4-chloro-3-(3,8-diazabicyclo[3.2.1]octan-3-ylsulfonyl)-2-hydroxyphenyl]-3-(2-chloropyridin-3-yl)urea Chemical compound C1=CC(Cl)=C(S(=O)(=O)N2CC3CCC(N3)C2)C(O)=C1NC(=O)NC1=CC=CN=C1Cl OZVJRQMLLBIHEU-UHFFFAOYSA-N 0.000 claims 1
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| TWI421252B (zh) | 2009-07-09 | 2014-01-01 | Irm Llc | 用於治療寄生蟲疾病之化合物及組合物 |
| CA2791884C (en) * | 2010-03-01 | 2018-04-24 | Novadrug, Llc | Compositions and methods for treating viral diseases |
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| US8648118B2 (en) * | 2010-12-17 | 2014-02-11 | Boehringer Ingelheim International Gmbh | Bicyclic ring system substituted amide functionalised phenols as medicaments |
| CN103957911A (zh) | 2011-08-24 | 2014-07-30 | Novadrug有限责任公司 | 用于治疗病毒性疾病的组合物及方法 |
| CA2867175A1 (en) | 2012-03-28 | 2013-10-03 | Neuropore Therapies, Inc. | Phenyl-urea and phenyl-carbamate derivatives as inhibitors of protein aggregation |
| US10167293B2 (en) * | 2016-05-26 | 2019-01-01 | Bayer Pharma Aktiengesellschaft | [8-(phenylsulfonyl)-3,8-diazabicyclo[3.2.1]oct-3-yl](1H-1,2,3-triazol-4-yl)methanones |
| EA036824B1 (ru) * | 2016-07-11 | 2020-12-24 | Байер Фарма Акциенгезельшафт | [8-(фенилсульфонил)-3,8-диазабицикло[3.2.1]окт-3-ил](1н-1,2,3-триазол-4-ил)метаноны |
| BR112019019109B1 (pt) * | 2017-03-15 | 2023-11-07 | Lunella Biotech, Inc | Compostos mitorriboscina, composição farmacêutica compreendendo os mesmos, e seus usos direcionados para células cancerosas, bactérias e levedura patogênica |
| TWI791515B (zh) | 2017-04-24 | 2023-02-11 | 瑞士商諾華公司 | 治療療法 |
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| US6767922B2 (en) * | 2000-03-14 | 2004-07-27 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
| US6664259B2 (en) * | 2000-03-16 | 2003-12-16 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
| AR031098A1 (es) * | 2000-03-16 | 2003-09-10 | Smithkline Beecham Corp | Compuestos de hidroxifenil urea sustituidos con sulfonamidas, composiciones farmaceuticas que los comprenden, y uso de los mismos en la fabricacion de medicamentos para tratar una enfermedad mediada por una quimioquina |
| UY26627A1 (es) * | 2000-03-24 | 2001-09-28 | Smithkline Beecham Corp | Antagonistas de receptores de il-8 |
| EP1274428A4 (en) * | 2000-04-07 | 2003-05-02 | Smithkline Beecham Corp | INTERLEUKIN-8 (IL-8) RECEPTOR ANTAGONISTS |
| US6432960B2 (en) * | 2000-05-10 | 2002-08-13 | Bristol-Myers Squibb Company | Squarate derivatives of dihydropyridine NPY antagonists |
| MXPA02011868A (es) * | 2000-05-30 | 2003-04-10 | Smithkline Beecham Corp | Antagonistas de receptor de interleucina 8. |
| US20040048897A1 (en) * | 2001-01-16 | 2004-03-11 | Mccleland Brent | Il-8 receptor antagonists |
| DE60230722D1 (de) * | 2001-01-16 | 2009-02-26 | Smithkline Beecham Corp | Il-8-rezeptor-antagonisten |
| US20030204085A1 (en) * | 2001-02-02 | 2003-10-30 | Taveras Arthur G. | 3, 4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor antagonists |
| RU2003126913A (ru) * | 2001-02-02 | 2005-03-10 | Шеринг Корпорейшн (US) | 3,4-дизамещенные циклобутен-1,2-дионы, как антагонисты хемокинового рецептора схс |
| CZ20032639A3 (cs) * | 2001-03-30 | 2004-04-14 | Smithkline Beecham Corporation | Způsoby přípravy sloučenin obsahujících fenol |
| AU2002310156A1 (en) * | 2001-06-05 | 2002-12-16 | Boehringer Ingelheim Pharmaceuticals, Inc. | 1,4-disubstituted benzo-fused cycloalkyl urea compounds |
| US20040038854A1 (en) * | 2001-07-16 | 2004-02-26 | Dillon Susan B. | Use of il-8 receptor antagonists in the treatment of virus infections |
| US20030032802A1 (en) * | 2002-08-30 | 2003-02-13 | Palovich Michael R. | IL8-receptor antagonists |
| US20030028042A1 (en) | 2002-08-30 | 2003-02-06 | Palovich Michael R. | Il8-receptor antagonists |
| US20030065170A1 (en) * | 2002-09-05 | 2003-04-03 | Widdowson Katherine Louisa | Il-8 receptor antagonists |
| TW200418812A (en) * | 2002-10-29 | 2004-10-01 | Smithkline Beecham Corp | IL-8 receptor antagonists |
| TW200510311A (en) * | 2002-12-23 | 2005-03-16 | Millennium Pharm Inc | CCr8 inhibitors |
| JP2006527201A (ja) * | 2003-06-06 | 2006-11-30 | スミスクライン・ビーチャム・コーポレイション | Ｉｌ−８受容体アンタゴニスト |
| WO2006043950A1 (en) * | 2004-10-20 | 2006-04-27 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
| AR060562A1 (es) * | 2006-04-21 | 2008-06-25 | Smithkline Beecham Corp | Compuestos heterociclicos como antagonistas del receptor il-8. procesos de obtencion y composiciones farmaceuticas. |
| US8097626B2 (en) | 2006-04-21 | 2012-01-17 | Glaxosmithkline Llc | IL-8 receptor antagonists |
| AR061571A1 (es) | 2006-06-23 | 2008-09-03 | Smithkline Beecham Corp | Compuesto sal del acido toluenosulfonico de 4-{[6-cloro-3-({[(2- cloro-3-fluorofenil) amino]carbonil} amino)- 2- hidroxifenil]sulfonil] -1- piperazinacarbxilato de 1.1-dimetiletilo, composicion farmaceutica que lo comprende su uso para la fabricacion de un medicamento combinacion farmaceutica con un |
| US8044075B2 (en) | 2006-12-05 | 2011-10-25 | Glaxosmithkline | IL-8 receptor antagonists |
-
2007
- 2007-04-20 US US12/297,917 patent/US8097626B2/en not_active Expired - Fee Related
- 2007-04-20 CN CNA2007800232115A patent/CN101495113A/zh active Pending
- 2007-04-20 MX MX2008013599A patent/MX2008013599A/es not_active Application Discontinuation
- 2007-04-20 AU AU2007240364A patent/AU2007240364A1/en not_active Abandoned
- 2007-04-20 RU RU2008145871/04A patent/RU2008145871A/ru not_active Application Discontinuation
- 2007-04-20 JP JP2009506793A patent/JP2009534420A/ja active Pending
- 2007-04-20 CA CA002650007A patent/CA2650007A1/en not_active Abandoned
- 2007-04-20 EP EP07761016A patent/EP2010180A4/en not_active Withdrawn
- 2007-04-20 BR BRPI0710559-2A patent/BRPI0710559A2/pt not_active IP Right Cessation
- 2007-04-20 WO PCT/US2007/067088 patent/WO2007124423A2/en not_active Ceased
-
2008
- 2008-10-12 IL IL194700A patent/IL194700A0/en unknown
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