JP2011518163A5 - - Google Patents

Info

Publication number

JP2011518163A5

JP2011518163A5 JP2011505096A JP2011505096A JP2011518163A5 JP 2011518163 A5 JP2011518163 A5 JP 2011518163A5 JP 2011505096 A JP2011505096 A JP 2011505096A JP 2011505096 A JP2011505096 A JP 2011505096A JP 2011518163 A5 JP2011518163 A5 JP 2011518163A5

Authority

JP

Japan

Prior art keywords

alkyl

cycloalkyl

heterocyclyl

aryl

pharmaceutically acceptable

Prior art date

2009-04-09

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.)

Granted

Links

• Espacenet
• Global Dossier
• Discuss

• 125000000217 alkyl group Chemical group 0.000 claims 29
• 125000000753 cycloalkyl group Chemical group 0.000 claims 23
• 125000000623 heterocyclic group Chemical group 0.000 claims 18
• 125000003118 aryl group Chemical group 0.000 claims 14
• 150000001875 compounds Chemical class 0.000 claims 14
• 150000003839 salts Chemical class 0.000 claims 13
• 125000003710 aryl alkyl group Chemical group 0.000 claims 11
• 125000001188 haloalkyl group Chemical group 0.000 claims 10
• 125000003545 alkoxy group Chemical group 0.000 claims 9
• 125000005843 halogen group Chemical group 0.000 claims 9
• 108010050904 Interferons Proteins 0.000 claims 8
• 102000014150 Interferons Human genes 0.000 claims 8
• 125000004438 haloalkoxy group Chemical group 0.000 claims 8
• 239000001257 hydrogen Substances 0.000 claims 8
• 229910052739 hydrogen Inorganic materials 0.000 claims 8
• 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 8
• 229940079322 interferon Drugs 0.000 claims 8
• 229910052757 nitrogen Inorganic materials 0.000 claims 8
• 229910052760 oxygen Inorganic materials 0.000 claims 8
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 7
• 229910052717 sulfur Chemical group 0.000 claims 7
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 6
• 125000003342 alkenyl group Chemical group 0.000 claims 6
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 6
• 125000004448 alkyl carbonyl group Chemical group 0.000 claims 6
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 6
• 125000005842 heteroatom Chemical group 0.000 claims 6
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 6
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 6
• 239000001301 oxygen Chemical group 0.000 claims 6
• 239000011593 sulfur Chemical group 0.000 claims 6
• 125000004093 cyano group Chemical group *C#N 0.000 claims 5
• 125000004356 hydroxy functional group Chemical group O* 0.000 claims 5
• 108010047761 Interferon-alpha Proteins 0.000 claims 4
• 102000006992 Interferon-alpha Human genes 0.000 claims 4
• 125000004183 alkoxy alkyl group Chemical group 0.000 claims 4
• 125000004414 alkyl thio group Chemical group 0.000 claims 4
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 4
• 125000000000 cycloalkoxy group Chemical group 0.000 claims 4
• 239000003814 drug Substances 0.000 claims 4
• 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 4
• 229940124597 therapeutic agent Drugs 0.000 claims 4
• 125000001424 substituent group Chemical group 0.000 claims 3
• 102100040018 Interferon alpha-2 Human genes 0.000 claims 2
• 108010079944 Interferon-alpha2b Proteins 0.000 claims 2
• IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical compound N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 claims 2
• 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 2
• 125000005129 aryl carbonyl group Chemical group 0.000 claims 2
• 125000004104 aryloxy group Chemical group 0.000 claims 2
• 230000000694 effects Effects 0.000 claims 2
• 125000004994 halo alkoxy alkyl group Chemical group 0.000 claims 2
• 125000004993 haloalkoxycarbonyl group Chemical group 0.000 claims 2
• 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 2
• 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 2
• 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 2
• 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
• 229960000329 ribavirin Drugs 0.000 claims 2
• HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 claims 2
• 229920006395 saturated elastomer Polymers 0.000 claims 2
• 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 1
• 125000004391 aryl sulfonyl group Chemical group 0.000 claims 1
• 125000005243 carbonyl alkyl group Chemical group 0.000 claims 1
• 125000004181 carboxyalkyl group Chemical group 0.000 claims 1
• 125000004966 cyanoalkyl group Chemical group 0.000 claims 1
• 125000000392 cycloalkenyl group Chemical group 0.000 claims 1
• 239000003937 drug carrier Substances 0.000 claims 1
• 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
• 208000015181 infectious disease Diseases 0.000 claims 1
• 0 CCc1c(-c(cc2)ccc2OC)nc(N[C@@](C(C)(C)C)C(N(C[C@@](C2)Oc(c3c4ccc(Cl)c3)ncc4OC)[C@@]2C(*[C@](C2)([C@]2C=C)C(N[S@@](C2CC2)=CC)=O)=O)=O)[s]1 Chemical compound CCc1c(-c(cc2)ccc2OC)nc(N[C@@](C(C)(C)C)C(N(C[C@@](C2)Oc(c3c4ccc(Cl)c3)ncc4OC)[C@@]2C(*[C@](C2)([C@]2C=C)C(N[S@@](C2CC2)=CC)=O)=O)=O)[s]1 0.000 description 3