JP2012532883A5 - - Google Patents

Info

Publication number

JP2012532883A5

JP2012532883A5 JP2012519731A JP2012519731A JP2012532883A5 JP 2012532883 A5 JP2012532883 A5 JP 2012532883A5 JP 2012519731 A JP2012519731 A JP 2012519731A JP 2012519731 A JP2012519731 A JP 2012519731A JP 2012532883 A5 JP2012532883 A5 JP 2012532883A5

Authority

JP

Japan

Prior art keywords

compound according

compound

independently

unsubstituted

substituted

Prior art date

2010-07-08

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

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• 150000001875 compounds Chemical class 0.000 claims 18
• 125000000217 alkyl group Chemical group 0.000 claims 5
• 125000004450 alkenylene group Chemical group 0.000 claims 4
• 125000004419 alkynylene group Chemical group 0.000 claims 4
• 229910052736 halogen Inorganic materials 0.000 claims 4
• 150000002367 halogens Chemical class 0.000 claims 4
• 125000005842 heteroatom Chemical group 0.000 claims 4
• -1 n-octyl Chemical group 0.000 claims 4
• 206010002091 Anaesthesia Diseases 0.000 claims 3
• 230000037005 anaesthesia Effects 0.000 claims 3
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 3
• 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims 2
• IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 claims 2
• HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 2
• 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 2
• 125000005865 C2-C10alkynyl group Chemical group 0.000 claims 2
• 125000002947 alkylene group Chemical group 0.000 claims 2
• 239000000203 mixture Substances 0.000 claims 2
• 239000008194 pharmaceutical composition Substances 0.000 claims 2
• 150000003839 salts Chemical class 0.000 claims 2
• 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 1
• 239000003937 drug carrier Substances 0.000 claims 1
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
• 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims 1
• 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1