TH62683A - - Google Patents

Info

Publication number

TH62683A

TH62683A TH301000319A TH0301000319A TH62683A TH 62683 A TH62683 A TH 62683A TH 301000319 A TH301000319 A TH 301000319A TH 0301000319 A TH0301000319 A TH 0301000319A TH 62683 A TH62683 A TH 62683A

Authority

TH

Thailand

Prior art keywords

butyl

cyclopentyl

alkyl

chemical formula

structural formula

Prior art date

2003-01-31

Links

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• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims abstract 5
• 150000001875 compounds Chemical class 0.000 claims abstract 3
• 239000000126 substance Substances 0.000 claims abstract 3
• 229940079593 drug Drugs 0.000 claims abstract 2
• 239000003814 drug Substances 0.000 claims abstract 2
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
• 125000004093 cyano group Chemical group *C#N 0.000 claims 2
• 125000000753 cycloalkyl group Chemical group 0.000 claims 2
• 125000001475 halogen functional group Chemical group 0.000 claims 2
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
• 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 1
• USSIQXCVUWKGNF-UHFFFAOYSA-N 6-(dimethylamino)-4,4-diphenylheptan-3-one Chemical compound C=1C=CC=CC=1C(CC(C)N(C)C)(C(=O)CC)C1=CC=CC=C1 USSIQXCVUWKGNF-UHFFFAOYSA-N 0.000 claims 1
• 206010011703 Cyanosis Diseases 0.000 claims 1
• -1 O- (C1-6) Alkyls Chemical group 0.000 claims 1
• 125000003368 amide group Chemical group 0.000 claims 1
• 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
• HFFXLYHRNRKAPM-UHFFFAOYSA-N 2,4,5-trichloro-n-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide Chemical group O1C(C)=CC(NS(=O)(=O)C=2C(=CC(Cl)=C(Cl)C=2)Cl)=N1 HFFXLYHRNRKAPM-UHFFFAOYSA-N 0.000 abstract 2
• 101800001838 Serine protease/helicase NS3 Proteins 0.000 abstract 2
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 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 abstract 2
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
• 150000003839 salts Chemical class 0.000 abstract 2
• 229940124158 Protease/peptidase inhibitor Drugs 0.000 abstract 1
• 239000003112 inhibitor Substances 0.000 abstract 1
• 239000000137 peptide hydrolase inhibitor Substances 0.000 abstract 1