CA2850779A1 - Substituted aminothiazoles as inhibitors of cancers, including hepatocellular carcinoma, and as inhibitors of hepatitis virus replication - Google Patents
Substituted aminothiazoles as inhibitors of cancers, including hepatocellular carcinoma, and as inhibitors of hepatitis virus replication Download PDFInfo
- Publication number
- CA2850779A1 CA2850779A1 CA2850779A CA2850779A CA2850779A1 CA 2850779 A1 CA2850779 A1 CA 2850779A1 CA 2850779 A CA2850779 A CA 2850779A CA 2850779 A CA2850779 A CA 2850779A CA 2850779 A1 CA2850779 A1 CA 2850779A1
- Authority
- CA
- Canada
- Prior art keywords
- pyridin
- pyrimidin
- thiazol
- amine
- ylamino
- 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
Links
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical class NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 title claims abstract description 19
- 208000006454 hepatitis Diseases 0.000 title claims abstract description 14
- 231100000283 hepatitis Toxicity 0.000 title claims abstract description 14
- 206010028980 Neoplasm Diseases 0.000 title claims abstract description 12
- 206010073071 hepatocellular carcinoma Diseases 0.000 title abstract description 4
- 231100000844 hepatocellular carcinoma Toxicity 0.000 title abstract description 3
- 239000003112 inhibitor Substances 0.000 title 2
- 230000029812 viral genome replication Effects 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 49
- 201000010099 disease Diseases 0.000 claims abstract description 46
- 241000700605 Viruses Species 0.000 claims abstract description 27
- 230000010261 cell growth Effects 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims description 68
- 150000001875 compounds Chemical class 0.000 claims description 56
- 239000000203 mixture Substances 0.000 claims description 37
- -1 (4-(pyridin-2-yl)thiazol-2-yl)(pyrimidin-2-yl)amino Chemical group 0.000 claims description 35
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 28
- 239000002253 acid Substances 0.000 claims description 20
- 150000003839 salts Chemical class 0.000 claims description 18
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 12
- 210000004185 liver Anatomy 0.000 claims description 12
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 12
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 11
- 229910052794 bromium Inorganic materials 0.000 claims description 10
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 9
- 208000015181 infectious disease Diseases 0.000 claims description 9
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
- 201000011510 cancer Diseases 0.000 claims description 8
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 7
- 206010006187 Breast cancer Diseases 0.000 claims description 6
- 208000026310 Breast neoplasm Diseases 0.000 claims description 6
- 206010033128 Ovarian cancer Diseases 0.000 claims description 6
- 206010061535 Ovarian neoplasm Diseases 0.000 claims description 5
- 150000004677 hydrates Chemical class 0.000 claims description 4
- 206010061289 metastatic neoplasm Diseases 0.000 claims description 4
- 239000012453 solvate Substances 0.000 claims description 4
- CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical compound COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 claims description 3
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 3
- 208000006359 hepatoblastoma Diseases 0.000 claims description 3
- 201000007270 liver cancer Diseases 0.000 claims description 3
- 201000005202 lung cancer Diseases 0.000 claims description 3
- 208000020816 lung neoplasm Diseases 0.000 claims description 3
- 201000009030 Carcinoma Diseases 0.000 claims description 2
- 241000701076 Macacine alphaherpesvirus 1 Species 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- JLBSDCDXDAOFJE-UHFFFAOYSA-N methyl 4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazole-5-carboxylate Chemical compound N=1C(C=2N=CC=CC=2)=C(C(=O)OC)SC=1NC1=NC=CC=N1 JLBSDCDXDAOFJE-UHFFFAOYSA-N 0.000 claims 7
- WZDDCNUYYXWDSE-UHFFFAOYSA-N n-(4-methylpyrimidin-2-yl)-4-pyridin-2-yl-1,3-thiazol-2-amine Chemical compound CC1=CC=NC(NC=2SC=C(N=2)C=2N=CC=CC=2)=N1 WZDDCNUYYXWDSE-UHFFFAOYSA-N 0.000 claims 7
- UKGBKXNZHVJTOF-UHFFFAOYSA-N n-pyrimidin-2-yl-4-quinolin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C(C=2N=C3C=CC=CC3=CC=2)=CSC=1NC1=NC=CC=N1 UKGBKXNZHVJTOF-UHFFFAOYSA-N 0.000 claims 7
- QERRMNCBNQADTC-UHFFFAOYSA-N 4-(3,5-dimethylpyridin-2-yl)-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CN=C1C1=CSC(NC=2N=CC=CN=2)=N1 QERRMNCBNQADTC-UHFFFAOYSA-N 0.000 claims 6
- MLUDUQIKZCQSFJ-UHFFFAOYSA-N 4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazole-5-carboxamide Chemical compound N=1C(C=2N=CC=CC=2)=C(C(=O)N)SC=1NC1=NC=CC=N1 MLUDUQIKZCQSFJ-UHFFFAOYSA-N 0.000 claims 6
- JOWNSKXJCUZVAR-UHFFFAOYSA-N 4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazole-5-carboxylic acid Chemical compound N=1C(C=2N=CC=CC=2)=C(C(=O)O)SC=1NC1=NC=CC=N1 JOWNSKXJCUZVAR-UHFFFAOYSA-N 0.000 claims 6
- HFABGDPBRCVHKI-UHFFFAOYSA-N 4-pyridin-2-yl-n-[4-(trifluoromethyl)pyrimidin-2-yl]-1,3-thiazol-2-amine Chemical compound FC(F)(F)C1=CC=NC(NC=2SC=C(N=2)C=2N=CC=CC=2)=N1 HFABGDPBRCVHKI-UHFFFAOYSA-N 0.000 claims 6
- WMWWFLUMIMEMLP-UHFFFAOYSA-N 5-propan-2-yl-4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C(C=2N=CC=CC=2)=C(C(C)C)SC=1NC1=NC=CC=N1 WMWWFLUMIMEMLP-UHFFFAOYSA-N 0.000 claims 6
- IENJOXRGJKIPRK-UHFFFAOYSA-N 6-methyl-n-(4-pyridin-2-yl-1,3-thiazol-2-yl)-1,3-benzothiazol-2-amine Chemical compound S1C2=CC(C)=CC=C2N=C1NC(SC=1)=NC=1C1=CC=CC=N1 IENJOXRGJKIPRK-UHFFFAOYSA-N 0.000 claims 6
- QZPXTNVERNDKCO-UHFFFAOYSA-N 4-(4-methylpyridin-2-yl)-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound CC1=CC=NC(C=2N=C(NC=3N=CC=CN=3)SC=2)=C1 QZPXTNVERNDKCO-UHFFFAOYSA-N 0.000 claims 5
- BKGZDPJCXISOJV-UHFFFAOYSA-N 5-bromo-4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C(C=2N=CC=CC=2)=C(Br)SC=1NC1=NC=CC=N1 BKGZDPJCXISOJV-UHFFFAOYSA-N 0.000 claims 5
- FFCNHBKDZGXAEB-UHFFFAOYSA-N 5-cyclohexyl-4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound C1CCCCC1C1=C(C=2N=CC=CC=2)N=C(NC=2N=CC=CN=2)S1 FFCNHBKDZGXAEB-UHFFFAOYSA-N 0.000 claims 5
- BBRGRJOZVHSCPX-UHFFFAOYSA-N 5-methyl-4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C(C=2N=CC=CC=2)=C(C)SC=1NC1=NC=CC=N1 BBRGRJOZVHSCPX-UHFFFAOYSA-N 0.000 claims 5
- SHDLBBBNPZBTDJ-UHFFFAOYSA-N 6-[2-(pyrimidin-2-ylamino)-1,3-thiazol-4-yl]-1h-pyridin-2-one Chemical compound OC1=CC=CC(C=2N=C(NC=3N=CC=CN=3)SC=2)=N1 SHDLBBBNPZBTDJ-UHFFFAOYSA-N 0.000 claims 5
- RXLFKSFMSCGFBD-UHFFFAOYSA-N [4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazol-5-yl]methanol Chemical compound N=1C(C=2N=CC=CC=2)=C(CO)SC=1NC1=NC=CC=N1 RXLFKSFMSCGFBD-UHFFFAOYSA-N 0.000 claims 5
- RGZMYQPBLDEPQB-UHFFFAOYSA-N [4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazol-5-yl]methyl butanoate Chemical compound N=1C(C=2N=CC=CC=2)=C(COC(=O)CCC)SC=1NC1=NC=CC=N1 RGZMYQPBLDEPQB-UHFFFAOYSA-N 0.000 claims 5
- KMRVCRSSXCJYOF-UHFFFAOYSA-N ethyl 2-[(4-methylpyrimidin-2-yl)amino]-4-pyridin-2-yl-1,3-thiazole-5-carboxylate Chemical compound N=1C(C=2N=CC=CC=2)=C(C(=O)OCC)SC=1NC1=NC=CC(C)=N1 KMRVCRSSXCJYOF-UHFFFAOYSA-N 0.000 claims 5
- YOTCDUGBYAOKIV-UHFFFAOYSA-N ethyl 4-(6-methylpyridin-2-yl)-2-(pyrimidin-2-ylamino)-1,3-thiazole-5-carboxylate Chemical compound N=1C(C=2N=C(C)C=CC=2)=C(C(=O)OCC)SC=1NC1=NC=CC=N1 YOTCDUGBYAOKIV-UHFFFAOYSA-N 0.000 claims 5
- YOGMJDLDADTOPF-UHFFFAOYSA-N n-benzyl-4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazole-5-carboxamide Chemical compound S1C(NC=2N=CC=CN=2)=NC(C=2N=CC=CC=2)=C1C(=O)NCC1=CC=CC=C1 YOGMJDLDADTOPF-UHFFFAOYSA-N 0.000 claims 5
- PMGMBUWSZZUMTO-UHFFFAOYSA-N n-benzyl-4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound C=1C=CC=CC=1CN(C=1N=CC=CN=1)C(SC=1)=NC=1C1=CC=CC=N1 PMGMBUWSZZUMTO-UHFFFAOYSA-N 0.000 claims 5
- AGQNMYLPVLOPBV-UHFFFAOYSA-N 3-[(4-phenyl-1,3-thiazol-2-yl)amino]phenol Chemical compound OC1=CC=CC(NC=2SC=C(N=2)C=2C=CC=CC=2)=C1 AGQNMYLPVLOPBV-UHFFFAOYSA-N 0.000 claims 4
- IZLGVISZPCTBOM-UHFFFAOYSA-N 4-(6-bromopyridin-2-yl)-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound BrC1=CC=CC(C=2N=C(NC=3N=CC=CN=3)SC=2)=N1 IZLGVISZPCTBOM-UHFFFAOYSA-N 0.000 claims 4
- LJDMFGGAHQJRIW-UHFFFAOYSA-N 4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazole-5-carbonitrile Chemical compound N=1C(C=2N=CC=CC=2)=C(C#N)SC=1NC1=NC=CC=N1 LJDMFGGAHQJRIW-UHFFFAOYSA-N 0.000 claims 4
- QAINFPRHEISSOY-UHFFFAOYSA-N 4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C=CC=NC=1NC(SC=1)=NC=1C1=CC=CC=N1 QAINFPRHEISSOY-UHFFFAOYSA-N 0.000 claims 4
- SWTCIZZQJZZPHQ-UHFFFAOYSA-N 5-ethyl-4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C(C=2N=CC=CC=2)=C(CC)SC=1NC1=NC=CC=N1 SWTCIZZQJZZPHQ-UHFFFAOYSA-N 0.000 claims 4
- JLKXZQUQIBQRJX-UHFFFAOYSA-N 5-nonyl-4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C(C=2N=CC=CC=2)=C(CCCCCCCCC)SC=1NC1=NC=CC=N1 JLKXZQUQIBQRJX-UHFFFAOYSA-N 0.000 claims 4
- XLWUIVIANDMKLA-UHFFFAOYSA-N 5-pentyl-4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C(C=2N=CC=CC=2)=C(CCCCC)SC=1NC1=NC=CC=N1 XLWUIVIANDMKLA-UHFFFAOYSA-N 0.000 claims 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 4
- 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 4
- UOZGFTNEUUUFGL-UHFFFAOYSA-N ethyl 4-(4-methylpyridin-2-yl)-2-(pyrimidin-2-ylamino)-1,3-thiazole-5-carboxylate Chemical compound N=1C(C=2N=CC=C(C)C=2)=C(C(=O)OCC)SC=1NC1=NC=CC=N1 UOZGFTNEUUUFGL-UHFFFAOYSA-N 0.000 claims 4
- PWVAPGWIKKAAMS-UHFFFAOYSA-N ethyl 4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazole-5-carboxylate Chemical compound N=1C(C=2N=CC=CC=2)=C(C(=O)OCC)SC=1NC1=NC=CC=N1 PWVAPGWIKKAAMS-UHFFFAOYSA-N 0.000 claims 4
- YVEBSOQNIVRDRH-UHFFFAOYSA-N n-(5-bromopyrimidin-2-yl)-4-pyridin-2-yl-1,3-thiazol-2-amine Chemical compound N1=CC(Br)=CN=C1NC1=NC(C=2N=CC=CC=2)=CS1 YVEBSOQNIVRDRH-UHFFFAOYSA-N 0.000 claims 4
- AOPIPGKZJOHGOY-UHFFFAOYSA-N n-methyl-4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazole-5-carboxamide Chemical compound N=1C(C=2N=CC=CC=2)=C(C(=O)NC)SC=1NC1=NC=CC=N1 AOPIPGKZJOHGOY-UHFFFAOYSA-N 0.000 claims 4
- XOTDCNMYRMZMQI-UHFFFAOYSA-N n-methyl-4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C=CC=NC=1N(C)C(SC=1)=NC=1C1=CC=CC=N1 XOTDCNMYRMZMQI-UHFFFAOYSA-N 0.000 claims 4
- DYPIPKBSINXYKJ-UHFFFAOYSA-N n-propan-2-yl-4-pyridin-2-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C=CC=NC=1N(C(C)C)C(SC=1)=NC=1C1=CC=CC=N1 DYPIPKBSINXYKJ-UHFFFAOYSA-N 0.000 claims 4
- IJEVNRAIXXCJEN-UHFFFAOYSA-N tert-butyl 2-[tert-butyl(pyrimidin-2-yl)amino]-4-pyridin-2-yl-1,3-thiazole-5-carboxylate Chemical compound CC(C)(C)OC(=O)C=1SC(N(C=2N=CC=CN=2)C(C)(C)C)=NC=1C1=CC=CC=N1 IJEVNRAIXXCJEN-UHFFFAOYSA-N 0.000 claims 4
- NKZCXGIZJHEBIX-UHFFFAOYSA-N 4-pyridin-2-yl-n-pyrimidin-4-yl-1,3-thiazol-2-amine Chemical compound C=1C=NC=NC=1NC(SC=1)=NC=1C1=CC=CC=N1 NKZCXGIZJHEBIX-UHFFFAOYSA-N 0.000 claims 3
- NYGKCRRUCANIBJ-UHFFFAOYSA-N 4-pyridin-4-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C=CC=NC=1NC(SC=1)=NC=1C1=CC=NC=C1 NYGKCRRUCANIBJ-UHFFFAOYSA-N 0.000 claims 3
- MADRSCSVNCWXAW-UHFFFAOYSA-N [4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazol-5-yl]methyl acetate Chemical compound N=1C(C=2N=CC=CC=2)=C(COC(=O)C)SC=1NC1=NC=CC=N1 MADRSCSVNCWXAW-UHFFFAOYSA-N 0.000 claims 3
- FAXWKQAPUYLLPC-UHFFFAOYSA-N n,4-diphenyl-1,3-thiazol-2-amine Chemical compound C=1C=CC=CC=1NC(SC=1)=NC=1C1=CC=CC=C1 FAXWKQAPUYLLPC-UHFFFAOYSA-N 0.000 claims 3
- RYCUBTFYRLAMFA-UHFFFAOYSA-N n,4-dipyridin-2-yl-1,3-thiazol-2-amine Chemical compound C=1C=CC=NC=1NC(SC=1)=NC=1C1=CC=CC=N1 RYCUBTFYRLAMFA-UHFFFAOYSA-N 0.000 claims 3
- FZGLXJIEPKFFOC-UHFFFAOYSA-N n-pyrazin-2-yl-4-pyridin-2-yl-1,3-thiazol-2-amine Chemical compound C=1N=CC=NC=1NC(SC=1)=NC=1C1=CC=CC=N1 FZGLXJIEPKFFOC-UHFFFAOYSA-N 0.000 claims 3
- 229940002612 prodrug Drugs 0.000 claims 3
- 239000000651 prodrug Substances 0.000 claims 3
- HXWIHKLVPKVLFO-UHFFFAOYSA-N 2-[(4-pyridin-2-yl-1,3-thiazol-2-yl)-pyrimidin-2-ylamino]ethanol Chemical compound N=1C=CC=NC=1N(CCO)C(SC=1)=NC=1C1=CC=CC=N1 HXWIHKLVPKVLFO-UHFFFAOYSA-N 0.000 claims 2
- RSMGISWQUHCXEP-UHFFFAOYSA-N 2-[[4-[(2,4-diaminopteridin-6-yl)methyl-methylamino]benzoyl]amino]-5-oxo-5-[2-[2-[2-[2-[2-[2-[[4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-1,3-thiazole-5-carbonyl]amino]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethylamino]pentanoic acid Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C(C=C1)=CC=C1C(=O)NC(C(O)=O)CCC(=O)NCCOCCOCCOCCOCCOCCNC(=O)C(=C(N=1)C=2N=CC=CC=2)SC=1NC1=NC=CC=N1 RSMGISWQUHCXEP-UHFFFAOYSA-N 0.000 claims 2
- VSKCWIXMOBTHAR-UHFFFAOYSA-N 4-pyridin-3-yl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C=CC=NC=1NC(SC=1)=NC=1C1=CC=CN=C1 VSKCWIXMOBTHAR-UHFFFAOYSA-N 0.000 claims 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims 2
- PWLNAUNEAKQYLH-UHFFFAOYSA-N butyric acid octyl ester Natural products CCCCCCCCOC(=O)CCC PWLNAUNEAKQYLH-UHFFFAOYSA-N 0.000 claims 2
- FXXYURIGCUUXRW-UHFFFAOYSA-N n-(3-chloro-2-methylphenyl)-4-pyridin-2-yl-1,3-thiazol-2-amine Chemical compound CC1=C(Cl)C=CC=C1NC1=NC(C=2N=CC=CC=2)=CS1 FXXYURIGCUUXRW-UHFFFAOYSA-N 0.000 claims 2
- NIBXGRDCQVHBHE-UHFFFAOYSA-N n-(5-chloropyrimidin-2-yl)-4-pyridin-2-yl-1,3-thiazol-2-amine Chemical compound N1=CC(Cl)=CN=C1NC1=NC(C=2N=CC=CC=2)=CS1 NIBXGRDCQVHBHE-UHFFFAOYSA-N 0.000 claims 2
- UUIQMZJEGPQKFD-UHFFFAOYSA-N n-butyric acid methyl ester Natural products CCCC(=O)OC UUIQMZJEGPQKFD-UHFFFAOYSA-N 0.000 claims 2
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 claims 2
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims 2
- GGNIKGLUPSHSBV-UHFFFAOYSA-N thiazole-5-carboxamide Chemical compound NC(=O)C1=CN=CS1 GGNIKGLUPSHSBV-UHFFFAOYSA-N 0.000 claims 2
- FMLLSOIFCVZTFJ-UHFFFAOYSA-N 4-phenyl-n-pyrimidin-2-yl-1,3-thiazol-2-amine Chemical compound N=1C=CC=NC=1NC(SC=1)=NC=1C1=CC=CC=C1 FMLLSOIFCVZTFJ-UHFFFAOYSA-N 0.000 claims 1
- CYORKSDZNSVZCP-UHFFFAOYSA-N 5-[17-(hydroxyamino)heptadecylamino]pentanoic acid Chemical compound ONCCCCCCCCCCCCCCCCCNCCCCC(=O)O CYORKSDZNSVZCP-UHFFFAOYSA-N 0.000 claims 1
- JGFBQFKZKSSODQ-UHFFFAOYSA-N Isothiocyanatocyclopropane Chemical compound S=C=NC1CC1 JGFBQFKZKSSODQ-UHFFFAOYSA-N 0.000 claims 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 1
- 208000006990 cholangiocarcinoma Diseases 0.000 claims 1
- 208000032839 leukemia Diseases 0.000 claims 1
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 claims 1
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 claims 1
- 230000009471 action Effects 0.000 abstract description 3
- 208000036142 Viral infection Diseases 0.000 abstract 1
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- 230000009385 viral infection Effects 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 description 41
- 238000003786 synthesis reaction Methods 0.000 description 38
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 33
- 210000004027 cell Anatomy 0.000 description 29
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- 239000000047 product Substances 0.000 description 21
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- 239000007788 liquid Substances 0.000 description 17
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- 235000019198 oils Nutrition 0.000 description 13
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- 125000003118 aryl group Chemical group 0.000 description 11
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Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- A61K31/33—Heterocyclic compounds
- 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
- A61K31/425—Thiazoles
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- 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
- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
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- A—HUMAN NECESSITIES
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/42—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Molecular Biology (AREA)
- Hematology (AREA)
- Gastroenterology & Hepatology (AREA)
- Biotechnology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161542907P | 2011-10-04 | 2011-10-04 | |
| US61/542,907 | 2011-10-04 | ||
| PCT/US2012/058674 WO2013052613A1 (en) | 2011-10-04 | 2012-10-04 | Substituted aminothiazoles as inhibitors of cancers, including hepatocellular carcinoma, and as inhibitors of hepatitis virus replication |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2850779A1 true CA2850779A1 (en) | 2013-04-11 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2850779A Abandoned CA2850779A1 (en) | 2011-10-04 | 2012-10-04 | Substituted aminothiazoles as inhibitors of cancers, including hepatocellular carcinoma, and as inhibitors of hepatitis virus replication |
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| Country | Link |
|---|---|
| US (2) | US20140249154A1 (OSRAM) |
| EP (1) | EP2763674A4 (OSRAM) |
| JP (2) | JP6240078B2 (OSRAM) |
| KR (1) | KR20140071472A (OSRAM) |
| CN (1) | CN103957908A (OSRAM) |
| AU (1) | AU2012318670B2 (OSRAM) |
| BR (1) | BR112014007963A2 (OSRAM) |
| CA (1) | CA2850779A1 (OSRAM) |
| HK (1) | HK1200361A1 (OSRAM) |
| IL (1) | IL231923A0 (OSRAM) |
| PH (1) | PH12014500724A1 (OSRAM) |
| SG (1) | SG11201401207XA (OSRAM) |
| WO (1) | WO2013052613A1 (OSRAM) |
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| US9582896B2 (en) * | 2011-09-02 | 2017-02-28 | Qualcomm Incorporated | Line tracking with automatic model initialization by graph matching and cycle detection |
| IN2015DN03235A (OSRAM) | 2012-11-07 | 2015-10-02 | Karus Therapeutics Ltd | |
| WO2014159938A1 (en) * | 2013-03-13 | 2014-10-02 | The Broad Institute, Inc. | Substituted aminothiazoles for the treatment of tuberculosis |
| PT2994465T (pt) | 2013-05-10 | 2018-10-25 | Karus Therapeutics Ltd | Novos inibidores de histona desacetilase |
| WO2016046759A2 (en) | 2014-09-22 | 2016-03-31 | Fratagene Therapeutics Ltd. | Compositions and methods for treating friedreich's ataxia |
| US10442779B2 (en) | 2014-09-22 | 2019-10-15 | Fratagene Therapeutics S.R.L. | Compositions and methods for treating Friedreich's ataxia |
| GB201419228D0 (en) | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
| GB201419264D0 (en) | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
| HK1252120A1 (zh) * | 2015-04-29 | 2019-05-17 | Takeda Pharmaceutical Company Limited | 抗病毒和抗炎疗法的治疗组合 |
| CN105524056A (zh) * | 2016-01-05 | 2016-04-27 | 中山大学肿瘤防治中心 | 一种氨基噻唑化合物及其制备方法和应用 |
| EP3481810A4 (en) * | 2016-07-11 | 2019-05-29 | Baruch S. Blumberg Institute | SUBSTITUTED AMINOTHIAZOLE |
| MY198676A (en) * | 2017-06-22 | 2023-09-15 | Celgene Corp | Treatment of hepatocellular carcinoma characterized by hepatitis b virus infection |
| US10426775B2 (en) | 2017-09-11 | 2019-10-01 | Fratagene Therapeutics Srl | Methods for treating Friedreich's ataxia with etravirine |
| WO2022087326A1 (en) * | 2020-10-23 | 2022-04-28 | Celgene Corporation | Heterocyclic compounds and their use for treatment of helminthic infections and diseases |
| WO2025017207A1 (en) | 2023-07-20 | 2025-01-23 | Cemm - Forschungszentrum Für Molekulare Medizin Gmbh | Inhibitors of smndc1 and their therapeutic use |
| WO2025151517A1 (en) * | 2024-01-08 | 2025-07-17 | Wavebreak Therapeutics Limited | Thiazole compounds, compositions and methods of treating disorders associated with missfolding of alpha-synuclein protein |
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| DE60136530D1 (de) * | 2000-03-01 | 2008-12-24 | Janssen Pharmaceutica Nv | 2,4-disubstituierte thiazolyl derivate |
| HUP0401748A3 (en) * | 2001-08-13 | 2011-03-28 | Janssen Pharmaceutica Nv | 2-amino-4,5-trisubstituted thiazolyl derivatives, process for their preparation and pharmaceutical compositions containing them |
| EP1732906A4 (en) * | 2004-03-30 | 2007-11-21 | Merck & Co Inc | 2-AMINOTHIAZONE COMPOUNDS SUITABLE AS ASPARTYL PROTEASE INHIBITORS |
| AU2005232753A1 (en) * | 2004-04-13 | 2005-10-27 | Astellas Pharma Inc. | Polycylic thiazoles as potassium ion channel modulators |
| BRPI0608910A2 (pt) * | 2005-05-09 | 2010-02-17 | Achillion Pharmaceuticals Inc | uso de um composto da fórmula ou um sal ou hidrato farmaceuticamente aceitável desse, composto ou sal ou hidrato do mesmo, composição farmacêutica e composição farmacêutica embalada |
| EP1996565A2 (en) * | 2006-03-08 | 2008-12-03 | Achillion Pharmaceuticals, Inc. | Substituted aminothiazole derivatives with anti-hcv activity |
| WO2008083098A1 (en) * | 2006-12-27 | 2008-07-10 | The Johns Hopkins University | Agents for reversing epigenetic silencing of genes |
| WO2009114552A1 (en) * | 2008-03-10 | 2009-09-17 | The Board Of Trustees Of The Leland Stanford Junior University | Heteroaryl compounds, compositions, and methods of use in cancer treatment |
| EP2411526A4 (en) * | 2009-03-27 | 2012-09-19 | Zacharon Pharmaceuticals Inc | MODULATORS OF GANGLIOSID BIOSYNTHESIS |
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2012
- 2012-10-04 JP JP2014534680A patent/JP6240078B2/ja not_active Expired - Fee Related
- 2012-10-04 CA CA2850779A patent/CA2850779A1/en not_active Abandoned
- 2012-10-04 KR KR1020147011691A patent/KR20140071472A/ko not_active Ceased
- 2012-10-04 PH PH1/2014/500724A patent/PH12014500724A1/en unknown
- 2012-10-04 US US14/349,014 patent/US20140249154A1/en not_active Abandoned
- 2012-10-04 HK HK15101053.5A patent/HK1200361A1/xx unknown
- 2012-10-04 BR BR112014007963A patent/BR112014007963A2/pt not_active IP Right Cessation
- 2012-10-04 CN CN201280059490.1A patent/CN103957908A/zh active Pending
- 2012-10-04 EP EP12838333.8A patent/EP2763674A4/en not_active Withdrawn
- 2012-10-04 AU AU2012318670A patent/AU2012318670B2/en not_active Ceased
- 2012-10-04 SG SG11201401207XA patent/SG11201401207XA/en unknown
- 2012-10-04 WO PCT/US2012/058674 patent/WO2013052613A1/en not_active Ceased
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2014
- 2014-04-03 IL IL231923A patent/IL231923A0/en unknown
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2016
- 2016-09-07 US US15/258,393 patent/US10087173B2/en not_active Expired - Fee Related
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2017
- 2017-04-13 JP JP2017079817A patent/JP2017149753A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| US20140249154A1 (en) | 2014-09-04 |
| CN103957908A (zh) | 2014-07-30 |
| IL231923A0 (en) | 2014-05-28 |
| BR112014007963A2 (pt) | 2013-04-11 |
| EP2763674A1 (en) | 2014-08-13 |
| JP6240078B2 (ja) | 2017-11-29 |
| JP2014528450A (ja) | 2014-10-27 |
| SG11201401207XA (en) | 2014-05-29 |
| WO2013052613A1 (en) | 2013-04-11 |
| AU2012318670A1 (en) | 2014-05-22 |
| AU2012318670B2 (en) | 2017-09-07 |
| KR20140071472A (ko) | 2014-06-11 |
| EP2763674A4 (en) | 2015-04-29 |
| US20170066758A1 (en) | 2017-03-09 |
| HK1200361A1 (en) | 2015-08-07 |
| PH12014500724A1 (en) | 2014-05-19 |
| US10087173B2 (en) | 2018-10-02 |
| JP2017149753A (ja) | 2017-08-31 |
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