DE60110262T2 - Thiazol und oxazol-derivate als aktivatoren von menschlichen peroxisom proliferator aktivierten rezeptoren - Google Patents
Thiazol und oxazol-derivate als aktivatoren von menschlichen peroxisom proliferator aktivierten rezeptoren Download PDFInfo
- Publication number
- DE60110262T2 DE60110262T2 DE60110262T DE60110262T DE60110262T2 DE 60110262 T2 DE60110262 T2 DE 60110262T2 DE 60110262 T DE60110262 T DE 60110262T DE 60110262 T DE60110262 T DE 60110262T DE 60110262 T2 DE60110262 T2 DE 60110262T2
- Authority
- DE
- Germany
- Prior art keywords
- methyl
- phenyl
- trifluoromethyl
- sulfanyl
- thiazol
- 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.)
- Expired - Lifetime
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- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 title description 3
- 150000007978 oxazole derivatives Chemical class 0.000 title 1
- 210000002824 peroxisome Anatomy 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 105
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 12
- 238000011282 treatment Methods 0.000 claims abstract description 11
- 208000024172 Cardiovascular disease Diseases 0.000 claims abstract description 6
- 208000035150 Hypercholesterolemia Diseases 0.000 claims abstract description 3
- -1 bromo, phenyl Chemical group 0.000 claims description 167
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 147
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 87
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 73
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 64
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 63
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 61
- 229910052739 hydrogen Inorganic materials 0.000 claims description 40
- 125000000217 alkyl group Chemical group 0.000 claims description 38
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 35
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 32
- 235000019260 propionic acid Nutrition 0.000 claims description 31
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 22
- 229910052757 nitrogen Inorganic materials 0.000 claims description 20
- 101000741788 Homo sapiens Peroxisome proliferator-activated receptor alpha Proteins 0.000 claims description 18
- 102100038831 Peroxisome proliferator-activated receptor alpha Human genes 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 16
- 150000002148 esters Chemical class 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 150000002367 halogens Chemical class 0.000 claims description 14
- 239000000556 agonist Substances 0.000 claims description 13
- 239000012453 solvate Substances 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 201000010099 disease Diseases 0.000 claims description 10
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 9
- 230000001404 mediated effect Effects 0.000 claims description 9
- 239000008194 pharmaceutical composition Substances 0.000 claims description 9
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 8
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 7
- 239000003814 drug Substances 0.000 claims description 7
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 7
- FVVACHCAVRTOQE-UHFFFAOYSA-N 2-methyl-2-[2-methyl-4-[[4-(thiophen-3-ylmethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]propanoic acid Chemical compound C1=C(OC(C)(C)C(O)=O)C(C)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CC2=CSC=C2)=C1 FVVACHCAVRTOQE-UHFFFAOYSA-N 0.000 claims description 6
- 125000001544 thienyl group Chemical group 0.000 claims description 6
- UTNZGBCCVVRBIW-UHFFFAOYSA-N 2-[4-[[4-[(4-methoxyphenyl)methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoic acid Chemical compound C1=CC(OC)=CC=C1CC1=C(CSC=2C=C(C)C(OC(C)(C)C(O)=O)=CC=2)SC(C=2C=CC(=CC=2)C(F)(F)F)=N1 UTNZGBCCVVRBIW-UHFFFAOYSA-N 0.000 claims description 5
- GWTXBGBDOIAZPQ-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoic acid Chemical compound C1=CC(OC)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=C(C)C(OC(C)(C)C(O)=O)=CC=2)CC1 GWTXBGBDOIAZPQ-UHFFFAOYSA-N 0.000 claims description 5
- BCTQCGIKVZFCLS-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]propanoic acid Chemical compound C1=CC(OC)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=C(C)C(OC(C)C(O)=O)=CC=2)CC1 BCTQCGIKVZFCLS-UHFFFAOYSA-N 0.000 claims description 5
- LPOBICWXXUKVPK-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]-2-methylpropanoic acid Chemical compound C1=CC(OC)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=CC(OC(C)(C)C(O)=O)=CC=2)CC1 LPOBICWXXUKVPK-UHFFFAOYSA-N 0.000 claims description 5
- JMZLZYWSHIVYQV-UHFFFAOYSA-N 2-methyl-2-[2-methyl-4-[[4-[[4-(trifluoromethoxy)phenyl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]propanoic acid Chemical compound C1=C(OC(C)(C)C(O)=O)C(C)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CC=2C=CC(OC(F)(F)F)=CC=2)=C1 JMZLZYWSHIVYQV-UHFFFAOYSA-N 0.000 claims description 5
- MVAGRNCLYNRSIU-UHFFFAOYSA-N 2-methyl-2-[4-[[4-[(4-pyrazin-2-ylpiperazin-1-yl)methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)(C)C(O)=O)=CC=C1SCC1=C(CN2CCN(CC2)C=2N=CC=NC=2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 MVAGRNCLYNRSIU-UHFFFAOYSA-N 0.000 claims description 5
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 5
- 208000011580 syndromic disease Diseases 0.000 claims description 5
- DIFNTPAWTGWFIQ-UHFFFAOYSA-N 2-[2-methyl-4-[[4-[(4-methylthiophen-2-yl)methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetic acid Chemical compound CC1=CSC(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=C(C)C(OCC(O)=O)=CC=2)=C1 DIFNTPAWTGWFIQ-UHFFFAOYSA-N 0.000 claims description 4
- BMNBRVGQZHPKHG-UHFFFAOYSA-N 2-[2-methyl-4-[[4-[(4-pyrimidin-2-ylpiperazin-1-yl)methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]propanoic acid Chemical compound C1=C(C)C(OC(C)C(O)=O)=CC=C1SCC1=C(CN2CCN(CC2)C=2N=CC=CN=2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 BMNBRVGQZHPKHG-UHFFFAOYSA-N 0.000 claims description 4
- XGTZMXYQJTZSCP-UHFFFAOYSA-N 2-[2-methyl-4-[[4-[[4-(4-propan-2-yloxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=C(C)C(OC(C)C(O)=O)=CC=2)CC1 XGTZMXYQJTZSCP-UHFFFAOYSA-N 0.000 claims description 4
- QUMUTAZYSUGGAM-UHFFFAOYSA-N 2-[4-[[4-[(4-methoxyphenyl)methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]acetic acid Chemical compound C1=CC(OC)=CC=C1CC1=C(CSC=2C=C(C)C(OCC(O)=O)=CC=2)SC(C=2C=CC(=CC=2)C(F)(F)F)=N1 QUMUTAZYSUGGAM-UHFFFAOYSA-N 0.000 claims description 4
- UQFYXXUDIYNDQH-UHFFFAOYSA-N 2-[4-[[4-[(4-tert-butylphenyl)methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoic acid Chemical compound C1=C(OC(C)(C)C(O)=O)C(C)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CC=2C=CC(=CC=2)C(C)(C)C)=C1 UQFYXXUDIYNDQH-UHFFFAOYSA-N 0.000 claims description 4
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 4
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims description 4
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims description 4
- 208000032928 Dyslipidaemia Diseases 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- 208000017170 Lipid metabolism disease Diseases 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- CESIUPFUCGHEPP-UHFFFAOYSA-N 2-[2-ethyl-4-[[4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetic acid Chemical compound C1=C(OCC(O)=O)C(CC)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CN2CCN(CC2)C=2C=CC(OC)=CC=2)=C1 CESIUPFUCGHEPP-UHFFFAOYSA-N 0.000 claims description 3
- AMWLERATXBSGQY-UHFFFAOYSA-N 2-[2-methyl-4-[[4-(2-phenylethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetic acid Chemical compound C1=C(OCC(O)=O)C(C)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CCC=2C=CC=CC=2)=C1 AMWLERATXBSGQY-UHFFFAOYSA-N 0.000 claims description 3
- FHWSXRDTCDHVOY-UHFFFAOYSA-N 2-[2-methyl-4-[[4-(thiophen-2-ylmethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]propanoic acid Chemical compound C1=C(C)C(OC(C)C(O)=O)=CC=C1SCC1=C(CC=2SC=CC=2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 FHWSXRDTCDHVOY-UHFFFAOYSA-N 0.000 claims description 3
- JYYLSMURAYLXRE-UHFFFAOYSA-N 2-[2-methyl-4-[[4-(thiophen-3-ylmethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetic acid Chemical compound C1=C(OCC(O)=O)C(C)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CC2=CSC=C2)=C1 JYYLSMURAYLXRE-UHFFFAOYSA-N 0.000 claims description 3
- GQDOHCPKHIILRT-UHFFFAOYSA-N 2-[2-methyl-4-[[4-[(4-phenylphenyl)methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetic acid Chemical compound C1=C(OCC(O)=O)C(C)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CC=2C=CC(=CC=2)C=2C=CC=CC=2)=C1 GQDOHCPKHIILRT-UHFFFAOYSA-N 0.000 claims description 3
- KRCKWKMHZJNRMT-UHFFFAOYSA-N 2-[2-methyl-4-[[4-[(4-pyrazin-2-ylpiperazin-1-yl)methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetic acid Chemical compound C1=C(OCC(O)=O)C(C)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CN2CCN(CC2)C=2N=CC=NC=2)=C1 KRCKWKMHZJNRMT-UHFFFAOYSA-N 0.000 claims description 3
- FTUDUVKEOPPRET-UHFFFAOYSA-N 2-[4-[[2-(4-fluorophenyl)-4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoic acid Chemical compound C1=CC(OC)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(F)=CC=2)CSC=2C=C(C)C(OC(C)(C)C(O)=O)=CC=2)CC1 FTUDUVKEOPPRET-UHFFFAOYSA-N 0.000 claims description 3
- WHHYTFSKYVBOTI-UHFFFAOYSA-N 2-[4-[[4-[[4-(2,4-dimethoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]propanoic acid Chemical compound COC1=CC(OC)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=C(C)C(OC(C)C(O)=O)=CC=2)CC1 WHHYTFSKYVBOTI-UHFFFAOYSA-N 0.000 claims description 3
- ZFXOVULAKVMWEM-UHFFFAOYSA-N 2-[4-[[4-[[4-(2-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]acetic acid Chemical compound COC1=CC=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=C(C)C(OCC(O)=O)=CC=2)CC1 ZFXOVULAKVMWEM-UHFFFAOYSA-N 0.000 claims description 3
- NAVWFKOQMRRKDH-UHFFFAOYSA-N 2-[4-[[4-[[4-(3-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]acetic acid Chemical compound COC1=CC=CC(N2CCN(CC3=C(SC(=N3)C=3C=CC(=CC=3)C(F)(F)F)CSC=3C=C(C)C(OCC(O)=O)=CC=3)CC2)=C1 NAVWFKOQMRRKDH-UHFFFAOYSA-N 0.000 claims description 3
- QDJZVWSCXMIPBV-UHFFFAOYSA-N 2-[4-[[4-[[4-(3-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]propanoic acid Chemical compound COC1=CC=CC(N2CCN(CC3=C(SC(=N3)C=3C=CC(=CC=3)C(F)(F)F)CSC=3C=C(C)C(OC(C)C(O)=O)=CC=3)CC2)=C1 QDJZVWSCXMIPBV-UHFFFAOYSA-N 0.000 claims description 3
- RJTOGUMCAKAOAU-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-acetylphenyl)piperazin-1-yl]methyl]-2-(4-fluorophenyl)-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoic acid Chemical compound C1=CC(C(=O)C)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(F)=CC=2)CSC=2C=C(C)C(OC(C)(C)C(O)=O)=CC=2)CC1 RJTOGUMCAKAOAU-UHFFFAOYSA-N 0.000 claims description 3
- LTCMMBCLNPSLPT-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-acetylphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoic acid Chemical compound C1=CC(C(=O)C)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=C(C)C(OC(C)(C)C(O)=O)=CC=2)CC1 LTCMMBCLNPSLPT-UHFFFAOYSA-N 0.000 claims description 3
- YQHDHUBEHGJCEC-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-acetylphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]propanoic acid Chemical compound C1=C(C)C(OC(C)C(O)=O)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=CC(=CC=2)C(C)=O)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 YQHDHUBEHGJCEC-UHFFFAOYSA-N 0.000 claims description 3
- KEGPZSDHNALZCV-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-acetylphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-propylphenoxy]propanoic acid Chemical compound C1=C(OC(C)C(O)=O)C(CCC)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CN2CCN(CC2)C=2C=CC(=CC=2)C(C)=O)=C1 KEGPZSDHNALZCV-UHFFFAOYSA-N 0.000 claims description 3
- LVRFCQZNPPFUEA-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-acetylphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]-2-methylpropanoic acid Chemical compound C1=CC(C(=O)C)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=CC(OC(C)(C)C(O)=O)=CC=2)CC1 LVRFCQZNPPFUEA-UHFFFAOYSA-N 0.000 claims description 3
- BOWUBEIOBIVSPN-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-ethoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]propanoic acid Chemical compound C1=CC(OCC)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=C(C)C(OC(C)C(O)=O)=CC=2)CC1 BOWUBEIOBIVSPN-UHFFFAOYSA-N 0.000 claims description 3
- NLAXBTJTOIJUJI-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-fluorophenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoic acid Chemical compound C1=C(OC(C)(C)C(O)=O)C(C)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CN2CCN(CC2)C=2C=CC(F)=CC=2)=C1 NLAXBTJTOIJUJI-UHFFFAOYSA-N 0.000 claims description 3
- GIIBXWSTEIQLJA-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-propan-2-ylphenoxy]acetic acid Chemical compound C1=CC(OC)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=C(C(OCC(O)=O)=CC=2)C(C)C)CC1 GIIBXWSTEIQLJA-UHFFFAOYSA-N 0.000 claims description 3
- JAQAQHYBXFOQIS-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-propan-2-ylphenoxy]propanoic acid Chemical compound C1=CC(OC)=CC=C1N1CCN(CC2=C(SC(=N2)C=2C=CC(=CC=2)C(F)(F)F)CSC=2C=C(C(OC(C)C(O)=O)=CC=2)C(C)C)CC1 JAQAQHYBXFOQIS-UHFFFAOYSA-N 0.000 claims description 3
- QVTXXICAWVRHIE-UHFFFAOYSA-N 2-[4-[[4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-propylphenoxy]propanoic acid Chemical compound C1=C(OC(C)C(O)=O)C(CCC)=CC(SCC2=C(N=C(S2)C=2C=CC(=CC=2)C(F)(F)F)CN2CCN(CC2)C=2C=CC(OC)=CC=2)=C1 QVTXXICAWVRHIE-UHFFFAOYSA-N 0.000 claims description 3
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- BXENIYIGPPXPNY-UHFFFAOYSA-N ethyl 2-(4-chlorosulfonyl-2-methylphenoxy)acetate Chemical compound CCOC(=O)COC1=CC=C(S(Cl)(=O)=O)C=C1C BXENIYIGPPXPNY-UHFFFAOYSA-N 0.000 description 1
- NZWJXSGPECGFJN-UHFFFAOYSA-N ethyl 2-(4-fluorophenyl)-4-(oxan-2-yloxymethyl)-1,3-thiazole-5-carboxylate Chemical compound CCOC(=O)C=1SC(C=2C=CC(F)=CC=2)=NC=1COC1CCCCO1 NZWJXSGPECGFJN-UHFFFAOYSA-N 0.000 description 1
- FKXLBALOGKPRIA-UHFFFAOYSA-N ethyl 2-[2-ethyl-4-[[4-(hydroxymethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetate Chemical compound C1=C(CC)C(OCC(=O)OCC)=CC=C1SCC1=C(CO)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 FKXLBALOGKPRIA-UHFFFAOYSA-N 0.000 description 1
- BZGISGMEFSCFEJ-UHFFFAOYSA-N ethyl 2-[2-ethyl-4-[[4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetate Chemical compound C1=C(CC)C(OCC(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=CC(OC)=CC=2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 BZGISGMEFSCFEJ-UHFFFAOYSA-N 0.000 description 1
- ZFZZHGGJCATVDV-UHFFFAOYSA-N ethyl 2-[2-methyl-4-[[4-(oxan-2-yloxymethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetate Chemical compound C1=C(C)C(OCC(=O)OCC)=CC=C1SCC1=C(COC2OCCCC2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 ZFZZHGGJCATVDV-UHFFFAOYSA-N 0.000 description 1
- JBYKJVHIUUPQRH-UHFFFAOYSA-N ethyl 2-[2-methyl-4-[[4-[[3-(5-methyl-1,2,4-oxadiazol-3-yl)phenoxy]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetate Chemical compound C1=C(C)C(OCC(=O)OCC)=CC=C1SCC1=C(COC=2C=C(C=CC=2)C=2N=C(C)ON=2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 JBYKJVHIUUPQRH-UHFFFAOYSA-N 0.000 description 1
- ALYBYBNSOOLVJT-UHFFFAOYSA-N ethyl 2-[4-[[2-(4-fluorophenyl)-4-[[4-(3-methoxyphenyl)piperazin-1-yl]methyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoate Chemical compound C1=C(C)C(OC(C)(C)C(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=C(OC)C=CC=2)N=C(C=2C=CC(F)=CC=2)S1 ALYBYBNSOOLVJT-UHFFFAOYSA-N 0.000 description 1
- HBWBRZWUEUESSR-UHFFFAOYSA-N ethyl 2-[4-[[2-(4-fluorophenyl)-4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoate Chemical compound C1=C(C)C(OC(C)(C)C(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=CC(OC)=CC=2)N=C(C=2C=CC(F)=CC=2)S1 HBWBRZWUEUESSR-UHFFFAOYSA-N 0.000 description 1
- CCASPDORVYFQLY-UHFFFAOYSA-N ethyl 2-[4-[[4-[[4-(2-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]-2-methylpropanoate Chemical compound C1=CC(OC(C)(C)C(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C(=CC=CC=2)OC)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 CCASPDORVYFQLY-UHFFFAOYSA-N 0.000 description 1
- WOALJTSWPXTRPB-UHFFFAOYSA-N ethyl 2-[4-[[4-[[4-(3-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoate Chemical compound C1=C(C)C(OC(C)(C)C(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=C(OC)C=CC=2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 WOALJTSWPXTRPB-UHFFFAOYSA-N 0.000 description 1
- NYMLQCYOBOBBAC-UHFFFAOYSA-N ethyl 2-[4-[[4-[[4-(3-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]-2-methylpropanoate Chemical compound C1=CC(OC(C)(C)C(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=C(OC)C=CC=2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 NYMLQCYOBOBBAC-UHFFFAOYSA-N 0.000 description 1
- MPAJNJRCNBEJNL-UHFFFAOYSA-N ethyl 2-[4-[[4-[[4-(4-acetylphenyl)piperazin-1-yl]methyl]-2-(4-fluorophenyl)-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoate Chemical compound C1=C(C)C(OC(C)(C)C(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=CC(=CC=2)C(C)=O)N=C(C=2C=CC(F)=CC=2)S1 MPAJNJRCNBEJNL-UHFFFAOYSA-N 0.000 description 1
- JXAMESYPHLHMSV-UHFFFAOYSA-N ethyl 2-[4-[[4-[[4-(4-acetylphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]-2-methylpropanoate Chemical compound C1=CC(OC(C)(C)C(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=CC(=CC=2)C(C)=O)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 JXAMESYPHLHMSV-UHFFFAOYSA-N 0.000 description 1
- OTWAYAIYWCVHLT-UHFFFAOYSA-N ethyl 2-[4-[[4-[[4-(4-chlorophenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]-2-methylpropanoate Chemical compound C1=CC(OC(C)(C)C(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=CC(Cl)=CC=2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 OTWAYAIYWCVHLT-UHFFFAOYSA-N 0.000 description 1
- SADGKXGQHJQWQC-UHFFFAOYSA-N ethyl 2-[4-[[4-[[4-(4-fluorophenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoate Chemical compound C1=C(C)C(OC(C)(C)C(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=CC(F)=CC=2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 SADGKXGQHJQWQC-UHFFFAOYSA-N 0.000 description 1
- FUBPBUZNRDBPDT-UHFFFAOYSA-N ethyl 2-[4-[[4-[[4-(4-methoxyphenyl)piperazin-1-yl]methyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]-2-methylphenoxy]-2-methylpropanoate Chemical compound C1=C(C)C(OC(C)(C)C(=O)OCC)=CC=C1SCC1=C(CN2CCN(CC2)C=2C=CC(OC)=CC=2)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 FUBPBUZNRDBPDT-UHFFFAOYSA-N 0.000 description 1
- IOLQWGVDEFWYNP-UHFFFAOYSA-N ethyl 2-bromo-2-methylpropanoate Chemical compound CCOC(=O)C(C)(C)Br IOLQWGVDEFWYNP-UHFFFAOYSA-N 0.000 description 1
- JMTJAPHJNNZWII-UHFFFAOYSA-N ethyl 2-chloro-3-oxo-4-(2-phenylethoxy)butanoate Chemical compound CCOC(=O)C(Cl)C(=O)COCCC1=CC=CC=C1 JMTJAPHJNNZWII-UHFFFAOYSA-N 0.000 description 1
- RBJYBVPPUKQOQO-UHFFFAOYSA-N ethyl 2-chloro-3-oxo-4-phenylbutanoate Chemical compound CCOC(=O)C(Cl)C(=O)CC1=CC=CC=C1 RBJYBVPPUKQOQO-UHFFFAOYSA-N 0.000 description 1
- AXESJJDMDNBIBX-UHFFFAOYSA-N ethyl 2-chloro-3-oxo-4-phenylmethoxybutanoate Chemical compound CCOC(=O)C(Cl)C(=O)COCC1=CC=CC=C1 AXESJJDMDNBIBX-UHFFFAOYSA-N 0.000 description 1
- RICCWHIBTQBAMF-UHFFFAOYSA-N ethyl 2-chloro-3-oxo-5-phenylpentanoate Chemical compound CCOC(=O)C(Cl)C(=O)CCC1=CC=CC=C1 RICCWHIBTQBAMF-UHFFFAOYSA-N 0.000 description 1
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- DWGNORJGZURHSW-UHFFFAOYSA-N tert-butyl 4-[[5-[[4-(2-methoxy-2-oxoethoxy)-3-methylphenyl]sulfanylmethyl]-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-4-yl]methyl]piperazine-1-carboxylate Chemical compound C1=C(C)C(OCC(=O)OC)=CC=C1SCC1=C(CN2CCN(CC2)C(=O)OC(C)(C)C)N=C(C=2C=CC(=CC=2)C(F)(F)F)S1 DWGNORJGZURHSW-UHFFFAOYSA-N 0.000 description 1
- MHYGQXWCZAYSLJ-UHFFFAOYSA-N tert-butyl-chloro-diphenylsilane Chemical compound C=1C=CC=CC=1[Si](Cl)(C(C)(C)C)C1=CC=CC=C1 MHYGQXWCZAYSLJ-UHFFFAOYSA-N 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 150000007979 thiazole derivatives Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 230000002103 transcriptional effect Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- GXPHKUHSUJUWKP-UHFFFAOYSA-N troglitazone Chemical compound C1CC=2C(C)=C(O)C(C)=C(C)C=2OC1(C)COC(C=C1)=CC=C1CC1SC(=O)NC1=O GXPHKUHSUJUWKP-UHFFFAOYSA-N 0.000 description 1
- 229960001641 troglitazone Drugs 0.000 description 1
- GXPHKUHSUJUWKP-NTKDMRAZSA-N troglitazone Natural products C([C@@]1(OC=2C(C)=C(C(=C(C)C=2CC1)O)C)C)OC(C=C1)=CC=C1C[C@H]1SC(=O)NC1=O GXPHKUHSUJUWKP-NTKDMRAZSA-N 0.000 description 1
- 229940116269 uric acid Drugs 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000008215 water for injection Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- 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
- C07D417/06—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 carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- C07D277/22—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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/24—Radicals substituted by oxygen atoms
-
- 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
- C07D277/22—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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/26—Radicals substituted by sulfur atoms
-
- 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
- C07D277/22—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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/28—Radicals substituted by nitrogen atoms
-
- 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
- C07D417/10—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 carbon chain containing aromatic rings
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Neurology (AREA)
- Hospice & Palliative Care (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Biomedical Technology (AREA)
- Endocrinology (AREA)
- Neurosurgery (AREA)
- Nutrition Science (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 Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0031103.5A GB0031103D0 (en) | 2000-12-20 | 2000-12-20 | Chemical compounds |
| GB0031103 | 2000-12-20 | ||
| PCT/US2001/051056 WO2002059098A1 (en) | 2000-12-20 | 2001-12-19 | Thiazole and oxazole derivatives as activators of human peroxisome proliferator activated receptors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60110262D1 DE60110262D1 (de) | 2005-05-25 |
| DE60110262T2 true DE60110262T2 (de) | 2006-03-09 |
Family
ID=9905490
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60110262T Expired - Lifetime DE60110262T2 (de) | 2000-12-20 | 2001-12-19 | Thiazol und oxazol-derivate als aktivatoren von menschlichen peroxisom proliferator aktivierten rezeptoren |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP1349843B1 (enExample) |
| JP (1) | JP4234431B2 (enExample) |
| AT (1) | ATE293611T1 (enExample) |
| DE (1) | DE60110262T2 (enExample) |
| DK (1) | DK1349843T3 (enExample) |
| ES (1) | ES2240558T3 (enExample) |
| GB (1) | GB0031103D0 (enExample) |
| PT (1) | PT1349843E (enExample) |
| WO (1) | WO2002059098A1 (enExample) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US7041691B1 (en) | 1999-06-30 | 2006-05-09 | Amgen Inc. | Compounds for the modulation of PPARγ activity |
| US20030171399A1 (en) | 2000-06-28 | 2003-09-11 | Tularik Inc. | Quinolinyl and benzothiazolyl modulators |
| US7105551B2 (en) | 2000-12-20 | 2006-09-12 | Smithkline Beecham Corporation | Thiazole derivatives for treating PPAR related disorders |
| GB0031109D0 (en) | 2000-12-20 | 2001-01-31 | Glaxo Group Ltd | Chemical compounds |
| HRP20040098B1 (en) * | 2001-08-13 | 2012-08-31 | Janssen Pharmaceutica N.V. | 2,4,5-TRlSUBSTITUTED THIAZOLYL DERIVATIVES AND THEIR ANTIINFLAMMATORY ACTIVITY |
| US7259175B2 (en) | 2002-02-25 | 2007-08-21 | Eli Lilly And Company | Peroxisome proliferator activated receptor modulators |
| GB0214139D0 (en) | 2002-06-19 | 2002-07-31 | Glaxo Group Ltd | Chemical compounds |
| PL375700A1 (en) | 2002-09-05 | 2005-12-12 | Novo Nordisk A/S | Novel vinyl carboxylic acid derivatives and their therapeutical use |
| EP1535915A4 (en) | 2002-09-06 | 2005-10-05 | Takeda Pharmaceutical | FURANOIC OR THIOPHENE DERIVATIVES AND THEIR MEDICAL USE |
| JP2005035966A (ja) * | 2002-09-06 | 2005-02-10 | Takeda Chem Ind Ltd | フランまたはチオフェン誘導体およびその医薬用途 |
| EP1546124A1 (en) * | 2002-09-19 | 2005-06-29 | SmithKline Beecham Corporation | Process for preparing substituted phenoxy-acetic acids from phenols |
| US7129268B2 (en) | 2002-10-28 | 2006-10-31 | Novo Nordisk A/S | Peroxisome proliferator activated receptor-active arylene acetic acid derivatives |
| CN1708479A (zh) | 2002-10-28 | 2005-12-14 | 诺沃挪第克公司 | 可用于治疗ppar所介导的疾病的新颖化合物 |
| EP1558572B1 (en) | 2002-10-28 | 2010-06-30 | High Point Pharmaceuticals, LLC | Novel compounds and their use as prar-modulators |
| US20050080115A1 (en) | 2002-10-28 | 2005-04-14 | Lone Jeppesen | Novel compounds, their preparation and use |
| DE10308355A1 (de) * | 2003-02-27 | 2004-12-23 | Aventis Pharma Deutschland Gmbh | Aryl-cycloalkyl substituierte Alkansäurederivate, Verfahren zu ihrer Herstellung und ihre Anwendung als Arzneimittel |
| US7223761B2 (en) | 2003-10-03 | 2007-05-29 | Amgen Inc. | Salts and polymorphs of a potent antidiabetic compound |
| EP1745003B1 (en) | 2004-05-05 | 2010-10-27 | High Point Pharmaceuticals, LLC | Novel compounds, their preparation and use |
| WO2005105736A1 (en) | 2004-05-05 | 2005-11-10 | Novo Nordisk A/S | Novel compounds, their preparation and use |
| JPWO2006126714A1 (ja) * | 2005-05-25 | 2008-12-25 | 日本ケミファ株式会社 | ペルオキシソーム増殖剤活性化受容体の活性化剤 |
| EP2298742B1 (en) | 2005-06-30 | 2014-01-08 | High Point Pharmaceuticals, LLC | phenoxy acetic acids as PPAR delta activators |
| EP2386540A1 (en) | 2005-12-22 | 2011-11-16 | High Point Pharmaceuticals, LLC | Novel compounds, their preparation and use |
| JP2009132620A (ja) * | 2006-03-07 | 2009-06-18 | Astellas Pharma Inc | フェニルチアゾール誘導体 |
| WO2007101864A2 (en) | 2006-03-09 | 2007-09-13 | High Point Pharmaceuticals, Llc | Compounds that modulate ppar activity, their preparation and use |
| ZA200809148B (en) | 2006-04-18 | 2010-01-27 | Nippon Chemiphar Co | Activating agent for peroxisome proliferator activated receptor delta |
| EA200900392A1 (ru) | 2006-09-07 | 2010-06-30 | Никомед Гмбх | Комбинированное лечение сахарного диабета |
| FR2910893A1 (fr) * | 2006-12-29 | 2008-07-04 | Genfit Sa | Derives de (phenylthiazolyl)-phenyl-propan-1-one et de (phenyloxazolyl)-phenyl-propan-1-one substitues, preparations et utilisations. |
| AU2008259342B2 (en) | 2007-06-04 | 2014-07-10 | Ben-Gurion University Of The Negev Research And Development Authority | Tri-aryl compounds and compositions comprising the same |
| BRPI0911197A2 (pt) | 2008-04-15 | 2015-10-13 | Nippon Chemiphar Co | composto, ativador de receptor ativado pelo proliferador de peroxissoma, e, medicamento para o tratamento e /ou profilaxia de uma doença. |
| US20120094959A1 (en) | 2010-10-19 | 2012-04-19 | Bonnie Blazer-Yost | Treatment of cystic diseases |
| US9688673B2 (en) | 2011-03-08 | 2017-06-27 | The Regents Of The University Of California | Deoxycytidine kinase binding compounds |
| ES2811087T3 (es) | 2013-09-09 | 2021-03-10 | Vtv Therapeutics Llc | Uso de agonistas de PPAR-delta para tratar la atrofia muscular |
| EA201690938A1 (ru) | 2013-11-05 | 2016-11-30 | Бен-Гурион Юниверсити Оф Дзе Негев Рисерч Энд Дивелопмент Оторити | Соединения для лечения диабета и осложнений, возникающих из-за этого заболевания |
| ES3041492T3 (en) | 2019-12-18 | 2025-11-12 | Stinginn Llc | Substituted 1,2, 4-triazoles and methods of use |
| MX2023005056A (es) | 2020-11-02 | 2023-07-24 | Trethera Corp | Formas cristalinas de un inhibidor de cinasa de desoxicitidina y sus usos. |
| AU2022277578A1 (en) * | 2021-05-19 | 2023-12-14 | Stinginn Inc | Small molecular inhibitors of sting signaling compositions and methods of use |
| WO2023147309A1 (en) | 2022-01-25 | 2023-08-03 | Reneo Pharmaceuticals, Inc. | Use of ppar-delta agonists in the treatment of disease |
Family Cites Families (4)
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| US6028052A (en) * | 1995-09-18 | 2000-02-22 | Ligand Pharmaceuticals Incorporated | Treating NIDDM with RXR agonists |
| GB9817118D0 (en) * | 1998-08-07 | 1998-10-07 | Glaxo Group Ltd | Pharmaceutical compounds |
| GB9914977D0 (en) * | 1999-06-25 | 1999-08-25 | Glaxo Group Ltd | Chemical compounds |
| PE20011010A1 (es) * | 1999-12-02 | 2001-10-18 | Glaxo Group Ltd | Oxazoles y tiazoles sustituidos como agonista del receptor activado por el proliferador de peroxisomas humano |
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2000
- 2000-12-20 GB GBGB0031103.5A patent/GB0031103D0/en not_active Ceased
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- 2001-12-19 AT AT01994514T patent/ATE293611T1/de not_active IP Right Cessation
- 2001-12-19 EP EP01994514A patent/EP1349843B1/en not_active Expired - Lifetime
- 2001-12-19 PT PT01994514T patent/PT1349843E/pt unknown
- 2001-12-19 JP JP2002559400A patent/JP4234431B2/ja not_active Expired - Fee Related
- 2001-12-19 DE DE60110262T patent/DE60110262T2/de not_active Expired - Lifetime
- 2001-12-19 ES ES01994514T patent/ES2240558T3/es not_active Expired - Lifetime
- 2001-12-19 DK DK01994514T patent/DK1349843T3/da active
- 2001-12-19 WO PCT/US2001/051056 patent/WO2002059098A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| PT1349843E (pt) | 2005-09-30 |
| EP1349843A1 (en) | 2003-10-08 |
| JP2004520377A (ja) | 2004-07-08 |
| DE60110262D1 (de) | 2005-05-25 |
| ATE293611T1 (de) | 2005-05-15 |
| EP1349843B1 (en) | 2005-04-20 |
| GB0031103D0 (en) | 2001-01-31 |
| ES2240558T3 (es) | 2005-10-16 |
| WO2002059098A1 (en) | 2002-08-01 |
| JP4234431B2 (ja) | 2009-03-04 |
| DK1349843T3 (da) | 2005-08-15 |
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