CA2510793A1 - Indane acetic acid derivatives and their use as pharmaceutical agents, intermediates, and method of preparation - Google Patents
Indane acetic acid derivatives and their use as pharmaceutical agents, intermediates, and method of preparation Download PDFInfo
- Publication number
- CA2510793A1 CA2510793A1 CA002510793A CA2510793A CA2510793A1 CA 2510793 A1 CA2510793 A1 CA 2510793A1 CA 002510793 A CA002510793 A CA 002510793A CA 2510793 A CA2510793 A CA 2510793A CA 2510793 A1 CA2510793 A1 CA 2510793A1
- Authority
- CA
- Canada
- Prior art keywords
- propoxy
- acetic acid
- indanyl
- cndot
- mmol
- 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
- 238000000034 method Methods 0.000 title claims abstract description 113
- 239000008177 pharmaceutical agent Substances 0.000 title claims description 13
- 238000002360 preparation method Methods 0.000 title abstract description 154
- BUVKILSTJGGJJN-UHFFFAOYSA-N acetic acid;2,3-dihydro-1h-indene Chemical class CC(O)=O.C1=CC=C2CCCC2=C1 BUVKILSTJGGJJN-UHFFFAOYSA-N 0.000 title abstract description 7
- 239000012450 pharmaceutical intermediate Substances 0.000 title description 2
- 206010012601 diabetes mellitus Diseases 0.000 claims abstract description 40
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 26
- 238000011282 treatment Methods 0.000 claims abstract description 12
- 208000008589 Obesity Diseases 0.000 claims abstract description 7
- 235000020824 obesity Nutrition 0.000 claims abstract description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 309
- 150000001875 compounds Chemical class 0.000 claims description 293
- 239000000203 mixture Substances 0.000 claims description 187
- -1 3-methyl-7-propyl-1,2-benzisoxazol-6-yl Chemical group 0.000 claims description 60
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 60
- 229910052786 argon Inorganic materials 0.000 claims description 55
- 229910052760 oxygen Inorganic materials 0.000 claims description 39
- 229910052717 sulfur Inorganic materials 0.000 claims description 38
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims description 37
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 claims description 30
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 28
- 125000005843 halogen group Chemical group 0.000 claims description 24
- 229920006395 saturated elastomer Polymers 0.000 claims description 23
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 21
- 150000002148 esters Chemical class 0.000 claims description 20
- 150000003839 salts Chemical class 0.000 claims description 20
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 16
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 16
- 102000004877 Insulin Human genes 0.000 claims description 15
- 108090001061 Insulin Proteins 0.000 claims description 15
- 229940125396 insulin Drugs 0.000 claims description 15
- 125000002837 carbocyclic group Chemical group 0.000 claims description 14
- 239000003814 drug Substances 0.000 claims description 14
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 14
- 208000035475 disorder Diseases 0.000 claims description 13
- 125000005842 heteroatom Chemical group 0.000 claims description 13
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 12
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 11
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 11
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 10
- 239000008103 glucose Substances 0.000 claims description 10
- 206010022489 Insulin Resistance Diseases 0.000 claims description 9
- 229940079593 drug Drugs 0.000 claims description 9
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 9
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 8
- 125000001072 heteroaryl group Chemical group 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 208000002705 Glucose Intolerance Diseases 0.000 claims description 7
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 claims description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 7
- 230000002440 hepatic effect Effects 0.000 claims description 7
- 201000009104 prediabetes syndrome Diseases 0.000 claims description 7
- 125000004001 thioalkyl group Chemical group 0.000 claims description 7
- 206010060378 Hyperinsulinaemia Diseases 0.000 claims description 6
- 206010056997 Impaired fasting glucose Diseases 0.000 claims description 6
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 230000003451 hyperinsulinaemic effect Effects 0.000 claims description 6
- 201000008980 hyperinsulinism Diseases 0.000 claims description 6
- 229910052727 yttrium Inorganic materials 0.000 claims description 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 5
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
- 125000002619 bicyclic group Chemical group 0.000 claims description 5
- 208000006575 hypertriglyceridemia Diseases 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 208000011580 syndromic disease Diseases 0.000 claims description 5
- 208000024172 Cardiovascular disease Diseases 0.000 claims description 4
- 208000032928 Dyslipidaemia Diseases 0.000 claims description 4
- 208000017170 Lipid metabolism disease Diseases 0.000 claims description 4
- 208000035180 MODY Diseases 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 201000001421 hyperglycemia Diseases 0.000 claims description 4
- 230000003914 insulin secretion Effects 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 201000006950 maturity-onset diabetes of the young Diseases 0.000 claims description 4
- 125000002950 monocyclic group Chemical group 0.000 claims description 4
- 235000001968 nicotinic acid Nutrition 0.000 claims description 4
- 239000011664 nicotinic acid Substances 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- NRMLKMKBUYOILR-QFIPXVFZSA-N 2-[(1s)-5-[3-[[2-(4-ethoxyphenyl)-5-methylpyrimidin-4-yl]methylamino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1=CC(OCC)=CC=C1C1=NC=C(C)C(CNCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)=N1 NRMLKMKBUYOILR-QFIPXVFZSA-N 0.000 claims description 3
- FKPYJIJYMXBAFW-IBGZPJMESA-N 2-[4-[3-[[(1s)-1-(carboxymethyl)-2,3-dihydro-1h-inden-5-yl]oxy]propoxy]-3-propylphenyl]-4-methyl-1,3-thiazole-5-carboxylic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC(C)=C(C(O)=O)S1 FKPYJIJYMXBAFW-IBGZPJMESA-N 0.000 claims description 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 3
- 208000004104 gestational diabetes Diseases 0.000 claims description 3
- 239000003862 glucocorticoid Substances 0.000 claims description 3
- 229960003512 nicotinic acid Drugs 0.000 claims description 3
- JIBRBEPRUAKTNJ-AHWVRZQESA-N (2s)-2-[(1s)-5-[2-[6-(4-ethylphenyl)pyridin-2-yl]ethoxy]-2,3-dihydro-1h-inden-1-yl]butanoic acid Chemical compound C([C@H](C1=CC=2)[C@H](CC)C(O)=O)CC1=CC=2OCCC(N=1)=CC=CC=1C1=CC=C(CC)C=C1 JIBRBEPRUAKTNJ-AHWVRZQESA-N 0.000 claims description 2
- WYZVWTYQKOZQQS-NRFANRHFSA-N 2-[(1s)-5-[2-[6-(4-acetylphenyl)pyridin-2-yl]ethoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1=CC(C(=O)C)=CC=C1C1=CC=CC(CCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)=N1 WYZVWTYQKOZQQS-NRFANRHFSA-N 0.000 claims description 2
- GYLMBHYEEPSETC-KRWDZBQOSA-N 2-[(1s)-5-[3-[(3,7-dimethyl-1,2-benzoxazol-6-yl)oxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1=C2[C@H](CC(O)=O)CCC2=CC(OCCCOC=2C(C)=C3ON=C(C3=CC=2)C)=C1 GYLMBHYEEPSETC-KRWDZBQOSA-N 0.000 claims description 2
- KHWSFWPKNKLKPX-FQEVSTJZSA-N 2-[(1s)-5-[3-[2-ethoxy-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(OCC)=C1 KHWSFWPKNKLKPX-FQEVSTJZSA-N 0.000 claims description 2
- HGRRXAJCQVQKSP-HSYKDVHTSA-N 2-[(1s)-5-[3-[2-methoxy-4-(3,5,6,7-tetrahydro-2h-pyrano[2,3-d][1,3]thiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(OC)=CC=1C(S1)NC2=C1CCCO2 HGRRXAJCQVQKSP-HSYKDVHTSA-N 0.000 claims description 2
- NPZMDWHUIIGJNS-IBGZPJMESA-N 2-[(1s)-5-[3-[2-methoxy-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(OC)=C1 NPZMDWHUIIGJNS-IBGZPJMESA-N 0.000 claims description 2
- BLJVVKCIOACNOQ-IBGZPJMESA-N 2-[(1s)-5-[3-[2-methoxy-4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1CCCC(O2)=C1N=C2C1=CC=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(OC)=C1 BLJVVKCIOACNOQ-IBGZPJMESA-N 0.000 claims description 2
- YUWKOSPDHRFEEF-KRWDZBQOSA-N 2-[(1s)-5-[3-[2-methoxy-4-(4-methoxy-1,3-thiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound COC1=CSC(C=2C=C(OC)C(OCCCOC=3C=C4CC[C@@H](CC(O)=O)C4=CC=3)=CC=2)=N1 YUWKOSPDHRFEEF-KRWDZBQOSA-N 0.000 claims description 2
- SLUNRBMNJCMKOE-NRFANRHFSA-N 2-[(1s)-5-[3-[2-propoxy-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(OCCC)=C1 SLUNRBMNJCMKOE-NRFANRHFSA-N 0.000 claims description 2
- VCBBROSSYZDABH-IBGZPJMESA-N 2-[(1s)-5-[3-[2-propyl-4-(1,3-thiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC=CS1 VCBBROSSYZDABH-IBGZPJMESA-N 0.000 claims description 2
- DPXRRYRDBWDWRM-NRFANRHFSA-N 2-[(1s)-5-[3-[2-propyl-4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1CCCC(O2)=C1N=C2C1=CC=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=C1 DPXRRYRDBWDWRM-NRFANRHFSA-N 0.000 claims description 2
- HEGJINSQHTYDEX-SFHVURJKSA-N 2-[(1s)-5-[3-[2-propyl-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC(C(F)(F)F)=CS1 HEGJINSQHTYDEX-SFHVURJKSA-N 0.000 claims description 2
- NTVBAWSNQRKVKF-FQEVSTJZSA-N 2-[(1s)-5-[3-[4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C(C=C1)=CC=C1OCCCOC1=CC=C2[C@H](CC(=O)O)CCC2=C1 NTVBAWSNQRKVKF-FQEVSTJZSA-N 0.000 claims description 2
- ZZKJSMBFWZMRRS-FQEVSTJZSA-N 2-[(1s)-5-[3-[4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1CCCC(O2)=C1N=C2C(C=C1)=CC=C1OCCCOC1=CC=C2[C@H](CC(=O)O)CCC2=C1 ZZKJSMBFWZMRRS-FQEVSTJZSA-N 0.000 claims description 2
- ZBFIQWUEGZKBFS-IBGZPJMESA-N 2-[(1s)-5-[3-[4-(4,5-dimethyl-1,3-thiazol-2-yl)-2-methoxyphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(OC)=CC=1C1=NC(C)=C(C)S1 ZBFIQWUEGZKBFS-IBGZPJMESA-N 0.000 claims description 2
- KZAIHPRSXFXXNU-FQEVSTJZSA-N 2-[(1s)-5-[3-[4-(4,5-dimethyl-1,3-thiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound S1C(C)=C(C)N=C1C(C=C1)=CC=C1OCCCOC1=CC=C([C@H](CC(O)=O)CC2)C2=C1 KZAIHPRSXFXXNU-FQEVSTJZSA-N 0.000 claims description 2
- DTSZUNRPQWYGHX-FQEVSTJZSA-N 2-[(1s)-5-[3-[4-(4-ethoxy-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC(OCC)=CS1 DTSZUNRPQWYGHX-FQEVSTJZSA-N 0.000 claims description 2
- UQFZTBWTJZBMDL-IBGZPJMESA-N 2-[(1s)-5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-methoxyphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound S1C(C)=C(OCC)N=C1C(C=C1OC)=CC=C1OCCCOC1=CC=C([C@H](CC(O)=O)CC2)C2=C1 UQFZTBWTJZBMDL-IBGZPJMESA-N 0.000 claims description 2
- XFEBTJLTAZGGPY-NRFANRHFSA-N 2-[(1s)-5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC(OCC)=C(C)S1 XFEBTJLTAZGGPY-NRFANRHFSA-N 0.000 claims description 2
- KKELJTWGLRARIG-FQEVSTJZSA-N 2-[(1s)-5-[3-[4-(4-ethyl-1,3-oxazol-2-yl)-2-propylphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC(CC)=CO1 KKELJTWGLRARIG-FQEVSTJZSA-N 0.000 claims description 2
- HBKNDUAKMHVGNM-SFHVURJKSA-N 2-[(1s)-5-[3-[4-(4-methoxy-1,3-thiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound COC1=CSC(C=2C=CC(OCCCOC=3C=C4CC[C@@H](CC(O)=O)C4=CC=3)=CC=2)=N1 HBKNDUAKMHVGNM-SFHVURJKSA-N 0.000 claims description 2
- DABDLIFECGXQNC-NRFANRHFSA-N 2-[(1s)-5-[3-[4-(4-propan-2-yloxy-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC(OC(C)C)=CS1 DABDLIFECGXQNC-NRFANRHFSA-N 0.000 claims description 2
- ZTQUDSFSSMPWPD-NRFANRHFSA-N 2-[(1s)-5-[3-[4-(4-tert-butyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC(C(C)(C)C)=CS1 ZTQUDSFSSMPWPD-NRFANRHFSA-N 0.000 claims description 2
- QJKOTSRVMJGHRK-NRFANRHFSA-N 2-[(1s)-5-[3-[4-(5,5-dimethyl-7-oxo-4,6-dihydro-1,3-benzothiazol-2-yl)-2-propylphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1C(C)(C)CC(=O)C(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=C1 QJKOTSRVMJGHRK-NRFANRHFSA-N 0.000 claims description 2
- IELCDGLGXNKKIF-SFHVURJKSA-N 2-[(1s)-5-[3-[4-(5,6-dihydro-4h-cyclopenta[d][1,3]thiazol-2-yl)-2-methoxyphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1=C2[C@H](CC(O)=O)CCC2=CC(OCCCOC2=CC=C(C=C2OC)C=2SC=3CCCC=3N=2)=C1 IELCDGLGXNKKIF-SFHVURJKSA-N 0.000 claims description 2
- FQTHEIJACHCXRP-FQEVSTJZSA-N 2-[(1s)-5-[3-[4-(5,6-dihydro-4h-cyclopenta[d][1,3]thiazol-2-yl)-2-propylphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C1=C2[C@H](CC(O)=O)CCC2=CC(OCCCOC2=CC=C(C=C2CCC)C=2SC=3CCCC=3N=2)=C1 FQTHEIJACHCXRP-FQEVSTJZSA-N 0.000 claims description 2
- XUJUKBDYMUPHEK-NRFANRHFSA-N 2-[(1s)-5-[3-[4-(5-acetyl-4-methyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3CC[C@@H](CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC(C)=C(C(C)=O)S1 XUJUKBDYMUPHEK-NRFANRHFSA-N 0.000 claims description 2
- NDSVGELSLGUYIY-KRWDZBQOSA-N 2-[(1s)-5-[3-[5-(4-ethyl-1,3-thiazol-2-yl)pyridin-2-yl]oxypropoxy]-2,3-dihydro-1h-inden-1-yl]acetic acid Chemical compound CCC1=CSC(C=2C=NC(OCCCOC=3C=C4CC[C@@H](CC(O)=O)C4=CC=3)=CC=2)=N1 NDSVGELSLGUYIY-KRWDZBQOSA-N 0.000 claims description 2
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- ZQJNIOMFZXVCBT-LBPRGKRZSA-N ethyl 2-[(1s)-5-(dimethylcarbamoylsulfanyl)-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound CN(C)C(=O)SC1=CC=C2[C@H](CC(=O)OCC)CCC2=C1 ZQJNIOMFZXVCBT-LBPRGKRZSA-N 0.000 description 1
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- RSTNPBLZECBJJZ-SFHVURJKSA-N ethyl 2-[(1s)-5-[2-(2,6-dimethylpyridin-3-yl)oxyethoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCOC1=CC=C(C)N=C1C RSTNPBLZECBJJZ-SFHVURJKSA-N 0.000 description 1
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- AFNWAIAAHZFZIP-KRWDZBQOSA-N ethyl 2-[(1s)-5-[3-(4-bromo-2-methoxyphenoxy)propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCOC1=CC=C(Br)C=C1OC AFNWAIAAHZFZIP-KRWDZBQOSA-N 0.000 description 1
- QYJWYZNJWXKFBN-IBGZPJMESA-N ethyl 2-[(1s)-5-[3-(4-cyano-2-methoxyphenoxy)propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCOC1=CC=C(C#N)C=C1OC QYJWYZNJWXKFBN-IBGZPJMESA-N 0.000 description 1
- OXFGMXNRJOGAAJ-NRFANRHFSA-N ethyl 2-[(1s)-5-[3-(4-cyano-2-propylphenoxy)propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound CCCC1=CC(C#N)=CC=C1OCCCOC1=CC=C([C@H](CC(=O)OCC)CC2)C2=C1 OXFGMXNRJOGAAJ-NRFANRHFSA-N 0.000 description 1
- FUZIUVUUBORFIZ-INIZCTEOSA-N ethyl 2-[(1s)-5-[3-(5-carbamothioylpyridin-2-yl)oxypropoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCOC1=CC=C(C(N)=S)C=N1 FUZIUVUUBORFIZ-INIZCTEOSA-N 0.000 description 1
- RZEIMQVFPNYIJO-IBGZPJMESA-N ethyl 2-[(1s)-5-[3-[(2-chloro-5-methylpyrimidin-4-yl)-propylamino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@@H](CC(=O)OCC)C1=CC=2)CC1=CC=2OCCCN(CCC)C1=NC(Cl)=NC=C1C RZEIMQVFPNYIJO-IBGZPJMESA-N 0.000 description 1
- DHBCKKDSUSOBJR-INIZCTEOSA-N ethyl 2-[(1s)-5-[3-[(2-chloro-5-methylpyrimidin-4-yl)amino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCNC1=NC(Cl)=NC=C1C DHBCKKDSUSOBJR-INIZCTEOSA-N 0.000 description 1
- ZEDRDCQJIXRFQV-INIZCTEOSA-N ethyl 2-[(1s)-5-[3-[(2-methylpropan-2-yl)oxycarbonylamino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound CC(C)(C)OC(=O)NCCCOC1=CC=C2[C@H](CC(=O)OCC)CCC2=C1 ZEDRDCQJIXRFQV-INIZCTEOSA-N 0.000 description 1
- RKJDXDZDDCZVEB-IBGZPJMESA-N ethyl 2-[(1s)-5-[3-[(3-methyl-1-benzofuran-6-yl)oxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C1=C2C(C)=COC2=CC(OCCCOC=2C=C3CC[C@H](C3=CC=2)CC(=O)OCC)=C1 RKJDXDZDDCZVEB-IBGZPJMESA-N 0.000 description 1
- FYXCHNPRDRXEGM-HNNXBMFYSA-N ethyl 2-[(1s)-5-[3-[(5-bromopyrimidin-2-yl)amino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCNC1=NC=C(Br)C=N1 FYXCHNPRDRXEGM-HNNXBMFYSA-N 0.000 description 1
- LRMIRQMEIJHFGI-INIZCTEOSA-N ethyl 2-[(1s)-5-[3-[(6-chloro-5-cyano-3-fluoropyridin-2-yl)-methylamino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCN(C)C1=NC(Cl)=C(C#N)C=C1F LRMIRQMEIJHFGI-INIZCTEOSA-N 0.000 description 1
- LSWLQWKRSXHOCO-FQEVSTJZSA-N ethyl 2-[(1s)-5-[3-[2-hydroxy-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C1CCCC(S2)=C1N=C2C(C=C1O)=CC=C1OCCCOC1=CC=C2[C@H](CC(=O)OCC)CCC2=C1 LSWLQWKRSXHOCO-FQEVSTJZSA-N 0.000 description 1
- GBDVXAIYMJKHPU-NRFANRHFSA-N ethyl 2-[(1s)-5-[3-[2-methoxy-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C1CCCC(S2)=C1N=C2C(C=C1OC)=CC=C1OCCCOC1=CC=C2[C@H](CC(=O)OCC)CCC2=C1 GBDVXAIYMJKHPU-NRFANRHFSA-N 0.000 description 1
- YBAZXMMBDKDXFP-QHCPKHFHSA-N ethyl 2-[(1s)-5-[3-[2-propoxy-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3CC[C@@H](CC(=O)OCC)C3=CC=2)C(OCCC)=C1 YBAZXMMBDKDXFP-QHCPKHFHSA-N 0.000 description 1
- NZEAYHVHEKKTCH-FQEVSTJZSA-N ethyl 2-[(1s)-5-[3-[4-(4-ethyl-1,3-oxazol-2-yl)-2-methoxyphenoxy]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCOC(C(=C1)OC)=CC=C1C1=NC(CC)=CO1 NZEAYHVHEKKTCH-FQEVSTJZSA-N 0.000 description 1
- CQSOZXXADFESOE-QFIPXVFZSA-N ethyl 2-[(1s)-5-[3-[[2-(3-methoxyphenoxy)-5-methylpyrimidin-4-yl]-methylamino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCN(C)C(C(=CN=1)C)=NC=1OC1=CC=CC(OC)=C1 CQSOZXXADFESOE-QFIPXVFZSA-N 0.000 description 1
- GAEZDOOLLYTODD-VWLOTQADSA-N ethyl 2-[(1s)-5-[3-[[2-(4-ethylphenyl)-5-methylpyrimidin-4-yl]-methylamino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCN(C)C(C(=CN=1)C)=NC=1C1=CC=C(CC)C=C1 GAEZDOOLLYTODD-VWLOTQADSA-N 0.000 description 1
- XBEQGWKONJTILY-NRFANRHFSA-N ethyl 2-[(1s)-5-[3-[[2-chloro-5-(4-methoxyphenyl)pyrimidin-4-yl]-methylamino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCN(C)C1=NC(Cl)=NC=C1C1=CC=C(OC)C=C1 XBEQGWKONJTILY-NRFANRHFSA-N 0.000 description 1
- GTEHAGDLOOJYML-FQEVSTJZSA-N ethyl 2-[(1s)-5-[3-[[4-(1,3-benzodioxol-5-yl)pyrimidin-2-yl]-methylamino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C1=C2OCOC2=CC(C=2C=CN=C(N=2)N(C)CCCOC=2C=C3CC[C@H](C3=CC=2)CC(=O)OCC)=C1 GTEHAGDLOOJYML-FQEVSTJZSA-N 0.000 description 1
- AAXWYPVECKZKCP-IBGZPJMESA-N ethyl 2-[(1s)-5-[3-[[4-(1,3-benzodioxol-5-yl)pyrimidin-2-yl]amino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C1=C2OCOC2=CC(C=2C=CN=C(N=2)NCCCOC=2C=C3CC[C@H](C3=CC=2)CC(=O)OCC)=C1 AAXWYPVECKZKCP-IBGZPJMESA-N 0.000 description 1
- AKRHJIIRAMOAET-QFIPXVFZSA-N ethyl 2-[(1s)-5-[3-[[5-cyano-3-fluoro-6-(4-methoxyphenyl)pyridin-2-yl]-methylamino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCN(C)C(C(=CC=1C#N)F)=NC=1C1=CC=C(OC)C=C1 AKRHJIIRAMOAET-QFIPXVFZSA-N 0.000 description 1
- GCXBLTCOKZPRLH-DEOSSOPVSA-N ethyl 2-[(1s)-5-[3-[[6-(4-ethylphenyl)-3-(trifluoromethyl)pyridin-2-yl]-methylamino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCN(C)C(C(=CC=1)C(F)(F)F)=NC=1C1=CC=C(CC)C=C1 GCXBLTCOKZPRLH-DEOSSOPVSA-N 0.000 description 1
- HLNGLJYZXKPUGS-NRFANRHFSA-N ethyl 2-[(1s)-5-[3-[[6-(4-methoxyphenyl)-5-(trifluoromethyl)pyridin-2-yl]amino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCNC(N=1)=CC=C(C(F)(F)F)C=1C1=CC=C(OC)C=C1 HLNGLJYZXKPUGS-NRFANRHFSA-N 0.000 description 1
- MIXXZCOIUYNKAT-HNNXBMFYSA-N ethyl 2-[(1s)-5-[3-[[6-chloro-5-(trifluoromethyl)pyridin-2-yl]amino]propoxy]-2,3-dihydro-1h-inden-1-yl]acetate Chemical compound C([C@H](C1=CC=2)CC(=O)OCC)CC1=CC=2OCCCNC1=CC=C(C(F)(F)F)C(Cl)=N1 MIXXZCOIUYNKAT-HNNXBMFYSA-N 0.000 description 1
- 239000002024 ethyl acetate extract Substances 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
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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
- A61P3/04—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
- A61P3/08—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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/44—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to only one six-membered aromatic ring
- C07C211/45—Monoamines
- C07C211/48—N-alkylated amines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
- C07C217/14—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring
- C07C217/24—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring being part of a condensed ring system containing rings other than six-membered aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/54—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C07C327/38—Amides of thiocarboxylic acids
- C07C327/48—Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Quinoline Compounds (AREA)
- Indole Compounds (AREA)
- Furan Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US43531002P | 2002-12-20 | 2002-12-20 | |
| US60/435,310 | 2002-12-20 | ||
| PCT/US2003/040842 WO2004058174A2 (en) | 2002-12-20 | 2003-12-19 | Indane acetic acid derivatives and their use as pharmaceutical agents, intermediates, and method of preparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2510793A1 true CA2510793A1 (en) | 2004-07-15 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002510793A Abandoned CA2510793A1 (en) | 2002-12-20 | 2003-12-19 | Indane acetic acid derivatives and their use as pharmaceutical agents, intermediates, and method of preparation |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US7714004B2 (enExample) |
| EP (1) | EP1578715B1 (enExample) |
| JP (1) | JP4974463B2 (enExample) |
| AU (1) | AU2003299790A1 (enExample) |
| CA (1) | CA2510793A1 (enExample) |
| DE (1) | DE60336264D1 (enExample) |
| WO (1) | WO2004058174A2 (enExample) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT1599468E (pt) | 2003-01-14 | 2008-01-14 | Arena Pharm Inc | Derivados de arilo e heteroarilo 1,2,3.-trissubstituídos comomoduladores do metabolismo, e profilaxia e tratamento dedesordens relacionadas tais como diabetes e hiperglicemia |
| JP2006523698A (ja) * | 2003-04-17 | 2006-10-19 | カリプシス・インコーポレーテッド | Ppar変調薬としての(3−{3−(2,4−ビス−トリフルオロメチル−ベンジル)−(5−エチル−ピリミジン−2−イル)−アミノ−プロポキシ}−フェニル)−酢酸および関連化合物、ならびに代謝性障害の処置方法 |
| WO2004106276A1 (ja) * | 2003-05-30 | 2004-12-09 | Takeda Pharmaceutical Company Limited | 縮合環化合物 |
| JP4805552B2 (ja) * | 2003-05-30 | 2011-11-02 | 武田薬品工業株式会社 | 縮合環化合物 |
| EP2287165A3 (en) | 2003-07-14 | 2011-06-22 | Arena Pharmaceuticals, Inc. | Fused-aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto |
| AU2004285530A1 (en) * | 2003-10-31 | 2005-05-12 | Janssen Pharmaceutica N.V. | Phenoxyacetic acids derivatives useful as peroxisome proliferator-activated receptor (PPAR) dual agonists |
| EP1687274A1 (en) * | 2003-11-20 | 2006-08-09 | Warner-Lambert Company LLC | Androgen receptor modulators |
| US7622491B2 (en) * | 2004-08-13 | 2009-11-24 | Metabolex Inc. | Modulators of PPAR and methods of their preparation |
| MY148521A (en) | 2005-01-10 | 2013-04-30 | Arena Pharm Inc | Substituted pyridinyl and pyrimidinyl derivatives as modulators of metabolism and the treatment of disorders related thereto |
| US20100130737A1 (en) * | 2005-02-18 | 2010-05-27 | Takeda Pharmaceutical Company Limited | Regulating Agent of GPR34 Receptor Function |
| EP1866293A1 (en) * | 2005-03-31 | 2007-12-19 | UCB Pharma, S.A. | Compounds comprising an oxazole or thiazole moiety, processes for making them, and their uses |
| US7816536B2 (en) | 2005-06-10 | 2010-10-19 | The Research Foundation Of State University Of New York | 4-substituted and 7-substituted indoles, benzofurans, benzothiophenes, benzimidazoles, benzoxazoles, and benzothiazoles and methods for making same |
| US8653115B2 (en) | 2006-06-13 | 2014-02-18 | Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences | Heterocyclic non-nucleoside compounds, their preparation, pharmaceutical composition and their use as antiviral agents |
| TW200936130A (en) * | 2008-02-26 | 2009-09-01 | Lundbeck & Co As H | Uses of indane compounds |
| EP2389368B1 (en) | 2009-01-23 | 2015-06-17 | Merck Sharp & Dohme Corp. | Bridged and fused antidiabetic compounds |
| AU2010206786A1 (en) * | 2009-01-23 | 2011-07-28 | Merck Sharp & Dohme Corp. | Bridged and fused heterocyclic antidiabetic compounds |
| TW201040186A (en) | 2009-02-05 | 2010-11-16 | Schering Corp | Phthalazine-containing antidiabetic compounds |
| WO2010141696A1 (en) * | 2009-06-04 | 2010-12-09 | Dara Biosciences, Inc. | Methods of treating or preventing psoriasis, and/or alzheimer's disease using indane acetic acid derivatives |
| JP2012188352A (ja) * | 2009-07-13 | 2012-10-04 | Dainippon Sumitomo Pharma Co Ltd | 3−(4−置換アルキル−フェニル)−2−フランカルボン酸誘導体およびその薬学的に許容される塩 |
| JP5941916B2 (ja) | 2010-09-22 | 2016-06-29 | アリーナ ファーマシューティカルズ, インコーポレイテッド | Gpr119レセプターのモジュレーターおよびそれに関連する障害の処置 |
| WO2012074980A2 (en) * | 2010-12-01 | 2012-06-07 | Dara Biosciences, Inc. | Methods of treating or preventing autoimmune disorders and liver disorders using indane acetic acid derivatives |
| PL3242666T3 (pl) | 2015-01-06 | 2025-02-17 | Arena Pharmaceuticals, Inc. | Związek do zastosowania w leczeniu dolegliwości związanych z receptorem s1p1 |
| DK3310760T3 (da) | 2015-06-22 | 2022-10-24 | Arena Pharm Inc | Krystallinsk L-argininsalt af (R)-2-(7-(4-cyclopentyl-3-(trifluormethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3- yl)eddikesyre til anvendelse ved S1P1-receptor-associerede lidelser |
| CN110520124A (zh) | 2017-02-16 | 2019-11-29 | 艾尼纳制药公司 | 用于治疗原发性胆汁性胆管炎的化合物和方法 |
| BR112020024762A2 (pt) | 2018-06-06 | 2021-03-23 | Arena Pharmaceuticals, Inc. | métodos de tratamento de condições relacionadas ao receptor s1p1 |
| BR112021013807A2 (pt) * | 2019-01-18 | 2021-11-30 | Astrazeneca Ab | Inibidores de pcsk9 e seus métodos de uso |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6197241A (ja) * | 1984-10-16 | 1986-05-15 | Yamanouchi Pharmaceut Co Ltd | 新規カルボン酸誘導体 |
| CA1314224C (en) * | 1987-07-07 | 1993-03-09 | Shinichiro Ashida | Antidiabetic agent |
| AR036237A1 (es) * | 2001-07-27 | 2004-08-25 | Bayer Corp | Derivados del acido indan acetico, intermediarios, y metodo para su preparacion, composicion farmaceutica y el uso de dichos derivados para la manufactura de un medicamento |
| UA79755C2 (en) | 2002-04-16 | 2007-07-25 | Bayer Pharmaceuticals Corp | Indane acetic acid derivatives and their use as pharmaceutical agents, intermediates, and method of preparation |
-
2003
- 2003-12-19 WO PCT/US2003/040842 patent/WO2004058174A2/en not_active Ceased
- 2003-12-19 EP EP03800063A patent/EP1578715B1/en not_active Expired - Lifetime
- 2003-12-19 CA CA002510793A patent/CA2510793A1/en not_active Abandoned
- 2003-12-19 US US10/537,630 patent/US7714004B2/en not_active Expired - Fee Related
- 2003-12-19 AU AU2003299790A patent/AU2003299790A1/en not_active Abandoned
- 2003-12-19 JP JP2004563903A patent/JP4974463B2/ja not_active Expired - Fee Related
- 2003-12-19 DE DE60336264T patent/DE60336264D1/de not_active Expired - Lifetime
-
2010
- 2010-04-13 US US12/759,328 patent/US7906653B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| AU2003299790A1 (en) | 2004-07-22 |
| US20060084680A1 (en) | 2006-04-20 |
| WO2004058174A2 (en) | 2004-07-15 |
| WO2004058174A3 (en) | 2004-12-02 |
| EP1578715A2 (en) | 2005-09-28 |
| JP2006516251A (ja) | 2006-06-29 |
| AU2003299790A8 (en) | 2004-07-22 |
| JP4974463B2 (ja) | 2012-07-11 |
| US20100204472A1 (en) | 2010-08-12 |
| US7906653B2 (en) | 2011-03-15 |
| EP1578715B1 (en) | 2011-03-02 |
| DE60336264D1 (de) | 2011-04-14 |
| US7714004B2 (en) | 2010-05-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |
Effective date: 20131219 |