CA2523245C - Indole acetic acid derivatives and their use as pharmaceutical agents - Google Patents
Indole acetic acid derivatives and their use as pharmaceutical agents Download PDFInfo
- Publication number
- CA2523245C CA2523245C CA2523245A CA2523245A CA2523245C CA 2523245 C CA2523245 C CA 2523245C CA 2523245 A CA2523245 A CA 2523245A CA 2523245 A CA2523245 A CA 2523245A CA 2523245 C CA2523245 C CA 2523245C
- Authority
- CA
- Canada
- Prior art keywords
- propoxy
- cndot
- phenoxy
- indol
- acetic acid
- 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 - Fee Related
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- 239000008177 pharmaceutical agent Substances 0.000 title claims description 10
- BOIZHGCLUSQNLD-UHFFFAOYSA-N acetic acid;1h-indole Chemical class CC(O)=O.C1=CC=C2NC=CC2=C1 BOIZHGCLUSQNLD-UHFFFAOYSA-N 0.000 title abstract description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 34
- 206010012601 diabetes mellitus Diseases 0.000 claims abstract description 34
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 29
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 24
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract description 22
- 238000011282 treatment Methods 0.000 claims abstract description 22
- 201000010099 disease Diseases 0.000 claims abstract description 17
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 15
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 12
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 12
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 8
- 125000002252 acyl group Chemical group 0.000 claims abstract description 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 199
- -1 .beta.-blocker Substances 0.000 claims description 79
- 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 40
- 125000005843 halogen group Chemical group 0.000 claims description 31
- 239000003112 inhibitor Substances 0.000 claims description 31
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 29
- 239000003814 drug Substances 0.000 claims description 29
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 25
- 229940079593 drug Drugs 0.000 claims description 22
- 229920006395 saturated elastomer Polymers 0.000 claims description 22
- 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 21
- 229910052786 argon Inorganic materials 0.000 claims description 21
- 125000002837 carbocyclic group Chemical group 0.000 claims description 21
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 20
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 20
- 125000005842 heteroatom Chemical group 0.000 claims description 18
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- 102000004877 Insulin Human genes 0.000 claims description 17
- 108090001061 Insulin Proteins 0.000 claims description 17
- 150000002148 esters Chemical class 0.000 claims description 17
- 150000003839 salts Chemical class 0.000 claims description 17
- 239000008103 glucose Substances 0.000 claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims description 16
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 14
- 239000000194 fatty acid Substances 0.000 claims description 14
- 229930195729 fatty acid Natural products 0.000 claims description 14
- 208000035475 disorder Diseases 0.000 claims description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims description 12
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 claims description 11
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 11
- 229910052717 sulfur Inorganic materials 0.000 claims description 11
- 125000002619 bicyclic group Chemical group 0.000 claims description 10
- 150000004665 fatty acids Chemical class 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 9
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 9
- 208000002705 Glucose Intolerance Diseases 0.000 claims description 9
- 102000003728 Peroxisome Proliferator-Activated Receptors Human genes 0.000 claims description 9
- 108090000029 Peroxisome Proliferator-Activated Receptors Proteins 0.000 claims description 9
- 125000002950 monocyclic group Chemical group 0.000 claims description 9
- 201000009104 prediabetes syndrome Diseases 0.000 claims description 9
- 125000004001 thioalkyl group Chemical group 0.000 claims description 9
- 206010056997 Impaired fasting glucose Diseases 0.000 claims description 8
- 239000003085 diluting agent Substances 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- 239000003446 ligand Substances 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 7
- 239000003937 drug carrier Substances 0.000 claims description 7
- 230000002440 hepatic effect Effects 0.000 claims description 7
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 7
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 6
- 239000005541 ACE inhibitor Substances 0.000 claims description 6
- 206010020772 Hypertension Diseases 0.000 claims description 6
- 229940122355 Insulin sensitizer Drugs 0.000 claims description 6
- 208000035180 MODY Diseases 0.000 claims description 6
- 229940100389 Sulfonylurea Drugs 0.000 claims description 6
- 229940044094 angiotensin-converting-enzyme inhibitor Drugs 0.000 claims description 6
- 230000003579 anti-obesity Effects 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 201000006950 maturity-onset diabetes of the young Diseases 0.000 claims description 6
- 235000001968 nicotinic acid Nutrition 0.000 claims description 6
- 239000011664 nicotinic acid Substances 0.000 claims description 6
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 6
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims description 6
- 125000006823 (C1-C6) acyl group Chemical group 0.000 claims description 5
- ILPUOPPYSQEBNJ-UHFFFAOYSA-N 2-methyl-2-phenoxypropanoic acid Chemical class OC(=O)C(C)(C)OC1=CC=CC=C1 ILPUOPPYSQEBNJ-UHFFFAOYSA-N 0.000 claims description 5
- 102000016622 Dipeptidyl Peptidase 4 Human genes 0.000 claims description 5
- 101000930822 Giardia intestinalis Dipeptidyl-peptidase 4 Proteins 0.000 claims description 5
- 229940121710 HMGCoA reductase inhibitor Drugs 0.000 claims description 5
- 229940122199 Insulin secretagogue Drugs 0.000 claims description 5
- 102000002072 Non-Receptor Type 1 Protein Tyrosine Phosphatase Human genes 0.000 claims description 5
- 108010015847 Non-Receptor Type 1 Protein Tyrosine Phosphatase Proteins 0.000 claims description 5
- 239000000556 agonist Substances 0.000 claims description 5
- 229940125753 fibrate Drugs 0.000 claims description 5
- 239000002471 hydroxymethylglutaryl coenzyme A reductase inhibitor Substances 0.000 claims description 5
- 229960003512 nicotinic acid Drugs 0.000 claims description 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 5
- 239000002464 receptor antagonist Substances 0.000 claims description 5
- 229940044551 receptor antagonist Drugs 0.000 claims description 5
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 claims description 4
- 229940123208 Biguanide Drugs 0.000 claims description 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 4
- 229940127291 Calcium channel antagonist Drugs 0.000 claims description 4
- 229910002651 NO3 Inorganic materials 0.000 claims description 4
- 102000003729 Neprilysin Human genes 0.000 claims description 4
- 108090000028 Neprilysin Proteins 0.000 claims description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 4
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims description 4
- 239000005557 antagonist Substances 0.000 claims description 4
- 239000003613 bile acid Substances 0.000 claims description 4
- 229920000080 bile acid sequestrant Polymers 0.000 claims description 4
- 239000000480 calcium channel blocker Substances 0.000 claims description 4
- 239000002934 diuretic Substances 0.000 claims description 4
- 150000002632 lipids Chemical class 0.000 claims description 4
- 230000003228 microsomal effect Effects 0.000 claims description 4
- 239000002461 renin inhibitor Substances 0.000 claims description 4
- 229940086526 renin-inhibitors Drugs 0.000 claims description 4
- 208000001145 Metabolic Syndrome Diseases 0.000 claims description 3
- 201000010390 abdominal obesity-metabolic syndrome 1 Diseases 0.000 claims description 3
- 239000002333 angiotensin II receptor antagonist Substances 0.000 claims description 3
- 208000004104 gestational diabetes Diseases 0.000 claims description 3
- 208000011661 metabolic syndrome X Diseases 0.000 claims description 3
- 108090000189 Neuropeptides Proteins 0.000 claims description 2
- 102000003797 Neuropeptides Human genes 0.000 claims description 2
- 239000002830 appetite depressant Substances 0.000 claims description 2
- 150000004283 biguanides Chemical class 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 229940097420 Diuretic Drugs 0.000 claims 3
- 239000003524 antilipemic agent Substances 0.000 claims 3
- 230000001882 diuretic effect Effects 0.000 claims 3
- 239000004026 insulin derivative Substances 0.000 claims 3
- ODNZGJDBOJGCIF-LJQANCHMSA-N (2r)-2-[5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]indol-1-yl]propanoic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=CN(C3=CC=2)[C@H](C)C(O)=O)C(CCC)=CC=1C1=NC(OCC)=C(C)S1 ODNZGJDBOJGCIF-LJQANCHMSA-N 0.000 claims 2
- NZHCHGSBOJVZMG-NRFANRHFSA-N (2s)-2-[3-methyl-5-[3-[2-propyl-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]indol-1-yl]propanoic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C(C)=CN(C3=CC=2)[C@@H](C)C(O)=O)C(CCC)=C1 NZHCHGSBOJVZMG-NRFANRHFSA-N 0.000 claims 2
- ODNZGJDBOJGCIF-IBGZPJMESA-N (2s)-2-[5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]indol-1-yl]propanoic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=CN(C3=CC=2)[C@@H](C)C(O)=O)C(CCC)=CC=1C1=NC(OCC)=C(C)S1 ODNZGJDBOJGCIF-IBGZPJMESA-N 0.000 claims 2
- 229940124681 11 beta HSD inhibitor Drugs 0.000 claims 2
- AATUKXAMWPBQCI-UHFFFAOYSA-N 2-[3-ethyl-5-[3-[2-propyl-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]indol-1-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C(CC)=CN(CC(O)=O)C3=CC=2)C(CCC)=C1 AATUKXAMWPBQCI-UHFFFAOYSA-N 0.000 claims 2
- DNOSAZIJZXQJPY-UHFFFAOYSA-N 2-[3-methyl-5-[3-[2-propyl-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C(C)=C(CC(O)=O)NC3=CC=2)C(CCC)=C1 DNOSAZIJZXQJPY-UHFFFAOYSA-N 0.000 claims 2
- HPENJUSOGRHJOD-UHFFFAOYSA-N 2-[3-methyl-5-[3-[2-propyl-4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound C1CCCC(O2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C(C)=C(C(C)C(O)=O)NC3=CC=2)C(CCC)=C1 HPENJUSOGRHJOD-UHFFFAOYSA-N 0.000 claims 2
- ZDFMZJPKRSPQKY-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C=C(CC(O)=O)NC3=CC=2)C(OC)=C1 ZDFMZJPKRSPQKY-UHFFFAOYSA-N 0.000 claims 2
- XIYFJXWZEKSXDD-UHFFFAOYSA-N 2-[5-[3-[2-propyl-4-(1,3-thiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=C(CC(O)=O)NC3=CC=2)C(CCC)=CC=1C1=NC=CS1 XIYFJXWZEKSXDD-UHFFFAOYSA-N 0.000 claims 2
- YRMNKMPRDAQXDC-UHFFFAOYSA-N 2-[5-[3-[2-propyl-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C=C(CC(O)=O)NC3=CC=2)C(CCC)=C1 YRMNKMPRDAQXDC-UHFFFAOYSA-N 0.000 claims 2
- NNCMAOPUOZJPQR-UHFFFAOYSA-N 2-[5-[3-[2-propyl-4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]indol-1-yl]acetic acid Chemical compound C1CCCC(O2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C=CN(CC(O)=O)C3=CC=2)C(CCC)=C1 NNCMAOPUOZJPQR-UHFFFAOYSA-N 0.000 claims 2
- CWQWKEHJHNRXJT-UHFFFAOYSA-N 2-[5-[3-[4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]indol-1-yl]acetic acid Chemical compound C1CCCC(O2)=C1N=C2C(C=C1)=CC=C1OCCCOC1=CC=C2N(CC(=O)O)C=CC2=C1 CWQWKEHJHNRXJT-UHFFFAOYSA-N 0.000 claims 2
- SBACZFSBEXLNAO-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=C(CC(O)=O)NC3=CC=2)C(CCC)=CC=1C1=NC(OCC)=C(C)S1 SBACZFSBEXLNAO-UHFFFAOYSA-N 0.000 claims 2
- ZQWMVCCGKMAIIC-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethyl-1,3-oxazol-2-yl)-2-propylphenoxy]propoxy]-3-methyl-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C(C)=C(CC(O)=O)NC3=CC=2)C(CCC)=CC=1C1=NC(CC)=CO1 ZQWMVCCGKMAIIC-UHFFFAOYSA-N 0.000 claims 2
- IMDOFSUZTMLYHH-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethyl-1,3-oxazol-2-yl)-2-propylphenoxy]propoxy]indol-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=CN(CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC(CC)=CO1 IMDOFSUZTMLYHH-UHFFFAOYSA-N 0.000 claims 2
- FBOPTUMPRDCVNM-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]indol-1-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=CN(CC(O)=O)C3=CC=2)C(CCC)=CC=1C1=NC(CC)=CS1 FBOPTUMPRDCVNM-UHFFFAOYSA-N 0.000 claims 2
- LCZCQUCAQSAYAG-UHFFFAOYSA-N 2-[5-[3-[4-(4-tert-butyl-1,3-oxazol-2-yl)-2-propylphenoxy]propoxy]-3-methyl-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C(C)=C(CC(O)=O)NC3=CC=2)C(CCC)=CC=1C1=NC(C(C)(C)C)=CO1 LCZCQUCAQSAYAG-UHFFFAOYSA-N 0.000 claims 2
- LKLAYFOHAOUMQE-UHFFFAOYSA-N 2-[5-[3-[4-(6,7-dihydro-5h-pyrano[2,3-d][1,3]thiazol-2-yl)-2-propylphenoxy]propoxy]indol-1-yl]acetic acid Chemical compound O1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C=CN(CC(O)=O)C3=CC=2)C(CCC)=C1 LKLAYFOHAOUMQE-UHFFFAOYSA-N 0.000 claims 2
- KOTREZXUBKZABP-UHFFFAOYSA-N 2-[5-[3-[4-[5-(dimethylcarbamoyl)-4-methyl-1,3-thiazol-2-yl]-2-propylphenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=C(CC(O)=O)NC3=CC=2)C(CCC)=CC=1C1=NC(C)=C(C(=O)N(C)C)S1 KOTREZXUBKZABP-UHFFFAOYSA-N 0.000 claims 2
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- 239000002671 adjuvant Substances 0.000 claims 2
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- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 2
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- YPPLMIJSLLUULP-AWEZNQCLSA-N (2s)-2-[5-[2-(1,6-dibromonaphthalen-2-yl)oxyethoxy]indol-1-yl]propanoic acid Chemical compound C1=C(Br)C=CC2=C(Br)C(OCCOC=3C=C4C=CN(C4=CC=3)[C@H](C(O)=O)C)=CC=C21 YPPLMIJSLLUULP-AWEZNQCLSA-N 0.000 claims 1
- PHWXBGHCPQZYHT-FQEVSTJZSA-N (2s)-2-[5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]-3-methylindol-1-yl]propanoic acid Chemical compound C=1C=C(OCCCOC=2C=C3C(C)=CN(C3=CC=2)[C@@H](C)C(O)=O)C(CCC)=CC=1C1=NC(OCC)=C(C)S1 PHWXBGHCPQZYHT-FQEVSTJZSA-N 0.000 claims 1
- URSAHEHEQDXFNL-INIZCTEOSA-N (2s)-2-[5-[3-[5-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)pyridin-2-yl]oxypropoxy]indol-1-yl]propanoic acid Chemical compound S1C(C)=C(OCC)N=C1C(C=N1)=CC=C1OCCCOC1=CC=C(N(C=C2)[C@@H](C)C(O)=O)C2=C1 URSAHEHEQDXFNL-INIZCTEOSA-N 0.000 claims 1
- OFIXDYUSKPEGEB-HNNXBMFYSA-N (2s)-2-[5-[3-[5-(4-ethyl-1,3-thiazol-2-yl)pyridin-2-yl]oxypropoxy]-1h-indol-2-yl]propanoic acid Chemical compound CCC1=CSC(C=2C=NC(OCCCOC=3C=C4C=C(NC4=CC=3)[C@H](C)C(O)=O)=CC=2)=N1 OFIXDYUSKPEGEB-HNNXBMFYSA-N 0.000 claims 1
- YJGZYIKAKURKSX-UHFFFAOYSA-N 2-[3-methyl-5-[3-[2-propyl-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C(C)=C(C(C)C(O)=O)NC3=CC=2)C(CCC)=C1 YJGZYIKAKURKSX-UHFFFAOYSA-N 0.000 claims 1
- PGQBCFCAQQADKO-UHFFFAOYSA-N 2-[3-methyl-5-[3-[4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound C1CCCC(S2)=C1N=C2C(C=C1)=CC=C1OCCCOC1=CC=C2NC(C(C(O)=O)C)=C(C)C2=C1 PGQBCFCAQQADKO-UHFFFAOYSA-N 0.000 claims 1
- AILXSUVUFWYHII-UHFFFAOYSA-N 2-[3-methyl-5-[3-[4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]indol-1-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C(C=C1)=CC=C1OCCCOC1=CC=C2N(CC(O)=O)C=C(C)C2=C1 AILXSUVUFWYHII-UHFFFAOYSA-N 0.000 claims 1
- UEHFTPSYYYQTIK-UHFFFAOYSA-N 2-[3-methyl-5-[3-[4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound C1CCCC(O2)=C1N=C2C(C=C1)=CC=C1OCCCOC1=CC=C2NC(C(C(O)=O)C)=C(C)C2=C1 UEHFTPSYYYQTIK-UHFFFAOYSA-N 0.000 claims 1
- VXXQSUTWHAEQIQ-UHFFFAOYSA-N 2-[3-methyl-5-[3-[4-[4-(trifluoromethyl)-1,3-oxazol-2-yl]phenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound C1=C2C(C)=C(C(C(O)=O)C)NC2=CC=C1OCCCOC(C=C1)=CC=C1C1=NC(C(F)(F)F)=CO1 VXXQSUTWHAEQIQ-UHFFFAOYSA-N 0.000 claims 1
- SLLMODALLXHKMU-UHFFFAOYSA-N 2-[5-[2-(1,6-dibromonaphthalen-2-yl)oxyethoxy]indol-1-yl]acetic acid Chemical compound C1=C(Br)C=CC2=C(Br)C(OCCOC=3C=C4C=CN(C4=CC=3)CC(=O)O)=CC=C21 SLLMODALLXHKMU-UHFFFAOYSA-N 0.000 claims 1
- YPPLMIJSLLUULP-UHFFFAOYSA-N 2-[5-[2-(1,6-dibromonaphthalen-2-yl)oxyethoxy]indol-1-yl]propanoic acid Chemical compound C1=C(Br)C=CC2=C(Br)C(OCCOC=3C=C4C=CN(C4=CC=3)C(C(O)=O)C)=CC=C21 YPPLMIJSLLUULP-UHFFFAOYSA-N 0.000 claims 1
- PCFHAMNJZRVJRX-UHFFFAOYSA-N 2-[5-[2-(2-chloro-4-methylphenoxy)ethoxy]indol-1-yl]propanoic acid Chemical compound C=1C=C2N(C(C(O)=O)C)C=CC2=CC=1OCCOC1=CC=C(C)C=C1Cl PCFHAMNJZRVJRX-UHFFFAOYSA-N 0.000 claims 1
- UFRQWCJIWPKCMN-UHFFFAOYSA-N 2-[5-[2-(2-cyano-4-methoxyphenoxy)ethoxy]indol-1-yl]propanoic acid Chemical compound N#CC1=CC(OC)=CC=C1OCCOC1=CC=C(N(C=C2)C(C)C(O)=O)C2=C1 UFRQWCJIWPKCMN-UHFFFAOYSA-N 0.000 claims 1
- VAZYQNYYLFKNEX-UHFFFAOYSA-N 2-[5-[2-(2-methoxy-4-methylphenoxy)ethoxy]indol-1-yl]propanoic acid Chemical compound COC1=CC(C)=CC=C1OCCOC1=CC=C(N(C=C2)C(C)C(O)=O)C2=C1 VAZYQNYYLFKNEX-UHFFFAOYSA-N 0.000 claims 1
- FFPKMVJVRGFEKY-UHFFFAOYSA-N 2-[5-[2-(4-bromo-2-chlorophenoxy)ethoxy]indol-1-yl]propanoic acid Chemical compound C=1C=C2N(C(C(O)=O)C)C=CC2=CC=1OCCOC1=CC=C(Br)C=C1Cl FFPKMVJVRGFEKY-UHFFFAOYSA-N 0.000 claims 1
- KAEIBQCEFVWOMQ-UHFFFAOYSA-N 2-[5-[2-(4-ethyl-2-methoxyphenoxy)ethoxy]indol-1-yl]propanoic acid Chemical compound COC1=CC(CC)=CC=C1OCCOC1=CC=C(N(C=C2)C(C)C(O)=O)C2=C1 KAEIBQCEFVWOMQ-UHFFFAOYSA-N 0.000 claims 1
- FPNFQGNJYCSCFK-UHFFFAOYSA-N 2-[5-[3-(2-methoxy-4-methylphenoxy)propoxy]indol-1-yl]propanoic acid Chemical compound COC1=CC(C)=CC=C1OCCCOC1=CC=C(N(C=C2)C(C)C(O)=O)C2=C1 FPNFQGNJYCSCFK-UHFFFAOYSA-N 0.000 claims 1
- BWMVLYNSNQSSOB-UHFFFAOYSA-N 2-[5-[3-(4-cyano-2-methoxyphenoxy)propoxy]-3-methylindol-1-yl]acetic acid Chemical compound COC1=CC(C#N)=CC=C1OCCCOC1=CC=C(N(CC(O)=O)C=C2C)C2=C1 BWMVLYNSNQSSOB-UHFFFAOYSA-N 0.000 claims 1
- WZGOWFVNXXRRNQ-UHFFFAOYSA-N 2-[5-[3-[(2-chloro-5-fluoropyrimidin-4-yl)methylamino]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C=1C=C2NC(CC(=O)O)=CC2=CC=1OCCCNCC1=NC(Cl)=NC=C1F WZGOWFVNXXRRNQ-UHFFFAOYSA-N 0.000 claims 1
- OKOHDNZQYAOZCV-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(1,3-thiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=C(CC(O)=O)NC3=CC=2)C(OC)=CC=1C1=NC=CS1 OKOHDNZQYAOZCV-UHFFFAOYSA-N 0.000 claims 1
- DQDVRMLOLHTFGE-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C=C(NC3=CC=2)C(C)C(O)=O)C(OC)=C1 DQDVRMLOLHTFGE-UHFFFAOYSA-N 0.000 claims 1
- DNBINYJLSKXAAH-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-3-methyl-1h-indol-2-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C(C)=C(CC(O)=O)NC3=CC=2)C(OC)=C1 DNBINYJLSKXAAH-UHFFFAOYSA-N 0.000 claims 1
- LJLHBGHCXVYRDS-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-3-methyl-1h-indol-2-yl]propanoic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C(C)=C(C(C)C(O)=O)NC3=CC=2)C(OC)=C1 LJLHBGHCXVYRDS-UHFFFAOYSA-N 0.000 claims 1
- QSZPYETXLXOAAZ-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]-3-methyl-1h-indol-2-yl]propanoic acid Chemical compound C1CCCC(O2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C(C)=C(C(C)C(O)=O)NC3=CC=2)C(OC)=C1 QSZPYETXLXOAAZ-UHFFFAOYSA-N 0.000 claims 1
- SWBAMIAUTFUWBP-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]indol-1-yl]acetic acid Chemical compound C1CCCC(O2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C=CN(CC(O)=O)C3=CC=2)C(OC)=C1 SWBAMIAUTFUWBP-UHFFFAOYSA-N 0.000 claims 1
- SILRVUXIKXQRLY-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]indol-1-yl]propanoic acid Chemical compound C1CCCC(O2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C=CN(C3=CC=2)C(C)C(O)=O)C(OC)=C1 SILRVUXIKXQRLY-UHFFFAOYSA-N 0.000 claims 1
- PWIPJLAZPPLQLD-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4-propan-2-yloxy-1,3-thiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=C(CC(O)=O)NC3=CC=2)C(OC)=CC=1C1=NC(OC(C)C)=CS1 PWIPJLAZPPLQLD-UHFFFAOYSA-N 0.000 claims 1
- WQDUPFBHFAAWET-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4-propan-2-yloxy-1,3-thiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=C(NC3=CC=2)C(C)C(O)=O)C(OC)=CC=1C1=NC(OC(C)C)=CS1 WQDUPFBHFAAWET-UHFFFAOYSA-N 0.000 claims 1
- GOIGQDQZPCOKBM-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4-propan-2-yloxy-1,3-thiazol-2-yl)phenoxy]propoxy]-3-methyl-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C(C)=C(CC(O)=O)NC3=CC=2)C(OC)=CC=1C1=NC(OC(C)C)=CS1 GOIGQDQZPCOKBM-UHFFFAOYSA-N 0.000 claims 1
- HHTZRBVLBKDVPO-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-(4-propan-2-yloxy-1,3-thiazol-2-yl)phenoxy]propoxy]-3-methyl-1h-indol-2-yl]propanoic acid Chemical compound C=1C=C(OCCCOC=2C=C3C(C)=C(C(C)C(O)=O)NC3=CC=2)C(OC)=CC=1C1=NC(OC(C)C)=CS1 HHTZRBVLBKDVPO-UHFFFAOYSA-N 0.000 claims 1
- BKHVOWMAHOJHBA-UHFFFAOYSA-N 2-[5-[3-[2-methoxy-4-[4-(trifluoromethyl)-1,3-oxazol-2-yl]phenoxy]propoxy]-3-methyl-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C(C)=C(CC(O)=O)NC3=CC=2)C(OC)=CC=1C1=NC(C(F)(F)F)=CO1 BKHVOWMAHOJHBA-UHFFFAOYSA-N 0.000 claims 1
- XIFRKQFBYGLXEZ-UHFFFAOYSA-N 2-[5-[3-[2-propyl-4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C=C(NC3=CC=2)C(C)C(O)=O)C(CCC)=C1 XIFRKQFBYGLXEZ-UHFFFAOYSA-N 0.000 claims 1
- KDVSSIISVPCOPA-UHFFFAOYSA-N 2-[5-[3-[2-propyl-4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound C1CCCC(O2)=C1N=C2C1=CC=C(OCCCOC=2C=C3C=C(NC3=CC=2)C(C)C(O)=O)C(CCC)=C1 KDVSSIISVPCOPA-UHFFFAOYSA-N 0.000 claims 1
- KOQDJIBDTMHMBI-UHFFFAOYSA-N 2-[5-[3-[3-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]indol-1-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C1=CC(OCCCOC=2C=C3C=CN(C3=CC=2)CC(=O)O)=CC=C1 KOQDJIBDTMHMBI-UHFFFAOYSA-N 0.000 claims 1
- RTEYHAXXIZGOEX-UHFFFAOYSA-N 2-[5-[3-[3-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]indol-1-yl]acetic acid Chemical compound C1CCCC(O2)=C1N=C2C1=CC(OCCCOC=2C=C3C=CN(C3=CC=2)CC(=O)O)=CC=C1 RTEYHAXXIZGOEX-UHFFFAOYSA-N 0.000 claims 1
- DYYNPNQBMHHUMT-UHFFFAOYSA-N 2-[5-[3-[3-(4-ethyl-1,3-oxazol-2-yl)phenoxy]propoxy]indol-1-yl]acetic acid Chemical compound CCC1=COC(C=2C=C(OCCCOC=3C=C4C=CN(CC(O)=O)C4=CC=3)C=CC=2)=N1 DYYNPNQBMHHUMT-UHFFFAOYSA-N 0.000 claims 1
- RXGJBXAYZLNSHX-UHFFFAOYSA-N 2-[5-[3-[3-[5-hydroxy-4-(trifluoromethyl)-4,5-dihydro-1,3-oxazol-2-yl]phenoxy]propoxy]indol-1-yl]acetic acid Chemical compound FC(F)(F)C1C(O)OC(C=2C=C(OCCCOC=3C=C4C=CN(CC(O)=O)C4=CC=3)C=CC=2)=N1 RXGJBXAYZLNSHX-UHFFFAOYSA-N 0.000 claims 1
- FVSRYXIRHGVJII-UHFFFAOYSA-N 2-[5-[3-[4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C1CCCC(S2)=C1N=C2C(C=C1)=CC=C1OCCCOC1=CC=C(NC(CC(=O)O)=C2)C2=C1 FVSRYXIRHGVJII-UHFFFAOYSA-N 0.000 claims 1
- ZHLAZEYLKZOMAG-UHFFFAOYSA-N 2-[5-[3-[4-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)phenoxy]propoxy]indol-1-yl]propanoic acid Chemical compound C1CCCC(S2)=C1N=C2C(C=C1)=CC=C1OCCCOC1=CC=C2N(C(C(O)=O)C)C=CC2=C1 ZHLAZEYLKZOMAG-UHFFFAOYSA-N 0.000 claims 1
- MWSBOCHSQMWYSW-UHFFFAOYSA-N 2-[5-[3-[4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)phenoxy]propoxy]indol-1-yl]propanoic acid Chemical compound C1CCCC(O2)=C1N=C2C(C=C1)=CC=C1OCCCOC1=CC=C2N(C(C(O)=O)C)C=CC2=C1 MWSBOCHSQMWYSW-UHFFFAOYSA-N 0.000 claims 1
- NAJMKBLJANHEDO-UHFFFAOYSA-N 2-[5-[3-[4-(4,5-dimethyl-1,3-thiazol-2-yl)-2-methoxyphenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=C(CC(O)=O)NC3=CC=2)C(OC)=CC=1C1=NC(C)=C(C)S1 NAJMKBLJANHEDO-UHFFFAOYSA-N 0.000 claims 1
- JKFUMYIFHLKJFO-UHFFFAOYSA-N 2-[5-[3-[4-(4,5-dimethyl-1,3-thiazol-2-yl)-2-methoxyphenoxy]propoxy]-3-methyl-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C(C)=C(CC(O)=O)NC3=CC=2)C(OC)=CC=1C1=NC(C)=C(C)S1 JKFUMYIFHLKJFO-UHFFFAOYSA-N 0.000 claims 1
- QZFSJDZOVYYABF-UHFFFAOYSA-N 2-[5-[3-[4-(4,5-dimethyl-1,3-thiazol-2-yl)-2-methoxyphenoxy]propoxy]-3-methyl-1h-indol-2-yl]propanoic acid Chemical compound C=1C=C(OCCCOC=2C=C3C(C)=C(C(C)C(O)=O)NC3=CC=2)C(OC)=CC=1C1=NC(C)=C(C)S1 QZFSJDZOVYYABF-UHFFFAOYSA-N 0.000 claims 1
- OVQWEUPUEHRADA-UHFFFAOYSA-N 2-[5-[3-[4-(4,5-dimethyl-1,3-thiazol-2-yl)phenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound S1C(C)=C(C)N=C1C(C=C1)=CC=C1OCCCOC1=CC=C(NC(CC(O)=O)=C2)C2=C1 OVQWEUPUEHRADA-UHFFFAOYSA-N 0.000 claims 1
- PPVMBJPBMLUWOK-UHFFFAOYSA-N 2-[5-[3-[4-(4,5-dimethyl-1,3-thiazol-2-yl)phenoxy]propoxy]-3-methyl-1h-indol-2-yl]acetic acid Chemical compound S1C(C)=C(C)N=C1C(C=C1)=CC=C1OCCCOC1=CC=C(NC(CC(O)=O)=C2C)C2=C1 PPVMBJPBMLUWOK-UHFFFAOYSA-N 0.000 claims 1
- NWSWKRSRNXBBAU-UHFFFAOYSA-N 2-[5-[3-[4-(4,5-dimethyl-1,3-thiazol-2-yl)phenoxy]propoxy]-3-methyl-1h-indol-2-yl]propanoic acid Chemical compound C1=C2C(C)=C(C(C(O)=O)C)NC2=CC=C1OCCCOC(C=C1)=CC=C1C1=NC(C)=C(C)S1 NWSWKRSRNXBBAU-UHFFFAOYSA-N 0.000 claims 1
- AYIUCJYGOFUDAW-UHFFFAOYSA-N 2-[5-[3-[4-(4,5-dimethyl-1,3-thiazol-2-yl)phenoxy]propoxy]indol-1-yl]propanoic acid Chemical compound C=1C=C2N(C(C(O)=O)C)C=CC2=CC=1OCCCOC(C=C1)=CC=C1C1=NC(C)=C(C)S1 AYIUCJYGOFUDAW-UHFFFAOYSA-N 0.000 claims 1
- LDWOXKRBMLMTKC-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-methoxyphenoxy]propoxy]-1h-indol-2-yl]acetic acid Chemical compound S1C(C)=C(OCC)N=C1C(C=C1OC)=CC=C1OCCCOC1=CC=C(NC(CC(O)=O)=C2)C2=C1 LDWOXKRBMLMTKC-UHFFFAOYSA-N 0.000 claims 1
- MWNKSMSKOCCMLZ-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-methoxyphenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound S1C(C)=C(OCC)N=C1C(C=C1OC)=CC=C1OCCCOC1=CC=C(NC(=C2)C(C)C(O)=O)C2=C1 MWNKSMSKOCCMLZ-UHFFFAOYSA-N 0.000 claims 1
- BEDPRHZBSAORIV-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-methoxyphenoxy]propoxy]-3-methyl-1h-indol-2-yl]propanoic acid Chemical compound S1C(C)=C(OCC)N=C1C(C=C1OC)=CC=C1OCCCOC1=CC=C(NC(C(C)C(O)=O)=C2C)C2=C1 BEDPRHZBSAORIV-UHFFFAOYSA-N 0.000 claims 1
- MJOIEFBCNWLCNK-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound C=1C=C(OCCCOC=2C=C3C=C(NC3=CC=2)C(C)C(O)=O)C(CCC)=CC=1C1=NC(OCC)=C(C)S1 MJOIEFBCNWLCNK-UHFFFAOYSA-N 0.000 claims 1
- CMPRWFRWRAQFGI-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]-3-methyl-1h-indol-2-yl]acetic acid Chemical compound C=1C=C(OCCCOC=2C=C3C(C)=C(CC(O)=O)NC3=CC=2)C(CCC)=CC=1C1=NC(OCC)=C(C)S1 CMPRWFRWRAQFGI-UHFFFAOYSA-N 0.000 claims 1
- DPFSSBSOJZYPGF-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethoxy-5-methyl-1,3-thiazol-2-yl)-2-propylphenoxy]propoxy]-3-methyl-1h-indol-2-yl]propanoic acid Chemical compound C=1C=C(OCCCOC=2C=C3C(C)=C(C(C)C(O)=O)NC3=CC=2)C(CCC)=CC=1C1=NC(OCC)=C(C)S1 DPFSSBSOJZYPGF-UHFFFAOYSA-N 0.000 claims 1
- FBIFZHWJADOOCW-UHFFFAOYSA-N 2-[5-[3-[4-(4-ethyl-1,3-oxazol-2-yl)-2-methoxyphenoxy]propoxy]-1h-indol-2-yl]propanoic acid Chemical compound CCC1=COC(C=2C=C(OC)C(OCCCOC=3C=C4C=C(NC4=CC=3)C(C)C(O)=O)=CC=2)=N1 FBIFZHWJADOOCW-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- 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
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- A—HUMAN NECESSITIES
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- 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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- A—HUMAN NECESSITIES
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- 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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
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- 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
- C07D417/14—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Indole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US46614303P | 2003-04-28 | 2003-04-28 | |
| US60/466,143 | 2003-04-28 | ||
| PCT/US2004/012959 WO2004098498A2 (en) | 2003-04-28 | 2004-04-28 | Indole acetic acid derivatives and their use as pharmaceutical agents |
Publications (2)
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| CA2523245A1 CA2523245A1 (en) | 2004-11-18 |
| CA2523245C true CA2523245C (en) | 2012-03-06 |
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| Application Number | Title | Priority Date | Filing Date |
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| CA2523245A Expired - Fee Related CA2523245C (en) | 2003-04-28 | 2004-04-28 | Indole acetic acid derivatives and their use as pharmaceutical agents |
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| Country | Link |
|---|---|
| US (2) | US7592361B2 (https=) |
| EP (1) | EP1620088A4 (https=) |
| JP (2) | JP4828414B2 (https=) |
| CA (1) | CA2523245C (https=) |
| WO (1) | WO2004098498A2 (https=) |
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| EP1630152A4 (en) * | 2003-05-30 | 2009-09-23 | Takeda Pharmaceutical | CONDENSED CYCLIC COMPOUND |
| JP4805552B2 (ja) * | 2003-05-30 | 2011-11-02 | 武田薬品工業株式会社 | 縮合環化合物 |
| JP4641942B2 (ja) | 2003-10-03 | 2011-03-02 | フェーイレン・ナムローゼ・フェンノートシャップ | ヒトおよび動物におけるigf−1血清レベルの低下と関連した種々の疾患状態の治療用の治療用組成物の製造のための血清中igf−1レベルを増加できる化合物の使用 |
| US7622491B2 (en) * | 2004-08-13 | 2009-11-24 | Metabolex Inc. | Modulators of PPAR and methods of their preparation |
| CA2602336A1 (en) | 2005-03-31 | 2006-10-05 | Ucb Pharma S.A. | Compounds comprising an oxazole or thiazole moiety, processes for making them, and their uses |
| EP2759533B1 (en) | 2011-09-22 | 2017-08-02 | Takeda Pharmaceutical Company Limited | Condensed heterocyclic compound |
| KR101808196B1 (ko) * | 2016-01-08 | 2017-12-14 | 대한민국(농촌진흥청장) | 왕지네 유래 신규 화합물 및 이의 항혈전 용도 |
| CN106702003B (zh) * | 2017-02-28 | 2021-02-12 | 固安博健生物技术有限公司 | Hsdl1在诊治骨肉瘤中的应用 |
| CN117326903B (zh) * | 2023-09-27 | 2025-05-02 | 常州大学 | 一种高立体选择性合成n-烷基化吲哚衍生物的方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| WO1996014843A2 (en) * | 1994-11-10 | 1996-05-23 | Cor Therapeutics, Inc. | Pharmaceutical pyrazole compositions useful as inhibitors of protein kinases |
| CA2383983C (en) * | 1998-03-31 | 2009-09-29 | The Institutes For Pharmaceutical Discovery, Llc | Substituted indolealkanoic acids |
| GB9820113D0 (en) * | 1998-09-15 | 1998-11-11 | Merck Sharp & Dohme | Therapeutic agents |
| TNSN99224A1 (fr) * | 1998-12-01 | 2005-11-10 | Inst For Pharm Discovery Inc | Methodes de reduction des niveaux de glucose et triglyceride en serum et pour suppression de l'antigenese utilisant les acides la indolealkanoique |
| DE10006139A1 (de) * | 2000-02-11 | 2001-08-16 | Merck Patent Gmbh | Indol-3-yl-Derivate |
| MXPA03000488A (es) * | 2000-07-19 | 2003-06-24 | Procter & Gamble | Composiciones para el lavado automatico de trastes en forma de gel, metodos de preparacion y uso de las mismas. |
| US20020072518A1 (en) * | 2000-08-29 | 2002-06-13 | Khanna Ish Kumar | Bicyclic alphavbeta3 antagonists |
| NZ539682A (en) * | 2001-01-29 | 2006-03-31 | Dimensional Pharm Inc | Substituted indoles and their use as integrin antagonists |
| HRP20040164A2 (en) * | 2001-08-29 | 2004-10-31 | Warner Lambert Co | Oral antidiabetic agents |
| US20070208026A1 (en) * | 2003-04-07 | 2007-09-06 | Liu Kevin | N-Containing Heteroaromatic Compounds As Modulators Of Ppars And Methods Of Treating Metabolic Disorders |
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2004
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- 2004-04-28 CA CA2523245A patent/CA2523245C/en not_active Expired - Fee Related
- 2004-04-28 JP JP2006513366A patent/JP4828414B2/ja not_active Expired - Fee Related
- 2004-04-28 WO PCT/US2004/012959 patent/WO2004098498A2/en not_active Ceased
- 2004-04-28 EP EP04750750A patent/EP1620088A4/en not_active Withdrawn
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2009
- 2009-07-23 US US12/508,314 patent/US7964622B2/en not_active Expired - Fee Related
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2010
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Also Published As
| Publication number | Publication date |
|---|---|
| JP2006524709A (ja) | 2006-11-02 |
| JP2011063613A (ja) | 2011-03-31 |
| CA2523245A1 (en) | 2004-11-18 |
| US7592361B2 (en) | 2009-09-22 |
| WO2004098498A3 (en) | 2005-07-28 |
| EP1620088A2 (en) | 2006-02-01 |
| US20090298854A1 (en) | 2009-12-03 |
| WO2004098498A2 (en) | 2004-11-18 |
| EP1620088A4 (en) | 2007-08-29 |
| US20060264486A1 (en) | 2006-11-23 |
| US7964622B2 (en) | 2011-06-21 |
| JP4828414B2 (ja) | 2011-11-30 |
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