JP2009507846A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2009507846A5 JP2009507846A5 JP2008530176A JP2008530176A JP2009507846A5 JP 2009507846 A5 JP2009507846 A5 JP 2009507846A5 JP 2008530176 A JP2008530176 A JP 2008530176A JP 2008530176 A JP2008530176 A JP 2008530176A JP 2009507846 A5 JP2009507846 A5 JP 2009507846A5
- Authority
- JP
- Japan
- Prior art keywords
- fluoro
- substituted
- group
- optionally
- cycloalkyl
- 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.)
- Pending
Links
- 125000000217 alkyl group Chemical group 0.000 claims 267
- 125000001424 substituent group Chemical group 0.000 claims 204
- 125000003545 alkoxy group Chemical group 0.000 claims 193
- 125000004414 alkyl thio group Chemical group 0.000 claims 185
- 125000003342 alkenyl group Chemical group 0.000 claims 156
- 125000001153 fluoro group Chemical group F* 0.000 claims 155
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 122
- 125000000304 alkynyl group Chemical group 0.000 claims 121
- 125000000753 cycloalkyl group Chemical group 0.000 claims 120
- 125000003118 aryl group Chemical group 0.000 claims 119
- 125000001072 heteroaryl group Chemical group 0.000 claims 101
- 229910052799 carbon Inorganic materials 0.000 claims 100
- 229910052736 halogen Inorganic materials 0.000 claims 72
- 150000002367 halogens Chemical class 0.000 claims 72
- 150000001875 compounds Chemical class 0.000 claims 71
- 229910052739 hydrogen Inorganic materials 0.000 claims 70
- 239000001257 hydrogen Substances 0.000 claims 70
- 125000006578 monocyclic heterocycloalkyl group Chemical group 0.000 claims 59
- 150000002431 hydrogen Chemical class 0.000 claims 51
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 47
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 47
- -1 alkynyl carbon Chemical compound 0.000 claims 30
- 229910052717 sulfur Inorganic materials 0.000 claims 29
- 150000001336 alkenes Chemical class 0.000 claims 22
- 150000001345 alkine derivatives Chemical class 0.000 claims 22
- 229910052757 nitrogen Inorganic materials 0.000 claims 21
- 229910052760 oxygen Inorganic materials 0.000 claims 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 18
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 17
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 13
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 13
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 6
- 201000010099 disease Diseases 0.000 claims 5
- 125000005843 halogen group Chemical group 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 5
- 239000000126 substance Substances 0.000 claims 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 4
- 125000000732 arylene group Chemical group 0.000 claims 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 3
- 125000005549 heteroarylene group Chemical group 0.000 claims 3
- 239000000651 prodrug Substances 0.000 claims 3
- 229940002612 prodrug Drugs 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 201000004624 Dermatitis Diseases 0.000 claims 2
- 206010019280 Heart failures Diseases 0.000 claims 2
- 102000003728 Peroxisome Proliferator-Activated Receptors Human genes 0.000 claims 2
- 108090000029 Peroxisome Proliferator-Activated Receptors Proteins 0.000 claims 2
- 125000003107 substituted aryl group Chemical group 0.000 claims 2
- 208000011580 syndromic disease Diseases 0.000 claims 2
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 2
- IHJHHCVJCWPZSS-UHFFFAOYSA-N 2-[3-(2-methoxyethoxy)-5-[4-[4-(trifluoromethoxy)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound COCCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(OC(F)(F)F)=CC=3)=CC=2)=C1 IHJHHCVJCWPZSS-UHFFFAOYSA-N 0.000 claims 1
- CEKHZFHIHJERHQ-UHFFFAOYSA-N 2-[3-(2-methoxyethoxy)-5-[4-[4-(trifluoromethyl)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound COCCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(=CC=3)C(F)(F)F)=CC=2)=C1 CEKHZFHIHJERHQ-UHFFFAOYSA-N 0.000 claims 1
- GQDMBZOZBCUGQK-UHFFFAOYSA-N 2-[3-butoxy-5-(3-methoxyphenyl)sulfonylphenyl]acetic acid Chemical compound CCCCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=C(OC)C=CC=2)=C1 GQDMBZOZBCUGQK-UHFFFAOYSA-N 0.000 claims 1
- WTELPLYTCOFJFY-UHFFFAOYSA-N 2-[3-butoxy-5-(4-methoxyphenyl)sulfonylphenyl]acetic acid Chemical compound CCCCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC)=CC=2)=C1 WTELPLYTCOFJFY-UHFFFAOYSA-N 0.000 claims 1
- MRSHRGKNKISYBA-UHFFFAOYSA-N 2-[3-butoxy-5-[4-(trifluoromethoxy)phenyl]sulfonylphenyl]acetic acid Chemical compound CCCCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC(F)(F)F)=CC=2)=C1 MRSHRGKNKISYBA-UHFFFAOYSA-N 0.000 claims 1
- IJOLUFWMGKWNPI-UHFFFAOYSA-N 2-[3-butoxy-5-[4-(trifluoromethyl)phenyl]sulfonylphenyl]acetic acid Chemical compound CCCCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(=CC=2)C(F)(F)F)=C1 IJOLUFWMGKWNPI-UHFFFAOYSA-N 0.000 claims 1
- BQAWBJUQGUXEQK-UHFFFAOYSA-N 2-[3-butoxy-5-[4-[4-(trifluoromethoxy)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound CCCCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(OC(F)(F)F)=CC=3)=CC=2)=C1 BQAWBJUQGUXEQK-UHFFFAOYSA-N 0.000 claims 1
- HWWVMIYSYZMXEK-UHFFFAOYSA-N 2-[3-butoxy-5-[4-[4-(trifluoromethyl)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound CCCCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(=CC=3)C(F)(F)F)=CC=2)=C1 HWWVMIYSYZMXEK-UHFFFAOYSA-N 0.000 claims 1
- GFTGSSOVYIDTQX-UHFFFAOYSA-N 2-[3-ethoxy-5-[3-[4-(trifluoromethoxy)phenyl]phenyl]sulfonylphenyl]acetic acid Chemical compound CCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=C(C=CC=2)C=2C=CC(OC(F)(F)F)=CC=2)=C1 GFTGSSOVYIDTQX-UHFFFAOYSA-N 0.000 claims 1
- JKCQLPOSPFIXDP-UHFFFAOYSA-N 2-[3-ethoxy-5-[3-[4-(trifluoromethyl)phenyl]phenyl]sulfonylphenyl]acetic acid Chemical compound CCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=C(C=CC=2)C=2C=CC(=CC=2)C(F)(F)F)=C1 JKCQLPOSPFIXDP-UHFFFAOYSA-N 0.000 claims 1
- ZRFIFPKHFSIRSB-UHFFFAOYSA-N 2-[3-ethoxy-5-[4-[4-(trifluoromethoxy)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound CCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(OC(F)(F)F)=CC=3)=CC=2)=C1 ZRFIFPKHFSIRSB-UHFFFAOYSA-N 0.000 claims 1
- XOJKBKULRZPPPY-UHFFFAOYSA-N 2-[3-ethoxy-5-[4-[4-(trifluoromethyl)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound CCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(=CC=3)C(F)(F)F)=CC=2)=C1 XOJKBKULRZPPPY-UHFFFAOYSA-N 0.000 claims 1
- BAARUDNIARHAJS-UHFFFAOYSA-N 2-[3-methoxy-5-[4-[4-(trifluoromethoxy)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound COC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(OC(F)(F)F)=CC=3)=CC=2)=C1 BAARUDNIARHAJS-UHFFFAOYSA-N 0.000 claims 1
- HMQOFLFXBQSSIO-UHFFFAOYSA-N 2-[3-methoxy-5-[4-[4-(trifluoromethyl)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound COC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(=CC=3)C(F)(F)F)=CC=2)=C1 HMQOFLFXBQSSIO-UHFFFAOYSA-N 0.000 claims 1
- FUSQDOIFQZHNPK-UHFFFAOYSA-N 2-[3-phenylmethoxy-5-[4-[4-(trifluoromethyl)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound C=1C(S(=O)(=O)C=2C=CC(OC=3C=CC(=CC=3)C(F)(F)F)=CC=2)=CC(CC(=O)O)=CC=1OCC1=CC=CC=C1 FUSQDOIFQZHNPK-UHFFFAOYSA-N 0.000 claims 1
- YDUHFCTYFILBMK-UHFFFAOYSA-N 2-[3-propoxy-5-[3-[4-(trifluoromethyl)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound CCCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=C(OC=3C=CC(=CC=3)C(F)(F)F)C=CC=2)=C1 YDUHFCTYFILBMK-UHFFFAOYSA-N 0.000 claims 1
- ASJOVILUAIGECY-UHFFFAOYSA-N 2-[3-propoxy-5-[4-[4-(trifluoromethoxy)phenoxy]phenyl]sulfonylphenyl]acetic acid Chemical compound CCCOC1=CC(CC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(OC(F)(F)F)=CC=3)=CC=2)=C1 ASJOVILUAIGECY-UHFFFAOYSA-N 0.000 claims 1
- WHGZCAWAMSJCBT-UHFFFAOYSA-N 3-[3-ethoxy-5-[4-[4-(trifluoromethyl)phenoxy]phenyl]sulfonylphenyl]propanoic acid Chemical compound CCOC1=CC(CCC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(=CC=3)C(F)(F)F)=CC=2)=C1 WHGZCAWAMSJCBT-UHFFFAOYSA-N 0.000 claims 1
- AFSOYHDWYCTBQG-UHFFFAOYSA-N 3-[3-propoxy-5-[4-[4-(trifluoromethyl)phenoxy]phenyl]sulfonylphenyl]propanoic acid Chemical compound CCCOC1=CC(CCC(O)=O)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(=CC=3)C(F)(F)F)=CC=2)=C1 AFSOYHDWYCTBQG-UHFFFAOYSA-N 0.000 claims 1
- TVEXGJYMHHTVKP-UHFFFAOYSA-N 6-oxabicyclo[3.2.1]oct-3-en-7-one Chemical compound C1C2C(=O)OC1C=CC2 TVEXGJYMHHTVKP-UHFFFAOYSA-N 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 208000000103 Anorexia Nervosa Diseases 0.000 claims 1
- 206010003210 Arteriosclerosis Diseases 0.000 claims 1
- 201000001320 Atherosclerosis Diseases 0.000 claims 1
- 208000023328 Basedow disease Diseases 0.000 claims 1
- 208000032841 Bulimia Diseases 0.000 claims 1
- 206010006550 Bulimia nervosa Diseases 0.000 claims 1
- 206010007559 Cardiac failure congestive Diseases 0.000 claims 1
- 206010007749 Cataract diabetic Diseases 0.000 claims 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 1
- 208000026372 Congenital cystic kidney disease Diseases 0.000 claims 1
- 208000011231 Crohn disease Diseases 0.000 claims 1
- 208000026292 Cystic Kidney disease Diseases 0.000 claims 1
- 208000002249 Diabetes Complications Diseases 0.000 claims 1
- 206010012655 Diabetic complications Diseases 0.000 claims 1
- 208000008960 Diabetic foot Diseases 0.000 claims 1
- 208000032928 Dyslipidaemia Diseases 0.000 claims 1
- 208000010228 Erectile Dysfunction Diseases 0.000 claims 1
- 208000002705 Glucose Intolerance Diseases 0.000 claims 1
- 208000015023 Graves' disease Diseases 0.000 claims 1
- 208000031886 HIV Infections Diseases 0.000 claims 1
- 208000037357 HIV infectious disease Diseases 0.000 claims 1
- 208000001204 Hashimoto Disease Diseases 0.000 claims 1
- 208000030836 Hashimoto thyroiditis Diseases 0.000 claims 1
- 206010019375 Helicobacter infections Diseases 0.000 claims 1
- 208000035150 Hypercholesterolemia Diseases 0.000 claims 1
- 206010060378 Hyperinsulinaemia Diseases 0.000 claims 1
- 208000031226 Hyperlipidaemia Diseases 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- 206010061218 Inflammation Diseases 0.000 claims 1
- 206010065390 Inflammatory pain Diseases 0.000 claims 1
- 206010022489 Insulin Resistance Diseases 0.000 claims 1
- 208000017170 Lipid metabolism disease Diseases 0.000 claims 1
- 208000001145 Metabolic Syndrome Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 208000000693 Neurogenic Urinary Bladder Diseases 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- 206010061876 Obstruction Diseases 0.000 claims 1
- 206010033307 Overweight Diseases 0.000 claims 1
- 206010033645 Pancreatitis Diseases 0.000 claims 1
- 208000018737 Parkinson disease Diseases 0.000 claims 1
- 208000034038 Pathologic Neovascularization Diseases 0.000 claims 1
- 241000721454 Pemphigus Species 0.000 claims 1
- 208000018262 Peripheral vascular disease Diseases 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- 201000004681 Psoriasis Diseases 0.000 claims 1
- 208000001647 Renal Insufficiency Diseases 0.000 claims 1
- 208000017442 Retinal disease Diseases 0.000 claims 1
- 206010038923 Retinopathy Diseases 0.000 claims 1
- 206010039710 Scleroderma Diseases 0.000 claims 1
- 208000021386 Sjogren Syndrome Diseases 0.000 claims 1
- 208000006011 Stroke Diseases 0.000 claims 1
- 208000007536 Thrombosis Diseases 0.000 claims 1
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims 1
- 206010046543 Urinary incontinence Diseases 0.000 claims 1
- 206010046851 Uveitis Diseases 0.000 claims 1
- 206010047642 Vitiligo Diseases 0.000 claims 1
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims 1
- 208000002552 acute disseminated encephalomyelitis Diseases 0.000 claims 1
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims 1
- 208000011775 arteriosclerosis disease Diseases 0.000 claims 1
- 208000006673 asthma Diseases 0.000 claims 1
- 208000010668 atopic eczema Diseases 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 208000026106 cerebrovascular disease Diseases 0.000 claims 1
- 230000001684 chronic effect Effects 0.000 claims 1
- 208000029078 coronary artery disease Diseases 0.000 claims 1
- 201000001981 dermatomyositis Diseases 0.000 claims 1
- 201000007025 diabetic cataract Diseases 0.000 claims 1
- 208000035475 disorder Diseases 0.000 claims 1
- 208000006454 hepatitis Diseases 0.000 claims 1
- 231100000283 hepatitis Toxicity 0.000 claims 1
- 208000033519 human immunodeficiency virus infectious disease Diseases 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 230000003451 hyperinsulinaemic effect Effects 0.000 claims 1
- 201000008980 hyperinsulinism Diseases 0.000 claims 1
- 208000006575 hypertriglyceridemia Diseases 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 201000001881 impotence Diseases 0.000 claims 1
- 201000008319 inclusion body myositis Diseases 0.000 claims 1
- 208000015181 infectious disease Diseases 0.000 claims 1
- 208000000509 infertility Diseases 0.000 claims 1
- 230000036512 infertility Effects 0.000 claims 1
- 231100000535 infertility Toxicity 0.000 claims 1
- 230000002757 inflammatory effect Effects 0.000 claims 1
- 230000004054 inflammatory process Effects 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 208000017169 kidney disease Diseases 0.000 claims 1
- 201000006370 kidney failure Diseases 0.000 claims 1
- 210000002429 large intestine Anatomy 0.000 claims 1
- 208000002780 macular degeneration Diseases 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- VEKBGZJJJKZNBI-UHFFFAOYSA-N methyl 2-[3-ethoxy-5-[4-[4-(trifluoromethoxy)phenoxy]phenyl]sulfonylphenyl]acetate Chemical compound CCOC1=CC(CC(=O)OC)=CC(S(=O)(=O)C=2C=CC(OC=3C=CC(OC(F)(F)F)=CC=3)=CC=2)=C1 VEKBGZJJJKZNBI-UHFFFAOYSA-N 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- 201000006417 multiple sclerosis Diseases 0.000 claims 1
- 208000010125 myocardial infarction Diseases 0.000 claims 1
- 201000008383 nephritis Diseases 0.000 claims 1
- 208000004296 neuralgia Diseases 0.000 claims 1
- 230000002981 neuropathic effect Effects 0.000 claims 1
- 208000021722 neuropathic pain Diseases 0.000 claims 1
- 201000001119 neuropathy Diseases 0.000 claims 1
- 230000007823 neuropathy Effects 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- 125000002971 oxazolyl group Chemical group 0.000 claims 1
- 208000033808 peripheral neuropathy Diseases 0.000 claims 1
- 201000010065 polycystic ovary syndrome Diseases 0.000 claims 1
- 208000005987 polymyositis Diseases 0.000 claims 1
- 201000009104 prediabetes syndrome Diseases 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 1
- 210000000813 small intestine Anatomy 0.000 claims 1
- 208000020431 spinal cord injury Diseases 0.000 claims 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 1
- 201000000596 systemic lupus erythematosus Diseases 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 230000029663 wound healing Effects 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71521405P | 2005-09-07 | 2005-09-07 | |
| US78938706P | 2006-04-05 | 2006-04-05 | |
| PCT/US2006/034764 WO2007030567A2 (en) | 2005-09-07 | 2006-09-06 | Pparactive compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009507846A JP2009507846A (ja) | 2009-02-26 |
| JP2009507846A5 true JP2009507846A5 (enExample) | 2009-11-05 |
Family
ID=37831846
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008530176A Pending JP2009507846A (ja) | 2005-09-07 | 2006-09-06 | Ppar活性化合物 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20080249137A1 (enExample) |
| EP (1) | EP1940767A2 (enExample) |
| JP (1) | JP2009507846A (enExample) |
| KR (1) | KR20080042170A (enExample) |
| AR (1) | AR057800A1 (enExample) |
| AU (1) | AU2006287521A1 (enExample) |
| BR (1) | BRPI0615948A2 (enExample) |
| CA (1) | CA2621406A1 (enExample) |
| CR (1) | CR9869A (enExample) |
| EC (1) | ECSP088254A (enExample) |
| GT (1) | GT200600407A (enExample) |
| IL (1) | IL189775A0 (enExample) |
| NO (1) | NO20081042L (enExample) |
| PE (1) | PE20071185A1 (enExample) |
| RU (1) | RU2008108221A (enExample) |
| TW (1) | TW200800872A (enExample) |
| WO (1) | WO2007030567A2 (enExample) |
Families Citing this family (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2502649A1 (en) | 2005-02-03 | 2012-09-26 | TopoTarget UK Limited | Combination therapy using HDAC inhibitors and erlotinib for treating cancer |
| ATE542527T1 (de) * | 2005-05-13 | 2012-02-15 | Topotarget Uk Ltd | Pharmazeutische formulierungen von hdac-hemmern |
| US7642259B2 (en) | 2005-07-09 | 2010-01-05 | Astrazeneca Ab | Heteroaryl benzamide derivatives for use as GLK activators in the treatment of diabetes |
| CA2621164A1 (en) | 2005-08-26 | 2007-03-01 | Shionogi & Co., Ltd. | Derivative having ppar agonistic activity |
| CA2627923C (en) * | 2005-11-10 | 2016-01-12 | Topotarget Uk Limited | Histone deacetylase (hdac) inhibitors (pxdlol) for the treatment of cancer |
| WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| AU2007326395B2 (en) * | 2006-12-01 | 2012-10-11 | Msd K.K. | Novel phenyl-isoxazol-3-ol derivative |
| FR2917084B1 (fr) * | 2007-06-05 | 2009-07-17 | Galderma Res & Dev | Nouveaux derives d'acide 3-phenyl propanoique activateurs des recpteurs de type ppar, leur methode de preparation et leur utilisation dans des compositions cosmetiques ou pharmaceutiques. |
| FR2917086B1 (fr) * | 2007-06-05 | 2009-07-17 | Galderma Res & Dev | Nouveaux derives d'acide 3-phenyl acrylique activateurs des recepteurs de type ppar, leur methode de preparation et leur utilisation dans des compositions cosmetiques ou pharmaceutiques. |
| MX2010000617A (es) | 2007-07-17 | 2010-05-17 | Plexxikon Inc | Compuestos y metodos para modulacion de cinasa, e indicaciones de estos. |
| US8642809B2 (en) * | 2007-09-25 | 2014-02-04 | Topotarget Uk Ltd. | Methods of synthesis of certain hydroxamic acid compounds |
| AU2009220942B2 (en) * | 2008-03-07 | 2015-05-28 | Onxeo Dk, Branch Of Onxeo S.A., France | Methods of treatment employing prolonged continuous infusion of Belinostat |
| US8158636B2 (en) | 2008-05-19 | 2012-04-17 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| JP2012506386A (ja) * | 2008-10-21 | 2012-03-15 | メタボレックス, インコーポレイテッド | アリールgpr120受容体アゴニストおよびその使用 |
| GB0900555D0 (en) * | 2009-01-14 | 2009-02-11 | Topotarget As | New methods |
| US8778939B2 (en) * | 2009-09-29 | 2014-07-15 | Glaxo Group Limited | Compounds |
| CN104292154A (zh) * | 2009-09-29 | 2015-01-21 | 葛兰素集团有限公司 | 新化合物 |
| KR20120097512A (ko) | 2009-11-18 | 2012-09-04 | 플렉시콘, 인코퍼레이티드 | 키나제 조절을 위한 화합물 및 방법, 및 그에 대한 적응증 |
| CN102753549A (zh) | 2009-12-23 | 2012-10-24 | 普莱希科公司 | 用于激酶调节的化合物和方法及其适应症 |
| TWI619713B (zh) | 2010-04-21 | 2018-04-01 | 普雷辛肯公司 | 用於激酶調節的化合物和方法及其適應症 |
| CN102285933B (zh) | 2010-06-18 | 2016-03-09 | 浙江海正药业股份有限公司 | 一种对亚型过氧化物酶增殖物激活受体具有激动作用的化合物、其制备方法和应用 |
| WO2012008549A1 (ja) * | 2010-07-15 | 2012-01-19 | 武田薬品工業株式会社 | 複素環化合物 |
| PL2672967T3 (pl) | 2011-02-07 | 2019-04-30 | Plexxikon Inc | Związki i sposoby modulacji kinaz i wskazania ku temu |
| SG194847A1 (en) | 2011-05-17 | 2013-12-30 | Plexxikon Inc | Kinase modulation and indications therefor |
| WO2013037705A2 (en) | 2011-09-16 | 2013-03-21 | Fovea Pharmaceuticals | Aniline derivatives,their preparation and their therapeutic application |
| US9358235B2 (en) | 2012-03-19 | 2016-06-07 | Plexxikon Inc. | Kinase modulation, and indications therefor |
| HK1211589A1 (zh) | 2012-08-23 | 2016-05-27 | Alios Biopharma, Inc. | 用於治疗副粘病毒病毒性感染的化合物 |
| AU2013312477B2 (en) | 2012-09-06 | 2018-05-31 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| RU2641916C2 (ru) | 2012-10-02 | 2018-01-23 | Байер Кропсайенс Аг | Гетероциклические соединения в качестве пестицидов |
| KR102212923B1 (ko) | 2012-12-21 | 2021-02-04 | 플렉시콘 인코퍼레이티드 | 키나제 조절을 위한 화합물 및 방법, 및 그에 대한 적응증 |
| US20140303121A1 (en) | 2013-03-15 | 2014-10-09 | Plexxikon Inc. | Heterocyclic compounds and uses thereof |
| JP6325078B2 (ja) | 2013-03-15 | 2018-05-16 | プレキシコン インコーポレーテッドPlexxikon Inc. | ヘテロ環式化合物およびその使用 |
| KR20160013028A (ko) | 2013-05-30 | 2016-02-03 | 플렉시콘, 인코퍼레이티드 | 키나제 조정을 위한 화합물 및 그에 대한 적응증 |
| WO2015134536A1 (en) | 2014-03-04 | 2015-09-11 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| US9856259B2 (en) | 2014-09-15 | 2018-01-02 | Plexxikon Inc. | Heterocyclic compounds and uses thereof |
| WO2016164641A1 (en) | 2015-04-08 | 2016-10-13 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| US10829484B2 (en) | 2015-07-28 | 2020-11-10 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| SG10201912386RA (en) | 2015-09-21 | 2020-02-27 | Plexxikon Inc | Heterocyclic compounds and uses thereof |
| UA122237C2 (uk) * | 2015-10-07 | 2020-10-12 | Мітобрідж, Інк. | Агоністи ppar, сполуки, фармацевтичні композиції та способи їх застосування |
| MX2018006856A (es) | 2015-12-07 | 2018-08-01 | Plexxikon Inc | Compuestos y metodos para modulacion de la quinasa, e indicaciones de los mismos. |
| ES2904615T3 (es) | 2016-03-16 | 2022-04-05 | Plexxikon Inc | Compuestos y métodos para la modulación de quinasas e indicaciones al respecto |
| MX380531B (es) | 2016-04-13 | 2025-03-12 | Mitobridge Inc | Agonistas del receptor activado por proliferador de peroxisoma (ppar), compuestos, composiciones farmacéuticas y métodos para usar los mismos. |
| TW201815766A (zh) | 2016-09-22 | 2018-05-01 | 美商普雷辛肯公司 | 用於ido及tdo調節之化合物及方法以及其適應症 |
| WO2018136202A2 (en) | 2016-12-23 | 2018-07-26 | Plexxikon Inc. | Compounds and methods for cdk8 modulation and indications therefor |
| ES2896502T3 (es) | 2017-03-20 | 2022-02-24 | Plexxikon Inc | Formas cristalinas de ácido 4-(1-(1,1-di(piridin-2-il) etil)-6-(3,5-dimetilisoxazol-4-il)-1H-pirrolo[3,2-b]piridin-3- il)benzoico que inhiben el bromodominio |
| US10428067B2 (en) | 2017-06-07 | 2019-10-01 | Plexxikon Inc. | Compounds and methods for kinase modulation |
| CA3069720A1 (en) | 2017-07-11 | 2019-01-17 | Vertex Pharmaceuticals Incorporated | Carboxamides as modulators of sodium channels |
| KR102615829B1 (ko) | 2017-07-25 | 2023-12-20 | 플렉시콘 인코퍼레이티드 | 키나제를 조정하는 화합물의 제제 |
| EP3694855A1 (en) | 2017-10-13 | 2020-08-19 | Plexxikon Inc. | Solid forms of a compound for modulating kinases |
| AU2018354423B2 (en) | 2017-10-27 | 2024-11-07 | Plexxikon Inc. | Formulations of a compound modulating kinases |
| JP2021518367A (ja) | 2018-03-20 | 2021-08-02 | プレキシコン インコーポレーテッドPlexxikon Inc. | Idoおよびtdo調節のための化合物および方法、ならびにそれらのための兆候 |
| US12441703B2 (en) | 2019-01-10 | 2025-10-14 | Vertex Pharmaceuticals Incorporated | Carboxamides as modulators of sodium channels |
| WO2020146612A1 (en) | 2019-01-10 | 2020-07-16 | Vertex Pharmaceuticals Incorporated | Esters and carbamates as modulators of sodium channels |
| US11091447B2 (en) | 2020-01-03 | 2021-08-17 | Berg Llc | UBE2K modulators and methods for their use |
| BR112022021920A2 (pt) | 2020-04-29 | 2023-01-17 | Plexxikon Inc | Síntese de compostos heterocíclicos |
Family Cites Families (89)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3489767A (en) * | 1966-01-12 | 1970-01-13 | Sumitomo Chemical Co | 1-(phenylsulfonyl)-3-indolyl aliphatic acid derivatives |
| US3511841A (en) * | 1967-05-29 | 1970-05-12 | Sterling Drug Inc | 1-((4-,5-,6-,and 7-azaindolyl)-lower-alkyl)- 4-substituted-piperazines |
| GB1210252A (en) * | 1967-06-16 | 1970-10-28 | Agfa Gevaert Nv | Methine dyes and colloid layers containing them |
| CA1041531A (en) * | 1973-10-29 | 1978-10-31 | Eisai Co. Ltd. | M-phenoxyphenyl propionic acid derivatives and preparation thereof |
| JPS5936979B2 (ja) * | 1980-11-17 | 1984-09-06 | 住友化学工業株式会社 | ジフェニルスルホン誘導体、その製造法およびこれらを有効成分として含有する除草剤 |
| US5516931A (en) * | 1982-02-01 | 1996-05-14 | Northeastern University | Release tag compounds producing ketone signal groups |
| DE3571432D1 (en) * | 1984-05-18 | 1989-08-17 | Asahi Chemical Ind | 2-nitro-5-(2'-chloro-4'trifluoromethylphenoxy)phenylacetic ester, thioester and amide, process for preparation therof, herbicidal composition, and method for destruction of undesirable weeds |
| US4683241A (en) * | 1984-05-21 | 1987-07-28 | G. D. Searle & Co. | Phenolic ester derivatives as elastase inhibitors |
| DE3419952A1 (de) * | 1984-05-28 | 1985-11-28 | Bayer Ag, 5090 Leverkusen | Substituierte phenoxyphenylpropionsaeure-derivate |
| US4990526A (en) * | 1985-06-18 | 1991-02-05 | Merck Frosst Canada, Inc. | Leukotriene antagonists, compositions and methods of use thereof |
| US4992576A (en) * | 1987-01-12 | 1991-02-12 | Eli Lilly And Company | Intermediates for leukotriene antagonists |
| US4826990A (en) * | 1987-09-30 | 1989-05-02 | American Home Products Corporation | 2-aryl substituted heterocyclic compounds as antiallergic and antiinflammatory agents |
| US5103014A (en) * | 1987-09-30 | 1992-04-07 | American Home Products Corporation | Certain 3,3'-[[[(2-phenyl-4-thiazolyl)methoxy]phenyl]methylene]dithiobis-propanoic acid derivatives |
| US4895953A (en) * | 1987-09-30 | 1990-01-23 | American Home Products Corporation | 2-Aryl substituted heterocyclic compounds as antiallergic and antiinflammatory agents |
| US4920131A (en) * | 1987-11-03 | 1990-04-24 | Rorer Pharmaceutical Corp. | Quinoline derivatives and use thereof as antagonists of leukotriene D4 |
| US5405851A (en) * | 1990-06-19 | 1995-04-11 | Burroughs Wellcome Co. | Pharmaceutical compounds |
| US5075313A (en) * | 1990-09-13 | 1991-12-24 | Eli Lilly And Company | 3-aryl-4(3H)quinazolinone CCK antagonists and pharmaceutical formulations thereof |
| EP0540165A1 (en) * | 1991-10-03 | 1993-05-05 | Zeneca Limited | Alkanoic acid derivatives |
| US5424280A (en) * | 1993-10-07 | 1995-06-13 | American Cyanamid Company | Aryloxybenzene herbicidal agents |
| US5523302A (en) * | 1993-11-24 | 1996-06-04 | The Du Pont Merck Pharmaceutical Company | Aromatic compounds containing basic and acidic termini useful as fibrinogen receptor antagonists |
| US5453443A (en) * | 1994-07-20 | 1995-09-26 | Merck Frosst Canada, Inc. | Bis(aryloxy)alkanes as inhibitors of phospholipase A2 enzymes |
| US5883106A (en) * | 1994-10-18 | 1999-03-16 | Pfizer Inc. | 5-lipoxygenase inhibitors |
| JP3400392B2 (ja) * | 1994-10-18 | 2003-04-28 | ファイザー製薬株式会社 | 5−リポキシゲナーゼ阻害剤及び新規医薬組成物 |
| US5977117A (en) * | 1996-01-05 | 1999-11-02 | Texas Biotechnology Corporation | Substituted phenyl compounds and derivatives thereof that modulate the activity of endothelin |
| US5859051A (en) * | 1996-02-02 | 1999-01-12 | Merck & Co., Inc. | Antidiabetic agents |
| US5854245A (en) * | 1996-06-28 | 1998-12-29 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| FR2755965B1 (fr) * | 1996-11-19 | 1998-12-18 | Cird Galderma | Composes biaromatiques, compositions pharmaceutiques et cosmetiques les contenant et utilisations |
| US6794511B2 (en) * | 1997-03-04 | 2004-09-21 | G. D. Searle | Sulfonyl aryl or heteroaryl hydroxamic acid compounds |
| HUP0101022A1 (hu) * | 1997-10-17 | 2001-10-28 | Aventis Pharmaceuticals Products Inc. | Kinolinszármazékok gyógyászati alkalmazása |
| CA2315736A1 (en) * | 1998-01-05 | 1999-07-15 | Eisai Co., Ltd. | Purine compounds and adenosine a2 receptor antagonist as preventive or therapeutic for diabetes mellitus |
| US6080587A (en) * | 1998-01-23 | 2000-06-27 | Eli Lilly And Company | Method for preparing and selecting pharmaceutically useful sulfur-bridged bi- and triaromatic ring compounds from a structurally diverse universal library |
| EA005244B1 (ru) * | 1998-02-23 | 2004-12-30 | Саут Алабама Медикал Сайенс Фаундейшн | Индол-3-пропионовые кислоты, их соли и эфиры, используемые в качестве лекарств |
| US6506757B1 (en) * | 1998-03-10 | 2003-01-14 | Ono Pharmaceutical Co., Ltd. | Carboxylic acid derivatives and drugs containing the same as the active ingredient |
| EP1070054A1 (en) * | 1998-04-08 | 2001-01-24 | Takeda Chemical Industries, Ltd. | Amine compounds, their production and their use as somatostatin receptor antagonists or agonists |
| CN1189166C (zh) * | 1998-09-11 | 2005-02-16 | 伊来克萨斯独资有限公司 | Fc受体调节剂及其应用 |
| WO2000064876A1 (en) * | 1999-04-28 | 2000-11-02 | Aventis Pharma Deutschland Gmbh | Tri-aryl acid derivatives as ppar receptor ligands |
| EP1177187B1 (en) * | 1999-04-28 | 2007-07-25 | Sanofi-Aventis Deutschland GmbH | Di-aryl acid derivatives as ppar receptor ligands |
| US7041691B1 (en) * | 1999-06-30 | 2006-05-09 | Amgen Inc. | Compounds for the modulation of PPARγ activity |
| HUP0202731A3 (en) * | 1999-09-17 | 2003-10-28 | Kyorin Seiyaku Kk | O-anisamide derivatives, process for their preparation and pharmaceutical compositions containing them |
| TWI262185B (en) * | 1999-10-01 | 2006-09-21 | Eisai Co Ltd | Carboxylic acid derivatives having anti-hyperglycemia and anti-hyperlipemia action, and pharmaceutical composition containing the derivatives |
| JP2004500389A (ja) * | 2000-03-09 | 2004-01-08 | アベンティス・ファーマ・ドイチユラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | Pparメディエーターの治療での使用 |
| WO2001082916A2 (en) * | 2000-05-03 | 2001-11-08 | Tularik Inc. | Combination therapeutic compositions and methods of use |
| SI1285908T1 (sl) * | 2000-05-29 | 2008-12-31 | Kyorin Seiyaku Kk | Substituirani fenilpropionski kislinski derivati |
| EP1310494B1 (en) * | 2000-08-11 | 2012-01-25 | Nippon Chemiphar Co., Ltd. | PPAR (delta) ACTIVATORS |
| MXPA03003021A (es) * | 2000-10-11 | 2003-07-14 | Esperion Therapeutics Inc | Compuestos de eter y composiciones para el control del colesterol y usos relacionados. |
| JP4148681B2 (ja) * | 2000-12-28 | 2008-09-10 | 武田薬品工業株式会社 | アルカン酸誘導体、その製造法および用途 |
| ATE433964T1 (de) * | 2000-12-28 | 2009-07-15 | Takeda Pharmaceutical | Alkansäurederivate, verfahren zu deren herstellung und deren verwendung |
| WO2002076957A1 (en) * | 2001-03-23 | 2002-10-03 | Nippon Chemiphar Co.,Ltd. | Activator for peroxisome proliferator-activated receptor |
| CA2445515A1 (en) * | 2001-05-04 | 2002-11-04 | Paratek Pharmaceuticals, Inc. | Transcription factor modulating compounds and methods of use thereof |
| KR100965201B1 (ko) * | 2001-06-12 | 2010-06-24 | 웰스테트 테라퓨틱스 코포레이션 | 대사 질환의 치료용 화합물 |
| IL160304A0 (en) * | 2001-08-10 | 2004-07-25 | Nippon Chemiphar Co | ACTIVATOR FOR PEROXISOME PROLIFERATOR-RESPONSIVE RECEPTOR delta |
| JP4825375B2 (ja) * | 2001-08-28 | 2011-11-30 | 株式会社 資生堂 | ジチアゾール化合物及びマトリックスメタロプロテアーゼ活性阻害剤、皮膚外用剤 |
| US6869975B2 (en) * | 2001-09-14 | 2005-03-22 | Tularik Inc. | Linked biaryl compounds |
| ES2316736T3 (es) * | 2002-02-25 | 2009-04-16 | Eli Lilly And Company | Moduladores de receptores activados por proliferador de peroxisoma. |
| US6875780B2 (en) * | 2002-04-05 | 2005-04-05 | Warner-Lambert Company | Compounds that modulate PPAR activity and methods for their preparation |
| US6806265B2 (en) * | 2002-05-16 | 2004-10-19 | Boehringer Ingelheim International Gmbh | Non-nucleoside reverse transcriptase inhibitors |
| WO2003099793A1 (en) * | 2002-05-24 | 2003-12-04 | Takeda Pharmaceutical Company Limited | 1,2-azole derivatives with hypoglycemic and hypolipidemic activity |
| JP2004277397A (ja) * | 2002-05-24 | 2004-10-07 | Takeda Chem Ind Ltd | 1,2−アゾール誘導体 |
| US20030229149A1 (en) * | 2002-05-28 | 2003-12-11 | Werner Baschong | Anti-inflammatory agents |
| SE0201937D0 (sv) * | 2002-06-20 | 2002-06-20 | Astrazeneca Ab | Therapeutic agents |
| WO2004007439A1 (ja) * | 2002-07-10 | 2004-01-22 | Sumitomo Pharmaceuticals Co., Ltd. | ビアリール誘導体 |
| SE0202241D0 (sv) * | 2002-07-17 | 2002-07-17 | Astrazeneca Ab | Novel Compounds |
| US7393960B2 (en) * | 2002-08-29 | 2008-07-01 | Merck & Co., Inc. | Indoles having anti-diabetic activity |
| KR101476067B1 (ko) * | 2002-09-06 | 2014-12-23 | 인설트 테라페틱스, 인코퍼레이티드 | 공유결합된 치료제 전달을 위한 사이클로덱스트린-기초 중합체 |
| WO2004022551A1 (ja) * | 2002-09-06 | 2004-03-18 | Takeda Pharmaceutical Company Limited | フランまたはチオフェン誘導体およびその医薬用途 |
| WO2004024705A1 (ja) * | 2002-09-10 | 2004-03-25 | Takeda Pharmaceutical Company Limited | 5員複素環化合物 |
| EP1572629A1 (en) * | 2002-12-12 | 2005-09-14 | Galderma Research & Development, S.N.C. | COMPOUNDS WHICH MODULATE PPARϝ TYPE RECEPTORS, AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS |
| EP1578716A1 (en) * | 2002-12-20 | 2005-09-28 | Novo Nordisk A/S | Dicarboxylic acid derivatives as ppar-agonists |
| AU2003296404A1 (en) * | 2003-01-06 | 2004-08-10 | Eli Lilly And Company | Heterocyclic ppar modulators |
| WO2004063155A1 (en) * | 2003-01-06 | 2004-07-29 | Eli Lilly And Company | Fused heterocyclic derivatives as ppar modulators |
| TWI328009B (en) * | 2003-05-21 | 2010-08-01 | Glaxo Group Ltd | Quinoline derivatives as phosphodiesterase inhibitors |
| US7268174B2 (en) * | 2003-07-11 | 2007-09-11 | Siemens Power Generation, Inc. | Homogeneous alumoxane-LCT-epoxy polymers and methods for making the same |
| JP4845730B2 (ja) * | 2003-07-17 | 2011-12-28 | プレキシコン,インコーポレーテッド | Ppar活性化合物 |
| US7348338B2 (en) * | 2003-07-17 | 2008-03-25 | Plexxikon, Inc. | PPAR active compounds |
| PT1658263E (pt) * | 2003-07-24 | 2010-09-06 | Leo Pharma As | Novos compostos de aminobenzofenona |
| US20100267778A1 (en) * | 2003-08-04 | 2010-10-21 | Shinya Kusuda | Diphenyl ether compound, process for producing the same, and use |
| JP4661595B2 (ja) * | 2003-09-22 | 2011-03-30 | 小野薬品工業株式会社 | フェニル酢酸誘導体、その製造方法および用途 |
| WO2005037763A1 (en) * | 2003-10-14 | 2005-04-28 | Eli Lilly And Company | Phenoxyether derivatives as ppar modulators |
| GB0324886D0 (en) * | 2003-10-24 | 2003-11-26 | Glaxo Group Ltd | Medicinal compounds |
| BRPI0416283A (pt) * | 2003-11-05 | 2007-01-23 | Hoffmann La Roche | compostos, processo para a fabricação de compostos, composição farmacêutica, método para o tratamento e/ou prevenção de doenças que são moduladas por agonistas de ppar(delta) e/ou ppar(alfa) e uso destes compostos |
| ES2299906T3 (es) * | 2003-11-25 | 2008-06-01 | Eli Lilly And Company | Moduladores de receptores activados por proliferadores de peroxisomas. |
| US20050203151A1 (en) * | 2003-12-19 | 2005-09-15 | Kalypsys, Inc. | Novel compounds, compositions and uses thereof for treatment of metabolic disorders and related conditions |
| BRPI0507734A (pt) * | 2004-02-18 | 2007-07-10 | Astrazeneca Ab | composto ou um sal, pró-droga ou solvato do mesmo, método de tratar doenças mediadas por glk, e, processo para a preparação de um composto |
| US7262318B2 (en) * | 2004-03-10 | 2007-08-28 | Pfizer, Inc. | Substituted heteroaryl- and phenylsulfamoyl compounds |
| AR048523A1 (es) * | 2004-04-07 | 2006-05-03 | Kalypsys Inc | Compuestos con estructura de aril sulfonamida y sulfonilo como moduladores de ppar y metodos para tratar trastornos metabolicos |
| US20050288340A1 (en) * | 2004-06-29 | 2005-12-29 | Pfizer Inc | Substituted heteroaryl- and phenylsulfamoyl compounds |
| US7622491B2 (en) * | 2004-08-13 | 2009-11-24 | Metabolex Inc. | Modulators of PPAR and methods of their preparation |
| EP1887000A4 (en) * | 2005-05-27 | 2011-09-07 | Shionogi & Co | ARYLACETATE DERIVATIVES WITH ISOXAZO EASY |
| BRPI0612513A2 (pt) * | 2005-06-20 | 2010-11-30 | Playtex Products Inc | composições não irritantes |
-
2006
- 2006-09-06 KR KR1020087008156A patent/KR20080042170A/ko not_active Withdrawn
- 2006-09-06 TW TW095132980A patent/TW200800872A/zh unknown
- 2006-09-06 WO PCT/US2006/034764 patent/WO2007030567A2/en not_active Ceased
- 2006-09-06 JP JP2008530176A patent/JP2009507846A/ja active Pending
- 2006-09-06 CA CA002621406A patent/CA2621406A1/en not_active Abandoned
- 2006-09-06 US US11/517,572 patent/US20080249137A1/en not_active Abandoned
- 2006-09-06 AU AU2006287521A patent/AU2006287521A1/en not_active Abandoned
- 2006-09-06 EP EP06803072A patent/EP1940767A2/en not_active Withdrawn
- 2006-09-06 RU RU2008108221/04A patent/RU2008108221A/ru not_active Application Discontinuation
- 2006-09-06 GT GT200600407A patent/GT200600407A/es unknown
- 2006-09-06 BR BRPI0615948-6A patent/BRPI0615948A2/pt not_active IP Right Cessation
- 2006-09-07 AR ARP060103888A patent/AR057800A1/es unknown
- 2006-09-07 PE PE2006001078A patent/PE20071185A1/es not_active Application Discontinuation
-
2008
- 2008-02-26 IL IL189775A patent/IL189775A0/en unknown
- 2008-02-28 NO NO20081042A patent/NO20081042L/no not_active Application Discontinuation
- 2008-03-07 EC EC2008008254A patent/ECSP088254A/es unknown
- 2008-04-04 CR CR9869A patent/CR9869A/es not_active Application Discontinuation
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2009507846A5 (enExample) | ||
| JP2009509932A5 (enExample) | ||
| JP5299810B2 (ja) | 代謝疾患の治療に使用するための、化合物、薬学的組成物及び方法 | |
| US7582803B2 (en) | Conformationally constrained 3-(4-hydroxy-phenyl)-substituted-propanoic acids useful for treating metabolic disorders | |
| RU2008108221A (ru) | Соединения, активные в отношении ppar (рецепторов активаторов пролиферации пероксисом) | |
| CA2662242C (en) | Benzo-fused compounds for use in treating metabolic disorders | |
| JP2008521829A5 (enExample) | ||
| AU2006251768B2 (en) | Compounds, pharmaceutical compositions and methods for their use in treating metabolic disorders | |
| JP3490704B2 (ja) | チアゾールおよびオキサゾール誘導体ならびにそれらの医薬的使用 | |
| JP2007525516A5 (enExample) | ||
| RU2009137124A (ru) | Соединения, активные в отношении ppar | |
| JP2005528348A (ja) | Ppar活性を変調するチアゾールおよびオキサゾール誘導体 | |
| JP2010520303A (ja) | Ppar活性化合物 | |
| JP2010539083A5 (enExample) | ||
| EP2139843A1 (en) | Substituted biphenyl phenoxy-, thiophenyl- and aminophenylpropanoic acid gpr40 modulators | |
| JP2007500720A5 (enExample) | ||
| JP2005505616A5 (enExample) | ||
| CA2397234A1 (en) | Novel use of phenylheteroalkylamine derivatives | |
| JPH11515008A (ja) | イミダゾール誘導体及びその一酸化窒素合成酵素阻害剤としての使用 | |
| CA2563461A1 (en) | Pyrazole phenyl derivatives as ppar activators | |
| JPH0519543B2 (enExample) |