JP2004517852A5 - - Google Patents
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- Publication number
- JP2004517852A5 JP2004517852A5 JP2002552939A JP2002552939A JP2004517852A5 JP 2004517852 A5 JP2004517852 A5 JP 2004517852A5 JP 2002552939 A JP2002552939 A JP 2002552939A JP 2002552939 A JP2002552939 A JP 2002552939A JP 2004517852 A5 JP2004517852 A5 JP 2004517852A5
- Authority
- JP
- Japan
- Prior art keywords
- diabetes
- inden
- cyclopenta
- aza
- dihydro
- 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.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims 34
- -1 3-oxetanyl Chemical group 0.000 claims 13
- 206010012601 diabetes mellitus Diseases 0.000 claims 12
- 230000002265 prevention Effects 0.000 claims 12
- 239000003814 drug Substances 0.000 claims 10
- 239000008194 pharmaceutical composition Substances 0.000 claims 10
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 8
- 238000004519 manufacturing process Methods 0.000 claims 8
- 208000035475 disorder Diseases 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 229940086609 Lipase inhibitor Drugs 0.000 claims 5
- 125000001153 fluoro group Chemical group F* 0.000 claims 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 4
- 230000003542 behavioural effect Effects 0.000 claims 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- 208000002249 Diabetes Complications Diseases 0.000 claims 3
- 206010012655 Diabetic complications Diseases 0.000 claims 3
- 206010022489 Insulin Resistance Diseases 0.000 claims 3
- 229940127470 Lipase Inhibitors Drugs 0.000 claims 3
- 208000008589 Obesity Diseases 0.000 claims 3
- 208000016222 Pancreatic disease Diseases 0.000 claims 3
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims 3
- 102100026383 Vasopressin-neurophysin 2-copeptin Human genes 0.000 claims 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 3
- 201000010064 diabetes insipidus Diseases 0.000 claims 3
- 229940079593 drug Drugs 0.000 claims 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 3
- 201000001421 hyperglycemia Diseases 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 235000020824 obesity Nutrition 0.000 claims 3
- AHLBNYSZXLDEJQ-FWEHEUNISA-N orlistat Chemical group CCCCCCCCCCC[C@H](OC(=O)[C@H](CC(C)C)NC=O)C[C@@H]1OC(=O)[C@H]1CCCCCC AHLBNYSZXLDEJQ-FWEHEUNISA-N 0.000 claims 3
- 229960001243 orlistat Drugs 0.000 claims 3
- 150000003431 steroids Chemical class 0.000 claims 3
- 125000006224 2-tetrahydrofuranylmethyl group Chemical group [H]C([H])(*)C1([H])OC([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 208000007848 Alcoholism Diseases 0.000 claims 2
- 208000000103 Anorexia Nervosa Diseases 0.000 claims 2
- 208000019901 Anxiety disease Diseases 0.000 claims 2
- 208000020925 Bipolar disease Diseases 0.000 claims 2
- 208000032841 Bulimia Diseases 0.000 claims 2
- 206010006550 Bulimia nervosa Diseases 0.000 claims 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 2
- 208000024172 Cardiovascular disease Diseases 0.000 claims 2
- 206010008874 Chronic Fatigue Syndrome Diseases 0.000 claims 2
- 206010012289 Dementia Diseases 0.000 claims 2
- 208000030814 Eating disease Diseases 0.000 claims 2
- 208000019454 Feeding and Eating disease Diseases 0.000 claims 2
- 208000018522 Gastrointestinal disease Diseases 0.000 claims 2
- 206010019233 Headaches Diseases 0.000 claims 2
- 206010022773 Intracranial pressure increased Diseases 0.000 claims 2
- 201000009906 Meningitis Diseases 0.000 claims 2
- 208000019695 Migraine disease Diseases 0.000 claims 2
- 208000027626 Neurocognitive disease Diseases 0.000 claims 2
- 208000021384 Obsessive-Compulsive disease Diseases 0.000 claims 2
- 208000002193 Pain Diseases 0.000 claims 2
- 206010036618 Premenstrual syndrome Diseases 0.000 claims 2
- 208000028017 Psychotic disease Diseases 0.000 claims 2
- 201000001880 Sexual dysfunction Diseases 0.000 claims 2
- 206010041250 Social phobia Diseases 0.000 claims 2
- 208000006011 Stroke Diseases 0.000 claims 2
- 201000007930 alcohol dependence Diseases 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 208000025748 atypical depressive disease Diseases 0.000 claims 2
- 210000003169 central nervous system Anatomy 0.000 claims 2
- 208000015114 central nervous system disease Diseases 0.000 claims 2
- 235000014632 disordered eating Nutrition 0.000 claims 2
- 206010014599 encephalitis Diseases 0.000 claims 2
- 206010015037 epilepsy Diseases 0.000 claims 2
- 231100000869 headache Toxicity 0.000 claims 2
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 208000014674 injury Diseases 0.000 claims 2
- 206010027175 memory impairment Diseases 0.000 claims 2
- 206010027599 migraine Diseases 0.000 claims 2
- 208000029766 myalgic encephalomeyelitis/chronic fatigue syndrome Diseases 0.000 claims 2
- 230000004770 neurodegeneration Effects 0.000 claims 2
- 208000015122 neurodegenerative disease Diseases 0.000 claims 2
- 208000022821 personality disease Diseases 0.000 claims 2
- 201000000484 premenstrual tension Diseases 0.000 claims 2
- 208000020016 psychiatric disease Diseases 0.000 claims 2
- 201000000980 schizophrenia Diseases 0.000 claims 2
- 231100000872 sexual dysfunction Toxicity 0.000 claims 2
- 201000002859 sleep apnea Diseases 0.000 claims 2
- 208000019116 sleep disease Diseases 0.000 claims 2
- 208000020685 sleep-wake disease Diseases 0.000 claims 2
- 230000008733 trauma Effects 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- DSDJWMWJRKCKCE-VIFPVBQESA-N (2s)-1-(5-fluoro-6-methoxy-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl)propan-2-amine Chemical compound COC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1F DSDJWMWJRKCKCE-VIFPVBQESA-N 0.000 claims 1
- FWXXHTBFBYUWTJ-NSHDSACASA-N (2s)-1-(6-cyclopropyloxy-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl)propan-2-amine Chemical compound C1=C2C(C[C@@H](N)C)=C3CCCN3C2=CC=C1OC1CC1 FWXXHTBFBYUWTJ-NSHDSACASA-N 0.000 claims 1
- IMDCAWVCNYESQC-JTQLQIEISA-N (2s)-1-(6-cyclopropyloxy-5-fluoro-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl)propan-2-amine Chemical compound FC1=C2C(C[C@@H](N)C)=C3CCCN3C2=CC=C1OC1CC1 IMDCAWVCNYESQC-JTQLQIEISA-N 0.000 claims 1
- QCPKALQXQKTTQB-NSHDSACASA-N (2s)-1-(6-ethoxy-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl)propan-2-amine Chemical compound CCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1 QCPKALQXQKTTQB-NSHDSACASA-N 0.000 claims 1
- SLLLMJVQCBMSLS-JTQLQIEISA-N (2s)-1-(6-ethoxy-5-fluoro-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl)propan-2-amine Chemical compound CCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1F SLLLMJVQCBMSLS-JTQLQIEISA-N 0.000 claims 1
- ZHZJODQADCZMHK-JTQLQIEISA-N (2s)-1-(6-ethoxy-7-fluoro-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl)propan-2-amine Chemical compound C1=C(F)C(OCC)=CC2=C1N1CCCC1=C2C[C@H](C)N ZHZJODQADCZMHK-JTQLQIEISA-N 0.000 claims 1
- XDEGBBONBCMCHL-NSHDSACASA-N (2s)-1-[5-fluoro-6-(2-methoxyethoxy)-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound COCCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1F XDEGBBONBCMCHL-NSHDSACASA-N 0.000 claims 1
- JYZQZNBKKFSHLV-LBPRGKRZSA-N (2s)-1-[5-fluoro-6-(3-methoxypropoxy)-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound COCCCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1F JYZQZNBKKFSHLV-LBPRGKRZSA-N 0.000 claims 1
- SWVILPKDPUXYKT-ZDUSSCGKSA-N (2s)-1-[6-(2-ethoxyethoxy)-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound CCOCCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1 SWVILPKDPUXYKT-ZDUSSCGKSA-N 0.000 claims 1
- YZMZCUJIBWXFLB-LBPRGKRZSA-N (2s)-1-[6-(2-methoxyethoxy)-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound COCCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1 YZMZCUJIBWXFLB-LBPRGKRZSA-N 0.000 claims 1
- LWJJTMYOGQVLNI-AWEZNQCLSA-N (2s)-1-[6-(3-ethoxypropoxy)-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound CCOCCCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1 LWJJTMYOGQVLNI-AWEZNQCLSA-N 0.000 claims 1
- OLMCBWTZMZYKJY-ZDUSSCGKSA-N (2s)-1-[6-(3-methoxypropoxy)-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound COCCCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1 OLMCBWTZMZYKJY-ZDUSSCGKSA-N 0.000 claims 1
- DETWXRAGLCWMEP-AWEZNQCLSA-N (2s)-1-[6-(4-methoxybutoxy)-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound COCCCCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1 DETWXRAGLCWMEP-AWEZNQCLSA-N 0.000 claims 1
- FOUAYMJKLOFDEH-AWEZNQCLSA-N (2s)-1-[6-[2-(2-methoxyethoxy)ethoxy]-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound COCCOCCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1 FOUAYMJKLOFDEH-AWEZNQCLSA-N 0.000 claims 1
- MYBNYWOIGBQJRH-HNNXBMFYSA-N (2s)-1-[6-[3-(2-methoxyethoxy)propoxy]-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound COCCOCCCOC1=CC=C2N(CCC3)C3=C(C[C@H](C)N)C2=C1 MYBNYWOIGBQJRH-HNNXBMFYSA-N 0.000 claims 1
- PDIUQBQZLVEAMP-NSHDSACASA-N (2s)-1-[7-fluoro-6-(2-methoxyethoxy)-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound C1=C(F)C(OCCOC)=CC2=C1N1CCCC1=C2C[C@H](C)N PDIUQBQZLVEAMP-NSHDSACASA-N 0.000 claims 1
- WVWSXKFURMFREJ-LBPRGKRZSA-N (2s)-1-[7-fluoro-6-(3-methoxypropoxy)-2,3-dihydro-1h-pyrrolo[1,2-a]indol-4-yl]propan-2-amine Chemical compound C1=C(F)C(OCCCOC)=CC2=C1N1CCCC1=C2C[C@H](C)N WVWSXKFURMFREJ-LBPRGKRZSA-N 0.000 claims 1
- PXMNBTNIDJTYFM-NSHDSACASA-N 2-[[4-[(2s)-2-aminopropyl]-2,3-dihydro-1h-pyrrolo[1,2-a]indol-6-yl]oxy]ethanol Chemical compound C12=CC=C(OCCO)C=C2C(C[C@@H](N)C)=C2N1CCC2 PXMNBTNIDJTYFM-NSHDSACASA-N 0.000 claims 1
- QHRMILCSVOCHAN-JTQLQIEISA-N 2-[[4-[(2s)-2-aminopropyl]-5-fluoro-2,3-dihydro-1h-pyrrolo[1,2-a]indol-6-yl]oxy]ethanol Chemical compound C12=CC=C(OCCO)C(F)=C2C(C[C@@H](N)C)=C2N1CCC2 QHRMILCSVOCHAN-JTQLQIEISA-N 0.000 claims 1
- CZTBECHUFDKWPR-JTQLQIEISA-N 2-[[4-[(2s)-2-aminopropyl]-7-fluoro-2,3-dihydro-1h-pyrrolo[1,2-a]indol-6-yl]oxy]ethanol Chemical compound C12=CC(F)=C(OCCO)C=C2C(C[C@@H](N)C)=C2N1CCC2 CZTBECHUFDKWPR-JTQLQIEISA-N 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000006232 ethoxy propyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000012453 solvate Substances 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0031724A GB0031724D0 (en) | 2000-12-27 | 2000-12-27 | Indole derivatives |
| GB0119820A GB0119820D0 (en) | 2001-08-14 | 2001-08-14 | Indole derivatives |
| PCT/EP2001/014781 WO2002051844A1 (en) | 2000-12-27 | 2001-12-14 | Indole derivatives and their use as 5-ht2b and 5-ht2c receptor ligands |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004517852A JP2004517852A (ja) | 2004-06-17 |
| JP2004517852A5 true JP2004517852A5 (https=) | 2005-05-26 |
| JP4094950B2 JP4094950B2 (ja) | 2008-06-04 |
Family
ID=26245498
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002552939A Expired - Fee Related JP4094950B2 (ja) | 2000-12-27 | 2001-12-14 | インドール誘導体および5−ht2bおよび5−ht2c受容体リガンドとしてのそれらの使用 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6610685B2 (https=) |
| EP (1) | EP1347979B1 (https=) |
| JP (1) | JP4094950B2 (https=) |
| KR (1) | KR100539143B1 (https=) |
| CN (1) | CN1250549C (https=) |
| AR (1) | AR035722A1 (https=) |
| AT (1) | ATE369368T1 (https=) |
| AU (1) | AU2002228007B2 (https=) |
| BR (1) | BR0116605A (https=) |
| CA (1) | CA2432085C (https=) |
| DE (1) | DE60129841T2 (https=) |
| ES (1) | ES2291374T3 (https=) |
| MX (1) | MXPA03005915A (https=) |
| PE (1) | PE20020911A1 (https=) |
| UY (1) | UY27097A1 (https=) |
| WO (1) | WO2002051844A1 (https=) |
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100484933C (zh) | 2002-06-19 | 2009-05-06 | 比奥维特罗姆股份公开公司 | 新的吡嗪化合物及其在制备用于治疗与5-羟色胺相关的疾病的药物中的用途 |
| US7105526B2 (en) | 2002-06-28 | 2006-09-12 | Banyu Pharmaceuticals Co., Ltd. | Benzimidazole derivatives |
| US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
| CL2004000826A1 (es) | 2003-04-25 | 2005-03-04 | Pfizer | Uso de un agonista para el receptor 5-ht2c para preparar un medicamento util en el tratamiento de la incontinencia urinaria provocada por estres, con la condicion de que el agonista no sea 1-[6-cloro-5-(trifluorometil)-2-piridinil]piperazina (org-129 |
| GB0314967D0 (en) * | 2003-06-26 | 2003-07-30 | Hoffmann La Roche | Piperazine derivatives |
| AU2004274309B2 (en) | 2003-09-22 | 2010-04-08 | Msd K.K. | Novel piperidine derivative |
| US20080125403A1 (en) | 2004-04-02 | 2008-05-29 | Merck & Co., Inc. | Method of Treating Men with Metabolic and Anthropometric Disorders |
| EP2248524A3 (en) | 2004-08-25 | 2011-03-09 | Takeda Pharmaceutical Company Limited | Preventives/remedies for stress urinary incontinence and method of screening the same |
| WO2006050007A2 (en) * | 2004-11-01 | 2006-05-11 | Wyeth | Substituted indolizines and derivatives as cns agents |
| US8394765B2 (en) | 2004-11-01 | 2013-03-12 | Amylin Pharmaceuticals Llc | Methods of treating obesity with two different anti-obesity agents |
| EP2286840A3 (en) | 2004-11-01 | 2013-09-04 | Amylin Pharmaceuticals, LLC | Treatment of obesity and related diseases |
| US7737155B2 (en) | 2005-05-17 | 2010-06-15 | Schering Corporation | Nitrogen-containing heterocyclic compounds and methods of use thereof |
| CA2609388C (en) | 2005-05-30 | 2013-08-06 | Banyu Pharmaceutical Co., Ltd. | Novel piperidine derivative |
| JPWO2007018248A1 (ja) | 2005-08-10 | 2009-02-19 | 萬有製薬株式会社 | ピリドン化合物 |
| BRPI0614649A2 (pt) | 2005-08-11 | 2011-04-12 | Amylin Pharmaceuticals Inc | polipeptìdeos hìbridos com propriedades selecionáveis |
| EP2330124B1 (en) | 2005-08-11 | 2015-02-25 | Amylin Pharmaceuticals, LLC | Hybrid polypeptides with selectable properties |
| EP1921065B1 (en) | 2005-08-24 | 2010-10-20 | Banyu Pharmaceutical Co., Ltd. | Phenylpyridone derivative |
| WO2007029847A1 (ja) | 2005-09-07 | 2007-03-15 | Banyu Pharmaceutical Co., Ltd. | 二環性芳香族置換ピリドン誘導体 |
| BRPI0616463A2 (pt) | 2005-09-29 | 2011-06-21 | Merck & Co Inc | composto, composição farmacêutica, e, uso de um composto |
| WO2007048027A2 (en) | 2005-10-21 | 2007-04-26 | Novartis Ag | Combination of a renin-inhibitor and an anti-dyslipidemic agent and/or an antiobesity agent |
| AU2006307046A1 (en) | 2005-10-27 | 2007-05-03 | Msd K.K. | Novel benzoxathiin derivative |
| US8158791B2 (en) | 2005-11-10 | 2012-04-17 | Msd K.K. | Aza-substituted spiro derivatives |
| JP2009518351A (ja) | 2005-12-09 | 2009-05-07 | エフ.ホフマン−ラ ロシュ アーゲー | 肥満症の処置に有用な三環性アミド誘導体 |
| EP2742936A1 (en) | 2006-05-16 | 2014-06-18 | Takeda Pharmaceutical Company Limited | Fused heterocyclic compound and use thereof |
| JP5489333B2 (ja) | 2006-09-22 | 2014-05-14 | メルク・シャープ・アンド・ドーム・コーポレーション | 脂肪酸合成阻害剤を用いた治療の方法 |
| AU2007301126A1 (en) | 2006-09-28 | 2008-04-03 | Banyu Pharmaceutical Co., Ltd. | Diaryl ketimine derivative |
| CA2675638C (en) | 2007-01-16 | 2015-11-24 | Ipintl, Llc | Composition comprising serotonin for treating metabolic syndrome |
| CA2682727C (en) | 2007-04-02 | 2016-03-22 | Banyu Pharmaceutical Co., Ltd. | Indoledione derivative |
| EP2527360B1 (en) | 2007-06-04 | 2015-10-28 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
| US8969514B2 (en) | 2007-06-04 | 2015-03-03 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases |
| EP2789338A3 (en) | 2007-11-15 | 2015-01-14 | Takeda Pharmaceutical Company Limited | Condensed pyridine derivate and use thereof |
| US20110015181A1 (en) | 2008-03-06 | 2011-01-20 | Makoto Ando | Alkylaminopyridine derivative |
| EP2272841A1 (en) | 2008-03-28 | 2011-01-12 | Banyu Pharmaceutical Co., Ltd. | Diarylmethylamide derivative having antagonistic activity on melanin-concentrating hormone receptor |
| CA2666036C (en) | 2008-05-16 | 2017-09-12 | Chien-Hung Chen | Novel compositions and methods for treating hyperproliferative diseases |
| EP2810951B1 (en) | 2008-06-04 | 2017-03-15 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
| AU2009261248A1 (en) | 2008-06-19 | 2009-12-23 | Banyu Pharmaceutical Co., Ltd. | Spirodiamine-diarylketoxime derivative |
| EP3241839B1 (en) | 2008-07-16 | 2019-09-04 | Bausch Health Ireland Limited | Agonists of guanylate cyclase useful for the treatment of gastrointestinal, inflammation, cancer and other disorders |
| WO2010013595A1 (ja) | 2008-07-30 | 2010-02-04 | 萬有製薬株式会社 | 5員-5員又は5員-6員縮環シクロアルキルアミン誘導体 |
| WO2010047982A1 (en) | 2008-10-22 | 2010-04-29 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
| JP5635991B2 (ja) | 2008-10-30 | 2014-12-03 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | イソニコチンアミドオレキシン受容体アンタゴニスト |
| JP5557845B2 (ja) | 2008-10-31 | 2014-07-23 | メルク・シャープ・アンド・ドーム・コーポレーション | 糖尿病用剤として有用な新規環状ベンゾイミダゾール誘導体 |
| US20110245209A1 (en) | 2008-12-16 | 2011-10-06 | Schering Corporation | Pyridopyrimidine derivatives and methods of use thereof |
| WO2010075069A1 (en) | 2008-12-16 | 2010-07-01 | Schering Corporation | Bicyclic pyranone derivatives as nicotinic acid receptor agonists |
| JPWO2011071136A1 (ja) | 2009-12-11 | 2013-04-22 | アステラス製薬株式会社 | 線維筋痛症治療剤 |
| US8895596B2 (en) | 2010-02-25 | 2014-11-25 | Merck Sharp & Dohme Corp | Cyclic benzimidazole derivatives useful as anti-diabetic agents |
| US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
| BR112013021236B1 (pt) | 2011-02-25 | 2021-05-25 | Merck Sharp & Dohme Corp | composto derivado de benzimidazol, e, composição |
| ES2664873T3 (es) | 2011-03-01 | 2018-04-23 | Synergy Pharmaceuticals Inc. | Proceso de preparación de agonistas de guanilato ciclasa C |
| AR088352A1 (es) | 2011-10-19 | 2014-05-28 | Merck Sharp & Dohme | Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina |
| US9527875B2 (en) | 2012-08-02 | 2016-12-27 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
| WO2014139388A1 (en) | 2013-03-14 | 2014-09-18 | Merck Sharp & Dohme Corp. | Novel indole derivatives useful as anti-diabetic agents |
| CA2905435A1 (en) | 2013-03-15 | 2014-09-25 | Synergy Pharmaceuticals Inc. | Compositions useful for the treatment of gastrointestinal disorders |
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| SI3004138T1 (sl) | 2013-06-05 | 2024-07-31 | Bausch Health Ireland Limited | Ultra čisti agonisti gvanilat ciklaze C, postopek za njihovo pripravo in uporabo |
| KR102431436B1 (ko) | 2014-08-29 | 2022-08-10 | 테스 파마 에스.알.엘. | α-아미노-β-카복시뮤콘산 세미알데히드 데카복실라제의 억제제 |
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| EP3733204A4 (en) | 2017-12-27 | 2021-09-15 | Takeda Pharmaceutical Company Limited | THERAPEUTIC AGENT FOR URINARY INCONTINENCE OF STRESS AND FECAL INCONTINENCE |
| LT3810283T (lt) * | 2018-06-21 | 2023-08-25 | F. Hoffmann-La Roche Ag | 3-((1r,3r)-1-(2,6-difluor-4-((1-(3-fluorpropil)azetidin-3- il)amino) fenil)-3-metil-1,3,4,9-tetrahidro-2h-pirido[3,4-b]indol-2-il)- 2,2- difluorpropan-1-olio tartrato druskos kietosios formos, jų paruošimo procesas ir jų naudojimo būdai vėžiui gydyti |
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| CA1247547A (en) | 1983-06-22 | 1988-12-28 | Paul Hadvary | Leucine derivatives |
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| TW334423B (en) * | 1993-10-22 | 1998-06-21 | Hoffmann La Roche | Tricyclic 1-aminoethylpyrrole-derivatives |
| TW270114B (https=) | 1993-10-22 | 1996-02-11 | Hoffmann La Roche | |
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| US6004996A (en) | 1997-02-05 | 1999-12-21 | Hoffman-La Roche Inc. | Tetrahydrolipstatin containing compositions |
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| EP1132389A1 (en) * | 2000-03-06 | 2001-09-12 | Vernalis Research Limited | New aza-indolyl derivatives for the treatment of obesity |
-
2001
- 2001-12-14 WO PCT/EP2001/014781 patent/WO2002051844A1/en not_active Ceased
- 2001-12-14 BR BR0116605-0A patent/BR0116605A/pt not_active IP Right Cessation
- 2001-12-14 US US10/017,978 patent/US6610685B2/en not_active Expired - Fee Related
- 2001-12-14 KR KR10-2003-7008679A patent/KR100539143B1/ko not_active Expired - Fee Related
- 2001-12-14 AT AT01989597T patent/ATE369368T1/de not_active IP Right Cessation
- 2001-12-14 JP JP2002552939A patent/JP4094950B2/ja not_active Expired - Fee Related
- 2001-12-14 CN CNB018213510A patent/CN1250549C/zh not_active Expired - Fee Related
- 2001-12-14 AU AU2002228007A patent/AU2002228007B2/en not_active Ceased
- 2001-12-14 ES ES01989597T patent/ES2291374T3/es not_active Expired - Lifetime
- 2001-12-14 EP EP01989597A patent/EP1347979B1/en not_active Expired - Lifetime
- 2001-12-14 DE DE60129841T patent/DE60129841T2/de not_active Expired - Lifetime
- 2001-12-14 MX MXPA03005915A patent/MXPA03005915A/es active IP Right Grant
- 2001-12-14 CA CA002432085A patent/CA2432085C/en not_active Expired - Fee Related
- 2001-12-21 PE PE2001001298A patent/PE20020911A1/es not_active Application Discontinuation
- 2001-12-21 AR ARP010106000A patent/AR035722A1/es not_active Application Discontinuation
- 2001-12-26 UY UY27097A patent/UY27097A1/es not_active Application Discontinuation
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