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 (2) | 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 (2) |
| EP (1) | EP1347979B1 (2) |
| JP (1) | JP4094950B2 (2) |
| KR (1) | KR100539143B1 (2) |
| CN (1) | CN1250549C (2) |
| AR (1) | AR035722A1 (2) |
| AT (1) | ATE369368T1 (2) |
| AU (1) | AU2002228007B2 (2) |
| BR (1) | BR0116605A (2) |
| CA (1) | CA2432085C (2) |
| DE (1) | DE60129841T2 (2) |
| ES (1) | ES2291374T3 (2) |
| MX (1) | MXPA03005915A (2) |
| PE (1) | PE20020911A1 (2) |
| UY (1) | UY27097A1 (2) |
| WO (1) | WO2002051844A1 (2) |
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4460450B2 (ja) | 2002-06-19 | 2010-05-12 | ビオヴィトルム・アクチボラゲット(プブリクト) | 新規化合物、その使用および製造法 |
| 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 |
| ATE547404T1 (de) | 2003-09-22 | 2012-03-15 | Msd Kk | Piperidinderivate |
| EP1734963A4 (en) | 2004-04-02 | 2008-06-18 | Merck & Co Inc | METHOD FOR TREATING PEOPLE WITH METABOLIC AND ANTHROPOMETRIC DISORDER |
| JP5173190B2 (ja) | 2004-08-25 | 2013-03-27 | 武田薬品工業株式会社 | 腹圧性尿失禁の予防・治療剤及びそのスクリーニング方法 |
| US8394765B2 (en) | 2004-11-01 | 2013-03-12 | Amylin Pharmaceuticals Llc | Methods of treating obesity with two different anti-obesity agents |
| MX2007005199A (es) * | 2004-11-01 | 2007-05-11 | Wyeth Corp | Indolizinas sustituidas y derivados como agentes del sistema nervioso central. |
| CN101094689B (zh) | 2004-11-01 | 2013-06-12 | 安米林药品有限责任公司 | 治疗肥胖以及肥胖相关疾病和病症的方法 |
| WO2007022123A2 (en) | 2005-08-11 | 2007-02-22 | Amylin Pharmaceuticals, Inc. | Hybrid polypeptides with selectable properties |
| US7737155B2 (en) | 2005-05-17 | 2010-06-15 | Schering Corporation | Nitrogen-containing heterocyclic compounds and methods of use thereof |
| BRPI0610580B8 (pt) | 2005-05-30 | 2021-05-25 | Banyu Pharma Co Ltd | composto derivado de piperidina |
| JPWO2007018248A1 (ja) | 2005-08-10 | 2009-02-19 | 萬有製薬株式会社 | ピリドン化合物 |
| EP2330125A3 (en) | 2005-08-11 | 2012-12-12 | Amylin Pharmaceuticals, Inc. | Hybrid polypeptides with selectable properties |
| WO2007024004A1 (ja) | 2005-08-24 | 2007-03-01 | Banyu Pharmaceutical Co., Ltd. | フェニルピリドン誘導体 |
| 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 |
| EP1940842B1 (en) | 2005-09-29 | 2012-05-30 | Merck Sharp & Dohme Corp. | Acylated spiropiperidine derivatives as melanocortin-4 receptor modulators |
| JP2009512715A (ja) | 2005-10-21 | 2009-03-26 | ノバルティス アクチエンゲゼルシャフト | レニン阻害剤と抗異脂肪血症剤および/または抗肥満症剤の組み合わせ |
| EP1944301A4 (en) | 2005-10-27 | 2012-01-04 | Msd Kk | NEW BENZOXATHIIN DERIVATIVES |
| ES2381205T3 (es) | 2005-11-10 | 2012-05-24 | Msd K.K. | Derivado espiro aza-sustituido |
| DE602006010433D1 (de) | 2005-12-09 | 2009-12-24 | Hoffmann La Roche | Für die behandlung von obesitas geeignete tricyclische amidderivate |
| EP2727585A1 (en) | 2006-05-16 | 2014-05-07 | Takeda Pharmaceutical Company Limited | In-vivo screening method |
| US8173629B2 (en) | 2006-09-22 | 2012-05-08 | Merck Sharp & Dohme Corp. | Method of treatment using fatty acid synthesis inhibitors |
| US20090247560A1 (en) | 2006-09-28 | 2009-10-01 | Banyu Pharmaceutical Co., Ltd. | Diaryl ketimine derivative |
| ES2660173T3 (es) | 2007-01-16 | 2018-03-21 | Ipintl, Llc | Nueva composición para el tratamiento del síndrome metabólico |
| JP5319518B2 (ja) | 2007-04-02 | 2013-10-16 | Msd株式会社 | インドールジオン誘導体 |
| 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 |
| MX354786B (es) | 2007-06-04 | 2018-03-21 | Synergy Pharmaceuticals Inc | Agonistas de guanilato ciclasa utiles para el tratamiento de trastornos gastrointestinales, inflamacion, cancer y otros trastornos. |
| EP2789338A3 (en) | 2007-11-15 | 2015-01-14 | Takeda Pharmaceutical Company Limited | Condensed pyridine derivate and use thereof |
| EP2264026A4 (en) | 2008-03-06 | 2012-03-28 | Msd Kk | ALKYLAMINOPYRIDINDERIVATE |
| WO2009119726A1 (ja) | 2008-03-28 | 2009-10-01 | 萬有製薬株式会社 | メラニン凝集ホルモン受容体拮抗作用を有するジアリールメチルアミド誘導体 |
| CA2666036C (en) | 2008-05-16 | 2017-09-12 | Chien-Hung Chen | Novel compositions and methods for treating hyperproliferative diseases |
| ES2522968T3 (es) | 2008-06-04 | 2014-11-19 | Synergy Pharmaceuticals Inc. | Agonistas de guanilato ciclasa útiles para el tratamiento de trastornos gastrointestinales, inflamación, cáncer y otros trastornos |
| JPWO2009154132A1 (ja) | 2008-06-19 | 2011-12-01 | Msd株式会社 | スピロジアミン−ジアリールケトオキシム誘導体 |
| AU2009270833B2 (en) | 2008-07-16 | 2015-02-19 | Bausch Health Ireland Limited | Agonists of guanylate cyclase useful for the treatment of gastrointestinal, inflammation, cancer and other disorders |
| EP2319841A1 (en) | 2008-07-30 | 2011-05-11 | Msd K.K. | (5-membered)-(5-membered) or (5-membered)-(6-membered) fused ring cycloalkylamine derivative |
| EP2348857B1 (en) | 2008-10-22 | 2016-02-24 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
| MX2011004551A (es) | 2008-10-30 | 2011-05-25 | Merck Sharp & Dohme | Antagonistas del receptor de orexina de isonicotinamida. |
| US8329914B2 (en) | 2008-10-31 | 2012-12-11 | Merck Sharp & Dohme Corp | Cyclic benzimidazole derivatives useful as anti-diabetic agents |
| US20110243940A1 (en) | 2008-12-16 | 2011-10-06 | Schering Corporation | Bicyclic pyranone derivatives and methods of use thereof |
| EP2379547A1 (en) | 2008-12-16 | 2011-10-26 | Schering Corporation | Pyridopyrimidine derivatives and methods of use thereof |
| EP2510949A4 (en) | 2009-12-11 | 2013-11-13 | Astellas Pharma Inc | THERAPEUTICS FOR FIBROMYALGIA |
| JP2013520502A (ja) | 2010-02-25 | 2013-06-06 | メルク・シャープ・エンド・ドーム・コーポレイション | 有用な抗糖尿病薬である新規な環状ベンズイミダゾール誘導体 |
| US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
| SG192941A1 (en) | 2011-02-25 | 2013-09-30 | Merck Sharp & Dohme | Novel cyclic azabenzimidazole derivatives useful as anti-diabetic agents |
| DK2681236T3 (en) | 2011-03-01 | 2018-04-16 | Synergy Pharmaceuticals Inc | PROCEDURE FOR MANUFACTURING GUANYLATE CYCLASE-C-AGONISTS |
| AR088352A1 (es) | 2011-10-19 | 2014-05-28 | Merck Sharp & Dohme | Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina |
| RU2015106909A (ru) | 2012-08-02 | 2016-09-27 | Мерк Шарп И Доум Корп. | Антидиабетические трициклические соединения |
| WO2014139388A1 (en) | 2013-03-14 | 2014-09-18 | Merck Sharp & Dohme Corp. | Novel indole derivatives useful as anti-diabetic agents |
| AU2014235209B2 (en) | 2013-03-15 | 2018-06-14 | Bausch Health Ireland Limited | Guanylate cyclase receptor agonists combined with other drugs |
| AU2014235215A1 (en) | 2013-03-15 | 2015-10-01 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase and their uses |
| BR112015030326A2 (pt) | 2013-06-05 | 2017-08-29 | Synergy Pharmaceuticals Inc | Agonistas ultrapuros de guanilato ciclase c, método de fabricar e usar os mesmos |
| KR102431436B1 (ko) | 2014-08-29 | 2022-08-10 | 테스 파마 에스.알.엘. | α-아미노-β-카복시뮤콘산 세미알데히드 데카복실라제의 억제제 |
| WO2018069532A1 (en) | 2016-10-14 | 2018-04-19 | Tes Pharma S.R.L. | Inhibitors of alpha-amino-beta-carboxymuconic acid semialdehyde decarboxylase |
| US20210052600A1 (en) | 2017-12-27 | 2021-02-25 | Takeda Pharmaceutical Company Limited | Therapeutic agents for stress urinary incontinence and incotinence of feces |
| CR20200621A (es) * | 2018-06-21 | 2021-02-03 | Hoffmann La Roche | Formas sólidas de 3-((1r,3r)-1-(2,6-difluoro-4-((1-(3 fluoropropil)azetidin-3-il)amino)fenil)-3-(metil-1,3,4,9-tetrahidro-2h-pirido[3,4-b]indol-2-il)-2,2-difluoropropan-1-ol y procesos para preparar compuestos tricíclicos fusionados que comprenden un resto fenilo o piridinilo sustituido, incluidos métodos para su uso |
| AR117122A1 (es) | 2018-11-20 | 2021-07-14 | Tes Pharma S R L | INHIBIDORES DE LA ÁCIDO a-AMINO-b-CARBOXIMUCÓNICO SEMIALDEHÍDO DESCARBOXILASA |
| US11098029B2 (en) | 2019-02-13 | 2021-08-24 | Merck Sharp & Dohme Corp. | 5-alkyl pyrrolidine orexin receptor agonists |
| WO2020167701A1 (en) | 2019-02-13 | 2020-08-20 | Merck Sharp & Dohme Corp. | Pyrrolidine orexin receptor agonists |
| WO2021026047A1 (en) | 2019-08-08 | 2021-02-11 | Merck Sharp & Dohme Corp. | Heteroaryl pyrrolidine and piperidine orexin receptor agonists |
| BR112023002957A2 (pt) | 2020-08-18 | 2023-04-04 | Merck Sharp & Dohme Llc | Composto, composição farmacêutica, e, métodos para tratar narcolepsia e para tratar hipersonia em um sujeito mamífero |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1247547A (en) | 1983-06-22 | 1988-12-28 | Paul Hadvary | Leucine derivatives |
| CA1328881C (en) | 1984-12-21 | 1994-04-26 | Pierre Barbier | Process for the manufacture of oxetanones |
| CA1270837A (en) | 1984-12-21 | 1990-06-26 | Hoffmann-La Roche Limited | Oxetanones |
| CA2035972C (en) | 1990-02-23 | 2006-07-11 | Martin Karpf | Process for the preparation of oxetanones |
| US5274143A (en) | 1991-07-23 | 1993-12-28 | Hoffmann-La Roche Inc. | Process for the preparation of (R)-3-hexyl-5,6-dihydro-4-hydroxy-6-undecyl-2H-pyran-2-one and (R)-5,6-dihydro-6-undecyl-2H-pyran-2,4(3H)-dione |
| TW270114B (2) | 1993-10-22 | 1996-02-11 | Hoffmann La Roche | |
| TW334423B (en) * | 1993-10-22 | 1998-06-21 | Hoffmann La Roche | Tricyclic 1-aminoethylpyrrole-derivatives |
| WO1998030548A1 (en) | 1997-01-13 | 1998-07-16 | Yamanouchi Pharmaceutical Co., Ltd. | 5-HT2c RECEPTOR AGONISTS AND AMINOALKYLINDAZOLE DERIVATIVES |
| US6004996A (en) | 1997-02-05 | 1999-12-21 | Hoffman-La Roche Inc. | Tetrahydrolipstatin containing compositions |
| US6267952B1 (en) | 1998-01-09 | 2001-07-31 | Geltex Pharmaceuticals, Inc. | Lipase inhibiting polymers |
| TR200100471T2 (tr) | 1998-08-14 | 2001-07-23 | F.Hoffmann-La Roche Ag | Lipaz inhibitörleri içeren farmasötik bileşimler |
| WO2000009123A1 (en) | 1998-08-14 | 2000-02-24 | F. Hoffmann-La Roche Ag | Pharmaceutical compositions containing lipase inhibitors and chitosan |
| GB9819035D0 (en) * | 1998-09-01 | 1998-10-28 | Cerebrus Res Ltd | Chemical compounds VII |
| NZ512765A (en) | 1998-12-17 | 2003-10-31 | Wyeth Corp | 2,3,4,4A-tetrahydro-1H-pyrazino(1,2-A)quinoxalin- 5(6H)one derivatives being 5HT2C agonists |
| EP1132389A1 (en) * | 2000-03-06 | 2001-09-12 | Vernalis Research Limited | New aza-indolyl derivatives for the treatment of obesity |
-
2001
- 2001-12-14 KR KR10-2003-7008679A patent/KR100539143B1/ko not_active Expired - Fee Related
- 2001-12-14 DE DE60129841T patent/DE60129841T2/de not_active Expired - Lifetime
- 2001-12-14 AT AT01989597T patent/ATE369368T1/de not_active IP Right Cessation
- 2001-12-14 WO PCT/EP2001/014781 patent/WO2002051844A1/en not_active Ceased
- 2001-12-14 AU AU2002228007A patent/AU2002228007B2/en not_active Ceased
- 2001-12-14 JP JP2002552939A patent/JP4094950B2/ja not_active Expired - Fee Related
- 2001-12-14 ES ES01989597T patent/ES2291374T3/es not_active Expired - Lifetime
- 2001-12-14 CA CA002432085A patent/CA2432085C/en not_active Expired - Fee Related
- 2001-12-14 US US10/017,978 patent/US6610685B2/en not_active Expired - Fee Related
- 2001-12-14 EP EP01989597A patent/EP1347979B1/en not_active Expired - Lifetime
- 2001-12-14 CN CNB018213510A patent/CN1250549C/zh not_active Expired - Fee Related
- 2001-12-14 BR BR0116605-0A patent/BR0116605A/pt not_active IP Right Cessation
- 2001-12-14 MX MXPA03005915A patent/MXPA03005915A/es active IP Right Grant
- 2001-12-21 AR ARP010106000A patent/AR035722A1/es not_active Application Discontinuation
- 2001-12-21 PE PE2001001298A patent/PE20020911A1/es not_active Application Discontinuation
- 2001-12-26 UY UY27097A patent/UY27097A1/es not_active Application Discontinuation
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