JP2004517852A5 - - Google Patents
Download PDFInfo
- 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
Links
- 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 (enExample) | 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 (enExample) |
| EP (1) | EP1347979B1 (enExample) |
| JP (1) | JP4094950B2 (enExample) |
| KR (1) | KR100539143B1 (enExample) |
| CN (1) | CN1250549C (enExample) |
| AR (1) | AR035722A1 (enExample) |
| AT (1) | ATE369368T1 (enExample) |
| AU (1) | AU2002228007B2 (enExample) |
| BR (1) | BR0116605A (enExample) |
| CA (1) | CA2432085C (enExample) |
| DE (1) | DE60129841T2 (enExample) |
| ES (1) | ES2291374T3 (enExample) |
| MX (1) | MXPA03005915A (enExample) |
| PE (1) | PE20020911A1 (enExample) |
| UY (1) | UY27097A1 (enExample) |
| WO (1) | WO2002051844A1 (enExample) |
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2003243089B2 (en) | 2002-06-19 | 2010-01-07 | Biovitrum Ab (Publ) | Novel compounds, their use and preparation |
| 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 |
| JP4765627B2 (ja) | 2003-09-22 | 2011-09-07 | Ｍｓｄ株式会社 | 新規ピペリジン誘導体 |
| US20080125403A1 (en) | 2004-04-02 | 2008-05-29 | Merck & Co., Inc. | Method of Treating Men with Metabolic and Anthropometric Disorders |
| EP1792629A4 (en) | 2004-08-25 | 2010-08-25 | Takeda Pharmaceutical | MEANS FOR THE PREVENTION / TREATMENT OF STRESS-RELATED HARNINE INCONTINENCE AND PRECAUTIONARY METHOD FOR THIS |
| 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. |
| ES2325773T5 (es) | 2004-11-01 | 2014-02-24 | Amylin Pharmaceuticals, Llc. | Tratamiento de la obesidad y de los trastornos relacionados |
| US7737155B2 (en) | 2005-05-17 | 2010-06-15 | Schering Corporation | Nitrogen-containing heterocyclic compounds and methods of use thereof |
| US8138206B2 (en) | 2005-05-30 | 2012-03-20 | Msd. K.K. | Piperidine derivative |
| CA2618112A1 (en) | 2005-08-10 | 2007-02-15 | Banyu Pharmaceutical Co., Ltd. | Pyridone compound |
| AU2006279680B2 (en) | 2005-08-11 | 2012-12-06 | Amylin Pharmaceuticals, Llc | Hybrid polypeptides with selectable properties |
| BRPI0614649A2 (pt) | 2005-08-11 | 2011-04-12 | Amylin Pharmaceuticals Inc | polipeptìdeos hìbridos com propriedades selecionáveis |
| WO2007024004A1 (ja) | 2005-08-24 | 2007-03-01 | Banyu Pharmaceutical Co., Ltd. | フェニルピリドン誘導体 |
| AU2006288153A1 (en) | 2005-09-07 | 2007-03-15 | Msd K.K. | Bicyclic aromatic substituted pyridone derivative |
| KR20080048502A (ko) | 2005-09-29 | 2008-06-02 | 머크 앤드 캄파니 인코포레이티드 | 멜라노코르틴-4 수용체 조절제로서의 아실화스피로피페리딘 유도체 |
| RU2008119687A (ru) | 2005-10-21 | 2009-11-27 | Новартис АГ (CH) | Комбинации органических соединений |
| CA2627139A1 (en) | 2005-10-27 | 2007-05-03 | Banyu Pharmaceutical Co., Ltd. | Novel benzoxathiin derivative |
| ES2381205T3 (es) | 2005-11-10 | 2012-05-24 | Msd K.K. | Derivado espiro aza-sustituido |
| WO2007065820A1 (en) | 2005-12-09 | 2007-06-14 | F. Hoffmann-La Roche Ag | Tricyclic amide derivatives useful for treating obesity |
| 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 |
| WO2008047544A1 (en) | 2006-09-28 | 2008-04-24 | Banyu Pharmaceutical Co., Ltd. | Diaryl ketimine derivative |
| DK2118279T3 (en) | 2007-01-16 | 2018-02-26 | Ipintl Llc | HIS UNKNOWN COMPOSITION FOR TREATMENT OF METABOLIC SYNDROME |
| 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 |
| MX2009013293A (es) | 2007-06-04 | 2010-02-15 | Synergy Pharmaceuticals Inc | Agonistas de guanilato ciclasa útiles para el tratamiento de trastornos gastrointestinales, inflamación, cáncer y otros trastornos. |
| EP2216023A4 (en) | 2007-11-15 | 2013-03-13 | Takeda Pharmaceutical | CONDENSED PYRIDINE DERIVATIVE AND ITS USE |
| JPWO2009110510A1 (ja) | 2008-03-06 | 2011-07-14 | Ｍｓｄ株式会社 | アルキルアミノピリジン誘導体 |
| US20110015198A1 (en) | 2008-03-28 | 2011-01-20 | Banyu Pharmaceutical Co., Inc. | Diarylmethylamide derivative having melanin-concentrating hormone receptor antagonism |
| 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 |
| 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 |
| CA2730603C (en) | 2008-07-16 | 2019-09-24 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
| JPWO2010013595A1 (ja) | 2008-07-30 | 2012-01-12 | Ｍｓｄ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 |
| EP2348857B1 (en) | 2008-10-22 | 2016-02-24 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
| EP2350010B1 (en) | 2008-10-30 | 2014-03-26 | Merck Sharp & Dohme Corp. | Isonicotinamide orexin receptor antagonists |
| 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 |
| US20110243940A1 (en) | 2008-12-16 | 2011-10-06 | Schering Corporation | Bicyclic pyranone derivatives and methods of use thereof |
| 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 |
| AU2011218830B2 (en) | 2010-02-25 | 2014-07-24 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
| US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
| MX348131B (es) | 2011-02-25 | 2017-05-26 | Merck Sharp & Dohme | Novedosos derivados de azabencimidazol ciclico utiles como agentes antidiabeticos. |
| CA3100941C (en) | 2011-03-01 | 2024-03-05 | Synergy Pharmaceuticals Inc. | Process of preparing guanylate cyclase c agonists |
| AR088352A1 (es) | 2011-10-19 | 2014-05-28 | Merck Sharp & Dohme | Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina |
| WO2014022528A1 (en) | 2012-08-02 | 2014-02-06 | 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 |
| JP2016514671A (ja) | 2013-03-15 | 2016-05-23 | シナジー ファーマシューティカルズ インコーポレイテッド | グアニル酸シクラーゼのアゴニストおよびその使用 |
| JP2016514670A (ja) | 2013-03-15 | 2016-05-23 | シナジー ファーマシューティカルズ インコーポレイテッド | 他の薬物と組み合わせたグアニル酸シクラーゼ受容体アゴニスト |
| EA201592263A1 (ru) | 2013-06-05 | 2016-05-31 | Синерджи Фармасьютикалз, Инк. | Ультрачистые агонисты гуанилатциклазы c, способ их получения и использования |
| EP3186242B1 (en) | 2014-08-29 | 2021-10-06 | Tes Pharma S.r.l. | Inhibitors of alpha-amino-beta-carboxymuconic acid semialdehyde decarboxylase |
| AU2017342083A1 (en) | 2016-10-14 | 2019-04-11 | Tes Pharma S.R.L. | Inhibitors of alpha-amino-beta-carboxymuconic acid semialdehyde decarboxylase |
| JPWO2019131902A1 (ja) | 2017-12-27 | 2020-12-10 | 武田薬品工業株式会社 | 腹圧性尿失禁および便失禁の治療薬 |
| TWI915239B (zh) * | 2018-06-21 | 2026-02-11 | 瑞士商赫孚孟拉羅股份公司 | 3-((1r,3r)-1-(2,6-二氟-4-((1-(3-氟丙基)氮雜環丁-3-基)胺基)苯基)-3-甲基-1,3,4,9-四氫-2h-吡啶并[3,4-b]吲哚-2-基)-2,2-二氟丙-1-醇之固體形式及用於製備包含經取代苯基或吡啶基部分之稠合三環化合物之製程，包括其使用方法 |
| AR117122A1 (es) | 2018-11-20 | 2021-07-14 | Tes Pharma S R L | INHIBIDORES DE LA ÁCIDO a-AMINO-b-CARBOXIMUCÓNICO SEMIALDEHÍDO DESCARBOXILASA |
| TW202045476A (zh) | 2019-02-13 | 2020-12-16 | 美商默沙東藥廠 | 5-烷基吡咯啶食慾素受體促效劑 |
| EP3923933A4 (en) | 2019-02-13 | 2022-08-17 | Merck Sharp & Dohme Corp. | PYRROLIDINOREXINE RECEPTOR AGONISTS |
| WO2021026047A1 (en) | 2019-08-08 | 2021-02-11 | Merck Sharp & Dohme Corp. | Heteroaryl pyrrolidine and piperidine orexin receptor agonists |
| MX2023001840A (es) | 2020-08-18 | 2023-03-13 | Merck Sharp & Dohme Llc | Agonistas de bicicloheptano pirrolidina de los receptores de orexina. |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1247547A (en) | 1983-06-22 | 1988-12-28 | Paul Hadvary | Leucine derivatives |
| CA1270837A (en) | 1984-12-21 | 1990-06-26 | Hoffmann-La Roche Limited | Oxetanones |
| CA1328881C (en) | 1984-12-21 | 1994-04-26 | Pierre Barbier | Process for the manufacture of 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 (enExample) | 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 |
| DE69916288T2 (de) | 1998-08-14 | 2005-03-24 | F. Hoffmann-La Roche Ag | Lipasehemmer und chitosan enthaltende arzneimittel |
| BR9912980B1 (pt) | 1998-08-14 | 2013-10-22 | Composição farmacêutica administrável oralmente, tablete de mascar contendo a mesma e utilização da mesma | |
| GB9819035D0 (en) * | 1998-09-01 | 1998-10-28 | Cerebrus Res Ltd | Chemical compounds VII |
| IL143323A0 (en) * | 1998-12-17 | 2002-04-21 | American Home Prod | 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 EP EP01989597A patent/EP1347979B1/en not_active Expired - Lifetime
- 2001-12-14 AU AU2002228007A patent/AU2002228007B2/en not_active Ceased
- 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
- 2001-12-14 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 US US10/017,978 patent/US6610685B2/en not_active Expired - Fee Related
- 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 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 WO PCT/EP2001/014781 patent/WO2002051844A1/en not_active Ceased
- 2001-12-14 AT AT01989597T patent/ATE369368T1/de not_active IP Right Cessation
- 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
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2005521671A5 (enExample) | ||
| AU2018282336B2 (en) | Trk-inhibiting compound | |
| AU2014337298B2 (en) | Hepatitis B viral assembly effectors | |
| JP5952917B2 (ja) | ベンゾチオフェン化合物又はその塩の、二水和物、及びその製造方法 | |
| TWI568728B (zh) | 雜環化合物及彼之用途 | |
| JP2009538867A5 (enExample) | ||
| JP5654559B2 (ja) | キナゾリンジオン誘導体の治療での使用 | |
| JP2012526735A5 (enExample) | ||
| CN101263130A (zh) | 2-苯胺-4-芳基取代的噻唑衍生物 | |
| AR059183A1 (es) | Uso de derivados de 2- imidazol o imidazolina sustituidos para preparar medicamentos | |
| CN102639530A (zh) | 作为α7正向变构调节剂的吗啉代噻唑 | |
| JP2011509297A5 (enExample) | ||
| CN1706813A (zh) | 含长链脂肪酰基取代的文拉法辛前体药物及其制备方法和用途 | |
| CN1201461A (zh) | 用作神经递质重摄取抑制剂的稠合莨菪烷衍生物 | |
| US11390623B2 (en) | 6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine dopamine D3 ligands | |
| JP5564101B2 (ja) | キナゾリンジオン誘導体、その調製およびその様々な治療上の使用 | |
| CN1545411A (zh) | 环丙基和环丁基埃坡霉素类似物 | |
| EP2203438A1 (en) | Cyanoisoquinoline | |
| JP2019537590A5 (enExample) | ||
| JP5822079B2 (ja) | 疼痛治療剤 | |
| RU2011103759A (ru) | Замещенные 6-(1-пиперазинил)-пиридазины в качестве антагонистов 5-нт6 рецептора | |
| JP2008543782A (ja) | ５−ｈｔ１ａ受容体のピペラジン−ピペリジンアンタゴニストおよびアゴニスト | |
| JP2011116663A (ja) | ベンゾジアゼピン化合物 | |
| JP2008523075A5 (enExample) | ||
| JP2014508178A5 (enExample) |