JP2010536734A5 - - Google Patents
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- JP2010536734A5 JP2010536734A5 JP2010520595A JP2010520595A JP2010536734A5 JP 2010536734 A5 JP2010536734 A5 JP 2010536734A5 JP 2010520595 A JP2010520595 A JP 2010520595A JP 2010520595 A JP2010520595 A JP 2010520595A JP 2010536734 A5 JP2010536734 A5 JP 2010536734A5
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- Prior art keywords
- methyl
- pharmaceutical composition
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- inhibitor
- amino
- Prior art date
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- 239000008194 pharmaceutical composition Substances 0.000 claims 20
- -1 methoxy, trifluoromethoxy, ethoxy, ethyl Chemical group 0.000 claims 14
- 239000003112 inhibitor Substances 0.000 claims 12
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims 11
- 239000008103 glucose Substances 0.000 claims 11
- 108010067722 Dipeptidyl Peptidase 4 Proteins 0.000 claims 10
- 102100025012 Dipeptidyl peptidase 4 Human genes 0.000 claims 10
- 229940123518 Sodium/glucose cotransporter 2 inhibitor Drugs 0.000 claims 9
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 8
- 210000002237 B-cell of pancreatic islet Anatomy 0.000 claims 6
- 206010022489 Insulin Resistance Diseases 0.000 claims 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 6
- 239000008280 blood Substances 0.000 claims 5
- 210000004369 blood Anatomy 0.000 claims 5
- 208000024891 symptom Diseases 0.000 claims 5
- 208000004611 Abdominal Obesity Diseases 0.000 claims 4
- 208000002705 Glucose Intolerance Diseases 0.000 claims 4
- 208000001145 Metabolic Syndrome Diseases 0.000 claims 4
- 208000008589 Obesity Diseases 0.000 claims 4
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- 230000006870 function Effects 0.000 claims 4
- 230000002641 glycemic effect Effects 0.000 claims 4
- 201000001421 hyperglycemia Diseases 0.000 claims 4
- 235000020824 obesity Nutrition 0.000 claims 4
- 201000009104 prediabetes syndrome Diseases 0.000 claims 4
- 239000012453 solvate Substances 0.000 claims 4
- 206010033307 Overweight Diseases 0.000 claims 3
- 230000001771 impaired effect Effects 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 230000000291 postprandial effect Effects 0.000 claims 3
- 206010003210 Arteriosclerosis Diseases 0.000 claims 2
- XTNGUQKDFGDXSJ-ZXGKGEBGSA-N Canagliflozin Chemical compound CC1=CC=C([C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)C=C1CC(S1)=CC=C1C1=CC=C(F)C=C1 XTNGUQKDFGDXSJ-ZXGKGEBGSA-N 0.000 claims 2
- 208000002177 Cataract Diseases 0.000 claims 2
- 206010065941 Central obesity Diseases 0.000 claims 2
- JVHXJTBJCFBINQ-ADAARDCZSA-N Dapagliflozin Chemical compound C1=CC(OCC)=CC=C1CC1=CC([C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)=CC=C1Cl JVHXJTBJCFBINQ-ADAARDCZSA-N 0.000 claims 2
- 102000017011 Glycated Hemoglobin A Human genes 0.000 claims 2
- 108010014663 Glycated Hemoglobin A Proteins 0.000 claims 2
- 206010060378 Hyperinsulinaemia Diseases 0.000 claims 2
- 208000033463 Ischaemic neuropathy Diseases 0.000 claims 2
- 206010054805 Macroangiopathy Diseases 0.000 claims 2
- 208000030831 Peripheral arterial occlusive disease Diseases 0.000 claims 2
- 208000017442 Retinal disease Diseases 0.000 claims 2
- 206010038923 Retinopathy Diseases 0.000 claims 2
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims 2
- 230000002159 abnormal effect Effects 0.000 claims 2
- 238000009825 accumulation Methods 0.000 claims 2
- 208000011775 arteriosclerosis disease Diseases 0.000 claims 2
- 230000036765 blood level Effects 0.000 claims 2
- 230000003915 cell function Effects 0.000 claims 2
- 229960003834 dapagliflozin Drugs 0.000 claims 2
- 230000007423 decrease Effects 0.000 claims 2
- 230000007850 degeneration Effects 0.000 claims 2
- 206010012601 diabetes mellitus Diseases 0.000 claims 2
- 208000035475 disorder Diseases 0.000 claims 2
- 239000002552 dosage form Substances 0.000 claims 2
- 230000003451 hyperinsulinaemic effect Effects 0.000 claims 2
- 201000008980 hyperinsulinism Diseases 0.000 claims 2
- 230000003914 insulin secretion Effects 0.000 claims 2
- 208000028867 ischemia Diseases 0.000 claims 2
- 208000017169 kidney disease Diseases 0.000 claims 2
- 210000004185 liver Anatomy 0.000 claims 2
- 208000030159 metabolic disease Diseases 0.000 claims 2
- XZWYZXLIPXDOLR-UHFFFAOYSA-N metformin Chemical compound CN(C)C(=N)NC(N)=N XZWYZXLIPXDOLR-UHFFFAOYSA-N 0.000 claims 2
- 229960003105 metformin Drugs 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 208000010125 myocardial infarction Diseases 0.000 claims 2
- 229950011516 remogliflozin etabonate Drugs 0.000 claims 2
- 238000009097 single-agent therapy Methods 0.000 claims 2
- 208000023516 stroke disease Diseases 0.000 claims 2
- 230000004584 weight gain Effects 0.000 claims 2
- 235000019786 weight gain Nutrition 0.000 claims 2
- 230000004580 weight loss Effects 0.000 claims 2
- DNLMJEXNHFAGLZ-YMQHIKHWSA-N (2r,3r,4s,5s,6r)-2-[4-chloro-3-[(4-ethylphenyl)methyl]phenyl]-6-(hydroxymethyl)oxane-2,3,4,5-tetrol Chemical compound C1=CC(CC)=CC=C1CC1=CC([C@]2(O)[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)=CC=C1Cl DNLMJEXNHFAGLZ-YMQHIKHWSA-N 0.000 claims 1
- AGJJCLBOHJQGFA-ZQGJOIPISA-N (2s,3r,4r,5s,6r)-2-[5-(azulen-2-ylmethyl)-2-hydroxyphenyl]-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1C1=CC(CC=2C=C3C=CC=CC=C3C=2)=CC=C1O AGJJCLBOHJQGFA-ZQGJOIPISA-N 0.000 claims 1
- HAKJUVBTRWXTRU-QGZVFWFLSA-N 2-[(3r)-3-aminopiperidin-1-yl]-3-but-2-ynyl-5-[(4-methylquinazolin-2-yl)methyl]imidazo[4,5-d]pyridazin-4-one Chemical compound N=1C=2C=NN(CC=3N=C4C=CC=CC4=C(C)N=3)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 HAKJUVBTRWXTRU-QGZVFWFLSA-N 0.000 claims 1
- ZOTODWFVYUPZFO-GOSISDBHSA-N 2-[[8-[(3r)-3-aminopiperidin-1-yl]-7-but-2-ynyl-3-methyl-2,6-dioxopurin-1-yl]methyl]benzonitrile Chemical compound O=C1C=2N(CC#CC)C(N3C[C@H](N)CCC3)=NC=2N(C)C(=O)N1CC1=CC=CC=C1C#N ZOTODWFVYUPZFO-GOSISDBHSA-N 0.000 claims 1
- ISVBJQYIQQKSGK-MRXNPFEDSA-N 2-[[8-[(3r)-3-aminopiperidin-1-yl]-7-but-2-ynyl-3-methyl-2,6-dioxopurin-1-yl]methyl]pyridine-3-carbonitrile Chemical compound O=C1C=2N(CC#CC)C(N3C[C@H](N)CCC3)=NC=2N(C)C(=O)N1CC1=NC=CC=C1C#N ISVBJQYIQQKSGK-MRXNPFEDSA-N 0.000 claims 1
- HDARIOSGMVVPLE-LJQANCHMSA-N 2-[[8-[(3r)-3-aminopiperidin-1-yl]-7-but-2-ynyl-3-methyl-2,6-dioxopurin-1-yl]methyl]quinoline-3-carbonitrile Chemical compound N=1C=2N(C)C(=O)N(CC=3C(=CC4=CC=CC=C4N=3)C#N)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 HDARIOSGMVVPLE-LJQANCHMSA-N 0.000 claims 1
- BNPBEDWUQOSRHB-UHFFFAOYSA-N 8-[(2-amino-2-methylpropyl)-methylamino]-7-but-2-ynyl-3-methyl-1-[(4-methylquinazolin-2-yl)methyl]purine-2,6-dione Chemical compound C1=CC=CC2=NC(CN3C(=O)N(C)C=4N=C(N(C=4C3=O)CC#CC)N(C)CC(C)(C)N)=NC(C)=C21 BNPBEDWUQOSRHB-UHFFFAOYSA-N 0.000 claims 1
- ONMDRNPIEXAJEZ-MRXNPFEDSA-N 8-[(3r)-3-aminopiperidin-1-yl]-7-but-2-ynyl-1-[(4,6-dimethylpyrimidin-2-yl)methyl]-3-methylpurine-2,6-dione Chemical compound O=C1C=2N(CC#CC)C(N3C[C@H](N)CCC3)=NC=2N(C)C(=O)N1CC1=NC(C)=CC(C)=N1 ONMDRNPIEXAJEZ-MRXNPFEDSA-N 0.000 claims 1
- ILTRPILDWNCOMQ-QGZVFWFLSA-N 8-[(3r)-3-aminopiperidin-1-yl]-7-but-2-ynyl-3-methyl-1-(quinazolin-2-ylmethyl)purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3N=C4C=CC=CC4=CN=3)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 ILTRPILDWNCOMQ-QGZVFWFLSA-N 0.000 claims 1
- GFMVACPPQCXLGW-QGZVFWFLSA-N 8-[(3r)-3-aminopiperidin-1-yl]-7-but-2-ynyl-3-methyl-1-(quinoxalin-6-ylmethyl)purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C=C4N=CC=NC4=CC=3)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 GFMVACPPQCXLGW-QGZVFWFLSA-N 0.000 claims 1
- YLTXBUGZVMPESA-OAHLLOKOSA-N 8-[(3r)-3-aminopiperidin-1-yl]-7-but-2-ynyl-3-methyl-1-[(4-methylpyrimidin-2-yl)methyl]purine-2,6-dione Chemical compound O=C1C=2N(CC#CC)C(N3C[C@H](N)CCC3)=NC=2N(C)C(=O)N1CC1=NC=CC(C)=N1 YLTXBUGZVMPESA-OAHLLOKOSA-N 0.000 claims 1
- OWVQLTBTGFYAHU-HNNXBMFYSA-N 8-[[(2s)-2-aminopropyl]-methylamino]-7-but-2-ynyl-3-methyl-1-[(4-methylquinazolin-2-yl)methyl]purine-2,6-dione Chemical compound C1=CC=CC2=NC(CN3C(=O)N(C)C=4N=C(N(C=4C3=O)CC#CC)N(C)C[C@H](C)N)=NC(C)=C21 OWVQLTBTGFYAHU-HNNXBMFYSA-N 0.000 claims 1
- 102100036966 Dipeptidyl aminopeptidase-like protein 6 Human genes 0.000 claims 1
- 101710092625 Dipeptidyl aminopeptidase-like protein 6 Proteins 0.000 claims 1
- 108010023302 HDL Cholesterol Proteins 0.000 claims 1
- LTXREWYXXSTFRX-QGZVFWFLSA-N Linagliptin Chemical compound N=1C=2N(C)C(=O)N(CC=3N=C4C=CC=CC4=C(C)N=3)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 LTXREWYXXSTFRX-QGZVFWFLSA-N 0.000 claims 1
- GSINGUMRKGRYJP-VZWAGXQNSA-N Remogliflozin Chemical compound C1=CC(OC(C)C)=CC=C1CC1=C(C)N(C(C)C)N=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 GSINGUMRKGRYJP-VZWAGXQNSA-N 0.000 claims 1
- QLXKHBNJTPICNF-QMCAAQAGSA-N Sergliflozin etabonate Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](COC(=O)OCC)O[C@H]1OC1=CC=CC=C1CC1=CC=C(OC)C=C1 QLXKHBNJTPICNF-QMCAAQAGSA-N 0.000 claims 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims 1
- 230000037396 body weight Effects 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 230000035487 diastolic blood pressure Effects 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical group C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims 1
- 150000004677 hydrates Chemical class 0.000 claims 1
- AHFWIQIYAXSLBA-RQXATKFSSA-N ipragliflozin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1C1=CC=C(F)C(CC=2SC3=CC=CC=C3C=2)=C1 AHFWIQIYAXSLBA-RQXATKFSSA-N 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000006504 o-cyanobenzyl group Chemical group [H]C1=C([H])C(C#N)=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 230000001737 promoting effect Effects 0.000 claims 1
- UAOCLDQAQNNEAX-ABMICEGHSA-N remogliflozin etabonate Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](COC(=O)OCC)O[C@H]1OC1=NN(C(C)C)C(C)=C1CC1=CC=C(OC(C)C)C=C1 UAOCLDQAQNNEAX-ABMICEGHSA-N 0.000 claims 1
- 229940126842 sergliflozin Drugs 0.000 claims 1
- HFLCZNNDZKKXCS-OUUBHVDSSA-N sergliflozin Chemical compound C1=CC(OC)=CC=C1CC1=CC=CC=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HFLCZNNDZKKXCS-OUUBHVDSSA-N 0.000 claims 1
- 229950000378 sergliflozin etabonate Drugs 0.000 claims 1
- 210000002966 serum Anatomy 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 230000035488 systolic blood pressure Effects 0.000 claims 1
- 238000011287 therapeutic dose Methods 0.000 claims 1
- 150000003577 thiophenes Chemical class 0.000 claims 1
- 150000003626 triacylglycerols Chemical class 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 229940075420 xanthine Drugs 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07114458 | 2007-08-16 | ||
| EP07114458.8 | 2007-08-16 | ||
| PCT/EP2008/060744 WO2009022010A1 (en) | 2007-08-16 | 2008-08-15 | Pharmaceutical composition comprising a sglt2 inhibitor in combination with a dpp-iv inhibitor |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010536734A JP2010536734A (ja) | 2010-12-02 |
| JP2010536734A6 JP2010536734A6 (ja) | 2011-04-07 |
| JP2010536734A5 true JP2010536734A5 (enExample) | 2011-09-29 |
Family
ID=40002943
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010520595A Pending JP2010536734A (ja) | 2007-08-16 | 2008-08-15 | Ｄｐｐｉｖ阻害剤と併用するｓｇｌｔ２阻害剤を含む医薬組成物 |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US20110098240A1 (enExample) |
| EP (1) | EP2187966A1 (enExample) |
| JP (1) | JP2010536734A (enExample) |
| KR (1) | KR20100055422A (enExample) |
| CN (1) | CN101784286A (enExample) |
| AR (1) | AR067969A1 (enExample) |
| AU (1) | AU2008288410A1 (enExample) |
| BR (1) | BRPI0815170A2 (enExample) |
| CA (1) | CA2696271A1 (enExample) |
| CL (1) | CL2008002425A1 (enExample) |
| IL (1) | IL202748A0 (enExample) |
| MX (1) | MX2010001560A (enExample) |
| NZ (1) | NZ583240A (enExample) |
| PE (1) | PE20090603A1 (enExample) |
| RU (1) | RU2010109449A (enExample) |
| TW (1) | TW200914031A (enExample) |
| UY (1) | UY31295A1 (enExample) |
| WO (1) | WO2009022010A1 (enExample) |
| ZA (1) | ZA200908992B (enExample) |
Families Citing this family (83)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7407955B2 (en) | 2002-08-21 | 2008-08-05 | Boehringer Ingelheim Pharma Gmbh & Co., Kg | 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions |
| US7501426B2 (en) | 2004-02-18 | 2009-03-10 | Boehringer Ingelheim International Gmbh | 8-[3-amino-piperidin-1-yl]-xanthines, their preparation and their use as pharmaceutical compositions |
| DE102004054054A1 (de) | 2004-11-05 | 2006-05-11 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Verfahren zur Herstellung chiraler 8-(3-Amino-piperidin-1-yl)-xanthine |
| US7772191B2 (en) | 2005-05-10 | 2010-08-10 | Boehringer Ingelheim International Gmbh | Processes for preparing of glucopyranosyl-substituted benzyl-benzene derivatives and intermediates therein |
| DE102005035891A1 (de) | 2005-07-30 | 2007-02-08 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 8-(3-Amino-piperidin-1-yl)-xanthine, deren Herstellung und deren Verwendung als Arzneimittel |
| BRPI0615882A2 (pt) * | 2005-09-08 | 2011-05-31 | Boehringer Ingelheim Int | formas cristalinas de 1-cloro-4-(beta-d-glicopiranos-1-il)-2-(4-etinil-benzil)- benzeno, métodos para sua preparação e o uso para preparar medicamentos do mesmo |
| PE20080697A1 (es) * | 2006-05-03 | 2008-08-05 | Boehringer Ingelheim Int | Derivados de benzonitrilo sustituidos con glucopiranosilo, composiciones farmaceuticas que contienen compuestos de este tipo, su uso y procedimiento para su fabricacion |
| EP1852108A1 (en) | 2006-05-04 | 2007-11-07 | Boehringer Ingelheim Pharma GmbH & Co.KG | DPP IV inhibitor formulations |
| BRPI0711558A2 (pt) | 2006-05-04 | 2011-11-08 | Boeringer Ingelheim Internat Gmbh | polimorfos |
| PE20080251A1 (es) | 2006-05-04 | 2008-04-25 | Boehringer Ingelheim Int | Usos de inhibidores de dpp iv |
| US8039441B2 (en) * | 2006-08-15 | 2011-10-18 | Boehringer Ingelheim International Gmbh | Glucopyranosyl-substituted cyclopropylbenzene derivatives, pharmaceutical compositions containing such compounds, their use as SGLT inhibitors and process for their manufacture |
| US8283326B2 (en) * | 2006-10-27 | 2012-10-09 | Boehringer Ingelheim International Gmbh | Crystalline form of 4-(beta-D-glucopyranos-1-yl)-1-methyl-2-[4-((S)-tetrahydrofuran-3-yloxy)-benzyl]-benzene, a method for its preparation and the use thereof for preparing medicaments |
| PE20090938A1 (es) | 2007-08-16 | 2009-08-08 | Boehringer Ingelheim Int | Composicion farmaceutica que comprende un derivado de benceno sustituido con glucopiranosilo |
| HUE035130T2 (en) | 2007-09-10 | 2018-05-02 | Janssen Pharmaceutica Nv | A method for preparing compounds useful as SGLT inhibitors |
| PE20091211A1 (es) | 2007-11-30 | 2009-09-14 | Boehringer Ingelheim Int | Derivados de pirazolopirimidina como moduladores de pde9a |
| CL2008003653A1 (es) | 2008-01-17 | 2010-03-05 | Mitsubishi Tanabe Pharma Corp | Uso de un inhibidor de sglt derivado de glucopiranosilo y un inhibidor de dppiv seleccionado para tratar la diabetes; y composicion farmaceutica. |
| UA105362C2 (en) | 2008-04-02 | 2014-05-12 | Бьорингер Ингельхайм Интернациональ Гмбх | 1-heterocyclyl-1, 5-dihydro-pyrazolo [3, 4-d] pyrimidin-4-one derivatives and their use as pde9a modulators |
| PE20091730A1 (es) | 2008-04-03 | 2009-12-10 | Boehringer Ingelheim Int | Formulaciones que comprenden un inhibidor de dpp4 |
| KR20190016601A (ko) | 2008-08-06 | 2019-02-18 | 베링거 인겔하임 인터내셔날 게엠베하 | 메트포르민 요법이 부적합한 환자에서의 당뇨병 치료 |
| UY32030A (es) | 2008-08-06 | 2010-03-26 | Boehringer Ingelheim Int | "tratamiento para diabetes en pacientes inapropiados para terapia con metformina" |
| NZ604091A (en) * | 2008-08-15 | 2014-08-29 | Boehringer Ingelheim Int | Purin derivatives for use in the treatment of fab-related diseases |
| CN102149717B (zh) | 2008-08-28 | 2014-05-14 | 辉瑞大药厂 | 二氧杂-双环[3.2.1]辛烷-2，3，4-三醇衍生物 |
| CA2736304A1 (en) | 2008-09-08 | 2010-03-11 | Boehringer Ingelheim International Gmbh | Pyrazolopyrimidines and their use for the treatment of cns disorders |
| BRPI0919288A2 (pt) | 2008-09-10 | 2015-12-15 | Boehring Ingelheim Internat Gmbh | teriapia de combinação para tratamento de diabetes e condições relacionadas. |
| US20240148737A1 (en) * | 2008-10-16 | 2024-05-09 | Boehringer Ingelheim International Gmbh | Treatment for diabetes in patients with insufficient glycemic control despite therapy with an oral antidiabetic drug |
| US20200155558A1 (en) | 2018-11-20 | 2020-05-21 | Boehringer Ingelheim International Gmbh | Treatment for diabetes in patients with insufficient glycemic control despite therapy with an oral antidiabetic drug |
| US9056850B2 (en) | 2008-10-17 | 2015-06-16 | Janssen Pharmaceutica N.V. | Process for the preparation of compounds useful as inhibitors of SGLT |
| AU2009331471B2 (en) | 2008-12-23 | 2015-09-03 | Boehringer Ingelheim International Gmbh | Salt forms of organic compound |
| AR074990A1 (es) | 2009-01-07 | 2011-03-02 | Boehringer Ingelheim Int | Tratamiento de diabetes en pacientes con un control glucemico inadecuado a pesar de la terapia con metformina |
| PE20120017A1 (es) | 2009-02-13 | 2012-02-12 | Boehringer Ingelheim Int | Composicion farmaceutica que comprende un inhibidor de sglt2, un inhibidor de dpp-iv, opcionalmente, un agente antidiabetico adicional, y sus usos |
| FI2395968T3 (fi) * | 2009-02-13 | 2024-02-27 | Boehringer Ingelheim Int | Glukopyranosylidifenylimetaanijohdannaisia sisältävä farmaseuttinen koostumus, niiden farmaseuttinen annostusmuoto, niiden valmistusmenetelmä ja niiden käyttö potilaan glukemiasäädön parantamiseksi |
| UY32427A (es) * | 2009-02-13 | 2010-09-30 | Boheringer Ingelheim Internat Gmbh | Composicion farmaceutica, forma farmaceutica, procedimiento para su preparacion, metodos de tratamiento y usos de la misma |
| GEP20146098B (en) | 2009-03-31 | 2014-05-27 | Boehringer Ingelheim Int | 1-heterocyclyl-1, 5-dihydro-pyrazolo [3, 4-d] pyrimidin-4-one derivatives and their usage as pde9a modulators |
| TW201103534A (en) | 2009-04-16 | 2011-02-01 | Taisho Pharmaceutical Co Ltd | Pharmaceutical compositions |
| US20110009347A1 (en) | 2009-07-08 | 2011-01-13 | Yin Liang | Combination therapy for the treatment of diabetes |
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| US6515117B2 (en) * | 1999-10-12 | 2003-02-04 | Bristol-Myers Squibb Company | C-aryl glucoside SGLT2 inhibitors and method |
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| DE102004044221A1 (de) * | 2004-09-14 | 2006-03-16 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue 3-Methyl-7-butinyl-xanthine, deren Herstellung und deren Verwendung als Arzneimittel |
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| PE20090938A1 (es) * | 2007-08-16 | 2009-08-08 | Boehringer Ingelheim Int | Composicion farmaceutica que comprende un derivado de benceno sustituido con glucopiranosilo |
| PE20120017A1 (es) * | 2009-02-13 | 2012-02-12 | Boehringer Ingelheim Int | Composicion farmaceutica que comprende un inhibidor de sglt2, un inhibidor de dpp-iv, opcionalmente, un agente antidiabetico adicional, y sus usos |
| EP2368552A1 (en) * | 2010-03-25 | 2011-09-28 | Boehringer Ingelheim Vetmedica GmbH | 1-[(3-cyano-pyridin-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-[3-(r)-amino-piperidin-1-yl]-xanthine for the treatment of a metabolic disorder of a predominantly carnivorous non-human animal |
-
2008
- 2008-08-14 CL CL2008002425A patent/CL2008002425A1/es unknown
- 2008-08-14 PE PE2008001381A patent/PE20090603A1/es not_active Application Discontinuation
- 2008-08-15 RU RU2010109449/15A patent/RU2010109449A/ru unknown
- 2008-08-15 EP EP08787272A patent/EP2187966A1/en not_active Withdrawn
- 2008-08-15 AU AU2008288410A patent/AU2008288410A1/en not_active Abandoned
- 2008-08-15 BR BRPI0815170 patent/BRPI0815170A2/pt not_active IP Right Cessation
- 2008-08-15 UY UY31295A patent/UY31295A1/es not_active Application Discontinuation
- 2008-08-15 CN CN200880102900A patent/CN101784286A/zh active Pending
- 2008-08-15 AR ARP080103591A patent/AR067969A1/es unknown
- 2008-08-15 US US12/673,319 patent/US20110098240A1/en not_active Abandoned
- 2008-08-15 KR KR1020107003406A patent/KR20100055422A/ko not_active Ceased
- 2008-08-15 JP JP2010520595A patent/JP2010536734A/ja active Pending
- 2008-08-15 MX MX2010001560A patent/MX2010001560A/es not_active Application Discontinuation
- 2008-08-15 NZ NZ583240A patent/NZ583240A/xx not_active IP Right Cessation
- 2008-08-15 WO PCT/EP2008/060744 patent/WO2009022010A1/en not_active Ceased
- 2008-08-15 CA CA2696271A patent/CA2696271A1/en not_active Abandoned
- 2008-08-15 TW TW097131319A patent/TW200914031A/zh unknown
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2009
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- 2009-12-17 ZA ZA200908992A patent/ZA200908992B/xx unknown
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- 2012-12-04 US US13/693,239 patent/US20130096076A1/en not_active Abandoned
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