HRP20120006T1 - Derivat bicikloestera - Google Patents
Derivat bicikloestera Download PDFInfo
- Publication number
- HRP20120006T1 HRP20120006T1 HR20120006T HRP20120006T HRP20120006T1 HR P20120006 T1 HRP20120006 T1 HR P20120006T1 HR 20120006 T HR20120006 T HR 20120006T HR P20120006 T HRP20120006 T HR P20120006T HR P20120006 T1 HRP20120006 T1 HR P20120006T1
- Authority
- HR
- Croatia
- Prior art keywords
- group
- substituted
- unsubstituted
- amino
- pharmaceutically acceptable
- Prior art date
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- 150000003839 salts Chemical class 0.000 claims abstract 13
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract 5
- 125000005002 aryl methyl group Chemical group 0.000 claims abstract 3
- 125000001931 aliphatic group Chemical group 0.000 claims abstract 2
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims abstract 2
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 2
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims abstract 2
- 208000002249 Diabetes Complications Diseases 0.000 claims 3
- 206010012655 Diabetic complications Diseases 0.000 claims 2
- 239000004480 active ingredient Substances 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 230000002265 prevention Effects 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
- -1 2-ethylpropyl group Chemical group 0.000 claims 1
- MUWDEAKFEHCPNO-MVYVIFSASA-N 2-methylpropyl 4-[[2-[(2s,4s)-2-cyano-4-fluoropyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.2]octane-1-carboxylate Chemical compound C1CC(C(=O)OCC(C)C)(CC2)CCC12NCC(=O)N1C[C@@H](F)C[C@H]1C#N MUWDEAKFEHCPNO-MVYVIFSASA-N 0.000 claims 1
- 208000030507 AIDS Diseases 0.000 claims 1
- 206010006187 Breast cancer Diseases 0.000 claims 1
- 208000026310 Breast neoplasm Diseases 0.000 claims 1
- 208000035473 Communicable disease Diseases 0.000 claims 1
- 108010067722 Dipeptidyl Peptidase 4 Proteins 0.000 claims 1
- 102100025012 Dipeptidyl peptidase 4 Human genes 0.000 claims 1
- 208000031886 HIV Infections Diseases 0.000 claims 1
- 206010060378 Hyperinsulinaemia Diseases 0.000 claims 1
- 206010020751 Hypersensitivity Diseases 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- 206010020880 Hypertrophy Diseases 0.000 claims 1
- 206010061218 Inflammation Diseases 0.000 claims 1
- 206010027476 Metastases Diseases 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- 208000001132 Osteoporosis Diseases 0.000 claims 1
- 206010060862 Prostate cancer Diseases 0.000 claims 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 1
- 201000004681 Psoriasis Diseases 0.000 claims 1
- 208000002474 Tinea Diseases 0.000 claims 1
- 241000893966 Trichophyton verrucosum Species 0.000 claims 1
- 230000002159 abnormal effect Effects 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 230000007815 allergy Effects 0.000 claims 1
- 125000004657 aryl sulfonyl amino group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- GWOYOGIMHOBJDT-NAMINWQUSA-N benzyl 4-[[2-[(2s,4s)-2-cyano-4-fluoropyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.2]octane-1-carboxylate Chemical compound C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1(CC2)CCC2(C(=O)OCC=2C=CC=CC=2)CC1 GWOYOGIMHOBJDT-NAMINWQUSA-N 0.000 claims 1
- 210000000481 breast Anatomy 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
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- VLSUZOGRPARBMR-MVYVIFSASA-N cyclopropylmethyl 4-[[2-[(2s,4s)-2-cyano-4-fluoropyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.2]octane-1-carboxylate Chemical compound C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1(CC2)CCC2(C(=O)OCC2CC2)CC1 VLSUZOGRPARBMR-MVYVIFSASA-N 0.000 claims 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- KRTRGJFVBXQFEC-IGEOTXOUSA-N ethyl 4-[[2-[(2s)-2-cyanopyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.1]heptane-1-carboxylate Chemical compound C1CC(C(=O)OCC)(C2)CCC12NCC(=O)N1CCC[C@H]1C#N KRTRGJFVBXQFEC-IGEOTXOUSA-N 0.000 claims 1
- PKJVNACMRDIHDQ-NNGSBXSVSA-N ethyl 4-[[2-[(2s)-2-cyanopyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.2]octane-1-carboxylate Chemical compound C1CC(C(=O)OCC)(CC2)CCC12NCC(=O)N1CCC[C@H]1C#N PKJVNACMRDIHDQ-NNGSBXSVSA-N 0.000 claims 1
- JAKYINCJWPMHPA-SCQRFTTHSA-N ethyl 4-[[2-[(2s,4s)-2-cyano-4-fluoropyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.1]heptane-1-carboxylate Chemical compound C1CC(C(=O)OCC)(C2)CCC12NCC(=O)N1C[C@@H](F)C[C@H]1C#N JAKYINCJWPMHPA-SCQRFTTHSA-N 0.000 claims 1
- AKFNKZFJBFQFAA-DIOPXHOYSA-N ethyl 4-[[2-[(2s,4s)-2-cyano-4-fluoropyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.2]octane-1-carboxylate Chemical compound C1CC(C(=O)OCC)(CC2)CCC12NCC(=O)N1C[C@@H](F)C[C@H]1C#N AKFNKZFJBFQFAA-DIOPXHOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 201000001421 hyperglycemia Diseases 0.000 claims 1
- 230000003451 hyperinsulinaemic effect Effects 0.000 claims 1
- 201000008980 hyperinsulinism Diseases 0.000 claims 1
- 230000004054 inflammatory process Effects 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 230000037356 lipid metabolism Effects 0.000 claims 1
- 210000004072 lung Anatomy 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 201000006417 multiple sclerosis Diseases 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- 210000000056 organ Anatomy 0.000 claims 1
- RXICRMIKLNPVCW-UXGDZIPNSA-N oxan-2-yl 4-[[2-[(2s)-2-cyanopyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.2]octane-1-carboxylate Chemical compound N1([C@@H](CCC1)C#N)C(=O)CNC(CC1)(CC2)CCC12C(=O)OC1CCCCO1 RXICRMIKLNPVCW-UXGDZIPNSA-N 0.000 claims 1
- OCOAXKJWIGCWRW-MPXPMMRMSA-N oxan-2-yl 4-[[2-[(2s,4s)-2-cyano-4-fluoropyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.2]octane-1-carboxylate Chemical compound C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1(CC2)CCC2(C(=O)OC2OCCCC2)CC1 OCOAXKJWIGCWRW-MPXPMMRMSA-N 0.000 claims 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 229940127557 pharmaceutical product Drugs 0.000 claims 1
- LVNAZZKVKBXMQZ-GKVPXEHWSA-N propan-2-yl 4-[[2-[(2s,4s)-2-cyano-4-fluoropyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.2]octane-1-carboxylate Chemical compound C1CC(C(=O)OC(C)C)(CC2)CCC12NCC(=O)N1C[C@@H](F)C[C@H]1C#N LVNAZZKVKBXMQZ-GKVPXEHWSA-N 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 210000002307 prostate Anatomy 0.000 claims 1
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- VONCNLUSLCHFFS-VMEOHVCESA-N tert-butyl 4-[[2-[(2s)-2-cyanopyrrolidin-1-yl]-2-oxoethyl]amino]bicyclo[2.2.2]octane-1-carboxylate Chemical compound C1CC(C(=O)OC(C)(C)C)(CC2)CCC12NCC(=O)N1CCC[C@H]1C#N VONCNLUSLCHFFS-VMEOHVCESA-N 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 210000001519 tissue Anatomy 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
- A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/10—Antioedematous agents; Diuretics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004029856 | 2004-02-05 | ||
PCT/JP2005/001377 WO2005075421A1 (fr) | 2004-02-05 | 2005-02-01 | Dérivé de bicycloester |
Publications (1)
Publication Number | Publication Date |
---|---|
HRP20120006T1 true HRP20120006T1 (hr) | 2012-01-31 |
Family
ID=34835968
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20120006T HRP20120006T1 (hr) | 2004-02-05 | 2012-01-03 | Derivat bicikloestera |
Country Status (22)
Country | Link |
---|---|
US (2) | US7754757B2 (fr) |
EP (1) | EP1712547B1 (fr) |
JP (1) | JP3954626B2 (fr) |
KR (1) | KR101130433B1 (fr) |
CN (2) | CN101684089A (fr) |
AT (1) | ATE537141T1 (fr) |
AU (1) | AU2005210285B2 (fr) |
BR (1) | BRPI0506622A (fr) |
CA (1) | CA2554493C (fr) |
CY (1) | CY1112550T1 (fr) |
DK (1) | DK1712547T3 (fr) |
ES (1) | ES2375625T3 (fr) |
HK (1) | HK1100511A1 (fr) |
HR (1) | HRP20120006T1 (fr) |
NO (1) | NO20063486L (fr) |
NZ (1) | NZ548440A (fr) |
PL (1) | PL1712547T3 (fr) |
PT (1) | PT1712547E (fr) |
RS (1) | RS52163B (fr) |
SI (1) | SI1712547T1 (fr) |
WO (1) | WO2005075421A1 (fr) |
ZA (1) | ZA200606237B (fr) |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SI1712547T1 (sl) * | 2004-02-05 | 2012-04-30 | Kyorin Seiyaku Kk | Bicikloestrski derivat |
US7514571B2 (en) * | 2004-02-27 | 2009-04-07 | Kyorin Pharmaceutical Co., Ltd. | Bicyclo derivative |
GB0526291D0 (en) | 2005-12-23 | 2006-02-01 | Prosidion Ltd | Therapeutic method |
AU2007224066B2 (en) * | 2006-03-08 | 2011-10-27 | Kyorin Pharmaceutical Co., Ltd. | Method for producing aminoacetylpyrrolidinecarbonitrile derivative and production intermediate thereof |
JP2010120851A (ja) * | 2007-02-09 | 2010-06-03 | Kyorin Pharmaceut Co Ltd | 二量化シクロ誘導体 |
US8143427B2 (en) * | 2007-03-22 | 2012-03-27 | Kyorin Pharmaceutical Co., Ltd. | Method for producing aminoacetylpyrrolidinecarbonitrile derivative |
JP5616630B2 (ja) | 2007-04-03 | 2014-10-29 | 田辺三菱製薬株式会社 | ジペプチジルペプチダーゼ4阻害化合物と甘味料との併用 |
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. |
UY32030A (es) | 2008-08-06 | 2010-03-26 | Boehringer Ingelheim Int | "tratamiento para diabetes en pacientes inapropiados para terapia con metformina" |
JP5476305B2 (ja) | 2008-08-07 | 2014-04-23 | 杏林製薬株式会社 | ビシクロ[2.2.2]オクチルアミン誘導体の製造方法 |
WO2010018866A1 (fr) | 2008-08-14 | 2010-02-18 | 杏林製薬株式会社 | Composition pharmaceutique stabilisée |
CN102216267A (zh) * | 2008-09-16 | 2011-10-12 | 杏林制药株式会社 | 氨基乙酰基吡咯烷甲腈衍生物的纯化方法及其盐 |
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 |
UY32048A (es) | 2009-01-08 | 2010-03-26 | Boehringer Ingelheim Int | Derivados sustituido de 1-(sustituido)-3-metil-7-(sustituido)-8-(3-(R)-amino-piperidin-1-il)cantina y derivados sustituidos de 1-(sustituido) - 4 - fluoropirrolidin- 2 - carbonitrilo y sus sales famacéuticamente aceptables como inhibidores de DPP-4 y aplicaciones. |
CA2749301C (fr) * | 2009-01-09 | 2019-06-11 | Gopalan Balasubramanian | Inhibiteurs de l'enzyme dipeptidyl peptidase iv |
TWI466672B (zh) | 2009-01-29 | 2015-01-01 | Boehringer Ingelheim Int | 小兒科病人糖尿病之治療 |
NZ619520A (en) | 2009-02-13 | 2015-06-26 | Boehringer Ingelheim Int | Antidiabetic medications comprising a dpp-4 inhibitor (linagliptin) optionally in combination with other antidiabetics |
EP2412370A4 (fr) | 2009-03-27 | 2013-05-22 | Kyorin Seiyaku Kk | Préparation à libération prolongée de type matrice contenant un additif basique |
AR077642A1 (es) | 2009-07-09 | 2011-09-14 | Arena Pharm Inc | Moduladores del metabolismo y el tratamiento de trastornos relacionados con el mismo |
CN102753161A (zh) | 2009-11-27 | 2012-10-24 | 贝林格尔.英格海姆国际有限公司 | 基因型糖尿病患者利用dpp-iv抑制剂例如利拉利汀的治疗 |
WO2011113947A1 (fr) | 2010-03-18 | 2011-09-22 | Boehringer Ingelheim International Gmbh | Combinaisons d'agonistes de gpr119 et d'inhibiteurs de dpp-iv, linagliptine, pour le traitement du diabète et d'états apparentés |
BR112012025592A2 (pt) | 2010-04-06 | 2019-09-24 | Arena Pharm Inc | moduladores do receptor de gpr119 e o tratamento de distúrbios relacionados com os mesmos |
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-
2005
- 2005-02-01 SI SI200531480T patent/SI1712547T1/sl unknown
- 2005-02-01 CN CN200910175524A patent/CN101684089A/zh active Pending
- 2005-02-01 PT PT05704327T patent/PT1712547E/pt unknown
- 2005-02-01 BR BRPI0506622-0A patent/BRPI0506622A/pt not_active IP Right Cessation
- 2005-02-01 KR KR1020067015699A patent/KR101130433B1/ko not_active IP Right Cessation
- 2005-02-01 DK DK05704327.5T patent/DK1712547T3/da active
- 2005-02-01 CN CN2005800041918A patent/CN1918119B/zh not_active Expired - Fee Related
- 2005-02-01 RS RS20120076A patent/RS52163B/en unknown
- 2005-02-01 WO PCT/JP2005/001377 patent/WO2005075421A1/fr active Application Filing
- 2005-02-01 AU AU2005210285A patent/AU2005210285B2/en not_active Ceased
- 2005-02-01 AT AT05704327T patent/ATE537141T1/de active
- 2005-02-01 CA CA2554493A patent/CA2554493C/fr not_active Expired - Fee Related
- 2005-02-01 JP JP2005517671A patent/JP3954626B2/ja not_active Expired - Fee Related
- 2005-02-01 ES ES05704327T patent/ES2375625T3/es active Active
- 2005-02-01 EP EP05704327A patent/EP1712547B1/fr active Active
- 2005-02-01 US US10/588,660 patent/US7754757B2/en not_active Expired - Fee Related
- 2005-02-01 NZ NZ548440A patent/NZ548440A/xx not_active IP Right Cessation
- 2005-02-01 PL PL05704327T patent/PL1712547T3/pl unknown
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- 2006-07-27 ZA ZA200606237A patent/ZA200606237B/xx unknown
- 2006-07-31 NO NO20063486A patent/NO20063486L/no not_active Application Discontinuation
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2007
- 2007-05-30 HK HK07105747.8A patent/HK1100511A1/xx not_active IP Right Cessation
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- 2011-12-21 CY CY20111101277T patent/CY1112550T1/el unknown
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Also Published As
Publication number | Publication date |
---|---|
US20100093825A1 (en) | 2010-04-15 |
US7754757B2 (en) | 2010-07-13 |
AU2005210285A1 (en) | 2005-08-18 |
HK1100511A1 (en) | 2007-09-21 |
CN1918119A (zh) | 2007-02-21 |
WO2005075421A1 (fr) | 2005-08-18 |
JP3954626B2 (ja) | 2007-08-08 |
DK1712547T3 (da) | 2012-03-19 |
SI1712547T1 (sl) | 2012-04-30 |
US8053465B2 (en) | 2011-11-08 |
NZ548440A (en) | 2009-07-31 |
AU2005210285B2 (en) | 2008-01-24 |
KR101130433B1 (ko) | 2012-03-27 |
ZA200606237B (en) | 2007-12-27 |
JPWO2005075421A1 (ja) | 2007-10-11 |
NO20063486L (no) | 2006-08-29 |
BRPI0506622A (pt) | 2007-05-02 |
CN1918119B (zh) | 2011-08-31 |
EP1712547B1 (fr) | 2011-12-14 |
EP1712547A4 (fr) | 2007-09-26 |
KR20060130641A (ko) | 2006-12-19 |
CN101684089A (zh) | 2010-03-31 |
CA2554493C (fr) | 2012-06-26 |
US20080146818A1 (en) | 2008-06-19 |
EP1712547A1 (fr) | 2006-10-18 |
CY1112550T1 (el) | 2016-02-10 |
PT1712547E (pt) | 2012-03-06 |
PL1712547T3 (pl) | 2012-04-30 |
ES2375625T3 (es) | 2012-03-02 |
RS52163B (en) | 2012-08-31 |
ATE537141T1 (de) | 2011-12-15 |
CA2554493A1 (fr) | 2005-08-18 |
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