JP4651714B2 - 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 - Google Patents
糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 Download PDFInfo
- Publication number
- JP4651714B2 JP4651714B2 JP2008520936A JP2008520936A JP4651714B2 JP 4651714 B2 JP4651714 B2 JP 4651714B2 JP 2008520936 A JP2008520936 A JP 2008520936A JP 2008520936 A JP2008520936 A JP 2008520936A JP 4651714 B2 JP4651714 B2 JP 4651714B2
- Authority
- JP
- Japan
- Prior art keywords
- oxy
- methyl
- benzamide
- ylcarbonyl
- azetidin
- 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.)
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- 0 **NC(c1cc(*)cc(O*)c1)=O Chemical compound **NC(c1cc(*)cc(O*)c1)=O 0.000 description 1
- AZFVEGKOGUJUPQ-KTKRTIGZSA-N CC(C)Oc1cc(C(NC(/C=C\NC)=N)=O)cc(OCc2ccccc2)c1 Chemical compound CC(C)Oc1cc(C(NC(/C=C\NC)=N)=O)cc(OCc2ccccc2)c1 AZFVEGKOGUJUPQ-KTKRTIGZSA-N 0.000 description 1
- LTQFVLZJOCCMQK-UHFFFAOYSA-N CC(C)Oc1cc(C(Nc2nc(C)n[s]2)=O)cc(OCc2ccccc2)c1 Chemical compound CC(C)Oc1cc(C(Nc2nc(C)n[s]2)=O)cc(OCc2ccccc2)c1 LTQFVLZJOCCMQK-UHFFFAOYSA-N 0.000 description 1
- KMGPAEVLMSNBOK-UHFFFAOYSA-N CC(C)Oc1cc(C(Nc2ncc[s]2)=O)cc(O)c1 Chemical compound CC(C)Oc1cc(C(Nc2ncc[s]2)=O)cc(O)c1 KMGPAEVLMSNBOK-UHFFFAOYSA-N 0.000 description 1
- YHRXMGQEVPNUIL-UHFFFAOYSA-N CC(C)Oc1cc(C(O)=O)cc(OCc2ccccc2)c1 Chemical compound CC(C)Oc1cc(C(O)=O)cc(OCc2ccccc2)c1 YHRXMGQEVPNUIL-UHFFFAOYSA-N 0.000 description 1
- OSPMSLMDRDPIKH-PLNGDYQASA-N CC(C1)C1(CO)Oc1cc(C(NC(/C=C\NC)=N)=O)cc(Oc2ncc(C(N3CCC3)=O)nc2)c1 Chemical compound CC(C1)C1(CO)Oc1cc(C(NC(/C=C\NC)=N)=O)cc(Oc2ncc(C(N3CCC3)=O)nc2)c1 OSPMSLMDRDPIKH-PLNGDYQASA-N 0.000 description 1
- GYMIPFGZFZKEAW-UHFFFAOYSA-N CC(CO)Oc1cc(C(O)OC)cc(OCc2ccccc2)c1 Chemical compound CC(CO)Oc1cc(C(O)OC)cc(OCc2ccccc2)c1 GYMIPFGZFZKEAW-UHFFFAOYSA-N 0.000 description 1
- JQMMHEMOUUMQEK-SNGWPZLWSA-N CC[C@H](C)Oc1cc(C(NC(/C=C\NC)=N)=O)cc(OCc2ccccc2)c1 Chemical compound CC[C@H](C)Oc1cc(C(NC(/C=C\NC)=N)=O)cc(OCc2ccccc2)c1 JQMMHEMOUUMQEK-SNGWPZLWSA-N 0.000 description 1
- ZEKHRXYOKMAZHS-INIZCTEOSA-N C[C@@H](CO)Oc1cc(C(Nc2cnc(C)cn2)=O)cc(Oc2ccc(C(N3CCC3)=O)nc2)c1 Chemical compound C[C@@H](CO)Oc1cc(C(Nc2cnc(C)cn2)=O)cc(Oc2ccc(C(N3CCC3)=O)nc2)c1 ZEKHRXYOKMAZHS-INIZCTEOSA-N 0.000 description 1
- JGFLEQKTOAQBTD-ZDUSSCGKSA-N C[C@@H](CO)Oc1cc(C(Nc2nc(C)n[s]2)=O)cc(Oc(cc2)ncc2C(N2CCC2)=O)c1 Chemical compound C[C@@H](CO)Oc1cc(C(Nc2nc(C)n[s]2)=O)cc(Oc(cc2)ncc2C(N2CCC2)=O)c1 JGFLEQKTOAQBTD-ZDUSSCGKSA-N 0.000 description 1
- RJYXLRBXWKHMQG-CDNLZTBQSA-O C[C@@H](COC(F)F)Oc1cc(C(NC(/C=C\NC)=[NH2+])=O)cc(OCc2ccccc2)c1 Chemical compound C[C@@H](COC(F)F)Oc1cc(C(NC(/C=C\NC)=[NH2+])=O)cc(OCc2ccccc2)c1 RJYXLRBXWKHMQG-CDNLZTBQSA-O 0.000 description 1
- CTRPGUCLKVYLDD-LBPRGKRZSA-N C[C@@H](COC(F)F)Oc1cc(C(O)=O)cc(OCc2ccccc2)c1 Chemical compound C[C@@H](COC(F)F)Oc1cc(C(O)=O)cc(OCc2ccccc2)c1 CTRPGUCLKVYLDD-LBPRGKRZSA-N 0.000 description 1
- IQGFVLNMIZIDIV-JYBLJSLWSA-N C[C@@H](COC)Oc1cc(C(NC(/C=C\NC(OC(C)(C)C)=O)=N)=O)cc(OCc2ccccc2)c1 Chemical compound C[C@@H](COC)Oc1cc(C(NC(/C=C\NC(OC(C)(C)C)=O)=N)=O)cc(OCc2ccccc2)c1 IQGFVLNMIZIDIV-JYBLJSLWSA-N 0.000 description 1
- WBLSHTHJCONIQZ-PTZVLDCSSA-N C[C@@H](COC)Oc1cc(C(NC(/C=C\NC)=N)=O)cc(Oc(nc2)ccc2S(N2CCC2)(O)=O)c1 Chemical compound C[C@@H](COC)Oc1cc(C(NC(/C=C\NC)=N)=O)cc(Oc(nc2)ccc2S(N2CCC2)(O)=O)c1 WBLSHTHJCONIQZ-PTZVLDCSSA-N 0.000 description 1
- YLSJWVQMXSNSQT-KRWDZBQOSA-N C[C@@H](COC)Oc1cc(C(Nc2cnc(C)cn2)=O)cc(OCc2ccccc2)c1 Chemical compound C[C@@H](COC)Oc1cc(C(Nc2cnc(C)cn2)=O)cc(OCc2ccccc2)c1 YLSJWVQMXSNSQT-KRWDZBQOSA-N 0.000 description 1
- UFPFCGXFAMBNFB-AWEZNQCLSA-N C[C@@H](COC)Oc1cc(C(Nc2nc(C)n[s]2)=O)cc(OCc2ccccc2)c1 Chemical compound C[C@@H](COC)Oc1cc(C(Nc2nc(C)n[s]2)=O)cc(OCc2ccccc2)c1 UFPFCGXFAMBNFB-AWEZNQCLSA-N 0.000 description 1
- PJIAOAQBXXYLRX-ZDUSSCGKSA-N C[C@@H](COC)Oc1cc(C(O)=O)cc(OCc2ccccc2)c1 Chemical compound C[C@@H](COC)Oc1cc(C(O)=O)cc(OCc2ccccc2)c1 PJIAOAQBXXYLRX-ZDUSSCGKSA-N 0.000 description 1
- JGIXKHBUAQEBSU-QMMMGPOBSA-N C[C@@H](COC)Oc1cc(C(OC)=O)cc(O)c1 Chemical compound C[C@@H](COC)Oc1cc(C(OC)=O)cc(O)c1 JGIXKHBUAQEBSU-QMMMGPOBSA-N 0.000 description 1
- JCTASGQIZHOHNP-AWEZNQCLSA-N C[C@@H](COC)Oc1cc(C(OC)=O)cc(OCc2ccccc2)c1 Chemical compound C[C@@H](COC)Oc1cc(C(OC)=O)cc(OCc2ccccc2)c1 JCTASGQIZHOHNP-AWEZNQCLSA-N 0.000 description 1
- WSEZVZLEOHKDAU-BYCRGOAPSA-O C[C@@H](C[OH2+])Oc1cc(C(NC(/C=C\NC)=N)=O)cc(Oc(ncc(C(O)=O)c2)c2Cl)c1 Chemical compound C[C@@H](C[OH2+])Oc1cc(C(NC(/C=C\NC)=N)=O)cc(Oc(ncc(C(O)=O)c2)c2Cl)c1 WSEZVZLEOHKDAU-BYCRGOAPSA-O 0.000 description 1
- DOVSROFFBXZSGC-DFPOMNKCSA-N C[C@@H]([C@H](C)Oc1cc(C(NC(/C=C\NC)=N)=O)cc(Oc2ncc(C(O)=O)nc2)c1)O Chemical compound C[C@@H]([C@H](C)Oc1cc(C(NC(/C=C\NC)=N)=O)cc(Oc2ncc(C(O)=O)nc2)c1)O DOVSROFFBXZSGC-DFPOMNKCSA-N 0.000 description 1
- RNXKCNWSEMDEHK-LUNKNMTDSA-O C[C@@H]([C@H](C)Oc1cc(C(NC(/C=C\NC)=[NH2+])=O)cc(Oc2ncc(C(N3CCC3)=O)nc2)c1)O Chemical compound C[C@@H]([C@H](C)Oc1cc(C(NC(/C=C\NC)=[NH2+])=O)cc(Oc2ncc(C(N3CCC3)=O)nc2)c1)O RNXKCNWSEMDEHK-LUNKNMTDSA-O 0.000 description 1
- DZOHEBUAOAFYHG-HOTGVXAUSA-N C[C@@H]([C@H](C)Oc1cc(C(Nc2n[n](C)cc2)=O)cc(OCc2ccccc2)c1)O Chemical compound C[C@@H]([C@H](C)Oc1cc(C(Nc2n[n](C)cc2)=O)cc(OCc2ccccc2)c1)O DZOHEBUAOAFYHG-HOTGVXAUSA-N 0.000 description 1
- JGIXKHBUAQEBSU-MRVPVSSYSA-N C[C@H](COC)Oc1cc(C(OC)=O)cc(O)c1 Chemical compound C[C@H](COC)Oc1cc(C(OC)=O)cc(O)c1 JGIXKHBUAQEBSU-MRVPVSSYSA-N 0.000 description 1
- LPMFCHLFNDXJIY-UHFFFAOYSA-N Cc1c[s]c(NC(c2cc(Oc3ncc(C(N4CCC4)=O)nc3)cc(OC3COCC3)c2)=O)n1 Chemical compound Cc1c[s]c(NC(c2cc(Oc3ncc(C(N4CCC4)=O)nc3)cc(OC3COCC3)c2)=O)n1 LPMFCHLFNDXJIY-UHFFFAOYSA-N 0.000 description 1
- NZNGZXHTYDHHIV-UHFFFAOYSA-N Cc1ccccc1COc1cc(O)cc(C(OC)=O)c1 Chemical compound Cc1ccccc1COc1cc(O)cc(C(OC)=O)c1 NZNGZXHTYDHHIV-UHFFFAOYSA-N 0.000 description 1
- XCNGNCFTRWXUJT-UHFFFAOYSA-N Cc1ncc(NC(c2cc(Oc(c(Cl)c3)ncc3C(N3CCC3)=O)cc(OC(CF)CF)c2)=O)nc1 Chemical compound Cc1ncc(NC(c2cc(Oc(c(Cl)c3)ncc3C(N3CCC3)=O)cc(OC(CF)CF)c2)=O)nc1 XCNGNCFTRWXUJT-UHFFFAOYSA-N 0.000 description 1
- YLHRUBHZTFHXMG-UHFFFAOYSA-N O=C(c(cn1)cc(Cl)c1Cl)N1CCCC1 Chemical compound O=C(c(cn1)cc(Cl)c1Cl)N1CCCC1 YLHRUBHZTFHXMG-UHFFFAOYSA-N 0.000 description 1
- IRBWBVKFPWRLMF-UHFFFAOYSA-N O[SH+2](c(cn1)cc(Br)c1Cl)N1CCC1 Chemical compound O[SH+2](c(cn1)cc(Br)c1Cl)N1CCC1 IRBWBVKFPWRLMF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
-
- 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
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- 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
- C07D405/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0514173A GB0514173D0 (en) | 2005-07-09 | 2005-07-09 | Chemical compounds |
| GB0516297A GB0516297D0 (en) | 2005-08-09 | 2005-08-09 | Chemical compounds |
| GB0523862A GB0523862D0 (en) | 2005-11-24 | 2005-11-24 | Chemical compounds |
| GB0524589A GB0524589D0 (en) | 2005-12-02 | 2005-12-02 | Chemical compounds |
| GB0607977A GB0607977D0 (en) | 2006-04-22 | 2006-04-22 | Chemical compounds |
| PCT/GB2006/002471 WO2007007041A1 (en) | 2005-07-09 | 2006-07-03 | Heteroaryl benzamide derivatives for use as glk activators in the treatment of diabetes |
Related Child Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009157639A Division JP2009215320A (ja) | 2005-07-09 | 2009-07-02 | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
| JP2009157686A Division JP2009263390A (ja) | 2005-07-09 | 2009-07-02 | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
| JP2009157655A Division JP4651729B2 (ja) | 2005-07-09 | 2009-07-02 | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009500443A JP2009500443A (ja) | 2009-01-08 |
| JP2009500443A5 JP2009500443A5 (enExample) | 2010-08-19 |
| JP4651714B2 true JP4651714B2 (ja) | 2011-03-16 |
Family
ID=36809156
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008520936A Active JP4651714B2 (ja) | 2005-07-09 | 2006-07-03 | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
| JP2009157639A Pending JP2009215320A (ja) | 2005-07-09 | 2009-07-02 | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
| JP2009157655A Expired - Fee Related JP4651729B2 (ja) | 2005-07-09 | 2009-07-02 | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
| JP2009157686A Pending JP2009263390A (ja) | 2005-07-09 | 2009-07-02 | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
Family Applications After (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009157639A Pending JP2009215320A (ja) | 2005-07-09 | 2009-07-02 | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
| JP2009157655A Expired - Fee Related JP4651729B2 (ja) | 2005-07-09 | 2009-07-02 | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
| JP2009157686A Pending JP2009263390A (ja) | 2005-07-09 | 2009-07-02 | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
Country Status (19)
| Country | Link |
|---|---|
| US (4) | US7642259B2 (enExample) |
| EP (4) | EP2305674A1 (enExample) |
| JP (4) | JP4651714B2 (enExample) |
| KR (2) | KR20110084339A (enExample) |
| AR (1) | AR055074A1 (enExample) |
| AU (2) | AU2006268406C1 (enExample) |
| BR (3) | BRPI0613570B8 (enExample) |
| CA (1) | CA2614746C (enExample) |
| EC (1) | ECSP088164A (enExample) |
| ES (1) | ES2397648T3 (enExample) |
| IL (2) | IL188059A0 (enExample) |
| MX (1) | MX2008000172A (enExample) |
| MY (1) | MY147749A (enExample) |
| NO (1) | NO20076658L (enExample) |
| NZ (4) | NZ564608A (enExample) |
| SA (1) | SA06270215B1 (enExample) |
| TW (1) | TW200730174A (enExample) |
| UY (1) | UY29656A1 (enExample) |
| WO (1) | WO2007007041A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009263390A (ja) * | 2005-07-09 | 2009-11-12 | Astrazeneca Ab | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0102764D0 (sv) | 2001-08-17 | 2001-08-17 | Astrazeneca Ab | Compounds |
| EP1718624B1 (en) * | 2004-02-18 | 2009-03-25 | AstraZeneca AB | Benzamide derivatives and their use as glucokinase activating agents |
| TW200600086A (en) * | 2004-06-05 | 2006-01-01 | Astrazeneca Ab | Chemical compound |
| TW200714597A (en) * | 2005-05-27 | 2007-04-16 | Astrazeneca Ab | Chemical compounds |
| PE20080251A1 (es) | 2006-05-04 | 2008-04-25 | Boehringer Ingelheim Int | Usos de inhibidores de dpp iv |
| US7910747B2 (en) | 2006-07-06 | 2011-03-22 | Bristol-Myers Squibb Company | Phosphonate and phosphinate pyrazolylamide glucokinase activators |
| CA2657566A1 (en) | 2006-07-24 | 2008-01-31 | F. Hoffmann-La Roche Ag | Pyrazoles as glucokinase activators |
| TW200825063A (en) * | 2006-10-23 | 2008-06-16 | Astrazeneca Ab | Chemical compounds |
| SA07280576B1 (ar) * | 2006-10-26 | 2011-06-22 | استرازينيكا ايه بي | مركبات بنزويل أمينو سيكليل غير متجانسة بأعتبارها عوامل منشطة للجلوكوكيناز |
| TW200827346A (en) | 2006-11-03 | 2008-07-01 | Astrazeneca Ab | Chemical compounds |
| JP2010513445A (ja) * | 2006-12-21 | 2010-04-30 | アストラゼネカ アクチボラグ | Glkアクチベーターとして有用な新規結晶性化合物 |
| TW200836719A (en) | 2007-02-12 | 2008-09-16 | Astrazeneca Ab | Chemical compounds |
| EP2170852A1 (en) | 2007-06-11 | 2010-04-07 | Bristol-Myers Squibb Company | 1, 3 - dihydroxy substituted phenylamide glucokinase activators |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| AU2008310097B2 (en) * | 2007-10-09 | 2013-05-16 | Merck Patent Gmbh | Pyridine derivatives useful as glucokinase activators |
| AU2008310115B2 (en) | 2007-10-09 | 2013-06-27 | Merck Patent Gmbh | N- ( pyrazole- 3 -yl) -benzamide derivatives as glucokinase activators |
| US8258134B2 (en) | 2008-04-16 | 2012-09-04 | Hoffmann-La Roche Inc. | Pyridazinone glucokinase activators |
| US7741327B2 (en) | 2008-04-16 | 2010-06-22 | Hoffmann-La Roche Inc. | Pyrrolidinone glucokinase activators |
| JP2011529955A (ja) | 2008-08-04 | 2011-12-15 | アストラゼネカ アクチボラグ | 治療薬414 |
| GB0902434D0 (en) * | 2009-02-13 | 2009-04-01 | Astrazeneca Ab | Chemical process |
| GB0902406D0 (en) | 2009-02-13 | 2009-04-01 | Astrazeneca Ab | Crystalline polymorphic form |
| WO2010116176A1 (en) * | 2009-04-09 | 2010-10-14 | Astrazeneca Ab | Pyrazolo [4, 5-e] pyrimidine derivative and its use to treat diabetes and obesity |
| WO2010116177A1 (en) | 2009-04-09 | 2010-10-14 | Astrazeneca Ab | A pyrazolo [4,5-e] pyrimidine derivative and its use to treat diabetes and obesity |
| US8222416B2 (en) | 2009-12-14 | 2012-07-17 | Hoffmann-La Roche Inc. | Azaindole glucokinase activators |
| WO2011095997A1 (en) | 2010-02-08 | 2011-08-11 | Advinus Therapeutics Private Limited | Benzamide compounds as glucokinase activators and their pharmaceutical application |
| WO2011135355A1 (en) | 2010-04-29 | 2011-11-03 | Astrazeneca Ab | 3-{ [5 -(azetidin-1-ylcarbonyl)pyrazin-2 -yl] oxy} -5-{ [(1s) -2 -hydroxy- 1 -methylethyl]oxy} -n- (5 -methylpyrazin-2-) benzamid monohydrate |
| EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| WO2012007758A2 (en) | 2010-07-15 | 2012-01-19 | Astrazeneca Ab | Pharmaceutical formulations |
| CA2903572A1 (en) * | 2013-03-15 | 2014-10-23 | Epizyme, Inc. | Substituted benzene compounds |
| US9243001B2 (en) * | 2013-03-15 | 2016-01-26 | Epizyme, Inc. | Substituted benzene compounds |
| KR102513342B1 (ko) | 2016-07-22 | 2023-03-22 | 브리스톨-마이어스 스큅 컴퍼니 | 글루코키나제 활성화제 및 그의 사용 방법 |
| KR102836470B1 (ko) * | 2021-09-02 | 2025-07-22 | 콘두이트 유케이 매니지먼트 엘티디 | 3-{[5-(아제티딘-1-일카르보닐)피라진-2-일]옥시}-5-{[(1s)-1-메틸-2-(메틸옥시)에틸]옥시)-n-(5-메틸피라진-2-일)벤즈아미드의치료 공결정 |
Family Cites Families (210)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2750393A (en) | 1954-12-01 | 1956-06-12 | Sterling Drug Inc | Iodinated 5-henzamidotetrazoles and preparation thereof |
| US2967194A (en) | 1958-05-15 | 1961-01-03 | Pennsalt Chemicals Corp | 4-trifluoromethylsalicylamides |
| FR1526074A (fr) | 1967-03-22 | 1968-05-24 | Rech S Ind S O R I Soc D | Méthoxy-phényl-amino-2-thiazoles, leurs amides et leurs procédés de préparation |
| GB1352415A (en) | 1970-05-03 | 1974-05-08 | Boots Co Ltd | Esters of substituted nicotine acids |
| FR2088019A1 (en) | 1970-05-08 | 1972-01-07 | Rabot Ets David | Esters of 2 and 6-substituted nicotinic acids - with vasomotor active |
| CS173097B1 (enExample) | 1972-12-01 | 1977-02-28 | ||
| GB1400540A (en) | 1972-12-06 | 1975-07-16 | Smith Kline French Lab | Salicylamides and compositions thereof |
| US4009174A (en) | 1972-12-08 | 1977-02-22 | The Boots Company Limited | Esters of substituted nicotinic acids |
| GB1437800A (en) | 1973-08-08 | 1976-06-03 | Phavic Sprl | Derivatives of 2-benzamido-5-nitro-thiazoles |
| JPS5734314B2 (enExample) | 1973-12-22 | 1982-07-22 | ||
| GB1561350A (en) | 1976-11-05 | 1980-02-20 | May & Baker Ltd | Benzamide derivatives |
| FR2344284A1 (fr) | 1976-03-17 | 1977-10-14 | Cerm Cent Europ Rech Mauvernay | Nouveaux composes tricycliques a cycle furannique et leur application comme antidepresseurs |
| GB1588242A (en) | 1977-10-28 | 1981-04-23 | May & Baker Ltd | N-(tetrazol-5-yl)-salicylamide derivatives |
| US4474792A (en) | 1979-06-18 | 1984-10-02 | Riker Laboratories, Inc. | N-Tetrazolyl benzamides and anti-allergic use thereof |
| JPS5721320A (en) | 1980-07-11 | 1982-02-04 | Chugai Pharmaceut Co Ltd | Blood sugar level depressing agent |
| JPS5775962A (en) | 1980-10-29 | 1982-05-12 | Shionogi & Co Ltd | 2-alkoxybenzamide derivative |
| FR2493848B2 (fr) | 1980-11-07 | 1986-05-16 | Delalande Sa | Nouveaux derives des nor-tropane et granatane, leur procede de preparation et leur application en therapeutique |
| JPS5869812A (ja) | 1981-10-22 | 1983-04-26 | Chugai Pharmaceut Co Ltd | 血糖降下剤 |
| JPS59139357A (ja) | 1983-01-28 | 1984-08-10 | Torii Yakuhin Kk | アミジン誘導体 |
| JPS61205937A (ja) | 1985-03-09 | 1986-09-12 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀カラ−写真感光材料 |
| JPS62142168A (ja) | 1985-10-16 | 1987-06-25 | Mitsubishi Chem Ind Ltd | チアゾ−ル誘導体及びそれを有効成分とするロイコトリエンきつ抗剤 |
| JPS62158252A (ja) | 1985-12-28 | 1987-07-14 | Kirin Brewery Co Ltd | 4−アミノピリジンベンズアミド誘導体 |
| CA1327358C (en) | 1987-11-17 | 1994-03-01 | Morio Fujiu | Fluoro cytidine derivatives |
| JP2852659B2 (ja) | 1988-03-03 | 1999-02-03 | 富山化学工業株式会社 | ピペラジン誘導体およびその塩 |
| DE3822449A1 (de) | 1988-07-02 | 1990-01-04 | Henkel Kgaa | Oxidationshaarfaerbemittel mit neuen kupplern |
| JPH03181465A (ja) | 1989-12-11 | 1991-08-07 | Takeda Chem Ind Ltd | キノリン誘導体 |
| US6344213B1 (en) | 1996-03-29 | 2002-02-05 | Emisphere Technologies, Inc. | Compounds and compositions for delivering active agents |
| JPH04300874A (ja) | 1991-03-29 | 1992-10-23 | Tsumura & Co | 新規2,4−ジアミノ−1,3,5−トリアジン誘導体 |
| JPH04300832A (ja) | 1991-03-29 | 1992-10-23 | Tsumura & Co | 2,4−ジアミノ−1,3,5−トリアジン誘導体を有 効成分とするロイコトリエン拮抗剤 |
| US5258407A (en) | 1991-12-31 | 1993-11-02 | Sterling Winthrop Inc. | 3,4-disubstituted phenols-immunomodulating agents |
| US5466715A (en) | 1991-12-31 | 1995-11-14 | Sterling Winthrop Inc. | 3,4-disubstituted phenols-immunomodulating agents |
| US5273986A (en) | 1992-07-02 | 1993-12-28 | Hoffmann-La Roche Inc. | Cycloalkylthiazoles |
| JPH0627025A (ja) | 1992-07-06 | 1994-02-04 | Toto Ltd | 分子認識機能膜及びこれを用いたセンサー |
| US5498609A (en) | 1992-08-20 | 1996-03-12 | Otsuka Pharmaceutical Company, Limited | Benzoazepinyl compounds as oxytocin and vasopressin antagonists |
| CZ141795A3 (en) | 1992-12-02 | 1995-11-15 | Pfizer | 4-substituted catechol diethers as such and for treating diseases and pharmaceutical preparations based thereon |
| EP0619116A3 (en) | 1993-04-05 | 1994-11-23 | Hoechst Japan | Use of synthetic retinoids for osteopathy. |
| GB9307527D0 (en) | 1993-04-13 | 1993-06-02 | Fujisawa Pharmaceutical Co | New venzamide derivatives,processes for the preparation thereof and pharmaceutical composition comprising the same |
| GB9401460D0 (en) | 1994-01-26 | 1994-03-23 | Rhone Poulenc Rorer Ltd | Compositions of matter |
| DE69523864T2 (de) | 1994-06-21 | 2002-06-13 | Otsuka Pharmaceutical Factory, Inc. | PYRAZOLO[1,5-a] PYRIMIDIN-DERIVATE |
| US5661153A (en) | 1994-07-19 | 1997-08-26 | Japan Energy Corporation | 1-arylpyrimidine derivatives and pharmaceutical use thereof |
| US5792109A (en) | 1994-09-01 | 1998-08-11 | Leland L. Ladd | Irrigation pump and system |
| GB9420557D0 (en) | 1994-10-12 | 1994-11-30 | Zeneca Ltd | Aromatic compounds |
| JPH08143565A (ja) | 1994-11-16 | 1996-06-04 | Fujisawa Pharmaceut Co Ltd | ベンズアミド化合物 |
| US5510478A (en) | 1994-11-30 | 1996-04-23 | American Home Products Corporation | 2-arylamidothiazole derivatives with CNS activity |
| US5672750A (en) | 1994-12-16 | 1997-09-30 | Eastman Chemical Company | Preparation of aromatic amides from carbon monoxide, an amine and an aromatic chloride |
| ATE223899T1 (de) | 1994-12-20 | 2002-09-15 | Hoffmann La Roche | Aryl-und hetaryl-sulfonamid derivate, deren herstellung und deren verwendung als endothelin- antagonisten |
| US5536718A (en) | 1995-01-17 | 1996-07-16 | American Cyanamid Company | Tricyclic benzazepine vasopressin antagonists |
| US5753648A (en) | 1995-01-17 | 1998-05-19 | American Cyanamid Company | Tricyclic benzazepine vasopressin antagonists |
| US5696112A (en) | 1995-01-17 | 1997-12-09 | American Cyanamid Company | Fused heterocyclic azepines as vasopressin antagonists |
| US5849735A (en) | 1995-01-17 | 1998-12-15 | American Cyanamid Company | Tricyclic benzazepine vasopressin antagonists |
| AR002459A1 (es) | 1995-01-17 | 1998-03-25 | American Cyanamid Co | Antagonistas de vasopresina de benzacepina triciclicos, una composicion farmaceutica que los contiene, un metodo para tratar enfermedades y unprocedimiento para su preparacion. |
| US5700796A (en) | 1995-01-17 | 1997-12-23 | American Cyanamid Company | Tricyclic benzazepine vasopressin antagonists |
| US5532235A (en) | 1995-01-17 | 1996-07-02 | American Cyanamid Company | Tricyclic benzazepine vasopressin antagonists |
| JPH08301760A (ja) | 1995-05-10 | 1996-11-19 | Shiseido Co Ltd | 皮膚外用剤 |
| AU699008B2 (en) | 1995-05-18 | 1998-11-19 | Zeria Pharmaceutical Co., Ltd. | Aminothiazole derivative, medicament containing the same, and intermediate for preperation of said compound |
| JP3168915B2 (ja) | 1995-05-25 | 2001-05-21 | 田辺製薬株式会社 | 医薬組成物 |
| GB9511694D0 (en) | 1995-06-09 | 1995-08-02 | Fujisawa Pharmaceutical Co | Benzamide derivatives |
| US5712270A (en) | 1995-11-06 | 1998-01-27 | American Home Products Corporation | 2-arylamidothiazole derivatives with CNS activity |
| JP3735741B2 (ja) | 1995-11-24 | 2006-01-18 | 株式会社大塚製薬工場 | 縮環ピリミジン誘導体 |
| GB9526558D0 (en) | 1995-12-27 | 1996-02-28 | Fujisawa Pharmaceutical Co | Heterobicyclic derivatives |
| CA2257222C (en) | 1996-06-06 | 2002-08-20 | Otsuka Pharmaceutical Factory, Inc. | Amide derivatives |
| JPH10101672A (ja) | 1996-08-06 | 1998-04-21 | Otsuka Pharmaceut Factory Inc | アデノシン増強剤 |
| JPH10101671A (ja) | 1996-08-08 | 1998-04-21 | Otsuka Pharmaceut Factory Inc | 一酸化窒素合成酵素阻害剤 |
| AUPO395396A0 (en) | 1996-12-02 | 1997-01-02 | Fujisawa Pharmaceutical Co., Ltd. | Benzamide derivatives |
| FR2757852B1 (fr) | 1996-12-31 | 1999-02-19 | Cird Galderma | Composes stilbeniques a groupement adamantyl, compositions les contenant et utilisations |
| JPH10212271A (ja) | 1997-01-31 | 1998-08-11 | Zeria Pharmaceut Co Ltd | N−置換ベンゾイルアミン誘導体、それを含有する医薬及び該化合物の製造中間体 |
| EP0993831B1 (en) | 1997-02-07 | 2008-01-09 | Emisphere Technologies, Inc. | Compounds and compositions for delivering active agents |
| JPH10338658A (ja) | 1997-04-08 | 1998-12-22 | Hoechst Marion Roussel Kk | レチノイド作用調節剤 |
| JPH1129480A (ja) | 1997-05-12 | 1999-02-02 | Otsuka Pharmaceut Factory Inc | 縮環ピリミジン誘導体を含有する医薬組成物 |
| BR9810456A (pt) | 1997-06-27 | 2001-09-25 | Fujisawa Pharmaceutical Co | Composto de sulfonamida, método para sua obtenção e seu uso farmacêutico |
| DE69826286T2 (de) | 1997-06-27 | 2005-11-24 | Fujisawa Pharmaceutical Co., Ltd. | Derivate mit einem aromatischen ring |
| US6613942B1 (en) | 1997-07-01 | 2003-09-02 | Novo Nordisk A/S | Glucagon antagonists/inverse agonists |
| US6114483A (en) | 1997-08-27 | 2000-09-05 | E. I. Du Pont De Nemours And Company | Polymerization of olefins |
| JPH11171848A (ja) | 1997-09-26 | 1999-06-29 | Fujirebio Inc | 芳香族アミド誘導体 |
| US6297239B1 (en) | 1997-10-08 | 2001-10-02 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
| DK1025088T3 (da) | 1997-10-22 | 2001-11-12 | Astrazeneca Ab | Imidazolderivater og deres anvendelse som farnesylproteintransferaseinhibitorer |
| AU1052599A (en) | 1997-11-12 | 1999-05-31 | Institute Of Medicinal Molecular Design. Inc. | Retinoid receptor agonists |
| DE69803883T2 (de) | 1997-11-21 | 2002-09-19 | Astrazeneca Uk Ltd., London | Neue verbindungen, welche antagonisten sind für p2-purinorezeptor 7-transmembran (tm) g-protein gekoppelte rezeptoren |
| GB9725298D0 (en) | 1997-11-28 | 1998-01-28 | Zeneca Ltd | Insecticidal thiazole derivatives |
| PT1040108E (pt) | 1997-12-19 | 2004-06-30 | Schering Ag | Derivados de orto-antranilamida como anticoagulantes |
| US6200995B1 (en) | 1998-01-29 | 2001-03-13 | Tularik Inc. | PPAR-γ modulators |
| JP3937367B2 (ja) | 1998-02-05 | 2007-06-27 | 株式会社大塚製薬工場 | 一酸化窒素合成酵素阻害剤 |
| JPH11292879A (ja) | 1998-04-08 | 1999-10-26 | Otsuka Pharmaceut Factory Inc | カルボキサミド誘導体 |
| DE19816780A1 (de) | 1998-04-16 | 1999-10-21 | Bayer Ag | Substituierte 2-Oxo-alkansäure-[2-(indol-3-yl)-ethyl]amide |
| GB9811969D0 (en) | 1998-06-03 | 1998-07-29 | Celltech Therapeutics Ltd | Chemical compounds |
| DE19830431A1 (de) | 1998-07-08 | 2000-01-13 | Hoechst Marion Roussel De Gmbh | Sulfonylamino-carbonsäure-N-arylamide als Guanylatcyclase-Aktivatoren |
| US6197798B1 (en) | 1998-07-21 | 2001-03-06 | Novartis Ag | Amino-benzocycloalkane derivatives |
| JP4191825B2 (ja) | 1998-09-10 | 2008-12-03 | あすか製薬株式会社 | 5−アミノイソキサゾール誘導体 |
| GB9823871D0 (en) | 1998-10-30 | 1998-12-23 | Pharmacia & Upjohn Spa | 2-Amino-thiazole derivatives, process for their preparation, and their use as antitumour agents |
| WO2000039118A1 (en) | 1998-12-23 | 2000-07-06 | Eli Lilly And Company | Aromatic amides |
| WO2000046203A2 (en) | 1999-02-04 | 2000-08-10 | Millennium Pharmaceuticals, Inc. | G-protein coupled heptahelical receptor binding compounds and methods of use thereof |
| US6610846B1 (en) | 1999-03-29 | 2003-08-26 | Hoffman-La Roche Inc. | Heteroaromatic glucokinase activators |
| US6320050B1 (en) | 1999-03-29 | 2001-11-20 | Hoffmann-La Roche Inc. | Heteroaromatic glucokinase activators |
| RU2242469C2 (ru) | 1999-03-29 | 2004-12-20 | Ф.Хоффманн-Ля Рош Аг | Активаторы глюкокиназы |
| BR0009486B1 (pt) | 1999-03-29 | 2011-03-09 | composto que compreende uma amida, composição farmacêutica que compreende esse composto, seu uso e processo para a preparação do mesmo. | |
| JP4295458B2 (ja) | 1999-06-30 | 2009-07-15 | アムジェン インコーポレイテッド | Ppar−ガンマ活性調節用化合物 |
| AR032130A1 (es) | 1999-08-13 | 2003-10-29 | Vertex Pharma | Un compuesto inhibidor de quinasas proteicas, una composicion farmaceutica que lo incluye, y un metodo para tratar afecciones con dicho compuesto |
| AU775625B2 (en) | 1999-08-27 | 2004-08-05 | Sugen, Inc. | Phosphate mimics and methods of treatment using phosphatase inhibitors |
| GB9921684D0 (en) | 1999-09-15 | 1999-11-17 | Zeneca Ltd | Assays |
| EP1216228B1 (en) | 1999-09-17 | 2008-10-29 | Millennium Pharmaceuticals, Inc. | BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa |
| DE60029235T2 (de) | 1999-10-08 | 2007-06-14 | Affinium Pharmaceuticals, Inc., Toronto | Fab-i-hemmer |
| RU2002111660A (ru) | 1999-11-04 | 2003-11-27 | Орто-Макнейл Фармасьютикал, Инк. (Us) | Непептидные замещенные бензотиазепины в качестве антагонистов вазопрессина |
| AU1917201A (en) | 1999-11-18 | 2001-05-30 | Centaur Pharmaceuticals, Inc. | Amide therapeutics and methods for treating inflammatory bowel disease |
| US6353111B1 (en) | 1999-12-15 | 2002-03-05 | Hoffmann-La Roche Inc. | Trans olefinic glucokinase activators |
| AU2001245353A1 (en) | 2000-02-29 | 2001-09-12 | Cor Therapeutics, Inc. | Benzamides and related inhibitors of factor xa |
| EP1132381A1 (en) | 2000-03-08 | 2001-09-12 | Cermol S.A. | Ester derivatives of dimethylpropionic acid and pharmaceutical compositions containing them |
| AU776053B2 (en) | 2000-03-31 | 2004-08-26 | Astellas Pharma Inc. | Diazepan derivatives or salts thereof |
| US6534651B2 (en) | 2000-04-06 | 2003-03-18 | Inotek Pharmaceuticals Corp. | 7-Substituted isoindolinone inhibitors of inflammation and reperfusion injury and methods of use thereof |
| US6388071B2 (en) | 2000-05-03 | 2002-05-14 | Hoffmann-La Roche Inc. | Alkynyl phenyl heteroaromatic glucokinase activators |
| JP3842131B2 (ja) | 2000-05-03 | 2006-11-08 | エフ.ホフマン−ラ ロシュ アーゲー | ヒダントイン含有グルコキナーゼ活性化物質 |
| EP1282611B1 (en) | 2000-05-08 | 2004-10-20 | F. Hoffmann-La Roche Ag | Substituted phenylacetamides and their use as glucokinase activators |
| ATE398611T1 (de) | 2000-05-08 | 2008-07-15 | Hoffmann La Roche | Para-amin substituierte phenylamid glukokinase activatoren |
| BRPI0112115B8 (pt) | 2000-06-28 | 2021-05-25 | Japan Tobacco Inc | compostos moduladores ppar-gamma de quinolinil e benzotiazolil |
| DE60111534T2 (de) | 2000-07-20 | 2006-05-11 | F. Hoffmann-La Roche Ag | Alpha-acyl- und alpha-heteroatom-substituierte benzenacetamide verwendbar als glucokinase-aktivatoren |
| US6369232B1 (en) | 2000-08-15 | 2002-04-09 | Hoffmann-La Roche Inc. | Tetrazolyl-phenyl acetamide glucokinase activators |
| EP1322635B1 (en) | 2000-09-25 | 2006-03-22 | Janssen Pharmaceutica N.V. | Farnesyl transferase inhibiting quinoline and quinazoline derivatives as farnesyl transferase inhibitors |
| AU2002214546A1 (en) | 2000-09-29 | 2002-04-08 | Cor Therapeutics, Inc. | Bicyclic pyrimidin-4-one based inhibitors of factor xa |
| US20040077690A1 (en) | 2000-09-29 | 2004-04-22 | Bing-Yan Zhu | Quaternary amidino based inhibitors of factor xa |
| KR20030067675A (ko) | 2000-10-05 | 2003-08-14 | 후지사와 야꾸힝 고교 가부시키가이샤 | 벤자미드 화합물 |
| US7504417B2 (en) | 2000-11-22 | 2009-03-17 | Astellas Pharma Inc. | Substituted benzene derivatives or salts thereof |
| ES2256340T3 (es) | 2000-12-06 | 2006-07-16 | F. Hoffmann-La Roche Ag | Activadores heteroaromaticos fusionados de la glucoquinasa. |
| US6482951B2 (en) | 2000-12-13 | 2002-11-19 | Hoffmann-La Roche Inc. | Isoindolin-1-one glucokinase activators |
| GB0031301D0 (en) | 2000-12-21 | 2001-01-31 | Ici Plc | Process for the production of fluoromethyl hexafluoroisopropyl ether |
| CA2432713C (en) | 2000-12-22 | 2009-10-27 | Ishihara Sangyo Kaisha, Ltd. | Aniline derivatives or salts thereof and cytokine production inhibitors containing the same |
| EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
| US20040077697A1 (en) | 2001-02-02 | 2004-04-22 | Hiroyuki Koshio | 2-Acylaminothiazole derivative or its salt |
| TWI243164B (en) | 2001-02-13 | 2005-11-11 | Aventis Pharma Gmbh | Acylated indanyl amines and their use as pharmaceuticals |
| DE60221505D1 (de) | 2001-03-30 | 2007-09-13 | Millennium Pharm Inc | FAKTOR Xa BENZAMIDIN INHIBITOREN |
| SE0102300D0 (sv) | 2001-06-26 | 2001-06-26 | Astrazeneca Ab | Compounds |
| SE0102299D0 (sv) | 2001-06-26 | 2001-06-26 | Astrazeneca Ab | Compounds |
| PL368129A1 (en) | 2001-08-09 | 2005-03-21 | Ono Pharmaceutical Co, Ltd. | Carboxylic acid derivative compounds and drugs comprising these compounds as the active ingredient |
| TWI312274B (en) | 2001-08-13 | 2009-07-21 | Du Pont | Method for controlling particular insect pests by applying anthranilamide compounds |
| SE0102764D0 (sv) | 2001-08-17 | 2001-08-17 | Astrazeneca Ab | Compounds |
| EP1425286B1 (en) | 2001-09-12 | 2007-02-28 | Pharmacia & Upjohn Company LLC | Substituted 7-aza-[2.2.1]bicycloheptanes for the treatment of diseases |
| TW200724033A (en) | 2001-09-21 | 2007-07-01 | Du Pont | Anthranilamide arthropodicide treatment |
| HRP20080382A2 (en) | 2001-09-21 | 2008-12-31 | Bristol-Myers Squibb Company A Delaware (Usa) Corporation | LACTAM-CONTAINING COMPOUNDS AND DERIVATIVES THEREOF AS FACTOR Xa INHIBITORS |
| WO2003028641A2 (en) | 2001-10-01 | 2003-04-10 | Taisho Pharmaceutical Co., Ltd. | Mch receptor antagonists |
| EP1336607A1 (en) | 2002-02-19 | 2003-08-20 | Novo Nordisk A/S | Amide derivatives as glucokinase activators |
| AU2002349299A1 (en) | 2001-12-03 | 2003-06-17 | Novo Nordisk A/S | Use of a glucokinase activator in combination with a glucagon antagonist for treating type 2 diabetes |
| AU2002365611A1 (en) | 2001-12-05 | 2003-06-17 | F. Hoffmann - La Roche Ag | Inflammation modulators |
| US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
| DE10161765A1 (de) | 2001-12-15 | 2003-07-03 | Bayer Cropscience Gmbh | Substituierte Phenylderivate |
| US6911545B2 (en) | 2001-12-19 | 2005-06-28 | Hoffman-La Roche Inc. | Crystals of glucokinase and methods of growing them |
| IL162620A0 (en) | 2001-12-21 | 2005-11-20 | Novo Nordisk As | Amide derivatives as gk activators |
| GB0202873D0 (en) | 2002-02-07 | 2002-03-27 | Novartis Ag | Organic compounds |
| AU2003221140B9 (en) | 2002-03-26 | 2009-07-30 | Banyu Pharmaceutical Co., Ltd. | Novel aminobenzamide derivative |
| CN100357283C (zh) | 2002-04-02 | 2007-12-26 | 中国科学院上海药物研究所 | 一类甲硫氨酰氨肽酶抑制剂 |
| AU2003232204B8 (en) | 2002-04-26 | 2009-07-30 | F. Hoffmann-La Roche Ag | Substituted phenylacetamides and their use as glucokinase activators |
| CA2490023A1 (en) | 2002-05-16 | 2003-11-27 | Banyu Pharmaceutical Co., Ltd. | Crystal of glucokinase protein, and method for drug design using the crystal |
| KR101116627B1 (ko) | 2002-06-27 | 2012-10-09 | 노보 노르디스크 에이/에스 | 치료제로서 아릴 카르보닐 유도체 |
| JPWO2004007472A1 (ja) | 2002-07-10 | 2005-11-17 | 小野薬品工業株式会社 | Ccr4アンタゴニストおよびその医薬用途 |
| AU2003263393A1 (en) | 2002-09-04 | 2004-03-29 | Glenmark Pharmaceuticals Limited | New heterocyclic amide compounds useful for the treatment of inflammatory and allergic disorders: process for their preparation and pharmaceutical compositions containing them |
| NZ539013A (en) | 2002-10-03 | 2007-05-31 | Novartis Ag | Substituted (thiazol-2-yl) -amide or sulfonamide as glycokinase activators useful in the treatment of type 2 diabetes |
| MXPA05003391A (es) | 2002-10-03 | 2005-06-22 | Hoffmann La Roche | Indol-3-carboxamidas como activadores de glucocinasa. |
| GB0226931D0 (en) | 2002-11-19 | 2002-12-24 | Astrazeneca Ab | Chemical compounds |
| GB0226930D0 (en) | 2002-11-19 | 2002-12-24 | Astrazeneca Ab | Chemical compounds |
| US7132425B2 (en) | 2002-12-12 | 2006-11-07 | Hoffmann-La Roche Inc. | 5-substituted-six-membered heteroaromatic glucokinase activators |
| AU2003294376A1 (en) | 2003-01-06 | 2004-08-10 | Eli Lilly And Company | Heteroaryl compounds |
| EP1585739B1 (en) | 2003-01-06 | 2011-04-20 | Eli Lilly And Company | Substituted arylcyclopropylacetamides as glucokinase activators |
| EP1594863A1 (en) | 2003-02-11 | 2005-11-16 | Prosidion Limited | Tri(cyclo) substituted amide glucokinase activator compounds |
| PL378117A1 (pl) | 2003-02-11 | 2006-03-06 | Prosidion Limited | Tricyklopodstawione związki amidowe |
| MXPA05008619A (es) | 2003-02-13 | 2005-11-04 | Banyu Pharma Co Ltd | Derivados novedosos de 2-piridincarboxamida. |
| EP1600442B1 (en) | 2003-02-26 | 2018-01-17 | Msd K.K. | Heteroarylcarbamoylbenzene derivative |
| CA2517888C (en) | 2003-03-14 | 2012-05-01 | Ono Pharmaceutical Co., Ltd. | Nitrogen-containing heterocyclic derivatives and drugs containing the same as the active ingredient |
| TW200505902A (en) | 2003-03-20 | 2005-02-16 | Schering Corp | Cannabinoid receptor ligands |
| MXPA05010081A (es) | 2003-03-24 | 2005-11-23 | Hoffmann La Roche | Bencil-piridazinonas como inhibidores de transcriptasa inversa. |
| US7244739B2 (en) | 2003-05-14 | 2007-07-17 | Torreypines Therapeutics, Inc. | Compounds and uses thereof in modulating amyloid beta |
| EP1635832A2 (en) | 2003-06-06 | 2006-03-22 | Merck & Co., Inc. | Combination therapy for the treatment of diabetes |
| JP2007505888A (ja) | 2003-09-22 | 2007-03-15 | ファイザー インコーポレイテッド | オキシトシン拮抗薬としての置換トリアゾール誘導体 |
| EP1675844A1 (en) | 2003-10-23 | 2006-07-05 | Sterix Limited | Phenyl carboxamide and sulfonamide derivatives for use as 11-beta-hydroxysteroid dehydrogenase |
| GB0325402D0 (en) | 2003-10-31 | 2003-12-03 | Astrazeneca Ab | Compounds |
| US20050267182A1 (en) | 2003-11-13 | 2005-12-01 | Ambit Biosciences Corporation | Urea derivatives as FLT-3 modulators |
| EP1532980A1 (en) | 2003-11-24 | 2005-05-25 | Novo Nordisk A/S | N-heteroaryl indole carboxamides and analogues thereof, for use as glucokinase activators in the treatment of diabetes |
| GB0327761D0 (en) | 2003-11-29 | 2003-12-31 | Astrazeneca Ab | Compounds |
| GB0327760D0 (en) | 2003-11-29 | 2003-12-31 | Astrazeneca Ab | Compounds |
| GB0328178D0 (en) | 2003-12-05 | 2004-01-07 | Astrazeneca Ab | Compounds |
| EP1702919B1 (en) | 2003-12-29 | 2012-05-30 | Msd K.K. | Novel 2-heteroaryl-substituted benzimidazole derivative |
| MXPA06007667A (es) | 2004-01-06 | 2006-09-01 | Novo Nordisk As | Heteroaril-ureas y su uso como activadores de glucocinasa. |
| EP1718624B1 (en) * | 2004-02-18 | 2009-03-25 | AstraZeneca AB | Benzamide derivatives and their use as glucokinase activating agents |
| KR20070007104A (ko) | 2004-02-18 | 2007-01-12 | 아스트라제네카 아베 | 화합물 |
| EP1734040A4 (en) | 2004-03-23 | 2007-11-28 | Banyu Pharma Co Ltd | SUBSTITUTED CHINAZOLINE OR PYRIDOPYRIMIDINE DERIVATIVE |
| KR20070006816A (ko) | 2004-04-02 | 2007-01-11 | 노파르티스 아게 | 티아졸로피리딘 유도체, 이를 함유하는 제약 조성물 및글루코키나제 매개형 증상의 치료 방법 |
| KR100830007B1 (ko) | 2004-04-02 | 2008-05-15 | 노파르티스 아게 | 2형 당뇨병 치료에 유용한 글루코키나제 활성화제로서의술폰아미드-티아졸피리딘 유도체 |
| EA012204B1 (ru) | 2004-04-21 | 2009-08-28 | Прозидион Лимитед | Три(цикло)замещённые амидные соединения |
| TW200600086A (en) | 2004-06-05 | 2006-01-01 | Astrazeneca Ab | Chemical compound |
| WO2005123132A2 (en) | 2004-06-17 | 2005-12-29 | Novo Nordisk A/S | Use of liver-selective glucokinase activators |
| GB0418046D0 (en) | 2004-08-12 | 2004-09-15 | Prosidion Ltd | Eantioselective process |
| CN101035767A (zh) | 2004-08-12 | 2007-09-12 | 普洛希典有限公司 | 被取代的苯乙酰胺及其作为葡糖激酶激活剂的用途 |
| GB0418058D0 (en) | 2004-08-12 | 2004-09-15 | Prosidion Ltd | Fluorination process |
| PE20060598A1 (es) | 2004-09-13 | 2006-08-21 | Ono Pharmaceutical Co | Derivado heterociclo conteniendo nitrogeno como antagonista de quimiocina ccr5 |
| GB0423043D0 (en) | 2004-10-16 | 2004-11-17 | Astrazeneca Ab | Compounds |
| GB0423044D0 (en) | 2004-10-16 | 2004-11-17 | Astrazeneca Ab | Compounds |
| CA2581619A1 (en) | 2004-10-16 | 2006-04-20 | Astrazeneca Ab | Process for making phenoxy benzamide compounds |
| DE602004018552D1 (de) | 2004-12-24 | 2009-01-29 | Telecom Italia Spa | Verfahren zur optimierung des webseitenzugangs in drahtlosen netzwerken |
| JP5033119B2 (ja) | 2005-04-25 | 2012-09-26 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | キナーゼ阻害剤としての新規アザ複素環化合物 |
| WO2006125958A1 (en) | 2005-05-24 | 2006-11-30 | Astrazeneca Ab | 2-phenyl substituted imidazol [4 , 5b] pyridine/ pyrazine and purine derivatives as glucokinase modulators |
| TW200714597A (en) | 2005-05-27 | 2007-04-16 | Astrazeneca Ab | Chemical compounds |
| US20080234273A1 (en) | 2005-07-09 | 2008-09-25 | Mckerrecher Darren | Heteroaryl Benzamide Derivatives for Use as Glk Activators in the Treatment of Diabetes |
| JP2009500442A (ja) | 2005-07-09 | 2009-01-08 | アストラゼネカ アクチボラグ | 2型糖尿病を処置するためのグルコキナーゼのモジュレーターとしての2−ヘテロシクリルオキシベンゾイルアミノヘテロシクリル化合物 |
| NZ564608A (en) * | 2005-07-09 | 2009-09-25 | Astrazeneca Ab | Heteroaryl benzamide derivatives for use as GLK activators in the treatment of diabetes |
| US20100160286A1 (en) | 2005-08-09 | 2010-06-24 | Astrazeneca Uk Limited Ab | Heteroarylcarbamoylbenzene derivatives for the treatment of diabetes |
| JP2007063225A (ja) | 2005-09-01 | 2007-03-15 | Takeda Chem Ind Ltd | イミダゾピリジン化合物 |
| AU2006287521A1 (en) | 2005-09-07 | 2007-03-15 | Plexxikon, Inc. | PPARactive compounds |
| US20090105263A1 (en) | 2005-09-16 | 2009-04-23 | Peter William Rodney Caulkett | Heterobicyclic compounds as glucokinase activators |
| CA2627813A1 (en) | 2005-11-01 | 2007-05-10 | Janssen Pharmaceutica N.V. | Substituted pyrrolones as allosteric modulators of glucokinase |
| TW200738621A (en) | 2005-11-28 | 2007-10-16 | Astrazeneca Ab | Chemical process |
| KR20090008217A (ko) | 2006-03-10 | 2009-01-21 | 오노 야꾸힝 고교 가부시키가이샤 | 질소 함유 복소환 유도체 및 이들을 유효 성분으로 하는 약제 |
| TW200825063A (en) | 2006-10-23 | 2008-06-16 | Astrazeneca Ab | Chemical compounds |
| SA07280576B1 (ar) | 2006-10-26 | 2011-06-22 | استرازينيكا ايه بي | مركبات بنزويل أمينو سيكليل غير متجانسة بأعتبارها عوامل منشطة للجلوكوكيناز |
| JP2010513445A (ja) | 2006-12-21 | 2010-04-30 | アストラゼネカ アクチボラグ | Glkアクチベーターとして有用な新規結晶性化合物 |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009263390A (ja) * | 2005-07-09 | 2009-11-12 | Astrazeneca Ab | 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体 |
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