KR101616737B1 - 당뇨병 치료를 위한 옥사디아조안트라센 화합물 - Google Patents
당뇨병 치료를 위한 옥사디아조안트라센 화합물 Download PDFInfo
- Publication number
- KR101616737B1 KR101616737B1 KR1020107020688A KR20107020688A KR101616737B1 KR 101616737 B1 KR101616737 B1 KR 101616737B1 KR 1020107020688 A KR1020107020688 A KR 1020107020688A KR 20107020688 A KR20107020688 A KR 20107020688A KR 101616737 B1 KR101616737 B1 KR 101616737B1
- Authority
- KR
- South Korea
- Prior art keywords
- phenyl
- compound
- hexahydro
- group
- anthracene
- 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.)
- Expired - Fee Related
Links
- 0 CC*C(*)N* Chemical compound CC*C(*)N* 0.000 description 2
- SUGZPSIGVCAQSR-RXBHZZDJSA-N CC(C)(C)OC(N(Cc(c(C1)c2)cc(O[C@H]3c(cc4)ccc4OCc(cc4)cc(Cl)c4Cl)c2N(C)C3=O)C1C(OC)=O)=O Chemical compound CC(C)(C)OC(N(Cc(c(C1)c2)cc(O[C@H]3c(cc4)ccc4OCc(cc4)cc(Cl)c4Cl)c2N(C)C3=O)C1C(OC)=O)=O SUGZPSIGVCAQSR-RXBHZZDJSA-N 0.000 description 1
- GDSTZBBOSCMRPM-SBHBPGBTSA-N CC(C)(C)OC1OC1N(Cc(cc1O[C@@H]2c(cc3)ccc3OCc(cc3)cc(Cl)c3Cl)c(C3)cc1N(C)C2=O)[C@@H]3C(OC)=O Chemical compound CC(C)(C)OC1OC1N(Cc(cc1O[C@@H]2c(cc3)ccc3OCc(cc3)cc(Cl)c3Cl)c(C3)cc1N(C)C2=O)[C@@H]3C(OC)=O GDSTZBBOSCMRPM-SBHBPGBTSA-N 0.000 description 1
- XDELRCXZRZSPAW-HOUGNEDLSA-N CC(C)[C@H](CC[C@@H](C)C1)[C@@H]1OC(C(Cc(c(C1)c2)cc(N3C)c2O[C@@H](c(cc2)ccc2OCc(cc2Cl)ccc2Cl)C3=O)N1C(OC(C)(C)C)=O)=O Chemical compound CC(C)[C@H](CC[C@@H](C)C1)[C@@H]1OC(C(Cc(c(C1)c2)cc(N3C)c2O[C@@H](c(cc2)ccc2OCc(cc2Cl)ccc2Cl)C3=O)N1C(OC(C)(C)C)=O)=O XDELRCXZRZSPAW-HOUGNEDLSA-N 0.000 description 1
- ZXJQFMYVTDGFTB-MGCVPBOFSA-N CCC(c1ccccc1)N(Cc(c(C1)c2)cc(OC3c(cc4)ccc4OCc(cc4Cl)ccc4Cl)c2N(C)C3=O)C1C(N[C@@H](Cc(cc1)ccc1-c(cc1)ccc1C#N)C(O)=O)=O Chemical compound CCC(c1ccccc1)N(Cc(c(C1)c2)cc(OC3c(cc4)ccc4OCc(cc4Cl)ccc4Cl)c2N(C)C3=O)C1C(N[C@@H](Cc(cc1)ccc1-c(cc1)ccc1C#N)C(O)=O)=O ZXJQFMYVTDGFTB-MGCVPBOFSA-N 0.000 description 1
- GGMBMFPUDVMNNM-HKOMJGRFSA-N CCC(c1ccccc1)N(Cc(c(C1)c2)cc(O[C@@H]3c(cc4)ccc4OCc(cc4Cl)ccc4Cl)c2N(C)C3=O)C1C(N[C@@H](Cc(cc1)ccc1-c(cc1)ccc1OC)C(O)=O)=O Chemical compound CCC(c1ccccc1)N(Cc(c(C1)c2)cc(O[C@@H]3c(cc4)ccc4OCc(cc4Cl)ccc4Cl)c2N(C)C3=O)C1C(N[C@@H](Cc(cc1)ccc1-c(cc1)ccc1OC)C(O)=O)=O GGMBMFPUDVMNNM-HKOMJGRFSA-N 0.000 description 1
- IEYVTXNDBGMIHA-GVUKDKGQSA-N CC[C@@H](c1ccccc1)N(Cc(c(C1)c2)cc(O[C@H]3c(cc4)ccc4O)c2N(C)C3=O)[C@@H]1C(O)=O Chemical compound CC[C@@H](c1ccccc1)N(Cc(c(C1)c2)cc(O[C@H]3c(cc4)ccc4O)c2N(C)C3=O)[C@@H]1C(O)=O IEYVTXNDBGMIHA-GVUKDKGQSA-N 0.000 description 1
- IEYVTXNDBGMIHA-OVQDZVAUSA-N CC[C@H](c1ccccc1)N(Cc(c(C1)c2)cc(O[C@H]3c(cc4)ccc4O)c2N(C)C3=O)C1C(O)=O Chemical compound CC[C@H](c1ccccc1)N(Cc(c(C1)c2)cc(O[C@H]3c(cc4)ccc4O)c2N(C)C3=O)C1C(O)=O IEYVTXNDBGMIHA-OVQDZVAUSA-N 0.000 description 1
- RAPJHYSULICCKF-BBQXNDQXSA-N CN1c(cc(CC(C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(O)=O)=O)N(C2)C(C3)Cc4c3cccc4)c2c2)c2OC(c(cc2)ccc2OCc(cc2Cl)ccc2Cl)C1=O Chemical compound CN1c(cc(CC(C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(O)=O)=O)N(C2)C(C3)Cc4c3cccc4)c2c2)c2OC(c(cc2)ccc2OCc(cc2Cl)ccc2Cl)C1=O RAPJHYSULICCKF-BBQXNDQXSA-N 0.000 description 1
- XIQGCFQXNOOKPY-RYHBZWQBSA-N CN1c(cc(CC(C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(O)=O)=O)N(C2)C3CCCCC3)c2c2)c2OC(c(cc2)ccc2OCc(cc2Cl)ccc2Cl)C1=O Chemical compound CN1c(cc(CC(C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(O)=O)=O)N(C2)C3CCCCC3)c2c2)c2OC(c(cc2)ccc2OCc(cc2Cl)ccc2Cl)C1=O XIQGCFQXNOOKPY-RYHBZWQBSA-N 0.000 description 1
- QEADFMDCECLBCY-LFOSQWHESA-N CN1c(cc(C[C@@H](C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(OC)=O)=O)NC2)c2c2)c2OC(c(cc2)ccc2OCc(cc2)cc(Cl)c2Cl)C1=O Chemical compound CN1c(cc(C[C@@H](C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(OC)=O)=O)NC2)c2c2)c2OC(c(cc2)ccc2OCc(cc2)cc(Cl)c2Cl)C1=O QEADFMDCECLBCY-LFOSQWHESA-N 0.000 description 1
- GXGPHFVGRDJMNL-DHLKQENFSA-N CN1c(cc(C[C@@H](C(OC)=O)NC2)c2c2)c2O[C@@H](c(cc2)ccc2OCc(cc2)cc(Cl)c2Cl)C1=O Chemical compound CN1c(cc(C[C@@H](C(OC)=O)NC2)c2c2)c2O[C@@H](c(cc2)ccc2OCc(cc2)cc(Cl)c2Cl)C1=O GXGPHFVGRDJMNL-DHLKQENFSA-N 0.000 description 1
- GXGPHFVGRDJMNL-WIOPSUGQSA-N CN1c2cc(C[C@@H](C(OC)=O)NC3)c3cc2O[C@H](c(cc2)ccc2OCc(cc2)cc(Cl)c2Cl)C1=O Chemical compound CN1c2cc(C[C@@H](C(OC)=O)NC3)c3cc2O[C@H](c(cc2)ccc2OCc(cc2)cc(Cl)c2Cl)C1=O GXGPHFVGRDJMNL-WIOPSUGQSA-N 0.000 description 1
- BPMUWXQCBDAICY-SYVAAPJHSA-N CSc1nc(CN(Cc(c(C2)c3)cc(OC4c(cc5)ccc5OCc(cc5Cl)ccc5Cl)c3NC4=O)C2C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(O)=O)=O)ccc1C#N Chemical compound CSc1nc(CN(Cc(c(C2)c3)cc(OC4c(cc5)ccc5OCc(cc5Cl)ccc5Cl)c3NC4=O)C2C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(O)=O)=O)ccc1C#N BPMUWXQCBDAICY-SYVAAPJHSA-N 0.000 description 1
- YKJKZJCVIAUGMO-OUOXWZJQSA-N Cc1c(CN(Cc(c(C2)c3)cc(OC4c(cc5)ccc5OCc(cc5)cc(Cl)c5Cl)c3NC4=O)[C@@H]2C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(O)=O)=O)cccc1 Chemical compound Cc1c(CN(Cc(c(C2)c3)cc(OC4c(cc5)ccc5OCc(cc5)cc(Cl)c5Cl)c3NC4=O)[C@@H]2C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(O)=O)=O)cccc1 YKJKZJCVIAUGMO-OUOXWZJQSA-N 0.000 description 1
- KKOKPMHWXQRCPJ-SYVAAPJHSA-N Cc1nc(CN(Cc(c(C2)c3)cc(OC4c(cc5)ccc5OCc(cc5Cl)ccc5Cl)c3NC4=O)C2C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(O)=O)=O)ccc1 Chemical compound Cc1nc(CN(Cc(c(C2)c3)cc(OC4c(cc5)ccc5OCc(cc5Cl)ccc5Cl)c3NC4=O)C2C(N[C@@H](Cc(cc2)ccc2-c(cc2)ccc2C#N)C(O)=O)=O)ccc1 KKOKPMHWXQRCPJ-SYVAAPJHSA-N 0.000 description 1
- GPEIOOLHSPBFAP-UHFFFAOYSA-N N#Cc(cc1)ccc1-c1ccc(CC(C(O)=O)NC(C(Cc(cc2NC3O)c(C4)cc2OC3c(cc2)ccc2OCc(cc2Cl)ccc2Cl)N4S(c2cc([NH+]([O-])O)ccc2)(=O)=O)=O)cc1 Chemical compound N#Cc(cc1)ccc1-c1ccc(CC(C(O)=O)NC(C(Cc(cc2NC3O)c(C4)cc2OC3c(cc2)ccc2OCc(cc2Cl)ccc2Cl)N4S(c2cc([NH+]([O-])O)ccc2)(=O)=O)=O)cc1 GPEIOOLHSPBFAP-UHFFFAOYSA-N 0.000 description 1
- AWNUYDZNEQFJNN-GTAGSRNNSA-N N#Cc(cc1)ccc1-c1ccc(C[C@@H](C(O)=O)NC(C(Cc(c(C2)c3)cc(N4)c3OC(c(cc3)ccc3OCc(cn3)cc(Cl)c3Cl)C4=O)N2C(c2ccc[s]2)=O)=O)cc1 Chemical compound N#Cc(cc1)ccc1-c1ccc(C[C@@H](C(O)=O)NC(C(Cc(c(C2)c3)cc(N4)c3OC(c(cc3)ccc3OCc(cn3)cc(Cl)c3Cl)C4=O)N2C(c2ccc[s]2)=O)=O)cc1 AWNUYDZNEQFJNN-GTAGSRNNSA-N 0.000 description 1
- ZRLAMGNDDVCLCD-SYVAAPJHSA-N N#Cc(cc1)ccc1-c1ccc(C[C@@H](C(O)=O)NC(C(Cc2c3)N(Cc4ccccc4Cl)Cc2cc(OC2c(cc4)ccc4OCc(cc4Cl)ccc4Cl)c3NC2=O)=O)cc1 Chemical compound N#Cc(cc1)ccc1-c1ccc(C[C@@H](C(O)=O)NC(C(Cc2c3)N(Cc4ccccc4Cl)Cc2cc(OC2c(cc4)ccc4OCc(cc4Cl)ccc4Cl)c3NC2=O)=O)cc1 ZRLAMGNDDVCLCD-SYVAAPJHSA-N 0.000 description 1
- OJDOHMPBJTYOOR-PFYITYDVSA-N N#Cc(cc1)ccc1-c1ccc(C[C@@H](C(O)=O)NC([C@H](Cc(c(C2)c3)cc(N4)c3OC(c(cc3)ccc3OCc(cc3)cc(Cl)c3Cl)C4=O)N2C(c(c(F)cc(F)c2)c2F)=O)=O)cc1 Chemical compound N#Cc(cc1)ccc1-c1ccc(C[C@@H](C(O)=O)NC([C@H](Cc(c(C2)c3)cc(N4)c3OC(c(cc3)ccc3OCc(cc3)cc(Cl)c3Cl)C4=O)N2C(c(c(F)cc(F)c2)c2F)=O)=O)cc1 OJDOHMPBJTYOOR-PFYITYDVSA-N 0.000 description 1
- LMDCCBBADBDIGJ-ZKCOFTMWSA-N N#Cc(cc1)ccc1-c1ccc(C[C@@H](C(O)=O)NC([C@H](Cc(c(C2)c3)cc(N4)c3OC(c(cc3)ccc3OCc(cc3)cc(Cl)c3Cl)C4=O)N2S(c2ccccc2)(=O)=O)=O)cc1 Chemical compound N#Cc(cc1)ccc1-c1ccc(C[C@@H](C(O)=O)NC([C@H](Cc(c(C2)c3)cc(N4)c3OC(c(cc3)ccc3OCc(cc3)cc(Cl)c3Cl)C4=O)N2S(c2ccccc2)(=O)=O)=O)cc1 LMDCCBBADBDIGJ-ZKCOFTMWSA-N 0.000 description 1
- FPBZVDNUFCQOSU-FTSYTSSGSA-N N#Cc(cc1)ccc1-c1ccc(C[C@@H](C(O)=O)NC([C@H](Cc2c3)N(Cc4ccccc4F)Cc2cc(OC2c(cc4)ccc4OCc(cc4)cc(Cl)c4Cl)c3NC2=O)=O)cc1 Chemical compound N#Cc(cc1)ccc1-c1ccc(C[C@@H](C(O)=O)NC([C@H](Cc2c3)N(Cc4ccccc4F)Cc2cc(OC2c(cc4)ccc4OCc(cc4)cc(Cl)c4Cl)c3NC2=O)=O)cc1 FPBZVDNUFCQOSU-FTSYTSSGSA-N 0.000 description 1
- VBWXZTKGNUDUGJ-BGLVMXALSA-N OC([C@H](Cc(cc1)ccc1-c1ccncc1)NC(C(Cc(c(C1)c2)cc(N3)c2OC(c(cc2)ccc2OCc(cc2)cc(Cl)c2Cl)C3=O)N1C(c1ccccc1)=O)=O)=O Chemical compound OC([C@H](Cc(cc1)ccc1-c1ccncc1)NC(C(Cc(c(C1)c2)cc(N3)c2OC(c(cc2)ccc2OCc(cc2)cc(Cl)c2Cl)C3=O)N1C(c1ccccc1)=O)=O)=O VBWXZTKGNUDUGJ-BGLVMXALSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic 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
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/14—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Child & Adolescent Psychology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Emergency Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Gastroenterology & Hepatology (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3459908P | 2008-03-07 | 2008-03-07 | |
| US61/034,599 | 2008-03-07 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20100131455A KR20100131455A (ko) | 2010-12-15 |
| KR101616737B1 true KR101616737B1 (ko) | 2016-05-02 |
Family
ID=41056666
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020107020688A Expired - Fee Related KR101616737B1 (ko) | 2008-03-07 | 2009-03-06 | 당뇨병 치료를 위한 옥사디아조안트라센 화합물 |
Country Status (17)
| Country | Link |
|---|---|
| US (7) | US7727983B2 (enExample) |
| EP (1) | EP2262364B1 (enExample) |
| JP (1) | JP5382952B2 (enExample) |
| KR (1) | KR101616737B1 (enExample) |
| CN (1) | CN101959405B (enExample) |
| AU (1) | AU2009221722B2 (enExample) |
| BR (1) | BRPI0910282A2 (enExample) |
| CA (1) | CA2716664C (enExample) |
| DK (1) | DK2262364T3 (enExample) |
| EA (1) | EA018225B1 (enExample) |
| ES (1) | ES2567451T3 (enExample) |
| IL (1) | IL207570A (enExample) |
| MA (1) | MA32175B1 (enExample) |
| MX (1) | MX2010009752A (enExample) |
| NZ (1) | NZ587343A (enExample) |
| WO (1) | WO2009111700A2 (enExample) |
| ZA (1) | ZA201006367B (enExample) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009111700A2 (en) | 2008-03-07 | 2009-09-11 | Transtech Pharma, Inc. | Oxadiazoanthracene compounds for the treatment of diabetes |
| CN102378574B (zh) * | 2009-03-30 | 2013-11-20 | 转化技术制药公司 | 取代的偶氮蒽衍生物、药物组合物及其使用方法 |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| DE102010015123A1 (de) | 2010-04-16 | 2011-10-20 | Sanofi-Aventis Deutschland Gmbh | Benzylamidische Diphenylazetidinone, diese Verbindungen enthaltende Arzneimittel und deren Verwendung |
| 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 |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| JP5694561B2 (ja) | 2010-12-23 | 2015-04-01 | ファイザー・インク | グルカゴン受容体モジュレーター |
| WO2012096824A1 (en) * | 2011-01-12 | 2012-07-19 | Transtech Pharma, Inc. | Phenylglyoxylic acid derivatives and their preparation and use |
| KR101638671B1 (ko) | 2011-02-08 | 2016-07-11 | 화이자 인코포레이티드 | 글루카곤 수용체 조절자 |
| JP5647379B2 (ja) | 2011-07-22 | 2014-12-24 | ファイザー・インク | キノリニルグルカゴン受容体モジュレーター |
| EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| ES2674951T3 (es) * | 2012-03-22 | 2018-07-05 | Transtech Pharma, Llc | Sales de tris(hidroximetil)aminometano de un agonista de GLP1R de molécula pequeña y composiciones farmacéuticas y usos de las mismas |
| IN2015DN03795A (enExample) | 2012-10-24 | 2015-10-02 | Inserm Inst Nat De La Santé Et De La Rech Médicale | |
| KR102165434B1 (ko) * | 2013-01-17 | 2020-10-14 | 브이티브이 테라퓨틱스 엘엘씨 | 2형 당뇨병 및 다른 장애의 치료를 위한 glp1r 작용제 및 메트포민의 조합 및 이것들의 사용법 |
| AU2015292356B2 (en) * | 2014-07-25 | 2020-02-06 | Receptos Llc | Novel GLP-1 receptor modulators |
| WO2016151018A1 (en) | 2015-03-24 | 2016-09-29 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Method and pharmaceutical composition for use in the treatment of diabetes |
| JOP20190060A1 (ar) | 2016-09-26 | 2019-03-26 | Chugai Pharmaceutical Co Ltd | مشتق بيرازولو بيريدين له تأثير مساعد لمستقبل glp-1 |
| TW201925204A (zh) * | 2017-11-22 | 2019-07-01 | 日商第一三共股份有限公司 | 稠合三環化合物 |
| CA3090823A1 (en) | 2018-05-08 | 2019-11-14 | Vtv Therapeutics Llc | Therapeutic uses of glp1r agonists |
| AU2019382642B2 (en) | 2018-11-22 | 2025-05-29 | Qilu Regor Therapeutics Inc. | GLP-1R agonists and uses thereof |
| CU20210083A7 (es) * | 2019-04-12 | 2022-05-11 | Qilu Regor Therapeutics Inc | Agonistas de glp-1r |
| CN115461344B (zh) | 2020-04-01 | 2024-01-12 | 杭州中美华东制药有限公司 | 一种glp-1受体激动剂的晶型a及其制备方法 |
| WO2021196951A1 (zh) | 2020-04-01 | 2021-10-07 | 杭州中美华东制药有限公司 | Glp-1受体激动剂游离碱的药学上可接受的酸式盐及其制备方法 |
| TW202144340A (zh) | 2020-04-03 | 2021-12-01 | 大陸商江蘇恆瑞醫藥股份有限公司 | 稠合咪唑類衍生物、其製備方法及其在醫藥上的應用 |
| EP4159737A4 (en) * | 2020-05-28 | 2024-10-09 | Hangzhou Zhongmeihuadong Pharmaceutical Co., Ltd. | METHOD FOR PREPARING A GLP-1 RECEPTOR AGONIST-FREE BASE |
| TW202210461A (zh) * | 2020-05-28 | 2022-03-16 | 中國大陸商杭州中美華東製藥有限公司 | 一種(s)—2—胺基—3—(4—(2,3—二甲基吡啶—4—基)苯基)丙酸甲酯二酸鹽的製備方法 |
| JP2023539584A (ja) | 2020-09-01 | 2023-09-15 | 江蘇恒瑞医薬股▲ふん▼有限公司 | 縮合イミダゾール誘導体、その調製方法及びその医薬的応用 |
| WO2022078152A1 (zh) | 2020-10-12 | 2022-04-21 | 杭州中美华东制药有限公司 | 苯并咪唑酮类glp-1受体激动剂及其用途 |
| US20230382899A1 (en) * | 2020-10-14 | 2023-11-30 | Qilu Regor Therapeutics Inc. | Crystal forms of glp-1r agonists and uses thereof |
| US11851419B2 (en) | 2020-11-20 | 2023-12-26 | Gilead Sciences, Inc. | GLP-1R modulating compounds |
| US20240246959A1 (en) | 2020-11-27 | 2024-07-25 | Shenzhen Salubris Pharmaceuticals Co., Ltd. | Benzimidazole derivative and preparation method therefor and medical use thereof |
| US20240208952A1 (en) | 2021-03-22 | 2024-06-27 | Hangzhou Zhongmeihuadong Pharmaceutical Co., Ltd. | Thiophene glp-1 receptor agonist and use thereof |
| WO2022202864A1 (ja) | 2021-03-24 | 2022-09-29 | 塩野義製薬株式会社 | 縮合環を有するglp-1受容体作動薬を含有する医薬組成物 |
| WO2022262615A1 (zh) * | 2021-06-17 | 2022-12-22 | 杭州中美华东制药有限公司 | 蒽类化合物、其制备方法和医药用途 |
| CN117098758A (zh) | 2021-06-24 | 2023-11-21 | 杭州中美华东制药有限公司 | Glp-1受体激动剂及其组合物和用途 |
| CN115521320B (zh) * | 2021-06-25 | 2023-09-05 | 沈阳兴齐眼药股份有限公司 | 一种制备普拉洛芬的方法 |
| JPWO2024063143A1 (enExample) | 2022-09-22 | 2024-03-28 | ||
| WO2025057134A2 (en) | 2023-09-14 | 2025-03-20 | Ascletis Pharma (China) Co., Limited | Glp-1r agonist and therapeutic method thereof |
| US12291530B1 (en) | 2023-11-24 | 2025-05-06 | Ascletis Pharma (China) Co., Limited | GLP-1R agonist and therapeutic method thereof |
| WO2025158275A1 (en) | 2024-01-24 | 2025-07-31 | Pfizer Inc. | Combination therapy using glucose-dependent insulinotropic polypeptide receptor antagonist compounds and glp-1 receptor agonist compounds |
| WO2025189141A1 (en) | 2024-03-08 | 2025-09-12 | Annapurna Bio, Inc. | Methods for treating obesity and increasing weight loss |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4789675A (en) | 1986-02-11 | 1988-12-06 | Takeda Chemical Industries, Ltd. | 1,4-benzoxazine derivatives and pharmaceutical use |
| US6770656B2 (en) | 2000-02-15 | 2004-08-03 | Applied Research Systems Ars Holding N.V. | Amine derivatives for the treatment of apoptosis |
| US20050222036A1 (en) | 2000-08-24 | 2005-10-06 | Thomas Jefferson University | Peptide compositions with effects on blood glucose |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6345270A (ja) * | 1986-02-11 | 1988-02-26 | Takeda Chem Ind Ltd | 1,4−ベンゾオキサジン誘導体,その製造法およびそれを含有する医薬用組成物 |
| WO1997012853A1 (en) * | 1995-10-06 | 1997-04-10 | Ligand Pharmaceuticals Incorporated | Dimer-selective rxr modulators and methods for their use |
| WO2000042026A1 (en) * | 1999-01-15 | 2000-07-20 | Novo Nordisk A/S | Non-peptide glp-1 agonists |
| HUP0203431A3 (en) * | 1999-12-03 | 2003-11-28 | Kyoto Pharma Ind | Novel heterocyclic compounds and salts thereof and pharmaceutical compositions containing and use of the same |
| CN100432056C (zh) * | 2003-03-26 | 2008-11-12 | 埃科特莱茵药品有限公司 | 四氢异喹啉基乙酰胺衍生物作为阿立新受体拮抗剂的应用 |
| WO2009111700A2 (en) * | 2008-03-07 | 2009-09-11 | Transtech Pharma, Inc. | Oxadiazoanthracene compounds for the treatment of diabetes |
| US8501982B2 (en) | 2010-06-09 | 2013-08-06 | Receptos, Inc. | GLP-1 receptor stabilizers and modulators |
-
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- 2009-03-06 ES ES09718287T patent/ES2567451T3/es active Active
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4789675A (en) | 1986-02-11 | 1988-12-06 | Takeda Chemical Industries, Ltd. | 1,4-benzoxazine derivatives and pharmaceutical use |
| US6770656B2 (en) | 2000-02-15 | 2004-08-03 | Applied Research Systems Ars Holding N.V. | Amine derivatives for the treatment of apoptosis |
| US20050222036A1 (en) | 2000-08-24 | 2005-10-06 | Thomas Jefferson University | Peptide compositions with effects on blood glucose |
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| JP5755217B2 (ja) | 置換アゾアントラセン誘導体、その医薬組成物とその使用の方法 | |
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