KR100619515B1 - 디아미노티아졸 - Google Patents
디아미노티아졸 Download PDFInfo
- Publication number
- KR100619515B1 KR100619515B1 KR1020047018605A KR20047018605A KR100619515B1 KR 100619515 B1 KR100619515 B1 KR 100619515B1 KR 1020047018605 A KR1020047018605 A KR 1020047018605A KR 20047018605 A KR20047018605 A KR 20047018605A KR 100619515 B1 KR100619515 B1 KR 100619515B1
- Authority
- KR
- South Korea
- Prior art keywords
- amino
- thiazol
- phenylamino
- phenyl
- methanone
- 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 *c1c2nc[n](*)c2nc(NC(CC2)CCC2N)n1 Chemical compound *c1c2nc[n](*)c2nc(NC(CC2)CCC2N)n1 0.000 description 7
- WKGAFKNWVGABDG-UHFFFAOYSA-N S=C=Nc(cc1)ccc1OCCN1CCCC1 Chemical compound S=C=Nc(cc1)ccc1OCCN1CCCC1 WKGAFKNWVGABDG-UHFFFAOYSA-N 0.000 description 2
- CACYXEKEQMWJHH-QHVLENNUSA-N C/C=N/CCOC1C=C(C)C(Nc2nc(N)c(C(c(cc3F)ccc3O)=O)[s]2)=CC1 Chemical compound C/C=N/CCOC1C=C(C)C(Nc2nc(N)c(C(c(cc3F)ccc3O)=O)[s]2)=CC1 CACYXEKEQMWJHH-QHVLENNUSA-N 0.000 description 1
- XRRXRQJQQKMFBC-UHFFFAOYSA-N CC(C)(C)OC(N(C1)CC1O)=O Chemical compound CC(C)(C)OC(N(C1)CC1O)=O XRRXRQJQQKMFBC-UHFFFAOYSA-N 0.000 description 1
- KDZPPCZEGQIGFU-UHFFFAOYSA-N CC(C=CC(C1)C(CBr)=O)=C1F Chemical compound CC(C=CC(C1)C(CBr)=O)=C1F KDZPPCZEGQIGFU-UHFFFAOYSA-N 0.000 description 1
- PBKGYWLWIJLDGZ-UHFFFAOYSA-N CC(CO)N(C)C Chemical compound CC(CO)N(C)C PBKGYWLWIJLDGZ-UHFFFAOYSA-N 0.000 description 1
- VWWWMRLYMSSIPU-UHFFFAOYSA-N CC(COc(cc1)ccc1[NH+2][O-])N(C)C Chemical compound CC(COc(cc1)ccc1[NH+2][O-])N(C)C VWWWMRLYMSSIPU-UHFFFAOYSA-N 0.000 description 1
- GSWTXZXGONEVJC-UHFFFAOYSA-N CC(c(cc1)cc(F)c1O)=O Chemical compound CC(c(cc1)cc(F)c1O)=O GSWTXZXGONEVJC-UHFFFAOYSA-N 0.000 description 1
- MMVUJVASBDVNGJ-UHFFFAOYSA-N CC(c(cc1)cc2c1OCC2)=O Chemical compound CC(c(cc1)cc2c1OCC2)=O MMVUJVASBDVNGJ-UHFFFAOYSA-N 0.000 description 1
- MNMQFOPYFREFRS-UHFFFAOYSA-N CCN(CC)CCOc(cc1)ccc1N=S Chemical compound CCN(CC)CCOc(cc1)ccc1N=S MNMQFOPYFREFRS-UHFFFAOYSA-N 0.000 description 1
- DKPVUBGBTUCNBO-UHFFFAOYSA-N CCN(CCC1)CC1Oc(cc1)ccc1NC(NC(SCC1CCCCCCC1)=N)=S Chemical compound CCN(CCC1)CC1Oc(cc1)ccc1NC(NC(SCC1CCCCCCC1)=N)=S DKPVUBGBTUCNBO-UHFFFAOYSA-N 0.000 description 1
- MIFQZEOWWYEATC-VAWYXSNFSA-N CCN/C=C/Oc(cc1)ccc1NC1SC(C(c2cccc(OC)c2)=O)=C(N)N1 Chemical compound CCN/C=C/Oc(cc1)ccc1NC1SC(C(c2cccc(OC)c2)=O)=C(N)N1 MIFQZEOWWYEATC-VAWYXSNFSA-N 0.000 description 1
- YWAKBDMZSWBMMS-UHFFFAOYSA-N CCOc1cccc(C(c2c(N)nc(Nc(cc3)ccc3OCCN3CCCC3)[s]2)=O)c1 Chemical compound CCOc1cccc(C(c2c(N)nc(Nc(cc3)ccc3OCCN3CCCC3)[s]2)=O)c1 YWAKBDMZSWBMMS-UHFFFAOYSA-N 0.000 description 1
- MPJMUPXNCBXSED-UHFFFAOYSA-N CCc(c(F)c1)ccc1C(c1c(N)nc(Nc(cc2)ccc2OCCN2CCCC2)[s]1)=O Chemical compound CCc(c(F)c1)ccc1C(c1c(N)nc(Nc(cc2)ccc2OCCN2CCCC2)[s]1)=O MPJMUPXNCBXSED-UHFFFAOYSA-N 0.000 description 1
- NXQXXOCEQZUJPF-UHFFFAOYSA-N CCc(ccc(/C(/C[Br]=C)=[O]\C)c1)c1F Chemical compound CCc(ccc(/C(/C[Br]=C)=[O]\C)c1)c1F NXQXXOCEQZUJPF-UHFFFAOYSA-N 0.000 description 1
- DXSZJARENLJWFV-UHFFFAOYSA-N CCc1cc(C(CBr)=O)ccc1F Chemical compound CCc1cc(C(CBr)=O)ccc1F DXSZJARENLJWFV-UHFFFAOYSA-N 0.000 description 1
- TVWMOJNVQLTJJG-AATRIKPKSA-N CN(CCC1)/C1=C/O Chemical compound CN(CCC1)/C1=C/O TVWMOJNVQLTJJG-AATRIKPKSA-N 0.000 description 1
- BIIVYFLTOXDAOV-UHFFFAOYSA-N CN(CCC1c(c(OC(c(cccc2)c2Cl)=C2)c(c(O)c3)C2=O)c3O)CC1O Chemical compound CN(CCC1c(c(OC(c(cccc2)c2Cl)=C2)c(c(O)c3)C2=O)c3O)CC1O BIIVYFLTOXDAOV-UHFFFAOYSA-N 0.000 description 1
- QBYXQRFFZGNKDK-NSHDSACASA-N CN1[C@H](COc(cc2)ccc2N=O)CCC1 Chemical compound CN1[C@H](COc(cc2)ccc2N=O)CCC1 QBYXQRFFZGNKDK-NSHDSACASA-N 0.000 description 1
- CSOZXOOJJJKJDT-UHFFFAOYSA-N COc(c(NO)c1)ccc1C(CBr)=O Chemical compound COc(c(NO)c1)ccc1C(CBr)=O CSOZXOOJJJKJDT-UHFFFAOYSA-N 0.000 description 1
- ZIUOGXYQWQLNQL-SECBINFHSA-N C[C@H](COc(cc1)ccc1N)N(C)C Chemical compound C[C@H](COc(cc1)ccc1N)N(C)C ZIUOGXYQWQLNQL-SECBINFHSA-N 0.000 description 1
- PPZSZPJJTNMYIR-LLVKDONJSA-N C[C@H](COc(cc1)ccc1N)N1CCCC1 Chemical compound C[C@H](COc(cc1)ccc1N)N1CCCC1 PPZSZPJJTNMYIR-LLVKDONJSA-N 0.000 description 1
- ZLQXZTCEZZIVRB-LLVKDONJSA-N C[C@H](COc(cc1)ccc1NO)N1CCCC1 Chemical compound C[C@H](COc(cc1)ccc1NO)N1CCCC1 ZLQXZTCEZZIVRB-LLVKDONJSA-N 0.000 description 1
- NCLDOAPBCXAMNW-OAHLLOKOSA-N C[C@H](COc(cc1)ccc1Nc1nc(N)c(C(c2cc(C3CC3)ccc2)=O)[s]1)N(C)C Chemical compound C[C@H](COc(cc1)ccc1Nc1nc(N)c(C(c2cc(C3CC3)ccc2)=O)[s]1)N(C)C NCLDOAPBCXAMNW-OAHLLOKOSA-N 0.000 description 1
- NMESODTXRYGDRX-SECBINFHSA-N C[C@H](COc(cc1)ccc1[NH+]([O-])O)N(C)C Chemical compound C[C@H](COc(cc1)ccc1[NH+]([O-])O)N(C)C NMESODTXRYGDRX-SECBINFHSA-N 0.000 description 1
- LLFNATBDUKLSGB-UHFFFAOYSA-N Cc1cccc(C(c2c(N)nc(Nc(cc3)ccc3OCC3N(C)CCC3)[s]2)=O)c1 Chemical compound Cc1cccc(C(c2c(N)nc(Nc(cc3)ccc3OCC3N(C)CCC3)[s]2)=O)c1 LLFNATBDUKLSGB-UHFFFAOYSA-N 0.000 description 1
- OTYZNDKWNPQQJP-UHFFFAOYSA-N Nc(cc1)ccc1OCCN1CCCC1 Chemical compound Nc(cc1)ccc1OCCN1CCCC1 OTYZNDKWNPQQJP-UHFFFAOYSA-N 0.000 description 1
- ZHFFNLQQANCJEQ-UHFFFAOYSA-N Nc(cc1)ccc1OCCN1CCOCC1 Chemical compound Nc(cc1)ccc1OCCN1CCOCC1 ZHFFNLQQANCJEQ-UHFFFAOYSA-N 0.000 description 1
- QMKKCOSTWZHORQ-UHFFFAOYSA-N Nc1c(C(c2ccc3OCCOc3c2)=O)[s]c(Nc(cc2)ccc2OCCN2CCOCC2)n1 Chemical compound Nc1c(C(c2ccc3OCCOc3c2)=O)[s]c(Nc(cc2)ccc2OCCN2CCOCC2)n1 QMKKCOSTWZHORQ-UHFFFAOYSA-N 0.000 description 1
- AMCOONRENOMFCT-UHFFFAOYSA-N O=C(CBr)c1cc(C2CC2)ccc1 Chemical compound O=C(CBr)c1cc(C2CC2)ccc1 AMCOONRENOMFCT-UHFFFAOYSA-N 0.000 description 1
- CZRHIPGIDWESKD-UHFFFAOYSA-N O=C(CBr)c1ccc2OCCc2c1 Chemical compound O=C(CBr)c1ccc2OCCc2c1 CZRHIPGIDWESKD-UHFFFAOYSA-N 0.000 description 1
- DTQVDTLACAAQTR-UHFFFAOYSA-N OC(C(F)(F)F)=O Chemical compound OC(C(F)(F)F)=O DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 1
- BHIKGDGTKBQDGJ-UHFFFAOYSA-N Oc(ccc(C(CBr)=O)c1)c1F Chemical compound Oc(ccc(C(CBr)=O)c1)c1F BHIKGDGTKBQDGJ-UHFFFAOYSA-N 0.000 description 1
- ZABHIIMPGGXEKO-UHFFFAOYSA-N S=C=Nc(cc1)ccc1OCCN1CCOCC1 Chemical compound S=C=Nc(cc1)ccc1OCCN1CCOCC1 ZABHIIMPGGXEKO-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
- C07D417/02—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 two hetero rings
- C07D417/06—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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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
- C07D277/38—Nitrogen atoms
- C07D277/42—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- 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
- C07D417/02—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 two hetero rings
- C07D417/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38151302P | 2002-05-17 | 2002-05-17 | |
| US60/381,513 | 2002-05-17 | ||
| PCT/EP2003/004939 WO2003097048A1 (en) | 2002-05-17 | 2003-05-12 | Diaminothiazoles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20050006261A KR20050006261A (ko) | 2005-01-15 |
| KR100619515B1 true KR100619515B1 (ko) | 2006-09-08 |
Family
ID=29550137
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020047018605A Expired - Fee Related KR100619515B1 (ko) | 2002-05-17 | 2003-05-12 | 디아미노티아졸 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6818663B2 (https=) |
| EP (1) | EP1507530B1 (https=) |
| JP (1) | JP4308133B2 (https=) |
| KR (1) | KR100619515B1 (https=) |
| CN (1) | CN100400041C (https=) |
| AR (1) | AR040078A1 (https=) |
| AT (1) | ATE308323T1 (https=) |
| AU (1) | AU2003232754B2 (https=) |
| BR (1) | BR0310081A (https=) |
| CA (1) | CA2485367A1 (https=) |
| DE (1) | DE60302152T2 (https=) |
| ES (1) | ES2251697T3 (https=) |
| MX (1) | MXPA04011372A (https=) |
| PL (1) | PL374581A1 (https=) |
| RU (1) | RU2311414C2 (https=) |
| WO (1) | WO2003097048A1 (https=) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070167329A1 (en) * | 2003-12-24 | 2007-07-19 | Bayer Cropscience Gmbh | Plant growth regulation |
| US7211576B2 (en) * | 2004-04-20 | 2007-05-01 | Hoffmann-La Roche Inc. | Diaminothiazoles |
| US7405220B2 (en) | 2004-06-09 | 2008-07-29 | Hoffmann-La Roche Inc. | Pyrazolopyrimidines |
| US7705009B2 (en) * | 2005-11-22 | 2010-04-27 | Hoffman-La Roche Inc. | 4-aminopyrimidine-5-thione derivatives |
| CA2668210C (en) | 2006-10-31 | 2013-03-12 | Schering Corporation | Anilinopiperazine derivatives and methods of use thereof |
| AR063531A1 (es) | 2006-10-31 | 2009-01-28 | Schering Corp | Derivados de anilinopiperazina y composicion farmaceutica |
| US8502401B2 (en) * | 2008-08-12 | 2013-08-06 | Delsper LP | Polymeric compositions comprising per(phenylethynyl) arene derivatives |
| ES2718637T3 (es) * | 2010-08-24 | 2019-07-03 | Gtx Inc | Compuestos para el tratamiento del cáncer |
| WO2013074120A1 (en) | 2011-11-18 | 2013-05-23 | Greene, Tweed & Co. | Crosslinking compounds for high glass transition temperature polymers |
| CA2909683A1 (en) | 2013-04-16 | 2014-10-23 | Memorial Sloan-Kettering Cancer Center | Companion diagnostic for cdk4 inhibitors |
| WO2015051525A1 (en) * | 2013-10-11 | 2015-04-16 | Rhodia Operations | Synthesis of acetal/ketal |
| WO2017156263A1 (en) | 2016-03-09 | 2017-09-14 | Memorial Sloan-Kettering Cancer Center | Enigma and cdh18 as companion diagnostics for cdk4 inhibitors |
| WO2017158147A1 (en) | 2016-03-18 | 2017-09-21 | Savira Pharmaceuticals Gmbh | Pyrimidone derivatives and their use in the treatment, amelioration or prevention of a viral disease |
| WO2018089902A1 (en) * | 2016-11-13 | 2018-05-17 | Apogee Biotechnology Corporation | Diaminothiazole compounds, compositions and methods of use |
| CN110950848B (zh) * | 2018-09-27 | 2024-03-26 | 徐诺药业 | 新型氨基吡唑类衍生物的合成与应用 |
| AU2020266083A1 (en) | 2019-04-30 | 2021-09-23 | Instituto de Medicina Molecular João Lobo Antunes | Rank pathway inhibitors in combination with CDK inhibitors |
| WO2026024674A1 (en) | 2024-07-22 | 2026-01-29 | Genesis Therapeutics, Inc. | Methods of treating skp2-associated cancers |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2714059B1 (fr) * | 1993-12-21 | 1996-03-08 | Sanofi Elf | Dérivés amino ramifiés du thiazole, leurs procédés de préparation et les compositions pharmaceutiques qui les contiennent. |
| NZ503788A (en) * | 1997-10-27 | 2002-11-26 | Agouron Pharma | 4-aminothiazole derivatives and their use as inhibitors of cyclin-dependent kinases |
| UA71971C2 (en) * | 1999-06-04 | 2005-01-17 | Agoron Pharmaceuticals Inc | Diaminothiazoles, composition based thereon, a method for modulation of protein kinases activity, a method for the treatment of diseases mediated by protein kinases |
| EP1307462A2 (en) * | 2000-08-09 | 2003-05-07 | Agouron Pharmaceuticals, Inc. | Pyrazole-thiazole compounds, pharmaceutical compositions containing them, and methods of their use for inhibiting cyclin-dependent kinases |
| US6756374B2 (en) | 2001-01-22 | 2004-06-29 | Hoffmann-La Roche Inc. | Diaminothiazoles having antiproliferative activity |
-
2003
- 2003-05-05 US US10/429,551 patent/US6818663B2/en not_active Expired - Fee Related
- 2003-05-12 EP EP03752731A patent/EP1507530B1/en not_active Expired - Lifetime
- 2003-05-12 AT AT03752731T patent/ATE308323T1/de not_active IP Right Cessation
- 2003-05-12 DE DE60302152T patent/DE60302152T2/de not_active Expired - Fee Related
- 2003-05-12 KR KR1020047018605A patent/KR100619515B1/ko not_active Expired - Fee Related
- 2003-05-12 AU AU2003232754A patent/AU2003232754B2/en not_active Ceased
- 2003-05-12 CN CNB038111314A patent/CN100400041C/zh not_active Expired - Fee Related
- 2003-05-12 MX MXPA04011372A patent/MXPA04011372A/es active IP Right Grant
- 2003-05-12 CA CA002485367A patent/CA2485367A1/en not_active Abandoned
- 2003-05-12 JP JP2004505047A patent/JP4308133B2/ja not_active Expired - Fee Related
- 2003-05-12 PL PL03374581A patent/PL374581A1/xx not_active Application Discontinuation
- 2003-05-12 BR BR0310081-2A patent/BR0310081A/pt not_active IP Right Cessation
- 2003-05-12 ES ES03752731T patent/ES2251697T3/es not_active Expired - Lifetime
- 2003-05-12 RU RU2004137110/04A patent/RU2311414C2/ru active
- 2003-05-12 WO PCT/EP2003/004939 patent/WO2003097048A1/en not_active Ceased
- 2003-05-15 AR ARP030101692A patent/AR040078A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| RU2311414C2 (ru) | 2007-11-27 |
| JP4308133B2 (ja) | 2009-08-05 |
| CA2485367A1 (en) | 2003-11-27 |
| WO2003097048A1 (en) | 2003-11-27 |
| AU2003232754A1 (en) | 2003-12-02 |
| CN1652780A (zh) | 2005-08-10 |
| RU2004137110A (ru) | 2005-08-20 |
| AR040078A1 (es) | 2005-03-16 |
| US6818663B2 (en) | 2004-11-16 |
| KR20050006261A (ko) | 2005-01-15 |
| PL374581A1 (en) | 2005-10-31 |
| ES2251697T3 (es) | 2006-05-01 |
| DE60302152T2 (de) | 2006-07-13 |
| BR0310081A (pt) | 2005-02-15 |
| DE60302152D1 (de) | 2005-12-08 |
| JP2005530783A (ja) | 2005-10-13 |
| US20040006058A1 (en) | 2004-01-08 |
| ATE308323T1 (de) | 2005-11-15 |
| EP1507530B1 (en) | 2005-11-02 |
| AU2003232754B2 (en) | 2009-03-12 |
| EP1507530A1 (en) | 2005-02-23 |
| MXPA04011372A (es) | 2005-08-15 |
| CN100400041C (zh) | 2008-07-09 |
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| AU2002242687A1 (en) | Diaminothiazoles and their use as inhibitors of cyclin-dependent kinase | |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
St.27 status event code: A-0-1-A10-A15-nap-PA0105 |
|
| A201 | Request for examination | ||
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| PA0201 | Request for examination |
St.27 status event code: A-1-2-D10-D11-exm-PA0201 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| PG1501 | Laying open of application |
St.27 status event code: A-1-1-Q10-Q12-nap-PG1501 |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
St.27 status event code: A-1-2-D10-D21-exm-PE0902 |
|
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
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