KR101435231B1 - 증식성 질환의 치료에 유용한 모르폴리노 피리미딘 유도체 - Google Patents
증식성 질환의 치료에 유용한 모르폴리노 피리미딘 유도체 Download PDFInfo
- Publication number
- KR101435231B1 KR101435231B1 KR1020097005961A KR20097005961A KR101435231B1 KR 101435231 B1 KR101435231 B1 KR 101435231B1 KR 1020097005961 A KR1020097005961 A KR 1020097005961A KR 20097005961 A KR20097005961 A KR 20097005961A KR 101435231 B1 KR101435231 B1 KR 101435231B1
- Authority
- KR
- South Korea
- Prior art keywords
- phenyl
- urea
- pyrimidin
- methyl
- alkyl
- 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 C**c(*c1N*)*c(*2[C@](*)COCC2)*1N Chemical compound C**c(*c1N*)*c(*2[C@](*)COCC2)*1N 0.000 description 6
- FEIBXQFRSZUXQZ-UHFFFAOYSA-N CC(C)(c1cc(N2CCOCC2)nc(C)n1)S(C)(=O)=O Chemical compound CC(C)(c1cc(N2CCOCC2)nc(C)n1)S(C)(=O)=O FEIBXQFRSZUXQZ-UHFFFAOYSA-N 0.000 description 1
- YFQUQOCRSGDZBP-UHFFFAOYSA-N CC(C)(c1nc(-c(cc2)ccc2NC(Oc2ccccc2)=O)nc(N2CCOCC2)c1)S(c(cc1)ccc1F)(=O)=O Chemical compound CC(C)(c1nc(-c(cc2)ccc2NC(Oc2ccccc2)=O)nc(N2CCOCC2)c1)S(c(cc1)ccc1F)(=O)=O YFQUQOCRSGDZBP-UHFFFAOYSA-N 0.000 description 1
- DZQVSRMLIWIZAM-UHFFFAOYSA-N CC(C)(c1nc(-c(cc2)ccc2NC(Oc2ccccc2)=O)nc(N2CCOCC2)c1)S(c1ccccn1)(=O)=O Chemical compound CC(C)(c1nc(-c(cc2)ccc2NC(Oc2ccccc2)=O)nc(N2CCOCC2)c1)S(c1ccccn1)(=O)=O DZQVSRMLIWIZAM-UHFFFAOYSA-N 0.000 description 1
- FCDQSNWGKUQWLI-UHFFFAOYSA-N CC(C)S(C(C)(C)c1cc(N2CCOCC2)nc(Cl)n1)(=O)=O Chemical compound CC(C)S(C(C)(C)c1cc(N2CCOCC2)nc(Cl)n1)(=O)=O FCDQSNWGKUQWLI-UHFFFAOYSA-N 0.000 description 1
- MYYDNSZZGRLEBB-UHFFFAOYSA-N CC1(CCNC(Nc(cc2)ccc2-c2nc(CS(C)(=O)=O)cc(N3CCOCC3)n2)=O)NC=CC=C1 Chemical compound CC1(CCNC(Nc(cc2)ccc2-c2nc(CS(C)(=O)=O)cc(N3CCOCC3)n2)=O)NC=CC=C1 MYYDNSZZGRLEBB-UHFFFAOYSA-N 0.000 description 1
- PBHGQPNXTZYQJX-YFHOEESVSA-O CC1OC1NCCS(Cc1cc(N(CCOC2)C2=C)nc(-c(cc2)ccc2NC(NC(/C=C\O)=[NH2+])=O)n1)(=O)=O Chemical compound CC1OC1NCCS(Cc1cc(N(CCOC2)C2=C)nc(-c(cc2)ccc2NC(NC(/C=C\O)=[NH2+])=O)n1)(=O)=O PBHGQPNXTZYQJX-YFHOEESVSA-O 0.000 description 1
- WINJETYZKZQUHA-VIFPVBQESA-N CCS(Cc1cc(N2[C@@H](C)COCC2)nc(Cl)n1)(=O)=O Chemical compound CCS(Cc1cc(N2[C@@H](C)COCC2)nc(Cl)n1)(=O)=O WINJETYZKZQUHA-VIFPVBQESA-N 0.000 description 1
- IQXVGJKHRMGZKY-UHFFFAOYSA-N CNC(Nc(cc1)ccc1-c1nc(N2CCOCC2)cc(CSC2CCCCC2)n1)=O Chemical compound CNC(Nc(cc1)ccc1-c1nc(N2CCOCC2)cc(CSC2CCCCC2)n1)=O IQXVGJKHRMGZKY-UHFFFAOYSA-N 0.000 description 1
- PPWFALYFZNXFCH-UHFFFAOYSA-N CNC(Nc1ncc(-c2nc(CS(C)(=O)=O)cc(N3CCOCC3)n2)[s]1)=O Chemical compound CNC(Nc1ncc(-c2nc(CS(C)(=O)=O)cc(N3CCOCC3)n2)[s]1)=O PPWFALYFZNXFCH-UHFFFAOYSA-N 0.000 description 1
- XJZYFWNWTOAHTR-UHFFFAOYSA-N CSc1nc(O)cc(CCl)n1 Chemical compound CSc1nc(O)cc(CCl)n1 XJZYFWNWTOAHTR-UHFFFAOYSA-N 0.000 description 1
- KWPMJEUHYJIPAX-QFIPXVFZSA-N C[C@@H](COCC1)N1c1cc(C(C)(C)S(C2CCCCC2)(=O)=O)nc(-c(cc2)ccc2NC(Oc2ccccc2)=O)n1 Chemical compound C[C@@H](COCC1)N1c1cc(C(C)(C)S(C2CCCCC2)(=O)=O)nc(-c(cc2)ccc2NC(Oc2ccccc2)=O)n1 KWPMJEUHYJIPAX-QFIPXVFZSA-N 0.000 description 1
- QXKIUQZHKYTFFV-IBGZPJMESA-N C[C@@H](COCC1)N1c1cc(CS(c2cc(F)cc(F)c2)(O)O)nc(-c(cc2)ccc2NC(Oc2ccccc2)=O)n1 Chemical compound C[C@@H](COCC1)N1c1cc(CS(c2cc(F)cc(F)c2)(O)O)nc(-c(cc2)ccc2NC(Oc2ccccc2)=O)n1 QXKIUQZHKYTFFV-IBGZPJMESA-N 0.000 description 1
- XBZSYENJVCXROM-KRWDZBQOSA-N C[C@@H](COCC1)N1c1nc(-c(cc2)ccc2NC(NC2CC2)=O)nc(CN(CC2)CCS2(=O)=O)c1 Chemical compound C[C@@H](COCC1)N1c1nc(-c(cc2)ccc2NC(NC2CC2)=O)nc(CN(CC2)CCS2(=O)=O)c1 XBZSYENJVCXROM-KRWDZBQOSA-N 0.000 description 1
- AYGRQBVXVAGJRQ-HNNXBMFYSA-N C[C@@H](COCC1)N1c1nc(-c(cc2)ccc2NC(NC2CC2)=O)nc(CS(C2CC2)(=O)=O)c1 Chemical compound C[C@@H](COCC1)N1c1nc(-c(cc2)ccc2NC(NC2CC2)=O)nc(CS(C2CC2)(=O)=O)c1 AYGRQBVXVAGJRQ-HNNXBMFYSA-N 0.000 description 1
- QGPPQMWGRIABSS-INIZCTEOSA-N C[C@@H](COCC1)N1c1nc(-c(cc2)ccc2NC(Oc2ccccc2)=O)nc(C(OC)=O)c1 Chemical compound C[C@@H](COCC1)N1c1nc(-c(cc2)ccc2NC(Oc2ccccc2)=O)nc(C(OC)=O)c1 QGPPQMWGRIABSS-INIZCTEOSA-N 0.000 description 1
- UTTLSNRUKXDGHO-LBPRGKRZSA-N C[C@@H](COCC1)N1c1nc(-c2cccc(N)c2)nc(CS(C)(=O)=O)c1 Chemical compound C[C@@H](COCC1)N1c1nc(-c2cccc(N)c2)nc(CS(C)(=O)=O)c1 UTTLSNRUKXDGHO-LBPRGKRZSA-N 0.000 description 1
- KUOZNFZZJHCLRN-JTQLQIEISA-N C[C@@H](COCC1)N1c1nc(-c2cnc(N)[s]2)nc(C(C)(C)S(C)(=O)=O)c1 Chemical compound C[C@@H](COCC1)N1c1nc(-c2cnc(N)[s]2)nc(C(C)(C)S(C)(=O)=O)c1 KUOZNFZZJHCLRN-JTQLQIEISA-N 0.000 description 1
- LVKVZWUJJIKRMY-QMMMGPOBSA-N C[C@@H](COCC1)N1c1nc(Cl)nc(COS(C)(O)O)c1 Chemical compound C[C@@H](COCC1)N1c1nc(Cl)nc(COS(C)(O)O)c1 LVKVZWUJJIKRMY-QMMMGPOBSA-N 0.000 description 1
- OAKDFDJCLAQSMY-JTQLQIEISA-N C[C@@H](COCC1)N1c1nc(Cl)nc(CSc2cc(F)cc(F)c2)c1 Chemical compound C[C@@H](COCC1)N1c1nc(Cl)nc(CSc2cc(F)cc(F)c2)c1 OAKDFDJCLAQSMY-JTQLQIEISA-N 0.000 description 1
- DHEYPLFMZJKMNQ-UHFFFAOYSA-O C[n]1ncc(CNC(Nc(cc2)ccc2-c2nc(C[OH2+])cc(N3CCOCC3)n2)=O)c1 Chemical compound C[n]1ncc(CNC(Nc(cc2)ccc2-c2nc(C[OH2+])cc(N3CCOCC3)n2)=O)c1 DHEYPLFMZJKMNQ-UHFFFAOYSA-O 0.000 description 1
- IIMLAOZJLPDSHH-UHFFFAOYSA-N Cc1nc(N2CCOCC2)cc(CS(C)(=O)=O)n1 Chemical compound Cc1nc(N2CCOCC2)cc(CS(C)(=O)=O)n1 IIMLAOZJLPDSHH-UHFFFAOYSA-N 0.000 description 1
- WQRCKPGNFKRKSK-UHFFFAOYSA-N Clc1nc(Cl)nc(CSC2CCCCC2)c1 Chemical compound Clc1nc(Cl)nc(CSC2CCCCC2)c1 WQRCKPGNFKRKSK-UHFFFAOYSA-N 0.000 description 1
- BBFOWPATSGSRRQ-UHFFFAOYSA-N O=C(Nc(cc1)ccc1-c1nc(N2CCOCC2)cc(CS(c2ccccc2)(=O)=O)n1)Oc1ccccc1 Chemical compound O=C(Nc(cc1)ccc1-c1nc(N2CCOCC2)cc(CS(c2ccccc2)(=O)=O)n1)Oc1ccccc1 BBFOWPATSGSRRQ-UHFFFAOYSA-N 0.000 description 1
- MLAWQZZFIAKYTG-UHFFFAOYSA-N O=S(Cc1cc(N2CCOCC2)nc(Cl)n1)(c1ccccc1)=O Chemical compound O=S(Cc1cc(N2CCOCC2)nc(Cl)n1)(c1ccccc1)=O MLAWQZZFIAKYTG-UHFFFAOYSA-N 0.000 description 1
- CQZDHYUKDWGDFH-UHFFFAOYSA-N O=[S](Cc1cc(N2CCOCC2)nc(Cl)n1)(C1CC1)#[O] Chemical compound O=[S](Cc1cc(N2CCOCC2)nc(Cl)n1)(C1CC1)#[O] CQZDHYUKDWGDFH-UHFFFAOYSA-N 0.000 description 1
- KZTPORGJBFSKKU-UHFFFAOYSA-O O[S+](Cc1cc(Cl)nc(Cl)n1)(c(cc1)ccc1F)=O Chemical compound O[S+](Cc1cc(Cl)nc(Cl)n1)(c(cc1)ccc1F)=O KZTPORGJBFSKKU-UHFFFAOYSA-O 0.000 description 1
Classifications
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D403/02—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 two hetero rings
- C07D403/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- 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)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0616747.2 | 2006-08-24 | ||
| GB0616747A GB0616747D0 (en) | 2006-08-24 | 2006-08-24 | Novel compounds |
| US94854407P | 2007-07-09 | 2007-07-09 | |
| US60/948,544 | 2007-07-09 | ||
| PCT/GB2007/003173 WO2008023159A1 (en) | 2006-08-24 | 2007-08-21 | Morpholino pyrimidine derivatives useful in the treatment of proliferative disorders |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20090053928A KR20090053928A (ko) | 2009-05-28 |
| KR101435231B1 true KR101435231B1 (ko) | 2014-10-02 |
Family
ID=38720451
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020097005961A Expired - Fee Related KR101435231B1 (ko) | 2006-08-24 | 2007-08-21 | 증식성 질환의 치료에 유용한 모르폴리노 피리미딘 유도체 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7750003B2 (https=) |
| EP (1) | EP2057140B1 (https=) |
| JP (1) | JP5534811B2 (https=) |
| KR (1) | KR101435231B1 (https=) |
| AR (1) | AR062526A1 (https=) |
| AU (1) | AU2007287428B2 (https=) |
| CA (1) | CA2660758A1 (https=) |
| CL (1) | CL2007002446A1 (https=) |
| CO (1) | CO6150160A2 (https=) |
| IL (1) | IL196998A0 (https=) |
| MX (1) | MX2009002046A (https=) |
| NO (1) | NO20090631L (https=) |
| PE (1) | PE20081362A1 (https=) |
| UY (1) | UY30559A1 (https=) |
| WO (1) | WO2008023159A1 (https=) |
Families Citing this family (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4903164A (en) | 1988-12-08 | 1990-02-20 | Texas Instruments Incorporated | O-ring/back-up ring seal for high pressure transducers |
| CA2264819C (en) * | 1996-09-04 | 2010-03-23 | Intertrust Technologies Corp. | Trusted infrastructure support systems, methods and techniques for secure electronic commerce, electronic transactions, commerce process control and automation, distributed computing, and rights management |
| CA2657247A1 (en) | 2006-07-28 | 2008-01-31 | Boehringer Ingelheim International Gmbh | Compounds which modulate the cb2 receptor |
| AU2007287428B2 (en) | 2006-08-24 | 2011-08-11 | Astrazeneca Ab | Morpholino pyrimidine derivatives useful in the treatment of proliferative disorders |
| US7928123B2 (en) | 2006-09-25 | 2011-04-19 | Boehringer Ingelheim International Gmbh | Compounds which modulate the CB2 receptor |
| AU2008205252B2 (en) * | 2007-01-09 | 2013-02-21 | Amgen Inc. | Bis-aryl amide derivatives useful for the treatment of cancer |
| WO2008098058A1 (en) * | 2007-02-06 | 2008-08-14 | Novartis Ag | Pi 3-kinase inhibitors and methods of their use |
| AU2008273889B2 (en) * | 2007-07-09 | 2012-03-08 | Astrazeneca Ab | Trisubstituted pyrimidine derivatives for the treatment of proliferative diseases |
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