AU2015366190B2 - Imidazopyridazine derivatives as P13Kbeta inhibitors - Google Patents
Imidazopyridazine derivatives as P13Kbeta inhibitors Download PDFInfo
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- AU2015366190B2 AU2015366190B2 AU2015366190A AU2015366190A AU2015366190B2 AU 2015366190 B2 AU2015366190 B2 AU 2015366190B2 AU 2015366190 A AU2015366190 A AU 2015366190A AU 2015366190 A AU2015366190 A AU 2015366190A AU 2015366190 B2 AU2015366190 B2 AU 2015366190B2
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- 4alkyl
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- 0 CC(*)(C*C1(*)*)c2c1cccc2C Chemical compound CC(*)(C*C1(*)*)c2c1cccc2C 0.000 description 9
- GCXKULANKFAPOX-UHFFFAOYSA-N Cc1c(C(F)(F)F)cccc1Cc1c(CO)nc(c(N)c2)[n]1nc2N1CCOCC1 Chemical compound Cc1c(C(F)(F)F)cccc1Cc1c(CO)nc(c(N)c2)[n]1nc2N1CCOCC1 GCXKULANKFAPOX-UHFFFAOYSA-N 0.000 description 2
- YLJOWVAMJHSMBO-UHFFFAOYSA-N CC(C)(C)Nc1cc(N2CCOCC2)n[n]2c1nc(COC(C)=O)c2Cc1cccc(F)c1CCl Chemical compound CC(C)(C)Nc1cc(N2CCOCC2)n[n]2c1nc(COC(C)=O)c2Cc1cccc(F)c1CCl YLJOWVAMJHSMBO-UHFFFAOYSA-N 0.000 description 1
- CCCJQWDWPSRCOO-UHFFFAOYSA-N CC(C)(C)Nc1cc(N2CCOCC2)n[n]2c1nc(COC(C)=O)c2Cc1cccc(F)c1COC1OCCCC1 Chemical compound CC(C)(C)Nc1cc(N2CCOCC2)n[n]2c1nc(COC(C)=O)c2Cc1cccc(F)c1COC1OCCCC1 CCCJQWDWPSRCOO-UHFFFAOYSA-N 0.000 description 1
- NKWFHGLXOGRYIS-UHFFFAOYSA-N CC(C)(C)[Si+](C)(C)OCc(nc1[n]2nc(C)cc1)c2Br Chemical compound CC(C)(C)[Si+](C)(C)OCc(nc1[n]2nc(C)cc1)c2Br NKWFHGLXOGRYIS-UHFFFAOYSA-N 0.000 description 1
- ZTMGQYZCWPUNLZ-UHFFFAOYSA-N CC(C)(C)[Si+](C)(C)OCc(nc1c(C)c2)c(Cc3cccc(F)c3C)[n]1nc2N1CCOCC1 Chemical compound CC(C)(C)[Si+](C)(C)OCc(nc1c(C)c2)c(Cc3cccc(F)c3C)[n]1nc2N1CCOCC1 ZTMGQYZCWPUNLZ-UHFFFAOYSA-N 0.000 description 1
- YSSZOMJFOJHNHC-UHFFFAOYSA-N CC(C)(C)[Si+](C)(C)OCc(nc1cc2)c(Cc3cccc(F)c3C)[n]1nc2N1CCOCC1 Chemical compound CC(C)(C)[Si+](C)(C)OCc(nc1cc2)c(Cc3cccc(F)c3C)[n]1nc2N1CCOCC1 YSSZOMJFOJHNHC-UHFFFAOYSA-N 0.000 description 1
- BCQDQPPHFBQTQE-UHFFFAOYSA-N CC(C1)OCCN1c(cc1-c2c[nH]cn2)n[n]2c1nc(CO)c2Cc1cccc(C(F)(F)F)c1C Chemical compound CC(C1)OCCN1c(cc1-c2c[nH]cn2)n[n]2c1nc(CO)c2Cc1cccc(C(F)(F)F)c1C BCQDQPPHFBQTQE-UHFFFAOYSA-N 0.000 description 1
- XZTNFRIOXXOUTK-UHFFFAOYSA-N CC(C1)OCCN1c(cc1N)n[n]2c1nc(COS(C)C(C)(C)C(C)(C)C)c2Cc1c(C)c(C(F)(F)F)ccc1 Chemical compound CC(C1)OCCN1c(cc1N)n[n]2c1nc(COS(C)C(C)(C)C(C)(C)C)c2Cc1c(C)c(C(F)(F)F)ccc1 XZTNFRIOXXOUTK-UHFFFAOYSA-N 0.000 description 1
- BWCCGIXXYMCMIM-ZSNJKBEMSA-N CC(CO[Si+](C)(C)C(C)(C)C)NCc(c(C(F)(F)F)ccc1)c1Nc1c(C)nc(c(/N=C/N(C)C)c2)[n]1nc2N1CCOCC1 Chemical compound CC(CO[Si+](C)(C)C(C)(C)C)NCc(c(C(F)(F)F)ccc1)c1Nc1c(C)nc(c(/N=C/N(C)C)c2)[n]1nc2N1CCOCC1 BWCCGIXXYMCMIM-ZSNJKBEMSA-N 0.000 description 1
- UPOGDYLFJGRLLD-UHFFFAOYSA-N CC(CO[Si+](C)(C)C(C)(C)C)NCc(c(C(F)(F)F)ccc1)c1Nc1c(C)nc(c(N)c2)[n]1nc2N1CCOCC1 Chemical compound CC(CO[Si+](C)(C)C(C)(C)C)NCc(c(C(F)(F)F)ccc1)c1Nc1c(C)nc(c(N)c2)[n]1nc2N1CCOCC1 UPOGDYLFJGRLLD-UHFFFAOYSA-N 0.000 description 1
- YGJUIAATWHOCPQ-UHFFFAOYSA-N CC(NCc(nc1c(C(N)=N)c2)c(Cc3c(C)c(C(F)(F)F)ccc3)[n]1nc2N1CCOCC1)=O Chemical compound CC(NCc(nc1c(C(N)=N)c2)c(Cc3c(C)c(C(F)(F)F)ccc3)[n]1nc2N1CCOCC1)=O YGJUIAATWHOCPQ-UHFFFAOYSA-N 0.000 description 1
- GNBINIPALPKLRK-UHFFFAOYSA-N CC(OCc(nc1cc2)c(Cc3cccc(C(F)(F)F)c3C)[n]1nc2Cl)=O Chemical compound CC(OCc(nc1cc2)c(Cc3cccc(C(F)(F)F)c3C)[n]1nc2Cl)=O GNBINIPALPKLRK-UHFFFAOYSA-N 0.000 description 1
- HYNSADPKMFEZDJ-UHFFFAOYSA-N CC(OCc1c[n](C)c(C(N)=C)n1)=O Chemical compound CC(OCc1c[n](C)c(C(N)=C)n1)=O HYNSADPKMFEZDJ-UHFFFAOYSA-N 0.000 description 1
- VHLZWMIVBXCKPF-UHFFFAOYSA-N CC(c(nc1c(N)c2)c(Cc3c(C)c(C(F)(F)F)ccc3)[n]1nc2N1CCOCC1)O[Si+](C)(C)C(C)(C)C Chemical compound CC(c(nc1c(N)c2)c(Cc3c(C)c(C(F)(F)F)ccc3)[n]1nc2N1CCOCC1)O[Si+](C)(C)C(C)(C)C VHLZWMIVBXCKPF-UHFFFAOYSA-N 0.000 description 1
- FWUVRPSBNNJXBK-UHFFFAOYSA-N CC(c(nc1cc2)c(Cc3c(C)c(C(F)(F)F)ccc3)[n]1nc2N1CCOCC1)O[Si](C)(C)C(C)(C)C Chemical compound CC(c(nc1cc2)c(Cc3c(C)c(C(F)(F)F)ccc3)[n]1nc2N1CCOCC1)O[Si](C)(C)C(C)(C)C FWUVRPSBNNJXBK-UHFFFAOYSA-N 0.000 description 1
- GJKWJXQMIQTGOR-UHFFFAOYSA-N CCOC(c(nc1cc2)c[n]1nc2N1CCOCC1)=O Chemical compound CCOC(c(nc1cc2)c[n]1nc2N1CCOCC1)=O GJKWJXQMIQTGOR-UHFFFAOYSA-N 0.000 description 1
- ZVWJTTCBRKVWBH-UHFFFAOYSA-N Cc(nc12)c(Cc3c(C)c(C)ccc3)[n]1nc(C)cc2N Chemical compound Cc(nc12)c(Cc3c(C)c(C)ccc3)[n]1nc(C)cc2N ZVWJTTCBRKVWBH-UHFFFAOYSA-N 0.000 description 1
- MKOIELRPPKJYKF-UHFFFAOYSA-N Cc(nc1c(-c(nc2)c[n]2S=O)c2)c(Nc3cccc(C(F)(F)F)c3C)[n]1nc2N1CCOCC1 Chemical compound Cc(nc1c(-c(nc2)c[n]2S=O)c2)c(Nc3cccc(C(F)(F)F)c3C)[n]1nc2N1CCOCC1 MKOIELRPPKJYKF-UHFFFAOYSA-N 0.000 description 1
- PAUFOFKHBORNLA-UHFFFAOYSA-N Cc(nc1c(C#N)c2)c(Cc3cccc(Cl)c3C)[n]1nc2N1CCOCC1 Chemical compound Cc(nc1c(C#N)c2)c(Cc3cccc(Cl)c3C)[n]1nc2N1CCOCC1 PAUFOFKHBORNLA-UHFFFAOYSA-N 0.000 description 1
- AGFMFGYOSGMEBJ-UHFFFAOYSA-N Cc(nc1c(C(N)=O)c2)c(Nc(cccc3)c3N3CCOCC3)[n]1nc2N1CCOCC1 Chemical compound Cc(nc1c(C(N)=O)c2)c(Nc(cccc3)c3N3CCOCC3)[n]1nc2N1CCOCC1 AGFMFGYOSGMEBJ-UHFFFAOYSA-N 0.000 description 1
- VDVWHINMCCZRAK-UHFFFAOYSA-N Cc(nc1c(C(N)=O)c2)c(Nc3cccc(C(F)(F)F)c3C)[n]1nc2N1CCOCC1 Chemical compound Cc(nc1c(C(N)=O)c2)c(Nc3cccc(C(F)(F)F)c3C)[n]1nc2N1CCOCC1 VDVWHINMCCZRAK-UHFFFAOYSA-N 0.000 description 1
- DKTMKUHYROTKCJ-UHFFFAOYSA-N Cc(nc1c(C(O)=O)c2)c(Cc3cccc(C(F)(F)F)c3C)[n]1nc2N1CCOCC1 Chemical compound Cc(nc1c(C(O)=O)c2)c(Cc3cccc(C(F)(F)F)c3C)[n]1nc2N1CCOCC1 DKTMKUHYROTKCJ-UHFFFAOYSA-N 0.000 description 1
- JMVSBGCKLJWTKO-UHFFFAOYSA-N Cc(nc1c(C(O)=O)c2)c(Nc(cccc3)c3N3CCOCC3)[n]1nc2N1CCOCC1 Chemical compound Cc(nc1c(C(O)=O)c2)c(Nc(cccc3)c3N3CCOCC3)[n]1nc2N1CCOCC1 JMVSBGCKLJWTKO-UHFFFAOYSA-N 0.000 description 1
- JXEGIOGTWFVNHY-UHFFFAOYSA-N Cc(nc1c(C(OC)=O)c2)c(Cc3cccc(Cl)c3C)[n]1nc2N1CCOCC1 Chemical compound Cc(nc1c(C(OC)=O)c2)c(Cc3cccc(Cl)c3C)[n]1nc2N1CCOCC1 JXEGIOGTWFVNHY-UHFFFAOYSA-N 0.000 description 1
- XHADQZSGBXAFFU-UHFFFAOYSA-N Cc(nc1c(N)c2)c(Nc3c(CN(C4)CC4O)c(C(F)(F)F)ccc3)[n]1nc2N1CCOCC1 Chemical compound Cc(nc1c(N)c2)c(Nc3c(CN(C4)CC4O)c(C(F)(F)F)ccc3)[n]1nc2N1CCOCC1 XHADQZSGBXAFFU-UHFFFAOYSA-N 0.000 description 1
- QWCBKTWFMVTWCY-UHFFFAOYSA-N Cc(nc1c(N)c2)c(Nc3c(CN(CC4)CCS4(=O)=O)c(C(F)(F)F)ccc3)[n]1nc2N1CCOCC1 Chemical compound Cc(nc1c(N)c2)c(Nc3c(CN(CC4)CCS4(=O)=O)c(C(F)(F)F)ccc3)[n]1nc2N1CCOCC1 QWCBKTWFMVTWCY-UHFFFAOYSA-N 0.000 description 1
- AJDOIAFEXAYFJT-UHFFFAOYSA-N Cc(nc1c(N)c2)c(Nc3cccc(C)c3C)[n]1nc2N1CCOCC1 Chemical compound Cc(nc1c(N)c2)c(Nc3cccc(C)c3C)[n]1nc2N1CCOCC1 AJDOIAFEXAYFJT-UHFFFAOYSA-N 0.000 description 1
- UVAGRDRUDQKLJZ-UHFFFAOYSA-N Cc1c(C(F)(F)F)cccc1Cc1c(CN)nc(c(I)c2)[n]1nc2N1CCOCC1 Chemical compound Cc1c(C(F)(F)F)cccc1Cc1c(CN)nc(c(I)c2)[n]1nc2N1CCOCC1 UVAGRDRUDQKLJZ-UHFFFAOYSA-N 0.000 description 1
- RGPSLKYWZVHAAZ-UHFFFAOYSA-N Cc1c(C(F)(F)F)cccc1Cc1c(CNCCO)nc(c(N)c2)[n]1nc2N1CCOCC1 Chemical compound Cc1c(C(F)(F)F)cccc1Cc1c(CNCCO)nc(c(N)c2)[n]1nc2N1CCOCC1 RGPSLKYWZVHAAZ-UHFFFAOYSA-N 0.000 description 1
- VZJYQILDWNTSIE-UHFFFAOYSA-N Cc1c(C(F)(F)F)cccc1Cc1c(CO)nc(c(-c2cnc[nH]2)c2)[n]1nc2N1CCOCC1 Chemical compound Cc1c(C(F)(F)F)cccc1Cc1c(CO)nc(c(-c2cnc[nH]2)c2)[n]1nc2N1CCOCC1 VZJYQILDWNTSIE-UHFFFAOYSA-N 0.000 description 1
- OVYGHUZLXOWUDG-UHFFFAOYSA-N Cc1c(C(F)(F)F)cccc1Cc1c(COC(C(Cc2ccccc2)N)=O)nc(c(N)c2)[n]1nc2N1CCOCC1 Chemical compound Cc1c(C(F)(F)F)cccc1Cc1c(COC(C(Cc2ccccc2)N)=O)nc(c(N)c2)[n]1nc2N1CCOCC1 OVYGHUZLXOWUDG-UHFFFAOYSA-N 0.000 description 1
- FDTNOUSUIUPLIR-UHFFFAOYSA-N Cc1c(CN2CCCC2)c(N)ccc1 Chemical compound Cc1c(CN2CCCC2)c(N)ccc1 FDTNOUSUIUPLIR-UHFFFAOYSA-N 0.000 description 1
- XKVUYEYANWFIJX-UHFFFAOYSA-N Cc1ccn[nH]1 Chemical compound Cc1ccn[nH]1 XKVUYEYANWFIJX-UHFFFAOYSA-N 0.000 description 1
- XLSZMDLNRCVEIJ-UHFFFAOYSA-N Cc1cnc[nH]1 Chemical compound Cc1cnc[nH]1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N Cc1ncc[nH]1 Chemical compound Cc1ncc[nH]1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- IKAVXGZBOWYERZ-UHFFFAOYSA-N [O-][N+](c1c(CN(CCC2)CS2(=O)=O)c(C(F)(F)F)ccc1)=O Chemical compound [O-][N+](c1c(CN(CCC2)CS2(=O)=O)c(C(F)(F)F)ccc1)=O IKAVXGZBOWYERZ-UHFFFAOYSA-N 0.000 description 1
- OKSPTBLAYWOHTJ-UHFFFAOYSA-N [O-][N+](c1cccc(C(F)(F)F)c1CN(C1)CC1O)=O Chemical compound [O-][N+](c1cccc(C(F)(F)F)c1CN(C1)CC1O)=O OKSPTBLAYWOHTJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07D487/04—Ortho-condensed systems
-
- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring 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
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
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- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
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- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P37/02—Immunomodulators
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- A—HUMAN NECESSITIES
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- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- 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
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Reproductive Health (AREA)
- Rheumatology (AREA)
- Pregnancy & Childbirth (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Psychiatry (AREA)
- Gynecology & Obstetrics (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Taps Or Cocks (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14199322 | 2014-12-19 | ||
| EPEP14199322.0 | 2014-12-19 | ||
| PCT/EP2015/080604 WO2016097347A1 (en) | 2014-12-19 | 2015-12-18 | IMIDAZOPYRIDAZINE DERIVATIVES AS ΡΙ3Κβ INHIBITORS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2015366190A1 AU2015366190A1 (en) | 2017-05-25 |
| AU2015366190B2 true AU2015366190B2 (en) | 2020-01-23 |
Family
ID=52134002
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2015366190A Ceased AU2015366190B2 (en) | 2014-12-19 | 2015-12-18 | Imidazopyridazine derivatives as P13Kbeta inhibitors |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US10087187B2 (enExample) |
| EP (1) | EP3233862B1 (enExample) |
| JP (1) | JP6568588B2 (enExample) |
| KR (1) | KR20170095239A (enExample) |
| CN (1) | CN107108634B (enExample) |
| AU (1) | AU2015366190B2 (enExample) |
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| BR112018007068B1 (pt) | 2015-10-09 | 2024-01-02 | Janssen Pharmaceutica N.V. | Derivados de quinoxalina e piridopirazina como inibidores de pi3kbeta, seu uso e composição farmacêutica que os compreende |
| CN109311875A (zh) | 2016-06-16 | 2019-02-05 | 詹森药业有限公司 | 作为PI3Kβ抑制剂的二环吡啶、二环吡嗪、和二环嘧啶衍生物 |
| EP3601254B1 (en) | 2017-03-29 | 2022-05-25 | Janssen Pharmaceutica NV | Quinoxaline and pyridopyrazine derivatives as pi3k-beta inhibitors |
| KR102853071B1 (ko) * | 2019-02-07 | 2025-09-02 | 베이진 엘티디 | Tlr7 작용제로서의 이미다조[2,1-f][1,2,4]트리아진-4-아민 유도체 |
| CN110128505A (zh) * | 2019-05-21 | 2019-08-16 | 梯尔希(南京)药物研发有限公司 | 一种戈舍瑞林杂质的合成方法 |
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| WO2010007099A1 (en) * | 2008-07-15 | 2010-01-21 | Cellzome Limited | 2-aminoimidazo[1,2-b]pyridazine derivatives as pi3k inhibitors |
| WO2011047770A2 (de) * | 2009-10-19 | 2011-04-28 | Merck Patent Gmbh | Pyrazolopyrimidinderivate |
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| US10087187B2 (en) | 2018-10-02 |
| RS59301B1 (sr) | 2019-10-31 |
| EA029789B1 (ru) | 2018-05-31 |
| ME03517B (me) | 2020-04-20 |
| MD3233862T2 (ro) | 2019-11-30 |
| US20180002336A1 (en) | 2018-01-04 |
| HRP20191550T1 (hr) | 2019-11-29 |
| CN107108634B (zh) | 2020-09-15 |
| AU2015366190A1 (en) | 2017-05-25 |
| IL252866B (en) | 2020-09-30 |
| KR20170095239A (ko) | 2017-08-22 |
| JP2017538734A (ja) | 2017-12-28 |
| EP3233862A1 (en) | 2017-10-25 |
| PL3233862T3 (pl) | 2020-01-31 |
| IL252866A0 (en) | 2017-08-31 |
| HUE045220T2 (hu) | 2019-12-30 |
| CA2967551A1 (en) | 2016-06-23 |
| WO2016097347A1 (en) | 2016-06-23 |
| PT3233862T (pt) | 2019-10-09 |
| SMT201900509T1 (it) | 2019-11-13 |
| DK3233862T3 (da) | 2019-10-07 |
| SI3233862T1 (sl) | 2019-09-30 |
| EP3233862B1 (en) | 2019-07-03 |
| EA201791396A1 (ru) | 2017-10-31 |
| CY1122381T1 (el) | 2021-01-27 |
| MX2017008074A (es) | 2018-01-09 |
| JP6568588B2 (ja) | 2019-08-28 |
| ES2761051T3 (es) | 2020-05-18 |
| MA41174A (fr) | 2017-10-25 |
| BR112017012930A2 (pt) | 2018-01-09 |
| LT3233862T (lt) | 2019-09-10 |
| MA41174B1 (fr) | 2019-09-30 |
| CN107108634A (zh) | 2017-08-29 |
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