ES2759240T3 - Compuestos de piridina 2,3-disustituidos como inhibidores de TGF-beta - Google Patents
Compuestos de piridina 2,3-disustituidos como inhibidores de TGF-beta Download PDFInfo
- Publication number
- ES2759240T3 ES2759240T3 ES15716690T ES15716690T ES2759240T3 ES 2759240 T3 ES2759240 T3 ES 2759240T3 ES 15716690 T ES15716690 T ES 15716690T ES 15716690 T ES15716690 T ES 15716690T ES 2759240 T3 ES2759240 T3 ES 2759240T3
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- Prior art keywords
- pyridin
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- dmso
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- 0 CC(CC1)C(*)CCC1C1NCCCC1C(N1)=CCNC1O Chemical compound CC(CC1)C(*)CCC1C1NCCCC1C(N1)=CCNC1O 0.000 description 16
- FAVPCWISDNFGNT-UHFFFAOYSA-N BrC(CC1)=Cc2c1[s]cn2 Chemical compound BrC(CC1)=Cc2c1[s]cn2 FAVPCWISDNFGNT-UHFFFAOYSA-N 0.000 description 1
- STVHMYNPQCLUNJ-UHFFFAOYSA-N Brc(cc1)cc2c1[nH]nc2 Chemical compound Brc(cc1)cc2c1[nH]nc2 STVHMYNPQCLUNJ-UHFFFAOYSA-N 0.000 description 1
- LBFRLXVNPMYUKI-UHFFFAOYSA-N Brc(cc1)cc2c1nccc2N1CCOCC1 Chemical compound Brc(cc1)cc2c1nccc2N1CCOCC1 LBFRLXVNPMYUKI-UHFFFAOYSA-N 0.000 description 1
- UWSPDJMUUIISBL-UHFFFAOYSA-N C#Cc1cc(-c2ncccc2-c(cc2)cc3c2NCS3)ccc1 Chemical compound C#Cc1cc(-c2ncccc2-c(cc2)cc3c2NCS3)ccc1 UWSPDJMUUIISBL-UHFFFAOYSA-N 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N C1NCCOC1 Chemical compound C1NCCOC1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
- ACMZWBHMOZWEQO-UHFFFAOYSA-N CC(C(C=C1)Br)N2C1=[N]=C2CO Chemical compound CC(C(C=C1)Br)N2C1=[N]=C2CO ACMZWBHMOZWEQO-UHFFFAOYSA-N 0.000 description 1
- RGSURBDWRSGXTG-UHFFFAOYSA-N CC(C)(C)OC([n-]1ccc2c1ccc(Br)c2)=O Chemical compound CC(C)(C)OC([n-]1ccc2c1ccc(Br)c2)=O RGSURBDWRSGXTG-UHFFFAOYSA-N 0.000 description 1
- DCMHFTLQFLQCML-UHFFFAOYSA-N CC(C)(C)[O-][N+]([O-][N+](OC(C)(C)C)=O)=O Chemical compound CC(C)(C)[O-][N+]([O-][N+](OC(C)(C)C)=O)=O DCMHFTLQFLQCML-UHFFFAOYSA-N 0.000 description 1
- YMCJGUPZLPUHSZ-UHFFFAOYSA-N CC(C1=CCN=C1)=C Chemical compound CC(C1=CCN=C1)=C YMCJGUPZLPUHSZ-UHFFFAOYSA-N 0.000 description 1
- BLTWXUMTQDUCLE-UHFFFAOYSA-N CC(CC(Br)=C[n]12)c1ccc2I Chemical compound CC(CC(Br)=C[n]12)c1ccc2I BLTWXUMTQDUCLE-UHFFFAOYSA-N 0.000 description 1
- QAJSUUZQMKMDSH-UHFFFAOYSA-N CC(CC/N=C(\N)/Cl)C1=CCCNC1C(CCC1C)C=CC1F Chemical compound CC(CC/N=C(\N)/Cl)C1=CCCNC1C(CCC1C)C=CC1F QAJSUUZQMKMDSH-UHFFFAOYSA-N 0.000 description 1
- QWVNPVYGZBWSFB-UHFFFAOYSA-N CCc1cccc(-c2ncccc2-c2cc3c(N)ncnc3cc2)c1 Chemical compound CCc1cccc(-c2ncccc2-c2cc3c(N)ncnc3cc2)c1 QWVNPVYGZBWSFB-UHFFFAOYSA-N 0.000 description 1
- CFRVIJOWQYONDU-GRCOWADOSA-N CN(C)/C=N/C(/C=C\C(Br)=N)=N Chemical compound CN(C)/C=N/C(/C=C\C(Br)=N)=N CFRVIJOWQYONDU-GRCOWADOSA-N 0.000 description 1
- ZNTKFBADUAXKLG-UHFFFAOYSA-N Cc(cc(c1c2)ncnc1N)c2-c1cccnc1-c(cc1)cc(Cl)c1F Chemical compound Cc(cc(c1c2)ncnc1N)c2-c1cccnc1-c(cc1)cc(Cl)c1F ZNTKFBADUAXKLG-UHFFFAOYSA-N 0.000 description 1
- CYLLVWFFBMIJGJ-UHFFFAOYSA-N Cc(cc(cc1)-c2ncccc2-c2c[nH]c3ncccc23)c1F Chemical compound Cc(cc(cc1)-c2ncccc2-c2c[nH]c3ncccc23)c1F CYLLVWFFBMIJGJ-UHFFFAOYSA-N 0.000 description 1
- PGHUUQJAEYZEGT-UHFFFAOYSA-N Cc(cc(cc1C=N)Br)c1N Chemical compound Cc(cc(cc1C=N)Br)c1N PGHUUQJAEYZEGT-UHFFFAOYSA-N 0.000 description 1
- AZZMRAKBRBTBIG-UHFFFAOYSA-N Cc1cc(-c(nccc2)c2-c2ccc3nc[n](CCN4CCOCC4)c3c2)ccc1F Chemical compound Cc1cc(-c(nccc2)c2-c2ccc3nc[n](CCN4CCOCC4)c3c2)ccc1F AZZMRAKBRBTBIG-UHFFFAOYSA-N 0.000 description 1
- DIMKCPXKVHTLMK-UHFFFAOYSA-N Cc1cc(F)c(C)cc1-c1ncccc1C1=CC2=NCNN2C=C1 Chemical compound Cc1cc(F)c(C)cc1-c1ncccc1C1=CC2=NCNN2C=C1 DIMKCPXKVHTLMK-UHFFFAOYSA-N 0.000 description 1
- YOXRAFDMJPRNKF-UHFFFAOYSA-N Cc1cccc(-c2ccncc2)c1-c1ccc2[o]ccc2c1 Chemical compound Cc1cccc(-c2ccncc2)c1-c1ccc2[o]ccc2c1 YOXRAFDMJPRNKF-UHFFFAOYSA-N 0.000 description 1
- BQXATJMGEVEOEW-UHFFFAOYSA-N Cc1cnc(-c2cc(O)ccc2)c(-c(cc2)cc3c2ncnc3N)c1 Chemical compound Cc1cnc(-c2cc(O)ccc2)c(-c(cc2)cc3c2ncnc3N)c1 BQXATJMGEVEOEW-UHFFFAOYSA-N 0.000 description 1
- ASQZDQWGTCJNBZ-UHFFFAOYSA-N Cc1nc(Nc2c[nH]nc2)c(cc(cc2)-c3cccnc3-c(cc(cc3)Cl)c3F)c2n1 Chemical compound Cc1nc(Nc2c[nH]nc2)c(cc(cc2)-c3cccnc3-c(cc(cc3)Cl)c3F)c2n1 ASQZDQWGTCJNBZ-UHFFFAOYSA-N 0.000 description 1
- SILJPOMUZOWVHS-UHFFFAOYSA-N ClC1=CC=C=Cc(cc2)c1cc2Br Chemical compound ClC1=CC=C=Cc(cc2)c1cc2Br SILJPOMUZOWVHS-UHFFFAOYSA-N 0.000 description 1
- SUEOFXZHGLPDPU-UHFFFAOYSA-N Clc(nccc1)c1-c(cc1)c[n]2c1ncc2 Chemical compound Clc(nccc1)c1-c(cc1)c[n]2c1ncc2 SUEOFXZHGLPDPU-UHFFFAOYSA-N 0.000 description 1
- XYXSUSFJXFFUHE-UHFFFAOYSA-N Clc1ccccc1-c(c(Cl)c1)c[n]2c1ccc2 Chemical compound Clc1ccccc1-c(c(Cl)c1)c[n]2c1ccc2 XYXSUSFJXFFUHE-UHFFFAOYSA-N 0.000 description 1
- GOPPZSDJSADGKT-UHFFFAOYSA-N FC(c1ccc(cc2)[n]1cc2Br)(F)F Chemical compound FC(c1ccc(cc2)[n]1cc2Br)(F)F GOPPZSDJSADGKT-UHFFFAOYSA-N 0.000 description 1
- AYUHRCDACUVWIA-UHFFFAOYSA-N Fc(cc1-c2ncccc2-c2nc3ccn[n]3cc2)cc(F)c1F Chemical compound Fc(cc1-c2ncccc2-c2nc3ccn[n]3cc2)cc(F)c1F AYUHRCDACUVWIA-UHFFFAOYSA-N 0.000 description 1
- WGOLHUGPTDEKCF-UHFFFAOYSA-N Nc(nc1)ccc1Br Chemical compound Nc(nc1)ccc1Br WGOLHUGPTDEKCF-UHFFFAOYSA-N 0.000 description 1
- XNQKMHOHLWJGTD-UHFFFAOYSA-N Nc1ncnc(cc2)c1cc2-c1cccnc1-c(cc(c(F)c1)O)c1Cl Chemical compound Nc1ncnc(cc2)c1cc2-c1cccnc1-c(cc(c(F)c1)O)c1Cl XNQKMHOHLWJGTD-UHFFFAOYSA-N 0.000 description 1
- NDVIEBMUURLVLG-UHFFFAOYSA-N Nc1ncnc(cc2)c1nc2-c1c(-c2cc(Cl)ccc2F)nccc1 Chemical compound Nc1ncnc(cc2)c1nc2-c1c(-c2cc(Cl)ccc2F)nccc1 NDVIEBMUURLVLG-UHFFFAOYSA-N 0.000 description 1
- IOGMMRUUNUKFFD-UHFFFAOYSA-N OC(C1=CNC(C=C2)N1C=C2Br)=O Chemical compound OC(C1=CNC(C=C2)N1C=C2Br)=O IOGMMRUUNUKFFD-UHFFFAOYSA-N 0.000 description 1
- GKYWOKFQMHFPSL-PLNGDYQASA-N [N-]=C(/C=C\C1=CCC=C(C#N)N1)Br Chemical compound [N-]=C(/C=C\C1=CCC=C(C#N)N1)Br GKYWOKFQMHFPSL-PLNGDYQASA-N 0.000 description 1
- FBOVQHNYFFCKEM-UHFFFAOYSA-N [O-][N+](C(C=CC(C1)Br)=C1F)=O Chemical compound [O-][N+](C(C=CC(C1)Br)=C1F)=O FBOVQHNYFFCKEM-UHFFFAOYSA-N 0.000 description 1
- CMQKBJCYVCHVKL-UHFFFAOYSA-N [O-][N+](c(ccc(-c1cccnc1Cl)c1)c1F)=O Chemical compound [O-][N+](c(ccc(-c1cccnc1Cl)c1)c1F)=O CMQKBJCYVCHVKL-UHFFFAOYSA-N 0.000 description 1
- LAIZZVRZPGYRJE-UHFFFAOYSA-N c1c[o]c2c1cccc2-c1ncccc1-c1ccncc1 Chemical compound c1c[o]c2c1cccc2-c1ncccc1-c1ccncc1 LAIZZVRZPGYRJE-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
- A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
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- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/39541—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against normal tissues, cells
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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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
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- 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
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2803—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
- C07K16/2818—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against CD28 or CD152
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- A—HUMAN NECESSITIES
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- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Oncology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461976880P | 2014-04-08 | 2014-04-08 | |
| US201462019577P | 2014-07-01 | 2014-07-01 | |
| PCT/US2015/024146 WO2015157093A1 (en) | 2014-04-08 | 2015-04-02 | 2,3-disubstituted pyridine compounds as tgf-beta inhibitors and methods of use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
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| WO2015157093A1 (en) * | 2014-04-08 | 2015-10-15 | Rigel Pharmaceuticals, Inc. | 2,3-disubstituted pyridine compounds as tgf-beta inhibitors and methods of use |
| CN107531666A (zh) * | 2015-02-20 | 2018-01-02 | 里格尔药品股份有限公司 | Gdf‑8抑制剂 |
| BR112018003588A2 (pt) | 2015-08-26 | 2018-09-25 | Blueprint Medicines Corp | compostos e composições úteis para tratamento de distúrbios relacionados ao ntrk |
| RU2018122089A (ru) | 2015-11-19 | 2019-12-25 | Блюпринт Медсинс Корпорейшн | Соединения и композиции, подходящие для лечения расстройств, связанных с ntrk |
| US10508106B2 (en) * | 2015-11-25 | 2019-12-17 | Convergene Llc | Bicyclic BET bromodomain inhibitors and uses thereof |
| ES2941687T3 (es) * | 2016-03-24 | 2023-05-24 | Cothera Bioscience Inc | Tratamiento del cáncer con TG02 |
| TWI808055B (zh) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Hdac 抑制劑與 pd-1 抑制劑之組合治療 |
| TWI794171B (zh) | 2016-05-11 | 2023-03-01 | 美商滬亞生物國際有限公司 | Hdac抑制劑與pd-l1抑制劑之組合治療 |
| WO2018013430A2 (en) | 2016-07-12 | 2018-01-18 | Arisan Therapeutics Inc. | Heterocyclic compounds for the treatment of arenavirus infection |
| CA3039220A1 (en) * | 2016-10-26 | 2018-05-03 | Icahn School Of Medicine At Mount Sinai | Method for increasing cell proliferation in pancreatic beta cells, treatment method, and composition |
| MX393780B (es) | 2017-01-17 | 2025-03-24 | Heparegenix Gmbh | Inhibidores de proteina cinasa para promover la regeneracion hepatica o reducir o prevenir la muerte de hepatocitos |
| KR20190110588A (ko) * | 2017-01-23 | 2019-09-30 | 레볼루션 메디슨즈, 인크. | 알로스테릭 shp2 억제제로서의 피리딘 화합물 |
| WO2018161876A1 (zh) * | 2017-03-08 | 2018-09-13 | 中国科学院上海药物研究所 | 二氢喹喔啉类溴结构域识别蛋白抑制剂及制备方法和用途 |
| CN107118210A (zh) * | 2017-04-28 | 2017-09-01 | 贵州大学 | 一种3‑碘‑6‑(三氟甲基)咪唑并[1,2‑a]吡啶的制备工艺 |
| US11547712B2 (en) | 2017-11-20 | 2023-01-10 | Icahn School Of Medicine At Mount Sinai | Kinase inhibitor compounds and compositions and methods of use |
| CN111819193A (zh) | 2018-01-05 | 2020-10-23 | 西奈山伊坎医学院 | 增加胰腺β细胞增殖的方法、治疗方法以及组合物 |
| AU2019240065A1 (en) | 2018-03-20 | 2020-09-24 | Icahn School Of Medicine At Mount Sinai | Kinase inhibitor compounds and compositions and methods of use |
| US12419865B2 (en) | 2018-12-06 | 2025-09-23 | Arisan Therapeutics Inc. | Compounds for the treatment of arenavirus infection |
| MX2021007738A (es) | 2018-12-27 | 2021-08-05 | Nexys Therapeutics Inc | Derivados de (piridin-2-il)amina como inhibidores de tgf-beta r1 (alk5) para el tratamiento de cancer. |
| US20220017483A1 (en) * | 2018-12-28 | 2022-01-20 | Sichuan-Kelun-Biotech Biopharmaceutical Co., Ltd | Aminopyridine compound, preparation method therefor and use thereof |
| PH12021500043A1 (en) | 2019-03-29 | 2022-06-06 | Sumitomo Chemical Co | Heterocyclic compound and harmful arthropod pest control composition containing same |
| US12247015B2 (en) | 2019-04-29 | 2025-03-11 | Solent Therapeutics, Llc | 3-amino-4H-benzo[e][1,2,4]thiadiazine 1,1-dioxide derivatives as inhibitors of MRGX2 |
| US12441707B2 (en) | 2019-12-30 | 2025-10-14 | Tyra Biosciences, Inc. | Indazole compounds |
| CN115916759B (zh) * | 2020-06-19 | 2025-07-15 | 泰州红云制药有限公司 | 取代喹唑啉类化合物、其制备方法、药物组合及应用 |
| US20230234935A1 (en) * | 2020-06-26 | 2023-07-27 | Icahn School Of Medicine At Mount Sinai | Kinase inhibitor compounds and compositions and methods of use |
| BR112023005876A2 (pt) | 2020-09-30 | 2023-05-02 | Sumitomo Chemical Co | Composto heterocíclico e composição de controle de artrópode nocivo contendo o mesmo |
| CN112225736B (zh) * | 2020-11-12 | 2022-04-15 | 山东省科学院菏泽分院 | 一种6-溴咪唑并[1.2-a]吡啶-3-甲醛的制备方法 |
| US20240277852A1 (en) * | 2021-05-20 | 2024-08-22 | Dana-Farber Cancer Institute, Inc. | Inhibitors and degraders of pip4k protein |
| CN113416181B (zh) * | 2021-08-02 | 2022-05-03 | 四川大学 | 喹唑啉类衍生物及其用途 |
| CN114292259B (zh) * | 2021-11-30 | 2023-06-27 | 西安交通大学 | 4-氨基酸侧链取代的喹唑啉衍生物及其应用 |
| WO2023107714A2 (en) * | 2021-12-10 | 2023-06-15 | Prothena Biosciences Limited | Methods for treating neurological disorders |
| EP4596547A1 (en) | 2022-09-30 | 2025-08-06 | Sumitomo Chemical Company, Limited | Heterocyclic compound and harmful arthropod-controlling composition containing same |
| WO2024096093A1 (ja) | 2022-11-04 | 2024-05-10 | 住友化学株式会社 | 複素環化合物及びそれを含有する有害節足動物防除組成物 |
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| US7320789B2 (en) * | 2001-09-26 | 2008-01-22 | Wyeth | Antibody inhibitors of GDF-8 and uses thereof |
| EP1720855A4 (en) * | 2004-03-02 | 2008-12-17 | Smithkline Beecham Corp | HEMMER OF ACT ACTIVITY |
| AU2005295734A1 (en) * | 2004-10-15 | 2006-04-27 | Biogen Idec Ma Inc. | Methods of treating vascular injuries |
| US9259426B2 (en) * | 2006-07-20 | 2016-02-16 | Gilead Sciences, Inc. | 4,6-di- and 2,4,6-trisubstituted quinazoline derivatives useful for treating viral infections |
| ATE522249T1 (de) * | 2007-07-26 | 2011-09-15 | Novartis Ag | Organische verbindungen |
| WO2009032653A1 (en) | 2007-08-31 | 2009-03-12 | Smith Kline Beecham Corporation | Inhibitors of akt activity |
| EA201201081A1 (ru) * | 2010-02-05 | 2013-03-29 | Мерк Патент Гмбх | Производные гетарил[1,8]нафтиридина |
| JP6104824B2 (ja) * | 2011-03-09 | 2017-03-29 | 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Merck Patent Gesellschaft mit beschraenkter Haftung | ピリド[2,3−b]ピラジン誘導体およびそれらの治療的使用 |
| TR201808033T4 (tr) * | 2011-07-13 | 2018-06-21 | Tiumbio Co Ltd | Alk5 ve veya alk4 inhibitörleri olarak 2 pridil ikameli imidazollar. |
| CN104837832B (zh) * | 2012-10-05 | 2019-04-26 | 里格尔药品股份有限公司 | Gdf-8抑制剂 |
| WO2015157093A1 (en) * | 2014-04-08 | 2015-10-15 | Rigel Pharmaceuticals, Inc. | 2,3-disubstituted pyridine compounds as tgf-beta inhibitors and methods of use |
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| WO2015157093A1 (en) | 2015-10-15 |
| CN106536507B (zh) | 2020-04-07 |
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| EP3129367A1 (en) | 2017-02-15 |
| JP2019196387A (ja) | 2019-11-14 |
| TW201623279A (zh) | 2016-07-01 |
| US10233170B2 (en) | 2019-03-19 |
| US20170096409A1 (en) | 2017-04-06 |
| EP3129367B1 (en) | 2019-09-04 |
| JP2017515802A (ja) | 2017-06-15 |
| JP6767875B2 (ja) | 2020-10-14 |
| CN106536507A (zh) | 2017-03-22 |
| US10858335B2 (en) | 2020-12-08 |
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