CN106132950B - 氨基吡啶类化合物和使用方法 - Google Patents
氨基吡啶类化合物和使用方法 Download PDFInfo
- Publication number
- CN106132950B CN106132950B CN201480075343.2A CN201480075343A CN106132950B CN 106132950 B CN106132950 B CN 106132950B CN 201480075343 A CN201480075343 A CN 201480075343A CN 106132950 B CN106132950 B CN 106132950B
- Authority
- CN
- China
- Prior art keywords
- chloro
- phenyl
- reaction
- pyridyl
- fluoro
- 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*C1(C)C=C(C=NC=C2)C2=NC=C1 Chemical compound C*C1(C)C=C(C=NC=C2)C2=NC=C1 0.000 description 28
- LICNVQCUUJKYJN-UHFFFAOYSA-N CC(c(c(Cl)c1)cnc1-c(cc(cc1)Cl)c1F)=C Chemical compound CC(c(c(Cl)c1)cnc1-c(cc(cc1)Cl)c1F)=C LICNVQCUUJKYJN-UHFFFAOYSA-N 0.000 description 3
- JZIQNDFHVVKMQW-UHFFFAOYSA-N CC(c(cnc(Cl)c1)c1Cl)=C Chemical compound CC(c(cnc(Cl)c1)c1Cl)=C JZIQNDFHVVKMQW-UHFFFAOYSA-N 0.000 description 2
- ZNYPPYODHXZNGD-UHFFFAOYSA-N Bc(nc1)ccc1Br Chemical compound Bc(nc1)ccc1Br ZNYPPYODHXZNGD-UHFFFAOYSA-N 0.000 description 1
- JFJGLXKWFMEPAO-UHFFFAOYSA-N CC(C(C(C1)Cl)=CN=C1c1ncccc1F)=C Chemical compound CC(C(C(C1)Cl)=CN=C1c1ncccc1F)=C JFJGLXKWFMEPAO-UHFFFAOYSA-N 0.000 description 1
- RKENEPILWUYPEP-UHFFFAOYSA-N CC(C)c(c(Nc1c(CCN2)c2ncc1)c1)cnc1-c1ncccc1F Chemical compound CC(C)c(c(Nc1c(CCN2)c2ncc1)c1)cnc1-c1ncccc1F RKENEPILWUYPEP-UHFFFAOYSA-N 0.000 description 1
- JJYZCPRITYKJAQ-UHFFFAOYSA-N CC(C)c(c(Nc1c(cc[nH]2)c2ncn1)c1)cnc1-c(cc(cc1)Cl)c1F Chemical compound CC(C)c(c(Nc1c(cc[nH]2)c2ncn1)c1)cnc1-c(cc(cc1)Cl)c1F JJYZCPRITYKJAQ-UHFFFAOYSA-N 0.000 description 1
- BAZCIOSBHUYZDR-UHFFFAOYSA-N CC(C)c(cc1)c(Nc(ccnc2)c2C(OC)=O)nc1-c1cc(Cl)ccc1F Chemical compound CC(C)c(cc1)c(Nc(ccnc2)c2C(OC)=O)nc1-c1cc(Cl)ccc1F BAZCIOSBHUYZDR-UHFFFAOYSA-N 0.000 description 1
- QPWBBPDULLEDDG-UHFFFAOYSA-N CC(NC(CO)CO)=O Chemical compound CC(NC(CO)CO)=O QPWBBPDULLEDDG-UHFFFAOYSA-N 0.000 description 1
- ZPQRGAFJWCVRLD-UHFFFAOYSA-O CC(c(c(Nc1c(C=C[NH2+]2)c2ncc1)c1)cnc1-c1ncccc1F)=C Chemical compound CC(c(c(Nc1c(C=C[NH2+]2)c2ncc1)c1)cnc1-c1ncccc1F)=C ZPQRGAFJWCVRLD-UHFFFAOYSA-O 0.000 description 1
- JNZUMXMEZFSESD-UHFFFAOYSA-N CC(c(cnc(-c1cc(C(F)(F)F)ccc1F)c1)c1Cl)=C Chemical compound CC(c(cnc(-c1cc(C(F)(F)F)ccc1F)c1)c1Cl)=C JNZUMXMEZFSESD-UHFFFAOYSA-N 0.000 description 1
- BRTXEUFBRDXZGV-UHFFFAOYSA-N CC(c(cnc(-c1cc(Cl)ccc1F)c1)c1Nc1ccnc2c1cccc2)=C Chemical compound CC(c(cnc(-c1cc(Cl)ccc1F)c1)c1Nc1ccnc2c1cccc2)=C BRTXEUFBRDXZGV-UHFFFAOYSA-N 0.000 description 1
- CZUXSKYVBFLUOG-UHFFFAOYSA-N CC1(C)C=C(C=CC=C2)C2=NC=C1 Chemical compound CC1(C)C=C(C=CC=C2)C2=NC=C1 CZUXSKYVBFLUOG-UHFFFAOYSA-N 0.000 description 1
- QVXREMRTDQTPQJ-UHFFFAOYSA-N CC1(C)N=CN=C(C=CN2)C2=C1 Chemical compound CC1(C)N=CN=C(C=CN2)C2=C1 QVXREMRTDQTPQJ-UHFFFAOYSA-N 0.000 description 1
- NVCIOJVTULGLGW-UHFFFAOYSA-N CC1(CC(C)=C)C=C(C=CN=C2)C2=NC=C1 Chemical compound CC1(CC(C)=C)C=C(C=CN=C2)C2=NC=C1 NVCIOJVTULGLGW-UHFFFAOYSA-N 0.000 description 1
- JMGQKVXGIZQIGS-UHFFFAOYSA-N CC1Nc([n](Cc(cc2)ccc2O)cc2)c2C(NS(C(C)(C)C)=O)=C1 Chemical compound CC1Nc([n](Cc(cc2)ccc2O)cc2)c2C(NS(C(C)(C)C)=O)=C1 JMGQKVXGIZQIGS-UHFFFAOYSA-N 0.000 description 1
- ITUOESSMMRUYQG-UHFFFAOYSA-N COC1=CC=C(C[n]2c3nccc(Cl)c3cc2)CC1 Chemical compound COC1=CC=C(C[n]2c3nccc(Cl)c3cc2)CC1 ITUOESSMMRUYQG-UHFFFAOYSA-N 0.000 description 1
- YJPVAMGGHWRIBR-LURJTMIESA-N C[C@@H](CNC(c1cnccc1N)=O)O Chemical compound C[C@@H](CNC(c1cnccc1N)=O)O YJPVAMGGHWRIBR-LURJTMIESA-N 0.000 description 1
- HNTZVGMWXCFCTA-UHFFFAOYSA-N Clc1c(cc[nH]2)c2ncc1 Chemical compound Clc1c(cc[nH]2)c2ncc1 HNTZVGMWXCFCTA-UHFFFAOYSA-N 0.000 description 1
- YFFUYGSLQXVHMB-UHFFFAOYSA-N Fc(c(Br)c1)ccc1Cl Chemical compound Fc(c(Br)c1)ccc1Cl YFFUYGSLQXVHMB-UHFFFAOYSA-N 0.000 description 1
- FQYRLEXKXQRZDH-UHFFFAOYSA-N Nc1c(cccc2)c2ncc1 Chemical compound Nc1c(cccc2)c2ncc1 FQYRLEXKXQRZDH-UHFFFAOYSA-N 0.000 description 1
- XMIAFAKRAAMSGX-UHFFFAOYSA-N Nc1c(cccn2)c2ccc1 Chemical compound Nc1c(cccn2)c2ccc1 XMIAFAKRAAMSGX-UHFFFAOYSA-N 0.000 description 1
- KUHVVLFCTMTYGR-UHFFFAOYSA-N OB(c(cc(C(F)(F)F)cc1)c1F)O Chemical compound OB(c(cc(C(F)(F)F)cc1)c1F)O KUHVVLFCTMTYGR-UHFFFAOYSA-N 0.000 description 1
- GGTUVWGMCFXUAS-UHFFFAOYSA-N OB(c1cc(Cl)ccc1F)O Chemical compound OB(c1cc(Cl)ccc1F)O GGTUVWGMCFXUAS-UHFFFAOYSA-N 0.000 description 1
- PCTOQRHZVLEWPR-UHFFFAOYSA-N OCC(CO)NC(c(cncc1)c1Nc1c(C2CC2)cnc(-c2cc(Cl)ccc2F)c1)=O Chemical compound OCC(CO)NC(c(cncc1)c1Nc1c(C2CC2)cnc(-c2cc(Cl)ccc2F)c1)=O PCTOQRHZVLEWPR-UHFFFAOYSA-N 0.000 description 1
- FLBAYUMRQUHISI-UHFFFAOYSA-N c(cn1)cc2c1nccc2 Chemical compound c(cn1)cc2c1nccc2 FLBAYUMRQUHISI-UHFFFAOYSA-N 0.000 description 1
- LBZYKNAEJRHENJ-UHFFFAOYSA-N c1c[nH]c2ccnnc12 Chemical compound c1c[nH]c2ccnnc12 LBZYKNAEJRHENJ-UHFFFAOYSA-N 0.000 description 1
- WCZVZNOTHYJIEI-UHFFFAOYSA-N c1cc2ccnnc2cc1 Chemical compound c1cc2ccnnc2cc1 WCZVZNOTHYJIEI-UHFFFAOYSA-N 0.000 description 1
- BEJXOECDIXUTLN-UHFFFAOYSA-N c1cc2ccnnc2nc1 Chemical compound c1cc2ccnnc2nc1 BEJXOECDIXUTLN-UHFFFAOYSA-N 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N c1cc2cncnc2cc1 Chemical compound c1cc2cncnc2cc1 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- UDJFFSGCRRMVFH-UHFFFAOYSA-N c1cc2cncnc2nc1 Chemical compound c1cc2cncnc2nc1 UDJFFSGCRRMVFH-UHFFFAOYSA-N 0.000 description 1
- PAQYIEZTLSDLQO-UHFFFAOYSA-N c1cncc2c1cncn2 Chemical compound c1cncc2c1cncn2 PAQYIEZTLSDLQO-UHFFFAOYSA-N 0.000 description 1
- PLZDHJUUEGCXJH-UHFFFAOYSA-N c1cncc2c1ncnc2 Chemical compound c1cncc2c1ncnc2 PLZDHJUUEGCXJH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- A61K31/435—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
-
- 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
- A61K31/435—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
- A61K31/444—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
-
- 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
- A61K31/435—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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61K31/435—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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- 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
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
- 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
- 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
-
- 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
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- 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
-
- 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
- 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
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical 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)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Otolaryngology (AREA)
- Ophthalmology & Optometry (AREA)
- Gastroenterology & Hepatology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201810955135.1A CN109045032A (zh) | 2014-01-01 | 2014-12-31 | 氨基吡啶类化合物和使用方法 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN6/DEL/2014 | 2014-01-01 | ||
| IN6DE2014 | 2014-01-01 | ||
| PCT/US2014/072922 WO2015103355A1 (en) | 2014-01-01 | 2014-12-31 | Compounds and methods of use |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201810955135.1A Division CN109045032A (zh) | 2014-01-01 | 2014-12-31 | 氨基吡啶类化合物和使用方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN106132950A CN106132950A (zh) | 2016-11-16 |
| CN106132950B true CN106132950B (zh) | 2018-11-09 |
Family
ID=52293317
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201480075343.2A Expired - Fee Related CN106132950B (zh) | 2014-01-01 | 2014-12-31 | 氨基吡啶类化合物和使用方法 |
| CN201810955135.1A Pending CN109045032A (zh) | 2014-01-01 | 2014-12-31 | 氨基吡啶类化合物和使用方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201810955135.1A Pending CN109045032A (zh) | 2014-01-01 | 2014-12-31 | 氨基吡啶类化合物和使用方法 |
Country Status (17)
| Country | Link |
|---|---|
| US (4) | US10030004B2 (https=) |
| EP (1) | EP3089971B1 (https=) |
| JP (2) | JP6474166B2 (https=) |
| CN (2) | CN106132950B (https=) |
| AU (2) | AU2014373773C1 (https=) |
| CA (1) | CA2935392C (https=) |
| CY (1) | CY1123290T1 (https=) |
| DK (1) | DK3089971T3 (https=) |
| ES (1) | ES2813875T3 (https=) |
| HR (1) | HRP20201384T1 (https=) |
| HU (1) | HUE050761T2 (https=) |
| LT (1) | LT3089971T (https=) |
| PL (1) | PL3089971T3 (https=) |
| PT (1) | PT3089971T (https=) |
| RS (1) | RS60718B1 (https=) |
| SI (1) | SI3089971T1 (https=) |
| WO (1) | WO2015103355A1 (https=) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL3089971T3 (pl) | 2014-01-01 | 2021-01-25 | Medivation Technologies Llc | Związki i sposoby ich zastosowania |
| JP6952747B2 (ja) | 2018-09-18 | 2021-10-20 | ファイザー・インク | がん処置のためのTGFβ阻害剤およびCDK阻害剤の組合せ |
| US12427147B2 (en) | 2018-10-31 | 2025-09-30 | Senju Pharmaceutical Co., Ltd. | Retinal ganglion cell death inhibitor |
| MA54526A (fr) * | 2018-12-20 | 2022-03-30 | Pfizer | NOUVELLES FORMES POLYMORPHES D'UN INHIBITEUR DE TGFBeta |
| AU2019417418B2 (en) * | 2018-12-27 | 2025-02-27 | Nexys Therapeutics, Inc. | (pyridin-2-yl)amine derivatives as ΤGFβR1 (Alk5) inhibitors for the treatment of cancer |
| EP4041399A1 (en) | 2019-10-02 | 2022-08-17 | Tolremo Therapeutics AG | Heterocyclic derivatives, pharmaceutical compositions and their use in the treatment or amelioration of cancer |
| CN111116565B (zh) * | 2020-04-01 | 2020-07-14 | 中科利健制药(广州)有限公司 | 2-芳基-4-(4-吡唑氧基)吡啶类化合物、其制备方法、药物组合物与应用 |
| KR20230028798A (ko) | 2020-06-25 | 2023-03-02 | 톨레모 테라퓨틱스 아게 | 암 치료를 위한 CBP/p300 브로모도메인 억제제 및 KRAS 억제제의 조합물 |
| WO2021260110A1 (en) * | 2020-06-25 | 2021-12-30 | Tolremo Therapeutics Ag | Heterocyclic derivatives, pharmaceutical compositions and their use in the treatment, amelioration or prevention of fibrotic disease |
| EP4182308B1 (en) * | 2020-07-15 | 2024-09-04 | Chiesi Farmaceutici S.p.A. | Pyridazinyl amino derivatives as alk5 inhibitors |
| CN114369083B (zh) * | 2020-10-15 | 2026-02-27 | 四川科伦博泰生物医药股份有限公司 | 杂环类化合物、包含其的药物组合物、其制备方法及其用途 |
| EP4251625A4 (en) * | 2020-11-24 | 2024-10-09 | Aligos Therapeutics, Inc. | Tricyclic compounds |
| WO2022130206A1 (en) | 2020-12-16 | 2022-06-23 | Pfizer Inc. | TGFβr1 INHIBITOR COMBINATION THERAPIES |
| CN112843058A (zh) * | 2021-01-27 | 2021-05-28 | 复旦大学附属华山医院 | 烟酰胺类化合物在制备治疗抗脊索肿瘤药物中的应用 |
| IL307402A (en) | 2021-04-07 | 2023-12-01 | Tolremo Therapeutics Ag | The tercyclic derivatives, pharmaceutical compounds and their use in the treatment or amelioration of cancer |
| WO2022229846A1 (en) | 2021-04-29 | 2022-11-03 | Pfizer Inc. | Treatment of cancer using a transforming growth factor beta receptor type 1 inhibitor |
| WO2023054712A1 (ja) | 2021-09-30 | 2023-04-06 | ペプチドリーム株式会社 | ペプチド |
| CN115353326A (zh) * | 2022-07-27 | 2022-11-18 | 魏玉芝 | 一种反光防车印沥青及其制备方法 |
| CN116606244A (zh) * | 2023-05-26 | 2023-08-18 | 康化(上海)新药研发有限公司 | 一种6-溴-5-甲氧基吡啶-3-胺的合成方法 |
| CN117865965B (zh) * | 2024-01-08 | 2024-06-28 | 贵州省天然产物研究中心 | 吡咯并嘧啶-4-胺和吡唑并嘧啶-4-胺衍生物及制备方法和应用 |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040198728A1 (en) * | 2003-04-04 | 2004-10-07 | Cell Therapeutics, Inc. | Pyridines and uses thereof |
| WO2005033105A2 (en) * | 2003-09-30 | 2005-04-14 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
| WO2005065691A1 (en) * | 2003-12-24 | 2005-07-21 | Scios, Inc. | Treatment of malignant gliomas with tgf-beta inhibitors |
| WO2009012375A2 (en) * | 2007-07-19 | 2009-01-22 | Wyeth | Squarate kinase inhibitors |
| WO2011044181A1 (en) * | 2009-10-08 | 2011-04-14 | Schering Corporation | Iminothiadiazine dioxide compounds as bace inhibitors, compositions, and their use |
| WO2011054433A1 (en) * | 2009-11-07 | 2011-05-12 | Merck Patent Gmbh | Heteroarylaminoquinolines as tgf-beta receptor kinase inhibitors |
| WO2011146287A1 (en) * | 2010-05-20 | 2011-11-24 | Takeda Pharmaceutical Company Limited | Pyrazolo[4,3-b]pyridine-7-amine inhibitors of alk5 |
Family Cites Families (91)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5714493A (en) | 1991-05-10 | 1998-02-03 | Rhone-Poulenc Rorer Pharmaceuticals, Inc. | Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase |
| US6645969B1 (en) | 1991-05-10 | 2003-11-11 | Aventis Pharmaceuticals Inc. | Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase |
| US5710158A (en) | 1991-05-10 | 1998-01-20 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
| DK0640599T3 (da) | 1993-08-26 | 1998-09-28 | Ono Pharmaceutical Co | 4-Aminopyrimidin-derivater |
| US6184226B1 (en) | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
| WO2000047102A2 (en) | 1999-02-11 | 2000-08-17 | The General Hospital Corporation | COMPOSITIONS AND METHODS FOR MODULATING TGF-β SIGNALING |
| GB9922171D0 (en) | 1999-09-21 | 1999-11-17 | Zeneca Ltd | Chemical compounds |
| US6660731B2 (en) | 2000-09-15 | 2003-12-09 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| US6613776B2 (en) | 2000-09-15 | 2003-09-02 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| WO2002022605A1 (en) * | 2000-09-15 | 2002-03-21 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| US6989385B2 (en) | 2000-12-21 | 2006-01-24 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| CA2468159A1 (en) | 2001-11-27 | 2003-06-05 | Merck & Co., Inc. | 4-aminoquinoline compounds |
| US20040006030A1 (en) | 2002-07-02 | 2004-01-08 | Isis Pharmaceuticals Inc. | Antisense modulation of TGF-beta 2 expression |
| US20030225089A1 (en) | 2002-04-10 | 2003-12-04 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Pharmaceutical compositions based on anticholinergics and p38 kinase inhibitors |
| AU2003229305A1 (en) | 2002-05-17 | 2003-12-02 | Scios, Inc. | TREATMENT OF FIBROPROLIFERATIVE DISORDERS USING TGF-Beta INHIBITORS |
| US20040146509A1 (en) | 2002-07-25 | 2004-07-29 | Zhihe Li | Methods for improvement of lung function using TGF-beta inhibitors |
| BR0314196A (pt) | 2002-09-10 | 2005-07-26 | Scios Inc | Inibidores de tgf-beta |
| CA2496295C (en) | 2002-09-18 | 2010-11-23 | Michael John Munchhof | Novels pyrazole compounds as transforming growth factor (tgf) inhibitors |
| MXPA05002981A (es) | 2002-09-18 | 2005-06-22 | Pfizer Prod Inc | Nuevos compuestos de imidazol como inhibidores del factor de crecimiento transformante (tgf). |
| AU2003256003A1 (en) | 2002-09-18 | 2004-04-08 | Pfizer Products Inc. | Novel oxazole and thiazole compounds as transforming growth factor (TGF) inhibitors |
| EP1542995A1 (en) | 2002-09-18 | 2005-06-22 | Pfizer Products Inc. | Novel isothiazole and isoxazole compounds as transforming growth factor (tgf) inhibitors |
| CA2497971A1 (en) | 2002-09-18 | 2004-04-01 | Pfizer Products Inc. | Triazole derivatives as transforming growth factor (tgf) inhibitors |
| WO2004048930A2 (en) | 2002-11-22 | 2004-06-10 | Scios, Inc. | METHOD FOR COUNTERACTING A PATHOLOGIC CHANGE IN THE ß-ADRENERGIC PATHWAY |
| WO2004047818A2 (en) | 2002-11-22 | 2004-06-10 | Scios, Inc. | USE OF TFG-β INHIBITORSTO COUNTERACT PATHOLOGIC CHANGES IN THE LEVEL OR FUNCTION OF STEROID/THYROID RECEPTORS |
| AU2003297460A1 (en) | 2002-12-19 | 2004-07-14 | Scios, Inc. | TREATMENT OF OBESITY AND ASSOCIATED CONDITIONS WITH TGF-Beta INHIBITORS |
| AU2003300099A1 (en) | 2003-01-02 | 2004-07-29 | Millennium Pharmaceuticals, Inc. | COMPOSITIONS AND METHODS FOR INHIBITING TGF-Beta |
| WO2004065392A1 (en) | 2003-01-24 | 2004-08-05 | Smithkline Beecham Corporation | Condensed pyridines and pyrimidines and their use as alk-5 receptor ligands |
| PA8595001A1 (es) | 2003-03-04 | 2004-09-28 | Pfizer Prod Inc | Nuevos compuestos heteroaromaticos condensados que son inhibidores del factor de crecimiento transforante (tgf) |
| WO2004080982A1 (en) | 2003-03-11 | 2004-09-23 | Pfizer Products Inc. | Pyrazine compounds as transforming growth factor (tgf) inhibitors |
| DE602004014347D1 (de) | 2003-03-12 | 2008-07-24 | Millennium Pharm Inc | Chinazolin-derivate als tgf-beta-inhibitoren |
| US7223766B2 (en) | 2003-03-28 | 2007-05-29 | Scios, Inc. | Bi-cyclic pyrimidine inhibitors of TGFβ |
| US20050014753A1 (en) | 2003-04-04 | 2005-01-20 | Irm Llc | Novel compounds and compositions as protein kinase inhibitors |
| ES2389258T3 (es) | 2003-06-17 | 2012-10-24 | Millennium Pharmaceuticals, Inc. | Composiciones y métodos para inhibir TGF-s |
| WO2005007646A1 (en) | 2003-07-10 | 2005-01-27 | Neurogen Corporation | Substituted heterocyclic diarylamine analogues |
| TW200510373A (en) | 2003-07-14 | 2005-03-16 | Neurogen Corp | Substituted quinolin-4-ylamine analogues |
| DE602004027048D1 (de) | 2003-07-16 | 2010-06-17 | Resverlogix Inc | Verbindungen und methoden für das downregulating der effekte von tgf-beta |
| WO2005018677A2 (en) | 2003-08-01 | 2005-03-03 | Wyeth Holdings Corporation | Use of combination of an epidermal growth factor receptor kinase inhibitor and cytotoxic agents for treatment and inhibition of cancer |
| WO2005032481A2 (en) | 2003-09-30 | 2005-04-14 | Scios Inc. | Quinazoline derivatives as medicaments |
| ES2576195T3 (es) | 2003-10-15 | 2016-07-06 | National Jewish Health | Cistatina C como antagonista de TGF-B y métodos relacionados con la misma |
| AR046324A1 (es) | 2003-11-10 | 2005-11-30 | Merck Sharp & Dohme | Heterociclos nitrogenados de seis miembros aminosustituidos que contienen sustituyentes de quinolina o isoquinolina |
| WO2005047279A1 (en) | 2003-11-10 | 2005-05-26 | Merck Sharp & Dohme Limited | Substituted nitrogen-containing six-membered amino-heterocycles as vanilloid-1 receptor antagonists for treating pain |
| US20070099950A1 (en) | 2003-11-21 | 2007-05-03 | Jongwon Lim | Pyridin-4-ylamine compounds useful in the treatment of neuropathic pain |
| WO2005069935A2 (en) | 2004-01-20 | 2005-08-04 | University Of Medicine And Dentistry Of New Jersey | METHODS FOR MEASURING TRANSFORMING GROWTH FACTOR BETA (TGF-β) RECEPTOR SIGNALING ACTIVITY AND USES THEREOF |
| EP1723146A1 (en) | 2004-03-01 | 2006-11-22 | Eli Lilly And Company | Fused pyrazole derivatives as tgf-beta signal transduction inhibitors for the treatment of fibrosis and neoplasms |
| EP1794135A1 (en) * | 2004-09-27 | 2007-06-13 | Amgen Inc. | Substituted heterocyclic compounds and methods of use |
| KR20070058602A (ko) | 2004-09-30 | 2007-06-08 | 티보텍 파마슈티칼즈 리미티드 | Hcv 저해 바이-사이클릭 피리미딘 |
| EP1812450A2 (en) | 2004-11-10 | 2007-08-01 | Eli Lilly And Company | Tgf-beta inhibitors |
| US7767687B2 (en) | 2004-12-13 | 2010-08-03 | Biogen Idec Ma Inc. | Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as RAF kinase inhibitors |
| WO2006102102A2 (en) | 2005-03-17 | 2006-09-28 | Marshfield Clinic | Tgf-beta modulators and methods for using the same |
| WO2006105222A2 (en) * | 2005-03-25 | 2006-10-05 | Scios Inc. | Carboxamide inhibitors of tgfb |
| US8030318B2 (en) | 2005-03-25 | 2011-10-04 | Tibotec Pharmaceuticals Ltd. | Fused bicyclic inhibitors of HCV |
| CN101189234B (zh) | 2005-03-25 | 2011-08-17 | 泰博特克药品有限公司 | Hcv的杂二环抑制剂 |
| MX2007013595A (es) | 2005-05-04 | 2008-01-24 | Renovis Inc | Compuestos heterociclicos fusionados y composiciones y usos de estos. |
| TW200716631A (en) | 2005-05-12 | 2007-05-01 | Tibotec Pharm Ltd | Pyrido[2,3-d]pyrimidines useful as HCV inhibitors, and methods for the preparation thereof |
| WO2007145862A2 (en) | 2006-06-05 | 2007-12-21 | Genentech, Inc. | Extending survival of cancer patients with elevated levels of egf or tgf-alpha |
| US20080280891A1 (en) | 2006-06-27 | 2008-11-13 | Locus Pharmaceuticals, Inc. | Anti-cancer agents and uses thereof |
| CA2665438C (en) | 2006-10-04 | 2014-12-02 | Tibotec Pharmaceuticals Ltd. | Carboxamide 4-[(4-pyridyl)amino]pyrimidines useful as hcv inhibitors |
| WO2008057402A2 (en) | 2006-11-02 | 2008-05-15 | Cytovia, Inc. | N-aryl-isoxazolopyrimidin-4-amines and related compounds as activators of caspases and inducers of apoptosis and the use thereof |
| ES2347721T3 (es) | 2006-12-19 | 2010-11-03 | Vertex Pharmaceuticals, Inc. | Aminopirimidinas utiles como inhibidores de proteina quinasas. |
| GB0702871D0 (en) | 2007-02-14 | 2007-03-28 | Tcp Innovations Ltd | Improved compositions and combinations 1 |
| EP2166849A4 (en) | 2007-06-11 | 2010-09-15 | Miikana Therapeutics Inc | SUBSTITUTED PYRAZOL COMPOUNDS |
| WO2009022171A1 (en) * | 2007-08-13 | 2009-02-19 | Astrazeneca Ab | Pyridinyiioxy pyridines as alk5 inhibitors |
| NZ603525A (en) | 2008-06-27 | 2015-02-27 | Celgene Avilomics Res Inc | Pyrimidine based compound and uses thereof |
| US20110257208A1 (en) | 2008-11-19 | 2011-10-20 | Matthew Duncton | Compounds useful as faah modulators and uses thereof |
| EP2241565A1 (en) | 2009-01-15 | 2010-10-20 | Universität Leipzig | Aurora kinase inhibitors compounds |
| WO2010102267A2 (en) | 2009-03-06 | 2010-09-10 | Ipierian, Inc. | Tgf-beta pathway inhibitors for enhancement of cellular reprogramming of human cells |
| US9908884B2 (en) | 2009-05-05 | 2018-03-06 | Dana-Farber Cancer Institute, Inc. | EGFR inhibitors and methods of treating disorders |
| US20120101095A1 (en) | 2009-06-22 | 2012-04-26 | Guenter Hoelzemann | Alkoxy-thienopyrimidines as tgf-beta receptor kinase modulators |
| AR079814A1 (es) | 2009-12-31 | 2012-02-22 | Otsuka Pharma Co Ltd | Compuestos heterociclicos, composiciones farmaceuticas que los contienen y sus usos |
| SG183233A1 (en) | 2010-02-22 | 2012-09-27 | Merck Patent Gmbh | Hetarylaminonaphthyridines |
| MX2012015147A (es) | 2010-06-30 | 2013-05-01 | Amgen Inc | Compuestos heterociclicos y su uso como inhibidores de la actividad pi3k. |
| ES2689103T3 (es) * | 2010-06-30 | 2018-11-08 | Fujifilm Corporation | Nuevo derivado de nicotinamida o sal del mismo |
| EP2441755A1 (en) | 2010-09-30 | 2012-04-18 | Almirall, S.A. | Pyridine- and isoquinoline-derivatives as Syk and JAK kinase inhibitors |
| CA2816219C (en) * | 2010-11-01 | 2019-10-29 | Portola Pharmaceuticals, Inc. | Nicotinamides as syk modulators |
| ES2542647T3 (es) | 2011-03-09 | 2015-08-07 | Merck Patent Gmbh | Derivados de pirido[2,3 b]pirazina y sus usos terapéuticos |
| MX2013011908A (es) * | 2011-04-12 | 2014-03-27 | Alzheimer S Inst Of America Inc | Composiciones y usos terapeuticos de inhibidores de cinasa epsilon relacionados con cinasa i-kappa b (ikk) y cinasa 1 de union tank. |
| CA2874998A1 (en) * | 2011-05-27 | 2012-12-06 | Cytocure Llc | Methods, compositions, and kits for the treatment of cancer |
| WO2012177624A2 (en) * | 2011-06-21 | 2012-12-27 | The Johns Hopkins University | Focused radiation for augmenting immune-based therapies against neoplasms |
| CA2849168A1 (en) * | 2011-09-22 | 2013-03-28 | Merck Sharp & Dohme Corp. | Cycloalkylnitrile pyrazole carboxamides as janus kinase inhibitors |
| WO2013078286A1 (en) | 2011-11-22 | 2013-05-30 | Cornell University | Methods for stimulating hematopoietic recovery by inhibiting tgf beta signaling |
| WO2013158422A1 (en) | 2012-04-17 | 2013-10-24 | E. I. Du Pont De Nemours And Company | Heterocyclic compounds for controlling invertebrate pests |
| WO2013175415A1 (en) * | 2012-05-23 | 2013-11-28 | Piramal Enterprises Limited | Substituted pyrimidine compounds and uses thereof |
| EP2863914B1 (en) * | 2012-06-20 | 2018-10-03 | Merck Sharp & Dohme Corp. | Pyrazolyl derivatives as syk inhibitors |
| WO2014091330A1 (en) * | 2012-12-11 | 2014-06-19 | Koninklijke Philips N.V. | Assisting apparatus for assisting in performing a brachytherapy |
| HK1218750A1 (zh) | 2013-03-21 | 2017-03-10 | Bayer Pharma Aktiengesellschaft | 3-杂芳基取代的吲唑 |
| WO2014181287A1 (en) | 2013-05-09 | 2014-11-13 | Piramal Enterprises Limited | Heterocyclyl compounds and uses thereof |
| PL3089971T3 (pl) | 2014-01-01 | 2021-01-25 | Medivation Technologies Llc | Związki i sposoby ich zastosowania |
| UY35935A (es) | 2014-01-03 | 2015-06-30 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | Compuestos de nicotinamida sustituida con heteroarilo como inhibidores de quinasa y moduladores de irak-4 |
| TWI582083B (zh) | 2014-10-07 | 2017-05-11 | 美國禮來大藥廠 | 胺基吡啶基氧基吡唑化合物 |
| AR103232A1 (es) | 2014-12-22 | 2017-04-26 | Bristol Myers Squibb Co | ANTAGONISTAS DE TGFbR |
| EP3744716A1 (en) | 2016-09-21 | 2020-12-02 | Celanese International Corporation | Acesulfame potassium compositions and processes for producing same |
-
2014
- 2014-12-31 PL PL14824755T patent/PL3089971T3/pl unknown
- 2014-12-31 CA CA2935392A patent/CA2935392C/en active Active
- 2014-12-31 HR HRP20201384TT patent/HRP20201384T1/hr unknown
- 2014-12-31 CN CN201480075343.2A patent/CN106132950B/zh not_active Expired - Fee Related
- 2014-12-31 JP JP2016544111A patent/JP6474166B2/ja not_active Expired - Fee Related
- 2014-12-31 SI SI201431651T patent/SI3089971T1/sl unknown
- 2014-12-31 HU HUE14824755A patent/HUE050761T2/hu unknown
- 2014-12-31 ES ES14824755T patent/ES2813875T3/es active Active
- 2014-12-31 RS RS20201011A patent/RS60718B1/sr unknown
- 2014-12-31 WO PCT/US2014/072922 patent/WO2015103355A1/en not_active Ceased
- 2014-12-31 LT LTEP14824755.4T patent/LT3089971T/lt unknown
- 2014-12-31 CN CN201810955135.1A patent/CN109045032A/zh active Pending
- 2014-12-31 EP EP14824755.4A patent/EP3089971B1/en active Active
- 2014-12-31 PT PT148247554T patent/PT3089971T/pt unknown
- 2014-12-31 DK DK14824755.4T patent/DK3089971T3/da active
- 2014-12-31 AU AU2014373773A patent/AU2014373773C1/en not_active Ceased
- 2014-12-31 US US15/109,013 patent/US10030004B2/en active Active
-
2018
- 2018-03-23 US US15/933,532 patent/US10501436B2/en active Active
- 2018-12-20 AU AU2018282363A patent/AU2018282363B2/en not_active Ceased
-
2019
- 2019-01-04 JP JP2019000208A patent/JP2019048899A/ja active Pending
- 2019-10-22 US US16/659,775 patent/US11053216B2/en active Active
-
2020
- 2020-08-28 CY CY20201100809T patent/CY1123290T1/el unknown
-
2021
- 2021-05-22 US US17/327,705 patent/US11702401B2/en active Active
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040198728A1 (en) * | 2003-04-04 | 2004-10-07 | Cell Therapeutics, Inc. | Pyridines and uses thereof |
| WO2005033105A2 (en) * | 2003-09-30 | 2005-04-14 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
| WO2005065691A1 (en) * | 2003-12-24 | 2005-07-21 | Scios, Inc. | Treatment of malignant gliomas with tgf-beta inhibitors |
| WO2009012375A2 (en) * | 2007-07-19 | 2009-01-22 | Wyeth | Squarate kinase inhibitors |
| WO2011044181A1 (en) * | 2009-10-08 | 2011-04-14 | Schering Corporation | Iminothiadiazine dioxide compounds as bace inhibitors, compositions, and their use |
| WO2011054433A1 (en) * | 2009-11-07 | 2011-05-12 | Merck Patent Gmbh | Heteroarylaminoquinolines as tgf-beta receptor kinase inhibitors |
| WO2011146287A1 (en) * | 2010-05-20 | 2011-11-24 | Takeda Pharmaceutical Company Limited | Pyrazolo[4,3-b]pyridine-7-amine inhibitors of alk5 |
Non-Patent Citations (3)
| Title |
|---|
| Diamino-C,N-diarylpyridine positional isomers as inhibitors of lysophosphatidic acid acyltransferase-β;Feng Hong等;《Bioorganic & Medicinal Chemistry Letters》;20050906;第15卷(第21期);4703-4707 * |
| Identification and SAR of squarate inhibitors of mitogen activated protein kinase-activated protein kinase 2 (MK-2);Frank Lovering等;《Bioorganic & Medicinal Chemistry》;20090326;第17卷(第9期);3342-3351 * |
| Novel Vanilloid Receptor-1 Antagonists: 1. Conformationally Restricted Analogues of trans-Cinnamides;Mark H. Norman等;《J. Med. Chem.》;20070622;第50卷(第15期);3497-3514 * |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN106132950B (zh) | 氨基吡啶类化合物和使用方法 | |
| CN107108561B (zh) | 用作irak抑制剂的杂芳基化合物及其用途 | |
| US11208403B2 (en) | Pyridone derivatives having tetrahydropyranylmethyl groups | |
| EP2763976B1 (en) | 2-pyridyl carboxamide-containing spleen tyrosine kinase (syk) inhibitors | |
| JP2010132689A (ja) | ジヒドロピラゾロピリミジノン誘導体 | |
| KR20240075952A (ko) | Fgfr 억제제 및 이의 사용 방법 | |
| TW201710250A (zh) | 經取代之喹喏啉衍生物 | |
| CN111094244A (zh) | 吡啶基吡啶酮化合物 | |
| CN121969622A (zh) | 取代的双环杂环yap-tead和/或taz-tead抑制剂 | |
| HK1230619B (zh) | 氨基吡啶類化合物和使用方法 | |
| HK1262758A1 (en) | Aminopyridines compounds and methods of use | |
| HK1230619A1 (en) | Aminopyridines compounds and methods of use | |
| HK40058077A (en) | Pyridone derivative having tetrahydropyranylmethyl group | |
| HK1238630B (en) | Pyridone derivative having tetrahydropyranyl methyl group | |
| HK1238630A1 (en) | Pyridone derivative having tetrahydropyranyl methyl group | |
| HK1242303B (zh) | 用作irak抑制剂的杂芳基化合物及其用途 | |
| HK1242303A1 (en) | Heteroaryl compounds as irak inhibitors and uses thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| CB02 | Change of applicant information |
Address after: Delaware Applicant after: Maddie Weber Technology Co.,Ltd. Address before: California, USA Applicant before: MEDIVATION TECHNOLOGIES, Inc. |
|
| CB02 | Change of applicant information | ||
| REG | Reference to a national code |
Ref country code: HK Ref legal event code: DE Ref document number: 1230619 Country of ref document: HK |
|
| CB02 | Change of applicant information |
Address after: Delaware Applicant after: Medivation Technologies LLC Address before: Delaware Applicant before: Maddie Weber Technology Co.,Ltd. |
|
| CB02 | Change of applicant information | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20181109 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |