CA3029630A1 - Biarylmethyl heterocycles - Google Patents
Biarylmethyl heterocycles Download PDFInfo
- Publication number
- CA3029630A1 CA3029630A1 CA3029630A CA3029630A CA3029630A1 CA 3029630 A1 CA3029630 A1 CA 3029630A1 CA 3029630 A CA3029630 A CA 3029630A CA 3029630 A CA3029630 A CA 3029630A CA 3029630 A1 CA3029630 A1 CA 3029630A1
- Authority
- CA
- Canada
- Prior art keywords
- alkyl
- cycloalkyl
- haloalkyl
- hydroxyalkyl
- mmol
- 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.)
- Pending
Links
- 0 CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC1OC1CO*)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC1OC1CO*)(=O)=O 0.000 description 3
- IVCQHSXQUGAWAZ-UHFFFAOYSA-N CCCCCC(NS(c(ccc(CN1CCCC1)c1)c1-c1ccc(C[n]2c3nc(C)cc(C)c3nc2CC)cc1)(=O)=O)=O Chemical compound CCCCCC(NS(c(ccc(CN1CCCC1)c1)c1-c1ccc(C[n]2c3nc(C)cc(C)c3nc2CC)cc1)(=O)=O)=O IVCQHSXQUGAWAZ-UHFFFAOYSA-N 0.000 description 1
- NXVWCYUJVUSWCD-UHFFFAOYSA-N CCc1nc(c(C)cc(C)c2)c2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(c1cccc(-c(cc2C)cc3c2nc(CC)[n]3Cc(cc2)ccc2-c(cc(Cc2ccccc2)[s]2)c2S(NC(c2ccccc2)=O)(=O)=O)c1)=O)(=O)=O Chemical compound CCc1nc(c(C)cc(C)c2)c2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(c1cccc(-c(cc2C)cc3c2nc(CC)[n]3Cc(cc2)ccc2-c(cc(Cc2ccccc2)[s]2)c2S(NC(c2ccccc2)=O)(=O)=O)c1)=O)(=O)=O NXVWCYUJVUSWCD-UHFFFAOYSA-N 0.000 description 1
- HXZIRMOMABVAND-UHFFFAOYSA-N CCc1nc2c(C)cc(C(N(C)C)=O)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC1OC1c1ccccc1)(=O)=O Chemical compound CCc1nc2c(C)cc(C(N(C)C)=O)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC1OC1c1ccccc1)(=O)=O HXZIRMOMABVAND-UHFFFAOYSA-N 0.000 description 1
- BJXFTPUVBSFEOV-UHFFFAOYSA-N CCc1nc2c(C)cc(C)cc2[n]1Cc(cc1)ccc1C(CC(C)(CN1CCOCC1)S1)=C1S(NC(C(c1ccccc1)C1=CCC(C)C(Cc(cc2C)cc3c2nc(CC)[n]3Cc(cc2)ccc2-c(cc(Cc2ccccc2)[s]2)c2S(NC(c2ccccc2)=O)(=O)=O)=C1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)cc2[n]1Cc(cc1)ccc1C(CC(C)(CN1CCOCC1)S1)=C1S(NC(C(c1ccccc1)C1=CCC(C)C(Cc(cc2C)cc3c2nc(CC)[n]3Cc(cc2)ccc2-c(cc(Cc2ccccc2)[s]2)c2S(NC(c2ccccc2)=O)(=O)=O)=C1)=O)(=O)=O BJXFTPUVBSFEOV-UHFFFAOYSA-N 0.000 description 1
- CCJGLSZNKAYAAD-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(CCc1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(CCc1ccccc1)=O)(=O)=O CCJGLSZNKAYAAD-UHFFFAOYSA-N 0.000 description 1
- VUGNWEUFBXVLPS-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(c(cccc1)c1Oc1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(c(cccc1)c1Oc1ccccc1)=O)(=O)=O VUGNWEUFBXVLPS-UHFFFAOYSA-N 0.000 description 1
- XBPDOYQLLZWIGG-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(c1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCCC1)cc1)c1S(NC(c1ccccc1)=O)(=O)=O XBPDOYQLLZWIGG-UHFFFAOYSA-N 0.000 description 1
- IMNRNJIVXFJTCL-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(Cc1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(Cc1ccccc1)=O)(=O)=O IMNRNJIVXFJTCL-UHFFFAOYSA-N 0.000 description 1
- QOUGSHMWCZQBOM-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(CN1CCOCC1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O QOUGSHMWCZQBOM-UHFFFAOYSA-N 0.000 description 1
- SFJQWEVGLDUGLM-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(C1CC1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(C1CC1)=O)(=O)=O SFJQWEVGLDUGLM-UHFFFAOYSA-N 0.000 description 1
- OVYVZRZLFTWXDU-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O OVYVZRZLFTWXDU-UHFFFAOYSA-N 0.000 description 1
- MVDOITYZIMLXLE-UHFFFAOYSA-N CCc1nc2c(C)cc(C)nc2[n]1Cc1ccc(C(C)(C(C=C2)S(NC(c3cc(Cc(cc4C)nc5c4nc(CC)[n]5Cc(cc4)ccc4C(C(C)C(CN4CCOCC4)C=C4)=C4S(NC(c4ccccc4)=O)(=O)=O)ccc3)=O)(=O)=O)C=C2c2ccccc2)cc1 Chemical compound CCc1nc2c(C)cc(C)nc2[n]1Cc1ccc(C(C)(C(C=C2)S(NC(c3cc(Cc(cc4C)nc5c4nc(CC)[n]5Cc(cc4)ccc4C(C(C)C(CN4CCOCC4)C=C4)=C4S(NC(c4ccccc4)=O)(=O)=O)ccc3)=O)(=O)=O)C=C2c2ccccc2)cc1 MVDOITYZIMLXLE-UHFFFAOYSA-N 0.000 description 1
- YFSODJRLDIOLRT-UHFFFAOYSA-N CCc1nc2c(C)ccnc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O Chemical compound CCc1nc2c(C)ccnc2[n]1Cc(cc1)ccc1-c(cc(Cc1ccccc1)[s]1)c1S(NC(c1ccccc1)=O)(=O)=O YFSODJRLDIOLRT-UHFFFAOYSA-N 0.000 description 1
- AVFLSYMKOGBIER-UHFFFAOYSA-N CCc1nc2c(C)ccnc2[n]1Cc(cc1)ccc1-c1c(-c2n[nH]nn2)[s]c(Cc2ccccc2)c1 Chemical compound CCc1nc2c(C)ccnc2[n]1Cc(cc1)ccc1-c1c(-c2n[nH]nn2)[s]c(Cc2ccccc2)c1 AVFLSYMKOGBIER-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
- C07D401/14—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
- 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
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4245—Oxadiazoles
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed 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
- A61K31/435—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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/47—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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines 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
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/26—Oxygen atoms
-
- 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
- C07D239/20—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
- C07D271/07—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
-
- 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
- C07D401/10—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 carbon chain containing aromatic rings
-
- 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
- C07D403/10—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 carbon chain containing aromatic rings
-
- 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
- C07D403/14—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 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
- C07D413/02—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
- C07D413/10—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 carbon chain containing aromatic 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Cardiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicinal Preparation (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662356215P | 2016-06-29 | 2016-06-29 | |
| US62/356,215 | 2016-06-29 | ||
| PCT/US2017/039646 WO2018005591A1 (en) | 2016-06-29 | 2017-06-28 | Biarylmethyl heterocycles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA3029630A1 true CA3029630A1 (en) | 2018-01-04 |
Family
ID=59297443
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA3029630A Pending CA3029630A1 (en) | 2016-06-29 | 2017-06-28 | Biarylmethyl heterocycles |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US11407733B2 (https=) |
| EP (1) | EP3478672B1 (https=) |
| JP (1) | JP7231414B2 (https=) |
| KR (1) | KR102538999B1 (https=) |
| CN (1) | CN109715615A (https=) |
| AR (1) | AR108906A1 (https=) |
| AU (1) | AU2017289974B2 (https=) |
| BR (1) | BR112018077075A2 (https=) |
| CA (1) | CA3029630A1 (https=) |
| EA (1) | EA039493B1 (https=) |
| ES (1) | ES2984389T3 (https=) |
| IL (1) | IL263499B (https=) |
| MX (1) | MX2018015247A (https=) |
| SG (1) | SG11201810837QA (https=) |
| TW (1) | TW201811759A (https=) |
| WO (1) | WO2018005591A1 (https=) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018010622A1 (zh) * | 2016-07-11 | 2018-01-18 | 武汉朗来科技发展有限公司 | 化合物的晶型及其制备方法、组合物和应用 |
| AU2018346597B2 (en) | 2017-10-06 | 2023-07-13 | Forma Therapeutics, Inc. | Inhibiting Ubiquitin Specific Peptidase 30 |
| CN109956870A (zh) * | 2017-12-14 | 2019-07-02 | 南京卡文迪许生物工程技术有限公司 | 一种罗沙司他的合成方法及其中间体化合物 |
| EP3556760A1 (en) * | 2018-04-19 | 2019-10-23 | F. Hoffmann-La Roche AG | Spiro compounds |
| EP3781156A4 (en) | 2018-04-16 | 2022-05-18 | C4 Therapeutics, Inc. | SPIROCYCLIC COMPOUNDS |
| JP7449242B2 (ja) | 2018-05-17 | 2024-03-13 | フォーマ セラピューティクス,インコーポレイテッド | ユビキチン特異的ペプチダーゼ30(usp30)阻害剤として有用な縮合二環化合物 |
| JP7530889B2 (ja) | 2018-10-05 | 2024-08-08 | フォーマ セラピューティクス,インコーポレイテッド | ユビキチン特異的プロテアーゼ30(usp30)阻害剤として作用する縮合ピロリン |
| ES2960987T3 (es) | 2019-04-12 | 2024-03-07 | Riboscience Llc | Derivados de heteroarilo bicíclicos como inhibidores de la ectonucleótido pirofosfatasa fosfodiesterasa 1 |
| WO2020257549A2 (en) * | 2019-06-20 | 2020-12-24 | Chemocentryx, Inc. | Compounds for treatment of pd-l1 diseases |
| CN110479182A (zh) * | 2019-09-10 | 2019-11-22 | 肯特催化材料股份有限公司 | 一种多氨基双子表面活性剂及其制备方法与应用 |
| GB201913603D0 (en) | 2019-09-20 | 2019-11-06 | Vicore Pharma Ab | New compounds |
| GB202104033D0 (en) * | 2021-03-23 | 2021-05-05 | Vicore Pharma Ab | New compounds |
| PE20241304A1 (es) * | 2021-07-30 | 2024-06-24 | Confo Therapeutics N V | Compuestos para el tratamiento del dolor, en particular el dolor neuropatico, y/u otras enfermedades o trastornos que se asocian con at2r y/o senalizacion mediada por at2r |
| KR20240051999A (ko) * | 2021-08-26 | 2024-04-22 | 상하이 한서 바이오메디컬 컴퍼니 리미티드 | 방향족 고리 함유 생물학적 길항제, 이의 제조 방법 및 용도 |
| CN115321495B (zh) * | 2022-07-28 | 2023-07-21 | 东北石油大学 | 一种金属富氮化合物FeN8的合成方法 |
Family Cites Families (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4444770A (en) | 1980-05-29 | 1984-04-24 | Bayer Aktiengesellschaft | New imidazoazole-alkenoic acid amide compounds, intermediate products for their production, their production, and their medicinal use |
| CA1338238C (en) | 1988-01-07 | 1996-04-09 | David John Carini | Angiotensin ii receptor blocking imidazoles and combinations thereof with diuretics and nsaids |
| EP0400835A1 (en) | 1989-05-15 | 1990-12-05 | Merck & Co. Inc. | Substituted benzimidazoles as angiotensin II antagonists |
| GB8911854D0 (en) | 1989-05-23 | 1989-07-12 | Ici Plc | Heterocyclic compounds |
| IE64514B1 (en) | 1989-05-23 | 1995-08-09 | Zeneca Ltd | Azaindenes |
| US5332744A (en) | 1989-05-30 | 1994-07-26 | Merck & Co., Inc. | Substituted imidazo-fused 6-membered heterocycles as angiotensin II antagonists |
| IL94390A (en) | 1989-05-30 | 1996-03-31 | Merck & Co Inc | The 6-membered trans-nitrogen-containing heterocycles are compressed with imidazo and pharmaceutical preparations containing them |
| US5223499A (en) | 1989-05-30 | 1993-06-29 | Merck & Co., Inc. | 6-amino substituted imidazo[4,5-bipyridines as angiotensin II antagonists |
| US5411980A (en) | 1989-07-28 | 1995-05-02 | Merck & Co., Inc. | Substituted triazolinones, triazolinethiones, and triazolinimines as angiotensin II antagonists |
| EP0415886A3 (en) | 1989-08-30 | 1991-10-23 | Ciba-Geigy Ag | Aza compounds |
| US5140037A (en) | 1990-03-20 | 1992-08-18 | E. I. Du Pont De Nemours And Company | Treatment of central nervous system disorders with imidazole angiotensin-ii receptor antagonists |
| JPH05509086A (ja) | 1990-06-22 | 1993-12-16 | イー・アイ・デュポン・ドゥ・ヌムール・アンド・カンパニー | イミダゾールアンジオテンシン―2受容体拮抗薬による慢性腎不全の治療 |
| CA2062558A1 (en) * | 1991-03-08 | 1992-09-09 | Prasun K. Chakravarty | Heterocyclic compounds bearing acidic functional groups as angiotensin ii antagonists |
| US5177074A (en) * | 1991-03-26 | 1993-01-05 | Merck & Co., Inc. | Angiotensin ii antagonists incorporating a substituted thiophene or furan |
| US5798364A (en) | 1992-03-26 | 1998-08-25 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Imidazopyridines |
| DE4110019C2 (de) | 1991-03-27 | 2000-04-13 | Merck Patent Gmbh | Imidazopyridine, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Zubereitungen |
| TW274551B (https=) | 1991-04-16 | 1996-04-21 | Takeda Pharm Industry Co Ltd | |
| US5198438A (en) * | 1991-05-07 | 1993-03-30 | Merck & Co., Inc. | Angiotensin ii antagonists incorporating a substituted thiophene or furan |
| CA2109524A1 (en) | 1991-05-10 | 1992-11-11 | Prasun K. Chakravarty | Acidic aralkyl triazole derivatives active as angiotensin ii antagonists |
| WO1993001177A1 (en) | 1991-07-03 | 1993-01-21 | Merck & Co., Inc. | Substituted triazolinones |
| WO1993003033A1 (en) | 1991-07-26 | 1993-02-18 | G. D. Searle & Co. | CARBONATE-SUBSTITUTED IMIDAZO[4,5-d] PYRIDAZINE COMPOUNDS FOR TREATMENT OF CARDIOVASCULAR DISORDERS |
| WO1993004045A1 (en) | 1991-08-19 | 1993-03-04 | E.I. Du Pont De Nemours And Company | Angiotensin ii receptor blocking imidazolinone derivatives |
| AU2494792A (en) | 1991-08-19 | 1993-03-16 | E.I. Du Pont De Nemours And Company | Angiotensin ii receptor blocking imidazolinone derivatives |
| EP0531876B1 (en) | 1991-09-10 | 1996-12-18 | Tanabe Seiyaku Co., Ltd. | Imidazoindolizine derivatives and process for preparation thereof |
| IL103020A (en) | 1991-09-10 | 1998-10-30 | Tanabe Seiyaku Co | 3-(1,1'-Biphenyl-4-yl-methyl)-4,5,6,7-tetrahydro-3h-imidazo Ú4,5-c¾ pyridine-4-carboxylic acids their preparation and pharmaceutical compositions containing them |
| WO1993019067A1 (en) | 1991-09-12 | 1993-09-30 | Fujisawa Pharmaceutical Co., Ltd. | Imidazopyridine derivatives as angiotensin ii antagonists |
| US5256667A (en) | 1991-09-25 | 1993-10-26 | Merck & Co., Inc. | Quinazolinones and pyridopyrimidinones |
| GB2263637A (en) | 1992-01-28 | 1993-08-04 | Merck & Co Inc | Substituted imidazo-fused 6-membered carbocycle or heterocycle as neurotensin antagonists |
| NZ254112A (en) | 1992-07-10 | 1997-06-24 | Boots Co Plc | Dioxocyclobutene derivatives; compounds, preparation and pharmaceutical compositions |
| AU675660B2 (en) * | 1992-07-17 | 1997-02-13 | Merck & Co., Inc. | Substituted biphenylmethylimidazopyridines |
| GB2272899A (en) | 1992-11-30 | 1994-06-01 | Du Pont Merck Pharma | Angiotensin-11 receptor blocking cycloalkylbenzylimidazoles |
| JPH06312926A (ja) | 1993-03-04 | 1994-11-08 | Tanabe Seiyaku Co Ltd | アンジオテンシンii拮抗薬 |
| DE4320432A1 (de) | 1993-06-21 | 1994-12-22 | Bayer Ag | Substituierte Mono- und Bipyridylmethylderivate |
| US5444067A (en) | 1993-08-30 | 1995-08-22 | Merck & Co., Inc. | Pharmaceutical treatment methods using angiotensin II receptor agonists bearing a thiophene moiety |
| US5424432A (en) | 1994-05-26 | 1995-06-13 | Merck & Co., Inc. | Process for the preparation of imidazolutidine |
| KR19990022723A (ko) | 1995-06-07 | 1999-03-25 | 윌리암스 로저 에이 | 울혈성심부전의 치료를 위한 스피로노락톤 및 앤지오텐신 ii 길 항제 복합요법 |
| AU725689B2 (en) | 1995-06-07 | 2000-10-19 | G.D. Searle & Co. | Epoxy-steroidal aldosterone antagonist and angiotensin II antagonist combination therapy for treatment of congestive heart failure |
| WO1996040256A1 (en) | 1995-06-07 | 1996-12-19 | G.D. Searle & Co. | Method to treat cardiofibrosis with a combination of an angiotensin ii antagonist and spironolactone |
| ATE314097T1 (de) | 1996-10-28 | 2006-01-15 | Amersham Health As | Kontrastmittel |
| SK92899A3 (en) | 1997-01-10 | 2000-08-14 | Merck & Co Inc | Use of angiotensin ii antagonists to treat symptomatic heart failure |
| CA2318778A1 (en) | 1998-02-25 | 1999-09-02 | Merck & Co., Inc. | Method for decreasing qt dispersion or inhibiting the progression of qt dispersion with an angiotensin ii receptor antagonist |
| GB2337701A (en) | 1998-05-26 | 1999-12-01 | United Medical And Dental Schools Of Guys St Thomas Hospitals | Treatment of ischemia with an angiotensin II antagonist |
| YU78601A (sh) | 1999-05-05 | 2005-07-19 | Aventis Pharma Deutschland Gmbh. | 1-(p-tienilbenzil)-imidazoli kao agonisti angiotenzin-(1-7)- receptora, postupak za njihovu proizvodnju, njihova primena i farmaceutski preparati koji ih sadrže |
| DE19920815A1 (de) | 1999-05-05 | 2000-11-09 | Aventis Pharma Gmbh | 1-(p-Thienylbenzyl)-Imidazole als Agonisten von Angiotensin-(1-7)-Rezeptoren, Verfahren zu ihrer Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate |
| GB0014861D0 (en) | 2000-06-16 | 2000-08-09 | Pharmacia & Upjohn Spa | Novel telomerase inhibitors |
| DE10112041A1 (de) | 2001-03-14 | 2002-09-26 | Aventis Pharma Gmbh | p-Thienylbenzyl-Amide als Agonisten von Angiotensin-(1-7)-Rezeptoren, Verfahren zu ihrer Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate |
| CN1529697B (zh) | 2001-05-31 | 2010-09-22 | 维科尔药物公司 | 用作血管紧张素ⅱ激动剂的三环化合物 |
| JP2003034684A (ja) | 2001-06-29 | 2003-02-07 | Biofor Inc | 新規な種類の抗真菌剤 |
| WO2003064414A1 (en) | 2002-01-29 | 2003-08-07 | Vicore Pharma Ab. | Tricyclic compounds useful as angiotensin ii agonists |
| AU2003302027A1 (en) | 2002-11-21 | 2004-06-15 | Vicore Pharma Ab | New tricyclic angiotensin ii agonists |
| US7129264B2 (en) | 2003-04-16 | 2006-10-31 | Bristol-Myers Squibb Company | Biarylmethyl indolines and indoles as antithromboembolic agents |
| US20060211866A1 (en) | 2005-03-21 | 2006-09-21 | Glenmark Pharmaceuticals Limited | Process for the preparation of angiotensin receptor blockers and intermediates thereof |
| US20110046090A1 (en) | 2005-10-31 | 2011-02-24 | Braincells Inc. | Modulation of neurogenesis with gaba agents and gaba analogs |
| US20110269717A1 (en) | 2006-07-17 | 2011-11-03 | Braincells Inc. | Neurogenesis by modulating angiotensin |
| KR20090060333A (ko) | 2006-09-08 | 2009-06-11 | 노파르티스 아게 | 림프구 상호작용에 의해 매개되는 질환의 치료에 유용한 n-바이아릴 (헤테로)아릴술폰아미드 유도체 |
| HRP20151440T1 (hr) | 2008-12-29 | 2016-01-29 | Trevena, Inc. | Efektori beta-arestina i sastavi i metode u kojima se koriste |
| US8835471B2 (en) | 2010-06-11 | 2014-09-16 | Vicore Pharma Ab | Use of angiotensin II agonists |
| CN102816126A (zh) | 2011-06-07 | 2012-12-12 | 中国药科大学 | 具有心血管活性的胺磺酰芳基取代的三氮唑类衍生物、其制备方法及用途 |
| DE102012004589A1 (de) | 2012-03-09 | 2013-09-12 | Forschungszentrum Jülich GmbH | Agonisten des Angiotensin II AT2-Rezeptors zur Behandlung neurodegenerativer Erkrankungen |
| CN104583185A (zh) | 2012-08-31 | 2015-04-29 | 株式会社Api | 联芳基化合物的制造方法 |
| EP3935944A1 (en) | 2013-03-15 | 2022-01-12 | University Of Southern California, USC Stevens | Compounds for the treatment of musculoskeletal diseases |
| EP2832357A1 (en) | 2013-07-29 | 2015-02-04 | Charité - Universitätsmedizin Berlin | Selective AT2 receptor agonists for use in treatment of cachexia |
| DK3169405T3 (da) | 2014-07-17 | 2024-09-23 | Univ Southern California | Fremgangsmåder, forbindelser og sammensætninger til behandling af muskel- og skeletsygdomme |
-
2017
- 2017-06-28 ES ES17737187T patent/ES2984389T3/es active Active
- 2017-06-28 MX MX2018015247A patent/MX2018015247A/es unknown
- 2017-06-28 AU AU2017289974A patent/AU2017289974B2/en not_active Ceased
- 2017-06-28 EA EA201990159A patent/EA039493B1/ru unknown
- 2017-06-28 JP JP2018568791A patent/JP7231414B2/ja active Active
- 2017-06-28 WO PCT/US2017/039646 patent/WO2018005591A1/en not_active Ceased
- 2017-06-28 AR ARP170101789A patent/AR108906A1/es unknown
- 2017-06-28 CN CN201780041083.0A patent/CN109715615A/zh active Pending
- 2017-06-28 TW TW106121669A patent/TW201811759A/zh unknown
- 2017-06-28 CA CA3029630A patent/CA3029630A1/en active Pending
- 2017-06-28 BR BR112018077075-2A patent/BR112018077075A2/pt not_active Application Discontinuation
- 2017-06-28 US US16/311,835 patent/US11407733B2/en active Active
- 2017-06-28 EP EP17737187.9A patent/EP3478672B1/en active Active
- 2017-06-28 SG SG11201810837QA patent/SG11201810837QA/en unknown
- 2017-06-28 KR KR1020197002349A patent/KR102538999B1/ko active Active
-
2018
- 2018-12-04 IL IL263499A patent/IL263499B/en unknown
-
2022
- 2022-07-11 US US17/861,809 patent/US12037324B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| IL263499B (en) | 2022-04-01 |
| JP2019519586A (ja) | 2019-07-11 |
| BR112018077075A2 (pt) | 2019-04-30 |
| US12037324B2 (en) | 2024-07-16 |
| AU2017289974A1 (en) | 2019-01-17 |
| US11407733B2 (en) | 2022-08-09 |
| US20190202808A1 (en) | 2019-07-04 |
| EA201990159A1 (ru) | 2019-07-31 |
| WO2018005591A1 (en) | 2018-01-04 |
| US20230045357A1 (en) | 2023-02-09 |
| EA039493B1 (ru) | 2022-02-02 |
| EP3478672A1 (en) | 2019-05-08 |
| IL263499A (en) | 2019-01-31 |
| KR102538999B1 (ko) | 2023-05-31 |
| MX2018015247A (es) | 2019-08-12 |
| JP7231414B2 (ja) | 2023-03-01 |
| ES2984389T3 (es) | 2024-10-29 |
| TW201811759A (zh) | 2018-04-01 |
| KR20190025639A (ko) | 2019-03-11 |
| EP3478672B1 (en) | 2024-04-10 |
| SG11201810837QA (en) | 2018-12-28 |
| CN109715615A (zh) | 2019-05-03 |
| AU2017289974B2 (en) | 2021-08-12 |
| AR108906A1 (es) | 2018-10-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA3029630A1 (en) | Biarylmethyl heterocycles | |
| EP3538526B1 (en) | Cyclobutane- and azetidine-containing mono and spirocyclic compounds as alpha v integrin inhibitors | |
| US10590113B2 (en) | 6-hydroxy-4-oxo-1,4-dihydropyrimidine-5-carboxamides as APJ agonists | |
| US10508104B2 (en) | 6-hydroxy-5-(phenyl/heteroarylsulfonyl)pyrimidin-4(1H)-one as APJ agonists | |
| CN108368087B (zh) | 作为apj激动剂的2,4-二羟基-烟酰胺 | |
| WO2025076044A1 (en) | Kras proteolysis targeting chimeras | |
| CA3007280A1 (en) | Apelin receptor agonists and methods of use | |
| US11851428B2 (en) | Activator of TREK (TWIK RElated K+channels) channels | |
| JP7434281B2 (ja) | Pad酵素のベンズイミダゾール阻害剤 | |
| CA2988147A1 (en) | 4-hydroxy-3-(heteroaryl)pyridine-2-one apj agonists for use in the treatment of cardiovascular disorders | |
| CA3008630A1 (en) | Heteroarylhydroxypyrimidinones as agonists of the apj receptor | |
| AU2020204341B2 (en) | Naphthyridinone derivatives and their use in the treatment of arrhythmia | |
| CA3042693A1 (en) | Pyrrole amides as .alpha.v integrin inhibitors | |
| AU2019340173B2 (en) | Imidazopyridinone compound | |
| CN109641918A (zh) | 作为组蛋白去甲基化酶抑制剂的咪唑 | |
| CN118679163A (zh) | 双环杂芳基化合物及其用途 | |
| WO2017161145A1 (en) | Triazolopyridine inhibitors of myeloperoxidase and/or epx | |
| US11498903B2 (en) | 2-(1,1′-biphenyl)-1H-benzodimidazole derivatives and related compounds as apelin and APJ agonists for treating cardiovascular diseases | |
| CA3042707A1 (en) | 3-substituted propionic acids as .alpha.v integrin inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |
Effective date: 20220628 |
|
| B12 | Application deemed to be withdrawn, abandoned or lapsed |
Free format text: ST27 STATUS EVENT CODE: N-2-6-B10-B12-B303 (AS PROVIDED BY THE NATIONAL OFFICE); EVENT TEXT: DEEMED ABANDONED - FAILURE TO RESPOND TO AN EXAMINER'S REQUISITION Effective date: 20240917 |
|
| W00 | Other event occurred |
Free format text: ST27 STATUS EVENT CODE: A-2-2-W10-W00-W100 (AS PROVIDED BY THE NATIONAL OFFICE); EVENT TEXT: LETTER SENT Effective date: 20251229 |