JP6938628B2 - 造血器型プロスタグランジンdシンターゼ阻害剤としての1,3二置換シクロブタンまたはアゼチジン誘導体 - Google Patents
造血器型プロスタグランジンdシンターゼ阻害剤としての1,3二置換シクロブタンまたはアゼチジン誘導体 Download PDFInfo
- Publication number
- JP6938628B2 JP6938628B2 JP2019520150A JP2019520150A JP6938628B2 JP 6938628 B2 JP6938628 B2 JP 6938628B2 JP 2019520150 A JP2019520150 A JP 2019520150A JP 2019520150 A JP2019520150 A JP 2019520150A JP 6938628 B2 JP6938628 B2 JP 6938628B2
- Authority
- JP
- Japan
- Prior art keywords
- trans
- muscle
- mmol
- substituted
- azetidine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 C*=C(NC)N*1C(*N=O)C(*)C1 Chemical compound C*=C(NC)N*1C(*N=O)C(*)C1 0.000 description 41
- DTQVDTLACAAQTR-UHFFFAOYSA-N OC(C(F)(F)F)=O Chemical compound OC(C(F)(F)F)=O DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- OVCFFHUSKNRCBQ-UHFFFAOYSA-N C1NCC1Oc1c2nc[s]c2ccc1 Chemical compound C1NCC1Oc1c2nc[s]c2ccc1 OVCFFHUSKNRCBQ-UHFFFAOYSA-N 0.000 description 1
- YIHPWULVQBWRRH-UHFFFAOYSA-N CC(C)(C(C1)CC1N)O Chemical compound CC(C)(C(C1)CC1N)O YIHPWULVQBWRRH-UHFFFAOYSA-N 0.000 description 1
- MVQLKRMRMPARSZ-UHFFFAOYSA-N CC(C)(C)OC(N(C1)CC1Oc1c2nc[s]c2ccc1)=O Chemical compound CC(C)(C)OC(N(C1)CC1Oc1c2nc[s]c2ccc1)=O MVQLKRMRMPARSZ-UHFFFAOYSA-N 0.000 description 1
- SWAVHIHQDBLTLG-UHFFFAOYSA-N CC(C)(C)OC(NC(C1)CN1c1nc(C#N)ccn1)=O Chemical compound CC(C)(C)OC(NC(C1)CN1c1nc(C#N)ccn1)=O SWAVHIHQDBLTLG-UHFFFAOYSA-N 0.000 description 1
- IHWLNHWOHBBVBK-JOCQHMNTSA-N CC(C)(C)c1nnc(NC([C@H](C2)C[C@@H]2Oc(cc(C=C)cc2)c2OC(F)F)=O)[o]1 Chemical compound CC(C)(C)c1nnc(NC([C@H](C2)C[C@@H]2Oc(cc(C=C)cc2)c2OC(F)F)=O)[o]1 IHWLNHWOHBBVBK-JOCQHMNTSA-N 0.000 description 1
- KHJQGAGWVMFLMZ-YHBQERECSA-N CC(C)(CO[C@H](CC1)CC[C@@H]1N(Cc1ccccc1)Cc1ccccc1)O Chemical compound CC(C)(CO[C@H](CC1)CC[C@@H]1N(Cc1ccccc1)Cc1ccccc1)O KHJQGAGWVMFLMZ-YHBQERECSA-N 0.000 description 1
- GLQYJJIXLLMSGF-KYZUINATSA-N CC(C)(CO[C@H](CC1)CC[C@@H]1N)O Chemical compound CC(C)(CO[C@H](CC1)CC[C@@H]1N)O GLQYJJIXLLMSGF-KYZUINATSA-N 0.000 description 1
- DLQYYZMIOCHMML-UHFFFAOYSA-N CC(C)(Cc1cnc(N)[s]1)O Chemical compound CC(C)(Cc1cnc(N)[s]1)O DLQYYZMIOCHMML-UHFFFAOYSA-N 0.000 description 1
- UVQVYRPYXXBLQH-HZCBDIJESA-N CC(C)([C@H](CC1)CC[C@@H]1N(Cc1ccccc1)Cc1ccccc1)O Chemical compound CC(C)([C@H](CC1)CC[C@@H]1N(Cc1ccccc1)Cc1ccccc1)O UVQVYRPYXXBLQH-HZCBDIJESA-N 0.000 description 1
- OCDCUUMLAMRDBN-UHFFFAOYSA-N CC(Nc(c(C)ccc1)c1OC)=S Chemical compound CC(Nc(c(C)ccc1)c1OC)=S OCDCUUMLAMRDBN-UHFFFAOYSA-N 0.000 description 1
- CIUFYJPIKSPRBF-UHFFFAOYSA-N CCC(C(CC1)CCC1N)=O Chemical compound CCC(C(CC1)CCC1N)=O CIUFYJPIKSPRBF-UHFFFAOYSA-N 0.000 description 1
- LWUFIZPAKBBKHM-JOCQHMNTSA-N CCOC(Cc1nnc(NC([C@H](C2)C[C@@H]2Oc2cccc3c2[o]cc3)=O)[s]1)=O Chemical compound CCOC(Cc1nnc(NC([C@H](C2)C[C@@H]2Oc2cccc3c2[o]cc3)=O)[s]1)=O LWUFIZPAKBBKHM-JOCQHMNTSA-N 0.000 description 1
- ACOIPZNSWIWCKN-UHFFFAOYSA-N CCc1ccc(N(C2)CC2N)nc1Cl Chemical compound CCc1ccc(N(C2)CC2N)nc1Cl ACOIPZNSWIWCKN-UHFFFAOYSA-N 0.000 description 1
- NNLZJNWYGICOFQ-MGCOHNPYSA-N COC([C@H](C1)C[C@@H]1Oc(c1c2cccn1)ccc2F)=O Chemical compound COC([C@H](C1)C[C@@H]1Oc(c1c2cccn1)ccc2F)=O NNLZJNWYGICOFQ-MGCOHNPYSA-N 0.000 description 1
- QRNSGRXTEQPSQN-HAQNSBGRSA-N COC([C@H](C1)C[C@@H]1Oc(cc(C=C)cc1)c1OC)=O Chemical compound COC([C@H](C1)C[C@@H]1Oc(cc(C=C)cc1)c1OC)=O QRNSGRXTEQPSQN-HAQNSBGRSA-N 0.000 description 1
- WUOAGSZATMTAKV-JOCQHMNTSA-N COC([C@H](C1)C[C@@H]1Oc1cc(C=C)cc2c1[o]cc2)=O Chemical compound COC([C@H](C1)C[C@@H]1Oc1cc(C=C)cc2c1[o]cc2)=O WUOAGSZATMTAKV-JOCQHMNTSA-N 0.000 description 1
- IGHROCWURIRNKM-KYZUINATSA-N COC([C@H](C1)C[C@@H]1Oc1cccc2c1[o]cc2Br)=O Chemical compound COC([C@H](C1)C[C@@H]1Oc1cccc2c1[o]cc2Br)=O IGHROCWURIRNKM-KYZUINATSA-N 0.000 description 1
- PWGXDJZPCRZEHI-MGCOHNPYSA-N COc(c(O[C@H](C1)C[C@@H]1SOC)c1)ccc1Cl Chemical compound COc(c(O[C@H](C1)C[C@@H]1SOC)c1)ccc1Cl PWGXDJZPCRZEHI-MGCOHNPYSA-N 0.000 description 1
- FQZSVSBKOSJMQF-BEVBOREHSA-N C[C@@H](C(C1)(C2)C(C)(C)O)C12NC(N(C1)CC1Oc1c2nc[s]c2ccc1)=O Chemical compound C[C@@H](C(C1)(C2)C(C)(C)O)C12NC(N(C1)CC1Oc1c2nc[s]c2ccc1)=O FQZSVSBKOSJMQF-BEVBOREHSA-N 0.000 description 1
- CNPGLKPJXHDHLQ-MGCOHNPYSA-N C[C@H](CC1)CC[C@@H]1N(CCOC1)C1=O Chemical compound C[C@H](CC1)CC[C@@H]1N(CCOC1)C1=O CNPGLKPJXHDHLQ-MGCOHNPYSA-N 0.000 description 1
- YBTUVQBSQYYKBP-UHFFFAOYSA-N C[n](cc1)nc1NC(Oc1ccccc1)=O Chemical compound C[n](cc1)nc1NC(Oc1ccccc1)=O YBTUVQBSQYYKBP-UHFFFAOYSA-N 0.000 description 1
- YRURHMXQNDBGIS-MQMHXKEQSA-N Cc1ccc(CNC([C@H](C2)C[C@@H]2Oc2c3nc[s]c3ccc2)=O)[o]1 Chemical compound Cc1ccc(CNC([C@H](C2)C[C@@H]2Oc2c3nc[s]c3ccc2)=O)[o]1 YRURHMXQNDBGIS-MQMHXKEQSA-N 0.000 description 1
- YRUJPSOMURRNQU-UHFFFAOYSA-N Cc1ccc(N(C2)CC2N)[n+]([O-])c1 Chemical compound Cc1ccc(N(C2)CC2N)[n+]([O-])c1 YRUJPSOMURRNQU-UHFFFAOYSA-N 0.000 description 1
- HLBGAUHQMZXPRZ-UHFFFAOYSA-N O=C(NC(CC1)CCN1c(nc1)ncc1F)N(C1)CC1OC(CC=C1)c2c1[s]cn2 Chemical compound O=C(NC(CC1)CCN1c(nc1)ncc1F)N(C1)CC1OC(CC=C1)c2c1[s]cn2 HLBGAUHQMZXPRZ-UHFFFAOYSA-N 0.000 description 1
- REWXYAQHNOXLNZ-XYPYZODXSA-N O=C([C@H](C1)C[C@@H]1Oc(c1c2cccn1)ccc2F)Nc1ncc[s]1 Chemical compound O=C([C@H](C1)C[C@@H]1Oc(c1c2cccn1)ccc2F)Nc1ncc[s]1 REWXYAQHNOXLNZ-XYPYZODXSA-N 0.000 description 1
- VWERIJDEGAFAFE-MQMHXKEQSA-N O=C([C@H](C1)C[C@@H]1Oc1c2nc[s]c2ccc1)NC(C1)CN1c1ncccn1 Chemical compound O=C([C@H](C1)C[C@@H]1Oc1c2nc[s]c2ccc1)NC(C1)CN1c1ncccn1 VWERIJDEGAFAFE-MQMHXKEQSA-N 0.000 description 1
- KIDSQHGDFKWYGM-KYZUINATSA-N OC([C@H](C1)C[C@@H]1Oc(c1c2cccn1)ccc2F)=O Chemical compound OC([C@H](C1)C[C@@H]1Oc(c1c2cccn1)ccc2F)=O KIDSQHGDFKWYGM-KYZUINATSA-N 0.000 description 1
- PGXQUDGRSAFSRX-ZKCHVHJHSA-N OC([C@H](C1)C[C@@H]1Oc(cccc1)c1OC(F)(F)F)=O Chemical compound OC([C@H](C1)C[C@@H]1Oc(cccc1)c1OC(F)(F)F)=O PGXQUDGRSAFSRX-ZKCHVHJHSA-N 0.000 description 1
- LQYQYUACIVBKNW-ZKCHVHJHSA-N OC([C@H](C1)C[C@@H]1Oc1c2nc[s]c2ccc1)=O Chemical compound OC([C@H](C1)C[C@@H]1Oc1c2nc[s]c2ccc1)=O LQYQYUACIVBKNW-ZKCHVHJHSA-N 0.000 description 1
- IZTHOFPWTNXSEB-KYZUINATSA-N OC([C@H](C1)C[C@@H]1Oc1ccc[n]2c1ncc2)=O Chemical compound OC([C@H](C1)C[C@@H]1Oc1ccc[n]2c1ncc2)=O IZTHOFPWTNXSEB-KYZUINATSA-N 0.000 description 1
- ZKJJXBOSCGJQAY-GVJMRKKJSA-N OC([C@H](C1)C[C@@H]1Oc1cccc(F)c1)=O Chemical compound OC([C@H](C1)C[C@@H]1Oc1cccc(F)c1)=O ZKJJXBOSCGJQAY-GVJMRKKJSA-N 0.000 description 1
- CCZCXFHJMKINPE-UHFFFAOYSA-N Oc(cccc1)c1OCc1ccccc1 Chemical compound Oc(cccc1)c1OCc1ccccc1 CCZCXFHJMKINPE-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
-
- 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
- A61K31/4196—1,2,4-Triazoles
-
- 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
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles 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
- A61K31/41—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
- A61K31/41—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
- A61K31/428—Thiazoles condensed with carbocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
-
- 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
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/40—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/20—Oxygen atoms
- C07D215/24—Oxygen atoms attached in position 8
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
-
- 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
- C07D257/06—Five-membered rings with nitrogen atoms directly attached to the ring carbon atom
-
- 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
- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/64—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
-
- 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
-
- 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
- C07D403/04—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 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
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/04—Systems containing only non-condensed rings with a four-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/93—Spiro compounds
- C07C2603/94—Spiro compounds containing "free" spiro atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pulmonology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Furan Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Pyrrole Compounds (AREA)
- Indole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Quinoline Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662407634P | 2016-10-13 | 2016-10-13 | |
| US62/407,634 | 2016-10-13 | ||
| PCT/IB2017/056320 WO2018069863A1 (en) | 2016-10-13 | 2017-10-12 | 1,3 di-substituted cyclobutane or azetidine derivatives as hematopoietic prostaglandin d synthase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019536757A JP2019536757A (ja) | 2019-12-19 |
| JP2019536757A5 JP2019536757A5 (enExample) | 2020-12-24 |
| JP6938628B2 true JP6938628B2 (ja) | 2021-09-22 |
Family
ID=60320926
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019520150A Expired - Fee Related JP6938628B2 (ja) | 2016-10-13 | 2017-10-12 | 造血器型プロスタグランジンdシンターゼ阻害剤としての1,3二置換シクロブタンまたはアゼチジン誘導体 |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US11053234B2 (enExample) |
| EP (1) | EP3526206A1 (enExample) |
| JP (1) | JP6938628B2 (enExample) |
| KR (1) | KR20190072565A (enExample) |
| CN (1) | CN110072857A (enExample) |
| AR (1) | AR109931A1 (enExample) |
| AU (1) | AU2017342156B2 (enExample) |
| BR (1) | BR112019007609A2 (enExample) |
| CA (1) | CA3038756A1 (enExample) |
| CL (1) | CL2019000986A1 (enExample) |
| CO (1) | CO2019003482A2 (enExample) |
| CR (1) | CR20190174A (enExample) |
| DO (1) | DOP2019000087A (enExample) |
| EA (1) | EA201990904A1 (enExample) |
| IL (1) | IL265597A (enExample) |
| JO (1) | JOP20190072A1 (enExample) |
| MA (1) | MA46531A (enExample) |
| MX (1) | MX2019004320A (enExample) |
| PE (1) | PE20191020A1 (enExample) |
| PH (1) | PH12019500811A1 (enExample) |
| TW (1) | TW201827412A (enExample) |
| UY (1) | UY37440A (enExample) |
| WO (1) | WO2018069863A1 (enExample) |
| ZA (1) | ZA201901848B (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JOP20190072A1 (ar) | 2016-10-13 | 2019-04-07 | Glaxosmithkline Ip Dev Ltd | مشتقات 1، 3 سيكلوبوتان ثنائي الاستبدال أو آزيتيدين كمثبطات للإنزيم المخلق للبروستاجلاندين d المكون للدم |
| UY37764A (es) * | 2017-06-13 | 2019-01-02 | Glaxosmithkline Ip Dev Ltd | Nuevos compuestos inhibidores de la prostaglandina d sintasa hematopoyética (h-pgds) |
| KR102757890B1 (ko) * | 2017-08-09 | 2025-01-23 | 데날리 테라퓨틱스 인크. | 화합물, 조성물 및 방법 |
| TW201920129A (zh) | 2017-09-01 | 2019-06-01 | 美商戴納立製藥公司 | 化合物、組合物及方法 |
| WO2020168011A1 (en) | 2019-02-13 | 2020-08-20 | Denali Therapeutics Inc. | Compounds, compositions and methods |
| EP3924341A4 (en) | 2019-02-13 | 2022-11-02 | Denali Therapeutics Inc. | Compounds, compositions and methods |
| WO2021152113A1 (en) | 2020-01-31 | 2021-08-05 | Bayer Aktiengesellschaft | Substituted 2,3-benzodiazepines derivatives |
| TW202204334A (zh) | 2020-04-08 | 2022-02-01 | 美商阿吉歐斯製藥公司 | Menin抑制劑及治療癌症之使用方法 |
| CN113582880B (zh) * | 2020-04-30 | 2023-11-17 | 南京药石科技股份有限公司 | 一种(3-氨基二环[1.1.1]戊烷-1-基)氨基甲酸叔丁酯的制备方法 |
| CN111574473A (zh) * | 2020-06-04 | 2020-08-25 | 宁夏农林科学院农业资源与环境研究所(宁夏土壤与植物营养重点实验室) | 一种氨基噻唑类化合物的合成方法 |
| CA3179059A1 (en) * | 2020-06-09 | 2021-12-16 | Anima Biotech Inc. | Collagen 1 translation inhibitors and methods of use thereof |
| CN111549000B (zh) * | 2020-06-18 | 2022-07-29 | 中国医学科学院整形外科医院 | 一种过表达Hpgds的重组脂肪干细胞、制备方法及其应用 |
| KR20230027059A (ko) | 2020-06-19 | 2023-02-27 | 사토 세이야쿠 가부시키가이샤 | H-pgds를 저해하는 축환 화합물 |
| CN114085167A (zh) * | 2021-12-13 | 2022-02-25 | 华中药业股份有限公司 | 一种杂质ts-3a的制备方法 |
| KR20240121786A (ko) | 2021-12-17 | 2024-08-09 | 사토 세이야쿠 가부시키가이샤 | H-pgds를 저해하는 아자인돌 유도체 |
| EP4448492A1 (en) | 2021-12-17 | 2024-10-23 | Reglagene, Inc. | Compositions and methods of making and using small molecules in the treatment of cancer |
| US20250250265A1 (en) * | 2022-04-15 | 2025-08-07 | Vanderbilt University | Benzothiazole-phenylsulfonyl-piperidine analogs as activators of nacylphosphatidylethanolamine hydrolyzing phospholipase d |
| US12215102B2 (en) | 2023-02-28 | 2025-02-04 | Reglagene, Inc. | Compositions and methods for making and using small molecules for tubulin-targeted therapy in the treatment of cancers and related conditions |
Family Cites Families (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4031221A (en) * | 1974-06-17 | 1977-06-21 | American Hoechst Corporation | Method of treating pain and hypertension |
| US4956359A (en) | 1985-02-28 | 1990-09-11 | A. H. Robins Company, Inc. | 3-aryloxy and 3-arylthioazetidinecarboxamides as anticonvulsants and antiepileptics |
| IE58943B1 (en) | 1985-02-28 | 1993-12-01 | Robins Co Inc A H | 3-Aryloxy-azetidine-carboxamides |
| US6809088B2 (en) * | 1997-03-24 | 2004-10-26 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | Derivatives of 2-(iminomethyl)amino-phenyl, their preparation, their use as medicaments and the pharmaceutical compositions containing them |
| GB9801501D0 (en) * | 1998-01-23 | 1998-03-18 | Cerebrus Ltd | Chemical compounds - II |
| GB9917385D0 (en) | 1999-07-23 | 1999-09-22 | Cerebrus Ltd | Chemical compounds-I |
| US6576265B1 (en) | 1999-12-22 | 2003-06-10 | Acell, Inc. | Tissue regenerative composition, method of making, and method of use thereof |
| EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
| CA2556239A1 (en) * | 2004-02-11 | 2005-08-25 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
| WO2005094805A1 (ja) | 2004-04-01 | 2005-10-13 | Institute Of Medicinal Molecular Design. Inc. | イミン誘導体及びアミド誘導体 |
| MXPA06012510A (es) * | 2004-04-28 | 2006-12-15 | Pfizer | Derivados de 3-heterociclil-4-fenil-triazol como inhibidores del receptor de vasopresina via. |
| AP2007004047A0 (en) * | 2005-01-20 | 2007-06-30 | Pfizer Ltd | Substituted triazole derivatives as oxtocin antagonists |
| WO2007003961A2 (en) | 2005-06-30 | 2007-01-11 | Prosidion Limited | Gpcr agonists |
| GB0514017D0 (en) * | 2005-07-07 | 2005-08-17 | Ionix Pharmaceuticals Ltd | Chemical compounds |
| TW200720255A (en) | 2005-07-13 | 2007-06-01 | Taiho Pharmaceutical Co Ltd | Benzoimidazole compound capable of inhibiting prostaglandin d synthetase |
| JP2007051121A (ja) | 2005-07-22 | 2007-03-01 | Taiho Yakuhin Kogyo Kk | プロスタグランジンd合成酵素を阻害するピリミジン化合物 |
| PE20110118A1 (es) * | 2005-10-04 | 2011-03-08 | Aventis Pharma Inc | Compuestos de pirimidina amida como inhibidores de pgds |
| US20070208426A1 (en) * | 2006-03-03 | 2007-09-06 | Sdgi Holdings, Inc. | Spinal implant with improved surface properties for delivery |
| JP2009529577A (ja) * | 2006-03-10 | 2009-08-20 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 可溶性エポキシドヒドロラーゼインヒビター及びその使用方法 |
| EP2065369A4 (en) | 2006-08-23 | 2011-12-28 | Astellas Pharma Inc | UREA CONNECTION OR SALT THEREOF |
| JP2010513458A (ja) * | 2006-12-19 | 2010-04-30 | ファイザー・プロダクツ・インク | H−pgdsの阻害剤としてのニコチンアミド誘導体、およびプロスタグランジンd2の仲介による疾患を治療するためのその使用 |
| PE20090552A1 (es) | 2007-03-30 | 2009-06-01 | Sanofi Aventis | Compuestos de pirimidina hidrazida como inhibidores de pgds |
| GB0706793D0 (en) | 2007-04-05 | 2007-05-16 | Evotec Ag | Compounds |
| WO2009109743A1 (en) * | 2008-03-04 | 2009-09-11 | Vernalis (R&D) Ltd. | Azetidine derivatives |
| WO2009153720A1 (en) | 2008-06-18 | 2009-12-23 | Pfizer Limited | Nicotinamide derivatives |
| JP2011524894A (ja) | 2008-06-18 | 2011-09-08 | ファイザー・リミテッド | ニコチンアミド誘導体 |
| WO2010024903A1 (en) * | 2008-08-29 | 2010-03-04 | Yangbo Feng | BENZO[d]OXAZOLES AND BENZO[d]THIAZOLES AS KINASE INHIBITORS |
| AP3272A (en) | 2008-09-22 | 2015-05-31 | Cayman Chem Co | Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prosaglandin D2 mediated diseases |
| HUE027702T2 (en) * | 2009-03-09 | 2016-11-28 | Taiho Pharmaceutical Co Ltd | Piperazine compound capable of inhibiting prostaglandin D synthase |
| US20120196854A1 (en) | 2009-10-06 | 2012-08-02 | Kyowa Hakko Kirin Co., Ltd. | Pharmaceutical composition comprising aromatic heterocyclic compound |
| AR078552A1 (es) | 2009-10-08 | 2011-11-16 | Sanofi Aventis | Derivados de feniloxadiazol como agentes inhibidores de las pgds |
| KR101723707B1 (ko) | 2010-01-22 | 2017-04-05 | 다이호야쿠힌고교 가부시키가이샤 | Pgds 저해 작용을 갖는 피페라진 화합물 |
| WO2011143366A1 (en) * | 2010-05-13 | 2011-11-17 | Amgen Inc. | Heteroaryloxycarbocyclyl compounds as pde10 inhibitors |
| JP2013526546A (ja) | 2010-05-13 | 2013-06-24 | アムジエン・インコーポレーテツド | Pde10阻害剤としてのヘテロアリ−ルオキシヘテロシクリル化合物 |
| US9050334B2 (en) | 2010-07-16 | 2015-06-09 | Innov88 Llc | MIF inhibitors and their uses |
| PE20131377A1 (es) | 2010-09-13 | 2013-11-30 | Novartis Ag | Triazina-oxadiazoles |
| KR101400192B1 (ko) | 2010-12-31 | 2014-05-27 | 제일모직 주식회사 | 포지티브형 감광성 수지 조성물, 이를 사용하여 제조된 감광성 수지막 및 상기 감광성 수지막을 포함하는 반도체 소자 |
| US9133164B2 (en) | 2011-04-13 | 2015-09-15 | Innov88 Llc | MIF inhibitors and their uses |
| EP2714624B1 (en) | 2011-05-23 | 2017-12-27 | Sanofi | Process for the preparation of deuterated compounds containing n-alkyl groups |
| WO2013074387A1 (en) * | 2011-11-14 | 2013-05-23 | Merck Sharp & Dohme Corp. | Imidazole derivatives |
| US9499533B2 (en) * | 2012-03-27 | 2016-11-22 | Shionogi & Co., Ltd. | Aromatic 5-membered heterocyclic derivative having TRPV4-Inhibiting activity |
| TWI585088B (zh) * | 2012-06-04 | 2017-06-01 | 第一三共股份有限公司 | 作爲激酶抑制劑之咪唑并[1,2-b]嗒衍生物 |
| CN105263910A (zh) | 2013-02-18 | 2016-01-20 | 斯克利普斯研究所 | 具有治疗潜力的血管加压素受体调节剂 |
| WO2014179144A1 (en) | 2013-04-29 | 2014-11-06 | E. I. Du Pont De Nemours And Company | Fungicidal heterocyclic compounds |
| AU2015264336B2 (en) | 2014-05-19 | 2018-08-30 | Boehringer Ingelheim Animal Health USA Inc. | Anthelmintic compounds |
| TWI695831B (zh) * | 2014-09-13 | 2020-06-11 | 香港商南北兄弟藥業投資有限公司 | Crth2拮抗劑化合物及其用途 |
| EP3277677B9 (en) * | 2015-03-30 | 2021-07-14 | Mission Therapeutics Limited | 1-cyano-pyrrolidine compounds as usp30 inhibitors |
| US20210238162A1 (en) | 2015-12-17 | 2021-08-05 | Glaxosmithkline Intellectual Property Development Limited | Chemical compounds |
| JOP20190072A1 (ar) | 2016-10-13 | 2019-04-07 | Glaxosmithkline Ip Dev Ltd | مشتقات 1، 3 سيكلوبوتان ثنائي الاستبدال أو آزيتيدين كمثبطات للإنزيم المخلق للبروستاجلاندين d المكون للدم |
-
2017
- 2017-06-16 JO JOP/2019/0072A patent/JOP20190072A1/ar unknown
- 2017-10-11 TW TW106134668A patent/TW201827412A/zh unknown
- 2017-10-11 UY UY0001037440A patent/UY37440A/es unknown
- 2017-10-11 AR ARP170102843A patent/AR109931A1/es unknown
- 2017-10-12 CN CN201780075127.1A patent/CN110072857A/zh active Pending
- 2017-10-12 JP JP2019520150A patent/JP6938628B2/ja not_active Expired - Fee Related
- 2017-10-12 EP EP17797738.6A patent/EP3526206A1/en not_active Withdrawn
- 2017-10-12 MA MA046531A patent/MA46531A/fr unknown
- 2017-10-12 CR CR20190174A patent/CR20190174A/es unknown
- 2017-10-12 BR BR112019007609A patent/BR112019007609A2/pt not_active Application Discontinuation
- 2017-10-12 PE PE2019000741A patent/PE20191020A1/es unknown
- 2017-10-12 MX MX2019004320A patent/MX2019004320A/es unknown
- 2017-10-12 KR KR1020197013195A patent/KR20190072565A/ko not_active Ceased
- 2017-10-12 US US16/341,113 patent/US11053234B2/en not_active Expired - Fee Related
- 2017-10-12 EA EA201990904A patent/EA201990904A1/ru unknown
- 2017-10-12 CA CA3038756A patent/CA3038756A1/en not_active Abandoned
- 2017-10-12 AU AU2017342156A patent/AU2017342156B2/en not_active Ceased
- 2017-10-12 WO PCT/IB2017/056320 patent/WO2018069863A1/en not_active Ceased
-
2019
- 2019-03-25 IL IL265597A patent/IL265597A/en unknown
- 2019-03-26 ZA ZA2019/01848A patent/ZA201901848B/en unknown
- 2019-04-08 DO DO2019000087A patent/DOP2019000087A/es unknown
- 2019-04-08 CO CONC2019/0003482A patent/CO2019003482A2/es unknown
- 2019-04-11 CL CL2019000986A patent/CL2019000986A1/es unknown
- 2019-04-12 PH PH12019500811A patent/PH12019500811A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| UY37440A (es) | 2018-04-30 |
| DOP2019000087A (es) | 2019-06-16 |
| CN110072857A (zh) | 2019-07-30 |
| US11053234B2 (en) | 2021-07-06 |
| CA3038756A1 (en) | 2018-04-19 |
| AR109931A1 (es) | 2019-02-06 |
| PE20191020A1 (es) | 2019-07-18 |
| MA46531A (fr) | 2019-08-21 |
| EP3526206A1 (en) | 2019-08-21 |
| EA201990904A1 (ru) | 2019-08-30 |
| CO2019003482A2 (es) | 2019-04-12 |
| MX2019004320A (es) | 2019-06-12 |
| ZA201901848B (en) | 2021-01-27 |
| IL265597A (en) | 2019-05-30 |
| CR20190174A (es) | 2019-08-21 |
| AU2017342156B2 (en) | 2020-10-22 |
| TW201827412A (zh) | 2018-08-01 |
| KR20190072565A (ko) | 2019-06-25 |
| AU2017342156A1 (en) | 2019-04-18 |
| CL2019000986A1 (es) | 2019-06-21 |
| US20190241554A1 (en) | 2019-08-08 |
| BR112019007609A2 (pt) | 2019-07-02 |
| JP2019536757A (ja) | 2019-12-19 |
| PH12019500811A1 (en) | 2020-01-20 |
| WO2018069863A1 (en) | 2018-04-19 |
| JOP20190072A1 (ar) | 2019-04-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6938628B2 (ja) | 造血器型プロスタグランジンdシンターゼ阻害剤としての1,3二置換シクロブタンまたはアゼチジン誘導体 | |
| AU2016370779B2 (en) | Quinoline-3-carboxamides as H-PGDS inhibitors | |
| JP5745021B2 (ja) | トロパン化合物 | |
| KR20190063473A (ko) | 칼페인 조정자 및 그 치료학적 용도 | |
| EA027247B1 (ru) | Новые производные пиридина | |
| CA2917193A1 (en) | Substituted heterocyclic sulfonamide compounds useful as trpa1 modulators | |
| JP2020525490A (ja) | ヘテロアリールジヒドロピリミジン誘導体及びb型肝炎感染を治療する方法 | |
| US20210139507A1 (en) | Fused pyridines which act as inhibitors of h pgds | |
| US20250214970A1 (en) | Pyridinylacetamide derivatives as sodium channel activators | |
| JP2022506850A (ja) | 化学化合物 | |
| TW201321384A (zh) | 作為鈣通道阻斷劑之經取代之八氫吡咯并[1,2-a]吡□磺醯胺 | |
| JP2023527792A (ja) | Tlr2調節剤化合物、医薬組成物、及びそれらの使用 | |
| BR112021014539A2 (pt) | Composto, ativador sirt6, composição farmacêutica, método para tratar e/ou prevenir uma doença inflamatória periférica e uso do composto |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20201012 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20201012 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20201113 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20210803 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20210805 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20210901 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 6938628 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| LAPS | Cancellation because of no payment of annual fees |