KR101149379B1 - 벤즈이미다졸, 벤즈티아졸 및 벤즈옥사졸 유도체 및lta4 h 조정자로서의 그의 용도 - Google Patents
벤즈이미다졸, 벤즈티아졸 및 벤즈옥사졸 유도체 및lta4 h 조정자로서의 그의 용도 Download PDFInfo
- Publication number
- KR101149379B1 KR101149379B1 KR1020067002194A KR20067002194A KR101149379B1 KR 101149379 B1 KR101149379 B1 KR 101149379B1 KR 1020067002194 A KR1020067002194 A KR 1020067002194A KR 20067002194 A KR20067002194 A KR 20067002194A KR 101149379 B1 KR101149379 B1 KR 101149379B1
- Authority
- KR
- South Korea
- Prior art keywords
- ethyl
- yloxy
- benzothiazol
- phenyl
- phenoxy
- 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 ClC1=Nc2ccccc2*1 Chemical compound ClC1=Nc2ccccc2*1 0.000 description 12
- GZQOBERZNSEHFJ-UHFFFAOYSA-N BrCCCOc(cc1)ccc1OCc1ccccc1 Chemical compound BrCCCOc(cc1)ccc1OCc1ccccc1 GZQOBERZNSEHFJ-UHFFFAOYSA-N 0.000 description 1
- OYYUXPQRNJIYPV-UHFFFAOYSA-N C(CN1CCCCCC1)c(cc1)ccc1Oc1nc2ccccc2[nH]1 Chemical compound C(CN1CCCCCC1)c(cc1)ccc1Oc1nc2ccccc2[nH]1 OYYUXPQRNJIYPV-UHFFFAOYSA-N 0.000 description 1
- ZFOMZVAPHUXJNT-UHFFFAOYSA-N C(COc(cc1)ccc1Oc1nc(cccc2)c2[s]1)N1CCCCC1 Chemical compound C(COc(cc1)ccc1Oc1nc(cccc2)c2[s]1)N1CCCCC1 ZFOMZVAPHUXJNT-UHFFFAOYSA-N 0.000 description 1
- JDZUDVCYJPNUKO-UHFFFAOYSA-N C(COc(cc1)ccc1Oc1nc(cccc2)c2[s]1)N1CCCCCC1 Chemical compound C(COc(cc1)ccc1Oc1nc(cccc2)c2[s]1)N1CCCCCC1 JDZUDVCYJPNUKO-UHFFFAOYSA-N 0.000 description 1
- CISXJTCZYBKDPY-UHFFFAOYSA-N C(COc(cc1)ccc1Oc1nc2ccccc2[nH]1)N1CCCCC1 Chemical compound C(COc(cc1)ccc1Oc1nc2ccccc2[nH]1)N1CCCCC1 CISXJTCZYBKDPY-UHFFFAOYSA-N 0.000 description 1
- DCLVFUYFBIWTRM-UHFFFAOYSA-N C(Cc1n[nH]cn1)CN(CCc(cc1)ccc1Oc1nc2ccccc2[s]1)CC1CC1 Chemical compound C(Cc1n[nH]cn1)CN(CCc(cc1)ccc1Oc1nc2ccccc2[s]1)CC1CC1 DCLVFUYFBIWTRM-UHFFFAOYSA-N 0.000 description 1
- BNQMVWKSYURTPW-UHFFFAOYSA-N C=[Br]c1ccc(C2(CCN(CCOc(cc3)ccc3Oc3nc(cccc4)c4[nH]3)CC2)O)cc1 Chemical compound C=[Br]c1ccc(C2(CCN(CCOc(cc3)ccc3Oc3nc(cccc4)c4[nH]3)CC2)O)cc1 BNQMVWKSYURTPW-UHFFFAOYSA-N 0.000 description 1
- PQAUMKITGQKVPU-UHFFFAOYSA-N C=[Br]c1ccc(C2(CCN(CCOc(cc3)ccc3Oc3nc4ccccc4[s]3)CC2)O)cc1 Chemical compound C=[Br]c1ccc(C2(CCN(CCOc(cc3)ccc3Oc3nc4ccccc4[s]3)CC2)O)cc1 PQAUMKITGQKVPU-UHFFFAOYSA-N 0.000 description 1
- IARGUVZEWAKSLG-UHFFFAOYSA-N CC(C)(C)OC(NCC1CCN(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)=O Chemical compound CC(C)(C)OC(NCC1CCN(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)=O IARGUVZEWAKSLG-UHFFFAOYSA-N 0.000 description 1
- IOQAYYZCMIJSKU-UHFFFAOYSA-N CC(C)NC(NC1CCN(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)=O Chemical compound CC(C)NC(NC1CCN(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)=O IOQAYYZCMIJSKU-UHFFFAOYSA-N 0.000 description 1
- LJCQRMOXTNWQDA-UHFFFAOYSA-N CC(C1(CCN(CCOc(cc2)ccc2Oc2nc(cccc3)c3[o]2)CC1)c1ccccc1)=O Chemical compound CC(C1(CCN(CCOc(cc2)ccc2Oc2nc(cccc3)c3[o]2)CC1)c1ccccc1)=O LJCQRMOXTNWQDA-UHFFFAOYSA-N 0.000 description 1
- VJKCOKFFSRWBHL-UHFFFAOYSA-N CCC(NC1CCN(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)=O Chemical compound CCC(NC1CCN(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)=O VJKCOKFFSRWBHL-UHFFFAOYSA-N 0.000 description 1
- HJQIDMVXPRRKNS-UHFFFAOYSA-N CCCOC(NC1CCN(Cc(cc2)ccc2Oc2nc(cccc3)c3[s]2)CC1)=O Chemical compound CCCOC(NC1CCN(Cc(cc2)ccc2Oc2nc(cccc3)c3[s]2)CC1)=O HJQIDMVXPRRKNS-UHFFFAOYSA-N 0.000 description 1
- TYZMXGWKKHAJCW-UHFFFAOYSA-N CCCc(cc1)ccc1Oc1nc2ccccc2[s]1 Chemical compound CCCc(cc1)ccc1Oc1nc2ccccc2[s]1 TYZMXGWKKHAJCW-UHFFFAOYSA-N 0.000 description 1
- FOSPOHCMRIJVNH-UHFFFAOYSA-O CCN(CCOc(cc1)ccc1Oc1[nH+]c2ccccc2[nH]1)C1CCCCC1 Chemical compound CCN(CCOc(cc1)ccc1Oc1[nH+]c2ccccc2[nH]1)C1CCCCC1 FOSPOHCMRIJVNH-UHFFFAOYSA-O 0.000 description 1
- OOLHSFYZOUIRBV-UHFFFAOYSA-N CCN(CCOc(cc1)ccc1Oc1nc2ccccc2[o]1)C1CCCCC1 Chemical compound CCN(CCOc(cc1)ccc1Oc1nc2ccccc2[o]1)C1CCCCC1 OOLHSFYZOUIRBV-UHFFFAOYSA-N 0.000 description 1
- GGVBHBACWISUCI-UHFFFAOYSA-N CCOC(CCCCCCN(CCc(cc1)ccc1Oc1nc2ccccc2[s]1)C1CC1)=O Chemical compound CCOC(CCCCCCN(CCc(cc1)ccc1Oc1nc2ccccc2[s]1)C1CC1)=O GGVBHBACWISUCI-UHFFFAOYSA-N 0.000 description 1
- AYVVFQAFDYQHRG-UHFFFAOYSA-N CN(C1CCN(Cc(cc2)ccc2Oc2nc(cccc3)c3[s]2)CC1)C(OC)=O Chemical compound CN(C1CCN(Cc(cc2)ccc2Oc2nc(cccc3)c3[s]2)CC1)C(OC)=O AYVVFQAFDYQHRG-UHFFFAOYSA-N 0.000 description 1
- JHTONAOHIXKHMD-UHFFFAOYSA-N CS/C(/NC1CCN(CCc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)=N\C#N Chemical compound CS/C(/NC1CCN(CCc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)=N\C#N JHTONAOHIXKHMD-UHFFFAOYSA-N 0.000 description 1
- OAUXHFPOFOZZLZ-UHFFFAOYSA-N O=C(CCC1)N1C1CCN(CCOc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1 Chemical compound O=C(CCC1)N1C1CCN(CCOc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1 OAUXHFPOFOZZLZ-UHFFFAOYSA-N 0.000 description 1
- UBVVZACYWWPTID-UHFFFAOYSA-N O=C(CCC1)N1C1CCN(Cc(cc2)ccc2Oc2nc(cccc3)c3[s]2)CC1 Chemical compound O=C(CCC1)N1C1CCN(Cc(cc2)ccc2Oc2nc(cccc3)c3[s]2)CC1 UBVVZACYWWPTID-UHFFFAOYSA-N 0.000 description 1
- WVRPNEFAKCUFKR-UHFFFAOYSA-N O=C(COCC1)N1C1CCN(CCc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1 Chemical compound O=C(COCC1)N1C1CCN(CCc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1 WVRPNEFAKCUFKR-UHFFFAOYSA-N 0.000 description 1
- WOYNTMCZQXRYOO-UHFFFAOYSA-N O=C1NCCC11CCN(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1 Chemical compound O=C1NCCC11CCN(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1 WOYNTMCZQXRYOO-UHFFFAOYSA-N 0.000 description 1
- JMORICXARVLAAR-UHFFFAOYSA-N O=C1OC2(CCN(Cc(cc3)ccc3Oc3nc4ccccc4[s]3)CC2)c2ccccc12 Chemical compound O=C1OC2(CCN(Cc(cc3)ccc3Oc3nc4ccccc4[s]3)CC2)c2ccccc12 JMORICXARVLAAR-UHFFFAOYSA-N 0.000 description 1
- HGXCLIZMBKPLLN-UHFFFAOYSA-N O=CNC1CCN(CCc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1 Chemical compound O=CNC1CCN(CCc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1 HGXCLIZMBKPLLN-UHFFFAOYSA-N 0.000 description 1
- WMPGTMLVIHASJI-UHFFFAOYSA-N OC(C(NC1CCN(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)=O)=O Chemical compound OC(C(NC1CCN(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)=O)=O WMPGTMLVIHASJI-UHFFFAOYSA-N 0.000 description 1
- QJLVQPXNAJBHTN-UHFFFAOYSA-N OC(CCN(CCOc(cc1)ccc1Oc1nc(cccc2)c2[s]1)C1CC1)=O Chemical compound OC(CCN(CCOc(cc1)ccc1Oc1nc(cccc2)c2[s]1)C1CC1)=O QJLVQPXNAJBHTN-UHFFFAOYSA-N 0.000 description 1
- FDTVVMYDEDPLPY-UHFFFAOYSA-N OC1(CCN(CCc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)c1ccccc1 Chemical compound OC1(CCN(CCc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1)c1ccccc1 FDTVVMYDEDPLPY-UHFFFAOYSA-N 0.000 description 1
- FMPGQGRECBCTKX-UHFFFAOYSA-N OC1CCN(CCc(cc2)ccc2Oc2nc(cccc3)c3[o]2)CC1 Chemical compound OC1CCN(CCc(cc2)ccc2Oc2nc(cccc3)c3[o]2)CC1 FMPGQGRECBCTKX-UHFFFAOYSA-N 0.000 description 1
- HHJAPVOVRQGCFN-UHFFFAOYSA-N OC1CCN(CCc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1 Chemical compound OC1CCN(CCc(cc2)ccc2Oc2nc3ccccc3[s]2)CC1 HHJAPVOVRQGCFN-UHFFFAOYSA-N 0.000 description 1
- MVWHGHDOPRCATH-UHFFFAOYSA-N OCC1CCN(CCOc(cc2)ccc2Oc2nc3ccccc3[o]2)CC1 Chemical compound OCC1CCN(CCOc(cc2)ccc2Oc2nc3ccccc3[o]2)CC1 MVWHGHDOPRCATH-UHFFFAOYSA-N 0.000 description 1
- WXHRYHXKKQDISV-UHFFFAOYSA-O OCC1CCN(Cc(cc2)ccc2[OH+]c2nc(cccc3)c3[s]2)CC1 Chemical compound OCC1CCN(Cc(cc2)ccc2[OH+]c2nc(cccc3)c3[s]2)CC1 WXHRYHXKKQDISV-UHFFFAOYSA-O 0.000 description 1
- NJKYZVIKKITPKU-UHFFFAOYSA-N OCC1CN(CCOc(cc2)ccc2Oc2nc(cccc3)c3[s]2)CCC1 Chemical compound OCC1CN(CCOc(cc2)ccc2Oc2nc(cccc3)c3[s]2)CCC1 NJKYZVIKKITPKU-UHFFFAOYSA-N 0.000 description 1
- PTPDJDATJRANLS-UHFFFAOYSA-N OCC1N(CCOc(cc2)ccc2Oc2nc(cccc3)c3[o]2)CCCC1 Chemical compound OCC1N(CCOc(cc2)ccc2Oc2nc(cccc3)c3[o]2)CCCC1 PTPDJDATJRANLS-UHFFFAOYSA-N 0.000 description 1
- WPJDXRZEKUJUEO-UHFFFAOYSA-N OCCC1N(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CCCC1 Chemical compound OCCC1N(Cc(cc2)ccc2Oc2nc3ccccc3[s]2)CCCC1 WPJDXRZEKUJUEO-UHFFFAOYSA-N 0.000 description 1
- MBGDQOYOKOUJOX-GOSISDBHSA-N O[C@H](C1)CN(C2CCN(Cc(cc3)ccc3Oc3nc4ccccc4[s]3)CC2)C1=O Chemical compound O[C@H](C1)CN(C2CCN(Cc(cc3)ccc3Oc3nc4ccccc4[s]3)CC2)C1=O MBGDQOYOKOUJOX-GOSISDBHSA-N 0.000 description 1
- SIJRSDOJOBGBJP-UHFFFAOYSA-N Oc1ccc(CCCBr)cc1 Chemical compound Oc1ccc(CCCBr)cc1 SIJRSDOJOBGBJP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/632—Organic additives
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- 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
- A61P11/06—Antiasthmatics
-
- 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
- A61P11/08—Bronchodilators
-
- 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
- A61P17/06—Antipsoriatics
-
- 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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- 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
- 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
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles 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
-
- 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
- C07D277/68—Benzothiazoles 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
-
- 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
-
- 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
- C07D413/12—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 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
- C07D417/02—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
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Structural Engineering (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Immunology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Physical Education & Sports Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Epidemiology (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US49071003P | 2003-07-28 | 2003-07-28 | |
| US60/490,710 | 2003-07-28 | ||
| PCT/US2004/024309 WO2005012297A1 (en) | 2003-07-28 | 2004-07-27 | Benzimidazole, benzthiazole and benzoxazole derivatives and their use as lta4h modulators |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20060057593A KR20060057593A (ko) | 2006-05-26 |
| KR101149379B1 true KR101149379B1 (ko) | 2012-06-28 |
Family
ID=34115427
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020067002194A Expired - Fee Related KR101149379B1 (ko) | 2003-07-28 | 2004-07-27 | 벤즈이미다졸, 벤즈티아졸 및 벤즈옥사졸 유도체 및lta4 h 조정자로서의 그의 용도 |
| KR1020067002211A Ceased KR20060054408A (ko) | 2003-07-28 | 2004-07-27 | 벤즈이미다졸, 벤즈티아졸 및 벤즈옥사졸 유도체 및lta4 h 조정자로서의 그의 용도 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020067002211A Ceased KR20060054408A (ko) | 2003-07-28 | 2004-07-27 | 벤즈이미다졸, 벤즈티아졸 및 벤즈옥사졸 유도체 및lta4 h 조정자로서의 그의 용도 |
Country Status (28)
| Country | Link |
|---|---|
| US (2) | US20050043379A1 (enExample) |
| EP (2) | EP1660492B1 (enExample) |
| JP (2) | JP2007500703A (enExample) |
| KR (2) | KR101149379B1 (enExample) |
| CN (2) | CN100591679C (enExample) |
| AR (2) | AR045729A1 (enExample) |
| AT (2) | ATE405562T1 (enExample) |
| AU (2) | AU2004261628B2 (enExample) |
| BR (2) | BRPI0413072A (enExample) |
| CA (2) | CA2534212A1 (enExample) |
| CY (1) | CY1108560T1 (enExample) |
| DE (2) | DE602004015620D1 (enExample) |
| DK (2) | DK1660491T3 (enExample) |
| ES (2) | ES2311858T3 (enExample) |
| HR (2) | HRP20060041B1 (enExample) |
| IL (1) | IL173372A (enExample) |
| MY (1) | MY145080A (enExample) |
| NO (2) | NO20060771L (enExample) |
| NZ (2) | NZ544970A (enExample) |
| PL (2) | PL1660492T3 (enExample) |
| PT (2) | PT1660491E (enExample) |
| RU (2) | RU2373204C2 (enExample) |
| SG (2) | SG130192A1 (enExample) |
| SI (2) | SI1660492T1 (enExample) |
| TW (2) | TWI362383B (enExample) |
| UA (2) | UA82888C2 (enExample) |
| WO (2) | WO2005012297A1 (enExample) |
| ZA (2) | ZA200601716B (enExample) |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100591679C (zh) * | 2003-07-28 | 2010-02-24 | 詹森药业有限公司 | 苯并咪唑、苯并噻唑和苯并唑衍生物及其作为lta4h调节剂的应用 |
| CN101189012A (zh) * | 2005-03-31 | 2008-05-28 | 詹森药业有限公司 | 苯基和吡啶基lta4h调节剂 |
| ES2523565T3 (es) | 2005-04-13 | 2014-11-27 | Astex Therapeutics Limited | Derivados de hidroxibenzamida y sus usos como inhibidores de la hsp90 |
| EP1717235A3 (en) * | 2005-04-29 | 2007-02-28 | Bioprojet | Phenoxypropylpiperidines and -pyrrolidines and their use as histamine H3-receptor ligands |
| CA2620127A1 (en) * | 2005-09-02 | 2007-03-08 | F. Hoffmann-La Roche Ag | Benzooxazole, oxazolopyridine, benzothiazole and thiazolopyridine derivatives |
| UA101943C2 (ru) * | 2005-09-21 | 2013-05-27 | Декод Дженетикс Ехф | Биарилзамещенные гетероциклические ингибиторы lta4h для лечения воспаления |
| AU2006333522A1 (en) * | 2005-12-21 | 2007-07-12 | Decode Genetics, Ehf. | Biaryl nitrogen heterocycle inhibitors of LTA4H for treating inflammation |
| WO2007073405A1 (en) * | 2005-12-21 | 2007-06-28 | Decode Genetics Ehf | N-linked aryl heteroaryl inhibitors of lta4h for treating inflammation |
| CA2634701C (en) | 2005-12-21 | 2014-07-29 | Decode Genetics Ehf | Biaryl substituted nitrogen containing heterocycle inhibitors of lta4h for treating inflammation |
| HUE031972T2 (en) * | 2005-12-29 | 2017-08-28 | Celtaxsys Inc | Diamine derivatives as inhibitors of leukotriene a4 hydrolase |
| JP2009525269A (ja) * | 2006-01-30 | 2009-07-09 | ユーロ−セルティーク エス.エイ. | カルシウムチャネルブロッカーとしての環状尿素化合物 |
| US7754725B2 (en) | 2006-03-01 | 2010-07-13 | Astex Therapeutics Ltd. | Dihydroxyphenyl isoindolymethanones |
| US7951829B2 (en) * | 2006-05-03 | 2011-05-31 | Janssen Pharmaceutica Nv | Benzimidazole modulators of VR1 |
| US8299095B2 (en) * | 2006-06-16 | 2012-10-30 | H. Lundbeck A/S | Crystalline forms of 4-[2-(4-methylphenylsulfanyl)-phenyl] piperidine with combined serotonin and norepinephrine reuptake inhibition and uses thereof |
| US7728032B2 (en) * | 2006-08-04 | 2010-06-01 | Decode Genetics Ehf | Phenoxymethylalkyne inhibitors of LTA4H for treating inflammation |
| WO2008019302A1 (en) * | 2006-08-04 | 2008-02-14 | Decode Genetics Ehf | Pyrazolylphenyl and pyrrolylphenyl inhibitors of lta4h for treating inflammation |
| EP2066800A2 (en) * | 2006-08-04 | 2009-06-10 | Decode Genetics EHF | Aryl amino acid derivatives as inhibitors of lta4h (leukotriene a4 hydrolase) for treating inflammation |
| US8916552B2 (en) | 2006-10-12 | 2014-12-23 | Astex Therapeutics Limited | Pharmaceutical combinations |
| US8883790B2 (en) | 2006-10-12 | 2014-11-11 | Astex Therapeutics Limited | Pharmaceutical combinations |
| JP5518478B2 (ja) | 2006-10-12 | 2014-06-11 | アステックス、セラピューティックス、リミテッド | 医薬化合物 |
| WO2008044029A1 (en) | 2006-10-12 | 2008-04-17 | Astex Therapeutics Limited | Pharmaceutical combinations |
| GB0620259D0 (en) | 2006-10-12 | 2006-11-22 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| TW200906396A (en) * | 2007-02-14 | 2009-02-16 | Janssen Pharmaceutica Nv | LTA4H modulators and uses thereof |
| US20100120807A1 (en) * | 2007-03-08 | 2010-05-13 | Irm Llc | Compounds and compositions as modulators of gpr119 activity |
| WO2008120710A1 (ja) * | 2007-03-30 | 2008-10-09 | Panasonic Electric Works Co., Ltd. | 活動強度計 |
| UY31443A1 (es) * | 2007-10-31 | 2009-04-30 | Diaminas en puente o fusionadas sustituidas con arilo como moduladores de leucotrieno a4 hidrolasa | |
| US20090176785A1 (en) * | 2007-11-16 | 2009-07-09 | Abbott Laboratories | Method of treating arthritis |
| GB0806527D0 (en) | 2008-04-11 | 2008-05-14 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| MX2010011154A (es) * | 2008-04-11 | 2010-12-21 | Janssen Pharmaceutica Nv | Tiazolopiridin-2-iloxi-fenilo y tiazolopirazin-2-iloxifenilaminas como moduladores de la leucotrieno a4 hidrolasa. |
| PT2294066E (pt) | 2008-04-28 | 2014-11-21 | Janssen Pharmaceutica Nv | Benzoimidazoles como inibidores da prolil-hidroxilase |
| AU2010249041B2 (en) | 2009-05-14 | 2014-11-13 | Janssen Pharmaceutica Nv | Compounds with two fused bicyclic heteroaryl moieties as modulators of leukotriene A4 hydrolase |
| CN102442962A (zh) * | 2010-11-10 | 2012-05-09 | 江苏德峰药业有限公司 | 1-烷基四氮唑的生产方法 |
| CN102442961A (zh) * | 2010-11-10 | 2012-05-09 | 江苏德峰药业有限公司 | 1-甲基四氮唑的生产方法 |
| EP2776023B1 (en) | 2011-10-25 | 2016-03-09 | Janssen Pharmaceutica, N.V. | Meglumine salt formulations of 1-(5,6-dichloro-1h-benzo[d]imidazol-2-yl)-1h-pyrazole-4-carboxylic acid |
| CA2905340C (en) | 2013-03-12 | 2022-05-31 | Celtaxsys, Inc. | Low dose oral formulations of acebilustat |
| BR112015022226A2 (pt) | 2013-03-14 | 2017-07-18 | Celtaxsys Inc | inibidores de leucotrieno a4 hidrolase |
| KR20150131211A (ko) * | 2013-03-14 | 2015-11-24 | 켈탁시스, 인코퍼레이티드 | 류코트라이엔 a4 가수분해효소의 저해제 |
| BR112015022864A8 (pt) | 2013-03-14 | 2019-11-26 | Celtaxsys Inc | composto, composição farmacêutica e uso dos mesmos |
| WO2015094902A1 (en) * | 2013-12-17 | 2015-06-25 | Eli Lilly And Company | Phenoxyethyl cyclic amine derivatives and their activity as ep4 receptor modulators |
| EP3233077A4 (en) | 2014-12-19 | 2018-08-08 | The Broad Institute Inc. | Dopamine d2 receptor ligands |
| EP3233799B1 (en) | 2014-12-19 | 2021-05-19 | The Broad Institute, Inc. | Dopamine d2 receptor ligands |
| RU2715897C2 (ru) | 2015-06-09 | 2020-03-04 | Эббви Инк. | Модуляторы ядерных рецепторов |
| IL267352B2 (en) | 2016-12-21 | 2023-10-01 | Hoffmann La Roche | Method for in vitro glycoengineering of antibodies |
| WO2018114878A1 (en) | 2016-12-21 | 2018-06-28 | F. Hoffmann-La Roche Ag | Re-use of enzymes in in vitro glycoengineering of antibodies |
| CN107663192B (zh) * | 2017-11-03 | 2019-05-10 | 梯尔希(南京)药物研发有限公司 | 一种雷贝拉唑杂质的制备方法 |
| JP7386815B2 (ja) | 2018-05-31 | 2023-11-27 | セルタクシー、エルエルシー | 呼吸器疾患患者の肺増悪を軽減する方法 |
| WO2020087031A1 (en) | 2018-10-26 | 2020-04-30 | The Research Foundation For The State University Of New York | Combination serotonin specific reuptake inhibitor and serotonin 1a receptor partial agonist for reducing l-dopa-induced dyskinesia |
| CN113784713A (zh) * | 2019-01-11 | 2021-12-10 | 纳吉斯制药股份有限公司 | 白三烯合成抑制剂 |
| CN110026557B (zh) * | 2019-05-28 | 2021-08-27 | 南方科技大学 | 一种混合固体颗粒重熔的直写装置及成型方法 |
| TW202235071A (zh) * | 2020-11-19 | 2022-09-16 | 美商特洛治療公司 | 小分子化合物及組成物 |
| US11932630B2 (en) * | 2021-04-16 | 2024-03-19 | Novartis Ag | Heteroaryl aminopropanol derivatives |
| CN113683491A (zh) * | 2021-09-01 | 2021-11-23 | 王传良 | 一种4-(2-溴乙基)苯酚的制备方法 |
| CN113735798B (zh) * | 2021-09-27 | 2022-07-12 | 安徽美致诚药业有限公司 | 一种盐酸罗沙替丁醋酸酯的制备方法 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998040364A1 (en) * | 1997-03-12 | 1998-09-17 | G.D. Searle & Co. | Lta4 hydrolase inhibitors |
| EP1221441A2 (en) * | 1994-10-11 | 2002-07-10 | G.D. Searle & Co. | LTA4 Hydrolase inhibitors |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4873346A (en) * | 1985-09-20 | 1989-10-10 | The Upjohn Company | Substituted benzothiazoles, benzimidazoles, and benzoxazoles |
| DK171349B1 (da) * | 1986-11-14 | 1996-09-16 | Hoffmann La Roche | Tetrahydronaphthalenderivater, fremgangsmåde til fremstilling deraf, lægemidler indeholdende forbindelserne samt anvendelse af forbindelserne til fremstilling af lægemidler |
| IL90337A0 (en) * | 1988-05-24 | 1989-12-15 | Pfizer | Aromatic and heterocyclic carboxamide derivatives as antineoplastic agents |
| IT1240598B (it) * | 1990-03-13 | 1993-12-17 | Mini Ricerca Scient Tecnolog | Derivati amminici ad azione antifungina |
| IL117149A0 (en) * | 1995-02-23 | 1996-06-18 | Schering Corp | Muscarinic antagonists |
| US5889006A (en) * | 1995-02-23 | 1999-03-30 | Schering Corporation | Muscarinic antagonists |
| EP1062216A1 (en) * | 1998-02-25 | 2000-12-27 | Genetics Institute, Inc. | Inhibitors of phospholipase a2 |
| US6514964B1 (en) * | 1999-09-27 | 2003-02-04 | Amgen Inc. | Fused cycloheptane and fused azacycloheptane compounds and their methods of use |
| US20040110757A1 (en) * | 2002-03-21 | 2004-06-10 | Thomas Arrhenius | Flt-1 ligands and their uses in the treatment of diseases regulatable by angiogenesis |
| CN100591679C (zh) * | 2003-07-28 | 2010-02-24 | 詹森药业有限公司 | 苯并咪唑、苯并噻唑和苯并唑衍生物及其作为lta4h调节剂的应用 |
| US7541466B2 (en) * | 2003-12-23 | 2009-06-02 | Genzyme Corporation | Tetrahydroisoquinoline derivatives for treating protein trafficking diseases |
| HRP20160373T1 (hr) * | 2005-03-16 | 2016-05-06 | Meda Pharma Gmbh & Co. Kg | Kombinacija antikolinergika i antagonista leukotrien receptora za liječenje bolesti dišnog sustava |
| TW200906396A (en) * | 2007-02-14 | 2009-02-16 | Janssen Pharmaceutica Nv | LTA4H modulators and uses thereof |
-
2004
- 2004-07-27 CN CN200480028138A patent/CN100591679C/zh not_active Expired - Fee Related
- 2004-07-27 SG SG200700817-0A patent/SG130192A1/en unknown
- 2004-07-27 AT AT04779375T patent/ATE405562T1/de active
- 2004-07-27 RU RU2006102510/04A patent/RU2373204C2/ru not_active IP Right Cessation
- 2004-07-27 PL PL04779375T patent/PL1660492T3/pl unknown
- 2004-07-27 JP JP2006521973A patent/JP2007500703A/ja active Pending
- 2004-07-27 PL PL04779219T patent/PL1660491T3/pl unknown
- 2004-07-27 UA UAA200601432A patent/UA82888C2/uk unknown
- 2004-07-27 BR BRPI0413072-3A patent/BRPI0413072A/pt not_active IP Right Cessation
- 2004-07-27 HR HRP20060041AA patent/HRP20060041B1/hr not_active IP Right Cessation
- 2004-07-27 DK DK04779219T patent/DK1660491T3/da active
- 2004-07-27 DK DK04779375T patent/DK1660492T3/da active
- 2004-07-27 ES ES04779219T patent/ES2311858T3/es not_active Expired - Lifetime
- 2004-07-27 PT PT04779219T patent/PT1660491E/pt unknown
- 2004-07-27 HR HR20060039A patent/HRP20060039A2/xx not_active Application Discontinuation
- 2004-07-27 DE DE602004015620T patent/DE602004015620D1/de not_active Expired - Lifetime
- 2004-07-27 EP EP04779375A patent/EP1660492B1/en not_active Expired - Lifetime
- 2004-07-27 SI SI200430927T patent/SI1660492T1/sl unknown
- 2004-07-27 DE DE602004016002T patent/DE602004016002D1/de not_active Expired - Lifetime
- 2004-07-27 WO PCT/US2004/024309 patent/WO2005012297A1/en not_active Ceased
- 2004-07-27 KR KR1020067002194A patent/KR101149379B1/ko not_active Expired - Fee Related
- 2004-07-27 EP EP04779219A patent/EP1660491B1/en not_active Expired - Lifetime
- 2004-07-27 CA CA002534212A patent/CA2534212A1/en not_active Abandoned
- 2004-07-27 US US10/900,152 patent/US20050043379A1/en not_active Abandoned
- 2004-07-27 CN CNA2004800279067A patent/CN1856490A/zh active Pending
- 2004-07-27 WO PCT/US2004/024050 patent/WO2005012296A1/en not_active Ceased
- 2004-07-27 NZ NZ544970A patent/NZ544970A/en unknown
- 2004-07-27 CA CA002534228A patent/CA2534228A1/en not_active Abandoned
- 2004-07-27 BR BRPI0412345-0A patent/BRPI0412345A/pt not_active IP Right Cessation
- 2004-07-27 ES ES04779375T patent/ES2313079T3/es not_active Expired - Lifetime
- 2004-07-27 UA UAA200601433A patent/UA87986C2/uk unknown
- 2004-07-27 KR KR1020067002211A patent/KR20060054408A/ko not_active Ceased
- 2004-07-27 AU AU2004261628A patent/AU2004261628B2/en not_active Ceased
- 2004-07-27 SG SG200700691A patent/SG129449A1/en unknown
- 2004-07-27 AU AU2004261610A patent/AU2004261610B2/en not_active Ceased
- 2004-07-27 PT PT04779375T patent/PT1660492E/pt unknown
- 2004-07-27 US US10/900,103 patent/US20050043378A1/en not_active Abandoned
- 2004-07-27 SI SI200430904T patent/SI1660491T1/sl unknown
- 2004-07-27 RU RU2006102508/04A patent/RU2359970C2/ru not_active IP Right Cessation
- 2004-07-27 NZ NZ544938A patent/NZ544938A/en unknown
- 2004-07-27 JP JP2006522022A patent/JP4726238B2/ja not_active Expired - Fee Related
- 2004-07-27 AT AT04779219T patent/ATE403654T1/de not_active IP Right Cessation
- 2004-07-28 AR ARP040102682A patent/AR045729A1/es unknown
- 2004-07-28 TW TW093122570A patent/TWI362383B/zh not_active IP Right Cessation
- 2004-07-28 TW TW093122566A patent/TW200520756A/zh unknown
- 2004-07-28 MY MYPI20043045A patent/MY145080A/en unknown
- 2004-07-28 AR ARP040102683A patent/AR045730A1/es not_active Application Discontinuation
-
2006
- 2006-01-26 IL IL173372A patent/IL173372A/en not_active IP Right Cessation
- 2006-02-17 NO NO20060771A patent/NO20060771L/no not_active Application Discontinuation
- 2006-02-20 NO NO20060823A patent/NO20060823L/no not_active Application Discontinuation
- 2006-02-27 ZA ZA200601716A patent/ZA200601716B/en unknown
- 2006-02-27 ZA ZA200601720A patent/ZA200601720B/en unknown
-
2008
- 2008-10-27 CY CY20081101220T patent/CY1108560T1/el unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1221441A2 (en) * | 1994-10-11 | 2002-07-10 | G.D. Searle & Co. | LTA4 Hydrolase inhibitors |
| WO1998040364A1 (en) * | 1997-03-12 | 1998-09-17 | G.D. Searle & Co. | Lta4 hydrolase inhibitors |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101149379B1 (ko) | 벤즈이미다졸, 벤즈티아졸 및 벤즈옥사졸 유도체 및lta4 h 조정자로서의 그의 용도 | |
| US20080194630A1 (en) | LTA4H modulators and uses thereof | |
| KR20080003385A (ko) | 페닐 및 피리딜 lta4h 조절제 | |
| US20080171749A1 (en) | 1-Phenyl-1,2-Diaminoethane Derivatives As Modulators Of The Chemokine Receptor Activity | |
| MXPA06001121A (en) | Benzimidazole, benzthiazole and benzoxazole derivatives and their use as lta4h modulators | |
| HK1092790B (en) | Benzimidazole, benzthiazole and benzoxazole derivatives and their use as lta4h modulators | |
| MXPA06001122A (en) | Benzimidazole, benzthiazole and benzoxazole derivatives and their use as lta4h modulators | |
| US7157471B2 (en) | Haloalkyl- and piperidine-substituted benzimidazole-derivatives | |
| HK1090359B (en) | Benzimidazole, benzthiazole and benzoxazole derivatives and their use as lta4h modulators | |
| US20050014782A1 (en) | Novel n-(heterobicycloalkanes)-substituted indoles-or heteroderivatives thereof | |
| EP1496058A1 (en) | Novel N-(heterobicycloalkanes)-substituted Indoles or heteroderivatives thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
St.27 status event code: A-0-1-A10-A15-nap-PA0105 |
|
| PG1501 | Laying open of application |
St.27 status event code: A-1-1-Q10-Q12-nap-PG1501 |
|
| AMND | Amendment | ||
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| A201 | Request for examination | ||
| AMND | Amendment | ||
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| PA0201 | Request for examination |
St.27 status event code: A-1-2-D10-D11-exm-PA0201 |
|
| PE0801 | Dismissal of amendment |
St.27 status event code: A-2-2-P10-P12-nap-PE0801 |
|
| D12-X000 | Request for substantive examination rejected |
St.27 status event code: A-1-2-D10-D12-exm-X000 |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
St.27 status event code: A-1-2-D10-D21-exm-PE0902 |
|
| AMND | Amendment | ||
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| E601 | Decision to refuse application | ||
| PE0601 | Decision on rejection of patent |
St.27 status event code: N-2-6-B10-B15-exm-PE0601 |
|
| AMND | Amendment | ||
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| J201 | Request for trial against refusal decision | ||
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| PJ0201 | Trial against decision of rejection |
St.27 status event code: A-3-3-V10-V11-apl-PJ0201 |
|
| PB0901 | Examination by re-examination before a trial |
St.27 status event code: A-6-3-E10-E12-rex-PB0901 |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
St.27 status event code: A-1-2-D10-D21-exm-PE0902 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| B701 | Decision to grant | ||
| PB0701 | Decision of registration after re-examination before a trial |
St.27 status event code: A-3-4-F10-F13-rex-PB0701 |
|
| GRNT | Written decision to grant | ||
| PR0701 | Registration of establishment |
St.27 status event code: A-2-4-F10-F11-exm-PR0701 |
|
| PR1002 | Payment of registration fee |
St.27 status event code: A-2-2-U10-U12-oth-PR1002 Fee payment year number: 1 |
|
| PG1601 | Publication of registration |
St.27 status event code: A-4-4-Q10-Q13-nap-PG1601 |
|
| FPAY | Annual fee payment |
Payment date: 20150417 Year of fee payment: 4 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 4 |
|
| FPAY | Annual fee payment |
Payment date: 20160419 Year of fee payment: 5 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 5 |
|
| FPAY | Annual fee payment |
Payment date: 20170420 Year of fee payment: 6 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 6 |
|
| LAPS | Lapse due to unpaid annual fee | ||
| PC1903 | Unpaid annual fee |
St.27 status event code: A-4-4-U10-U13-oth-PC1903 Not in force date: 20180518 Payment event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE |
|
| PC1903 | Unpaid annual fee |
St.27 status event code: N-4-6-H10-H13-oth-PC1903 Ip right cessation event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE Not in force date: 20180518 |
|
| R18-X000 | Changes to party contact information recorded |
St.27 status event code: A-5-5-R10-R18-oth-X000 |