NO300732B1 - 1H-indol-3-acetamid sPLA2-inhibitorer, farmasöytiske preparater inneholdende forbindelsene samt anvendelse av forbindelsene for fremstilling av farmasöytiske preparater - Google Patents
1H-indol-3-acetamid sPLA2-inhibitorer, farmasöytiske preparater inneholdende forbindelsene samt anvendelse av forbindelsene for fremstilling av farmasöytiske preparater Download PDFInfo
- Publication number
- NO300732B1 NO300732B1 NO941361A NO941361A NO300732B1 NO 300732 B1 NO300732 B1 NO 300732B1 NO 941361 A NO941361 A NO 941361A NO 941361 A NO941361 A NO 941361A NO 300732 B1 NO300732 B1 NO 300732B1
- Authority
- NO
- Norway
- Prior art keywords
- indole
- methyl
- phenylmethyl
- amino
- oxy
- Prior art date
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- ZOAMBXDOGPRZLP-UHFFFAOYSA-N indole-3-acetamide Chemical compound C1=CC=C2C(CC(=O)N)=CNC2=C1 ZOAMBXDOGPRZLP-UHFFFAOYSA-N 0.000 title claims abstract description 39
- 150000001875 compounds Chemical class 0.000 title claims description 87
- 238000002360 preparation method Methods 0.000 title claims description 15
- 239000000825 pharmaceutical preparation Substances 0.000 title claims description 8
- 102000005473 Secretory Phospholipases A2 Human genes 0.000 title abstract description 12
- 108010031873 Secretory Phospholipases A2 Proteins 0.000 title abstract description 12
- 239000003112 inhibitor Substances 0.000 title description 6
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 150000003839 salts Chemical class 0.000 claims abstract description 36
- 238000011282 treatment Methods 0.000 claims abstract description 16
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 11
- 229930195729 fatty acid Natural products 0.000 claims abstract description 11
- 239000000194 fatty acid Substances 0.000 claims abstract description 11
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 11
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 10
- 230000001404 mediated effect Effects 0.000 claims abstract description 10
- 206010040070 Septic Shock Diseases 0.000 claims abstract description 7
- 230000036303 septic shock Effects 0.000 claims abstract description 7
- 239000011734 sodium Substances 0.000 claims description 75
- 239000001257 hydrogen Substances 0.000 claims description 64
- 229910052739 hydrogen Inorganic materials 0.000 claims description 64
- -1 C 1 -C 6 alkoxy Chemical group 0.000 claims description 57
- 150000002431 hydrogen Chemical class 0.000 claims description 52
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 46
- 125000000217 alkyl group Chemical group 0.000 claims description 35
- 229910052736 halogen Inorganic materials 0.000 claims description 32
- 150000002367 halogens Chemical class 0.000 claims description 32
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 30
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 28
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 24
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 18
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 16
- 229910052751 metal Inorganic materials 0.000 claims description 15
- 239000002184 metal Substances 0.000 claims description 15
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 14
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- 235000010290 biphenyl Nutrition 0.000 claims description 12
- 239000004305 biphenyl Substances 0.000 claims description 11
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- 229910006069 SO3H Inorganic materials 0.000 claims description 10
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
- 239000003814 drug Substances 0.000 claims description 9
- 125000004076 pyridyl group Chemical group 0.000 claims description 9
- 125000004414 alkyl thio group Chemical group 0.000 claims description 8
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 8
- 239000001294 propane Substances 0.000 claims description 8
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- LYSUZOPMYPBNJF-UHFFFAOYSA-N 2-[3-(2-amino-2-oxoethyl)-1-[(3-chlorophenyl)methyl]-2-ethylindol-4-yl]oxyacetic acid Chemical compound CCC1=C(CC(N)=O)C2=C(OCC(O)=O)C=CC=C2N1CC1=CC=CC(Cl)=C1 LYSUZOPMYPBNJF-UHFFFAOYSA-N 0.000 claims description 5
- HPYJQHRYCGNSRU-UHFFFAOYSA-N 2-[[3-(2-amino-2-oxoethyl)-1-benzyl-2-methylindol-5-yl]oxymethyl]benzoic acid Chemical compound C=1C=C2N(CC=3C=CC=CC=3)C(C)=C(CC(N)=O)C2=CC=1OCC1=CC=CC=C1C(O)=O HPYJQHRYCGNSRU-UHFFFAOYSA-N 0.000 claims description 5
- MAYQVXCEHNKYHR-UHFFFAOYSA-N 3-[3-(2-amino-2-oxoethyl)-1-benzyl-2-cyclopropylindol-5-yl]oxypropylphosphonic acid Chemical compound C=1C=CC=CC=1CN1C2=CC=C(OCCCP(O)(O)=O)C=C2C(CC(=O)N)=C1C1CC1 MAYQVXCEHNKYHR-UHFFFAOYSA-N 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- OYFJLSSCYHASQQ-UHFFFAOYSA-N 2-(1-benzyl-2-cyclopropyl-5-hydroxyindol-3-yl)acetamide Chemical compound C=1C=CC=CC=1CN1C2=CC=C(O)C=C2C(CC(=O)N)=C1C1CC1 OYFJLSSCYHASQQ-UHFFFAOYSA-N 0.000 claims description 4
- DLSBYQBSELZZOY-UHFFFAOYSA-N 2-[1-benzyl-2-ethyl-5-(4-hydrazinyl-4-oxobutoxy)indol-3-yl]acetamide Chemical compound CCC1=C(CC(N)=O)C2=CC(OCCCC(=O)NN)=CC=C2N1CC1=CC=CC=C1 DLSBYQBSELZZOY-UHFFFAOYSA-N 0.000 claims description 4
- WMFPGJIEXUIPGN-UHFFFAOYSA-N 2-[3-(2-amino-2-oxoethyl)-1-benzyl-2-methylindol-4-yl]oxyacetic acid Chemical compound CC1=C(CC(N)=O)C2=C(OCC(O)=O)C=CC=C2N1CC1=CC=CC=C1 WMFPGJIEXUIPGN-UHFFFAOYSA-N 0.000 claims description 4
- LMEUGHUVZLECBH-UHFFFAOYSA-N 4-[3-(2-amino-2-oxoethyl)-1-benzyl-2-bromoindol-5-yl]oxybutanoic acid Chemical compound C12=CC=C(OCCCC(O)=O)C=C2C(CC(=O)N)=C(Br)N1CC1=CC=CC=C1 LMEUGHUVZLECBH-UHFFFAOYSA-N 0.000 claims description 4
- CBBHYRRZBIRYKM-UHFFFAOYSA-N 4-[3-(2-amino-2-oxoethyl)-1-benzyl-2-chloroindol-5-yl]oxybutanoic acid Chemical compound C12=CC=C(OCCCC(O)=O)C=C2C(CC(=O)N)=C(Cl)N1CC1=CC=CC=C1 CBBHYRRZBIRYKM-UHFFFAOYSA-N 0.000 claims description 4
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- OPWQYOUZRHDKBR-UHFFFAOYSA-N 3-[3-(2-amino-2-oxoethyl)-1-benzyl-2-ethylindol-5-yl]oxypropylphosphonic acid Chemical compound CCC1=C(CC(N)=O)C2=CC(OCCCP(O)(O)=O)=CC=C2N1CC1=CC=CC=C1 OPWQYOUZRHDKBR-UHFFFAOYSA-N 0.000 claims description 2
- QJKYFHMCVRIEKU-UHFFFAOYSA-N 3-[3-(2-amino-2-oxoethyl)-1-benzylindol-5-yl]oxypropylphosphonic acid Chemical compound C12=CC=C(OCCCP(O)(O)=O)C=C2C(CC(=O)N)=CN1CC1=CC=CC=C1 QJKYFHMCVRIEKU-UHFFFAOYSA-N 0.000 claims description 2
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 3
- 125000006727 (C1-C6) alkenyl group Chemical group 0.000 claims 1
- 150000002475 indoles Chemical class 0.000 abstract description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 809
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 402
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 391
- 235000019439 ethyl acetate Nutrition 0.000 description 337
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 246
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 214
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 209
- 239000000243 solution Substances 0.000 description 206
- 239000000203 mixture Substances 0.000 description 199
- 238000004458 analytical method Methods 0.000 description 192
- 230000002829 reductive effect Effects 0.000 description 154
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 153
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 146
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 126
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 108
- 238000000034 method Methods 0.000 description 97
- 238000004519 manufacturing process Methods 0.000 description 91
- 238000002844 melting Methods 0.000 description 90
- 230000008018 melting Effects 0.000 description 90
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 86
- 239000000377 silicon dioxide Substances 0.000 description 71
- 239000000741 silica gel Substances 0.000 description 65
- 229910002027 silica gel Inorganic materials 0.000 description 65
- 239000002480 mineral oil Substances 0.000 description 64
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 63
- 235000010446 mineral oil Nutrition 0.000 description 63
- 239000012267 brine Substances 0.000 description 59
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 59
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 54
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 54
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 54
- 229910000104 sodium hydride Inorganic materials 0.000 description 54
- 238000010992 reflux Methods 0.000 description 49
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 48
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 43
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 43
- 239000003617 indole-3-acetic acid Substances 0.000 description 41
- 238000001816 cooling Methods 0.000 description 40
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 39
- 238000004587 chromatography analysis Methods 0.000 description 38
- 239000000460 chlorine Substances 0.000 description 36
- 239000000047 product Substances 0.000 description 34
- 239000002904 solvent Substances 0.000 description 34
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 29
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 28
- 239000000463 material Substances 0.000 description 27
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 26
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 25
- 239000003921 oil Substances 0.000 description 25
- 239000011541 reaction mixture Substances 0.000 description 24
- 238000002425 crystallisation Methods 0.000 description 22
- 230000008025 crystallization Effects 0.000 description 22
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 21
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 18
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 18
- 239000007868 Raney catalyst Substances 0.000 description 18
- 229910000564 Raney nickel Inorganic materials 0.000 description 18
- OBNCKNCVKJNDBV-UHFFFAOYSA-N ethyl butyrate Chemical compound CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 18
- 238000003756 stirring Methods 0.000 description 18
- 239000012044 organic layer Substances 0.000 description 17
- YLFBFPXKTIQSSY-UHFFFAOYSA-N dimethoxy(oxo)phosphanium Chemical compound CO[P+](=O)OC YLFBFPXKTIQSSY-UHFFFAOYSA-N 0.000 description 16
- 210000001519 tissue Anatomy 0.000 description 16
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 14
- 150000002148 esters Chemical class 0.000 description 14
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 14
- XNQULTQRGBXLIA-UHFFFAOYSA-O phosphonic anhydride Chemical compound O[P+](O)=O XNQULTQRGBXLIA-UHFFFAOYSA-O 0.000 description 14
- 229910015845 BBr3 Inorganic materials 0.000 description 13
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 13
- XBPOBCXHALHJFP-UHFFFAOYSA-N ethyl 4-bromobutanoate Chemical compound CCOC(=O)CCCBr XBPOBCXHALHJFP-UHFFFAOYSA-N 0.000 description 13
- 239000002198 insoluble material Substances 0.000 description 13
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 12
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 12
- 239000000543 intermediate Substances 0.000 description 12
- 239000010410 layer Substances 0.000 description 12
- YDCHPLOFQATIDS-UHFFFAOYSA-N methyl 2-bromoacetate Chemical compound COC(=O)CBr YDCHPLOFQATIDS-UHFFFAOYSA-N 0.000 description 12
- 239000011780 sodium chloride Substances 0.000 description 12
- AQRLNPVMDITEJU-UHFFFAOYSA-N triethylsilane Chemical compound CC[SiH](CC)CC AQRLNPVMDITEJU-UHFFFAOYSA-N 0.000 description 12
- IYYIVELXUANFED-UHFFFAOYSA-N bromo(trimethyl)silane Chemical compound C[Si](C)(C)Br IYYIVELXUANFED-UHFFFAOYSA-N 0.000 description 11
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 10
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 10
- MDEARKLIJNPQCN-UHFFFAOYSA-N ethyl 2-(5-methoxy-2-methyl-1h-indol-3-yl)acetate Chemical compound C1=C(OC)C=C2C(CC(=O)OCC)=C(C)NC2=C1 MDEARKLIJNPQCN-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 230000004044 response Effects 0.000 description 10
- DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 10
- XKITUVWHONUREI-UHFFFAOYSA-N 1-bromo-3-dimethoxyphosphorylpropane Chemical compound COP(=O)(OC)CCCBr XKITUVWHONUREI-UHFFFAOYSA-N 0.000 description 9
- GDDVEHDUMMPABM-UHFFFAOYSA-N 2-(1-benzyl-5-hydroxy-2-methylindol-3-yl)acetamide Chemical compound CC1=C(CC(N)=O)C2=CC(O)=CC=C2N1CC1=CC=CC=C1 GDDVEHDUMMPABM-UHFFFAOYSA-N 0.000 description 9
- YFIDROVIWDFKFW-UHFFFAOYSA-N 2-(1-benzyl-5-methoxyindol-3-yl)acetamide Chemical compound C1=C(CC(N)=O)C2=CC(OC)=CC=C2N1CC1=CC=CC=C1 YFIDROVIWDFKFW-UHFFFAOYSA-N 0.000 description 9
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 9
- 239000012043 crude product Substances 0.000 description 9
- WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 description 9
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 9
- 235000019341 magnesium sulphate Nutrition 0.000 description 9
- 239000002244 precipitate Substances 0.000 description 9
- 229910004373 HOAc Inorganic materials 0.000 description 8
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 8
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 239000000706 filtrate Substances 0.000 description 8
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical class C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 description 8
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 7
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 7
- 231100000673 dose–response relationship Toxicity 0.000 description 7
- 230000005764 inhibitory process Effects 0.000 description 7
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 7
- GEXXCDGXTJQPOR-UHFFFAOYSA-N 2-(1-benzyl-2-methyl-5-nitroindol-3-yl)-2-hydroxyacetamide Chemical compound CC1=C(C(O)C(N)=O)C2=CC([N+]([O-])=O)=CC=C2N1CC1=CC=CC=C1 GEXXCDGXTJQPOR-UHFFFAOYSA-N 0.000 description 6
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- 230000002378 acidificating effect Effects 0.000 description 6
- 150000001408 amides Chemical class 0.000 description 6
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000012279 sodium borohydride Substances 0.000 description 6
- 229910000033 sodium borohydride Inorganic materials 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 6
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 6
- LOALWRKDHWJUPZ-UHFFFAOYSA-N 2-(1-benzyl-2-bromo-5-methoxyindol-3-yl)acetamide Chemical compound BrC1=C(CC(N)=O)C2=CC(OC)=CC=C2N1CC1=CC=CC=C1 LOALWRKDHWJUPZ-UHFFFAOYSA-N 0.000 description 5
- ZTYYSJCGMURZQJ-UHFFFAOYSA-N 2-(1-benzyl-4-hydroxy-2-methylindol-3-yl)acetamide Chemical compound CC1=C(CC(N)=O)C2=C(O)C=CC=C2N1CC1=CC=CC=C1 ZTYYSJCGMURZQJ-UHFFFAOYSA-N 0.000 description 5
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 5
- 229940073608 benzyl chloride Drugs 0.000 description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 5
- OSQPUMRCKZAIOZ-UHFFFAOYSA-N carbon dioxide;ethanol Chemical compound CCO.O=C=O OSQPUMRCKZAIOZ-UHFFFAOYSA-N 0.000 description 5
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- FKHIFSZMMVMEQY-UHFFFAOYSA-N talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- CEKCIDIGSSYIMH-UHFFFAOYSA-N tert-butyl n-(4-ethoxy-2-methylphenyl)carbamate Chemical compound CCOC1=CC=C(NC(=O)OC(C)(C)C)C(C)=C1 CEKCIDIGSSYIMH-UHFFFAOYSA-N 0.000 description 1
- WISZFUKBWXQQKO-UHFFFAOYSA-N tert-butyl n-(5-methoxy-2-methylphenyl)carbamate Chemical compound COC1=CC=C(C)C(NC(=O)OC(C)(C)C)=C1 WISZFUKBWXQQKO-UHFFFAOYSA-N 0.000 description 1
- WWRURGHCIPXMFN-UHFFFAOYSA-N tert-butyl n-[3-methoxy-2-(2-oxobutyl)phenyl]carbamate Chemical compound CCC(=O)CC1=C(NC(=O)OC(C)(C)C)C=CC=C1OC WWRURGHCIPXMFN-UHFFFAOYSA-N 0.000 description 1
- BYSOTCWTIGNKFY-UHFFFAOYSA-N tert-butyl n-[5-methyl-2-(2-oxopropyl)phenyl]carbamate Chemical compound CC(=O)CC1=CC=C(C)C=C1NC(=O)OC(C)(C)C BYSOTCWTIGNKFY-UHFFFAOYSA-N 0.000 description 1
- KZZHPWMVEVZEFG-UHFFFAOYSA-N tert-butyl n-phenylcarbamate Chemical class CC(C)(C)OC(=O)NC1=CC=CC=C1 KZZHPWMVEVZEFG-UHFFFAOYSA-N 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- APJYDQYYACXCRM-UHFFFAOYSA-N tryptamine Chemical class C1=CC=C2C(CCN)=CNC2=C1 APJYDQYYACXCRM-UHFFFAOYSA-N 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 125000002256 xylenyl group Chemical group C1(C(C=CC=C1)C)(C)* 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—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 only aliphatic carbon atoms
-
- 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
-
- 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
- A61P11/08—Bronchodilators
-
- 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
- A61P11/16—Central respiratory analeptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/02—Nutrients, e.g. vitamins, minerals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/22—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with an aralkyl radical attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with an alkyl or cycloalkyl radical attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/572—Five-membered rings
- C07F9/5728—Five-membered rings condensed with carbocyclic rings or carbocyclic ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Nutrition Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4862993A | 1993-04-16 | 1993-04-16 | |
US20872194A | 1994-03-15 | 1994-03-15 |
Publications (3)
Publication Number | Publication Date |
---|---|
NO941361D0 NO941361D0 (no) | 1994-04-15 |
NO941361L NO941361L (no) | 1994-10-17 |
NO300732B1 true NO300732B1 (no) | 1997-07-14 |
Family
ID=26726342
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO941361A NO300732B1 (no) | 1993-04-16 | 1994-04-15 | 1H-indol-3-acetamid sPLA2-inhibitorer, farmasöytiske preparater inneholdende forbindelsene samt anvendelse av forbindelsene for fremstilling av farmasöytiske preparater |
Country Status (25)
Country | Link |
---|---|
US (1) | US5684034A (sv) |
EP (1) | EP0620215B1 (sv) |
JP (1) | JPH0725850A (sv) |
KR (1) | KR100317755B1 (sv) |
CN (1) | CN1068588C (sv) |
AT (1) | ATE183503T1 (sv) |
AU (1) | AU676884B2 (sv) |
BR (1) | BR9401482A (sv) |
CA (1) | CA2121323A1 (sv) |
CO (1) | CO4230092A1 (sv) |
CZ (1) | CZ289750B6 (sv) |
DE (1) | DE69420068T2 (sv) |
DK (1) | DK0620215T3 (sv) |
ES (1) | ES2138648T3 (sv) |
FI (1) | FI941767A (sv) |
GR (1) | GR3031783T3 (sv) |
HU (1) | HUT70836A (sv) |
IL (1) | IL109311A0 (sv) |
NO (1) | NO300732B1 (sv) |
NZ (1) | NZ260298A (sv) |
PL (1) | PL181319B1 (sv) |
RU (1) | RU2162463C2 (sv) |
TW (1) | TW268942B (sv) |
UA (1) | UA44218C2 (sv) |
YU (1) | YU20194A (sv) |
Families Citing this family (69)
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IL109309A (en) * | 1993-04-16 | 2000-06-29 | Lilly Co Eli | 1-H-indole-3-acetic acid hydrazide SPLA2 inhibitors and pharmaceutical compositions containing them |
IL109311A0 (en) * | 1993-04-16 | 1994-07-31 | Lilly Co Eli | 1H-indole-3-acetamide sPla2 inhibitors |
US6252084B1 (en) | 1994-03-15 | 2001-06-26 | Eli Lilly And Company | 1H-indole-3-acetamide sPLA2 inhibitors |
KR100368707B1 (ko) * | 1994-04-01 | 2003-06-02 | 일라이 릴리 앤드 캄파니 | 1H-인돌-3-글리옥실아미드sPLA2억제제 |
US5641800A (en) * | 1994-07-21 | 1997-06-24 | Eli Lilly And Company | 1H-indole-1-functional sPLA2 inhibitors |
US6214876B1 (en) | 1994-07-21 | 2001-04-10 | Eli Lilly And Company | Indene-1-acetamide sPLA2 inhibitors |
CA2264020A1 (en) * | 1996-08-26 | 1998-03-05 | Jean Bemis | Inhibitors of phospholipase enzymes |
US6630496B1 (en) | 1996-08-26 | 2003-10-07 | Genetics Institute Llc | Inhibitors of phospholipase enzymes |
YU19299A (sh) * | 1996-10-30 | 2000-03-21 | ELI LILLY AND COMPANY, Proizvodno i trgovinsko preduzeće organizovano po propisima države Indiana, US | Supstituisani tricikli |
US6713645B1 (en) * | 1996-10-30 | 2004-03-30 | Eli Lilly And Company | Substituted tricyclics |
US6569539B2 (en) | 1996-10-30 | 2003-05-27 | Tetra Level Holdings & Finance S.A. | Gas barrier packaging laminate method for production thereof and packaging containers |
US5919774A (en) * | 1996-12-10 | 1999-07-06 | Eli Lilly And Company | Pyrroles as sPLA2 inhibitors |
AU6229298A (en) * | 1997-02-20 | 1998-09-09 | Shionogi & Co., Ltd. | Indole dicarboxylic acid derivatives |
US6916841B2 (en) | 1998-02-25 | 2005-07-12 | Genetics Institute, Llc | Inhibitors of phospholipase enzymes |
CA2322162A1 (en) * | 1998-02-25 | 1999-09-02 | Genetics Institute, Llc | Inhibitors of phospholipase enzymes |
US6828344B1 (en) | 1998-02-25 | 2004-12-07 | Genetics Institute, Llc | Inhibitors of phospholipase enzymes |
CN1298404A (zh) * | 1998-02-25 | 2001-06-06 | 遗传研究所有限公司 | 磷脂酶a2的抑制剂 |
AU2782699A (en) * | 1998-02-25 | 1999-09-15 | Genetics Institute, Llc | Inhibitors of phospholipase enzymes |
US6500853B1 (en) | 1998-02-28 | 2002-12-31 | Genetics Institute, Llc | Inhibitors of phospholipase enzymes |
US6407104B1 (en) | 1998-03-31 | 2002-06-18 | Shionogi & Co., Ltd. | Pyrrolo[1,2-a]pyrazine spla2 inhibitor |
ID23219A (id) * | 1998-04-17 | 2000-03-30 | Lilly Co Eli | Trisiklik tersubstitusi |
DZ2769A1 (fr) * | 1998-04-17 | 2003-12-01 | Lilly Co Eli | Composés tricycliques substitués. |
KR20010034881A (ko) | 1998-05-21 | 2001-04-25 | 시오노 요시히코 | sPLA2 억제 효과를 갖는 피롤로[1,2-b]피리다진 유도체 |
AU5331499A (en) | 1998-08-03 | 2000-02-28 | Eli Lilly And Company | Indole spla2 inhibitors |
WO2000007590A1 (en) | 1998-08-03 | 2000-02-17 | Eli Lilly And Company | INDOLE sPLA2 INHIBITORS |
WO2000010568A1 (en) | 1998-08-24 | 2000-03-02 | Draheim Susan E | Methods and compositions for treating periodontal disease with an inhibitor of secretory phospholipase a¿2? |
AU6004799A (en) * | 1998-10-14 | 2000-05-01 | Shionogi & Co., Ltd. | Remedies or preventives for ischemic reflow failure |
DE69910432D1 (de) | 1998-12-22 | 2003-09-18 | Lilly Co Eli | Substituierte pyrroloindole |
US6706752B1 (en) | 1999-07-19 | 2004-03-16 | Eli Lilly And Company | sPLA2 inhibitors |
AU6015600A (en) | 1999-07-19 | 2001-02-05 | Shionogi & Co., Ltd. | Tricyclic compounds having spla2-inhibitory activities |
DE60032774D1 (de) * | 1999-07-19 | 2007-02-15 | Lilly Co Eli | Spla2 inhibitoren |
AU6023200A (en) | 1999-08-02 | 2001-02-19 | Shionogi & Co., Ltd. | Tricyclic compounds having spla2-inhibitory activities |
AU6473600A (en) | 1999-08-23 | 2001-03-19 | Shionogi & Co., Ltd. | Pyrrolotriazine derivatives having spla2-inhibitory activities |
EP1220839B1 (en) * | 1999-09-20 | 2006-12-06 | Eli Lilly And Company | Hydroxyfunctional amide 1h-indole derivatives active as spla2 inhibitors |
US6831095B1 (en) | 1999-09-20 | 2004-12-14 | Eli Lilly And Company | Hydroxyfunctional amide 1h-indole derivatives active as sPLA2 inhibitors |
WO2001026653A1 (fr) * | 1999-10-15 | 2001-04-19 | Shionogi & Co., Ltd. | Inhibiteurs spla2 du type v et/ou du type x |
AU1304801A (en) | 1999-11-15 | 2001-05-30 | Shionogi & Co., Ltd. | Tricyclic azaindolizine derivatives having an SPLA2- inhibiting effect |
DE19962300A1 (de) * | 1999-12-23 | 2001-06-28 | Asta Medica Ag | Substituierte N-Benzyl-Indol-3-yl-glyoxylsäure-Derivate mit Antitumorwirkung |
WO2002000646A1 (en) * | 2000-06-27 | 2002-01-03 | Smithkline Beecham Corporation | Fatty acid synthase inhibitors |
JPWO2002000621A1 (ja) * | 2000-06-29 | 2004-04-22 | 塩野義製薬株式会社 | X型sPLA2阻害作用を有する化合物 |
WO2002000256A1 (en) | 2000-06-29 | 2002-01-03 | Shionogi & Co., Ltd. | Remedies for cirrhosis |
US20050203166A1 (en) * | 2000-06-30 | 2005-09-15 | Cancer Research Technology Limited | Indole-3-acetic acid derivatives |
GB0016162D0 (en) * | 2000-06-30 | 2000-08-23 | Cancer Res Campaign Tech | Indole-3-acetic acid derivatives |
EP1303262A2 (en) * | 2000-07-14 | 2003-04-23 | Eli Lilly And Company | Use of a spla2 inhibitor for the treatment of sepsis |
AU2001282410A1 (en) * | 2000-08-24 | 2002-03-22 | Dublin City University | N-benzylindole-3-acetic acid derivatives for use in the treatment of drug resistan cancer |
US6974831B2 (en) * | 2000-12-18 | 2005-12-13 | Eli Lilly And Company | sPLA2 inhibitors |
JP2004520363A (ja) * | 2000-12-18 | 2004-07-08 | イーライ・リリー・アンド・カンパニー | 新規なsPLA2インヒビター |
TWI314457B (sv) | 2001-03-19 | 2009-09-11 | Shionogi & Co | |
US7101875B2 (en) | 2001-12-03 | 2006-09-05 | Wyeth | Methods for treating arthritic disorders |
US6635771B2 (en) | 2001-12-03 | 2003-10-21 | Wyeth | N-benzhydryl indole compounds |
US6797708B2 (en) | 2001-12-03 | 2004-09-28 | Wyeth | Inhibitors of cytosolic phospholipase A2 |
US7605156B2 (en) | 2001-12-03 | 2009-10-20 | Wyeth | Methods for the use of inhibitors of cytosolic phospholipase A2 |
US6984735B2 (en) | 2001-12-03 | 2006-01-10 | Wyeth | Process for making an aldehyde |
US7713964B2 (en) | 2001-12-03 | 2010-05-11 | Wyeth Llc | Methods for treating asthmatic conditions |
US7129264B2 (en) * | 2003-04-16 | 2006-10-31 | Bristol-Myers Squibb Company | Biarylmethyl indolines and indoles as antithromboembolic agents |
US20070161698A1 (en) * | 2003-05-30 | 2007-07-12 | Microbia, Inc. | Modulators of CRTH2 Activity |
WO2005002525A2 (en) * | 2003-07-01 | 2005-01-13 | Microbia, Inc. | Cox-2 and faah inhibitors |
US20070293542A1 (en) * | 2003-10-16 | 2007-12-20 | Cali Brian M | Selective Cox-2 Inhibitors |
US7417063B2 (en) * | 2004-04-13 | 2008-08-26 | Bristol-Myers Squibb Company | Bicyclic heterocycles useful as serine protease inhibitors |
US20050234030A1 (en) * | 2004-04-20 | 2005-10-20 | Wilmin Bartolini | Modulators of CRTH2, COX-2 and FAAH |
US20050234244A1 (en) * | 2004-04-20 | 2005-10-20 | Wilmin Bartolini | Synthesis of COX-2 and FAAH inhibitors |
TW200718687A (en) | 2005-05-27 | 2007-05-16 | Wyeth Corp | Inhibitors of cytosolic phospholipase A2 |
EP1931632A4 (en) * | 2005-08-18 | 2011-05-11 | Microbia Inc | USEFUL INDOOR CONNECTIONS |
AU2006311761A1 (en) * | 2005-11-03 | 2007-05-18 | Ilypsa, Inc. | Indole compounds having C4-amide substituents and use thereof as phospholipase-A2 inhibitors |
US7666898B2 (en) | 2005-11-03 | 2010-02-23 | Ilypsa, Inc. | Multivalent indole compounds and use thereof as phospholipase-A2 inhibitors |
GB2431927B (en) * | 2005-11-04 | 2010-03-17 | Amira Pharmaceuticals Inc | 5-Lipoxygenase-activating protein (FLAP) inhibitors |
US8048880B2 (en) * | 2007-05-03 | 2011-11-01 | Anthera Pharmaceuticals, Inc. | Treatment of cardiovascular disease and dyslipidemia using secretory phospholipase A2 (SPLA2) inhibitors and SPLA2 inhibitor combination therapies |
NZ624963A (en) | 2009-04-29 | 2016-07-29 | Amarin Pharmaceuticals Ie Ltd | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
CN105384619B (zh) * | 2014-08-22 | 2020-05-29 | 四川海思科制药有限公司 | 一种异丙基苯酚衍生物及其制备方法 |
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US2825734A (en) * | 1955-04-11 | 1958-03-04 | Upjohn Co | Reduction of carbonylic radicals in indolyl-3 compounds |
US2890223A (en) * | 1956-03-22 | 1959-06-09 | Research Corp | 1-benzyl, 2-methyl, 5-methoxy tryptamine |
US3196162A (en) * | 1961-03-13 | 1965-07-20 | Merck & Co Inc | Indolyl aliphatic acids |
US3242193A (en) * | 1961-03-13 | 1966-03-22 | Merck & Co Inc | Indolyl aliphatic acids |
US3242163A (en) * | 1961-03-13 | 1966-03-22 | Merck & Co Inc | Indolyl aliphatic acids |
US3242162A (en) * | 1961-03-13 | 1966-03-22 | Merck & Co Inc | Indolyl aliphatic acids |
US3271416A (en) * | 1961-10-24 | 1966-09-06 | Merck & Co Inc | Indolyl aliphatic acids |
US3259622A (en) * | 1962-09-07 | 1966-07-05 | Merck & Co Inc | 1-benzyl-3-indolyl-alpha-haloalkyl and alkylidenyl acetic acids |
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IL109311A0 (en) * | 1993-04-16 | 1994-07-31 | Lilly Co Eli | 1H-indole-3-acetamide sPla2 inhibitors |
-
1994
- 1994-04-12 IL IL10931194A patent/IL109311A0/xx unknown
- 1994-04-13 HU HU9401060A patent/HUT70836A/hu unknown
- 1994-04-13 NZ NZ260298A patent/NZ260298A/en unknown
- 1994-04-13 TW TW083103301A patent/TW268942B/zh active
- 1994-04-14 CA CA002121323A patent/CA2121323A1/en not_active Abandoned
- 1994-04-14 CZ CZ1994893A patent/CZ289750B6/cs not_active IP Right Cessation
- 1994-04-14 ES ES94302666T patent/ES2138648T3/es not_active Expired - Lifetime
- 1994-04-14 EP EP94302666A patent/EP0620215B1/en not_active Expired - Lifetime
- 1994-04-14 DK DK94302666T patent/DK0620215T3/da active
- 1994-04-14 BR BR9401482A patent/BR9401482A/pt not_active Application Discontinuation
- 1994-04-14 AT AT94302666T patent/ATE183503T1/de not_active IP Right Cessation
- 1994-04-14 DE DE69420068T patent/DE69420068T2/de not_active Expired - Fee Related
- 1994-04-14 CO CO94014981A patent/CO4230092A1/es unknown
- 1994-04-15 UA UA94005180A patent/UA44218C2/uk unknown
- 1994-04-15 AU AU59492/94A patent/AU676884B2/en not_active Ceased
- 1994-04-15 YU YU20194A patent/YU20194A/sh unknown
- 1994-04-15 NO NO941361A patent/NO300732B1/no not_active IP Right Cessation
- 1994-04-15 PL PL94303028A patent/PL181319B1/pl unknown
- 1994-04-15 FI FI941767A patent/FI941767A/sv unknown
- 1994-04-15 RU RU94012930/04A patent/RU2162463C2/ru active
- 1994-04-15 JP JP6077650A patent/JPH0725850A/ja active Pending
- 1994-04-15 KR KR1019940007935A patent/KR100317755B1/ko not_active IP Right Cessation
- 1994-04-15 CN CN94104434A patent/CN1068588C/zh not_active Expired - Fee Related
-
1995
- 1995-05-05 US US08/435,256 patent/US5684034A/en not_active Expired - Lifetime
-
1999
- 1999-11-08 GR GR990402875T patent/GR3031783T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
BR9401482A (pt) | 1994-10-18 |
CZ89394A3 (en) | 1994-12-15 |
EP0620215A1 (en) | 1994-10-19 |
CZ289750B6 (cs) | 2002-03-13 |
CN1068588C (zh) | 2001-07-18 |
CA2121323A1 (en) | 1994-10-17 |
AU676884B2 (en) | 1997-03-27 |
GR3031783T3 (en) | 2000-02-29 |
CN1098715A (zh) | 1995-02-15 |
DE69420068T2 (de) | 1999-12-23 |
CO4230092A1 (es) | 1995-10-19 |
RU2162463C2 (ru) | 2001-01-27 |
NZ260298A (en) | 1996-05-28 |
JPH0725850A (ja) | 1995-01-27 |
KR100317755B1 (ko) | 2002-08-09 |
EP0620215B1 (en) | 1999-08-18 |
YU20194A (sh) | 1997-09-30 |
DE69420068D1 (de) | 1999-09-23 |
DK0620215T3 (da) | 1999-12-06 |
US5684034A (en) | 1997-11-04 |
FI941767A (sv) | 1994-10-17 |
HUT70836A (en) | 1995-11-28 |
UA44218C2 (uk) | 2002-02-15 |
HU9401060D0 (en) | 1994-07-28 |
ATE183503T1 (de) | 1999-09-15 |
TW268942B (sv) | 1996-01-21 |
NO941361L (no) | 1994-10-17 |
IL109311A0 (en) | 1994-07-31 |
FI941767A0 (sv) | 1994-04-15 |
AU5949294A (en) | 1994-10-20 |
PL181319B1 (pl) | 2001-07-31 |
ES2138648T3 (es) | 2000-01-16 |
NO941361D0 (no) | 1994-04-15 |
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MM1K | Lapsed by not paying the annual fees |
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