IL103356A - History of Neptopyrins Preparation and Pharmaceutical Preparations Containing Them - Google Patents
History of Neptopyrins Preparation and Pharmaceutical Preparations Containing ThemInfo
- Publication number
- IL103356A IL103356A IL103356A IL10335692A IL103356A IL 103356 A IL103356 A IL 103356A IL 103356 A IL103356 A IL 103356A IL 10335692 A IL10335692 A IL 10335692A IL 103356 A IL103356 A IL 103356A
- Authority
- IL
- Israel
- Prior art keywords
- phenyl
- naphtho
- alkyl
- pyran
- amino
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title description 5
- VCMLCMCXCRBSQO-UHFFFAOYSA-N 3h-benzo[f]chromene Chemical class C1=CC=CC2=C(C=CCO3)C3=CC=C21 VCMLCMCXCRBSQO-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 57
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 35
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 26
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 14
- 239000001257 hydrogen Substances 0.000 claims abstract description 14
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 10
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 10
- 150000002825 nitriles Chemical class 0.000 claims abstract description 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 8
- 125000002541 furyl group Chemical group 0.000 claims abstract description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 5
- 125000001424 substituent group Chemical group 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 239000003085 diluting agent Substances 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 2
- -1 trifluoromethoxy, carboxy Chemical group 0.000 abstract description 35
- 125000004185 ester group Chemical group 0.000 abstract description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 5
- 125000004414 alkyl thio group Chemical group 0.000 abstract description 4
- 125000002947 alkylene group Chemical group 0.000 abstract description 2
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 abstract description 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 abstract description 2
- 125000004076 pyridyl group Chemical group 0.000 abstract description 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract description 2
- 125000001544 thienyl group Chemical group 0.000 abstract description 2
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 28
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 26
- PVLILYCJFFKRGB-UHFFFAOYSA-N 2h-pyran-3-carbonitrile Chemical compound N#CC1=CC=COC1 PVLILYCJFFKRGB-UHFFFAOYSA-N 0.000 description 19
- 239000000243 solution Substances 0.000 description 19
- 210000004027 cell Anatomy 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000004480 active ingredient Substances 0.000 description 11
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 10
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 125000005843 halogen group Chemical group 0.000 description 8
- 238000010992 reflux Methods 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- 229920002472 Starch Polymers 0.000 description 7
- 239000013078 crystal Substances 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 235000019698 starch Nutrition 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000008107 starch Substances 0.000 description 6
- 239000002775 capsule Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000007903 gelatin capsule Substances 0.000 description 5
- 235000019359 magnesium stearate Nutrition 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 4
- 239000006144 Dulbecco’s modified Eagle's medium Substances 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000004663 cell proliferation Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000005457 ice water Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 4
- 239000003826 tablet Substances 0.000 description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 3
- KLHQWXOILCCTOX-UHFFFAOYSA-N 2-amino-4-(3-nitrophenyl)-4h-benzo[h]chromene-3-carbonitrile Chemical compound C12=CC=C3C=CC=CC3=C2OC(N)=C(C#N)C1C1=CC=CC([N+]([O-])=O)=C1 KLHQWXOILCCTOX-UHFFFAOYSA-N 0.000 description 3
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 108010062580 Concanavalin A Proteins 0.000 description 3
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 3
- 229930182816 L-glutamine Natural products 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000012267 brine Substances 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 239000002552 dosage form Substances 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 230000035755 proliferation Effects 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- DMCALUGUAZZLFS-UHFFFAOYSA-N 2-amino-4-(4-chloro-3-nitrophenyl)-4h-benzo[h]chromene-3-carbonitrile Chemical compound C12=CC=C3C=CC=CC3=C2OC(N)=C(C#N)C1C1=CC=C(Cl)C([N+]([O-])=O)=C1 DMCALUGUAZZLFS-UHFFFAOYSA-N 0.000 description 2
- JDTUPLBMGDDPJS-UHFFFAOYSA-N 2-methoxy-2-phenylethanol Chemical compound COC(CO)C1=CC=CC=C1 JDTUPLBMGDDPJS-UHFFFAOYSA-N 0.000 description 2
- LZNNMMKMGKFYLL-UHFFFAOYSA-N 2h-pyran-3-carboxylic acid Chemical compound OC(=O)C1=CC=COC1 LZNNMMKMGKFYLL-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 206010016654 Fibrosis Diseases 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 description 2
- 229930182555 Penicillin Natural products 0.000 description 2
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 2
- 102000010780 Platelet-Derived Growth Factor Human genes 0.000 description 2
- 108010038512 Platelet-Derived Growth Factor Proteins 0.000 description 2
- 229920001030 Polyethylene Glycol 4000 Polymers 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 239000000908 ammonium hydroxide Substances 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 239000002026 chloroform extract Substances 0.000 description 2
- OQNGCCWBHLEQFN-UHFFFAOYSA-N chloroform;hexane Chemical compound ClC(Cl)Cl.CCCCCC OQNGCCWBHLEQFN-UHFFFAOYSA-N 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- UZLDAOIRJMPDOO-UHFFFAOYSA-N n-acetyl-n-[3-cyano-4-(3-nitrophenyl)-4h-benzo[h]chromen-2-yl]acetamide Chemical compound C12=CC=C3C=CC=CC3=C2OC(N(C(C)=O)C(=O)C)=C(C#N)C1C1=CC=CC([N+]([O-])=O)=C1 UZLDAOIRJMPDOO-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229940049954 penicillin Drugs 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 210000000329 smooth muscle myocyte Anatomy 0.000 description 2
- 229960005322 streptomycin Drugs 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- IQFYYKKMVGJFEH-OFKYTIFKSA-N 1-[(2r,4s,5r)-4-hydroxy-5-(tritiooxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione Chemical compound C1[C@H](O)[C@@H](CO[3H])O[C@H]1N1C(=O)NC(=O)C(C)=C1 IQFYYKKMVGJFEH-OFKYTIFKSA-N 0.000 description 1
- KZDCMKVLEYCGQX-UDPGNSCCSA-N 2-(diethylamino)ethyl 4-aminobenzoate;(2s,5r,6r)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;hydrate Chemical compound O.CCN(CC)CCOC(=O)C1=CC=C(N)C=C1.N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 KZDCMKVLEYCGQX-UDPGNSCCSA-N 0.000 description 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- QGESGQINLPXOJL-UHFFFAOYSA-N 2-[(2-nitrophenyl)methylidene]propanedinitrile Chemical compound [O-][N+](=O)C1=CC=CC=C1C=C(C#N)C#N QGESGQINLPXOJL-UHFFFAOYSA-N 0.000 description 1
- PFISAUZEHHNMIX-UHFFFAOYSA-N 2-[(3,4-dichlorophenyl)methylidene]-3-hydroxybutanedinitrile Chemical compound N#CC(O)C(C#N)=CC1=CC=C(Cl)C(Cl)=C1 PFISAUZEHHNMIX-UHFFFAOYSA-N 0.000 description 1
- KRUWRUCOSPJGML-UHFFFAOYSA-N 2-[(3,4-dimethoxyphenyl)methylidene]-3-hydroxybutanedinitrile Chemical compound COC1=CC=C(C=C(C#N)C(O)C#N)C=C1OC KRUWRUCOSPJGML-UHFFFAOYSA-N 0.000 description 1
- DFNFCGRXPLQYOH-UHFFFAOYSA-N 2-[(3-bromo-4-fluorophenyl)methylidene]propanedinitrile Chemical compound FC1=CC=C(C=C(C#N)C#N)C=C1Br DFNFCGRXPLQYOH-UHFFFAOYSA-N 0.000 description 1
- GURAFVQCXDAQDY-UHFFFAOYSA-N 2-[(3-chloro-4-fluorophenyl)methylidene]propanedinitrile Chemical compound FC1=CC=C(C=C(C#N)C#N)C=C1Cl GURAFVQCXDAQDY-UHFFFAOYSA-N 0.000 description 1
- CGLGAIINXSHQBP-UHFFFAOYSA-N 2-[(3-chlorophenyl)methylidene]propanedinitrile Chemical compound ClC1=CC=CC(C=C(C#N)C#N)=C1 CGLGAIINXSHQBP-UHFFFAOYSA-N 0.000 description 1
- BEIBHVQFFGGDLC-UHFFFAOYSA-N 2-[(3-hydroxyphenyl)methylidene]propanedinitrile Chemical compound OC1=CC=CC(C=C(C#N)C#N)=C1 BEIBHVQFFGGDLC-UHFFFAOYSA-N 0.000 description 1
- LZBVVVZUWLWGHM-UHFFFAOYSA-N 2-[(3-methoxyphenyl)methylidene]propanedinitrile Chemical compound COC1=CC=CC(C=C(C#N)C#N)=C1 LZBVVVZUWLWGHM-UHFFFAOYSA-N 0.000 description 1
- UQMJZLGIKHAOQZ-UHFFFAOYSA-N 2-[(3-nitrophenyl)methylidene]propanedinitrile Chemical compound [O-][N+](=O)C1=CC=CC(C=C(C#N)C#N)=C1 UQMJZLGIKHAOQZ-UHFFFAOYSA-N 0.000 description 1
- YJMAUPPEHPTNTJ-UHFFFAOYSA-N 2-[(4-chloro-3-nitrophenyl)methylidene]-3-hydroxybutanedinitrile Chemical compound N#CC(O)C(C#N)=CC1=CC=C(Cl)C([N+]([O-])=O)=C1 YJMAUPPEHPTNTJ-UHFFFAOYSA-N 0.000 description 1
- GHBRDJGZDJZLRI-UHFFFAOYSA-N 2-[(4-fluoro-3-nitrophenyl)methylidene]-3-hydroxybutanedinitrile Chemical compound N#CC(O)C(C#N)=CC1=CC=C(F)C([N+]([O-])=O)=C1 GHBRDJGZDJZLRI-UHFFFAOYSA-N 0.000 description 1
- BDTIGNGBIBFXSE-UHFFFAOYSA-N 2-[(4-nitrophenyl)methylidene]propanedinitrile Chemical compound [O-][N+](=O)C1=CC=C(C=C(C#N)C#N)C=C1 BDTIGNGBIBFXSE-UHFFFAOYSA-N 0.000 description 1
- ILHFXEHGTMBGEU-UHFFFAOYSA-N 2-[[3-(trifluoromethoxy)phenyl]methylidene]propanedinitrile Chemical compound FC(F)(F)OC1=CC=CC(C=C(C#N)C#N)=C1 ILHFXEHGTMBGEU-UHFFFAOYSA-N 0.000 description 1
- KOBCKAMPCIQPAW-UHFFFAOYSA-N 2-amino-4-(2-nitrophenyl)-4h-benzo[h]chromene-3-carbonitrile Chemical compound C12=CC=C3C=CC=CC3=C2OC(N)=C(C#N)C1C1=CC=CC=C1[N+]([O-])=O KOBCKAMPCIQPAW-UHFFFAOYSA-N 0.000 description 1
- VOWJLMKKBXGJMR-UHFFFAOYSA-N 2-amino-4-(3-bromo-4-fluorophenyl)-4h-benzo[h]chromene-3-carbonitrile Chemical compound C12=CC=C3C=CC=CC3=C2OC(N)=C(C#N)C1C1=CC=C(F)C(Br)=C1 VOWJLMKKBXGJMR-UHFFFAOYSA-N 0.000 description 1
- CGDVMGKWKXCXJT-UHFFFAOYSA-N 2-amino-4-(3-carboxyphenyl)-3-cyano-4h-benzo[h]chromene-6-carboxylic acid Chemical compound C12=CC(C(O)=O)=C3C=CC=CC3=C2OC(N)=C(C#N)C1C1=CC=CC(C(O)=O)=C1 CGDVMGKWKXCXJT-UHFFFAOYSA-N 0.000 description 1
- ZWCPQLKGMWGQTK-UHFFFAOYSA-N 2-amino-4-(3-chloro-4-fluorophenyl)-4h-benzo[h]chromene-3-carbonitrile Chemical compound C12=CC=C3C=CC=CC3=C2OC(N)=C(C#N)C1C1=CC=C(F)C(Cl)=C1 ZWCPQLKGMWGQTK-UHFFFAOYSA-N 0.000 description 1
- QMOAGEFZQCHUSG-UHFFFAOYSA-N 2-amino-4-(3-methoxyphenyl)-4h-benzo[h]chromene-3-carbonitrile Chemical compound COC1=CC=CC(C2C3=C(C4=CC=CC=C4C=C3)OC(N)=C2C#N)=C1 QMOAGEFZQCHUSG-UHFFFAOYSA-N 0.000 description 1
- ACGMQPXRVMJTKD-UHFFFAOYSA-N 2-amino-4-(4-nitrophenyl)-4h-benzo[h]chromene-3-carbonitrile Chemical compound C12=CC=C3C=CC=CC3=C2OC(N)=C(C#N)C1C1=CC=C([N+]([O-])=O)C=C1 ACGMQPXRVMJTKD-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
- C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
- C07D311/92—Naphthopyrans; Hydrogenated naphthopyrans
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Epidemiology (AREA)
- Vascular Medicine (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Transplantation (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrane Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Saccharide Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB919121358A GB9121358D0 (en) | 1991-10-09 | 1991-10-09 | Pharmaceutical compounds |
| GB929213058A GB9213058D0 (en) | 1992-06-19 | 1992-06-19 | Pharmaceutical compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL103356A0 IL103356A0 (en) | 1993-03-15 |
| IL103356A true IL103356A (en) | 1998-02-22 |
Family
ID=26299655
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL103356A IL103356A (en) | 1991-10-09 | 1992-10-05 | History of Neptopyrins Preparation and Pharmaceutical Preparations Containing Them |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US5284868A (fr) |
| EP (1) | EP0537949B1 (fr) |
| JP (1) | JPH05194477A (fr) |
| KR (1) | KR100228841B1 (fr) |
| CN (1) | CN1034938C (fr) |
| AT (1) | ATE167859T1 (fr) |
| AU (1) | AU658003B2 (fr) |
| CA (1) | CA2079428A1 (fr) |
| CZ (1) | CZ281688B6 (fr) |
| DE (1) | DE69226060T2 (fr) |
| DK (1) | DK0537949T3 (fr) |
| ES (1) | ES2117035T3 (fr) |
| FI (1) | FI924551A (fr) |
| HU (1) | HU218916B (fr) |
| IL (1) | IL103356A (fr) |
| MX (1) | MX9205714A (fr) |
| MY (1) | MY111368A (fr) |
| NO (1) | NO301587B1 (fr) |
| NZ (1) | NZ244627A (fr) |
| PH (1) | PH30659A (fr) |
| RU (1) | RU2071472C1 (fr) |
| TW (1) | TW221292B (fr) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9203497D0 (en) * | 1992-02-19 | 1992-04-08 | Lilly Industries Ltd | Pharmaceutical compounds |
| EP0599514A3 (en) * | 1992-11-18 | 1994-07-06 | Lilly Industries Ltd | Pyranoquinoline derivatives as inhibitors of cell proliferation. |
| GB9306062D0 (en) * | 1993-03-24 | 1993-05-12 | Lilly Industries Ltd | Pharmaceutical compounds |
| EP0619314A1 (fr) * | 1993-04-09 | 1994-10-12 | Eli Lilly And Company | Dérivés de 4-phényl-4H-naphtho 2,1-b pyran et leur utilisation pharmaceutique |
| WO1995008289A2 (fr) * | 1993-09-16 | 1995-03-30 | Scimed Life Systems, Inc. | Reparation percutanee d'anomalies cardio-vasculaires et compositions associees |
| US5407955A (en) * | 1994-02-18 | 1995-04-18 | Eli Lilly And Company | Methods for lowering serum cholesterol and inhibiting smooth muscle cell proliferation, restenosis, endometriosis, and uterine fibroid disease |
| US5665591A (en) * | 1994-12-06 | 1997-09-09 | Trustees Of Boston University | Regulation of smooth muscle cell proliferation |
| NZ505584A (en) * | 1996-05-24 | 2002-04-26 | Univ British Columbia | Delivery of a therapeutic agent to the smooth muscle cells of a body passageway via an adventia |
| IL119069A0 (en) * | 1996-08-14 | 1996-11-14 | Mor Research Applic Ltd | Pharmaceutical composition comprising tyrphostins |
| AU781986B2 (en) | 1999-11-05 | 2005-06-23 | Cytovia, Inc. | Substituted 4H-chromene and analogs as activators of caspases and inducers of apoptosis and the use thereof |
| US6858607B1 (en) | 2001-05-16 | 2005-02-22 | Cytovia, Inc. | 7,8-fused 4H-chromene and analogs as activators of caspases and inducers of apoptosis and the use thereof |
| WO2002092594A1 (fr) * | 2001-05-16 | 2002-11-21 | Cytovia, Inc. | Chromenes subtitues 4h et leurs analogues en tant qu'activateurs de caspases et inducteurs d'apoptose, et leur utilisation |
| WO2002092076A1 (fr) * | 2001-05-16 | 2002-11-21 | Cytovia, Inc. | Coumarines et quinolines substituees utilisees comme activateurs des caspases |
| AU2003241482A1 (en) * | 2002-05-16 | 2003-12-02 | Cytovia, Inc. | Substituted 4h-chromenes, 2h-chromenes, chromans and analogs as activators of caspases and inducers of apoptosis and the use thereof |
| AU2003230411A1 (en) * | 2002-05-16 | 2003-12-02 | Cytovia, Inc. | Substituted 4-aryl-4h-pyrrolo(2,3-h)chromenes and analogs as activators of caspases and inducers of apoptosis and the use thereof |
| US20040127511A1 (en) * | 2002-12-12 | 2004-07-01 | Pharmacia Corporation | Tricyclic aminocyanopyridine inhibitors of mitogen activated protein kinase-activated protein kinase-2 |
| US20040127519A1 (en) * | 2002-12-12 | 2004-07-01 | Pharmacia Corporation | Method of using aminocyanopyridine compounds as mitogen activated protein kinase-activated protein kinase-2 inhibitors |
| ZA200702041B (en) * | 2004-09-09 | 2008-09-25 | Florey Howard Inst | Enzyme inhibitors and uses thereof |
| EP2532390B1 (fr) * | 2005-02-16 | 2016-08-17 | Md Bioalpha Co., Ltd. | Composition pharmaceutique pour les maladies du foie. |
| US20080183282A1 (en) * | 2006-03-09 | 2008-07-31 | Saul Yedgar | Use of lipid conjugates for the coating of stents and catheters |
| NZ585338A (en) | 2007-11-19 | 2012-08-31 | Howard Florey Inst | Insulin-regulated aminopeptidase (irap) inhibitors and uses thereof |
| EA015364B1 (ru) * | 2009-03-18 | 2011-06-30 | Учреждение Российской Академии Наук Институт Элементоорганических Соединений Им. А.Н. Несмеянова Ран (Инэос Ран) | 6,6'-диизопропил-8,8'-диметил-2,2'-динитро-3,3'-бис(трифторметил)- 3н,3'н-[9,9']ди[бензо(f)хроменил]-5,10,5',10'-тетраол, обладающий противоопухолевой и противогрибковой активностью, и способ его получения |
| US9371333B2 (en) | 2010-11-12 | 2016-06-21 | Deutsches Krebsforschungszentrum | Chromene derivatives and their analoga as Wnt pathway antagonists |
| CN104185631A (zh) * | 2011-11-10 | 2014-12-03 | 纪念斯隆-凯特琳癌症中心 | 用2-氨基-4H-萘并[1,2-b]吡喃-3-甲腈治疗卵巢癌 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU724509A1 (ru) * | 1978-09-21 | 1980-03-30 | Пермский государственный фармацевтический институт | Способ получени 2-ароил-3н- нафто 2,1-в пиранонов-3 |
| US5232942A (en) * | 1988-04-14 | 1993-08-03 | Yamanouchi Pharmaceutical Co., Ltd. | Q-2819 substance and the use thereof |
-
1992
- 1992-09-25 US US07/951,629 patent/US5284868A/en not_active Expired - Fee Related
- 1992-09-29 CA CA002079428A patent/CA2079428A1/fr not_active Abandoned
- 1992-10-05 CZ CS923035A patent/CZ281688B6/cs not_active IP Right Cessation
- 1992-10-05 PH PH45043A patent/PH30659A/en unknown
- 1992-10-05 AU AU26216/92A patent/AU658003B2/en not_active Ceased
- 1992-10-05 IL IL103356A patent/IL103356A/en not_active IP Right Cessation
- 1992-10-05 TW TW081107894A patent/TW221292B/zh active
- 1992-10-06 NZ NZ244627A patent/NZ244627A/en unknown
- 1992-10-06 MX MX9205714A patent/MX9205714A/es not_active IP Right Cessation
- 1992-10-06 RU SU925052861A patent/RU2071472C1/ru active
- 1992-10-07 MY MYPI92001807A patent/MY111368A/en unknown
- 1992-10-07 KR KR1019920018309A patent/KR100228841B1/ko not_active IP Right Cessation
- 1992-10-08 HU HU9203183A patent/HU218916B/hu not_active IP Right Cessation
- 1992-10-08 JP JP4269002A patent/JPH05194477A/ja active Pending
- 1992-10-08 FI FI924551A patent/FI924551A/fi unknown
- 1992-10-08 DK DK92309169T patent/DK0537949T3/da active
- 1992-10-08 ES ES92309169T patent/ES2117035T3/es not_active Expired - Lifetime
- 1992-10-08 AT AT92309169T patent/ATE167859T1/de not_active IP Right Cessation
- 1992-10-08 DE DE69226060T patent/DE69226060T2/de not_active Expired - Fee Related
- 1992-10-08 CN CN92111625A patent/CN1034938C/zh not_active Expired - Fee Related
- 1992-10-08 EP EP92309169A patent/EP0537949B1/fr not_active Expired - Lifetime
- 1992-10-08 NO NO923910A patent/NO301587B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| MX9205714A (es) | 1993-04-01 |
| US5284868A (en) | 1994-02-08 |
| CN1034938C (zh) | 1997-05-21 |
| EP0537949A1 (fr) | 1993-04-21 |
| TW221292B (fr) | 1994-02-21 |
| HU9203183D0 (en) | 1992-12-28 |
| KR930007931A (ko) | 1993-05-20 |
| DE69226060T2 (de) | 1998-11-19 |
| CZ303592A3 (en) | 1993-12-15 |
| ES2117035T3 (es) | 1998-08-01 |
| HUT62281A (en) | 1993-04-28 |
| MY111368A (en) | 1999-12-31 |
| FI924551A (fi) | 1993-04-10 |
| CA2079428A1 (fr) | 1993-04-10 |
| NZ244627A (en) | 1994-12-22 |
| DE69226060D1 (de) | 1998-08-06 |
| NO301587B1 (no) | 1997-11-17 |
| AU658003B2 (en) | 1995-03-30 |
| CN1073437A (zh) | 1993-06-23 |
| DK0537949T3 (da) | 1999-02-15 |
| AU2621692A (en) | 1993-04-22 |
| NO923910D0 (no) | 1992-10-08 |
| FI924551A0 (fi) | 1992-10-08 |
| PH30659A (en) | 1997-09-16 |
| EP0537949B1 (fr) | 1998-07-01 |
| RU2071472C1 (ru) | 1997-01-10 |
| HU218916B (hu) | 2000-12-28 |
| IL103356A0 (en) | 1993-03-15 |
| CZ281688B6 (cs) | 1996-12-11 |
| JPH05194477A (ja) | 1993-08-03 |
| ATE167859T1 (de) | 1998-07-15 |
| NO923910L (no) | 1993-04-13 |
| KR100228841B1 (ko) | 1999-11-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FF | Patent granted | ||
| KB | Patent renewed | ||
| KB | Patent renewed | ||
| HC | Change of name of proprietor(s) | ||
| RH1 | Patent not in force |