NO317257B1 - Indolderivater og farmasoytiske sammensetninger omfattende det samme - Google Patents

Indolderivater og farmasoytiske sammensetninger omfattende det samme Download PDF

Info

Publication number: NO317257B1
Authority: NO; Norway
Prior art keywords: ethyl; propyl; compound; solution; amino
Prior art date: 1998-02-27

Application number

NO20004277A

Other languages

English (en)

Norwegian (no)

Other versions

NO20004277D0 (no

NO20004277L (no

Inventor

Makio Kitazawa

Toshiaki Yamaguchi

Yukiyoshi Ajisawa

Hiroshi Miyata

Original Assignee

Kissei Pharmaceutical Company

Priority date (The priority date 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 date listed.)

1998-02-27

Filing date

2000-08-25

Publication date

2004-09-27

2000-08-25 Application filed by Kissei Pharmaceutical Company filed Critical Kissei Pharmaceutical Company

2000-08-25 Publication of NO20004277D0 publication Critical patent/NO20004277D0/no

2000-09-11 Publication of NO20004277L publication Critical patent/NO20004277L/no

2004-09-27 Publication of NO317257B1 publication Critical patent/NO317257B1/no

Links

150000002475 indoles Chemical class 0.000 title claims description 21
239000008194 pharmaceutical composition Substances 0.000 title claims description 9
229940054051 antipsychotic indole derivative Drugs 0.000 title description 5
229910052799 carbon Inorganic materials 0.000 claims description 25
125000004432 carbon atom Chemical group C* 0.000 claims description 25
-1 pivaloyloxy group Chemical group 0.000 claims description 24
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 22
150000003839 salts Chemical class 0.000 claims description 21
125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 13
208000010412 Glaucoma Diseases 0.000 claims description 9
230000004410 intraocular pressure Effects 0.000 claims description 9
206010030043 Ocular hypertension Diseases 0.000 claims description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
238000002360 preparation method Methods 0.000 claims description 8
230000002265 prevention Effects 0.000 claims description 8
238000000034 method Methods 0.000 claims description 6
239000004480 active ingredient Substances 0.000 claims description 4
239000000470 constituent Substances 0.000 claims description 2
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 102
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 81
239000000243 solution Substances 0.000 description 54
150000001875 compounds Chemical class 0.000 description 49
239000000203 mixture Substances 0.000 description 36
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 28
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 21
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 21
229940126062 Compound A Drugs 0.000 description 19
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 19
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 19
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 17
239000002904 solvent Substances 0.000 description 17
238000012360 testing method Methods 0.000 description 16
238000005160 1H NMR spectroscopy Methods 0.000 description 15
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
230000000694 effects Effects 0.000 description 14
IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical class CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 14
235000017557 sodium bicarbonate Nutrition 0.000 description 14
229910000030 sodium bicarbonate Inorganic materials 0.000 description 14
239000012267 brine Substances 0.000 description 13
239000012530 fluid Substances 0.000 description 13
239000011541 reaction mixture Substances 0.000 description 13
229920006395 saturated elastomer Polymers 0.000 description 13
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 13
239000003889 eye drop Substances 0.000 description 12
229940012356 eye drops Drugs 0.000 description 12
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 12
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 11
239000003795 chemical substances by application Substances 0.000 description 11
238000001816 cooling Methods 0.000 description 10
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
239000013078 crystal Substances 0.000 description 8
238000004440 column chromatography Methods 0.000 description 7
229940079593 drug Drugs 0.000 description 7
239000003814 drug Substances 0.000 description 7
239000003480 eluent Substances 0.000 description 7
239000000741 silica gel Substances 0.000 description 7
229910002027 silica gel Inorganic materials 0.000 description 7
238000003756 stirring Methods 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
VZTDIZULWFCMLS-UHFFFAOYSA-N ammonium formate Chemical compound [NH4+].[O-]C=O VZTDIZULWFCMLS-UHFFFAOYSA-N 0.000 description 6
230000035699 permeability Effects 0.000 description 6
230000003389 potentiating effect Effects 0.000 description 6
238000010992 reflux Methods 0.000 description 6
101150041968 CDC13 gene Proteins 0.000 description 5
239000008280 blood Substances 0.000 description 5
210000004369 blood Anatomy 0.000 description 5
230000037396 body weight Effects 0.000 description 5
230000008602 contraction Effects 0.000 description 5
239000012153 distilled water Substances 0.000 description 5
238000004128 high performance liquid chromatography Methods 0.000 description 5
239000012528 membrane Substances 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
230000035515 penetration Effects 0.000 description 5
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 5
LPAJCOGMIXSKKG-GOSISDBHSA-N 5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-1-(3-hydroxypropyl)indole-7-carboxamide Chemical compound CCOC1=CC=CC=C1OCCN[C@H](C)CC1=CC(C(N)=O)=C(N(CCCO)C=C2)C2=C1 LPAJCOGMIXSKKG-GOSISDBHSA-N 0.000 description 4
208000001953 Hypotension Diseases 0.000 description 4
208000001089 Multiple system atrophy Diseases 0.000 description 4
238000005481 NMR spectroscopy Methods 0.000 description 4
206010031127 Orthostatic hypotension Diseases 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
IUGQFMIATSVYLK-UHFFFAOYSA-N benzyl 2-(4-hydroxyphenyl)acetate Chemical compound C1=CC(O)=CC=C1CC(=O)OCC1=CC=CC=C1 IUGQFMIATSVYLK-UHFFFAOYSA-N 0.000 description 4
229960003612 bunazosin hydrochloride Drugs 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
230000036543 hypotension Effects 0.000 description 4
QMKUYPGVVVLYSR-UHFFFAOYSA-N propyl 2,2-dimethylpropanoate Chemical compound CCCOC(=O)C(C)(C)C QMKUYPGVVVLYSR-UHFFFAOYSA-N 0.000 description 4
125000006239 protecting group Chemical group 0.000 description 4
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 4
UUQSFEQUZOKCHP-OAQYLSRUSA-N tert-butyl n-[(2r)-1-[7-carbamoyl-1-(3-hydroxypropyl)-2,3-dihydroindol-5-yl]propan-2-yl]-n-[2-(2-ethoxyphenoxy)ethyl]carbamate Chemical compound CCOC1=CC=CC=C1OCCN(C(=O)OC(C)(C)C)[C@H](C)CC(C=C1C(N)=O)=CC2=C1N(CCCO)CC2 UUQSFEQUZOKCHP-OAQYLSRUSA-N 0.000 description 4
SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 description 3
CTMYLDUPTAZFCT-OAQYLSRUSA-N 3-[7-carbamoyl-5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]indol-1-yl]propyl 2,2-dimethylpropanoate Chemical compound CCOC1=CC=CC=C1OCCN[C@H](C)CC1=CC(C(N)=O)=C(N(CCCOC(=O)C(C)(C)C)C=C2)C2=C1 CTMYLDUPTAZFCT-OAQYLSRUSA-N 0.000 description 3
OKXAFOMCBQVAHI-ZMBIFBSDSA-N 3-[7-carbamoyl-5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]indol-1-yl]propyl 2,2-dimethylpropanoate;hydrochloride Chemical compound Cl.CCOC1=CC=CC=C1OCCN[C@H](C)CC1=CC(C(N)=O)=C(N(CCCOC(=O)C(C)(C)C)C=C2)C2=C1 OKXAFOMCBQVAHI-ZMBIFBSDSA-N 0.000 description 3
ZYBXLNNJVLQAIN-GOSISDBHSA-N 5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-1-(3-hydroxypropyl)-2,3-dihydroindole-7-carboxamide Chemical compound CCOC1=CC=CC=C1OCCN[C@H](C)CC(C=C1C(N)=O)=CC2=C1N(CCCO)CC2 ZYBXLNNJVLQAIN-GOSISDBHSA-N 0.000 description 3
GPWOZMLUYFBWBB-GMUIIQOCSA-N 5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-1-(3-hydroxypropyl)indole-7-carboxamide;hydrochloride Chemical compound Cl.CCOC1=CC=CC=C1OCCN[C@H](C)CC1=CC(C(N)=O)=C(N(CCCO)C=C2)C2=C1 GPWOZMLUYFBWBB-GMUIIQOCSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
108090000604 Hydrolases Proteins 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
241000700159 Rattus Species 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
229910000147 aluminium phosphate Inorganic materials 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
230000000903 blocking effect Effects 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
235000015165 citric acid Nutrition 0.000 description 3
210000004087 cornea Anatomy 0.000 description 3
230000005284 excitation Effects 0.000 description 3
238000005558 fluorometry Methods 0.000 description 3
150000002476 indolines Chemical class 0.000 description 3
238000009434 installation Methods 0.000 description 3
229960002748 norepinephrine Drugs 0.000 description 3
SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 description 3
239000008363 phosphate buffer Substances 0.000 description 3
LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 3
239000011780 sodium chloride Substances 0.000 description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
VICSLOHTZDWOFF-QGZVFWFLSA-N 1-(3-hydroxypropyl)-5-[(2r)-2-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethylamino]propyl]indole-7-carboxamide Chemical compound N([C@@H](CC=1C=C2C=CN(CCCO)C2=C(C(N)=O)C=1)C)CCOC1=CC=CC=C1OCC(F)(F)F VICSLOHTZDWOFF-QGZVFWFLSA-N 0.000 description 2
OXQGTIUCKGYOAA-UHFFFAOYSA-N 2-Ethylbutanoic acid Chemical class CCC(CC)C(O)=O OXQGTIUCKGYOAA-UHFFFAOYSA-N 0.000 description 2
SMUKODJVMQOSAB-UHFFFAOYSA-N 2-ethylbutanoyl chloride Chemical compound CCC(CC)C(Cl)=O SMUKODJVMQOSAB-UHFFFAOYSA-N 0.000 description 2
SPIYQPPDQNLNDT-MRXNPFEDSA-N 3-[5-[(2r)-2-aminopropyl]-7-cyano-2,3-dihydroindol-1-yl]propyl benzoate Chemical compound C1=2C(C#N)=CC(C[C@H](N)C)=CC=2CCN1CCCOC(=O)C1=CC=CC=C1 SPIYQPPDQNLNDT-MRXNPFEDSA-N 0.000 description 2
CBFCMNHKMMHMPJ-XMMPIXPASA-N 3-[7-carbamoyl-5-[(2r)-2-[(2-methylpropan-2-yl)oxycarbonyl-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]amino]propyl]indol-1-yl]propyl 2-ethylbutanoate Chemical compound CC(C)(C)OC(=O)N([C@H](C)CC=1C=C2C=CN(C2=C(C(N)=O)C=1)CCCOC(=O)C(CC)CC)CCOC1=CC=CC=C1OCC(F)(F)F CBFCMNHKMMHMPJ-XMMPIXPASA-N 0.000 description 2
BSMVRQLNZFJKRJ-XMMPIXPASA-N 3-[7-carbamoyl-5-[(2r)-2-[2-(2-ethoxyphenoxy)ethyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propyl]-2,3-dihydroindol-1-yl]propyl 2,2-dimethylpropanoate Chemical compound CCOC1=CC=CC=C1OCCN(C(=O)OC(C)(C)C)[C@H](C)CC(C=C1C(N)=O)=CC2=C1N(CCCOC(=O)C(C)(C)C)CC2 BSMVRQLNZFJKRJ-XMMPIXPASA-N 0.000 description 2
IENUJLYMYCPJBQ-XMMPIXPASA-N 3-[7-cyano-5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-2,3-dihydroindol-1-yl]propyl benzoate Chemical compound CCOC1=CC=CC=C1OCCN[C@H](C)CC(C=C1C#N)=CC2=C1N(CCCOC(=O)C=1C=CC=CC=1)CC2 IENUJLYMYCPJBQ-XMMPIXPASA-N 0.000 description 2
DBQYWUDHQGTRCW-LJQANCHMSA-N 5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-1-(3-hydroxypropyl)-2,3-dihydroindole-7-carbonitrile Chemical compound CCOC1=CC=CC=C1OCCN[C@H](C)CC(C=C1C#N)=CC2=C1N(CCCO)CC2 DBQYWUDHQGTRCW-LJQANCHMSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
PCBZRNYXXCIELG-WYFCWLEVSA-N COC1=CC=C(C[C@H](NC(=O)OC2CCCC3(C2)OOC2(O3)C3CC4CC(C3)CC2C4)C(=O)N[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O)N2C=NC3=C2N=CN=C3N(C)C)C=C1 Chemical compound COC1=CC=C(C[C@H](NC(=O)OC2CCCC3(C2)OOC2(O3)C3CC4CC(C3)CC2C4)C(=O)N[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O)N2C=NC3=C2N=CN=C3N(C)C)C=C1 PCBZRNYXXCIELG-WYFCWLEVSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
241000283977 Oryctolagus Species 0.000 description 2
241000283973 Oryctolagus cuniculus Species 0.000 description 2
241000700157 Rattus norvegicus Species 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
BLGXFZZNTVWLAY-CCZXDCJGSA-N Yohimbine Natural products C1=CC=C2C(CCN3C[C@@H]4CC[C@@H](O)[C@H]([C@H]4C[C@H]33)C(=O)OC)=C3NC2=C1 BLGXFZZNTVWLAY-CCZXDCJGSA-N 0.000 description 2
239000008351 acetate buffer Substances 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
BLGXFZZNTVWLAY-UHFFFAOYSA-N beta-Yohimbin Natural products C1=CC=C2C(CCN3CC4CCC(O)C(C4CC33)C(=O)OC)=C3NC2=C1 BLGXFZZNTVWLAY-UHFFFAOYSA-N 0.000 description 2
230000036772 blood pressure Effects 0.000 description 2
231100000478 corneal permeability Toxicity 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000002198 insoluble material Substances 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
230000002035 prolonged effect Effects 0.000 description 2
239000012264 purified product Substances 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
230000001603 reducing effect Effects 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
235000019333 sodium laurylsulphate Nutrition 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
230000009885 systemic effect Effects 0.000 description 2
KOPCPLUGJAGRLM-HXUWFJFHSA-N tert-butyl n-[(2r)-1-[7-carbamoyl-1-(3-hydroxypropyl)-2,3-dihydroindol-5-yl]propan-2-yl]-n-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]carbamate Chemical compound CC(C)(C)OC(=O)N([C@@H](CC=1C=C(C=2N(CCCO)CCC=2C=1)C(N)=O)C)CCOC1=CC=CC=C1OCC(F)(F)F KOPCPLUGJAGRLM-HXUWFJFHSA-N 0.000 description 2
GGNNNBSQZZITCH-OAQYLSRUSA-N tert-butyl n-[(2r)-1-[7-carbamoyl-1-(3-hydroxypropyl)indol-5-yl]propan-2-yl]-n-[2-(2-ethoxyphenoxy)ethyl]carbamate Chemical compound CCOC1=CC=CC=C1OCCN(C(=O)OC(C)(C)C)[C@H](C)CC1=CC(C(N)=O)=C(N(CCCO)C=C2)C2=C1 GGNNNBSQZZITCH-OAQYLSRUSA-N 0.000 description 2
125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
238000011200 topical administration Methods 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
BLGXFZZNTVWLAY-SCYLSFHTSA-N yohimbine Chemical compound C1=CC=C2C(CCN3C[C@@H]4CC[C@H](O)[C@@H]([C@H]4C[C@H]33)C(=O)OC)=C3NC2=C1 BLGXFZZNTVWLAY-SCYLSFHTSA-N 0.000 description 2
229960000317 yohimbine Drugs 0.000 description 2
AADVZSXPNRLYLV-UHFFFAOYSA-N yohimbine carboxylic acid Natural products C1=CC=C2C(CCN3CC4CCC(C(C4CC33)C(O)=O)O)=C3NC2=C1 AADVZSXPNRLYLV-UHFFFAOYSA-N 0.000 description 2
BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
WLRMANUAADYWEA-NWASOUNVSA-N (S)-timolol maleate Chemical compound OC(=O)\C=C/C(O)=O.CC(C)(C)NC[C@H](O)COC1=NSN=C1N1CCOCC1 WLRMANUAADYWEA-NWASOUNVSA-N 0.000 description 1
VUAXHMVRKOTJKP-UHFFFAOYSA-N 2,2-dimethylbutyric acid Chemical class CCC(C)(C)C(O)=O VUAXHMVRKOTJKP-UHFFFAOYSA-N 0.000 description 1
JVSFQJZRHXAUGT-UHFFFAOYSA-N 2,2-dimethylpropanoyl chloride Chemical compound CC(C)(C)C(Cl)=O JVSFQJZRHXAUGT-UHFFFAOYSA-N 0.000 description 1
FKLQNFXTDRYXEV-UHFFFAOYSA-N 2-(2-ethoxyphenoxy)ethyl methanesulfonate Chemical compound CCOC1=CC=CC=C1OCCOS(C)(=O)=O FKLQNFXTDRYXEV-UHFFFAOYSA-N 0.000 description 1
KYUCVOVGODORNE-NUFNRNBZSA-N 3-[5-[(2r)-2-aminopropyl]-7-cyano-2,3-dihydroindol-1-yl]propyl benzoate;(2r,3r)-2,3-dihydroxybutanedioic acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O.C1=2C(C#N)=CC(C[C@H](N)C)=CC=2CCN1CCCOC(=O)C1=CC=CC=C1 KYUCVOVGODORNE-NUFNRNBZSA-N 0.000 description 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
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OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
229940122601 Esterase inhibitor Drugs 0.000 description 1
WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
206010020772 Hypertension Diseases 0.000 description 1
CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
229960000583 acetic acid Drugs 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
231100000215 acute (single dose) toxicity testing Toxicity 0.000 description 1
238000011047 acute toxicity test Methods 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
ZRYCZAWRXHAAPZ-UHFFFAOYSA-N alpha,alpha-dimethyl valeric acid Chemical class CCCC(C)(C)C(O)=O ZRYCZAWRXHAAPZ-UHFFFAOYSA-N 0.000 description 1
102000015007 alpha-adrenergic receptor activity proteins Human genes 0.000 description 1
108040006816 alpha-adrenergic receptor activity proteins Proteins 0.000 description 1
BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
230000002421 anti-septic effect Effects 0.000 description 1
229940064004 antiseptic throat preparations Drugs 0.000 description 1
210000001742 aqueous humor Anatomy 0.000 description 1
235000003704 aspartic acid Nutrition 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
229940092714 benzenesulfonic acid Drugs 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
UDEWPOVQBGFNGE-UHFFFAOYSA-N benzoic acid n-propyl ester Natural products CCCOC(=O)C1=CC=CC=C1 UDEWPOVQBGFNGE-UHFFFAOYSA-N 0.000 description 1
OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
210000004204 blood vessel Anatomy 0.000 description 1
239000000872 buffer Substances 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
OBNCKNCVKJNDBV-UHFFFAOYSA-N butanoic acid ethyl ester Natural products CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
210000002808 connective tissue Anatomy 0.000 description 1
230000009989 contractile response Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
206010013990 dysuria Diseases 0.000 description 1
239000002329 esterase inhibitor Substances 0.000 description 1
ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 1
230000029142 excretion Effects 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
229940013688 formic acid Drugs 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
235000011087 fumaric acid Nutrition 0.000 description 1
235000013922 glutamic acid Nutrition 0.000 description 1
239000004220 glutamic acid Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
229940071870 hydroiodic acid Drugs 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 1
125000001041 indolyl group Chemical group 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
238000003780 insertion Methods 0.000 description 1
230000037431 insertion Effects 0.000 description 1
XXUPXHKCPIKWLR-JHUOEJJVSA-N isopropyl unoprostone Chemical compound CCCCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(=O)OC(C)C XXUPXHKCPIKWLR-JHUOEJJVSA-N 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000007788 liquid Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000001630 malic acid Substances 0.000 description 1
235000011090 malic acid Nutrition 0.000 description 1
239000000463 material Substances 0.000 description 1
FBBDOOHMGLLEGJ-UHFFFAOYSA-N methane;hydrochloride Chemical compound C.Cl FBBDOOHMGLLEGJ-UHFFFAOYSA-N 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
OLXYLDUSSBULGU-UHFFFAOYSA-N methyl pyridine-4-carboxylate Chemical compound COC(=O)C1=CC=NC=C1 OLXYLDUSSBULGU-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
239000000843 powder Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
DZAQGDJIAAXOAG-UHFFFAOYSA-N propyl 2,2-dimethylbutanoate Chemical compound CCCOC(=O)C(C)(C)CC DZAQGDJIAAXOAG-UHFFFAOYSA-N 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000000284 resting effect Effects 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
230000007017 scission Effects 0.000 description 1
PNCPYILNMDWPEY-QGZVFWFLSA-N silodosin Chemical compound N([C@@H](CC=1C=C(C=2N(CCCO)CCC=2C=1)C(N)=O)C)CCOC1=CC=CC=C1OCC(F)(F)F PNCPYILNMDWPEY-QGZVFWFLSA-N 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000011775 sodium fluoride Substances 0.000 description 1
235000013024 sodium fluoride Nutrition 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
238000013112 stability test Methods 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
ZYCYVMNPICJOBM-HXUWFJFHSA-N tert-butyl n-[(2r)-1-[7-carbamoyl-1-(3-hydroxypropyl)indol-5-yl]propan-2-yl]-n-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]carbamate Chemical compound CC(C)(C)OC(=O)N([C@@H](CC=1C=C2C=CN(CCCO)C2=C(C(N)=O)C=1)C)CCOC1=CC=CC=C1OCC(F)(F)F ZYCYVMNPICJOBM-HXUWFJFHSA-N 0.000 description 1
210000001550 testis Anatomy 0.000 description 1
229960005221 timolol maleate Drugs 0.000 description 1
230000000699 topical effect Effects 0.000 description 1
229950008081 unoprostone isopropyl Drugs 0.000 description 1
210000001177 vas deferen Anatomy 0.000 description 1

Classifications

- 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
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Life Sciences & Earth Sciences (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Bioinformatics & Cheminformatics (AREA)
Pharmacology & Pharmacy (AREA)
Engineering & Computer Science (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Ophthalmology & Optometry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Indole Compounds (AREA)

NO20004277A 1998-02-27 2000-08-25 Indolderivater og farmasoytiske sammensetninger omfattende det samme NO317257B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP9057298		1998-02-27
PCT/JP1999/000732 WO1999043652A1 (en)	1998-02-27	1999-02-19	Indole derivatives and medicinal compositions containing the same

Publications (3)

Publication Number	Publication Date
NO20004277D0 NO20004277D0 (no)	2000-08-25
NO20004277L NO20004277L (no)	2000-09-11
NO317257B1 true NO317257B1 (no)	2004-09-27

Family

ID=14002150

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO20004277A NO317257B1 (no)	1998-02-27	2000-08-25	Indolderivater og farmasoytiske sammensetninger omfattende det samme

Country Status (23)

Country	Link
US (1)	US6310086B1 (ja)
EP (1)	EP1057813B1 (ja)
JP (1)	JP4342101B2 (ja)
KR (1)	KR100576207B1 (ja)
CN (1)	CN1157375C (ja)
AR (1)	AR014964A1 (ja)
AT (1)	ATE264841T1 (ja)
AU (1)	AU766088B2 (ja)
BR (1)	BR9908301A (ja)
CA (1)	CA2321547C (ja)
DE (1)	DE69916586T2 (ja)
DK (1)	DK1057813T3 (ja)
ES (1)	ES2220043T3 (ja)
HU (1)	HUP0100680A3 (ja)
NO (1)	NO317257B1 (ja)
NZ (1)	NZ506497A (ja)
PE (1)	PE20000329A1 (ja)
PL (1)	PL342477A1 (ja)
RU (1)	RU2212404C2 (ja)
SK (1)	SK12722000A3 (ja)
TW (2)	TWI249525B (ja)
WO (1)	WO1999043652A1 (ja)
ZA (1)	ZA991590B (ja)

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ATE264841T1 (de)	1998-02-27	2004-05-15	Kissei Pharmaceutical	Indol-derivate und medizinische zusammensetzungen die diese enthalten
JP4634560B2 (ja) *	2000-01-14	2011-02-16	キッセイ薬品工業株式会社	光学活性なインドリン誘導体の製造方法およびその製造中間体
EP1293206A4 (en) *	2000-05-15	2005-09-21	Kissei Pharmaceutical	LIQUID PREPARATION BASED ON WATER
CA2408913A1 (en)	2000-05-16	2001-11-22	Takeda Chemical Industries, Ltd.	Melanin-concentrating hormone antagonist
JP4921646B2 (ja) *	2001-03-08	2012-04-25	キッセイ薬品工業株式会社	１−（３−ベンジルオキシプロピル）−５−（２−置換プロピル）インドリン誘導体およびその使用方法
WO2003006061A1 (en) *	2001-07-13	2003-01-23	Kissei Pharmaceutical Co., Ltd.	Medicinal compositions for opthalmic use
UA78854C2 (en) *	2002-09-06	2007-04-25	Kissei Pharmaceutical	Crystal for an oral solid drug and oral solid drug for dysuria treatment containing the same
HU225505B1 (en) *	2002-09-09	2007-01-29	Richter Gedeon Vegyeszet	Process for the preparation of r-(-)-tamsulosin hydrochloride and novel intermediates
TW200616967A (en)	2004-06-24	2006-06-01	Smithkline Beecham Corp	Novel indazole carboxamides and their use
EP1806340B1 (en) *	2004-10-27	2011-05-04	Kissei Pharmaceutical Co., Ltd.	Indoline compound and process for producing the same
US8629161B2 (en)	2005-06-21	2014-01-14	Kowa Co., Ltd.	Preventive or remedy for glaucoma
US8063071B2 (en)	2007-10-31	2011-11-22	GlaxoSmithKline, LLC	Chemical compounds
US20100076010A1 (en) *	2007-02-26	2010-03-25	Concert Pharmaceuticals, Inc.	Alpha 1a-adrenoceptor antagonists
WO2008106125A2 (en) *	2007-02-26	2008-09-04	Concert Pharmaceuticals, Inc.	Deuterated derivatives of silodosin as alpha la-adrenoceptor antagonists
PE20081889A1 (es)	2007-03-23	2009-03-05	Smithkline Beecham Corp	Indol carboxamidas como inhibidores de ikk2
JP2012520257A (ja)	2009-03-10	2012-09-06	グラクソグループリミテッド	Ｉｋｋ２阻害剤としてのインドール誘導体
CN104211631A (zh) *	2013-05-30	2014-12-17	中国科学院上海药物研究所	一类吲哚类化合物、其制备方法、药物组合物及应用
WO2016042441A1 (en)	2014-09-18	2016-03-24	Mankind Research Centre	A novel process for the preparation of considerably pure silodosin
ES2607639B1 (es)	2015-09-30	2018-02-28	Urquima, S.A	Sal de ácido maleico de un intermedio de silodosina

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Publication number	Priority date	Publication date	Assignee	Title
US5021410A (en)	1989-05-22	1991-06-04	Allergan, Inc.	Combinations of selective alpha-adrenergic agonists and antagonists useful in lowering intraocular pressure
US5068234A (en) *	1990-02-26	1991-11-26	Sterling Drug Inc.	3-arylcarbonyl-1-(c-attached-n-heteryl)-1h-indoles
EP0600675B1 (en)	1992-12-02	1998-07-08	Kissei Pharmaceutical Co., Ltd.	Indoline compounds for the treatment of dysuria
JP3331047B2 (ja) *	1994-06-01	2002-10-07	キッセイ薬品工業株式会社	インドリン誘導体
JP3331048B2 (ja) *	1994-06-01	2002-10-07	キッセイ薬品工業株式会社	インドール誘導体
JPH08143557A (ja) *	1994-11-24	1996-06-04	Toyobo Co Ltd	新規なフェニルピペラジン誘導体、その塩及びその溶媒和物
JPH0912563A (ja) *	1995-06-30	1997-01-14	Toyobo Co Ltd	新規ベンジルアルコ−ル誘導体、その製造方法およびその用途
AU9095998A (en) *	1997-09-22	1999-04-12	Kissei Pharmaceutical Co. Ltd.	Remedies for dysuria resulting from prostatic hypertrophy
ATE264841T1 (de)	1998-02-27	2004-05-15	Kissei Pharmaceutical	Indol-derivate und medizinische zusammensetzungen die diese enthalten

1999
- 1999-02-19 AT AT99905242T patent/ATE264841T1/de not_active IP Right Cessation
- 1999-02-19 AU AU25478/99A patent/AU766088B2/en not_active Ceased
- 1999-02-19 WO PCT/JP1999/000732 patent/WO1999043652A1/ja not_active Ceased
- 1999-02-19 KR KR1020007009536A patent/KR100576207B1/ko not_active Expired - Fee Related
- 1999-02-19 DK DK99905242T patent/DK1057813T3/da active
- 1999-02-19 PL PL99342477A patent/PL342477A1/xx not_active Application Discontinuation
- 1999-02-19 BR BR9908301-9A patent/BR9908301A/pt not_active IP Right Cessation
- 1999-02-19 NZ NZ506497A patent/NZ506497A/xx unknown
- 1999-02-19 EP EP99905242A patent/EP1057813B1/en not_active Expired - Lifetime
- 1999-02-19 US US09/622,871 patent/US6310086B1/en not_active Expired - Lifetime
- 1999-02-19 RU RU2000122435/04A patent/RU2212404C2/ru not_active IP Right Cessation
- 1999-02-19 HU HU0100680A patent/HUP0100680A3/hu unknown
- 1999-02-19 DE DE69916586T patent/DE69916586T2/de not_active Expired - Lifetime
- 1999-02-19 JP JP2000533410A patent/JP4342101B2/ja not_active Expired - Fee Related
- 1999-02-19 ES ES99905242T patent/ES2220043T3/es not_active Expired - Lifetime
- 1999-02-19 SK SK1272-2000A patent/SK12722000A3/sk unknown
- 1999-02-19 CN CNB998033219A patent/CN1157375C/zh not_active Expired - Lifetime
- 1999-02-19 CA CA002321547A patent/CA2321547C/en not_active Expired - Fee Related
- 1999-02-22 TW TW088102531A patent/TWI249525B/zh active
- 1999-02-22 TW TW089116222A patent/TWI241293B/zh not_active IP Right Cessation
- 1999-02-26 ZA ZA9901590A patent/ZA991590B/xx unknown
- 1999-02-26 PE PE1999000167A patent/PE20000329A1/es not_active Application Discontinuation
- 1999-02-26 AR ARP990100809A patent/AR014964A1/es unknown
2000
- 2000-08-25 NO NO20004277A patent/NO317257B1/no unknown

Also Published As

Publication number	Publication date
NO20004277D0 (no)	2000-08-25
EP1057813A4 (en)	2001-11-21
CA2321547A1 (en)	1999-09-02
HK1036974A1 (en)	2002-01-25
DE69916586D1 (de)	2004-05-27
KR100576207B1 (ko)	2006-05-03
PE20000329A1 (es)	2000-04-13
HUP0100680A2 (hu)	2001-08-28
HUP0100680A3 (en)	2001-09-28
PL342477A1 (en)	2001-06-04
DE69916586T2 (de)	2004-09-16
DK1057813T3 (da)	2004-08-16
NO20004277L (no)	2000-09-11
WO1999043652A1 (en)	1999-09-02
CN1291976A (zh)	2001-04-18
EP1057813B1 (en)	2004-04-21
KR20010041403A (ko)	2001-05-15
SK12722000A3 (sk)	2001-03-12
EP1057813A1 (en)	2000-12-06
BR9908301A (pt)	2000-10-31
ES2220043T3 (es)	2004-12-01
CA2321547C (en)	2010-01-19
RU2212404C2 (ru)	2003-09-20
JP4342101B2 (ja)	2009-10-14
US6310086B1 (en)	2001-10-30
CN1157375C (zh)	2004-07-14
AR014964A1 (es)	2001-04-11
ZA991590B (en)	1999-08-27
AU766088B2 (en)	2003-10-09
AU2547899A (en)	1999-09-15
NZ506497A (en)	2004-12-24
TWI249525B (en)	2006-02-21
ATE264841T1 (de)	2004-05-15
TWI241293B (en)	2005-10-11

Publication	Publication Date	Title
NO317257B1 (no)	2004-09-27	Indolderivater og farmasoytiske sammensetninger omfattende det samme
EP0489579B1 (en)	1995-03-29	Peptidyl derivatives
CZ150596A3 (en)	1997-05-14	Tetrahydrocarbazole derivatives, process of their preparation and pharmaceutical compositions containing thereof
JPWO1999043652A1 (ja)	2002-10-08	インドール誘導体および当該誘導体を含有する医薬品組成物
BG97493A (bg)	1994-03-24	Сулфонамидокарбоксамиди
CS253702B2 (en)	1987-12-17	Process for preparing new 3-/1-imidazolylalkyl/indoles
DK164557B (da)	1992-07-13	Derivater af cis,endo-2-azabicyclo-oe5.3.0aa-decan-3-carboxylsyre samt laegemiddel indeholdende dem
US8980897B2 (en)	2015-03-17	Benzenesulfonamide compounds, method for synthesizing same, and use thereof in medicine as well as in cosmetics
US4071552A (en)	1978-01-31	Aryloxy aminobutanols, their preparation and use thereof
WO1998031669A1 (fr)	1998-07-23	Nouvelles arylpiperazines derivees de piperidine comme medicaments antidepresseurs
JPH047741B2 (ja)	1992-02-12
NO821651L (no)	1982-11-22	Substituerte tryptaminderivater av tienyloksypropanolaminer, fremgangsmaate til deres fremstilling, farmasoeytiske preparater paa basis av disse forbindelser samt deres anvendelse
CZ20003126A3 (cs)	2000-12-13	Deriváty indolu a farmaceutické prostředky, které je obsahují
FR2950057A1 (fr)	2011-03-18	Nouveaux composes benzene-carboxylamides, leur procede de synthese et leur utilisation en medecine ainsi qu'en cosmetique
MXPA00008396A (en)	2001-07-31	Indole derivatives and medicinal compositions containing the same
EP1415666A1 (en)	2004-05-06	Medicinal compositions for opthalmic use
WO1996026922A1 (fr)	1996-09-06	Nouveaux derives bi-tryptaminiques sulfonamides, leur procede de preparation et leur utilisation a titre de medicaments
IE921610A1 (en)	1992-12-16	Peptidyl derivatives
HK1036974B (en)	2004-12-24	Indole derivatives and medicinal compositions containing the same