KR920703040A - 진경 특성 및 신경보호특성을 갖는 아릴알킬-아민 및-아미드 - Google Patents
진경 특성 및 신경보호특성을 갖는 아릴알킬-아민 및-아미드Info
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- KR920703040A KR920703040A KR1019920701879A KR920701879A KR920703040A KR 920703040 A KR920703040 A KR 920703040A KR 1019920701879 A KR1019920701879 A KR 1019920701879A KR 920701879 A KR920701879 A KR 920701879A KR 920703040 A KR920703040 A KR 920703040A
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- phenyl
- amino
- acetamide
- methylethyl
- propylamine
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Abstract
내용 없음
Description
진경 특성 및 신경보호특성을 갖는 아릴알킬-아민 및-아미드
[도면의 간단한 설명]
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (8)
- 약제학적으로 허용되는 보조제, 희석제 또는 담체와 함께 하기 일반식(I)의 화합물 또는 이의 약제학적으로 허용되는 염을 포함하는 약제학적 조성물.상기식에서, Ar1및 Ar2는 동일하거나 상이할 수 있으며, 하나이상의 아미노, 니트로, 염소, 브롬, 하이드록시, C1-C6알콕시, C1-C6알킬 또는 시아노에 의해 독립적으로 치환된 페닐이거나 Ar1또는 Ar2는 또한 페닐일 수 있고; R1은 수소 또는 C1-C6알킬이며, R2는 수소 또는 COCH2NH2이고; R3는 수소 또는 C1-C6알킬이며; 단, R2가 수소인 경우, Ar1및 Ar2중의 하나 또는 모두는 또한 페닐, 플루오로페닐 또는 2-, 3- 또는 4-피리디닐일 수 있고 R1은 또한 C1-C6알콕시카보닐 또는 트리플루오로메틸이다.
- 하기 일반식(IA)의 화합물 및 이의 약제학적으로 허용되는 염.상기식에서, Ar1a, R1a, R2a및 R3a는 제1항의 Ar1, Ar2, R1, R2및 R3에 대해 각각 정의된 바와 같으며, 단, R2a가 수소인 경우, R1a는 C1-C6알킬이다.
- 제2항에 있어서, Ar1a및 Ar2a중의 하나 또는 모두가 4-하이드록시페닐인 화합물.
- 제2항에 있어서, Ar1a및 Ar2a가 일- 또는 이치환된 화합물.
- 제2항에 있어서, R1a가 메틸인 화합물.
- 제2항에 있어서, R3a가 메틸인 화합물.
- 신경계 질환으로 고통을 받는 환자에게, 제1항에서 정의한 바와 같은 일반식(I)의 화합물 또는 이의 약제학적으로 허용되는 염을 투여함을 특징으로 하여, 신경계 질환을 치료하거나 예방하는 방법.
- 제2항에 있어서, 화합물이:1-(4-하이드록시페닐)-2-페닐-2-프로필아민; 1-(4-하이드록시페닐)-2-페닐에틸아민; 1-페닐-2-(4-하이드록시페닐)에틸아민; 1,2-비스(4-하이드록시페닐)에틸아민; 1-페닐-2-(4-하이드록시페닐)-2-프로필아민; 1,2-비스(4-하이드록시페닐)-2-프로필아민; 1-(3-니트로페닐)-2-페닐-2-프로필아민; 1-(3-클로로페닐)-2-페닐-2-프로필아민; 1-(3-브로모페닐)-2-페닐-2-프로필아민; 1-(3-시아노페닐)-2-페닐-2-프로필아민; 2-(2-메틸페닐)-1-페닐-2-프로필아민; 1-(4-클로로페닐)-2-페닐-2-프로필아민; 1-페닐-2-(3,4-디클로로페닐)-2-프로필아민; 1-페닐-2-(3-메톡시페닐)-2-프로필아민; 1-페닐-2-[3-((2,2,2-트리클로로에톡시카보닐)아미노)페닐]-2-프로필아민; 2-(3-클로로페닐)-1-페닐-2-프로필아민; 1-(2-클로로페닐)-2-페닐-2-프로필아민; 2-(2-클로로페닐)-1-페닐-2-프로필아민; 1-(3-니트로페닐)-1-페닐-2-프로필아민; 2-(4-클로로페닐)-1-페닐-2-프로필아민; 2-(3,4-디메톡시페닐)-1-페닐-2-프로필아민; 2-(4-메틸페닐)-1-페닐-2-프로필아민; 2-(4-메톡시페닐)-1-페닐-2-프로필아민; 1-(3,4-디클로로페닐)-2-페닐-2-프로필아민; 1-(4-메톡시페닐)-2-페닐-2-프로필아민; 2-아미노-N-[1-(3-클로로페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[2-(2-클로로페닐)-1-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[2-(4-클로로페닐)-1-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(2-메틸페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(2-클로로페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[2-(3-클로로페닐)-1-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[2-(3-아미노페닐)-1-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[2-(3-브로모페닐)-1-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[2-(3-니트로페닐)-1-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(3-니트로페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(3-아미노페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(4- 클로로페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(3,4-디클로로페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(3,4-디메톡시페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[2-(3-시아노페닐)-1-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(4-메틸페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(4-하이드록시페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(4-하이드록시페닐)-2-페닐에틸]아세트아미드; 2-아미노-N-[1-(4-하이드록시페닐)-1-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[2-(4-하이드록시페닐)-1-페닐에틸]아세트아미드; 2-아미노-N-[1,2-비스(4-하이드록시페닐)-1-메틸에틸]아세트아미드; 2-아미노-N-[1,2-비스(4-하이드록시페닐)에틸]아세트아미드; 2-아미노-N-[1-(3-메톡시페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[1-(4-메톡시페닐)-2-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[2-(3,4-디클로로페닐)-1-페닐-1-메틸에틸]아세트아미드; 2-아미노-N-[2-(4-메톡시페닐)-1-페닐-1-메틸에틸]아세트아미드; 또는 이의 약제학적으로 허용되는 염인 화합물.※ 참고사항:최초출원 내용에 의하여 공개하는 것임.
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Application Number | Priority Date | Filing Date | Title |
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US23256688A | 1988-08-12 | 1988-08-12 | |
PCT/GB1990/000184 WO1991011995A1 (en) | 1988-08-12 | 1990-02-07 | Arylalkyl-amines and -amides having anticonvulsant and neuroprotective properties |
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KR920703040A true KR920703040A (ko) | 1992-12-17 |
KR0169998B1 KR0169998B1 (ko) | 1999-02-01 |
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KR1019920701879A KR0169998B1 (ko) | 1988-08-12 | 1990-02-07 | 진경 특성 및 신경보호 특성을 갖는 아릴알킬아민 및 아릴알킬아미드 |
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EP (3) | EP0356035B1 (ko) |
JP (2) | JP2846895B2 (ko) |
KR (1) | KR0169998B1 (ko) |
AT (1) | ATE135206T1 (ko) |
AU (1) | AU654802B2 (ko) |
CA (1) | CA1341136C (ko) |
DE (1) | DE68925933T2 (ko) |
DK (2) | DK175755B1 (ko) |
ES (1) | ES2083972T3 (ko) |
FI (1) | FI111712B (ko) |
GR (1) | GR3020407T3 (ko) |
HU (1) | HU211467A9 (ko) |
IE (3) | IE74216B1 (ko) |
LV (1) | LV11817B (ko) |
NO (1) | NO301974B1 (ko) |
PT (1) | PT91435B (ko) |
SG (1) | SG52662A1 (ko) |
WO (1) | WO1991011995A1 (ko) |
ZA (1) | ZA90878B (ko) |
Families Citing this family (13)
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GB9320273D0 (en) * | 1993-04-01 | 1993-11-17 | Fisons Corp | Compound useful in therapy |
US5455259A (en) * | 1987-02-06 | 1995-10-03 | Fisons Corporation | Compounds for the treatment of neurodegenerative disorders |
ZA908490B (en) * | 1989-10-27 | 1991-07-31 | Fisons Corp | Use of arylalkylamides in the treatment of neurodegenerative diseases |
EP0572560B1 (en) * | 1991-02-22 | 2003-01-29 | SHAPIRO, Howard, K. | Use of pharmaceutical compounds in the treatment of symptoms of disorders related to neurological diseases and etiologically related symptomology |
EP0540318A1 (en) * | 1991-10-30 | 1993-05-05 | Fisons Corporation | 2-Heterocyclicethylamine derivatives and their use as pharmaceuticals |
SG47948A1 (en) * | 1992-04-03 | 1998-04-17 | Astra Ab | Compounds for the treatment of neurodegenerative disorders |
ZA942140B (en) * | 1993-04-01 | 1994-10-03 | Fisons Corp | Salt of (S)-alpha-phenyl-2-pyridineethanamine useful in therapy |
GB9410320D0 (en) * | 1994-05-24 | 1994-07-13 | Fisons Corp | Novel therapeutic method |
SE9901237D0 (sv) * | 1999-04-06 | 1999-04-06 | Astra Ab | Novel use |
PT1545613E (pt) | 2002-07-31 | 2011-09-27 | Seattle Genetics Inc | Conjugados de auristatina e sua utilização para tratamento do cancro, de uma doença autoimune ou de uma doença infecciosa |
WO2007017652A2 (en) * | 2005-08-10 | 2007-02-15 | Astrazeneca Ab | Arylakylamines for the treatment of cancer |
MX2011006680A (es) | 2008-12-24 | 2011-07-12 | Astrazeneca Ab | Compuestos etanaminicos y su uso para tratar la depresion. |
TR201909632T4 (tr) * | 2013-11-05 | 2019-07-22 | Astrazeneca Ab | Nmda antagonisti ön ilaçları. |
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US2503285A (en) * | 1945-10-18 | 1950-04-11 | Winthrop Stearns Inc | Beta-substituted alpha, beta-diphenylethylamines and the preparation thereof |
US2691680A (en) * | 1951-06-16 | 1954-10-12 | George A Breon And Company | N-methyl-1-(3-hydroxyphenyl)-2-phenylethylamine and addition salts thereof |
CH343388A (de) * | 1956-03-09 | 1959-12-31 | Cilag Chemie Aktiengesellschaf | Verfahren zur Herstellung neuer Amide |
NL128079C (ko) * | 1958-04-02 | |||
NL6512616A (ko) * | 1964-09-30 | 1966-03-31 | ||
ES484553A1 (es) * | 1978-10-05 | 1980-05-16 | Hoechst Ag | Un metodo para preparar 4-fenil-1,3-benzodiazepinas |
US4757076A (en) * | 1984-06-18 | 1988-07-12 | Eli Lilly And Company | Method of inhibiting aromatase |
HU207280B (en) * | 1986-09-25 | 1993-03-29 | Chinoin Gyogyszer Es Vegyeszet | Process for producing new phenyl-alkyl-amines and pharmaceutical compositions containing them |
IL84305A (en) * | 1987-02-06 | 1992-01-15 | Fisons Corp | 2-aminoacetamide derivatives |
US4798687A (en) * | 1987-02-06 | 1989-01-17 | Pennwalt Corporation | 2-Amino-N-[1,2-Diphenyl-1-(thifluoromethyl)ethyl]acetamide derivatives |
GB9320273D0 (en) * | 1993-04-01 | 1993-11-17 | Fisons Corp | Compound useful in therapy |
US4769466A (en) * | 1987-02-06 | 1988-09-06 | Pennwalt Corporation | 2-aminoacetamide pyridinyl derivatives |
EP0322582A3 (en) * | 1987-12-07 | 1989-09-13 | Hoechst-Roussel Pharmaceuticals Incorporated | 4-heteroaryl-1,3-benzodiazepines and 2-substituted-alpha-(heteroaryl)benzeneethanamines, a process for their preparation and their use us medicaments |
EP0401253A1 (en) * | 1988-01-20 | 1990-12-12 | Fisons Corporation | 2-amino acetamide derivatives |
GB8801883D0 (en) * | 1988-01-28 | 1988-02-24 | Oldham Crompton Batteries Ltd | Improvements in/relating to clamp reflectors |
ZA908490B (en) * | 1989-10-27 | 1991-07-31 | Fisons Corp | Use of arylalkylamides in the treatment of neurodegenerative diseases |
SG47948A1 (en) * | 1992-04-03 | 1998-04-17 | Astra Ab | Compounds for the treatment of neurodegenerative disorders |
-
1989
- 1989-08-01 SG SG1996007517A patent/SG52662A1/en unknown
- 1989-08-01 EP EP89307815A patent/EP0356035B1/en not_active Expired - Lifetime
- 1989-08-01 EP EP94119942A patent/EP0648745A1/en not_active Withdrawn
- 1989-08-01 DE DE68925933T patent/DE68925933T2/de not_active Expired - Fee Related
- 1989-08-01 ES ES89307815T patent/ES2083972T3/es not_active Expired - Lifetime
- 1989-08-01 EP EP94119941A patent/EP0648489A1/en not_active Withdrawn
- 1989-08-01 AT AT89307815T patent/ATE135206T1/de not_active IP Right Cessation
- 1989-08-11 JP JP1207062A patent/JP2846895B2/ja not_active Expired - Fee Related
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- 1989-08-11 IE IE259689A patent/IE74216B1/en not_active IP Right Cessation
- 1989-08-11 IE IE960774A patent/IE960774L/xx unknown
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- 1989-08-11 IE IE960775A patent/IE960775L/xx unknown
- 1989-08-11 CA CA000608107A patent/CA1341136C/en not_active Expired - Fee Related
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1990
- 1990-02-06 ZA ZA90878A patent/ZA90878B/xx unknown
- 1990-02-07 AU AU50927/90A patent/AU654802B2/en not_active Ceased
- 1990-02-07 WO PCT/GB1990/000184 patent/WO1991011995A1/en active IP Right Grant
- 1990-02-07 KR KR1019920701879A patent/KR0169998B1/ko not_active IP Right Cessation
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1992
- 1992-07-30 NO NO923006A patent/NO301974B1/no unknown
- 1992-08-06 FI FI923540A patent/FI111712B/fi active
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1995
- 1995-06-12 HU HU95P/P00188P patent/HU211467A9/hu unknown
- 1995-07-05 DK DK078995A patent/DK78995A/da not_active Application Discontinuation
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1996
- 1996-03-26 JP JP8069758A patent/JPH08291112A/ja active Pending
- 1996-06-12 GR GR960401582T patent/GR3020407T3/el unknown
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1997
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