KR880009903A - 폴리아민 유도체 - Google Patents
폴리아민 유도체 Download PDFInfo
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- KR880009903A KR880009903A KR1019880000970A KR880000970A KR880009903A KR 880009903 A KR880009903 A KR 880009903A KR 1019880000970 A KR1019880000970 A KR 1019880000970A KR 880000970 A KR880000970 A KR 880000970A KR 880009903 A KR880009903 A KR 880009903A
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Abstract
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Claims (26)
- 일반식(Ⅰ)의 화합물 및 약제학적으로 허용되는 이의 염.상기식에거, n은 내지 6의 정수이고, m은 3 내지 12의 정수이며, R은 포화 또는 불포화된 C1-6하이드로카빌라디칼 또는 -(CH2)X-(Ar)-X이고, 여기에서 X는 0,1 또는 2이고, Ar은 페닐 또는 나프틸이며, X는 H, C1-6알콕시, 할로겐, C1-4알킬, -S(0)XR(여기서, R1은 C1-6알킬이다)이고, 단 n이 2이고 m이 6또는 10인 경우에는 R은 페닐 메틸인 수는 없다.
- 제1항에 있어서, m이 6내지 9의 정수인 화합물.
- 제2항에 있어서, n이 3인 화합물.
- 제2항에 있어서, R이 벤질인 화합물.
- 제2항에 있어서, R이 페닐인 화합물.
- 제2항에 있어서, R이 페닐에틸인 화합물.
- 제2항에 있어서, 비스-벤질-3-7-3인 화합물.
- 제2항에 있어서, 비스-벤질-3-6-3인 화합물.
- 제2항에 있어서, 비스-벤질-3-8-3인 화합물.
- 제1항의 화합물의 치료적 유효량을 투여함을 특징으로 하여, 원생동물에 의해 유발되는 감염증을 치료하는 방법.
- 제10항에 있어서, 오르니틴 데카복실라제 억제제 또는 아르기닌 데카복실라제 억제제와 병용하는 방법.
- 제10항에 있어서, 감염증이 플라스모듐(Plasmodium), 트리파노소마(Trupanosoma) 〔살리바리아(Salivaria) 및 스테르코라리아(Stercoraia)포함〕,레이샤마니아(Leishmania), 트리코모나스(Trichomonas), 바베시아(Babesia), 톡소플라슴마(Toxoplasma), 및 테일레리아(Theileria)로 이루어진 속중에서 선택되는 원생동물에 의해 유발되는 방법.
- 제12항에 있어서, 오르니틴 데카복실라제 억제제 또는 아르기닌 데카복실라제 억제제와 병용하는 방법.
- 제12항에 있어서, 원생동물 감염증에 걸린 숙주가 말라리아에 걸린 숙주인 방법.
- 제12항에 있어서, 원생동물 감염증에 걸린 숙주가 샤가(Chaga)질병에 걸린 숙주인 방법.
- 제14항에 있어서, 병용치료시 α-디플루오로메틸 오르니틴을 사용하는 방법.
- 제15항에 있어서, 병용치료시 α-디플루오로메틸 아르기닌을 사용하는 방법.
- 제16항에 있어서, 폴리아민이 N,N′-비스〔3-〔(페닐메틸)아미노〕프로필〕-1,6-헥산디아민인 방법.
- 제16항에 있어서, 폴리아민이 N,N′-비스〔3-〔(페닐메틸)아미노〕프로필〕-1,7-헵탄디아민인 방법.
- 적절한 N-보호된 테트라민을 일반식(Ⅳ)의 화합물로 반응시킨후, N-말단 알킬화된 생성물을 탈보호시키거나, 일반식(Ⅲ)의 화합물을 일반식(Ⅳ)의 적절한 알데히드로 환원적 알킬화시킨후, 알킬화된 생성물을 N-보호 및 메실화시키고, N-보호 및 메실화된 생성물을 일반식(Ⅴ)의 N-보호된 디아민과 반응시키거나, 부분적으로 N-보호된 테트라민을 아로일 클로라이드로 N-아로일화시킨후 N-아로일화된 생성물을 환원 및 탈보호시키거나, R이 X-(Ar)-(CH2)X(단 X는 0)인 일반식(Ⅰ)의 화합물을 제조하기 위해서 일반식(Ⅵ)의 N-보호된 화합물을 적절한 디할로알칸과 반응시킨후 탈보호시키거나, 또는 R이 불포화된 하이드로카빌 라디칼인 일반식(Ⅰ)의 화합물을 제조하기 위해서는, N-보호된 디아민 메실레이트를 적적한 불포화된 하이드로카빌잔기를 함유하는 N-보호된 아민과 반응시킨후 탈보호시킴을 특징으로하여 일반식(Ⅰ)의 화합물 및 약제학적으로 허용되는 이의 염을 제조하는 방법.상기식에서, n은 2내지 6의 정수이고, m은 3내지 12의 정수이며, R은 포화 또는 불포화된 C1-6하이드로카빌라디칼 또는-(CH2)X-(Ar)-X 이고, 여기에서 X는 0,1 또는 2이고, Ar은 페닐 또는 나프틸이며, X는 H,C1-6알콕시, 할로겐, C1-4알킬, 또는-S(0)XR1(여기에서, R1은 C1-6알킬이다.)이고, 단, n이 2이고 m이 6또는 10인 경우에는 R은 페닐메틸일 수는 없으며, R′는 R이 X-(Ar)-(CH2)X인 경우에 X가 0일 수는 없는 것을 제외하고는 R에 대해 정의한 바와 같고, 단 일반식(Ⅳ)에서는 X-(Ar)-(CH2)X(여기에서는 X는 0이 아니다)이며, n′는 0또는 양의 정수이며, Pro는 N-보호그룹이다.
- 제20항의 방법으로 제조되는 N,N′-비스〔3-〔(페닐메틸)아미노〕프로필〕-1,7-헵탄디아민.
- 제21항에 있어서, N,N′-비스〔3-(아미노)프로필〕-1,7-헵탄디아민을 (브로모메틸)벤젠으로 N-말단 알킬화시키는 방법으로 제조되는 화합물.
- 제20항의 방법으로 제조되는 N,N′-비스〔3-〔(페닐메틸)아미노〕프로필〕-1,8-옥탄디아민.
- 제23항에 있어서, N,N′-비스〔3-(아미노)프로필〕-1,8-옥탄디아민을 (브로모메틸)벤젠으로 N-말단 알킬화시키는 방법으로 제조되는 화합물.
- 제20항의 방법으로 제조되는 N,N′-비스〔3-〔(페닐메틸)아미노〕프로필〕-1,6-헥산디아민.
- 제21항에 있어서, N,N′-비스〔3-〔(아미노)-프로필〕-1,6〕-헥산디아민을 (브로모메틸)벤젠으로 N-말단 알킬화시키는 방법으로 제조되는 화합물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1038087A | 1987-02-03 | 1987-02-03 | |
US010,380 | 1987-02-03 | ||
US010380 | 1987-02-03 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR880009903A true KR880009903A (ko) | 1988-10-05 |
KR960006551B1 KR960006551B1 (ko) | 1996-05-17 |
Family
ID=21745504
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019880000970A KR960006551B1 (ko) | 1987-02-03 | 1988-02-03 | 폴리아민 유도체, 이의 제조방법 및 이를 포함하는 약제학적 조성물 |
Country Status (20)
Country | Link |
---|---|
EP (1) | EP0277635B1 (ko) |
JP (1) | JP2556720B2 (ko) |
KR (1) | KR960006551B1 (ko) |
CN (1) | CN1021817C (ko) |
AR (1) | AR246093A1 (ko) |
AT (1) | ATE99668T1 (ko) |
AU (1) | AU602186B2 (ko) |
CA (1) | CA1338764C (ko) |
DE (1) | DE3886784T2 (ko) |
DK (1) | DK174418B1 (ko) |
ES (1) | ES2061528T3 (ko) |
FI (1) | FI108030B (ko) |
HU (2) | HU202188B (ko) |
IE (1) | IE61496B1 (ko) |
IL (1) | IL85247A (ko) |
NO (1) | NO166362C (ko) |
NZ (1) | NZ223340A (ko) |
PH (1) | PH30970A (ko) |
PT (1) | PT86687B (ko) |
ZA (1) | ZA88600B (ko) |
Families Citing this family (25)
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US5109024A (en) * | 1987-02-03 | 1992-04-28 | Merrell Dow Pharmaceuticals Inc. | Polyamine derivatives as antineoplastic agents |
US5753714A (en) * | 1987-02-03 | 1998-05-19 | Merrell Pharmaceuticals Inc. | Polyamine derivatives |
ZA887410B (en) * | 1987-10-08 | 1989-06-28 | Merrell Dow Pharma | Polyamine derivatives as antineoplastic agents |
US4935449A (en) * | 1988-08-04 | 1990-06-19 | Merrell Dow Pharmaceuticals Inc. | N-2,3-butadienyl tri- and tetraaminoalkane derivatives |
EP0378146B1 (en) * | 1989-01-10 | 1995-03-29 | Merrell Pharmaceuticals Inc. | Polyamine derivatives as antineoplastic agents |
ZA903804B (en) * | 1989-05-23 | 1991-03-27 | Merrell Dow Pharma | A method of potentiating cell-mediated immunity utilizing polyamine derivatives |
US5079262A (en) * | 1989-07-28 | 1992-01-07 | Queen's University At Kingston | Method of detection and treatment of malignant and non-malignant lesions utilizing 5-aminolevulinic acid |
ZA919695B (en) * | 1990-12-13 | 1992-09-30 | Merrell Dow Pharma | Method of treating cancer by conjunctive therapy with n,n'-bis(3-(ethylamino)propyl)-1,7-heptanediamine and a cytotoxic agent |
US5561136A (en) * | 1990-12-13 | 1996-10-01 | Merrell Pharmaceuticals Inc. | Method of treating cancer by conjunctive therapy with N,N'-bis[ethylamino)propyl]-1,7-heptanediamine and a cytotoxic agent |
US5354782A (en) * | 1991-01-17 | 1994-10-11 | Merrell Dow Pharmaceuticals Inc. | Polyamine phenols as radioprotective agents |
US5217964A (en) * | 1991-01-23 | 1993-06-08 | Merrell Dow Pharmaceuticals Inc. | Polyamine thiols as radioprotective agents |
KR100311851B1 (ko) * | 1993-02-23 | 2002-04-24 | 슈테펜엘.네스비트 | 방사선보호제로서의폴리아민유도체 |
CA2155095A1 (en) * | 1993-12-27 | 1995-07-06 | Jorg Frei | Unsaturate amino compounds for use as anticancer and antiprotozoic agent |
US5516807A (en) * | 1994-10-25 | 1996-05-14 | Warner-Lambert Company | Method for treating vascular proliferative disorders following balloon angioplasty |
AU703340B2 (en) * | 1995-06-26 | 1999-03-25 | Chelator Llc | Compounds with chelation affinity and selectivity for first transition series elements, and their use in medical therapy and diagnosis |
FR2749845B1 (fr) * | 1996-06-18 | 1998-08-21 | Oreal | Nouveaux derives benzyl substitue(s) de polyalkylene-polyamines et leur utilisation dans des compositions cosmetiques et pharmaceutiques |
US7087648B1 (en) | 1997-10-27 | 2006-08-08 | The Regents Of The University Of California | Methods for modulating macrophage proliferation using polyamine analogs |
US8198334B2 (en) | 1997-10-27 | 2012-06-12 | Pathologica Llc | Methods for modulating macrophage proliferation in ocular disease using polyamine analogs |
WO2003013245A1 (en) | 2001-08-07 | 2003-02-20 | Wisconsin Alumni Research Foundation | Polyamines and analogs for protecting cells during cancer chemotherapy and radiotherapy |
BRPI0614805A2 (pt) * | 2005-08-10 | 2011-04-12 | Univ Johns Hopkins | poliaminas úteis como produtos terapêuticos antiparasìticos e anticáncer e como inibidores de demetilase lisina-especìficos |
EP2190404A1 (en) * | 2007-09-18 | 2010-06-02 | Fujifilm Manufacturing Europe B.V. | Uv absorbing compounds |
CN102753604B (zh) * | 2010-01-04 | 2015-01-21 | 罗地亚经营管理公司 | 多胺及其制造方法 |
CN103242256A (zh) * | 2013-05-21 | 2013-08-14 | 苏州科捷生物医药有限公司 | 一种3-胺甲基-异噁唑盐酸盐的合成方法 |
CN111989316B (zh) * | 2018-01-30 | 2023-09-08 | 潘贝拉治疗股份有限公司 | 用于生产(6s,15s)-3,8,13,18-四氮杂二十烷-6,15-二醇的方法 |
CN112218849B (zh) * | 2018-04-06 | 2023-08-18 | 巴斯夫欧洲公司 | 用于制备胺的方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3013020A (en) * | 1958-01-24 | 1961-12-12 | Miles Lab | N,n'-bis-phenyl-alkylene-diamines |
DE2458222A1 (de) * | 1973-12-19 | 1975-07-03 | Sandoz Ag | Verfahren zur herstellung neuer phenylaethylaminderivate |
DE2557657A1 (de) * | 1975-12-20 | 1977-06-30 | Knoll Ag | Neue spermin-derivate |
DE2938710A1 (de) * | 1979-09-25 | 1981-04-09 | Hoechst Ag, 6000 Frankfurt | N,n'-dialkylaminoalkylethylendiamine und verfahren zu deren herstellung |
NZ212053A (en) * | 1984-05-17 | 1988-02-29 | Merrell Dow Pharma | Polyamine containing pharmaceutical compositions for treating neoplasms |
GB8419103D0 (en) * | 1984-07-26 | 1984-08-30 | Beecham Wuelfing Gmbh & Co Kg | Compounds |
ZA887410B (en) * | 1987-10-08 | 1989-06-28 | Merrell Dow Pharma | Polyamine derivatives as antineoplastic agents |
-
1988
- 1988-01-28 NZ NZ223340A patent/NZ223340A/en unknown
- 1988-01-28 ZA ZA880600A patent/ZA88600B/xx unknown
- 1988-01-28 CA CA000557585A patent/CA1338764C/en not_active Expired - Fee Related
- 1988-01-28 AU AU10902/88A patent/AU602186B2/en not_active Ceased
- 1988-01-29 IL IL85247A patent/IL85247A/xx not_active IP Right Cessation
- 1988-02-01 AR AR88309985A patent/AR246093A1/es active
- 1988-02-02 NO NO880452A patent/NO166362C/no not_active IP Right Cessation
- 1988-02-02 ES ES88101472T patent/ES2061528T3/es not_active Expired - Lifetime
- 1988-02-02 EP EP88101472A patent/EP0277635B1/en not_active Expired - Lifetime
- 1988-02-02 PT PT86687A patent/PT86687B/pt not_active IP Right Cessation
- 1988-02-02 FI FI880469A patent/FI108030B/fi not_active IP Right Cessation
- 1988-02-02 AT AT88101472T patent/ATE99668T1/de not_active IP Right Cessation
- 1988-02-02 HU HU88453A patent/HU202188B/hu not_active IP Right Cessation
- 1988-02-02 IE IE28588A patent/IE61496B1/en not_active IP Right Cessation
- 1988-02-02 PH PH36445A patent/PH30970A/en unknown
- 1988-02-02 DE DE88101472T patent/DE3886784T2/de not_active Expired - Fee Related
- 1988-02-02 JP JP63021440A patent/JP2556720B2/ja not_active Expired - Fee Related
- 1988-02-02 DK DK198800523A patent/DK174418B1/da not_active IP Right Cessation
- 1988-02-03 CN CN88100500A patent/CN1021817C/zh not_active Expired - Fee Related
- 1988-02-03 KR KR1019880000970A patent/KR960006551B1/ko not_active IP Right Cessation
-
1994
- 1994-11-09 HU HU94P/P00043P patent/HU210205A9/hu unknown
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