KR20060052866A - 질환 및 상태의 치료 및 예방을 위한 플루오로 치환오메가-카르복시아릴 디페닐 우레아 - Google Patents
질환 및 상태의 치료 및 예방을 위한 플루오로 치환오메가-카르복시아릴 디페닐 우레아 Download PDFInfo
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- ZQHJPIPGBODVTG-UHFFFAOYSA-N CNC(c1nccc(Oc(cc2)cc(F)c2N)c1)=O Chemical compound CNC(c1nccc(Oc(cc2)cc(F)c2N)c1)=O ZQHJPIPGBODVTG-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
Claims (54)
- a) 염산, 브롬화수소산, 황산, 인산, 메탄술폰산, 트리플루오로메탄술폰산, 벤젠술폰산, p-톨루엔 술폰산 (토실레이트 염), 1-나프탈렌 술폰산, 2-나프탈렌 술폰산, 아세트산, 트리플루오로아세트산, 말산, 타르타르산, 시트르산, 락트산, 옥살산, 숙신산, 푸마르산, 말레산, 벤조산, 살리실산, 페닐아세트산 또는 만델산인 유기산 또는 무기산의 염기성 염, 또는b) 알칼리 금속 양이온, 알칼리 토금속 양이온, 암모늄 양이온, 지방족 치환된 암모늄 양이온 또는 방향족 치환된 암모늄 양이온을 함유하는 유기 염기 또는 무기 염기의 산성 염인 제1항의 화학식 I의 화합물의 제약학상 허용되는 염.
- 4-{4-[3-(4-클로로-3-트리플루오로메틸페닐)-우레이도]-3-플루오로페녹시}- 피리딘-2-카르복실산 메틸아미드인 화합물, 또는 그의 염.
- 염산, 브롬화수소산, 황산, 인산, 메탄술폰산, 트리플루오로메탄술폰산, 벤젠술폰산, p-톨루엔 술폰산 (토실레이트 염), 1-나프탈렌 술폰산, 2-나프탈렌 술폰산, 아세트산, 트리플루오로아세트산, 말산, 타르타르산, 시트르산, 락트산, 옥살산, 숙신산, 푸마르산, 말레산, 벤조산, 살리실산, 페닐아세트산 또는 만델산과 같은 유기산의 염기성 염인, 제3항의 화합물의 제약학상 허용되는 염.
- N-(4-클로로-3-(트리플루오로메틸)페닐)-N'-2-플루오로-(4-(2-(N-메틸카르바모일)-4-피리딜옥시)페닐) 우레아의 염산염, 벤젠술폰산염 또는 메탄술폰산염인 화합물.
- 제1항의 화합물 및 생리학상 허용되는 담체를 포함하는 제약 조성물.
- 제3항의 화합물 및 생리학상 허용되는 담체를 포함하는 제약 조성물.
- 제1항의 화합물 및 생리학상 허용되는 담체를 포함하는, 단백질 키나아제에 의하여 조절되며 단백질 키나아제 신호 전달 경로의 이상과 관련있는 인간 또는 다른 포유동물의 질환 치료용 제약 조성물.
- 제1항의 화합물 및 생리학상 허용되는 담체를 포함하는, 과증식성 장애 치료용 제약 조성물.
- 제1항의 화합물 및 생리학상 허용되는 담체를 포함하는, 암성 세포 성장 치료용 제약 조성물.
- N-(4-클로로-3-(트리플루오로메틸)페닐)-N'-2-플루오로-(4-(2-(N-메틸카르바모일)-4-피리딜옥시)페닐) 우레아의 제약학상 허용되는 염 및 생리학상 허용되는 담체를 포함하는 제약 조성물.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 티로신 키나아제 신호 전달의 조절 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 티로신 키나아제에 의하여 조절되며 티로신 키나아제 신호 전달 경로의 이상과 관련있는 인간 또는 다른 포유동물의 질환의 치료 또는 예방 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 및(또는) 다른 포유동물의 VEGFR-2 매개 장애의 치료 또는 예방 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 및(또는) 다른 포유동물의 PDGFR 매개 장애의 치료 또는 예방 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 또는 다른 포유동물의 raf-매개 장애의 치료 또는 예방 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 또는 다른 포유동물의 p38-매개 장애의 치료 또는 예방 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 또는 다른 포유동물의 VEGF-매개 장애의 치료 또는 예방 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 또는 다른 포유동물의 과증식성, 염증성 및(또는) 혈관신생 장애의 치료 또는 예방 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 또는 다른 포유동물의 과증식성 장애의 치료 또는 예방 방법.
- 제20항에 있어서, 과증식성 장애가 암인 방법.
- 제21항에 있어서, 제1항의 화합물을 인간 또는 다른 포유동물에게 1종 이상의 추가의 항암제와 병용하여 투여하는 것을 포함하는 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 비정상적인 혈관신생 또는 과투과성 과정을 특징으로 하는 인간 또는 다른 포유동물의 질환의 치료 또는 예방 방법.
- 제23항에 있어서, 제1항의 화합물을 인간 또는 다른 포유동물에 동일한 제제로 또는 별개의 제제로 다른 항혈관신생 제제와 동시에 투여하는 것을 포함하는, 비정상적인 혈관신생 또는 과투과성 과정을 특징으로 하는 인간 또는 다른 포유동물의 질환의 치료 또는 예방 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 또는 다른 포유동물의 종양 성장, 망막병증, 허혈성 망막-정맥 폐쇄증, 미숙아 망막병증, 노화성 황반 변성, 류마티스성 관절염, 건선, 수포성 유천포창, 다형 홍반, 또는 포진 피부염을 포함하는 표피하 수포 형성과 관련된 수포성 질환, 류마티스성 관절염, 골관절염, 패혈성 관절염, 종양 전이, 치주 질환, 각막 궤양, 단백뇨 및 죽상경화판으로 인한 심장 혈전증, 동맥류성 대동맥, 수태 조절, 이영양성 수포성표피 박리증, 외상성 관절 손상에 따른 퇴행성 연골 손실, MMP 활성 매개 골감소 증, 악관절 질환 또는 탈수초성 신경계 질환 중 하나 이상의 상태의 치료 또는 예방 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 및(또는) 다른 포유동물의 종양 성장, 망막병증, 허혈성 망막-정맥 폐쇄증, 미숙아 망막병증, 노화성 황반 변성, 류마티스성 관절염, 건선, 수포성 유천포창, 다형 홍반, 또는 포진 피부염을 포함하는 표피하 수포 형성과 관련된 수포성 질환 중 하나 이상의 상태를 류마티스열, 뼈 흡수, 폐경후 골다공증, 패혈증, 그람 음성 패혈증, 패혈성 쇼크, 내독소성 쇼크, 독성 쇼크 증후군, 전신 염증성 반응 증후군, 염증성 장질환 (크론병 및 궤양성 대장염), 야리시-헤륵스하이머 (Jarisch-Herxheimer) 반응, 천식, 성인성 호흡 곤란 증후군, 급성 폐섬유성 질환, 폐사르코이드증, 알레르기성 호흡기병, 규소폐증, 광부 진폐증, 폐포 손상, 간부전, 급성 염증 중의 간질환, 중증 알코올성 간염, 말라리아 (열대열원충 말라리아 및 뇌 말라리아), 인슐린 비의존성 당뇨병 (NIDDM), 울혈성 심부전, 심장 질환에 따르는 손상, 죽상경화증, 알츠하이머병, 급성 뇌염, 뇌 손상, 다발성 경화증 (다발성 경화증 중 탈수초화 및 희소돌기아교세포 손실), 진행성 암, 림프성 악성종양, 췌장염, 감염, 염증 및 암 중 악화된 상처 회복, 골수형성이상증후군, 전신 홍반 루푸스, 담즙성 간경변, 장 괴사, 모노클로날 항체의 투여에 따르는 방사선 손상/독성, 숙주 대 이식편 반응 (허혈성 관류 손상 및 신장, 간, 심장, 및 피부의 동종이식 거부), 폐 동종이식 거부 (폐색성 기관지염) 및 고관절 전치환으로 인한 합병증으로 이루어진 군으로부터 선택되는 다른 상태와 함께 치료 또는 예방하는 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 및(또는) 다른 포유동물의 종양 성장, 망막병증, 당뇨성 망막병증, 허혈성 망막-정맥 폐쇄증, 미숙아 망막병증, 노화성 황반 변성, 류마티스성 관절염, 건선, 표피하 수포 형성, 수포성 유천포창, 다형 홍반, 및 포진 피부염과 관련된 수포성 질환 중 하나 이상의 상태를 결핵, 소화 궤양병 중의 헬리코박터 파일로리 (Helicobacter pylori) 감염, 트리파노소마 크루지 (Trypanosoma cruzi) 감염에 기인한 샤가(Chaga) 병, 대장균 감염에 기인한 시가양 독소의 효과, 포도상구균 감염에 기인한 장독소 A의 효과, 수막구균 감염, 및 보렐리아 부르그도페리 (Borrelia burgdorferi), 트레포네마 펠리덤 (Treponema pallidum), 시토메갈로바이러스, 인플루엔자 바이러스, 테일러씨 (Theiler's) 뇌척수염 바이러스, 및 인간 면역결핍 바이러스 (HIV)의 감염으로 이루어진 군으로부터 선택되는 감염성 질환과 함께 치료 또는 예방하는 방법.
- 제22항에 있어서, 추가의 항암제가 아스파라기나제, 블레오마이신, 카르보플라틴, 카르무스틴, 클로람부실, 시스플라틴, 콜라스파제, 시클로포스파미드, 시타라빈, 다카르바진, 닥티노마이신, 다우노루비신, 독소루비신 (아드리아마이신), 에피루비신, 에토포시드, 5-플루오로우라실, 헥사메틸멜라민, 히드록시우레아, 이포스파미드, 이리노테칸, 류코보린, 로무스틴, 메클로르에타민, 6-메르캅토퓨린, 메 스나, 메토트렉세이트, 미토마이신 C, 미톡산트론, 프레드니솔론, 프레드니손, 프로카르바진, 랄록시펜, 스트렙토조신, 타목시펜, 티오구아닌, 토포테칸, 빈블라스틴, 빈크리스틴, 빈데신, 아미노글루테티미드, L-아스파라기나아제, 아자티오프린, 5-아자시티딘 클라드리빈, 부술판, 디에틸스틸베스트롤, 2',2'-디플루오로데옥시시티딘, 도세탁셀, 에리트로히드록시노닐 아데닌, 에티닐 에스트라디올, 5-플루오로데옥시우리딘, 5-플루오로데옥시우리딘 모노포스페이트, 플루다라빈 포스페이트, 플루옥시메스테론, 플루타미드, 히드록시프로게스테론 카프로에이트, 이다루비신, 인터페론, 메드록시프로게스테론 아세테이트, 메게스트롤 아세테이트, 멜팔란, 미토탄, 파클리탁셀, 펜토스타틴, N-포스포노아세틸-L-아스파테이트 (PALA), 플리카마이신, 세무스틴, 테니포시드, 테스토스테론 프로피오네이트, 티오테파, 트리메틸멜라민, 우리딘, 및 비노렐빈, 옥살리플라틴, 젬시타빈, 카페시타빈, 에포틸론 및 그의 천연 또는 합성 유도체, 토시투모마브, 트라베덱틴, 및 테모졸로미드, 트라스투주마브, 세툭시마브, 베바시주마브, 페르투주마브, ZD-1839 (이레사), OSI-774 (타르세바), CI-1033, GW-2016, CP-724,714, HKI-272, EKB-569, STI-571 (글리벡), PTK-787, SU-11248, ZD-6474, AG-13736, KRN-951, CP-547,632, CP-673,451, CHIR-258, MLN-518, AZD-2171, PD-325901, ARRY-142886, 수베로일아닐리드 히드록삼산 (SAHA), LAQ-824, LBH-589, MS-275, FR-901228, 보르테조미브, 및 CCI-779로 이루어진 군으로부터 선택되는 것인 방법.
- 제22항에 있어서, 추가의 항암제가 DNA 토포이소머라아제 I 및 II 억제제, DNA 중간삽입물질, 알킬화제, 항대사체, 세포 주기 차단제, 미세관 분해제, 및 Eg5 억제제로 이루어진 군으로부터 선택되는 세포독성 제제인 방법.
- 제22항에 있어서, 추가의 항암제가 성장 인자 수용체 신호의 억제제, 히스톤 데아세틸라아제 억제제, PKB 경로의 억제제, Raf/MEK/ERK 경로의 억제제, mTOR 경로의 억제제, 및 프로테아좀 억제제로 이루어진 군으로부터 선택되는 것인 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 및(또는) 다른 포유동물의 류마티스열, 뼈 흡수, 폐경후 골다공증, 패혈증, 그람 음성 패혈증, 패혈성 쇼크, 내독소성 쇼크, 독성 쇼크 증후군, 전신 염증성 반응 증후군, 염증성 장질환 (크론병 및 궤양성 대장염), 야리시-헤륵스하이머 (Jarisch-Herxheimer) 반응, 천식, 성인성 호흡 곤란 증후군, 급성 폐섬유성 질환, 폐사르코이드증, 알레르기성 호흡기병, 규소폐증, 광부 진폐증, 폐포 손상, 간부전, 급성 염증 중의 간질환, 중증 알코올성 간염, 말라리아 (열대열원충 말라리아 및 뇌 말라리아), 인슐린 비의존성 당뇨병 (NIDDM), 울혈성 심부전, 심장 질환에 따르는 손상, 죽상경화증, 알츠하이머병, 급성 뇌염, 뇌 손상, 다발성 경화증 (다발성 경화증 중 탈수초화 및 희소돌기아교세포 손실), 진행성 암, 림프성 악성종양, 췌장염, 감염, 염증 및 암 중 악화된 상처 회복, 골수형성이상 증후군, 전신 홍반 루푸스, 담즙성 간경변, 장 괴사, 건선, 모노클로날 항체 투여에 따르는 방사선 손상/독성, 숙주 대 이식편 반응 (허혈성 관류 손상 및 신장, 간, 심장, 및 피 부의 동종이식 거부), 폐 동종이식 거부 (폐색성 기관지염) 또는 고관절 전치환으로 인한 합병증 중 하나 이상의 상태의 치료 또는 예방 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 및(또는) 다른 포유동물의 결핵, 소화 궤양병 중의 헬리코박터 파일로리 (Helicobacter pylori) 감염, 트리파노소마 크루지 (Trypanosoma cruzi) 감염에 기인한 샤가(Chaga) 병, 대장균 감염에 기인한 시가양 독소의 효과, 포도상구균 감염에 기인한 장독소 A의 효과, 수막구균 감염, 및 보렐리아 부르그도르페리 (Borrelia burgdorferi), 트레포네마 펠리덤 (Treponema pallidum), 사이토메갈로바이러스, 인플루엔자 바이러스, 테일러씨 (Theiler's) 뇌척수염 바이러스, 및 인간 면역결핍 바이러스 (HIV)의 감염 중 하나 이상의 상태의 치료 또는 예방 방법.
- 제1항의 화합물의 유효량을 인간 및(또는) 다른 포유동물에 투여하여 상기 포유류의 골다공증, 염증 및 암을 제외한 혈관신생 장애를 치료 또는 예방하는 방법.
- (삭제)
- (삭제)
- (삭제)
- 제1항 또는 제2항의 화합물의 유효량을 투여하는 것을 포함하는, 치료 또는 예방이 필요한 대상의 질환 및(또는) 상태의 치료 및(또는) 예방 방법.
- 제37항에 있어서, 대상 또는 그의 세포에서 종양 퇴행을 일으키는 것을 포함하는 방법.
- 제37항에 있어서, 림프혈관신생을 억제하는 것을 포함하는 방법.
- 제37항에 있어서, 혈관신생을 억제하는 것을 포함하는 방법.
- 제37항에 있어서, 림프혈관신생 및 혈관신생을 억제하는 것을 포함하는 방법.
- 제37항에 있어서, 조혈모세포의 증식을 유발하는 것을 포함하는 방법.
- 제37항에 있어서, 포유동물 대상의 raf, VEGFR-2, VEGFR-3, PDGFR-베타, p38 및(또는) flt-3 매개 장애를 치료하는 것을 포함하는 방법.
- 제37항에 있어서, 상기 상태를 가진 대상 또는 세포로부터 얻은 세포 또는 세포 추출물을 포함하는 표본에서 raf, VEGFR-2, VEGFR-3, PDGFR-베타, p38 및(또는) flt-3의 발현 또는 활성을 측정하는 것을 포함하며, 상기 상태에서 발현 또는 활성이 정상 대조군과 비교하여 다른 경우 상기 상태가 상기 화합물에 의해 조절될 수 있는 것으로 결정하는, 상기 상태가 상기 화합물로 조절될 수 있는지 결정하는 것을 포함하는 방법.
- 제44항에 있어서, 상기 표본의 발현을 정상 대조군과 비교하는 것을 추가로 포함하는 방법.
- 제37항에 있어서, 상기 화합물을 투여하고, raf, VEGFR-2, VEGFR-3, PDGFR-베타, p38, 및(또는) flt-3의 발현 또는 활성을 측정하고, 상기 발현 또는 활성에 대한 화합물의 효과를 결정하는 것을 포함하는, 화합물 장애의 효능을 평가하는 것을 포함하는 방법.
- 제37항에 있어서, 생물학적 물질 표본에서 raf, VEGFR-2, VEGFR-3, PDGFR-베타, p38 및(또는) flt-3의 존재를 확인하고, 상기 화합물과 표본을 접촉시키고, 상기 화합물이 상기 물질에 결합하는지 여부를 확인하는 것을 포함하는 방법.
- 제37항에 있어서, 종양 세포 증식 및 혈관신생을 억제하는 데 효과적인 양인 효과량의 상기 화합물을 투여하는 것을 포함하는, 치료가 필요한 대상의 종양을 치료하는 것을 포함하는 방법.
- 제3항의 화합물의 천연 대사체인 화합물.
- 제49항에 있어서, 대사 부위가 두 개의 우레아 질소 원자 중 어느 하나, 또는 피리딘 질소 원자, 또는 메틸아미드 작용기, 또는 이들의 조합인 화합물.
- 제49항에 있어서, 우레아 질소 원자 중 어느 것이 히드록실기를 가지는 것이고(이거나) 피리딘 질소 원소가 산화된 것이고(이거나) 아미드 작용기가 탈메틸화된 것인 화합물.
- 제49항에 있어서,4-{4-[3-(4-클로로-3-트리플루오로메틸페닐)-우레이도]-3-플루오로페녹시}-피리딘-2-카르복실산 아미드,4-{4-[3-(4-클로로-3-트리플루오로메틸페닐)-우레이도]-3-플루오로페녹시}-1-히드록시-피리딘-2-카르복실산 메틸아미드, 또는4-{4-[3-(4-클로로-3-트리플루오로메틸페닐)-우레이도]-3-플루오로페녹시}-l-히드록시-피리딘-2-카르복실산 아미드로부터 선택되는 것인 화합물.
- 제19항에 있어서, 염증성 장애가 류마티스성 관절염, COPD, 크론병 및 건선으로부터 선택되는 것인 방법.
- 제1항의 화합물을 인간 또는 다른 포유동물에 투여하는 것을 포함하는, 인간 또는 다른 포유 동물의 flt-3 매개 장애의 치료 또는 예방 방법.
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Publication number | Priority date | Publication date | Assignee | Title |
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KR101374530B1 (ko) * | 2011-07-14 | 2014-03-14 | 연세대학교 원주산학협력단 | 디에틸스틸베스트롤을 함유하는 심혈관 질환의 예방 또는 치료용 조성물 |
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