RU2012127790A - Индуцирующие апоптоз агенты для лечения рака и иммунных и аутоиммунных заболеваний - Google Patents

Индуцирующие апоптоз агенты для лечения рака и иммунных и аутоиммунных заболеваний Download PDF

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RU2012127790A
RU2012127790A RU2012127790/04A RU2012127790A RU2012127790A RU 2012127790 A RU2012127790 A RU 2012127790A RU 2012127790/04 A RU2012127790/04 A RU 2012127790/04A RU 2012127790 A RU2012127790 A RU 2012127790A RU 2012127790 A RU2012127790 A RU 2012127790A
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methyl
cancer
chlorophenyl
piperazin
sulfonyl
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RU2012127790/04A
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RU2535203C2 (ru
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Милан БРАНКО
Юджиа ДАЙ
Хун ДИН
Джордж А. ДОУЭРТИ
Стивен В. ЭЛМОР
Лиза ХАСВОЛЬД
Лаура ХЕКСАМЕР
Аарон КАНЗЕР
Роберт А. МАНТЕЙ
Уилльям Дж. МАККЛЕЛЛАН
Чанг Х. ПАРК
Чеол-Мин ПАРК
Эндрю М. ПЕТРОС
Сяохун СУН
Эндрю Дж. САУЭРС
Джерард М. САЛЛИВАН
Чжи-фу ТАО
Гари Т. ВАН
Лэ ВАН
Силу ВАН
Майкл Д. УЭНДТ
Тодд М. ХАНСЕН
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Эбботт Лэборетриз
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Abstract

1. Соединение или его терапевтически приемлемая соль, где соединение выбрано из следующих:N-({3-хлор-4-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]фенил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индол-5-ил)окси]бензамид;N-({3-хлор-4-[(4-фтортетрагидро-2H-пиран-4-ил)метокси]фенил}сульфонил)-4-(4-{[4-(4-хлорфенил)-6,6-диметил-5,6-дигидро-2Н-пиран-3-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индол-5-ил)окси]бензамид;N-({5-хлор-6-[(транс-4-гидроксициклогексил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индазол-4-ил)окси]бензамид;N-({5-хлор-6-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индазол-4-ил)окси]бензамид;трет-бутил 5-[(4-{4-[({5-хлор-6-[(4-фтортетрагидро-2H-пиран-4-ил)метокси]пиридин-3-ил}сульфонил)карбамоил]-3-[(6-фтор-1Н-индол-5-ил)окси]фенил}пиперазин-1-ил)метил]-4-(4-хлорфенил)-3,6-дигидропиридин-1(2Н)-карбоксилат;N-({5-хлор-6-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[4-(4-хлорфенил)-1-(1,3-дифторпропан-2-ил)-1,2,5,6-тетрагидропиридин-3-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индол-5-ил)окси]бензамид;4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индазол-4-ил)окси]-N-[(4-{[(4-фтортетрагидро-2H-пиран-4-ил)метил]амино}-3-нитрофенил)сульфонил]бензамид;N-({5-хлор-6-[(транс-4-гидроксициклогексил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(7-фтор-1Н-индазол-4-ил)окси]бензамид;N-({5-хлор-6-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)

Claims (6)

1. Соединение или его терапевтически приемлемая соль, где соединение выбрано из следующих:
N-({3-хлор-4-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]фенил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индол-5-ил)окси]бензамид;
N-({3-хлор-4-[(4-фтортетрагидро-2H-пиран-4-ил)метокси]фенил}сульфонил)-4-(4-{[4-(4-хлорфенил)-6,6-диметил-5,6-дигидро-2Н-пиран-3-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индол-5-ил)окси]бензамид;
N-({5-хлор-6-[(транс-4-гидроксициклогексил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индазол-4-ил)окси]бензамид;
N-({5-хлор-6-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индазол-4-ил)окси]бензамид;
трет-бутил 5-[(4-{4-[({5-хлор-6-[(4-фтортетрагидро-2H-пиран-4-ил)метокси]пиридин-3-ил}сульфонил)карбамоил]-3-[(6-фтор-1Н-индол-5-ил)окси]фенил}пиперазин-1-ил)метил]-4-(4-хлорфенил)-3,6-дигидропиридин-1(2Н)-карбоксилат;
N-({5-хлор-6-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[4-(4-хлорфенил)-1-(1,3-дифторпропан-2-ил)-1,2,5,6-тетрагидропиридин-3-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индол-5-ил)окси]бензамид;
4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индазол-4-ил)окси]-N-[(4-{[(4-фтортетрагидро-2H-пиран-4-ил)метил]амино}-3-нитрофенил)сульфонил]бензамид;
N-({5-хлор-6-[(транс-4-гидроксициклогексил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(7-фтор-1Н-индазол-4-ил)окси]бензамид;
N-({5-хлор-6-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(7-фтор-1Н-индазол-4-ил)окси]бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-{[3-нитро-4-({[4-(оксетан-3-ил)морфолин-2-ил]метил}амино)фенил]сульфонил}бензамид;
4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индол-5-ил)окси]-N-{[3-нитро-4-({[4-(оксетан-3-ил)морфолин-2-ил]метил}амино)фенил]сульфонил}бензамид;
4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(7-фтор-1Н-индазол-4-ил)окси]-N-[(4-{[(4-фтортетрагидро-2H-пиран-4-ил)метил]амино}-3-нитрофенил)сульфонил]бензамид;
N-({5-хлор-6-[(транс-4-гидрокси-4-метилциклогексил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индазол-4-ил)окси]бензамид;
4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-{[5-хлор-6-(тетрагидро-2Н-пиран-4-илметокси)пиридин-3-ил]сульфонил}-2-[(3-метил-2-оксо-2,3-дигидро-1Н-бензимидазол-4-ил)окси]бензамид;
4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-({4-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]-3-нитрофенил}сульфонил)-2-[(3-метил-2-оксо-2,3-дигидро-1Н-бензимидазол-4-ил)окси]бензамид;
4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(4-{[(транс-4-
метоксициклогексил)метил]амино}-3-нитрофенил)сульфонил]-2-[(3-метил-2-оксо-2,3-дигидро-1Н-бензимидазол-4-ил)окси]бензамид;
2-[(3-амино-1Н-индазол-4-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(4-{[(4-фтортетрагидро-2Н-пиран-4-ил)метил]амино}-3-нитрофенил)сульфонил]бензамид;
2-[(3-амино-1Н-индазол-4-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-({4-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]-3-нитрофенил}сульфонил)бензамид;
2-[(3-амино-1Н-индазол-4-ил)окси]-N-({5-хлор-6-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)бензамид;
2-[(3-амино-1Н-индазол-4-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-({3-нитро-4-[(тетрагидро-2Н-пиран-4-илметил)амино]фенил}сульфонил)бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(4-{[4-фтор-1-(оксетан-3-ил)пиперидин-4-ил]метокси}-3-нитрофенил)сульфонил]бензамид;
4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-2-[(6-фтор-1Н-индазол-4-ил)окси]-N-({4-[(4-фтортетрагидро-2Н-пиран-4-ил)метокси]-3-нитрофенил}сульфонил)бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(4-{[(транс-4-гидрокси-4-метилциклогексил)метил]амино}-3-нитрофенил)сульфонил]бензамид;
2-[(3-амино-1Н-индазол-4-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(4-{[(транс-4-метоксициклогексил)метил]амино}-3-нитрофенил)сульфонил]бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-({4-[(цис-4-гидрокси-4-метилциклогексил)метокси]-3-нитрофенил}сульфонил)бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(4-{[(цис-4-гидрокси-4-метилциклогексил)метил]амино}-3-нитрофенил)сульфонил]бензамид;
4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-{[3-хлор-4-(тетрагидро-2Н-пиран-4-илметокси)фенил]сульфонил}-2-[(3-метил-2-оксо-2,3-дигидро-1Н-бензимидазол-4-ил)окси]бензамид;
4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(4-{[(4-циклопропилморфолин-2-ил)метил]амино}-3-нитрофенил)сульфонил]-2-[(3-метил-2-оксо-2,3-дигидро-1Н-бензимидазол-4-ил)окси]бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-{[3-нитро-4-(2-оксаспиро[3,5]non-7-илметокси)фенил]сульфонил}бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-({4-[(транс-4-гидрокси-4-метилциклогексил)метокси]-3-нитрофенил}сульфонил)бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-{[4-({[(2S)-4-циклопропилморфолин-2-ил]метил}амино)-3-нитрофенил]сульфонил}бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-N-({5-хлор-6-[(транс-1-фтор-4-гидрокси-4-метилциклогексил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-N-({5-хлор-6-[(цис-1-фтор-4-гидрокси-4-метилциклогексил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)бензамид;
2-[(3-амино-1Н-индазол-4-ил)окси]-N-({5-хлор-6-[(транс-4-гидрокси-4-метилциклогексил)метокси]пиридин-3-ил}сульфонил)-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)бензамид;
N-({5-хлор-6-[(транс-4-гидрокси-4-метилциклогексил)метокси]пиридин-3-ил}сульфонил)-2-[(3-хлор-1Н-индазол-4-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(4-{[(цис-4-этил-4-гидроксициклогексил)метил]амино}-3-нитрофенил)сульфонил]бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-{[3-нитро-4-({[(2S)-4-(оксетан-3-ил)морфолин-2-ил]метил}амино)фенил]сульфонил}бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-({5-нитро-6-[(тетрагидро-2Н-пиран-4-илметил)амино]пиридин-3ил }сульфонил)бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-({3-нитро-4-[(2-оксаспиро[3,5]non-7-илметил)амино]фенил}сульфонил)бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-{[4-({[транс-4-(морфолин-4-ил)циклогексил]метил}амино)-3-нитрофенил]сульфонил}бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(4-{[цис-4-(морфолин-4-ил)циклогексил]амино}-3-нитрофенил)сульфонил]бензамид;
4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-({5-циано-6-[(транс-4-гидрокси-4-метилциклогексил)метокси]пиридин-3-ил}сульфонил)-2-[(6-фтор-1Н-индазол-4-ил)окси]бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-{[4-({[4-({[4-(метоксиметил)циклогексил]метил}амино)-3-нитрофенил]сульфонил}амино)-3-нитрофенил]сульфонил}бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(3-нитро-4-{[(3R)-1-(оксетан-3-ил)пирролидин-3-ил]амино}фенил)сульфонил]бензамид;
2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)-N-[(3-нитро-4-{[(3S)-1-(оксетан-3-ил)пирролидин-3-ил]амино}фенил)сульфонил]бензамид;
N-[4-({2-[(6-амино-5-хлорпиридпин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)бензоил}сульфамоил)-2-нитрофенил]морфолин-4-карбоксамид;
и
N-[4-({2-[(6-амино-5-хлорпиридин-3-ил)окси]-4-(4-{[2-(4-хлорфенил)-4,4-диметилциклогекс-1-ен-1-ил]метил}пиперазин-1-ил)бензоил}сульфамоил)-2-нитрофенил]-4-цианопиперидин-1-карбоксамид.
2. Композиция для лечения рака мочевого пузыря, рака головного мозга, рака молочной железы, рака костного мозга, рака шейки матки, хронического лимфолейкоза, колоректального рака, рака пищевода, гепатоцеллюлярного рака, лимфобластного лейкоза, фолликулярной лимфомы, лимфобластного лейкоза из предшественников Т-клеток или В-клеток, меланомы, миелолейкоза, миеломы, рака ротовой полости, рака яичников, не мелкоклеточного рака легкого, рака простаты, мелкоклеточного рака легкого или рака поджелудочной железы, где указанная композиция содержит инертный наполнитель и терапевтически эффективное количество соединения по п.1.
3. Соединение по п.1 или его терапевтически приемлемая соль для лечения рака мочевого пузыря, рака головного мозга, рака молочной железы, рака костного мозга, рака шейки матки, хронического лимфолейкоза, колоректального рака, рака пищевода, гепатоцеллюлярного рака, лимфобластного лейкоза, фолликулярной лимфомы, лимфобластного лейкоза из предшественников Т-клеток или В-клеток, меланомы, миелолейкоза, миеломы, рака ротовой полости, рака яичников, не мелкоклеточного рака легкого, рака простаты, мелкоклеточного рака легкого или рака поджелудочной железы у пациента.
4. Соединение по п.1 или его терапевтически приемлемая соль и один дополнительный терапевтический агент или более одного дополнительного терапевтического агента для лечения рака мочевого пузыря, рака головного мозга, рака молочной железы, рака костного мозга, рака шейки матки, хронического лимфолейкоза, колоректального рака, рака пищевода, гепатоцеллюлярного рака, лимфобластного лейкоза, фолликулярной лимфомы, лимфобластного лейкоза из предшественников Т-клеток или В-клеток, меланомы, миелолейкоза, миеломы, рака ротовой полости, рака яичников, не мелкоклеточного рака легкого, рака простаты, мелкоклеточного рака легкого или рака поджелудочной железы у пациента.
5. Применение соединения по п.1 или его терапевтически приемлемой соли при получении лекарственного средства для лечения рака мочевого пузыря, рака головного мозга, рака молочной железы, рака костного мозга, рака шейки матки, хронического лимфолейкоза, колоректального рака, рака пищевода, гепатоцеллюлярного рака, лимфобластного лейкоза, фолликулярной лимфомы, лимфобластного лейкоза из предшественников Т-клеток или В-клеток, меланомы, миелолейкоза, миеломы, рака ротовой полости, рака яичников, не мелкоклеточного рака легкого, рака простаты, мелкоклеточного рака легкого или рака поджелудочной железы у пациента.
6. Применение соединения по п.1 или его терапевтически приемлемой соли и одного дополнительного терапевтического агента или более одного дополнительного терапевтического агента при получении лекарственного средства для лечения рака мочевого пузыря, рака головного мозга, рака молочной железы, рака костного мозга, рака шейки матки, хронического лимфолейкоза, колоректального рака, рака пищевода, гепатоцеллюлярного рака, лимфобластного лейкоза, фолликулярной лимфомы, лимфобластного лейкоза из предшественников Т-клеток или В-клеток, меланомы, миелолейкоза, миеломы, рака ротовой полости, рака яичников, не мелкоклеточного рака легкого, рака простаты, мелкоклеточного рака легкого или рака поджелудочной железы у пациента.
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Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9259399B2 (en) 2007-11-07 2016-02-16 Cornell University Targeting CDK4 and CDK6 in cancer therapy
US20100160322A1 (en) 2008-12-04 2010-06-24 Abbott Laboratories Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US8557983B2 (en) * 2008-12-04 2013-10-15 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US8586754B2 (en) 2008-12-05 2013-11-19 Abbvie Inc. BCL-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases
US8563735B2 (en) 2008-12-05 2013-10-22 Abbvie Inc. Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases
AU2010204554B2 (en) * 2009-01-19 2013-05-30 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
AU2010204555B2 (en) * 2009-01-19 2013-03-07 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US9034875B2 (en) 2009-05-26 2015-05-19 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US20220315555A1 (en) 2009-05-26 2022-10-06 Abbvie Inc. Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases
US8546399B2 (en) 2009-05-26 2013-10-01 Abbvie Inc. Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases
TWI476195B (zh) * 2009-05-26 2015-03-11 Abbvie Bahamas Ltd 用於治療癌症及免疫及自體免疫疾病之細胞凋亡誘發劑
NZ602055A (en) 2010-03-25 2014-08-29 Abbvie Inc Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
TWI520960B (zh) * 2010-05-26 2016-02-11 艾伯維有限公司 用於治療癌症及免疫及自體免疫疾病之細胞凋亡誘導劑
NZ717373A (en) 2010-06-03 2017-11-24 Pharmacyclics Llc The use of inhibitors of bruton’s tyrosine kinase (btk)
JP6068352B2 (ja) * 2010-10-29 2017-01-25 アッヴィ・インコーポレイテッド アポトーシス誘発剤を含む固体分散体
UA113500C2 (xx) * 2010-10-29 2017-02-10 Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб
PT2642999T (pt) 2010-11-23 2017-01-05 Abbvie Ireland Unlimited Co Métodos de tratamento que utilizam inibidores seletivos de bcl-2
PT2643322T (pt) * 2010-11-23 2017-11-13 Abbvie Inc Sais e formas cristalinas de um agente indutor de apoptose
US8940737B2 (en) 2011-10-14 2015-01-27 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
SG10201702913XA (en) * 2011-10-19 2017-06-29 Pharmacyclics Llc Use of inhibitors of bruton's tyrosine kinase (btk)
BR112015001690A2 (pt) 2012-07-24 2017-11-07 Pharmacyclics Inc mutações associadas com a resistência a inibidores da tirosina quinase de bruton (btk)
EP4019491A1 (en) * 2013-03-13 2022-06-29 AbbVie Ireland Unlimited Company Process for preparing a synthetic intermediate useful in the preparation of an apoptosis-inducing agent
US20140275082A1 (en) 2013-03-14 2014-09-18 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
WO2015116735A1 (en) 2014-01-28 2015-08-06 Mayo Foundation For Medical Education And Research Methods and combinations for killing senescent cells and for treating senescence-associated diseases and disorders
JP6688224B2 (ja) 2014-01-28 2020-04-28 バック インスティテュート フォー リサーチ オン エイジング Mdm2を阻害する手段の投与による関節における変形性関節症の処置
US10328058B2 (en) 2014-01-28 2019-06-25 Mayo Foundation For Medical Education And Research Treating atherosclerosis by removing senescent foam cell macrophages from atherosclerotic plaques
EP3119910A4 (en) 2014-03-20 2018-02-21 Pharmacyclics LLC Phospholipase c gamma 2 and resistance associated mutations
CA2946538A1 (en) 2014-04-04 2015-10-08 Del Mar Pharmaceuticals Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer
HRP20211813T1 (hr) 2014-08-11 2022-03-04 Acerta Pharma B.V. Terapeutske kombinacije inhibitora btk i inhibitora bcl-2
WO2016057572A1 (en) 2014-10-06 2016-04-14 Mark Thomas Miller Modulators of cystic fibrosis transmembrane conductance regulator
US10195213B2 (en) 2015-03-13 2019-02-05 Unity Biotechnology, Inc. Chemical entities that kill senescent cells for use in treating age-related disease
WO2017173274A1 (en) 2016-03-31 2017-10-05 Vertex Pharmaceuticals Incorporated Modulators of cystic fibrosis transmembrane conductance regulator
GEP20217329B (en) 2016-09-30 2021-12-10 Vertex Pharma Modulator of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator
EA202192783A1 (ru) 2016-12-09 2022-02-24 Вертекс Фармасьютикалз Инкорпорейтед Модулятор регулятора трансмембранной проводимости при муковисцидозе, фармацевтические композиции, способы лечения и способ получения указанного модулятора
AU2018279646B2 (en) 2017-06-08 2023-04-06 Vertex Pharmaceuticals Incorporated Methods of treatment for cystic fibrosis
CN110759908B (zh) * 2017-06-26 2021-03-12 深圳市塔吉瑞生物医药有限公司 用于抑制Bcl-2蛋白的N-苯磺酰基苯甲酰胺类化合物及其组合物及应用
CA3069226A1 (en) 2017-07-17 2019-01-24 Vertex Pharmaceuticals Incorporated Methods of treatment for cystic fibrosis
MX2020001302A (es) 2017-08-02 2020-03-20 Vertex Pharma Procesos para preparar compuestos de pirrolidina.
SG11202001553UA (en) 2017-08-23 2020-03-30 Newave Pharmaceutical Inc Condensed heterocyclic derivatives as bcl-2 inhibitors for the treatment of neoplastic diseases
TWI719349B (zh) 2017-10-19 2021-02-21 美商維泰克斯製藥公司 Cftr調節劑之結晶形式及組合物
CA3085006A1 (en) 2017-12-08 2019-06-13 Vertex Pharmaceuticals Incorporated Processes for making modulators of cystic fibrosis transmembrane conductance regulator
CN118084904A (zh) 2018-01-10 2024-05-28 里科瑞尔姆Ip控股有限责任公司 苯甲酰胺化合物
TWI810243B (zh) 2018-02-05 2023-08-01 美商維泰克斯製藥公司 用於治療囊腫纖化症之醫藥組合物
EP3774825A1 (en) 2018-04-13 2021-02-17 Vertex Pharmaceuticals Incorporated Modulators of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator
WO2020041406A1 (en) 2018-08-22 2020-02-27 Newave Pharmaceutical Inc. Bcl-2 inhibitors
CN109851535A (zh) * 2019-01-30 2019-06-07 天津现代职业技术学院 一种制备4-氟-3-(三氟甲磺酰基)苯磺酰胺的方法
CN113444078B (zh) * 2020-03-25 2023-07-07 中国科学院上海有机化学研究所 抗凋亡蛋白Bcl-2抑制剂及其制备方法和应用
CN111978246A (zh) * 2020-09-26 2020-11-24 安徽金禾实业股份有限公司 一种2-甲基-3-甲氧基-4-氯吡啶的纯化合成方法
CN117616023A (zh) * 2021-04-13 2024-02-27 爱新医药科技(香港)有限公司 Bcl-2或bcl-2/bcl-xl调节剂及其用途

Family Cites Families (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4126937A1 (de) 1991-08-10 1993-02-11 Basf Ag Salicyl(thio)etherderivate, verfahren und zwischenprodukte zu ihrer herstellung
JPH06510763A (ja) 1991-08-19 1994-12-01 イー・アイ・デュポン・ドゥ・ヌムール・アンド・カンパニー アンジオテンシン2受容体遮断イミダゾリノン誘導体
GB9203798D0 (en) 1992-02-21 1992-04-08 Fujisawa Pharmaceutical Co Quinolylbenzofuran derivatives,processes for preparation thereof and pharmaceutical composition comprising the same
MY115155A (en) 1993-09-09 2003-04-30 Upjohn Co Substituted oxazine and thiazine oxazolidinone antimicrobials.
ATE257829T1 (de) 1995-09-15 2004-01-15 Upjohn Co Aminoaryl oxazolidinone n-oxide
CN1265669A (zh) 1997-07-31 2000-09-06 伊兰药品公司 抑制由vla-4介导的白细胞粘着的化合物
US20030220234A1 (en) * 1998-11-02 2003-11-27 Selvaraj Naicker Deuterated cyclosporine analogs and their use as immunodulating agents
US6410584B1 (en) 1998-01-14 2002-06-25 Cell Pathways, Inc. Method for inhibiting neoplastic cells with indole derivatives
BR9909322A (pt) 1998-02-04 2000-12-05 Novartis Ag Derivados de sulfonilamino que inibem metaloproteinases de degradação de matriz
RU2001103044A (ru) 1998-07-06 2003-08-10 Бристол-Маерс Сквибб Ко. (Us) Бенилсульфонамиды в качестве двойных антагонистов ангиотензиновых эндотелиновых рецепторов
DE19830430A1 (de) * 1998-07-08 2000-01-13 Hoechst Marion Roussel De Gmbh Schwefelsubstituierte Sulfonylamino-carbonsäure-N-arylamide, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate
RU2232751C2 (ru) * 1998-12-22 2004-07-20 Ф.Хоффманн-Ля Рош Аг Производные сульфонамидов и фармацевтическая композиция
GB9918037D0 (en) * 1999-07-30 1999-09-29 Biochemie Gmbh Organic compounds
EP1202733B1 (en) 1999-08-12 2005-10-05 Pharmacia Italia S.p.A. 3(5)-amino-pyrazole derivatives, process for their preparation and their use as antitumor agents
JP2003528082A (ja) 2000-03-21 2003-09-24 ザ プロクター アンド ギャンブル カンパニー ニフッ化酪酸メタロプロテアーゼ阻害物質
MXPA02009311A (es) 2000-03-21 2003-03-12 Procter & Gamble Inhibidores de las metaloproteasas n-sustituidas que contienen cadenas laterales heterociclicas.
AR031130A1 (es) * 2000-09-20 2003-09-10 Abbott Lab N-acilsulfonamidas promotoras de la apoptosis
US20020055631A1 (en) * 2000-09-20 2002-05-09 Augeri David J. N-acylsulfonamide apoptosis promoters
US6720338B2 (en) * 2000-09-20 2004-04-13 Abbott Laboratories N-acylsulfonamide apoptosis promoters
US6995162B2 (en) 2001-01-12 2006-02-07 Amgen Inc. Substituted alkylamine derivatives and methods of use
EA005810B1 (ru) * 2001-06-06 2005-06-30 Эли Лилли Энд Компани Бензоилсульфонамиды и сульфонилбензамидины для применения в качестве противоопухолевых агентов
PE20030547A1 (es) 2001-09-24 2003-08-18 Bayer Corp Derivados de imidazol para el tratamiento de la obesidad
AR043059A1 (es) 2002-11-12 2005-07-13 Bayer Pharmaceuticals Corp Derivados de indolil pirazinona utiles para el tratamiento de trastornos hiper-proliferativos
WO2004048329A1 (en) 2002-11-22 2004-06-10 Eli Lilly And Company Antitumor benzoylsulfonamides
WO2005024636A1 (ja) 2003-09-04 2005-03-17 Hitachi Ulsi Systems Co., Ltd. 半導体装置
US8614318B2 (en) * 2003-11-13 2013-12-24 Abbvie Inc. Apoptosis promoters
WO2005049593A2 (en) * 2003-11-13 2005-06-02 Abbott Laboratories N-acylsulfonamide apoptosis promoters
US7642260B2 (en) * 2003-11-13 2010-01-05 Abbott Laboratories, Inc. Apoptosis promoters
US7767684B2 (en) 2003-11-13 2010-08-03 Abbott Laboratories Apoptosis promoters
US7973161B2 (en) 2003-11-13 2011-07-05 Abbott Laboratories Apoptosis promoters
JP2007512526A (ja) * 2003-11-20 2007-05-17 フレッシュポイント・ホールディングス・ソシエテ・アノニム 時間温度指標の状態を測定する方法及びシステム
RU2263666C1 (ru) 2004-04-08 2005-11-10 Общество с ограниченной ответственностью "Исследовательский Институт Химического Разнообразия" (ООО "Исследовательский Институт Химического Разнообразия") Гетероциклилсульфиновые кислоты и их производные, фокусированная библиотека и фармацевтическая композиция
WO2005099353A2 (en) 2004-04-19 2005-10-27 Symed Labs Limited A novel process for the preparation of linezolid and related compounds
RU2416606C2 (ru) 2004-06-17 2011-04-20 Инфинити Дискавери, Инк. Соединения и способы для ингибирования взаимодействия bcl белков с компонентами по связыванию
US7429661B2 (en) 2004-07-20 2008-09-30 Symed Labs Limited Intermediates for linezolid and related compounds
EP1804823A4 (en) * 2004-09-29 2010-06-09 Amr Technology Inc NEW CYCLOSPORIN ANALOGUE AND ITS PHARMACEUTICAL APPLICATIONS
US8624027B2 (en) 2005-05-12 2014-01-07 Abbvie Inc. Combination therapy for treating cancer and diagnostic assays for use therein
JP5132550B2 (ja) 2005-05-12 2013-01-30 アボット・ラボラトリーズ アポトーシス促進剤
TW200716636A (en) 2005-05-31 2007-05-01 Speedel Experimenta Ag Heterocyclic spiro-compounds
US7514068B2 (en) * 2005-09-14 2009-04-07 Concert Pharmaceuticals Inc. Biphenyl-pyrazolecarboxamide compounds
CN101534904B (zh) 2006-09-05 2013-11-06 Abbvie公司 治疗血小板过量的bcl抑制剂
US7813729B2 (en) 2006-09-08 2010-10-12 The Boeing Company System and method for associating a wireless mobile communications device with a specific vehicle
US8796267B2 (en) 2006-10-23 2014-08-05 Concert Pharmaceuticals, Inc. Oxazolidinone derivatives and methods of use
US20080182845A1 (en) 2006-11-16 2008-07-31 Abbott Laboratories Method of preventing or treating organ, hematopoietic stem cell or bone marrow transplant rejection
US20100087436A1 (en) 2006-11-16 2010-04-08 Abbott Laboratories Method of preventing or treating organ, hematopoietic stem cell or bone marrow transplant rejection
RU2460725C2 (ru) 2007-02-15 2012-09-10 Ф. Хоффманн-Ля Рош Аг Новые 2-аминооксазолины в качестве лигандов taar1
US7528131B2 (en) * 2007-04-19 2009-05-05 Concert Pharmaceuticals Inc. Substituted morpholinyl compounds
US7531685B2 (en) * 2007-06-01 2009-05-12 Protia, Llc Deuterium-enriched oxybutynin
US20090131485A1 (en) 2007-09-10 2009-05-21 Concert Pharmaceuticals, Inc. Deuterated pirfenidone
US20090118238A1 (en) 2007-09-17 2009-05-07 Protia, Llc Deuterium-enriched alendronate
US20090088416A1 (en) 2007-09-26 2009-04-02 Protia, Llc Deuterium-enriched lapaquistat
US20090082471A1 (en) 2007-09-26 2009-03-26 Protia, Llc Deuterium-enriched fingolimod
WO2009045476A1 (en) 2007-10-02 2009-04-09 Concert Pharmaceuticals, Inc. Pyrimidinedione derivatives
US8410124B2 (en) 2007-10-18 2013-04-02 Concert Pharmaceuticals Inc. Deuterated etravirine
US20090105338A1 (en) 2007-10-18 2009-04-23 Protia, Llc Deuterium-enriched gabexate mesylate
WO2009055006A1 (en) 2007-10-26 2009-04-30 Concert Pharmaceuticals, Inc. Deuterated darunavir
CN101969951B (zh) 2007-11-16 2012-10-31 雅培制药有限公司 化合物在制备治疗关节炎的药物中的方法
US20100160322A1 (en) 2008-12-04 2010-06-24 Abbott Laboratories Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
UA108193C2 (uk) * 2008-12-04 2015-04-10 Апоптозіндукуючий засіб для лікування раку і імунних і аутоімунних захворювань
US8557983B2 (en) * 2008-12-04 2013-10-15 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US8563735B2 (en) 2008-12-05 2013-10-22 Abbvie Inc. Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases
CN102307872B (zh) 2008-12-05 2016-06-15 Abbvie公司 作为用于治疗癌症和免疫疾病的bcl-2-选择性诱发细胞凋亡药剂的磺酰胺衍生物
US8586754B2 (en) 2008-12-05 2013-11-19 Abbvie Inc. BCL-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases
AU2010204554B2 (en) 2009-01-19 2013-05-30 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
AU2010204555B2 (en) 2009-01-19 2013-03-07 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US9034875B2 (en) 2009-05-26 2015-05-19 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US8546399B2 (en) 2009-05-26 2013-10-01 Abbvie Inc. Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases
TWI476195B (zh) * 2009-05-26 2015-03-11 Abbvie Bahamas Ltd 用於治療癌症及免疫及自體免疫疾病之細胞凋亡誘發劑

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