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    • 1. 发明授权
    • Thrombin receptor antagonists
    • 凝血酶受体拮抗剂
    • US06326380B1
    • 2001-12-04
    • US09545720
    • 2000-04-07
    • Samuel ChackalamannilTheodros AsberomYan XiaDario DollerMartin C. ClasbyMichael F. Czarniecki
    • Samuel ChackalamannilTheodros AsberomYan XiaDario DollerMartin C. ClasbyMichael F. Czarniecki
    • A61K3147
    • C07D405/06C07D405/14C07D409/14C07D413/06C07D417/06C07D471/04C07D491/04C07D493/10
    • Heterocyclic-substituted tricyclics of the formula or a pharmaceutically acceptable salt thereof, wherein: the single dotted line represents an optional double bond; the double dotted line represents an optional single bond; n is 0-2; Q is optionally substituted cycloalkyl, heterocycloalkyl, aryl or heteroaryl; Het is an optionally substituted mono-, bi- or tricyclic heteroaromatic group; B is —(CH2)n3—, wherein n3 is 0-5, —CH2—O—, —CH2S—, —CH2—NR6—, —C(O)NR6—, —NR6C(O)—,  optionally substituted alkenyl or optionally substituted alkynyl; X is —O— or —NR6— when the double dotted line represents a single bond, or X is —OH or —NHR20 when the bond is absent; Y is ═O, ═S, (H, H), (H, OH) or (H, C1-C6 alkoxy) when the double dotted line represents a single bond, or when the bond is absent, Y is ═O, (H, H), (H, OH), (H, SH) or (H, C1-C6 alkoxy); R15 is absent when the double dotted line represents a single bond and is H, —NR18R19, or —OR17 when the bond is absent; or Y is  or  and R15 is H or C1-C6 alkyl; are disclosed, as well as pharmaceutical compositions containing them and a method of treating diseases associated with thrombosis, atherosclerosis, restenosis, hypertension, angina pectoris, arrhythmia, heart failure, and cancer by administering said compounds.
    • 式2的杂环取代的三环或其药学上可接受的盐,其中:单点线表示任选的双键;双点划线表示任选的单键; n为0-2; Q为任选取代的环烷基,杂环烷基,芳基 或杂芳基; Het是任选取代的单,双或三环杂芳族基团; B是 - (CH 2)n3-,其中n3是0-5,-CH2-O-,-CH2S-,-CH2-NR6-, -C(O)NR 6 - ,-NR 6 C(O) - ,任选取代的烯基或任选取代的炔基;当双点划线表示单键时,X为-O-或-NR6-,或X为-OH或-NHR20 当双键虚线表示单键时,当不存在键时,Y为= O,= S,(H,H),(H,OH)或(H,C 1 -C 6烷氧基) ,Y为= O,(H,H),(H,OH),(H,SH)或(H,C1-C6烷氧基);当双点表示单键且为H时, NR18R19或-OR17,当该键不存在时; 或Y为或R 15为H或C 1 -C 6烷基;以及含有它们的药物组合物和治疗与血栓形成,动脉粥样硬化,再狭窄,高血压,心绞痛,心律失常,心力衰竭和癌症相关的疾病的方法 通过施用所述化合物。
    • 2. 发明授权
    • Thrombin receptor antagonists
    • 凝血酶受体拮抗剂
    • US6063847A
    • 2000-05-16
    • US197442
    • 1998-11-23
    • Samuel ChackalamannilTheodros AsberomYan XiaDario DollerMartin C. ClasbyMichael F. Czarniecki
    • Samuel ChackalamannilTheodros AsberomYan XiaDario DollerMartin C. ClasbyMichael F. Czarniecki
    • C07D405/06C07D405/14C07D409/14C07D413/06C07D417/06C07D471/04C07D491/04C07D493/10A61K31/44A61K31/423A61K31/47C02D213/60
    • C07D405/06C07D405/14C07D409/14C07D413/06C07D417/06C07D471/04C07D491/04C07D493/10
    • Heterocyclic-substituted tricyclics of the formula ##STR1## or a pharmaceutically acceptable salt thereof, wherein: the single dotted line represents an optional double bond;the double dotted line represents an optional single bond;n is 0-2;Q is optionally substituted cycloalkyl, heterocycloalkyl, aryl or heteroaryl;Het is an optionally substituted mono-, bi- or tricyclic heteroaromatic group;B is --(CH.sub.2).sub.n3 --, wherein n.sub.3 is 0-5, --CH.sub.2 --O--, --CH.sub.2 S--, --CH.sub.2 --NR.sup.6 --, --C(O)NR.sup.6 --. --NR.sup.6 C(O)--, ##STR2## optionally substituted alkenyl or optionally substituted alkynyl; X is --O-- or --NR.sup.6 -- when the double dotted line represents a single bond, or X is --OH or --NHR.sup.20 when the bond is absent;Y is .dbd.O, .dbd.S, (H, H), (H, OH) or (H, C.sub.1 -C.sub.6 alkoxy) when the double dotted line represents a single bond, or when the bond is absent, Y is .dbd.O, (H, H), (H, OH), (H, SH) or (H, C.sub.1 -C.sub.6 alkoxy);R.sup.15 is absent when the double dotted line represents a single bond and is H, --NR.sup.18 R.sup.19, or --OR.sup.17 when the bond is absent; or Y is ##STR3## and R.sup.15 is H or C.sub.1 -C.sub.6 alkyl; are disclosed, as well as pharmaceutical compositions containing them and a method of treating diseases associated with thrombosis, atherosclerosis, restenosis, hypertension, angina pectoris, arrhythmia, heart failure, and cancer by administering said compounds.
    • 具有下式的杂环取代的三环或其药学上可接受的盐,其中:单个虚线表示任选的双键; 双点划线表示可选的单键; n为0-2; Q是任选取代的环烷基,杂环烷基,芳基或杂芳基; Het是任选取代的单,双或三环杂芳族基团; B是 - (CH 2)n3-,其中n3是0-5,-CH2-O-,-CH2S-,-CH2-NR6-, - C(O)NR6-。 -NR 6 C(O) - ,任选取代的烯基或任选取代的炔基; 当双点划线表示单键时,X是-O-或-NR6-,或者当不存在键时X是-OH或-NHR 20; 当双点划线表示单键时,Y为= O,= S,(H,H),(H,OH)或(H,C 1 -C 6烷氧基),或当不存在键时,Y为= (H,H),(H,OH),(H,SH)或(H,C 1 -C 6烷氧基); 当双重虚线表示单键并且当不存在键时,R 15不存在且为H,-NR 18 R 19或-OR 17; 或Y为R 15为H或C 1 -C 6烷基; 以及含有它们的药物组合物以及通过施用所述化合物治疗与血栓形成,动脉粥样硬化,再狭窄,高血压,心绞痛,心律失常,心力衰竭和癌症相关的疾病的方法。