Aminoguanidines and alkoxyguanidines as protease inhibitors
    1.
    发明授权
    Aminoguanidines and alkoxyguanidines as protease inhibitors 有权
    氨基胍和烷氧基胍作为蛋白酶抑制剂

    公开(公告)号:US06638931B1

    公开(公告)日:2003-10-28

    申请号:US09722363

    申请日:2000-11-28

    IPC分类号: A61K31255

    摘要: Aminoguanidine and alkoxyguanidine compounds, including compounds of the formula: wherein X is O or NR9 and R1-R4, R6-R9, R11, R12, Ra, Rb, Rc, Y, Z, n and m are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhibit proteolytic enzymes such as thrombin are described. Also described are methods for preparing the compounds of Formula I. The novel compounds of the present invention are potent inhibitors of proteases, especially trypsin-like serine proteases, such as chymotrypsin, trypsin, thrombin, plasmin and factor Xa. Certain of the compounds exhibit antithrombotic activity via direct, selective inhibition of thrombin, or are intermediates useful for forming compounds having antithrombotic activity. The invention includes a composition for inhibiting loss of blood platelets, inhibiting formation of blood platelet aggregates, inhibiting formation of fibrin, inhibiting thrombus formation, and inhibiting embolus formation in a mammal, comprising a compound of the invention in a pharmaceutically acceptable carrier. Other uses of compounds of the invention are as anticoagulants either embedded in or physically linked to materials used in the manufacture of devices used in blood collection, blood circulation, and blood storage, such as catheters, blood dialysis machines, blood collection syringes and tubes, blood lines and stents.

    摘要翻译: 氨基胍和烷氧基胍化合物,包括下式的化合物:其中X是O或NR 9和R 1 -R 4,R 6 -R 9,R 11,R 12, 说明书中列出的R a,R b,R c,Y,Z,n和m以及抑制蛋白水解酶如凝血酶的水合物,溶剂合物或其药学上可接受的盐是 描述。 还描述了制备式I化合物的方法。本发明的新化合物是蛋白酶的有效抑制剂,特别是胰蛋白酶样丝氨酸蛋白酶,例如胰凝乳蛋白酶,胰蛋白酶,凝血酶,纤溶酶和因子Xa。 某些化合物通过直接,选择性抑制凝血酶表现出抗血栓形成活性,或者是用于形成具有抗血栓形成活性的化合物的中间体。 本发明包括用于抑制血小板损失,抑制血小板聚集体形成,抑制纤维蛋白形成,抑制血栓形成和抑制哺乳动物栓塞形成的组合物,其包含本发明化合物在药学上可接受的载体中。 本发明化合物的其它用途是作为凝血剂或者物理上连接于用于血液收集,血液循环和血液储存(例如导管,血液透析机,采血注射器和管)中使用的装置的制造中使用的材料的抗凝剂, 血线和支架。

    Aminoguanidines and alkoxyguanidines as protease inhibitors
    2.
    发明授权
    Aminoguanidines and alkoxyguanidines as protease inhibitors 有权
    氨基胍和烷氧基胍作为蛋白酶抑制剂

    公开(公告)号:US06518310B2

    公开(公告)日:2003-02-11

    申请号:US09809293

    申请日:2001-03-16

    IPC分类号: A61K31255

    摘要: Aminoguanidine and alkoxyguanidine compounds, including compounds of the formula: wherein X is O or NR9 and R1-R4, R6-R9, R11, R12, Ra, Rb, Rc, Y, Z, n and m are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhibit proteolytic enzymes such as thrombin are described. Also described are methods for preparing the compounds of Formula I. The novel compounds of the present invention are potent inhibitors of proteases, especially trypsin-like serine proteases, such as chymotrypsin, trypsin, thrombin, plasmin and factor Xa. Certain of the compounds exhibit antithrombotic activity via direct, selective inhibition of thrombin, or are intermediates useful for forming compounds having antithrombotic activity. The invention includes a composition for inhibiting loss of blood platelets, inhibiting formation of blood platelet aggregates, inhibiting formation of fibrin, inhibiting thrombus formation, and inhibiting embolus formation in a mammal, comprising a compound of the invention in a pharmaceutically acceptable carrier. Other uses of compounds of the invention are as anticoagulants either embedded in or physically linked to materials used in the manufacture of devices used in blood collection, blood circulation, and blood storage, such as catheters, blood dialysis machines, blood collection syringes and tubes, blood lines and stents.

    摘要翻译: 氨基胍和烷氧基胍化合物,包括下式的化合物:其中X为O或NR 9,R 1 -R 4,R 6 -R 9,R 11,R 12,R a,R b,R c,Y,Z,n和m在说明书中阐述, 以及抑制蛋白水解酶如凝血酶的水合物,溶剂合物或其药学上可接受的盐。 还描述了制备式I化合物的方法。本发明的新化合物是蛋白酶的有效抑制剂,特别是胰蛋白酶样丝氨酸蛋白酶,例如胰凝乳蛋白酶,胰蛋白酶,凝血酶,纤溶酶和因子Xa。 某些化合物通过直接,选择性抑制凝血酶表现出抗血栓形成活性,或者是用于形成具有抗血栓形成活性的化合物的中间体。 本发明包括用于抑制血小板损失,抑制血小板聚集体形成,抑制纤维蛋白形成,抑制血栓形成和抑制哺乳动物栓塞形成的组合物,其包含本发明化合物在药学上可接受的载体中。 本发明化合物的其它用途是作为凝血剂或者物理上连接于用于血液收集,血液循环和血液储存(例如导管,血液透析机,采血注射器和管)中使用的装置的制造中使用的材料的抗凝剂, 血线和支架。

    Heteroaryl aminoguanidines and alkoxyguanidines and their use as protease inhibitors
    3.
    发明授权
    Heteroaryl aminoguanidines and alkoxyguanidines and their use as protease inhibitors 有权
    杂芳基氨基胍和烷氧基胍及其作为蛋白酶抑制剂的用途

    公开(公告)号:US06350764B2

    公开(公告)日:2002-02-26

    申请号:US09827292

    申请日:2001-04-06

    IPC分类号: A61K314412

    摘要: Aminoguanidine and alkoxyguanidine compounds are described, including compounds of the Formula VII: wherein X is O or NR9 and Het, R1, R7, R8, R12-R15, Ra, Rb, Rc, Z, and n are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhibit proteolytic enzymes such as thrombin. Also described are methods for preparing such compounds. The compounds of the invention are potent inhibitors of proteases, especially trypsin-like serine proteases, such as chymotrypsin, trypsin, thrombin, plasmin and factor Xa. Certain of the compounds exhibit antithrombotic activity via direct, selective inhibition of thrombin. The invention includes a composition for inhibiting loss of blood platelets, inhibiting formation of blood platelet aggregates, inhibiting formation of fibrin, inhibiting thrombus formation, and inhibiting embolus formation in a mammal, comprising a compound of the invention in a pharmaceutically acceptable carrier. Other uses of compounds of the invention are as anticoagulants either embedded in or physically linked to materials used in the manufacture of devices used in blood collection, blood circulation, and blood storage, such as catheters, blood dialysis machines, blood collection syringes and tubes, blood lines and stents. Additionally, the compounds can be detectably labeled and employed for in vivo imaging of thrombi.

    摘要翻译: 描述了氨基胍和烷氧基胍化合物,包括式VII的化合物:其中X是O或NR 9,Het,R 1,R 7,R 8,R 12 -R 15,R a,R b,R c,Z和n在说明书中阐述, 以及其抑制蛋白水解酶如凝血酶的水合物,溶剂合物或其药学上可接受的盐。 还描述了制备这些化合物的方法。 本发明的化合物是蛋白酶的有效抑制剂,特别是胰蛋白酶样丝氨酸蛋白酶,如胰凝乳蛋白酶,胰蛋白酶,凝血酶,纤溶酶和因子Xa。 某些化合物通过直接,选择性抑制凝血酶表现出抗血栓形成活性。 本发明包括用于抑制血小板损失,抑制血小板聚集体形成,抑制纤维蛋白形成,抑制血栓形成和抑制哺乳动物栓塞形成的组合物,其包含本发明化合物在药学上可接受的载体中。 本发明化合物的其它用途是作为凝血剂或者物理上连接于用于血液收集,血液循环和血液储存(例如导管,血液透析机,采血注射器和管)中使用的装置的制造中使用的材料的抗凝剂, 血线和支架。 另外,化合物可以被可检测地标记并用于血栓的体内成像。

    Benzamide and sulfonamide substituted aminoguanidines and alkoxyguanidines as protease inhibitors
    4.
    发明授权
    Benzamide and sulfonamide substituted aminoguanidines and alkoxyguanidines as protease inhibitors 有权
    苯甲酰胺和磺酰胺取代的氨基胍和烷氧基胍作为蛋白酶抑制剂

    公开(公告)号:US06344486B1

    公开(公告)日:2002-02-05

    申请号:US09283241

    申请日:1999-04-01

    IPC分类号: A61K31165

    摘要: The present invention is directed to aminoguanidine and alkoxyguanidine compounds, including compounds of Formula I: wherein X is O or NH, L is —O— or —SO2—, and R1-R4, R9-R19, Ra, Rb, Rc, Y, Z, n and m are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhibit proteolytic enzymes such as thrombin. Also described are methods for preparing the compounds of Formula I. Certain of the compounds exhibit antithrombotic activity via direct, selective inhibition of thrombin, or are intermediates useful for forming compounds having antithrombotic activity. The invention includes a composition for inhibiting loss of blood platelets, inhibiting formation of blood platelet aggregates, inhibiting formation of fibrin, inhibiting thrombus formation, and inhibiting embolus formation in a mammal. Other uses of compounds of the invention are as anticoagulants either embedded in or physically linked to materials used in the manufacture of devices used in blood collection, blood circulation, and blood storage.

    摘要翻译: 本发明涉及氨基胍和烷氧基胍化合物,包括式I化合物:其中X为O或NH,L为-O-或-SO 2 - ,R 1 -R 4,R 9 -R 19,R a,R b,R c,Y ,Z,n和m在说明书中列出,以及抑制蛋白水解酶如凝血酶的水合物,溶剂合物或其药学上可接受的盐。 还描述了制备式I化合物的方法。某些化合物通过直接,选择性抑制凝血酶表现出抗血栓形成活性,或者是用于形成具有抗血栓形成活性的化合物的中间体。 本发明包括用于抑制血小板损失,抑制血小板聚集体形成,抑制纤维蛋白形成,抑制血栓形成和抑制哺乳动物栓塞形成的组合物。 本发明化合物的其它用途是作为抗凝剂,其嵌入或用于制造用于采血,血液循环和血液储存中的装置的材料中物理连接。

    Heteroaryl aminoguanidines and alkoxyguanidines and their use as
protease inhibitors
    5.
    发明授权
    Heteroaryl aminoguanidines and alkoxyguanidines and their use as protease inhibitors 有权
    杂芳基氨基胍和烷氧基胍及其作为蛋白酶抑制剂的用途

    公开(公告)号:US6037356A

    公开(公告)日:2000-03-14

    申请号:US199167

    申请日:1998-11-25

    摘要: Aminoguanidine and alkoxyguanidine compounds are described, including compounds of the Formula VII: ##STR1## wherein X is O or NR.sup.9 and Het, R.sup.1, R.sup.7, R.sup.8, R.sup.12 -R.sup.15, R.sup.a, R.sup.b, R.sup.c, Z, and n are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhibit proteolytic enzymes such as thrombin. Also described are methods for preparing such compounds. The compounds of the invention are potent inhibitors of proteases, especially trypsin-like serine proteases, such as chymotrypsin, trypsin, thrombin, plasmin and factor Xa. Certain of the compounds exhibit antithrombotic activity via direct, selective inhibition of thrombin. The invention includes a composition for inhibiting loss of blood platelets, inhibiting formation of blood platelet aggregates, inhibiting formation of fibrin, inhibiting thrombus formation, and inhibiting embolus formation in a mammal, comprising a compound of the invention in a pharmaceutically acceptable carrier. Other uses of compounds of the invention are as anticoagulants either embedded in or physically linked to materials used in the manufacture of devices used in blood collection, blood circulation, and blood storage, such as catheters, blood dialysis machines, blood collection syringes and tubes, blood lines and stents. Additionally, the compounds can be detectably labeled and employed for in vivo imaging of thrombi.

    摘要翻译: 描述了氨基胍和烷氧基胍化合物,包括式VII的化合物:其中X是O或NR 9,Het,R 1,R 7,R 8,R 12 -R 15,R a,R b,R c,Z和n在说明书中阐述, 以及其抑制蛋白水解酶如凝血酶的水合物,溶剂合物或其药学上可接受的盐。 还描述了制备这些化合物的方法。 本发明的化合物是蛋白酶的有效抑制剂,特别是胰蛋白酶样丝氨酸蛋白酶,如胰凝乳蛋白酶,胰蛋白酶,凝血酶,纤溶酶和因子Xa。 某些化合物通过直接,选择性抑制凝血酶表现出抗血栓形成活性。 本发明包括用于抑制血小板损失,抑制血小板聚集体形成,抑制纤维蛋白形成,抑制血栓形成和抑制哺乳动物栓塞形成的组合物,其包含本发明化合物在药学上可接受的载体中。 本发明化合物的其它用途是作为凝血剂或者物理上连接于用于血液收集,血液循环和血液储存(例如导管,血液透析机,采血注射器和管)中使用的装置的制造中使用的材料的抗凝剂, 血线和支架。 另外,化合物可以被可检测地标记并用于血栓的体内成像。

    Thromboresistant materials incorporating pyrazinone protease inhibitors
    6.
    发明授权
    Thromboresistant materials incorporating pyrazinone protease inhibitors 有权
    结合吡嗪酮蛋白酶抑制剂的抗栓材料

    公开(公告)号:US06514978B2

    公开(公告)日:2003-02-04

    申请号:US09773730

    申请日:2001-02-02

    IPC分类号: A61K314965

    CPC分类号: C07K5/06139 A61K38/00

    摘要: Thromboresistant materials are described which incorporate pyrazinone compounds of the Formula I: wherein X is O, NR11 or CH═N, R3-R11, Ra, Rb, Rc, W, m, and n are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof. The compounds of the invention are potent inhibitors of proteases, especially trypsin-like serine proteases, such as chymotrypsin, trypsin, thrombin, plasmin and factor Xa. Certain of the compounds exhibit antithrombotic activity via direct, selective inhibition of thrombin. Compositions for inhibiting loss of blood platelets, inhibiting formation of blood platelet aggregates, inhibiting formation of fibrin, inhibiting thrombus formation, and inhibiting embolus formation are described. Other uses of compounds of the invention are as anticoagulants either embedded in or physically linked to materials used in the manufacture of devices used in blood collection, blood circulation, and blood storage, such as catheters, blood dialysis machines, blood collection syringes and tubes, blood lines and stents. Additionally, the compounds can be detectably labeled and employed for in vivo imaging of thrombi.

    摘要翻译: 描述了含有式I的吡嗪酮化合物的抗栓材料:其中X是O,NR 11或CH = N,R 3 -R 11,R a,R b,R c,W,m和n在说明书中列出,以及 水合物,溶剂合物或其药学上可接受的盐。 本发明的化合物是蛋白酶的有效抑制剂,特别是胰蛋白酶样丝氨酸蛋白酶,如胰凝乳蛋白酶,胰蛋白酶,凝血酶,纤溶酶和因子Xa。 某些化合物通过直接,选择性抑制凝血酶表现出抗血栓形成活性。 描述了抑制血小板损失,抑制血小板聚集体形成,抑制纤维蛋白形成,抑制血栓形成和抑制栓塞形成的组合物。 本发明化合物的其它用途是作为凝血剂或者物理上连接于用于血液收集,血液循环和血液储存(例如导管,血液透析机,采血注射器和管)中使用的装置的制造中使用的材料的抗凝剂, 血线和支架。 另外,化合物可以被可检测地标记并用于血栓的体内成像。

    Heteroaryl aminoguanidines and alkoxyguanidines and their use as protease inhibitors
    7.
    发明授权
    Heteroaryl aminoguanidines and alkoxyguanidines and their use as protease inhibitors 有权
    杂芳基氨基胍和烷氧基胍及其作为蛋白酶抑制剂的用途

    公开(公告)号:US06245763B1

    公开(公告)日:2001-06-12

    申请号:US09482540

    申请日:2000-01-14

    IPC分类号: A61K31501

    摘要: Aminoguanidine and alkoxyguanidine compounds are described, including compounds of the Formula VII: wherein X is O or NR9 and Het, R1, R7, R8, R12-R15, Ra, Rb, Rc, Z, and n are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhibit proteolytic enzymes such as thrombin. Also described are methods for preparing such compounds. The compounds of the invention are potent inhibitors of proteases, especially trypsin-like serine proteases, such as chymotrypsin, trypsin, thrombin, plasmin and factor Xa. Certain of the compounds exhibit antithrombotic activity via direct, selective inhibition of thrombin. The invention includes a composition for inhibiting loss of blood platelets, inhibiting formation of blood platelet aggregates, inhibiting formation of fibrin, inhibiting thrombus formation, and inhibiting embolus formation in a mammal, comprising a compound of the invention in a pharmaceutically acceptable carrier. Other uses of compounds of the invention are as anticoagulants either embedded in or physically linked to materials used in the manufacture of devices used in blood collection, blood circulation, and blood storage, such as catheters, blood dialysis machines, blood collection syringes and tubes, blood lines and stents. Additionally, the compounds can be detectably labeled and employed for in vivo imaging of thrombi.

    摘要翻译: 描述了氨基胍和烷氧基胍化合物,包括式VII的化合物:其中X是O或NR 9,Het,R 1,R 7,R 8,R 12 -R 15,R a,R b,R c,Z和n在说明书中阐述, 以及其抑制蛋白水解酶如凝血酶的水合物,溶剂合物或其药学上可接受的盐。 还描述了制备这些化合物的方法。 本发明的化合物是蛋白酶的有效抑制剂,特别是胰蛋白酶样丝氨酸蛋白酶,如胰凝乳蛋白酶,胰蛋白酶,凝血酶,纤溶酶和因子Xa。 某些化合物通过直接,选择性抑制凝血酶表现出抗血栓形成活性。 本发明包括用于抑制血小板损失,抑制血小板聚集体形成,抑制纤维蛋白形成,抑制血栓形成和抑制哺乳动物栓塞形成的组合物,其包含本发明化合物在药学上可接受的载体中。 本发明化合物的其它用途是作为凝血剂或者物理连接于制造用于血液收集,血液循环和血液储存中的装置的材料的抗凝剂,例如导管,血液透析机,采血注射器和管, 血线和支架。 另外,化合物可以被可检测地标记并用于血栓的体内成像。

    Heteroaryl aminoguanidines and alkoxyguanidines and their use as protease inhibitors
    8.
    发明授权
    Heteroaryl aminoguanidines and alkoxyguanidines and their use as protease inhibitors 有权
    杂芳基氨基胍和烷氧基胍及其作为蛋白酶抑制剂的用途

    公开(公告)号:US07029654B2

    公开(公告)日:2006-04-18

    申请号:US10714988

    申请日:2003-11-17

    IPC分类号: A61K49/00

    摘要: Aminoguanidine and alkoxyguanidine compounds are described, including compounds of the Formula VII: wherein X is O or NR9 and Het, R1, R7, R8, R12—R15, Ra, Rb, Rc, Z, and n are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhibit proteolytic enzymes such as thrombin. Also described are methods for preparing such compounds. The compounds of the invention are potent inhibitors of proteases, especially trypsin-like serine proteases, such as chymotrypsin, trypsin, thrombin, plasmin and factor Xa. Certain of the compounds exhibit antithrombotic activity via direct, selective inhibition of thrombin. The invention includes a composition for inhibiting loss of blood platelets, inhibiting formation of blood platelet aggregates, inhibiting formation of fibrin, inhibiting thrombus formation, and inhibiting embolus formation in a mammal, comprising a compound of the invention in a pharmaceutically acceptable carrier. Other uses of compounds of the invention are as anticoagulants either embedded in or physically linked to materials used in the manufacture of devices used in blood collection, blood circulation, and blood storage, such as catheters, blood dialysis machines, blood collection syringes and tubes, blood lines and stents. Additionally, the compounds can be detectably labeled and employed for in vivo imaging of thrombi.

    摘要翻译: 描述了氨基胍和烷氧基胍化合物,包括式VII的化合物:其中X是O或NR 9和Het,R 1,R 7, R 8,R 12,R 15,R 12,R 12,R 12, 说明书中描述的R,Z和n以及其抑制蛋白水解酶如凝血酶的水合物,溶剂合物或其药学上可接受的盐。 还描述了制备这些化合物的方法。 本发明的化合物是蛋白酶的有效抑制剂,特别是胰蛋白酶样丝氨酸蛋白酶,如胰凝乳蛋白酶,胰蛋白酶,凝血酶,纤溶酶和因子Xa。 某些化合物通过直接,选择性抑制凝血酶表现出抗血栓形成活性。 本发明包括用于抑制血小板损失,抑制血小板聚集体形成,抑制纤维蛋白形成,抑制血栓形成和抑制哺乳动物栓塞形成的组合物,其包含本发明化合物在药学上可接受的载体中。 本发明化合物的其它用途是作为凝血剂或者物理上连接于用于血液收集,血液循环和血液储存(例如导管,血液透析机,采血注射器和管)中使用的装置的制造中使用的材料的抗凝剂, 血线和支架。 另外,化合物可以被可检测地标记并用于血栓的体内成像。

    Benzamide and sulfonamide substituted aminoguanidines and alkoxyguanidines as protease inhibitors

    公开(公告)号:US06274628B1

    公开(公告)日:2001-08-14

    申请号:US09283241

    申请日:1999-04-01

    IPC分类号: A61K31165

    摘要: The present invention is directed to aminoguanidine and alkoxyguanidine compounds, including compounds of Formula I: wherein X is O or NH, L is —O— or —SO2—, and R1-R4, R9-R19, Ra, Rb, Rc, Y, Z, n and m are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhibit proteolytic enzymes such as thrombin. Also described are methods for preparing the compounds of Formula I. Certain of the compounds exhibit antithrombotic activity via direct, selective inhibition of thrombin, or are intermediates useful for forming compounds having antithrombotic activity. The invention includes a composition for inhibiting loss of blood platelets, inhibiting formation of blood platelet aggregates, inhibiting formation of fibrin, inhibiting thrombus formation, and inhibiting embolus formation in a mammal. Other uses of compounds of the invention are as anticoagulants either embedded in or physically linked to materials used in the manufacture of devices used in blood collection, blood circulation, and blood storage.

    Process for preparing aminoguanidines and alkoxyguanidines as protease inhibitors
    10.
    发明授权
    Process for preparing aminoguanidines and alkoxyguanidines as protease inhibitors 有权
    制备氨基胍和烷氧基胍作为蛋白酶抑制剂的方法

    公开(公告)号:US06730783B2

    公开(公告)日:2004-05-04

    申请号:US10419972

    申请日:2003-04-22

    IPC分类号: A61K31255

    摘要: Aminoguanidine and alkoxyguanidine compounds, including compounds of the formula: wherein X is O or NR9 and R1-R4, R6-R9, R11, R12, Ra, Rb, Rc, Y, Z, n and m are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhibit proteolytic enzymes such as thrombin are described. Also described are methods for preparing the compounds of Formula I. The novel compounds of the present invention are potent inhibitors of proteases, especially trypsin-like serine proteases, such as chymotrypsin, trypsin, thrombin, plasmin and factor Xa. Certain of the compounds exhibit antithrombotic activity via direct, selective inhibition of thrombin, or are intermediates useful for forming compounds having antithrombotic activity. The invention includes a composition for inhibiting loss of blood platelets, inhibiting formation of blood platelet aggregates, inhibiting formation of fibrin, inhibiting thrombus formation, and inhibiting embolus formation in a mammal, comprising a compound of the invention in a pharmaceutically acceptable carrier. Other uses of compounds of the invention are as anticoagulants either embedded in or physically linked to materials used in the manufacture of devices used in blood collection, blood circulation, and blood storage, such as catheters, blood dialysis machines, blood collection syringes and tubes, blood lines and stents.

    摘要翻译: 氨基胍和烷氧基胍化合物,包括下式的化合物:其中X是O或NR 9和R 1 -R 4,R 6 -R 9,R 11,R 12, 说明书中列出的R a,R b,R c,Y,Z,n和m以及抑制蛋白水解酶如凝血酶的水合物,溶剂合物或其药学上可接受的盐是 描述。 还描述了制备式I化合物的方法。本发明的新化合物是蛋白酶的有效抑制剂,特别是胰蛋白酶样丝氨酸蛋白酶,例如胰凝乳蛋白酶,胰蛋白酶,凝血酶,纤溶酶和因子Xa。 某些化合物通过直接,选择性抑制凝血酶表现出抗血栓形成活性,或者是用于形成具有抗血栓形成活性的化合物的中间体。 本发明包括用于抑制血小板损失,抑制血小板聚集体形成,抑制纤维蛋白形成,抑制血栓形成和抑制哺乳动物栓塞形成的组合物,其包含本发明化合物在药学上可接受的载体中。 本发明化合物的其它用途是作为凝血剂或者物理上连接于用于血液收集,血液循环和血液储存(例如导管,血液透析机,采血注射器和管)中使用的装置的制造中使用的材料的抗凝剂, 血线和支架。