-
1
-
-
33748686332
-
New dual pharmacophore 2-hydroxyethylamine derivatives are β-adrenergic antagonists and/or phosphodiesterase inhibitors - Useful for the treatment of cardiovascular diseases, stroke, epilepsy, ophthalmic disorders and migraine
-
Artesian Therapeutics Inc WO-2006060122
-
Artesian Therapeutics Inc (Taylor GM, Klenke B, Suzdak PD, Mazhari R): New dual pharmacophore 2-hydroxyethylamine derivatives are β-adrenergic antagonists and/or phosphodiesterase inhibitors - useful for the treatment of cardiovascular diseases, stroke, epilepsy, ophthalmic disorders and migraine. WO-2006060122 (2006).
-
(2006)
-
-
Taylor, G.M.1
Klenke, B.2
Suzdak, P.D.3
Mazhari, R.4
-
2
-
-
33748701828
-
New aryl substituted compounds - Useful for the treatment of cardiovascular disorders such as atherosclerosis, restenosis and hypertension
-
WO-2006063408
-
Stocker RO: New aryl substituted compounds - useful for the treatment of cardiovascular disorders such as atherosclerosis, restenosis and hypertension. WO-2006063408 (2006).
-
(2006)
-
-
Stocker, R.O.1
-
3
-
-
33748699768
-
New bicyclic [1,4]benzodiazepine derivatives are vasopressin V2 antagonists - Useful for the treatment of hypertension, cardiac insufficiency, coronary vasospasm, cirrhosis, renal failure, stroke, thrombosis and water retention
-
Janssen Pharmaceutica NV WO-2006049984
-
Janssen Pharmaceutica NV (Maryanoff B, Matthews J): New bicyclic [1,4]benzodiazepine derivatives are vasopressin V2 antagonists - useful for the treatment of hypertension, cardiac insufficiency, coronary vasospasm, cirrhosis, renal failure, stroke, thrombosis and water retention. WO-2006049984 (2006)
-
(2006)
-
-
Maryanoff, B.1
Matthews, J.2
-
4
-
-
33748695483
-
New fused pyrazole derivatives are RUP26 receptor agonists - Useful for the treatment of metabolic-related disorders such as atherosclerosis, dyslipidemia and coronary heart disease
-
Arena Pharmaceuticals Inc WO-2006069242
-
Arena Pharmaceuticals Inc (Boatman DP, Schrader TO, Semple G, Skinner PJ, Jung J-K): New fused pyrazole derivatives are RUP26 receptor agonists - useful for the treatment of metabolic-related disorders such as atherosclerosis, dyslipidemia and coronary heart disease. WO-2006069242 (2006).
-
(2006)
-
-
Boatman, D.P.1
Schrader, T.O.2
Semple, G.3
Skinner, P.J.4
Jung, J.-K.5
-
5
-
-
33748712611
-
New biaryl derivatives are niacin agonists - Useful for the treatment of dysilpidemia and atherosclerosis
-
Merck & Co Inc WO-2006057922
-
Merck & Co Inc (Colletti SL, Tata JR, Shen HC, Ding F-X, Frie JL, Imbriglio JE, Chen W): New biaryl derivatives are niacin agonists - useful for the treatment of dysilpidemia and atherosclerosis. WO-2006057922 (2006)
-
(2006)
-
-
Colletti, S.L.1
Tata, J.R.2
Shen, H.C.3
Ding, F.-X.4
Frie, J.L.5
Imbriglio, J.E.6
Chen, W.7
-
6
-
-
33748714085
-
New xanthine derivatives are HM74A receptor modulators - Useful for the treatment of eg diabetic dyslipidemia, heart failure and atherosclerosis
-
SmithKline Beecham Corp WO-2006045564
-
SmithKline Beecham Corp (Hatley RJD, Pinto IL): New xanthine derivatives are HM74A receptor modulators - useful for the treatment of eg diabetic dyslipidemia, heart failure and atherosclerosis. WO-2006045564 (2006).
-
(2006)
-
-
Hatley, R.J.D.1
Pinto, I.L.2
-
7
-
-
33748714085
-
New xanthine derivatives are HM74A receptor modulators - Useful for the treatment of, eg, diabetic dyslipidemia, heart failure and atherosclerosis
-
SmithKline Beecham Corp WO-2006045565
-
SmithKline Beecham Corp (Hatley RJD, Pinto IL): New xanthine derivatives are HM74A receptor modulators - useful for the treatment of, eg, diabetic dyslipidemia, heart failure and atherosclerosis. WO-2006045565 (2006).
-
(2006)
-
-
Hatley, R.J.D.1
Pinto, I.L.2
-
8
-
-
33748706327
-
New piperidine sulfonyl urea derivatives are blockers of ATP-sensitive potassium channels - Useful for the treatment of cardiovascular disorders
-
Sanofi-Aventis Deutschland GmbH WO-2006063722
-
Sanofi-Aventis Deutschland GmbH (Knieps S, Englert HC, Gerlach U, Goegelein H, Heitsch H, Lehr K-H, Pfeiffer-Marek S): New piperidine sulfonyl urea derivatives are blockers of ATP-sensitive potassium channels - useful for the treatment of cardiovascular disorders. WO-2006063722 (2006).
-
(2006)
-
-
Knieps, S.1
Englert, H.C.2
Gerlach, U.3
Goegelein, H.4
Heitsch, H.5
Lehr, K.-H.6
Pfeiffer-Marek, S.7
-
9
-
-
33748683935
-
New thieno[2,3-b]pyridine derivatives are potassium channel inhibitors - Useful for the treatment and prevention of arrhythmia, type 1 and 2 diabetes and immune, inflammatory bowel and demyelinating disorders
-
Xention Discovery Limited WO-2006061642
-
Xention Discovery Limited (Ford J, Madge DJ, Palmer NJ, Atherall JF, John D): New thieno[2,3-b]pyridine derivatives are potassium channel inhibitors - useful for the treatment and prevention of arrhythmia, type 1 and 2 diabetes and immune, inflammatory bowel and demyelinating disorders. WO-2006061642 (2006).
-
(2006)
-
-
Ford, J.1
Madge, D.J.2
Palmer, N.J.3
Atherall, J.F.4
John, D.5
-
10
-
-
33748697594
-
Novel thiazole-5-carboxamide derivatives are selective Kv channel blockers - Useful for the treatment of cardiac and central nervous system disorders
-
Devgen NV WO-2006068905
-
Devgen NV (Biom P, De Kerpel JO, Fourmaintraux E, René PP, Kaletta, TJ, Leysen D): Novel thiazole-5-carboxamide derivatives are selective Kv channel blockers - useful for the treatment of cardiac and central nervous system disorders. WO-2006068905 (2006).
-
(2006)
-
-
Biom, P.1
De Kerpel, J.O.2
Fourmaintraux, E.3
René, P.P.4
Kaletta, T.J.5
Leysen, D.6
-
11
-
-
33748704438
-
Composition comprising midklne protein - Useful for the treatment of heart disease
-
Cell Signals Inc/National University Corp/Nagoya University WO-2006062087
-
Cell Signals Inc/National University Corp/Nagoya University (Mitsuru H, Itsuo, K. Takashi M, Kenji K): Composition comprising midklne protein - useful for the treatment of heart disease. WO-2006062087 (2006).
-
(2006)
-
-
Mitsuru, H.1
Itsuo, K.2
Takashi, M.3
Kenji, K.4
-
12
-
-
33748682289
-
Use of a nitrogenous fused compound as a URAT1 Inhibitor - For treating, eg, hyperuricemia, gouty node, acute or chronic gouty arthritis, gouty kidney, urinary calcus, renal dysfunction, coronary artery disease and ischemic artery disease
-
Japan Tobacco Inc WO-2006057460
-
Japan Tobacco Inc (Hirata K, Ogawa N, Shinagawa Y, Kiguchi T, Inoue T, Matsuo A, Kosugi Y, Nomura Y, Kawahara I, Uehara H): Use of a nitrogenous fused compound as a URAT1 Inhibitor - for treating, eg, hyperuricemia, gouty node, acute or chronic gouty arthritis, gouty kidney, urinary calcus, renal dysfunction, coronary artery disease and ischemic artery disease. WO-2006057460 (2006).
-
(2006)
-
-
Hirata, K.1
Ogawa, N.2
Shinagawa, Y.3
Kiguchi, T.4
Inoue, T.5
Matsuo, A.6
Kosugi, Y.7
Nomura, Y.8
Kawahara, I.9
Uehara, H.10
-
13
-
-
33748706122
-
New 1H-pyrrol[2,3-b]pyridine derivatives are SGK-1 kinase inhibitors - Useful for the treatment of proliferative disorders, water retention, renal disease or cardiovascular disease
-
SmithKline Beecham Corp WO-2006063167
-
SmithKline Beecham Corp (Frazee JS, Hammond M, Kano K, Manns S, Nakamura H, Thompson SK, Washburn DG): New 1H-pyrrol[2,3-b]pyridine derivatives are SGK-1 kinase inhibitors - useful for the treatment of proliferative disorders, water retention, renal disease or cardiovascular disease. WO-2006063167 (2006).
-
(2006)
-
-
Frazee, J.S.1
Hammond, M.2
Kano, K.3
Manns, S.4
Nakamura, H.5
Thompson, S.K.6
Washburn, D.G.7
-
14
-
-
33748704904
-
New substituted 1,2,4-triazin-5(2H)-ones are PAF acetylhydrolase inhibit - Useful for the treatment of chronic inflammatory disease, cardiovascular disease and arteriosclerosis
-
Bayer Healthcare AG WO-2006063811
-
Bayer Healthcare AG (Hendrix M, Zimmermann K, Hirth-Dietrich C, Karig G, Karthaus D, Raabe M, Weber O, Zaiss S): New substituted 1,2,4-triazin-5(2H)-ones are PAF acetylhydrolase inhibit - useful for the treatment of chronic inflammatory disease, cardiovascular disease and arteriosclerosis. WO-2006063811 (2006).
-
(2006)
-
-
Hendrix, M.1
Zimmermann, K.2
Hirth-Dietrich, C.3
Karig, G.4
Karthaus, D.5
Raabe, M.6
Weber, O.7
Zaiss, S.8
-
15
-
-
33748704904
-
New 3-cycloalkyl-1,2,4-triazin-5(2H)-ones are PAF acetylhydrolase inhibitors - Useful for the treatment of chronic inflammatory disease, cardiovascular disease and arteriosclerosis
-
Bayer Healthcare AG WO-2006063812
-
Bayer Healthcare AG (Hendrix M, Zimmermann K, Hirth-Dietrich C, Karig G, Karthaus D, Raabe M, Weber O, Zaiss S): New 3-cycloalkyl-1,2,4-triazin-5(2H)-ones are PAF acetylhydrolase inhibitors - useful for the treatment of chronic inflammatory disease, cardiovascular disease and arteriosclerosis. WO-2006063812 (2006).
-
(2006)
-
-
Hendrix, M.1
Zimmermann, K.2
Hirth-Dietrich, C.3
Karig, G.4
Karthaus, D.5
Raabe, M.6
Weber, O.7
Zaiss, S.8
-
16
-
-
33748704904
-
New 3-arylalkyl-and 3-heteroarylalkyl-substituted 1,2,4-triazin-5(2H)-ones are PAF acetylhydrolase inhibitors - Useful for the treatment of chronic inflammatory disease, cardiovascular disease and arteriosclerosis
-
Bayer Healthcare AG WO-2006063813
-
Bayer Healthcare AG (Hendrix M, Zimmermann K, Hirth-Dietrich C, Karig G, Karthaus D, Raabe M, Weber O, Zaiss S): New 3-arylalkyl-and 3-heteroarylalkyl-substituted 1,2,4-triazin-5(2H)-ones are PAF acetylhydrolase inhibitors - useful for the treatment of chronic inflammatory disease, cardiovascular disease and arteriosclerosis. WO-2006063813 (2006).
-
(2006)
-
-
Hendrix, M.1
Zimmermann, K.2
Hirth-Dietrich, C.3
Karig, G.4
Karthaus, D.5
Raabe, M.6
Weber, O.7
Zaiss, S.8
-
17
-
-
33748704904
-
New 3-benzylthio-1,2,4-triazin-5(2H)-one compounds are PAF acetylhydrolase inhibitors - Useful for the treatment of chronic inflammatory disease, cardiovascular disease and arteriosclerosis
-
Bayer Healthcare AG WO-2006063791
-
Bayer Healthcare AG (Hendrix M, Zimmermann K, Flessner T, Hirth-Dietrich C, Karig G, Raabe M, Karthaus D, Michels M, Weber O, Zaiss S, Zumpe F): New 3-benzylthio-1,2,4-triazin-5(2H)-one compounds are PAF acetylhydrolase inhibitors - useful for the treatment of chronic inflammatory disease, cardiovascular disease and arteriosclerosis. WO-2006063791 (2006).
-
(2006)
-
-
Hendrix, M.1
Zimmermann, K.2
Flessner, T.3
Hirth-Dietrich, C.4
Karig, G.5
Raabe, M.6
Karthaus, D.7
Michels, M.8
Weber, O.9
Zaiss, S.10
Zumpe, F.11
-
18
-
-
33748706742
-
2 inhibitors - Useful for the prevention and treatment of cardiovascular disease such as hyperlipidemia, coronary artery heart disease and atherosclerosis
-
Korea Research Institute Of Bioscience And Biotechnology US-20060106017
-
2 inhibitors - Useful for the prevention and treatment of cardiovascular disease such as hyperlipidemia, coronary artery heart disease and atherosclerosis. US-20060106017 (2006).
-
(2006)
-
-
Jeong, T.S.1
Lee, W.S.2
Jeong, H.J.3
Park, Y.D.4
Han, J.M.5
Kim, H.C.6
Moon, O.S.7
Won, Y.S.8
-
19
-
-
33748714009
-
New macrocyclic macrophage foaming inhibitor - Useful for treating and preventing atherosclerosis, myocardial infarction, cerebral apoplexy and cerebral stroke
-
The Kitasato Institute WO-2006048947
-
The Kitasato Institute (Omura S, Tomoda H, Masuma R): New macrocyclic macrophage foaming inhibitor - useful for treating and preventing atherosclerosis, myocardial infarction, cerebral apoplexy and cerebral stroke. WO-2006048947 (2006).
-
(2006)
-
-
Omura, S.1
Tomoda, H.2
Masuma, R.3
-
20
-
-
33748707965
-
Antibodies directed against the FSAP Marburg I variant - Useful for diagnosing atherosclerotic disease
-
Dade Behring Marburgh GmbH US-20080045879
-
Dade Behring Marburgh GmbH (Althaus H, Schwarz H, Fischer B, Wissel T): Antibodies directed against the FSAP Marburg I variant - useful for diagnosing atherosclerotic disease. US-20080045879 (2006).
-
(2006)
-
-
Althaus, H.1
Schwarz, H.2
Fischer, B.3
Wissel, T.4
-
21
-
-
33748679098
-
New N-alkylguanadinylamino acid derivatives are dimethylarginine dimethylaminohydrolase inhibitors - Used to treat eg ischemia, sepsis, pain and neurodegeneration
-
UCL Biomedica plc WO-2006051314
-
UCL Biomedica plc (Vallance P, John T, Leiper J, Mitchell S, David L, Rossiter S, Hartzoulakis B): New N-alkylguanadinylamino acid derivatives are dimethylarginine dimethylaminohydrolase inhibitors - used to treat eg ischemia, sepsis, pain and neurodegeneration. WO-2006051314 (2006).
-
(2006)
-
-
Vallance, P.1
John, T.2
Leiper, J.3
Mitchell, S.4
David, L.5
Rossiter, S.6
Hartzoulakis, B.7
-
22
-
-
33748683724
-
Method for preventing or delaying damage to a cardiac cell induced by a supraventricular arrhythmia - Comprises increasing the amount of heat shock protein in the cardiac cell
-
Zernike Business Support BV WO-2006062402
-
Zernike Business Support BV (Henning RH, Kampinga HH, Brundel BJJM): Method for preventing or delaying damage to a cardiac cell induced by a supraventricular arrhythmia - comprises increasing the amount of heat shock protein in the cardiac cell. WO-2006062402 (2006).
-
(2006)
-
-
Henning, R.H.1
Kampinga, H.H.2
Brundel, B.J.J.M.3
-
23
-
-
33748694278
-
Use of a modulator of muscle selective calcineuron interacting protein (MCIP-1-38) - For the treatment of cardiovascular disease
-
Myogen Inc WO-2006034184
-
Myogen Inc (Bush E, Hood D): Use of a modulator of muscle selective calcineuron interacting protein (MCIP-1-38) - for the treatment of cardiovascular disease. WO-2006034184 (2006).
-
(2006)
-
-
Bush, E.1
Hood, D.2
-
24
-
-
33748706121
-
Methods for delivering RNAi agents to target genes in vascular and surrounding tissue - Useful for treating restenosis
-
Benitec Inc US-20060115454
-
Benitec Inc (Couto L, Brashears S, Cunningham SM): Methods for delivering RNAi agents to target genes in vascular and surrounding tissue - useful for treating restenosis. US-20060115454 (2006).
-
(2006)
-
-
Couto, L.1
Brashears, S.2
Cunningham, S.M.3
-
25
-
-
33748684985
-
Interfering RNA agent capable of reducing the amount of ApoB mRNA - Useful for treating lipid disorders, eg, hypercholesterolemia, hyperlipidemia and coronary artery disease
-
Alnylam Pharmaceuticals Inc WO-2006036916
-
Alnylam Pharmaceuticals Inc (Soutschek J, Vorniocher H-P, Hadwiger P, Elbashir S): Interfering RNA agent capable of reducing the amount of ApoB mRNA - useful for treating lipid disorders, eg, hypercholesterolemia, hyperlipidemia and coronary artery disease. WO-2006036916 (2006).
-
(2006)
-
-
Soutschek, J.1
Vorniocher, H.-P.2
Hadwiger, P.3
Elbashir, S.4
-
26
-
-
33748689713
-
Vasopressin-binding nucleic acids - Useful for treating, eg, congestive heart failure
-
Noxxon Pharma AG WO-2006058705
-
Noxxon Pharma AG (Purschke W, Eulberg D, Klussmann S, Röhl I, Vater A): Vasopressin-binding nucleic acids - useful for treating, eg, congestive heart failure. WO-2006058705 (2006).
-
(2006)
-
-
Purschke, W.1
Eulberg, D.2
Klussmann, S.3
Röhl, I.4
Vater, A.5
-
27
-
-
33748707757
-
Vector encoding an angiogenic cytokine - Useful in the gene therapy of heart disease
-
Anges MG Inc WO-2006046766
-
Anges MG Inc (Sam Y, Shirakawa Y, Tatsumi E, Taenaka Y, Matsuda H): Vector encoding an angiogenic cytokine - useful in the gene therapy of heart disease. WO-2006046766 (2006).
-
(2006)
-
-
Sam, Y.1
Shirakawa, Y.2
Tatsumi, E.3
Taenaka, Y.4
Matsuda, H.5
-
28
-
-
33748681260
-
Use of MAP kinase TNN13K - For the treatment of heart disease
-
Kumamoto University WO-2006057278
-
Kumamoto University (Yorinaka H, Ding J-F, Meng X-M): Use of MAP kinase TNN13K - for the treatment of heart disease. WO-2006057278 (2006).
-
(2006)
-
-
Yorinaka, H.1
Ding, J.-F.2
Meng, X.-M.3
-
29
-
-
33748682676
-
Use of colony stimulating factor-1 enhanced myoblasts - For the treatment of ischemic heart diseases and heart failure
-
WO-2006047799
-
Aharinejad S: Use of colony stimulating factor-1 enhanced myoblasts - for the treatment of ischemic heart diseases and heart failure. WO-2006047799 (2006).
-
(2006)
-
-
Aharinejad, S.1
-
30
-
-
33748681261
-
Use of a cardiogenic cell - For treating a cardiac disorder eg myocardial infarction
-
Columbia University In The City Of New York/The Research Foundation Of State University Of New York WO-2006032054
-
Columbia University In The City Of New York/The Research Foundation Of State University Of New York (Cohen IS, Rosen MR, Robinson RB, Brink PR, Gaudette G, Potapova I): Use of a cardiogenic cell - for treating a cardiac disorder eg myocardial infarction. WO-2006032054 (2006).
-
(2006)
-
-
Cohen, I.S.1
Rosen, M.R.2
Robinson, R.B.3
Brink, P.R.4
Gaudette, G.5
Potapova, I.6
-
31
-
-
33748684131
-
Method for modifying rhythmic electrical and contractile activities of in vivo cardiac tissue - Comprises integrating the donor cardiomyocytes derived from genetically engineered human embryonic stem cells into recipient cardiomyocytes
-
The Johns Hopkins University WO-2006017567
-
The Johns Hopkins University (Li RA, Akar FG, Cho H, Marban E, Tomaselli G): Method for modifying rhythmic electrical and contractile activities of in vivo cardiac tissue - comprises integrating the donor cardiomyocytes derived from genetically engineered human embryonic stem cells into recipient cardiomyocytes. WO-2006017567 (2006).
-
(2006)
-
-
Li, R.A.1
Akar, F.G.2
Cho, H.3
Marban, E.4
Tomaselli, G.5
-
32
-
-
33748691774
-
Methods for inducing differentiation of human embryonic stem cells - Useful for producing cardiomyocytes and cardiomyocyte progenitor cells
-
IP Organisers Pty Ltd/ ES Cell International Pte Ltd WO-2006066320
-
IP Organisers Pty Ltd/ ES Cell International Pte Ltd (Passier R, Mummery CL): Methods for inducing differentiation of human embryonic stem cells - useful for producing cardiomyocytes and cardiomyocyte progenitor cells. WO-2006066320 (2006).
-
(2006)
-
-
Passier, R.1
Mummery, C.L.2
-
33
-
-
33748707150
-
Method of generating vascular smooth muscle cells from vasculogenic progenitor cells - Comprises culturing the progenitor cells in a differentiating medium including a serum volume concentration higher than 5%
-
Technion Research & Development Foundation Ltd WO-2006040755
-
Technion Research & Development Foundation Ltd (Gerecht-Nir S, Itskovitz-Eldor J): Method of generating vascular smooth muscle cells from vasculogenic progenitor cells - comprises culturing the progenitor cells in a differentiating medium including a serum volume concentration higher than 5%. WO-2006040755 (2006).
-
(2006)
-
-
Gerecht-Nir, S.1
Itskovitz-Eldor, J.2
-
34
-
-
33748677870
-
Use of an antigen capable of activating in vitro a Tr1 cell population, and the Tr1 cell population activated by the antigen - For treating or preventing atherosclerosis
-
INSERM/TxCell WO-2006018674
-
INSERM/TxCell (Groux H, Tedgui A, Mallat Z, Brun V): Use of an antigen capable of activating in vitro a Tr1 cell population, and the Tr1 cell population activated by the antigen - for treating or preventing atherosclerosis. WO-2006018674 (2006).
-
(2006)
-
-
Groux, H.1
Tedgui, A.2
Mallat, Z.3
Brun, V.4
-
35
-
-
33748689510
-
New 1,5,6-substituted-2-oxo-3-cyano-1,6a-diaza-tetrahydro-fluoranthene derivatives are reverse transcriptase inhibitors - Useful for the treatment of retroviral diseases
-
Tibotec Pharmaceuticals Ltd WO-2006039630
-
Tibotec Pharmaceuticals Ltd (Kesteleyn BRR, Raboisson PJ-M, Van De Vreken W, Canard MFJ-MG): New 1,5,6-substituted-2-oxo-3-cyano-1,6a-diaza-tetrahydro-fluoranthene derivatives are reverse transcriptase inhibitors - useful for the treatment of retroviral diseases. WO-2006039630 (2006).
-
(2006)
-
-
Kesteleyn, B.R.R.1
Raboisson, P.J.-M.2
Van De Vreken, W.3
Canard, M.F.J.-M.G.4
-
36
-
-
33748682086
-
Method for identifying an agent for modulating cell growth or survival - Comprises determining the net ratio of nuclear-localized versus cytosolic-localized H11 kinase in a cell contacted with a test agent
-
University of Medicine and Dentistry of New Jersey WO-2006036822
-
University of Medicine and Dentistry of New Jersey (Vatner SF, Depre C): Method for identifying an agent for modulating cell growth or survival - comprises determining the net ratio of nuclear-localized versus cytosolic-localized H11 kinase in a cell contacted with a test agent. WO-2006036822 (2006).
-
(2006)
-
-
Vatner, S.F.1
Depre, C.2
-
37
-
-
33748680066
-
Method for identifying a compound for treating atrial fibrillation - Comprises selecting the compound that inhibits tachyarrhythmias in the atrial preparation isolated from the heart of the mammal
-
US-20060094003
-
Nattel S, Hebert T: Method for identifying a compound for treating atrial fibrillation - comprises selecting the compound that inhibits tachyarrhythmias in the atrial preparation isolated from the heart of the mammal. US-20060094003 (2006).
-
(2006)
-
-
Nattel, S.1
Hebert, T.2
-
38
-
-
33748688582
-
Transgenic non-human models of ischemia/reperfusion injury - Useful for screening for agents for treating ischemic disorders
-
University of Rochester WO-2006050532
-
University of Rochester (Berk BC, Abe J-I): Transgenic non-human models of ischemia/reperfusion injury - useful for screening for agents for treating ischemic disorders. WO-2006050532 (2006).
-
(2006)
-
-
Berk, B.C.1
Abe, J.-I.2
-
39
-
-
33748687154
-
Construction of arterial occlusive disease animal model
-
Japan Health Sciences Foundation WO-2006030737
-
Japan Health Sciences Foundation (Iida H, Ohta Y, Teramoto N, Hayashi T): Construction of arterial occlusive disease animal model. WO-2006030737 (2006).
-
(2006)
-
-
Iida, H.1
Ohta, Y.2
Teramoto, N.3
Hayashi, T.4
-
40
-
-
33748691773
-
Method of constructing animal model of atrial fibrillation, method of inducing atrial fibrillation and method of evaluating atrial fibrillation inhibitor
-
University of Yamanashi WO-2006025450
-
University of Yamanashi (Sugiyama A, Takahara A, Hashimoto K): Method of constructing animal model of atrial fibrillation, method of inducing atrial fibrillation and method of evaluating atrial fibrillation inhibitor. WO-2006025450 (2006).
-
(2006)
-
-
Sugiyama, A.1
Takahara, A.2
Hashimoto, K.3
-
41
-
-
33748692385
-
Method for evaluating pathologies in a rat carotid artery - Comprises endovascularly creating an injury within the carotid artery of a rat and evaluating the pathologies associated with the injury
-
Cordis Corp US-20060104903
-
Cordis Corp (Argentieri DC, Falotico R, Parry TJ, Zhao JZ): Method for evaluating pathologies in a rat carotid artery - comprises endovascularly creating an injury within the carotid artery of a rat and evaluating the pathologies associated with the injury. US-20060104903 (2006).
-
(2006)
-
-
Argentieri, D.C.1
Falotico, R.2
Parry, T.J.3
Zhao, J.Z.4
-
42
-
-
33748683934
-
New heteroarylacetamide derivates are Factor Xa inhibitors - Useful for treatment of thrombotic disorders and tumors
-
F Hoffmann-La Roche AG WO-2006066778
-
F Hoffmann-La Roche AG (Boehringer M, Groebke KZ, Haap W, Hilpert H, Panday N, Ricklin F): New heteroarylacetamide derivates are Factor Xa inhibitors - useful for treatment of thrombotic disorders and tumors. WO-2006066778 (2006).
-
(2006)
-
-
Boehringer, M.1
Groebke, K.Z.2
Haap, W.3
Hilpert, H.4
Panday, N.5
Ricklin, F.6
-
43
-
-
33748714704
-
Heteroarylacetamide inhibitors of Factor Xa
-
Hoffmann-La Roche Inc US-20060142362
-
Hoffmann-La Roche Inc (Boehringer M, Zbinden KG, Haap W, Hilpert H, Panday N, Ricklin F): Heteroarylacetamide inhibitors of Factor Xa. US-20060142362 (2006).
-
(2006)
-
-
Boehringer, M.1
Zbinden, K.G.2
Haap, W.3
Hilpert, H.4
Panday, N.5
Ricklin, F.6
-
44
-
-
33748683934
-
New dicarboxamide derivatives are Factor Xa antagonists - Useful for the treatment of, eg, thrombotic disorders, inflammation and tumors
-
F. Hoffmann-La Roche AG WO-2006048152
-
F Hoffmann-La Roche AG (Boehringer M, Groebke KZ, Haap W, Hilpert H, Himber J, Humm R, Iding H, Hilpert H, Knopp D, Panday N, Ricklin F, Stahl CM): New dicarboxamide derivatives are Factor Xa antagonists - useful for the treatment of, eg, thrombotic disorders, inflammation and tumors. WO-2006048152 (2006).
-
(2006)
-
-
Boehringer, M.1
Groebke, K.Z.2
Haap, W.3
Hilpert, H.4
Himber, J.5
Humm, R.6
Iding, H.7
Hilpert, H.8
Knopp, D.9
Panday, N.10
Ricklin, F.11
Stahl, C.M.12
-
45
-
-
33748703274
-
New 2-(3,4,6-trihydroxy-6-hydroxymethyl-tetrahydropyran-2- ylioxy)phenylalanine derivatives are Factor Xa inhibitors - Useful for the treatment and prevention of thromboembolytic diseases, arterial restenosis, blood poisoning, cancer and acute inflammation
-
Morphochem Aktiengesellschaft für Kombinatorische Chemie WO-2006008141
-
Morphochem Aktiengesellschaft für Kombinatorische Chemie (Fuchs T, Eckl R): New 2-(3,4,6-trihydroxy-6-hydroxymethyl-tetrahydropyran-2-ylioxy) phenylalanine derivatives are Factor Xa inhibitors - useful for the treatment and prevention of thromboembolytic diseases, arterial restenosis, blood poisoning, cancer and acute inflammation. WO-2006008141 (2006).
-
(2006)
-
-
Fuchs, T.1
Eckl, R.2
-
46
-
-
33748707151
-
New heterocyclic amine derivatives are inhibitors of Factor VIIa, IXa, Xa, XIa and/or plasma kalllkrein - Useful for the treatment of thromboembolic disorders
-
Bristol-Myers Squibb Co WO-2006062972
-
Bristol-Myers Squibb Co (Glunz PW, Wurtz N, Cheng X): New heterocyclic amine derivatives are inhibitors of Factor VIIa, IXa, Xa, XIa and/or plasma kalllkrein - useful for the treatment of thromboembolic disorders. WO-2006062972 (2006).
-
(2006)
-
-
Glunz, P.W.1
Wurtz, N.2
Cheng, X.3
-
47
-
-
33748694672
-
New tetrahydroisoquinoline derivatives are Factor Xa inhibitors - Useful for inhibiting blood coagulation and treating thrombotic disorders
-
Portola Pharmaceuticals Inc WO-2006055951
-
Portola Pharmaceuticals Inc (Song Y, Zhu B-Y, Wang S, Bauer S, Scarborough RM): New tetrahydroisoquinoline derivatives are Factor Xa inhibitors - useful for inhibiting blood coagulation and treating thrombotic disorders. WO-2006055951 (2006).
-
(2006)
-
-
Song, Y.1
Zhu, B.-Y.2
Wang, S.3
Bauer, S.4
Scarborough, R.M.5
-
48
-
-
33748694672
-
New urea derivatives are Factor Xa inhibitors - Useful for the treatment of thrombosis and related conditions
-
Portola Pharmaceuticals Inc WO-2006063113
-
Portola Pharmaceuticals Inc (Song Y, Zhu B-Y, Wang S, Bhakta C, Scarborough RM): New urea derivatives are Factor Xa inhibitors - useful for the treatment of thrombosis and related conditions. WO-2006063113 (2006).
-
(2006)
-
-
Song, Y.1
Zhu, B.-Y.2
Wang, S.3
Bhakta, C.4
Scarborough, R.M.5
-
49
-
-
33748694672
-
New thiourea derivatives are Factor Xa inhibitors - Useful for the treatment of thrombosis and related conditions
-
Portola Pharmaceuticals Inc WO-2006063293
-
Portola Pharmaceuticals Inc (Song Y, Zhu B-Y, Bhakta C, Scarborough RM): New thiourea derivatives are Factor Xa inhibitors - useful for the treatment of thrombosis and related conditions. WO-2006063293 (2006).
-
(2006)
-
-
Song, Y.1
Zhu, B.-Y.2
Bhakta, C.3
Scarborough, R.M.4
-
50
-
-
33748713598
-
New substituted 2H-1,3-benzoxazin-4(3H)-one derivatives are platelet ADP receptor inhibitors - Useful for treating thrombosis and secondary ischemic events
-
Portola Pharmaceuticals Inc US-20060069093
-
Portola Pharmaceuticals Inc (Scarborough RM, Venkatraman MS, Zhang X, Pandey A): New substituted 2H-1,3-benzoxazin-4(3H)-one derivatives are platelet ADP receptor inhibitors - useful for treating thrombosis and secondary ischemic events. US-20060069093 (2006).
-
(2006)
-
-
Scarborough, R.M.1
Venkatraman, M.S.2
Zhang, X.3
Pandey, A.4
-
51
-
-
33748693083
-
New cyclic iminocarbamate derivatives are Factor Xa inhibitors - Useful as anticoagulants for the treatment and prevention of thromboembolic disorders
-
Bayer Healthcare AG WO-2006058630
-
Bayer Healthcare AG (Röhrig S, Pohlmann J, Arndt S, Jeske M, Akbaba M, Perzborn E, Gerdes C, Schlemmer K-H, Tuch A, Lobell M, Nell P, Burkhardt N): New cyclic iminocarbamate derivatives are Factor Xa inhibitors - useful as anticoagulants for the treatment and prevention of thromboembolic disorders. WO-2006058630 (2006).
-
(2006)
-
-
Röhrig, S.1
Pohlmann, J.2
Arndt, S.3
Jeske, M.4
Akbaba, M.5
Perzborn, E.6
Gerdes, C.7
Schlemmer, K.-H.8
Tuch, A.9
Lobell, M.10
Nell, P.11
Burkhardt, N.12
-
52
-
-
33748694077
-
New bicyclic derivatives are Factor Xa inhibitors - Useful for the treatment of cardiovascular diseases associated with thromboses
-
Janssen Pharmaceutica NV WO-2006047415
-
Janssen Pharmaceutica NV (Lu T, Thieu TV, Player MR, Lee Y-K, Parks DJ, Markotan TP, Pan W, Milkiewicz KL): New bicyclic derivatives are Factor Xa inhibitors - useful for the treatment of cardiovascular diseases associated with thromboses. WO-2006047415 (2006).
-
(2006)
-
-
Lu, T.1
Thieu, T.V.2
Player, M.R.3
Lee, Y.-K.4
Parks, D.J.5
Markotan, T.P.6
Pan, W.7
Milkiewicz, K.L.8
-
53
-
-
33748701618
-
New 2-alkoxybenzamide and related derivatives are Factor Xa and/or thrombin inhibitors - Useful for the treatment of thromboembolic disorders
-
Eli Lilly & Co WO-2006057845
-
Eli Lilly & Co (Argade AB, Goodson T Jr, Herron DK, Joseph S, Lepore SD, Marquart AL, Masters JJ, Mendel DML, Ratz AM, Smith GF, Tebbe AL): New 2-alkoxybenzamide and related derivatives are Factor Xa and/or thrombin inhibitors - useful for the treatment of thromboembolic disorders. WO-2006057845 (2006).
-
(2006)
-
-
Argade, A.B.1
Goodson Jr., T.2
Herron, D.K.3
Joseph, S.4
Lepore, S.D.5
Marquart, A.L.6
Masters, J.J.7
Mendel, D.M.L.8
Ratz, A.M.9
Smith, G.F.10
Tebbe, A.L.11
-
54
-
-
33748684984
-
New 2-alkoxybenzamide derivatives are Factor Xa and/or thrombin inhibitors - Useful for the treatment of thromboembolic disorders
-
Eli Lilly & Co WO-2006057868
-
Eli Lilly & Co (Franciskovich JB, Herron DK, Wimkowski VJ, Marquart AL, Masters JJ, Mendel D, Ratz AM, Smith GF, Wiley MR, Yee YK): New 2-alkoxybenzamide derivatives are Factor Xa and/or thrombin inhibitors - useful for the treatment of thromboembolic disorders. WO-2006057868 (2006).
-
(2006)
-
-
Franciskovich, J.B.1
Herron, D.K.2
Wimkowski, V.J.3
Marquart, A.L.4
Masters, J.J.5
Mendel, D.6
Ratz, A.M.7
Smith, G.F.8
Wiley, M.R.9
Yee, Y.K.10
-
55
-
-
33748692669
-
Novel cyclic β-amino acid as inhibitors of Factor Xa and thrombin - Useful in the treatment of thromboembolic disorders
-
US-20060074103
-
Corte JR, Li Y-L: Novel cyclic β-amino acid as inhibitors of Factor Xa and thrombin - useful in the treatment of thromboembolic disorders. US-20060074103 (2006).
-
(2006)
-
-
Corte, J.R.1
Li, Y.-L.2
-
56
-
-
33748678494
-
New carbonyl compounds are Factor Xa and Factor VIIa antagonists - Useful for the treatment of, eg, thrombosis, myocardial infarction, inflammation, apoplexy, restenosis, migraine and tumor metastasis
-
Merck Patent GmbH WO-2006034769
-
Merck Patent GmbH (Cezanne B, Dorsch D, Mederski W, Tsaklakidis C, Gleitz J): New carbonyl compounds are Factor Xa and Factor VIIa antagonists - useful for the treatment of, eg, thrombosis, myocardial infarction, inflammation, apoplexy, restenosis, migraine and tumor metastasis. WO-2006034769 (2006).
-
(2006)
-
-
Cezanne, B.1
Dorsch, D.2
Mederski, W.3
Tsaklakidis, C.4
Gleitz, J.5
-
57
-
-
33748695691
-
New carbonyl compounds are coagulation inhibitors - Useful for the treatment of, eg, thrombosis, inflammation, restenosis, migraine and cancer
-
Merck Patent GmbH WO-2006032342
-
Merck Patent GmbH (Cezanne B, Dorsch D, Mederski W, Tsaklakidis C, Gleitz J): New carbonyl compounds are coagulation inhibitors - useful for the treatment of, eg, thrombosis, inflammation, restenosis, migraine and cancer. WO-2006032342 (2006).
-
(2006)
-
-
Cezanne, B.1
Dorsch, D.2
Mederski, W.3
Tsaklakidis, C.4
Gleitz, J.5
-
58
-
-
33748686552
-
New substituted thiophene carboxamides are thrombin and Factor Xa inhibitors - Useful for the treatment of, eg, DVT, reocclusions after bypass operations, pulmonary embolism and ulcerative colitis
-
Boehringer Ingelheim International GmbH US-20060069082
-
Boehringer Ingelheim International GmbH (Priepke H, Gerlach K, Pfau R, Wienen W, Schuler-Metz A, Nar H, Handschuh S): New substituted thiophene carboxamides are thrombin and Factor Xa inhibitors - useful for the treatment of, eg, DVT, reocclusions after bypass operations, pulmonary embolism and ulcerative colitis. US-20060069082 (2006).
-
(2006)
-
-
Priepke, H.1
Gerlach, K.2
Pfau, R.3
Wienen, W.4
Schuler-Metz, A.5
Nar, H.6
Handschuh, S.7
-
59
-
-
33748688985
-
New biotinylated hexadecasaccharide derivatives are Factor IIa and Factor Xa antagonists - Useful for the treatment of coagulation disorders
-
Sanofi-Aventis WO-2006030104
-
Sanofi-Aventis (Duchaussoy P, Herault JP, Herbert JM, Petitou M, Savi P): New biotinylated hexadecasaccharide derivatives are Factor IIa and Factor Xa antagonists - useful for the treatment of coagulation disorders. WO-2006030104 (2006).
-
(2006)
-
-
Duchaussoy, P.1
Herault, J.P.2
Herbert, J.M.3
Petitou, M.4
Savi, P.5
-
60
-
-
33748687553
-
New indole compounds - Useful for treating thromboembolic disorders
-
Daiamed Inc WO-2006012504
-
Daiamed Inc (Deng H, Lin J, Guo Z, Meyers HV, Abdel-Meguid SS, Babine RE): New indole compounds - useful for treating thromboembolic disorders. WO-2006012504 (2006).
-
(2006)
-
-
Deng, H.1
Lin, J.2
Guo, Z.3
Meyers, H.V.4
Abdel-Meguid, S.S.5
Babine, R.E.6
-
61
-
-
33748707358
-
New aminopyridines are thrombin antagonists - Useful for the treatment of thrombosis and cardiovascular diseases
-
Santhera Pharmaceuticals (Schweiz) GmbH WO-2006045459
-
Santhera Pharmaceuticals (Schweiz) GmbH (Bosio S, Bulat S, Feurer A, Rosenbaum C, Matassa VG): New aminopyridines are thrombin antagonists - useful for the treatment of thrombosis and cardiovascular diseases. WO-2006045459 (2006).
-
(2006)
-
-
Bosio, S.1
Bulat, S.2
Feurer, A.3
Rosenbaum, C.4
Matassa, V.G.5
-
62
-
-
33748698214
-
Isolated peptide derived from trocarin protein and capable of interacting with factor Va - Useful for preventing formation of intravascular blood clots in subjects having ischemic events
-
National University Of Singapore WO-2006049580
-
National University Of Singapore (Kini MR, Koh CY, Joseph JS): Isolated peptide derived from trocarin protein and capable of interacting with factor Va - useful for preventing formation of intravascular blood clots in subjects having ischemic events. WO-2006049580 (2006).
-
(2006)
-
-
Kini, M.R.1
Koh, C.Y.2
Joseph, J.S.3
-
63
-
-
33748694078
-
New hydrazide derivatives are activated Factor VII inhibitors and antithrombotic agents - Useful for treating diseases in which thrombosis is a factor such as deep vein thrombosis, pulmonary thrombosis, cerebral infarction, myocardial infarction and reperfusion disorder
-
Eisai Co Ltd WO-2006041119
-
Eisai Co Ltd (Clark R, Hirota S, Azuma H, Kira K, Watanabe N, Nagakura T, Harizoe T): New hydrazide derivatives are activated Factor VII inhibitors and antithrombotic agents - useful for treating diseases in which thrombosis is a factor such as deep vein thrombosis, pulmonary thrombosis, cerebral infarction, myocardial infarction and reperfusion disorder. WO-2006041119 (2006).
-
(2006)
-
-
Clark, R.1
Hirota, S.2
Azuma, H.3
Kira, K.4
Watanabe, N.5
Nagakura, T.6
Harizoe, T.7
-
64
-
-
33748687554
-
New pyrroionaphthalene derivatives are PAI-1 inhibitors - Useful for the treatment of eg fibrinolytic disorders and cardiovascular disease
-
Wyeth WO-2006023864
-
Wyeth (Commons TJ, Jenkins DJ): New pyrroionaphthalene derivatives are PAI-1 inhibitors - useful for the treatment of eg fibrinolytic disorders and cardiovascular disease. WO-2006023864 (2006).
-
(2006)
-
-
Commons, T.J.1
Jenkins, D.J.2
-
65
-
-
33748687554
-
New oxazolonaphthalene derivatives are PAI-1 inhibitors - Useful for the treatment of fibrinolytic disorders and cardiovascular disease
-
Wyeth WO-2006023865
-
Wyeth (Commons TJ, Woodworth RP Jr): New oxazolonaphthalene derivatives are PAI-1 inhibitors - useful for the treatment of fibrinolytic disorders and cardiovascular disease. WO-2006023865 (2006).
-
(2006)
-
-
Commons, T.J.1
Woodworth Jr, R.P.2
-
66
-
-
33748687554
-
New thiazolonaphthalene derivatives are PAI-1 inhibitors - Useful for the treatment of fibrinolytic disorders and cardiovascular disease
-
Wyeth WO-2006023866
-
Wyeth (Commons TJ): New thiazolonaphthalene derivatives are PAI-1 inhibitors - useful for the treatment of fibrinolytic disorders and cardiovascular disease WO-2006023866 (2006).
-
(2006)
-
-
Commons, T.J.1
-
67
-
-
33748700980
-
New pyrrolidine derivatives are renin inhibitors - Useful for the treatment of cardiovascular diseases, diabetic complications and cognitive disorders
-
Novartis AG, Novartis Pharma GmbH WO-2006066896
-
Novartis AG, Novartis Pharma GmbH (Breitenstein W, Cottens S, Ehrhardt C, Jacoby E, Lorthiois ELJ, Maibaum JK, Ostermann N, Sellner H, Simic O): New pyrrolidine derivatives are renin inhibitors - useful for the treatment of cardiovascular diseases, diabetic complications and cognitive disorders. WO-2006066896 (2006).
-
(2006)
-
-
Breitenstein, W.1
Cottens, S.2
Ehrhardt, C.3
Jacoby, E.4
Lorthiois, E.L.J.5
Maibaum, J.K.6
Ostermann, N.7
Sellner, H.8
Simic, O.9
-
68
-
-
33748702860
-
New diazabicyclononene derivative, a non-peptide renin inhibitor - Useful for the treatment of, eg, hypertension, congestive heart failure, renal insufficency, glaucoma and cognitive disorders
-
Actelion Pharmaceuticals Ltd WO-2006061791
-
Actelion Pharmaceuticals Ltd (Bezencon O, Bur D, Fischli W, Remen L, Richard-Bildstein S, Sifferlen T, Weber H-P, Weller T): New diazabicyclononene derivative, a non-peptide renin inhibitor - useful for the treatment of, eg, hypertension, congestive heart failure, renal insufficency, glaucoma and cognitive disorders. WO-2006061791 (2006).
-
(2006)
-
-
Bezencon, O.1
Bur, D.2
Fischli, W.3
Remen, L.4
Richard-Bildstein, S.5
Sifferlen, T.6
Weber, H.-P.7
Weller, T.8
-
69
-
-
33748684576
-
New lactam derivatives are renin inhibitors - Useful for the treatment of, eg, cardiovascular disorders, renal disease and diabetic complications
-
Actelion Pharmaceuticals Ltd WO-2006058546
-
Actelion Pharmaceuticals Ltd (Bezencon O, Remen L, Sifferlen T, Grisostomi C, Richard-Bildstein S, Bur D, Boss C, Corminboeuf O, Fischil W, Weller T): New lactam derivatives are renin inhibitors - useful for the treatment of, eg, cardiovascular disorders, renal disease and diabetic complications. WO-2006058546 (2006).
-
(2006)
-
-
Bezencon, O.1
Remen, L.2
Sifferlen, T.3
Grisostomi, C.4
Richard-Bildstein, S.5
Bur, D.6
Boss, C.7
Corminboeuf, O.8
Fischil, W.9
Weller, T.10
-
70
-
-
33748684576
-
New bicyclic derivatives are renin inhibitors - Useful for the treatment of, eg, cardiovascular disorders, renal disease and diabetic complications
-
Actelion Pharmaceuticals Ltd WO-2006059304
-
Actelion Pharmaceuticals Ltd (Bezencon O, Boss C, Bur D, Corminboeuf O, Fischli W, Grisostomi C, Remen L, Richard-Bildslein S, Sifferlen T, Weller T): New bicyclic derivatives are renin inhibitors - useful for the treatment of, eg, cardiovascular disorders, renal disease and diabetic complications. WO-2006059304 (2006).
-
(2006)
-
-
Bezencon, O.1
Boss, C.2
Bur, D.3
Corminboeuf, O.4
Fischli, W.5
Grisostomi, C.6
Remen, L.7
Richard-Bildslein, S.8
Sifferlen, T.9
Weller, T.10
-
71
-
-
33748684576
-
New diazabicyclononene and related derivatives are renin inhibitors - Useful for the treatment of, eg, cardiovascular diseases and renal failure
-
Actelion Pharmaceuticals Ltd WO-2006021399
-
Actelion Pharmaceuticals Ltd (Bezencon O, Boss C, Bur D, Corminboeuf O, Fischli W, Grisostomi C, Remen L, Richard S, Sifferlen T, Weller T): New diazabicyclononene and related derivatives are renin inhibitors - useful for the treatment of, eg, cardiovascular diseases and renal failure. WO-2006021399 (2006).
-
(2006)
-
-
Bezencon, O.1
Boss, C.2
Bur, D.3
Corminboeuf, O.4
Fischli, W.5
Grisostomi, C.6
Remen, L.7
Richard, S.8
Sifferlen, T.9
Weller, T.10
-
72
-
-
33748684576
-
New diazabicyclononene and related derivatives are renin inhibitors - Useful for the treatment of, eg, cardiovascular diseases and renal failure
-
Actelion Pharmaceuticals Ltd WO-2006021403
-
Actelion Pharmaceuticals Ltd (Bezencon O, Boss C, Bur D, Corminboeuf O, Fischli W, Grisostomi C, Remen L, Richard S, Sifferlen T, Weller T): New diazabicyclononene and related derivatives are renin inhibitors - useful for the treatment of, eg, cardiovascular diseases and renal failure. WO-2006021403 (2006).
-
(2006)
-
-
Bezencon, O.1
Boss, C.2
Bur, D.3
Corminboeuf, O.4
Fischli, W.5
Grisostomi, C.6
Remen, L.7
Richard, S.8
Sifferlen, T.9
Weller, T.10
-
73
-
-
33748684576
-
New diazabicyclononene and related derivatives are renin inhibitors - Useful for the treatment of, eg, cardiovascular diseases and renal failure
-
Actelion Pharmaceuticals Ltd WO-2006021402
-
Actelion Pharmaceuticals Ltd (Bezencon O, Boss C, Bur D, Corminboeuf O, Fischli W, Grisostomi C, Remen L, Richard S, Sifferlen T, Weller T): New diazabicyclononene and related derivatives are renin inhibitors - useful for the treatment of, eg, cardiovascular diseases and renal failure. WO-2006021402 (2006).
-
(2006)
-
-
Bezencon, O.1
Boss, C.2
Bur, D.3
Corminboeuf, O.4
Fischli, W.5
Grisostomi, C.6
Remen, L.7
Richard, S.8
Sifferlen, T.9
Weller, T.10
-
74
-
-
33748684576
-
New diazabicyclononene and related derivatives are renin inhibitors - Useful for the treatment of, eg, cardiovascular diseases and renal failure
-
Actelion Pharmaceuticals Ltd WO-2006021401
-
Actelion Pharmaceuticals Ltd (Bezencon O, Boss C, Bur D, Corminboeuf O, Fischli W, Grisostomi C, Remen L, Richard S, Sifferlen T, Weller T): New diazabicyclononene and related derivatives are renin inhibitors - useful for the treatment of, eg, cardiovascular diseases and renal failure. WO-2006021401 (2006).
-
(2006)
-
-
Bezencon, O.1
Boss, C.2
Bur, D.3
Corminboeuf, O.4
Fischli, W.5
Grisostomi, C.6
Remen, L.7
Richard, S.8
Sifferlen, T.9
Weller, T.10
-
75
-
-
33748689283
-
New ω-phenyloctanamide derivatives are renin inhibitors - Useful for the treatment of, eg, hypertension and heart failure
-
Speedel Experimenta AG WO-2006061426
-
Speedel Experimenta AG (Herold P, Stutz S, Mah R, Tschinke V, Marti C): New ω-phenyloctanamide derivatives are renin inhibitors - useful for the treatment of, eg, hypertension and heart failure. WO-2006061426 (2006).
-
(2006)
-
-
Herold, P.1
Stutz, S.2
Mah, R.3
Tschinke, V.4
Marti, C.5
-
76
-
-
33748689283
-
New 5-amino-4-hydroxy-2-isopropyl-7-[4-methoxy-3-(3-methoxypropoxy) benzyl]-8-methylnonanamide derivatives are renin inhibitors - Useful for the treatment of, eg, hypertension and heart failure
-
Speedel Experimenta AG WO-2006061427
-
Speedel Experimenta AG (Herold P, Stutz S, Mah R, Tschinke V, Marti C): New
-
(2006)
-
-
Herold, P.1
Stutz, S.2
Mah, R.3
Tschinke, V.4
Marti, C.5
|