-
1
-
-
33646799069
-
Global and regional burden of disease and risk factors, 2001: Systematic analysis of population health data
-
Lopez AD, Mathers CD, Ezzati M, Jamison DT, Murray CJL. Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data. Lancet 2006; 367: 1747-1757.
-
(2006)
Lancet
, vol.367
, pp. 1747-1757
-
-
Lopez, A.D.1
Mathers, C.D.2
Ezzati, M.3
Jamison, D.T.4
Murray, C.J.L.5
-
3
-
-
0021327417
-
-
2-[1,2,3,4-tetrahydro-8- quinolinyl)sulfonyl]-L-arginyl]-2-piperidinecarboxylic acid. Biochemistry 1984; 23: 85-90.
-
2-[1,2,3,4-tetrahydro-8- quinolinyl)sulfonyl]-L-arginyl]-2-piperidinecarboxylic acid. Biochemistry 1984; 23: 85-90.
-
-
-
-
4
-
-
33845480738
-
Direct thrombin inhibitors - a survey of recent developments
-
Schwienhorst A. Direct thrombin inhibitors - a survey of recent developments. Cell Mol. Life Sci. 2006; 63: 2773-2791.
-
(2006)
Cell Mol. Life Sci
, vol.63
, pp. 2773-2791
-
-
Schwienhorst, A.1
-
5
-
-
0033760658
-
Combination of a direct thrombin inhibitor and a platelet glycoprotein IIb/IIIa blocking peptide facilitates and maintaines reperfusion of platelet-rich thrombus with alteplase
-
Sabatine MS, Tu TM, Jang IK. Combination of a direct thrombin inhibitor and a platelet glycoprotein IIb/IIIa blocking peptide facilitates and maintaines reperfusion of platelet-rich thrombus with alteplase. J. Thromb. Thrombolysis 2000; 10: 189-196.
-
(2000)
J. Thromb. Thrombolysis
, vol.10
, pp. 189-196
-
-
Sabatine, M.S.1
Tu, T.M.2
Jang, I.K.3
-
6
-
-
0032895104
-
Clinical experience with combined treatment of thrombin inhibitors and GP IIb/IIIa inhibitors in patients with HIT
-
Wallenga JM, Jeske WP, Wallis DE, Bakhos M, Lewis BE, Leya F, Fareed J. Clinical experience with combined treatment of thrombin inhibitors and GP IIb/IIIa inhibitors in patients with HIT. Semin. Thromb. Haemostasis 1999; 25(Suppl. 1): 77-81.
-
(1999)
Semin. Thromb. Haemostasis
, vol.25
, Issue.SUPPL. 1
, pp. 77-81
-
-
Wallenga, J.M.1
Jeske, W.P.2
Wallis, D.E.3
Bakhos, M.4
Lewis, B.E.5
Leya, F.6
Fareed, J.7
-
7
-
-
0000319455
-
Hirudin as an inhibitor of thrombin
-
Marhardt F. Hirudin as an inhibitor of thrombin. Methods Enzymol. 1970; 19: 924-932.
-
(1970)
Methods Enzymol
, vol.19
, pp. 924-932
-
-
Marhardt, F.1
-
8
-
-
0025346345
-
Design and characterization of hirulogs: A Novel class of bivalent peptide inhibitors of thrombin
-
Maraganore JM, Bourdon P, Jablonski J, Ramachandran KL, Fenton JW II. Design and characterization of hirulogs: A Novel class of bivalent peptide inhibitors of thrombin. Biochemistry 1990; 29: 7095-7101.
-
(1990)
Biochemistry
, vol.29
, pp. 7095-7101
-
-
Maraganore, J.M.1
Bourdon, P.2
Jablonski, J.3
Ramachandran, K.L.4
Fenton II, J.W.5
-
9
-
-
0026483791
-
Hirudin-derived thrombin inhibitors with disintegrin activity
-
Knapp A, Degenhardt T, Dodt J. Hirudisins. Hirudin-derived thrombin inhibitors with disintegrin activity. J. Biol. Chem. 1992; 267: 24230-24234.
-
(1992)
J. Biol. Chem
, vol.267
, pp. 24230-24234
-
-
Knapp, A.1
Degenhardt, T.2
Dodt, J.3
Hirudisins4
-
10
-
-
0025951849
-
Chimeric antithrombin peptide-characterization of an Arg-Gly-Asp (RGD)-containing and hirudin carboxyl terminus-containing synthetic peptide
-
Church FC, Phillips JE, Woods JL. Chimeric antithrombin peptide-characterization of an Arg-Gly-Asp (RGD)-containing and hirudin carboxyl terminus-containing synthetic peptide. J. Biol. Chem. 1991; 266: 11975-11979.
-
(1991)
J. Biol. Chem
, vol.266
, pp. 11975-11979
-
-
Church, F.C.1
Phillips, J.E.2
Woods, J.L.3
-
11
-
-
50449088532
-
-
Owen TJ, Broersma RJ, Krstenansky JL. Trifunctional antithrombin and antiplatelet peptides, WO9429349, 1994.
-
Owen TJ, Broersma RJ, Krstenansky JL. Trifunctional antithrombin and antiplatelet peptides, WO9429349, 1994.
-
-
-
-
12
-
-
27144449695
-
Designed multiple ligands. An emerging drug discovery paradigm
-
Morphy R, Kay C, Rankovic Z. Designed multiple ligands. An emerging drug discovery paradigm. J. Med. Chem. 2005; 48: 6523-6543.
-
(2005)
J. Med. Chem
, vol.48
, pp. 6523-6543
-
-
Morphy, R.1
Kay, C.2
Rankovic, Z.3
-
13
-
-
0025095466
-
Rapid continuous peptide synthesis via Fmoc amino acid chloride coupling and 4-(aminomethyl)piperidine deblocking
-
Beyermann M, Bienert M, Niedrich H, Carpino LA, Sadat-Aalaee D. Rapid continuous peptide synthesis via Fmoc amino acid chloride coupling and 4-(aminomethyl)piperidine deblocking. J. Org. Chem. 1990; 55: 721-728.
-
(1990)
J. Org. Chem
, vol.55
, pp. 721-728
-
-
Beyermann, M.1
Bienert, M.2
Niedrich, H.3
Carpino, L.A.4
Sadat-Aalaee, D.5
-
14
-
-
0014772602
-
Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides
-
Kaiser E, Colescott RL, Bossinger CD, Cook PI. Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides. Anal. Biochem. 1970; 34: 595-598.
-
(1970)
Anal. Biochem
, vol.34
, pp. 595-598
-
-
Kaiser, E.1
Colescott, R.L.2
Bossinger, C.D.3
Cook, P.I.4
-
15
-
-
50449087918
-
-
Novabiochem Synthesis Notes, Attachment to hydroxymethyl resins using symmetrical anhydride. Catalog 2004/2005; 2.36.
-
Novabiochem Synthesis Notes, Attachment to hydroxymethyl resins using symmetrical anhydride. Catalog 2004/2005; 2.36.
-
-
-
-
17
-
-
19944429529
-
-
Anderluh M, Cesar J, Štefanič P, Kikelj D, Janeš D, Murn J, Nadrah K, Tominc M, Addicks E, Giannis A, Stegnar M, Sollner Dolenc M. Design and synthesis of novel platelet fibrinogen receptor antagonists with 2H-1,4-benzoxazine-3(4H)-one scaffold. A systematic study. Eur. J. Med. Chem. 2005; 40: 25-49.
-
Anderluh M, Cesar J, Štefanič P, Kikelj D, Janeš D, Murn J, Nadrah K, Tominc M, Addicks E, Giannis A, Stegnar M, Sollner Dolenc M. Design and synthesis of novel platelet fibrinogen receptor antagonists with 2H-1,4-benzoxazine-3(4H)-one scaffold. A systematic study. Eur. J. Med. Chem. 2005; 40: 25-49.
-
-
-
-
18
-
-
11644261806
-
Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function
-
Morris GM, Goodsell DS, Halliday RS, Huey R, Har TWE. Belew RK, Olson AJ. Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function. J. Comput. Chem. 1998; 19: 1639-1662.
-
(1998)
J. Comput. Chem
, vol.19
, pp. 1639-1662
-
-
Morris, G.M.1
Goodsell, D.S.2
Halliday, R.S.3
Huey, R.4
Har, T.W.E.5
Belew, R.K.6
Olson, A.J.7
-
19
-
-
50449093898
-
-
HyperChem Release 7.01 for Windows, Hypercube, Inc. 2002
-
HyperChem (Release 7.01 for Windows, Hypercube, Inc. 2002.
-
-
-
-
20
-
-
0037171819
-
Structure-based design of novel potent nonpeptide thrombin inhibitors
-
Hauel NH, Nar H, Priepke H, Ries U, Stassen J-M, Wienen W. Structure-based design of novel potent nonpeptide thrombin inhibitors. J. Med. Chem. 2002; 45: 1757-1766.
-
(2002)
J. Med. Chem
, vol.45
, pp. 1757-1766
-
-
Hauel, N.H.1
Nar, H.2
Priepke, H.3
Ries, U.4
Stassen, J.-M.5
Wienen, W.6
-
21
-
-
8544259562
-
Structural basis for allostery in integrins and binding to fibrinogen-mimetic therapeutics
-
Xiao T, Takagi J, Coller BS, Wang J-H, Springer TA. Structural basis for allostery in integrins and binding to fibrinogen-mimetic therapeutics. Nature 2004; 432: 59-67.
-
(2004)
Nature
, vol.432
, pp. 59-67
-
-
Xiao, T.1
Takagi, J.2
Coller, B.S.3
Wang, J.-H.4
Springer, T.A.5
-
22
-
-
18244394034
-
-
Anderluh Štefanič P, Anderluh M, Ilaš J, Mravljak J, Sollner Dolenc M, Stegnar M, Kikelj D. Toward a novel class of antithrombotic compounds with dual function. Discovery of 1,4-benzoxazin-3(4H)-one derivatives possessing thrombin inhibitory and fibrinogen receptor antagonistic activities. J. Med. Chem. 2005; 48: 3110-3113.
-
Anderluh Štefanič P, Anderluh M, Ilaš J, Mravljak J, Sollner Dolenc M, Stegnar M, Kikelj D. Toward a novel class of antithrombotic compounds with dual function. Discovery of 1,4-benzoxazin-3(4H)-one derivatives possessing thrombin inhibitory and fibrinogen receptor antagonistic activities. J. Med. Chem. 2005; 48: 3110-3113.
-
-
-
-
24
-
-
0023160794
-
i and inhibitor type from the concentration of inhibitor for 50-percent inhibition for Michaelis-Menten enzymes
-
i and inhibitor type from the concentration of inhibitor for 50-percent inhibition for Michaelis-Menten enzymes. Biochem. Med. Metab. Biol. 1987; 37: 344-349.
-
(1987)
Biochem. Med. Metab. Biol
, vol.37
, pp. 344-349
-
-
Brandt, R.B.1
Laux, J.E.2
Yates, S.W.3
-
25
-
-
0037021332
-
Synthesis and biological investigation of novel tricyclic benzodiazepinedione-based RGD analogue
-
Addicks E, Mazitschek R, Giannis A. Synthesis and biological investigation of novel tricyclic benzodiazepinedione-based RGD analogue. Chem BioChem 2002; 3: 1078-1088.
-
(2002)
Chem BioChem
, vol.3
, pp. 1078-1088
-
-
Addicks, E.1
Mazitschek, R.2
Giannis, A.3
-
26
-
-
0033624589
-
An activated O → N acyl transfer auxiliary: Efficient amide-backbone substitution of hindered "difficult" peptides
-
Miranda LP, Meutermans WDF, Smythe ML, Alewood PF. An activated O → N acyl transfer auxiliary: efficient amide-backbone substitution of hindered "difficult" peptides. J. Org. Chem. 2000; 65: 5460-5468.
-
(2000)
J. Org. Chem
, vol.65
, pp. 5460-5468
-
-
Miranda, L.P.1
Meutermans, W.D.F.2
Smythe, M.L.3
Alewood, P.F.4
-
27
-
-
0030765141
-
-
Nefzi AM, Ostresh JM, Houghten RA. Solid phase synthesis of 1,3,4,7-tetrasubstituted perhydro-1,4-diazepine-2,5-diones. Tetrahedron Lett. 1997; 38: 4943-4946.
-
Nefzi AM, Ostresh JM, Houghten RA. Solid phase synthesis of 1,3,4,7-tetrasubstituted perhydro-1,4-diazepine-2,5-diones. Tetrahedron Lett. 1997; 38: 4943-4946.
-
-
-
-
28
-
-
0035348720
-
Solid-phase synthesis of macrolide analogues
-
Akritopoulou-Zanze I, Sowin TJ. Solid-phase synthesis of macrolide analogues. J. Comb. Chem. 2001; 3: 301-311.
-
(2001)
J. Comb. Chem
, vol.3
, pp. 301-311
-
-
Akritopoulou-Zanze, I.1
Sowin, T.J.2
-
29
-
-
4644247209
-
Clinical potential of oral direct thrombin inhibitors in the prevention and treatment of venous thromboembolism
-
Agnelli G. Clinical potential of oral direct thrombin inhibitors in the prevention and treatment of venous thromboembolism. Drugs 2004; 64(Suppl. 1): 47-52.
-
(2004)
Drugs
, vol.64
, Issue.SUPPL. 1
, pp. 47-52
-
-
Agnelli, G.1
-
30
-
-
0027366387
-
Changes in interactions in complexes of hirudin derivatives and human α-thrombin due to different crystal forms
-
Priestle JP, Rahuel J, Rink HM, Tones M, Grutter MG. Changes in interactions in complexes of hirudin derivatives and human α-thrombin due to different crystal forms. Protein Sci. 1993; 2: 1630-1642.
-
(1993)
Protein Sci
, vol.2
, pp. 1630-1642
-
-
Priestle, J.P.1
Rahuel, J.2
Rink, H.M.3
Tones, M.4
Grutter, M.G.5
|