-
1
-
-
0029044322
-
Purification and characterization of TAFI, a thrombin-activatable fibrinolysis inhibitor
-
Bajzar, L.; Manuel, R.; Nesheim, M. E. Purification and characterization of TAFI, a thrombin-activatable fibrinolysis inhibitor. J. Biol. Chem. 1995, 270, 14477-14484.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 14477-14484
-
-
Bajzar, L.1
Manuel, R.2
Nesheim, M.E.3
-
3
-
-
0030742896
-
Thrombin, thrombomodulin and TAFI in the molecular link between coagulation and fibrinolysis
-
(b) Nesheim, M.; Wang, W.; Boffa, M.; Nagashima, M.; Morser, J.; Bajzar, L. Thrombin, thrombomodulin and TAFI in the molecular link between coagulation and fibrinolysis. Thromb. Haemostasis 1997, 78, 386-391.
-
(1997)
Thromb. Haemostasis
, vol.78
, pp. 386-391
-
-
Nesheim, M.1
Wang, W.2
Boffa, M.3
Nagashima, M.4
Morser, J.5
Bajzar, L.6
-
4
-
-
34147159934
-
A role for procarboxypeptidase U (TAFI) in thrombosis
-
For recent reviews on TAFI, see: a
-
For recent reviews on TAFI, see: (a) Willemse, J. L.; Hendriks, D. F. A role for procarboxypeptidase U (TAFI) in thrombosis. Front. Biosci. 2007, 12, 1973-1987.
-
(2007)
Front. Biosci
, vol.12
, pp. 1973-1987
-
-
Willemse, J.L.1
Hendriks, D.F.2
-
5
-
-
33750222459
-
Regulation of fibrinolysis by thrombin activatable fibrinolysis inhibitor, an unstable carboxypeptidase B that unites the pathways of coagulation and fibrinolysis
-
(b) Mosnier, L. O.; Bouma, B. N. Regulation of fibrinolysis by thrombin activatable fibrinolysis inhibitor, an unstable carboxypeptidase B that unites the pathways of coagulation and fibrinolysis. Arterioscler., Thromb., Vasc. Biol. 2006, 26, 2445-2453.
-
(2006)
Arterioscler., Thromb., Vasc. Biol
, vol.26
, pp. 2445-2453
-
-
Mosnier, L.O.1
Bouma, B.N.2
-
6
-
-
4444287314
-
Thrombin-activatable fibrinolysis inhibitor
-
(b) Marx, P. F. Thrombin-activatable fibrinolysis inhibitor. Curr. Med. Chem. 2004, 11, 2335-2348.
-
(2004)
Curr. Med. Chem
, vol.11
, pp. 2335-2348
-
-
Marx, P.F.1
-
7
-
-
0025748556
-
Isolation, molecular cloning, and partial characterisation of a novel carboxypeptidase B from human plasma
-
Eaton, D. L.; Malloy, B. E.; Tsai, S. P.; Henzel, W.; Dryana, D. Isolation, molecular cloning, and partial characterisation of a novel carboxypeptidase B from human plasma. J. Biol. Chem. 1991, 266, 21833-21838.
-
(1991)
J. Biol. Chem
, vol.266
, pp. 21833-21838
-
-
Eaton, D.L.1
Malloy, B.E.2
Tsai, S.P.3
Henzel, W.4
Dryana, D.5
-
8
-
-
0028222563
-
Carboxypeptidase U, a plasma carboxypeptidase with high affinity for plasminogen
-
Wang, W.; Hendriks, D. F.; Scharpe S. S. Carboxypeptidase U, a plasma carboxypeptidase with high affinity for plasminogen. J. Biol. Chem. 1994, 269, 15937-15944.
-
(1994)
J. Biol. Chem
, vol.269
, pp. 15937-15944
-
-
Wang, W.1
Hendriks, D.F.2
Scharpe, S.S.3
-
9
-
-
0033825322
-
Consequences of inhibition of plasma carboxypeptidase B on in vivo thrombolysis, thrombosis, and hemostasis
-
Refino, C. J.; DeGuzman, L.; Schmitt, D.; Smyth, R.; Jeet, S.; Lipari, M. T.; Eaton, D.; Bunting, S. Consequences of inhibition of plasma carboxypeptidase B on in vivo thrombolysis, thrombosis, and hemostasis. Fibrinolysis Proteolysis 2000, 14, 305-314.
-
(2000)
Fibrinolysis Proteolysis
, vol.14
, pp. 305-314
-
-
Refino, C.J.1
DeGuzman, L.2
Schmitt, D.3
Smyth, R.4
Jeet, S.5
Lipari, M.T.6
Eaton, D.7
Bunting, S.8
-
12
-
-
37849014517
-
-
Commercially available from Aldrich Chemical Company
-
Commercially available from Aldrich Chemical Company.
-
-
-
-
13
-
-
0029920476
-
Regiospecific alkylation of histidine and histamine at N-I (τ)
-
Jain, R.; Cohen, L. A. Regiospecific alkylation of histidine and histamine at N-I (τ). Tetrahedron 1996, 52, 5363-5370.
-
(1996)
Tetrahedron
, vol.52
, pp. 5363-5370
-
-
Jain, R.1
Cohen, L.A.2
-
14
-
-
0027746129
-
Efficient synthesis of azetidine through N-trityl- or N- dimethoxyttitylazetidines starting from 3-amino-1-propanol or 3-halopropylamine hydrohalides
-
Huszthy, P.; Bradshaw, J. S.; Krakowiak, K. E.; Wang, T.; Dalley, N. K. Efficient synthesis of azetidine through N-trityl- or N- dimethoxyttitylazetidines starting from 3-amino-1-propanol or 3-halopropylamine hydrohalides. J. Heterocycl. Chem. 1993, 30, 1197-1207.
-
(1993)
J. Heterocycl. Chem
, vol.30
, pp. 1197-1207
-
-
Huszthy, P.1
Bradshaw, J.S.2
Krakowiak, K.E.3
Wang, T.4
Dalley, N.K.5
-
16
-
-
0001346254
-
Selective reduction of aryl halides and a,b-unsaturated esters with sodium borohydride-cuprous chloride in methanol and its application to deuterium labeling
-
Nansada, M.; Horibe, I.; Watanabe, F.; Takeda, K. Selective reduction of aryl halides and a,b-unsaturated esters with sodium borohydride-cuprous chloride in methanol and its application to deuterium labeling. J. Org. Chem. 1989, 54, 5308-5313.
-
(1989)
J. Org. Chem
, vol.54
, pp. 5308-5313
-
-
Nansada, M.1
Horibe, I.2
Watanabe, F.3
Takeda, K.4
-
17
-
-
33845551642
-
-
Flynn, D. L.; Zelle, R. E.; Grieco, P. A. A mild two-step method for the hydrolysis/methanolysis of secondary amides and lactams. J. Org. Chem. 1983, 48, 2424-2426.
-
Flynn, D. L.; Zelle, R. E.; Grieco, P. A. A mild two-step method for the hydrolysis/methanolysis of secondary amides and lactams. J. Org. Chem. 1983, 48, 2424-2426.
-
-
-
-
18
-
-
21144447472
-
Efficient synthesis of an imidazole-substituted d-amino acid by the integration of chiral technologies
-
Appleby, I; Boulton, L. T.; Cobley, C. J.; Hill, C.; Hughes, M.; De Koning, P. D.; Lennon, I. C.; Praquin, C.; Ramsden, J. A.; Samuel, H. J.; Willis, N. Efficient synthesis of an imidazole-substituted d-amino acid by the integration of chiral technologies. Org. Lett. 2005, 7, 1931-1934.
-
(2005)
Org. Lett
, vol.7
, pp. 1931-1934
-
-
Appleby, I.1
Boulton, L.T.2
Cobley, C.J.3
Hill, C.4
Hughes, M.5
De Koning, P.D.6
Lennon, I.C.7
Praquin, C.8
Ramsden, J.A.9
Samuel, H.J.10
Willis, N.11
-
19
-
-
0029793068
-
-
The potato tuber carboxypeptidase inhibitor peptide (PCI) had been shown to be a potent inhibitor of TAFIa: Bajzar, L.; Nesheim, M. E.; Tracy, P. B. The profibrinolytic effect of activated protein C in clots formed from plasma is TAFI-dependent. Blood 1996, 88, 2093-2100.
-
The potato tuber carboxypeptidase inhibitor peptide (PCI) had been shown to be a potent inhibitor of TAFIa: Bajzar, L.; Nesheim, M. E.; Tracy, P. B. The profibrinolytic effect of activated protein C in clots formed from plasma is TAFI-dependent. Blood 1996, 88, 2093-2100.
-
-
-
-
20
-
-
10744228937
-
-
Over recent years, a number of nonpeptidic TAFIa inhibitors have been disclosed, including a related series of imidazole-based inhibitors from Merck; see: (a) Barrow, J. C.; Nantermet, P. G.; Stauffer, S. R.; Ngo, P. L.; Steinbeiser, M. A.; Mao, S.-S.; Carroll, S. S.; Bailey, C.; Colussi, D.; Bosserman, M.; Burlein, C.; Cook, J. J.; Sitko, G.; Tiller, P. R.; Miller-Stein, C. M.; Rose, M.; McMasters, D. R.; Vacca, J. P.; Selnick, H. G. Synthesis and evaluation of imidazole acetic acid inhibitors of activated thrombin-activatable fibrinolysis inhibitor as novel antithrombotics. J. Med. Chem. 2003, 46, 5294-5297.
-
Over recent years, a number of nonpeptidic TAFIa inhibitors have been disclosed, including a related series of imidazole-based inhibitors from Merck; see: (a) Barrow, J. C.; Nantermet, P. G.; Stauffer, S. R.; Ngo, P. L.; Steinbeiser, M. A.; Mao, S.-S.; Carroll, S. S.; Bailey, C.; Colussi, D.; Bosserman, M.; Burlein, C.; Cook, J. J.; Sitko, G.; Tiller, P. R.; Miller-Stein, C. M.; Rose, M.; McMasters, D. R.; Vacca, J. P.; Selnick, H. G. Synthesis and evaluation of imidazole acetic acid inhibitors of activated thrombin-activatable fibrinolysis inhibitor as novel antithrombotics. J. Med. Chem. 2003, 46, 5294-5297.
-
-
-
-
21
-
-
11144357139
-
Imidazole acetic acid TAFIa inhibitors: SAR studies centered around the basic P1′ group
-
(b) Nantermet, P. G.; Barrow, J. C.; Lindsley, S. R.; Young, M.; Mao, S.-S.; Carroll, S.; Bailey, C.; Bosserman, M.; Colussi, D.; McMasters, D. R.; Vacca, J. P.; Selnick, H. G. Imidazole acetic acid TAFIa inhibitors: SAR studies centered around the basic P1′ group, Bioorg. Med. Chem. Lett. 2004, 14, 2141-2145.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 2141-2145
-
-
Nantermet, P.G.1
Barrow, J.C.2
Lindsley, S.R.3
Young, M.4
Mao, S.-S.5
Carroll, S.6
Bailey, C.7
Bosserman, M.8
Colussi, D.9
McMasters, D.R.10
Vacca, J.P.11
Selnick, H.G.12
-
22
-
-
0015932710
-
Binding of the by-product analog benzylsuccinic acid by carboxypeptidase A
-
Byers, L. D. Wolfenden, R. Binding of the by-product analog benzylsuccinic acid by carboxypeptidase A. Biochemistry 1973, 12, 2070-2078.
-
(1973)
Biochemistry
, vol.12
, pp. 2070-2078
-
-
Byers, L.D.1
Wolfenden, R.2
-
23
-
-
0018794371
-
Design of potent and specific inhibitors of carboxypeptidases A and B
-
Ondetti, M. A.; Condon, M. E.; Reid, J.; Sabo, E. F.; Cheung, H. S.; Cushman, D. W. Design of potent and specific inhibitors of carboxypeptidases A and B. Biochemistry 1979, 18, 1427-1430.
-
(1979)
Biochemistry
, vol.18
, pp. 1427-1430
-
-
Ondetti, M.A.1
Condon, M.E.2
Reid, J.3
Sabo, E.F.4
Cheung, H.S.5
Cushman, D.W.6
-
24
-
-
0017578611
-
Design of specific inhibitors of angiotensin-converting enzyme: New class of orally active antihypertensive agents
-
Ondetti, M. A.; Rubin, B.; Cushman, D. W. Design of specific inhibitors of angiotensin-converting enzyme: New class of orally active antihypertensive agents. Science 1977, 196, 441-444.
-
(1977)
Science
, vol.196
, pp. 441-444
-
-
Ondetti, M.A.1
Rubin, B.2
Cushman, D.W.3
-
25
-
-
0019238621
-
Inhibitors of angiotensin-converting enzyme
-
Cushman, D. W.; Ondetti, M. A. Inhibitors of angiotensin-converting enzyme. Prog. Med. Chem. 1980, 17, 41-104.
-
(1980)
Prog. Med. Chem
, vol.17
, pp. 41-104
-
-
Cushman, D.W.1
Ondetti, M.A.2
-
26
-
-
0019890965
-
A potent mercapto bi-product analog inhibitor for human carboxypeptidase N
-
Plummer, T. H., Jr.; Ryan, T. J. A potent mercapto bi-product analog inhibitor for human carboxypeptidase N. Biochem. Biophys. Res. Commun. 1981, 98, 448-454.
-
(1981)
Biochem. Biophys. Res. Commun
, vol.98
, pp. 448-454
-
-
Plummer Jr., T.H.1
Ryan, T.J.2
-
27
-
-
0023690624
-
Basic carboxypeptidases: Regulators of peptide hormone activity
-
Skidgel, R. A. Basic carboxypeptidases: regulators of peptide hormone activity. TIPS 1988, 9, 299-304.
-
(1988)
TIPS
, vol.9
, pp. 299-304
-
-
Skidgel, R.A.1
-
28
-
-
0020595387
-
Potentiation of the anaphylatoxins in vivo using an inhibitor of serum carboxypeptidase N (SCPN). I. Lethality and pathological effects on pulmonary tissue
-
Huey, R.; Bloor, C. M.; Kawahara, M. S.; Hugh, T. E. Potentiation of the anaphylatoxins in vivo using an inhibitor of serum carboxypeptidase N (SCPN). I. Lethality and pathological effects on pulmonary tissue. Am. J. Pathol. 1983, 112, 48-60.
-
(1983)
Am. J. Pathol
, vol.112
, pp. 48-60
-
-
Huey, R.1
Bloor, C.M.2
Kawahara, M.S.3
Hugh, T.E.4
-
29
-
-
0001518155
-
A new type of carboxypeptidase A inhibitors designed using an imidazole as a zinc coordinating ligand
-
Lee, K. J.; Joo, K. C.; Kim, E.-J.; Lee, M.; Kim, D. H. A new type of carboxypeptidase A inhibitors designed using an imidazole as a zinc coordinating ligand. Bioorg. Med. Chem. 1997, 5, 1989-1998.
-
(1997)
Bioorg. Med. Chem
, vol.5
, pp. 1989-1998
-
-
Lee, K.J.1
Joo, K.C.2
Kim, E.-J.3
Lee, M.4
Kim, D.H.5
-
30
-
-
37849000777
-
-
The numbering system used is the same as that used for the deposited structure INSA
-
The numbering system used is the same as that used for the deposited structure INSA.
-
-
-
-
31
-
-
33846947189
-
-
Researchers at Merck have also shown the efficacy of TAFIa inhibition in a model of thrombosis in African green monkeys; see ref 17(a, In addition, researchers at Berlex have recently reported in vivo efficacy data for their TAFIa inhibitor, BX 528; see: Wang, Y.-X, da Cunha, V, Vincelette, J, Zhao, L, Nagashima, M, Kawai, K, Yuan, S, Emayan, K, Islam, I, Hosoya, J, Sullivan, M. E, Dole, W. P, Morser, J, Buckman, B. O, Vergona, R. A novel inhibitor of activated thrombin activatable fibrinolysis inhibitor (TAFIa, Part thrombosis. Thromb. Haemost. 2007, 971, 54-61
-
Researchers at Merck have also shown the efficacy of TAFIa inhibition in a model of thrombosis in African green monkeys; see ref 17(a). In addition, researchers at Berlex have recently reported in vivo efficacy data for their TAFIa inhibitor, BX 528; see: Wang, Y.-X.; da Cunha, V.; Vincelette, J.; Zhao, L.; Nagashima, M.; Kawai, K.; Yuan, S.; Emayan, K.; Islam, I.; Hosoya, J.; Sullivan, M. E.; Dole, W. P.; Morser, J.; Buckman, B. O.; Vergona, R. A novel inhibitor of activated thrombin activatable fibrinolysis inhibitor (TAFIa) - Part thrombosis. Thromb. Haemost. 2007, 97(1), 54-61.
-
-
-
-
32
-
-
0027312774
-
Selective paracellular permeability in two models of intestinal absorption: Cultured monolayers of human intestinal epithelial cells and rat intestinal segments
-
Artursson, P.; Ungell, A.-L.; Löfroth, J. E. Selective paracellular permeability in two models of intestinal absorption: cultured monolayers of human intestinal epithelial cells and rat intestinal segments. Pharm. Res. 1993, 10, 1123-1129.
-
(1993)
Pharm. Res
, vol.10
, pp. 1123-1129
-
-
Artursson, P.1
Ungell, A.-L.2
Löfroth, J.E.3
-
33
-
-
0031958251
-
Species differences in size discrimination in the paracellular pathway reflected by oral bioavailability of polyethylene glycol and D-peptides
-
He, Y.-L.; Murby, S.; Warhurst, G.; Gifford, L.; Walker, D.; Ayrton, J.; Eastmond, R.; Rowland, M. Species differences in size discrimination in the paracellular pathway reflected by oral bioavailability of polyethylene glycol and D-peptides. J. Pharm. Sci. 1998, 87, 626-633.
-
(1998)
J. Pharm. Sci
, vol.87
, pp. 626-633
-
-
He, Y.-L.1
Murby, S.2
Warhurst, G.3
Gifford, L.4
Walker, D.5
Ayrton, J.6
Eastmond, R.7
Rowland, M.8
-
34
-
-
0031059866
-
Processing of X-ray diffraction data collected in oscillation mode
-
Carter, C. W, Jr, Sweet, R. M, Eds, Academic Press: New York, Part A, pp
-
Otwinowski, Z.; Minor, W. Processing of X-ray diffraction data collected in oscillation mode. In Methods in Enzymology; Carter, C. W., Jr, Sweet, R. M., Eds.; Academic Press: New York, 1997; Vol. 276, Part A, pp 307-326.
-
(1997)
Methods in Enzymology
, vol.276
, pp. 307-326
-
-
Otwinowski, Z.1
Minor, W.2
-
35
-
-
0028103275
-
-
CCP4 suite. Acta Crystallogr. 1994, D50, 760-763.
-
CCP4 suite. Acta Crystallogr. 1994, D50, 760-763.
-
-
-
-
37
-
-
0026597444
-
R value: A novel statistical quantity for assessing the accuracy of crystal structures
-
Brunger, A. T. Free R value: A novel statistical quantity for assessing the accuracy of crystal structures. Nature 1992, 355, 472-475.
-
(1992)
Nature
, vol.355
, pp. 472-475
-
-
Brunger, A.1
Free, T.2
-
38
-
-
0000243829
-
A program to check the stereochemical quality of protein structure
-
Laskowski, R. A.; MacArthur, M. W.; Moss, D. S.; Thornton, J. M. PROCHECK: A program to check the stereochemical quality of protein structure. J. Appl. Crystallogr. 1993, 26, 283-291.
-
(1993)
J. Appl. Crystallogr
, vol.26
, pp. 283-291
-
-
Laskowski, R.A.1
MacArthur, M.W.2
Moss, D.S.3
Thornton, J.4
PROCHECK, M.5
-
39
-
-
37849043294
-
-
integration software; Bruker AXS, Inc, Madison, WI
-
SMART v5.618 (control) and SAINT v6.02 (integration) software; Bruker AXS, Inc.: Madison, WI, 1994.
-
(1994)
SMART v5.618 (control) and SAINT v6.02
-
-
-
40
-
-
37849038816
-
-
Sheldrick, G. M. SADABS: Program for Scaling and Correction of Area Detector Data; University of Göttingen: Göttingen, Germany, 1997 (based on the method of Blessing, R. H. Acta Cryst. 1995, A51, 33-38).
-
Sheldrick, G. M. SADABS: Program for Scaling and Correction of Area Detector Data; University of Göttingen: Göttingen, Germany, 1997 (based on the method of Blessing, R. H. Acta Cryst. 1995, A51, 33-38).
-
-
-
-
41
-
-
37849045102
-
-
Sheldrick, G. M. SHELXS-97: Program for Crystal Structure Solution; University of Göttingen: Göttingen, Germany, 1997 (release 97-2).
-
Sheldrick, G. M. SHELXS-97: Program for Crystal Structure Solution; University of Göttingen: Göttingen, Germany, 1997 (release 97-2).
-
-
-
-
42
-
-
37849025126
-
-
Sheldrick, G. M. SHELXL-97: Program for Crystal Structure Refinement; University of Göttingen: Göttingen, Germany, 1997 (release 97-2).
-
Sheldrick, G. M. SHELXL-97: Program for Crystal Structure Refinement; University of Göttingen: Göttingen, Germany, 1997 (release 97-2).
-
-
-
-
43
-
-
84944438568
-
-
Flack, H. D. Acta Cryst. 1983, A39, 876-881.
-
(1983)
Acta Cryst
, vol.A39
, pp. 876-881
-
-
Flack, H.D.1
|