-
1
-
-
34447135455
-
Characterization of subtilase protease in Cryptosporidium parvum and C.hominis
-
Feng X, Akiyoshi DE, Widmer G, Tzipori S. Characterization of subtilase protease in Cryptosporidium parvum and C.hominis. J Parasitol 2007;93:619-626
-
(2007)
J Parasitol
, vol.93
, pp. 619-626
-
-
Feng, X.1
Akiyoshi, D.E.2
Widmer, G.3
Tzipori, S.4
-
2
-
-
24044436201
-
A novel, potent dual inhibitor of the leukocyte proteases cathepsin G and chymase: Molecular mechanisms and anti-inflammatory activity in vivo
-
De Garavilla L, Greco MN, Sukumar N, Chen ZW, Pineda AO, Mathews FS, Di Cera E, Giardino EC, Wells GI, Haertlein BJ, Kauffman JA, Corcoran TW, Derian CK, Eckardt AJ, Damiano BP, Andrade-Gordon P, Maryanoff BE. A novel, potent dual inhibitor of the leukocyte proteases cathepsin G and chymase: molecular mechanisms and anti-inflammatory activity in vivo. J Biol Chem 2005;280:18001-18007
-
(2005)
J Biol Chem
, vol.280
, pp. 18001-18007
-
-
De Garavilla, L.1
Greco, M.N.2
Sukumar, N.3
Chen, Z.W.4
Pineda, A.O.5
Mathews, F.S.6
Di Cera, E.7
Giardino, E.C.8
Wells, G.I.9
Haertlein, B.J.10
Kauffman, J.A.11
Corcoran, T.W.12
Derian, C.K.13
Eckardt, A.J.14
Damiano, B.P.15
Andrade-Gordon, P.16
Maryanoff, B.E.17
-
3
-
-
34247223189
-
Discovery of potent, selective, orally active, nonpeptide inhibitors of human mast cell chymase
-
Greco MN, Hawkins MJ, Powell ET, Almond HR Jr, de Garavilla L, Hall J, Minor LK, Wang Y, Corcoran TW, Di Cera E, Cantwell AM, Savvides SN, Damiano BP, Maryanoff BE. Discovery of potent, selective, orally active, nonpeptide inhibitors of human mast cell chymase. J Med Chem 2007;50:1727-1730
-
(2007)
J Med Chem
, vol.50
, pp. 1727-1730
-
-
Greco, M.N.1
Hawkins, M.J.2
Powell, E.T.3
Almond Jr., H.R.4
De Garavilla, L.5
Hall, J.6
Minor, L.K.7
Wang, Y.8
Corcoran, T.W.9
Di Cera, E.10
Cantwell, A.M.11
Savvides, S.N.12
Damiano, B.P.13
Maryanoff, B.E.14
-
4
-
-
4644289087
-
Therapeutic applications of chymase inhibitors in cardiovascular diseases and fibrosis
-
Takai S, Jin D, Muramatsu M, Okamoto Y, Miyazaki M. Therapeutic applications of chymase inhibitors in cardiovascular diseases and fibrosis. Eur J Pharmacol 2004;501:1-8.
-
(2004)
Eur J Pharmacol
, vol.501
, pp. 1-8
-
-
Takai, S.1
Jin, D.2
Muramatsu, M.3
Okamoto, Y.4
Miyazaki, M.5
-
5
-
-
0024341633
-
Irreversible inhibition of serine proteases by peptidyl derivatives of alpha-aminoalkylphosphonate diphenyl esters
-
Oleksyszyn J, Powers JC. Irreversible inhibition of serine proteases by peptidyl derivatives of alpha-aminoalkylphosphonate diphenyl esters. Biochem Biophys Res Commun 1989;161:143-149
-
(1989)
Biochem Biophys Res Commun
, vol.161
, pp. 143-149
-
-
Oleksyszyn, J.1
Powers, J.C.2
-
6
-
-
0025979246
-
Irreversible inhibition of serine proteases by peptide derivatives of (alpha-aminoalkyl)phosphonate diphenyl esters
-
Oleksyszyn J, Powers JC. Irreversible inhibition of serine proteases by peptide derivatives of (alpha-aminoalkyl)phosphonate diphenyl esters. Biochemistry 1991;30:485-493
-
(1991)
Biochemistry
, vol.30
, pp. 485-493
-
-
Oleksyszyn, J.1
Powers, J.C.2
-
7
-
-
0028672813
-
Amino acid and peptide phosphonate derivatives as specific inhibitors of serine peptidases
-
Oleksyszyn J, Powers JC. Amino acid and peptide phosphonate derivatives as specific inhibitors of serine peptidases. Methods Enzymol 1994;244:423-441
-
(1994)
Methods Enzymol
, vol.244
, pp. 423-441
-
-
Oleksyszyn, J.1
Powers, J.C.2
-
8
-
-
0028172324
-
Alpha-aminoalkylphosphonate di(chlorophenyl) esters as inhibitors of serine proteases
-
Boduszek B, Brown AD, Powers JC. Alpha-aminoalkylphosphonate di(chlorophenyl) esters as inhibitors of serine proteases. J Enzyme Inhib 1994;8:147-158
-
(1994)
J Enzyme Inhib
, vol.8
, pp. 147-158
-
-
Boduszek, B.1
Brown, A.D.2
Powers, J.C.3
-
11
-
-
0002978054
-
The characterization of enzyme inhibition
-
Amsterdam: Elsevier
-
Knight CG. The characterization of enzyme inhibition. In: Proteinase Inhibitors. Amsterdam: Elsevier, 1986:23-51.
-
(1986)
Proteinase Inhibitors
, pp. 23-51
-
-
Knight, C.G.1
-
12
-
-
37449014883
-
Small, potent, and selective diaryl phosphonate inhibitors for urokinase-type plasminogen activator with in vivo antimetastatic properties
-
Joossens J, Ali OM, El-Sayed I, Surpateanu G, Van der Veken P, Lambeir AM, Setyono-Han B, Foekens JA, Schneider A, Schmalix W, Haemers A, Augustyns K. Small, potent, and selective diaryl phosphonate inhibitors for urokinase-type plasminogen activator with in vivo antimetastatic properties. J Med Chem 2007;50:6638-6646
-
(2007)
J Med Chem
, vol.50
, pp. 6638-6646
-
-
Joossens, J.1
Ali, O.M.2
El-Sayed, I.3
Surpateanu, G.4
Van Der Veken, P.5
Lambeir, A.M.6
Setyono-Han, B.7
Foekens, J.A.8
Schneider, A.9
Schmalix, W.10
Haemers, A.11
Augustyns, K.12
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