-
1
-
-
0011753217
-
Inhibitors of Elastases, Chymases and Cathepsin G
-
Sandler, M., Smith, H. J., Eds.; Oxford University Press: Oxford
-
Powers, J. C.; Zimmerman, M. Inhibitors of Elastases, Chymases and Cathepsin G. In Design of Enzyme Inhibitors as Drugs; Sandler, M., Smith, H. J., Eds.; Oxford University Press: Oxford, 1989; pp 596-619.
-
(1989)
Design of Enzyme Inhibitors as Drugs
, pp. 596-619
-
-
Powers, J.C.1
Zimmerman, M.2
-
2
-
-
0025364110
-
Recent Developments in Inhibiting Cysteine and Serine Proteases
-
Demuth, H.-U. Recent Developments in Inhibiting Cysteine and Serine Proteases. J. Enzyme Inhib. 1990, 3, 249-278.
-
(1990)
J. Enzyme Inhib.
, vol.3
, pp. 249-278
-
-
Demuth, H.-U.1
-
3
-
-
0027516156
-
Proteasomes: Multicatalytic Proteinase Complexes
-
Rivett, A. J. Proteasomes: Multicatalytic Proteinase Complexes. Biochem. J. 1993, 291, 1-10.
-
(1993)
Biochem. J.
, vol.291
, pp. 1-10
-
-
Rivett, A.J.1
-
5
-
-
0028186402
-
Inhibitors of Human Leukocyte Elastase
-
Ellis, G. P., Luscombe, D. K., Eds.; Elsevier: New York
-
Bernstein, P. R.; Edwards, P. D.; Williams, J. C. Inhibitors of Human Leukocyte Elastase. In Progress in Medicinal Chemistry, Vol. 31; Ellis, G. P., Luscombe, D. K., Eds.; Elsevier: New York, 1994; pp 59-120.
-
(1994)
Progress in Medicinal Chemistry
, vol.31
, pp. 59-120
-
-
Bernstein, P.R.1
Edwards, P.D.2
Williams, J.C.3
-
7
-
-
0021112874
-
Haloenol Lactones: Potent Enzyme-Activated Irreversible Inhibitors for α-Chymotrypsin
-
Daniels, S. B.; Cooney, E.; Sofia, M. J.; Chakravarty, P. K.; Katzenellenbogen, J. A. Haloenol Lactones: Potent Enzyme-Activated Irreversible Inhibitors for α-Chymotrypsin. J. Biol. Chem. 1983, 258, 15046-15053.
-
(1983)
J. Biol. Chem.
, vol.258
, pp. 15046-15053
-
-
Daniels, S.B.1
Cooney, E.2
Sofia, M.J.3
Chakravarty, P.K.4
Katzenellenbogen, J.A.5
-
8
-
-
0026445446
-
Enol Lactone Derivatives as Inhibitors of Human Neutrophil Elastase and Trypsin-like Proteases
-
Katzenellenbogen, J. A.; Rai, R.; Dai, W. Enol Lactone Derivatives as Inhibitors of Human Neutrophil Elastase and Trypsin-like Proteases. Bioorg. Med. Chem. Lett. 1992, 2, 1399-1404.
-
(1992)
Bioorg. Med. Chem. Lett.
, vol.2
, pp. 1399-1404
-
-
Katzenellenbogen, J.A.1
Rai, R.2
Dai, W.3
-
9
-
-
0021679050
-
Novel Suicide Inhibitors of Serine Proteinases. Inactivation of Human Leukocyte Elastase by Ynenol Lactones
-
Tam, T. F.; Spencer, R. W.; Thomas, E. M.; Copp, L. J.; Krantz, A. Novel Suicide Inhibitors of Serine Proteinases. Inactivation of Human Leukocyte Elastase by Ynenol Lactones. J. Am. Chem. Soc. 1984, 106, 6849-6851.
-
(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 6849-6851
-
-
Tam, T.F.1
Spencer, R.W.2
Thomas, E.M.3
Copp, L.J.4
Krantz, A.5
-
10
-
-
0022271601
-
Reaction of Serine Proteases with Substituted Isocoumarins. Discovery of 3, 4-Dichloroisocoumarin, a new general Mechanism Based Serine Protease Inhibitor
-
Harper, J. W.; Hemmi, K.; Powers, J. C. Reaction of Serine Proteases with Substituted Isocoumarins. Discovery of 3, 4-Dichloroisocoumarin, a new general Mechanism Based Serine Protease Inhibitor. Biochemistry 1985, 24, 1831-1841.
-
(1985)
Biochemistry
, vol.24
, pp. 1831-1841
-
-
Harper, J.W.1
Hemmi, K.2
Powers, J.C.3
-
11
-
-
0022396629
-
Reaction of Serine Proteases with Substituted 3-Alkoxy-4-chloroisocoumarins and 3-Alkoxy-7-amino-4-chloroisocoumarins. New Reactive Mechanism Based Inhibitors
-
Harper, J. W.; Powers, J. C. Reaction of Serine Proteases with Substituted 3-Alkoxy-4-chloroisocoumarins and 3-Alkoxy-7-amino-4-chloroisocoumarins. New Reactive Mechanism Based Inhibitors. Biochemistry 1985, 24, 7200-7213.
-
(1985)
Biochemistry
, vol.24
, pp. 7200-7213
-
-
Harper, J.W.1
Powers, J.C.2
-
12
-
-
0015847339
-
Inactivation of α-Chymotrypsin by a Bifunctional Reagent, 3, 4-Dihydro-3, 4-dibromo-6-bromo-methylcoumarin
-
Béchet, J.-J.; Dupaix, A.; Yon, J.; Wakselman, M.; Robert, J.-L.; Vilkas, M. Inactivation of α-Chymotrypsin by a Bifunctional Reagent, 3, 4-Dihydro-3, 4-dibromo-6-bromo-methylcoumarin. Eur. J. Biochem. 1973, 35, 527-539.
-
(1973)
Eur. J. Biochem.
, vol.35
, pp. 527-539
-
-
Béchet, J.-J.1
Dupaix, A.2
Yon, J.3
Wakselman, M.4
Robert, J.-L.5
Vilkas, M.6
-
13
-
-
0025219812
-
Reaction of Thrombin and Proteinases of the Fibrinolytic System with a Mechanism-Based Inhibitor, 3, 4-Dihydro-3-benzyl-6-chloromethylcoumarin
-
Mor, A.; Maillard, J.; Favreau, C.; Reboud-Ravaux, M. Reaction of Thrombin and Proteinases of the Fibrinolytic System with a Mechanism-Based Inhibitor, 3, 4-Dihydro-3-benzyl-6-chloromethylcoumarin. Biochim. Biophys. Acta 1990, 1038, 119-124.
-
(1990)
Biochim. Biophys. Acta
, vol.1038
, pp. 119-124
-
-
Mor, A.1
Maillard, J.2
Favreau, C.3
Reboud-Ravaux, M.4
-
14
-
-
0025912832
-
A Cyclopeptidic Suicide Substrate preferentially Inactivates Urokinase-type Plasminogen Activators
-
Reboud-Ravaux, M.; Vilain, A.-C.; Boggetto, N.; Maillard, J.; Favreau, C.; Xie, J.; Mazaleyrat, J.-P.; Wakselman, M. A Cyclopeptidic Suicide Substrate preferentially Inactivates Urokinase-type Plasminogen Activators. Biochem. Biophys. Res. Commun. 1991, 178, 352-359.
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.178
, pp. 352-359
-
-
Reboud-Ravaux, M.1
Vilain, A.-C.2
Boggetto, N.3
Maillard, J.4
Favreau, C.5
Xie, J.6
Mazaleyrat, J.-P.7
Wakselman, M.8
-
15
-
-
0027270445
-
New Mechanism-Based Inactivators of Trypsin-like Proteinases. Selective Inactivation of Urokinase by Functionalized Cyclopeptides Incorporating a Sulfoniomethyl-Substituted m-Aminobenzoic Acid Residue
-
Wakselman, M.; Xie, J.; Mazaleyrat, J.-P.; Boggetto, N.; Vilain, A.-C.; Montagne, J.-J.; Reboud-Ravaux, M. New Mechanism-Based Inactivators of Trypsin-like Proteinases. Selective Inactivation of Urokinase by Functionalized Cyclopeptides Incorporating a Sulfoniomethyl-Substituted m-Aminobenzoic Acid Residue. J. Med. Chem. 1993, 36, 1539-1547.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 1539-1547
-
-
Wakselman, M.1
Xie, J.2
Mazaleyrat, J.-P.3
Boggetto, N.4
Vilain, A.-C.5
Montagne, J.-J.6
Reboud-Ravaux, M.7
-
16
-
-
0022505992
-
Cephalosporin Antibiotics can be Modified to Inhibit Human Leucocyte Elastase
-
Doherty, J. B.; Ashe, B. M.; Argenbright, L. W.; Barker, P. L.; Bonney, R. J.; Chandler, G. O.; Dahlgren, M. E.; Dorn, C. P., Jr.; Finke, P. E.; Firestone, R. A.; Fletcher, D.; Hagmann, W. K.; Mumford, R.; O'Grady, L.; Maycock, A. L.; Pisano, J. M.; Shah, S. K.; Thompson, K. R.; Zimmerman, M. Cephalosporin Antibiotics can be Modified to Inhibit Human Leucocyte Elastase. Nature 1986, 322, 192-194.
-
(1986)
Nature
, vol.322
, pp. 192-194
-
-
Doherty, J.B.1
Ashe, B.M.2
Argenbright, L.W.3
Barker, P.L.4
Bonney, R.J.5
Chandler, G.O.6
Dahlgren, M.E.7
Dorn Jr., C.P.8
Finke, P.E.9
Firestone, R.A.10
Fletcher, D.11
Hagmann, W.K.12
Mumford, R.13
O'Grady, L.14
Maycock, A.L.15
Pisano, J.M.16
Shah, S.K.17
Thompson, K.R.18
Zimmerman, M.19
-
17
-
-
0026662213
-
Specificity, Stability and Potency of Monocyclic β-Lactam Inhibitors of Human Leucocyte Elastase
-
Knight, W. B.; Green, B. G.; Chablin, R. M.; Gale, P.; Maycock, A. L.; Weston, H.; Kuo, D. W.; Westler, W. M.; Dorn, C. P.; Finke, P. E.; Hagmann, W. K.; Hale, J. J.; Liesch, J.; MacCoss, M.; Navia, M. A.; Shah, S. K.; Underwood, D.; Doherty, J.B. Specificity, Stability and Potency of Monocyclic β-Lactam Inhibitors of Human Leucocyte Elastase. Biochemistry 1992, 31, 8160-8170.
-
(1992)
Biochemistry
, vol.31
, pp. 8160-8170
-
-
Knight, W.B.1
Green, B.G.2
Chablin, R.M.3
Gale, P.4
Maycock, A.L.5
Weston, H.6
Kuo, D.W.7
Westler, W.M.8
Dorn, C.P.9
Finke, P.E.10
Hagmann, W.K.11
Hale, J.J.12
Liesch, J.13
MacCoss, M.14
Navia, M.A.15
Shah, S.K.16
Underwood, D.17
Doherty, J.B.18
-
18
-
-
0025076178
-
Biological Evaluation of the Inhibition of Neutrophil Elastase by a Synthetic β-Lactam Derivative
-
Maillard, J.-L.; Favreau, C.; Reboud-Ravaux, M.; Kobaiter, R.; Joyau, R.; Wakselman, M. Biological Evaluation of the Inhibition of Neutrophil Elastase by a Synthetic β-Lactam Derivative. Eur. J. Biol. 1990, 52, 213-221.
-
(1990)
Eur. J. Biol.
, vol.52
, pp. 213-221
-
-
Maillard, J.-L.1
Favreau, C.2
Reboud-Ravaux, M.3
Kobaiter, R.4
Joyau, R.5
Wakselman, M.6
-
19
-
-
0025774784
-
Functionalized N-Arylazetidinones as Novel Mechanism-Based Inhibitors of Neutrophil Elastase
-
Wakselman, M.; Joyau, R.; Kobaiter, R.; Boggetto, N.; Vergely, I.; Maillard, J.; Okochi, V.; Montagne, J. J.; Reboud-Ravaux, M. Functionalized N-Arylazetidinones as Novel Mechanism-Based Inhibitors of Neutrophil Elastase. FEBS Lett. 1991, 282, 377-381.
-
(1991)
FEBS Lett.
, vol.282
, pp. 377-381
-
-
Wakselman, M.1
Joyau, R.2
Kobaiter, R.3
Boggetto, N.4
Vergely, I.5
Maillard, J.6
Okochi, V.7
Montagne, J.J.8
Reboud-Ravaux, M.9
-
20
-
-
0017399918
-
Inactivation of α-Chymotrypsin by New Bifunctional Reagents: Halomethylated Derivatives of Dihydrocoumarins
-
Béchet, J.-J.; Dupaix, A.; Blagoeva, I. Inactivation of α-Chymotrypsin by New Bifunctional Reagents: Halomethylated Derivatives of Dihydrocoumarins. Biochimie 1977, 59, 231-239.
-
(1977)
Biochimie
, vol.59
, pp. 231-239
-
-
Béchet, J.-J.1
Dupaix, A.2
Blagoeva, I.3
-
21
-
-
0017380435
-
Inactivation of Proteases and Esterases by Halomethylated Derivatives of Dihydrocoumarins
-
Béchet, J.-J.; Dupaix, A.; Roucous, C.; Bonamy, A.-M. Inactivation of Proteases and Esterases by Halomethylated Derivatives of Dihydrocoumarins. Biochimie 1977, 59, 241-246.
-
(1977)
Biochimie
, vol.59
, pp. 241-246
-
-
Béchet, J.-J.1
Dupaix, A.2
Roucous, C.3
Bonamy, A.-M.4
-
22
-
-
0026073616
-
Acyloxybenzyl Halides, Inhibitors of Elastases
-
Vilain, A.-C.; Okochi, V.; Vergely, I.; Reboud-Ravaux, M.; Mazaleyrat, J.-P.; Wakselman, M. Acyloxybenzyl Halides, Inhibitors of Elastases. Biochim. Biophys. Acta 1991, 119-127.
-
(1991)
Biochim. Biophys. Acta
, pp. 119-127
-
-
Vilain, A.-C.1
Okochi, V.2
Vergely, I.3
Reboud-Ravaux, M.4
Mazaleyrat, J.-P.5
Wakselman, M.6
-
23
-
-
0021745792
-
Inactivation of Human High-and Low-Molecular-Weight Urokinases. Analysis of their Active Site
-
Reboud-Ravaux, M.; Desvages, G. Inactivation of Human High-and Low-Molecular-Weight Urokinases. Analysis of their Active Site. Biochim. Biophys. Acta 1984, 791, 333-341.
-
(1984)
Biochim. Biophys. Acta
, vol.791
, pp. 333-341
-
-
Reboud-Ravaux, M.1
Desvages, G.2
-
24
-
-
0000231181
-
1,4- and 1,6-Eliminations from Hydroxy- and Amino-Substituted benzyl Systems: Chemical and Biochemical Application
-
Wakselman, M. 1,4- and 1,6-Eliminations from Hydroxy- and Amino-Substituted benzyl Systems: Chemical and Biochemical Application. Nouv. J. Chimie 1983, 7, 439-447.
-
(1983)
Nouv. J. Chimie
, vol.7
, pp. 439-447
-
-
Wakselman, M.1
-
25
-
-
84945103904
-
Synthese Aromatischer Alkohole mit Formaldehyd
-
Stoermer, R.; Behn, K. Synthese Aromatischer Alkohole mit Formaldehyd. Ber. 1901, 34, 2455-2460.
-
Ber. 1901
, vol.34
, pp. 2455-2460
-
-
Stoermer, R.1
Behn, K.2
-
27
-
-
5244323484
-
Uber den 2-Oxy-5-chloromethyl-benzaldehyd
-
Reichert, B.; Hoss, W. Uber den 2-Oxy-5-chloromethyl-benzaldehyd. Ber. 1942, 75, 157-171.
-
(1942)
Ber.
, vol.75
, pp. 157-171
-
-
Reichert, B.1
Hoss, W.2
|