-
1
-
-
0011753217
-
Inhibitors of elastases, chymases and cathepsin G
-
Sandler, M., Smith, H. J., Eds.; Oxford University Press: Oxford
-
Poweres, 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
-
-
Poweres, 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
-
-
0020077285
-
Studies on the pathogenesis of the adult respiratory distress syndrome
-
McGuire, W. W.; Spragg, R. G.; Cohen, A. B.; Cochrane, C. G. Studies on the Pathogenesis of the Adult Respiratory Distress Syndrome. J. Clin. Invest. 1982, 69, 543-553.
-
(1982)
J. Clin. Invest.
, vol.69
, pp. 543-553
-
-
McGuire, W.W.1
Spragg, R.G.2
Cohen, A.B.3
Cochrane, C.G.4
-
4
-
-
0028839246
-
The control of neutrophil chemotaxis by inhibitors of cathepsin G and chymotrypsin
-
Lomas, D. A.; Stone, S. R.; Llewellyn-Jones, C.; Keogan, M.-T.; Wang, Z.-m.; Rubin, H.; Carrell, R. W.; Stockley, R. A. The Control of Neutrophil Chemotaxis by Inhibitors of Cathepsin G and Chymotrypsin. J. Biol. Chem. 1995, 270, 23437-23443.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 23437-23443
-
-
Lomas, D.A.1
Stone, S.R.2
Llewellyn-Jones, C.3
Keogan, M.-T.4
Wang, Z.-M.5
Rubin, H.6
Carrell, R.W.7
Stockley, R.A.8
-
5
-
-
0030970908
-
Activation of angiotensin II-forming chymase in the cardiomyopathic hamster heart
-
Shiota, N.; Fukamizu, A.; Takai, S.; Okunishi, H.; Murakami, K.; Miyazaki, M. Activation of Angiotensin II-forming Chymase in the Cardiomyopathic Hamster Heart. J. Hypertension 1997, 15, 431-440.
-
(1997)
J. Hypertension
, vol.15
, pp. 431-440
-
-
Shiota, N.1
Fukamizu, A.2
Takai, S.3
Okunishi, H.4
Murakami, K.5
Miyazaki, M.6
-
7
-
-
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; Ellis, G. P., Luscombe, D. K., Eds.; Elsevier: New York, 1994; Vol. 31, 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
-
8
-
-
0011199743
-
Haloketone inhibitors of proteolytic enzyme
-
Weinstein, B., Ed.; Marcel Dekker: New York
-
Powers, J. C. Haloketone Inhibitors of Proteolytic Enzyme. In Chemistry and Biochemistry of Amino Acids, Peptides, and Proteins; Weinstein, B., Ed.; Marcel Dekker: New York, 1977; Vol. 4, pp 65-178.
-
(1977)
Chemistry and Biochemistry of Amino Acids, Peptides, and Proteins
, vol.4
, pp. 65-178
-
-
Powers, J.C.1
-
10
-
-
0031587424
-
Potent inactivator of α-chymotrypsin: 2,2-dimethyl-3-(N-4-cyanobenzoyl)amino-5-phenylpentanoic acid
-
Ito, K.; Igarashi, K.; Muramatsu, M.; Harada, T.; Hayashi, Y.; Katada, J.; Uno, I. Potent Inactivator of α-Chymotrypsin: 2,2-Dimethyl-3-(N-4-cyanobenzoyl)amino-5-phenylpentanoic Acid. Biochem. Biophys. Res. Commun. 1997, 240, 850-855.
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.240
, pp. 850-855
-
-
Ito, K.1
Igarashi, K.2
Muramatsu, M.3
Harada, T.4
Hayashi, Y.5
Katada, J.6
Uno, I.7
-
11
-
-
0029665670
-
From poor substrates to good inhibitors: Design of inhibitors for serine and thiol proteases
-
Baggio, R.; Shi, Y.-Q.; Wu, Y.-q.; Abeles, R. H. From Poor Substrates to Good Inhibitors: Design of Inhibitors for Serine and Thiol Proteases. Biochemistry 1996, 35, 3351-3353.
-
(1996)
Biochemistry
, vol.35
, pp. 3351-3353
-
-
Baggio, R.1
Shi, Y.-Q.2
Wu, Y.-Q.3
Abeles, R.H.4
-
12
-
-
0014942114
-
Mapping the active site of papain with the aid of peptide substrates and inhibitors
-
Schechter, I.; Berger, A. Mapping the Active Site of Papain with the Aid of Peptide Substrates and Inhibitors. Philos. Trans. R. Soc. London 1970, B257, 249-264.
-
(1970)
Philos. Trans. R. Soc. London
, vol.B257
, pp. 249-264
-
-
Schechter, I.1
Berger, A.2
-
13
-
-
0031031681
-
Development of the new potent non-peptide GpIIb/IIIa antagonist NSL-95301 by utilizing combinatorial technique
-
(a) Harada, T.; Katada, J.; Tachiki, A.; Asari, T.; Iijima, K.; Uno, I.; Ojima, I.; Hayashi, Y. Development of the New Potent Non-Peptide GpIIb/IIIa Antagonist NSL-95301 by Utilizing Combinatorial Technique. Bioorg. Med. Chem. Lett. 1997, 7, 209-212.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 209-212
-
-
Harada, T.1
Katada, J.2
Tachiki, A.3
Asari, T.4
Iijima, K.5
Uno, I.6
Ojima, I.7
Hayashi, Y.8
-
14
-
-
0031404346
-
Combinatorial chemical approaches as an efficient tool for discovering GPIIb/ IIIa antagonists
-
(b) Hayashi, Y.; Harada, T.; Katada, J.; Uno, I. Combinatorial Chemical Approaches as an Efficient Tool for Discovering GPIIb/ IIIa Antagonists. Drugs Future 1997, 22, 1367-1374.
-
(1997)
Drugs Future
, vol.22
, pp. 1367-1374
-
-
Hayashi, Y.1
Harada, T.2
Katada, J.3
Uno, I.4
-
15
-
-
15444346262
-
GPIIb/IIIa integrin antagonists with the new conformational restriction unit, trisubstituted β-amino acid derivatives, and a substituted benzamidine structure
-
Hayashi, Y.; Katada, J.; Harada, T.; Tachiki, A.; Iijima, K.; Takiguchi, Y.; Muramatsu, M.; Miyazaki, M.; Asari, T.; Okazaki, T.; Sato, Y.; Yasuda, E.; Yano, M.; Uno, I.; Ojima, I. GPIIb/IIIa Integrin Antagonists with the New Conformational Restriction Unit, Trisubstituted β-Amino Acid Derivatives, and a Substituted Benzamidine Structure. J. Med. Chem. 1998, 41, 2345-2360.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2345-2360
-
-
Hayashi, Y.1
Katada, J.2
Harada, T.3
Tachiki, A.4
Iijima, K.5
Takiguchi, Y.6
Muramatsu, M.7
Miyazaki, M.8
Asari, T.9
Okazaki, T.10
Sato, Y.11
Yasuda, E.12
Yano, M.13
Uno, I.14
Ojima, I.15
-
16
-
-
1842442545
-
A convenient synthesis of water-soluble carbodiimides
-
Sheehan, J. C.; Cruickshank, P. A.; Boshart, G. L. A Convenient Synthesis of Water-Soluble Carbodiimides. J. Org. Chem. 1961, 26, 2525-2528.
-
(1961)
J. Org. Chem.
, vol.26
, pp. 2525-2528
-
-
Sheehan, J.C.1
Cruickshank, P.A.2
Boshart, G.L.3
-
17
-
-
0014704672
-
New method for the synthesis of peptides: Activation of the carboxyl group with dicyclohexylcarbodiimide by using 1-hydroxybenzotriazoles as additives
-
König, W.; Geiger, R. New Method for the Synthesis of Peptides: Activation of the Carboxyl Group with Dicyclohexylcarbodiimide by Using 1-Hydroxybenzotriazoles as Additives. Chem. Ber. 1970, 703, 788-798.
-
(1970)
Chem. Ber.
, vol.703
, pp. 788-798
-
-
König, W.1
Geiger, R.2
-
18
-
-
0018637477
-
A sensitive new substrate for chymotrypsin
-
DelMar, E. G.; Largman, C.; Brodrick, J. W.; Geokas, M. C. A Sensitive New Substrate for Chymotrypsin. Anal. Biochem. 1979, 99, 316-320.
-
(1979)
Anal. Biochem.
, vol.99
, pp. 316-320
-
-
DelMar, E.G.1
Largman, C.2
Brodrick, J.W.3
Geokas, M.C.4
-
19
-
-
0015789712
-
Recording spectrophotometric method for determination of dissociation and phosphorylation constants for the inhibition of acetylcholinesterase by organophosphates in the presence of substrate
-
Hart, G. J.; O'Brien, R. D Recording Spectrophotometric Method for Determination of Dissociation and Phosphorylation Constants for the Inhibition of Acetylcholinesterase by Organophosphates in the Presence of Substrate. Biochemistry 1973 12 2940-2945.
-
(1973)
Biochemistry
, vol.12
, pp. 2940-2945
-
-
Hart, G.J.1
O'Brien, R.D.2
-
20
-
-
0025286470
-
Alternate substrate inhibitors of an α-chymotrypsin: Enantioselective interaction of aryl-substituted enol lactones
-
Baek, D.-J.; Reed, P. E.; Daniels, S. B.; Katzenellenbogen, J. A. Alternate Substrate Inhibitors of an α-Chymotrypsin: Enantioselective Interaction of Aryl-Substituted Enol Lactones. Biochemistry 1990, 29, 4305-4311.
-
(1990)
Biochemistry
, vol.29
, pp. 4305-4311
-
-
Baek, D.-J.1
Reed, P.E.2
Daniels, S.B.3
Katzenellenbogen, J.A.4
-
21
-
-
0019888592
-
Selective inhibition of human leukocyte elastase and bovine α-chymotrypsin by novel heterocycles
-
Ashe, B. M.; Clark, R. L.; Jones, H.; Zimmerman, M. Selective Inhibition of Human Leukocyte Elastase and Bovine α-Chymotrypsin by Novel Heterocycles. J. Biol. Chem. 1981, 256, 11603-11606.
-
(1981)
J. Biol. Chem.
, vol.256
, pp. 11603-11606
-
-
Ashe, B.M.1
Clark, R.L.2
Jones, H.3
Zimmerman, M.4
-
22
-
-
0000540529
-
A new class of serine protease inactivators based on isatoic anhydride
-
Moorman, A. R.; Abeles, R. H. A New Class of Serine Protease Inactivators Based on Isatoic Anhydride. J. Am. Chem. Soc 1982, 104, 6785-6786.
-
(1982)
J. Am. Chem. Soc
, vol.104
, pp. 6785-6786
-
-
Moorman, A.R.1
Abeles, R.H.2
-
23
-
-
0021759418
-
Suicide inactivation of chymotrypsin by benzoxazinones
-
Hedstrom, L.; Moorman, A. R.; Dobbs, J.; Abeles, R. H. Suicide Inactivation of Chymotrypsin by Benzoxazinones. Biochemistry 1984, 23, 1753-1759.
-
(1984)
Biochemistry
, vol.23
, pp. 1753-1759
-
-
Hedstrom, L.1
Moorman, A.R.2
Dobbs, J.3
Abeles, R.H.4
-
24
-
-
0021109430
-
Novel inactivators of serine proteases based on 6-chloro-2-pyrone
-
Westkaemper, R. B.; Abeles, R. H. Novel Inactivators of Serine Proteases Based on 6-Chloro-2-pyrone. Biochemistry 1983, 22, 3256-3264.
-
(1983)
Biochemistry
, vol.22
, pp. 3256-3264
-
-
Westkaemper, R.B.1
Abeles, R.H.2
-
25
-
-
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
-
26
-
-
0022481858
-
Substituted isatoic anhydrides: Selective inactivators of trypsin-like serine proteases
-
Gelb, M. H.; Abeles, R. H. Substituted Isatoic Anhydrides: Selective Inactivators of Trypsin-like Serine Proteases. J. Med. Chem. 1986, 29, 585-589.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 585-589
-
-
Gelb, M.H.1
Abeles, R.H.2
-
27
-
-
0023317381
-
Design of alternate substrate inhibitors of serine proteases. Synergistic use of alkyl substitution to impede enzymecatalyzed deacylation
-
Krantz, A.; Spencer, R. W.; Tam, T. F.; Thomas, E.; Copp, L. J. Design of Alternate Substrate Inhibitors of Serine Proteases. Synergistic Use of Alkyl Substitution to Impede Enzymecatalyzed Deacylation. J. Med. Chem. 1987, 30, 589-591.
-
(1987)
J. Med. Chem.
, vol.30
, pp. 589-591
-
-
Krantz, A.1
Spencer, R.W.2
Tam, T.F.3
Thomas, E.4
Copp, L.J.5
-
28
-
-
0014945734
-
Structure of crystalline a-chymotrypsin. IV. The structure of indoleacryloyl-α-chyotrypsin and its relevance to the hydrolytic mechanism of the enzyme
-
Henderson, R. Structure of Crystalline a-Chymotrypsin. IV. The Structure of Indoleacryloyl-α-chyotrypsin and its Relevance to the Hydrolytic Mechanism of the Enzyme. J. Mol. Biol. 1970, 54, 341-354.
-
(1970)
J. Mol. Biol.
, vol.54
, pp. 341-354
-
-
Henderson, R.1
-
29
-
-
0022261015
-
Inhibition of human leukocyte elastase, cathepsin G, chymotrypsin Aa, and porcine pancreatic elastase with substituted isobenzofuranones and benzopyrandiones
-
Hemmi, K.; Harper, J. W.; Powers, J. C. Inhibition of Human Leukocyte Elastase, Cathepsin G, Chymotrypsin Aa, and Porcine Pancreatic Elastase with Substituted Isobenzofuranones and Benzopyrandiones. Biochemistry 1985, 24, 1841-1848.
-
(1985)
Biochemistry
, vol.24
, pp. 1841-1848
-
-
Hemmi, K.1
Harper, J.W.2
Powers, J.C.3
-
30
-
-
0024571818
-
Human leukocyte and porcine pancreatic elastase: X-ray crystal structures, mechanism, substrate specificity, and mechanism-based inhibitors
-
Bode, W.; Meyer, E., Jr.; Powers, J. C. Human Leukocyte and Porcine Pancreatic Elastase: X-ray Crystal Structures, Mechanism, Substrate Specificity, and Mechanism-based Inhibitors. Biochemistry 1989, 28, 1951-1963.
-
(1989)
Biochemistry
, vol.28
, pp. 1951-1963
-
-
Bode, W.1
Meyer E., Jr.2
Powers, J.C.3
|