-
1
-
-
33746921221
-
α-Aminoalkyl-α-Halomethylketones: Preparation and Application to Pharmaceutically Interesting Compounds
-
Reeder, M. R.; Anderson, R. M. α-Aminoalkyl-α-Halomethylketones: Preparation and Application to Pharmaceutically Interesting Compounds. Chem. Rev., 2006, 106, 2828-2842.
-
(2006)
Chem. Rev
, vol.106
, pp. 2828-2842
-
-
Reeder, M.R.1
Anderson, R.M.2
-
2
-
-
47349130002
-
Synthesis and synthetic applications of amino ketones derived from natural alphα-Amino acids
-
Concellón, J. M.; Rodríguez-Solla, H. Synthesis and synthetic applications of amino ketones derived from natural alphα-Amino acids. Curr. Org. Chem., 2008, 12, 524-543.
-
(2008)
Curr. Org. Chem
, vol.12
, pp. 524-543
-
-
Concellón, J.M.1
Rodríguez-Solla, H.2
-
3
-
-
64849117664
-
Amino Carbonyl Compounds in Organic Synthesis
-
Baktharaman, S.; Hili, R.; Yudin, A. K. Amino Carbonyl Compounds in Organic Synthesis. Aldrichim. Acta, 2008, 41, 109-119.
-
(2008)
Aldrichim. Acta
, vol.41
, pp. 109-119
-
-
Baktharaman, S.1
Hili, R.2
Yudin, A.K.3
-
4
-
-
84944628716
-
The Chemistry of α-Haloketones, α -Haloaldehydes and α-Haloimines
-
α-Haloaldehydes and α-Haloimines, Patai, S., Ed. Wiley: Chichester
-
De Kimpe, N.; Verhé, R., The Chemistry of α-Haloketones, α -Haloaldehydes and α-Haloimines. In The Chemistry of α-Haloketones, α-Haloaldehydes and α-Haloimines, Patai, S., Ed. Wiley: Chichester, 1988; pp 1-119.
-
(1988)
The Chemistry of α-Haloketones
, pp. 1-119
-
-
de Kimpe, N.1
Verhé, R.2
-
5
-
-
0035825779
-
On the Inherent Instability of α-Amino α'-Fluoro Ketones. Evidence for Their Transformation to Reactive Oxyvinyliminium Ion Intermediates
-
Myers, A. G.; Barbay, J. K. On the Inherent Instability of α-Amino α'-Fluoro Ketones. Evidence for Their Transformation to Reactive Oxyvinyliminium Ion Intermediates. Org. Lett., 2001, 3, 425-428.
-
(2001)
Org. Lett
, vol.3
, pp. 425-428
-
-
Myers, A.G.1
Barbay, J.K.2
-
6
-
-
77957785439
-
First General Route to Substituted a-chloropropan-2-ones by Oxidation of N-Protected Aminohalohydrins: The Importance of Disrupting Hydrogen Bond Networks
-
Pace, V.; Cortés-Cabrera, Á.; Fernández, M.; Sinisterra, J. V.; Alcántara, A. R. First General Route to Substituted a-chloropropan-2-ones by Oxidation of N-Protected Aminohalohydrins: The Importance of Disrupting Hydrogen Bond Networks. Synthesis, 2010, 3545-3555.
-
(2010)
Synthesis
, pp. 3545-3555
-
-
Pace, V.1
Cortés-Cabrera, Á.2
Fernández, M.3
Sinisterra, J.V.4
Alcántara, A.R.5
-
7
-
-
5444236447
-
Asymmetric Transfer Hydrogenation of α-Aminoalkyl αâ-Chloromethyl Ketones with Chiral Rh Complexes
-
Hamada, T.; Torii, T.; Onishi, T.; Izawa, K.; Ikariya, T. Asymmetric Transfer Hydrogenation of α-Aminoalkyl αâ-Chloromethyl Ketones with Chiral Rh Complexes. J. Org. Chem., 2004, 69, 7391-7394.
-
(2004)
J. Org. Chem
, vol.69
, pp. 7391-7394
-
-
Hamada, T.1
Torii, T.2
Onishi, T.3
Izawa, K.4
Ikariya, T.5
-
8
-
-
33746893025
-
Industrial Syntheses of the Central Core Molecules of HIV Protease Inhibitors
-
Izawa, K.; Onishi, T. Industrial Syntheses of the Central Core Molecules of HIV Protease Inhibitors. Chem. Rev., 2006, 106, 2811-2827.
-
(2006)
Chem. Rev
, vol.106
, pp. 2811-2827
-
-
Izawa, K.1
Onishi, T.2
-
9
-
-
79952818361
-
Structural bases for understanding the stereoselectivity in ketone reductions with ADH from Thermus thermophilus: A quantitative model
-
Pace, V.; Cortés-Cabrera, Á.; Ferrario, V.; Sinisterra, J. V.; Ebert, C; Gardossi, L.; Braiuca, P.; Alcántara, A. R. Structural bases for understanding the stereoselectivity in ketone reductions with ADH from Thermus thermophilus: A quantitative model. J. Mol. Catal. B: Enzym., 2011, 70, 23-31.
-
(2011)
J. Mol. Catal. B: Enzym
, vol.70
, pp. 23-31
-
-
Pace, V.1
Cortés-Cabrera, Á.2
Ferrario, V.3
Sinisterra, J.V.4
Ebert, C.5
Gardossi, L.6
Braiuca, P.7
Alcántara, A.R.8
-
10
-
-
0029019630
-
A practical synthesis of an HIV protease inhibitor intermediate - diastereoselective epoxide formation from chiral [alpha]-aminoaldehydes
-
Ng, J. S.; Przybyla, C. A.; Liu, C; Yen, J. C; Muellner, F. W.; Weyker, C. L. A practical synthesis of an HIV protease inhibitor intermediate - diastereoselective epoxide formation from chiral [alpha]-aminoaldehydes. Tetrahedron, 1995, 51, 6397-6410.
-
(1995)
Tetrahedron
, vol.51
, pp. 6397-6410
-
-
Ng, J.S.1
Przybyla, C.A.2
Liu, C.3
Yen, J.C.4
Muellner, F.W.5
Weyker, C.L.6
-
11
-
-
14444281534
-
Viracept (Nelfinavir Mesylate, AG1343): A Potent, Orally Bioavailable Inhibitor of HIV-1 Protease
-
Kaldor, S. W.; Kalish, V. J.; Davies, J. F.; Shetty, B. V.; Fritz, J. E.; Appelt, K.; Burgess, J. A.; Campanale, K. M.; Chirgadze, N. Y.; Clawson, D. K.; Dressman, B. A.; Hatch, S. D.; Khalil, D. A.; Kosa, M. B.; Lubbehusen, P. P.; Muesing, M. A.; Patick, A. K.; Reich, S. H.; Su, K. S.; Tatlock, J. H. Viracept (Nelfinavir Mesylate, AG1343): A Potent, Orally Bioavailable Inhibitor of HIV-1 Protease. J. Med. Chem., 1997, 40, 3979-3985.
-
(1997)
J. Med. Chem
, vol.40
, pp. 3979-3985
-
-
Kaldor, S.W.1
Kalish, V.J.2
Davies, J.F.3
Shetty, B.V.4
Fritz, J.E.5
Appelt, K.6
Burgess, J.A.7
Campanale, K.M.8
Chirgadze, N.Y.9
Clawson, D.K.10
Dressman, B.A.11
Hatch, S.D.12
Khalil, D.A.13
Kosa, M.B.14
Lubbehusen, P.P.15
Muesing, M.A.16
Patick, A.K.17
Reich, S.H.18
Su, K.S.19
Tatlock, J.H.20
more..
-
12
-
-
0030834124
-
Preparation of chiral synthon for HIV protease inhibitor: Stereoselective microbial reduction of N-protected [alpha]-aminochloroketone
-
Patel, R. N.; Banerjee, A.; McNamee, C. G.; Brzozowski, D. B.; Szarka, L. J. Preparation of chiral synthon for HIV protease inhibitor: stereoselective microbial reduction of N-protected [alpha]-aminochloroketone. Tetrahedron: Asymmetry, 1997, 8, 2547-2552.
-
(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 2547-2552
-
-
Patel, R.N.1
Banerjee, A.2
McNamee, C.G.3
Brzozowski, D.B.4
Szarka, L.J.5
-
13
-
-
0008583584
-
Discovery of Ritonavir, a Potent Inhibitor of HIV Protease with High Oral Bioavailability and Clinical Efficacy
-
Kempf, D. J.; Sham, H. L.; Marsh, K. C; Flentge, C. A.; Betebenner, D.; Green, B. E.; McDonald, E.; Vasavanonda, S.; Saldivar, A.; Wideburg, N. E.; Kati, W. M.; Ruiz, L.; Zhao, C.; Fino, L.; Patterson, J.; Molla, A.; Plattner, J. J.; Norbeck, D. W. Discovery of Ritonavir, a Potent Inhibitor of HIV Protease with High Oral Bioavailability and Clinical Efficacy. J. Med. Chem., 1998, 41, 602-617.
-
(1998)
J. Med. Chem
, vol.41
, pp. 602-617
-
-
Kempf, D.J.1
Sham, H.L.2
Marsh, K.C.3
Flentge, C.A.4
Betebenner, D.5
Green, B.E.6
McDonald, E.7
Vasavanonda, S.8
Saldivar, A.9
Wideburg, N.E.10
Kati, W.M.11
Ruiz, L.12
Zhao, C.13
Fino, L.14
Patterson, J.15
Molla, A.16
Plattner, J.J.17
Norbeck, D.W.18
-
14
-
-
3843132927
-
New approaches to the industrial synthesis of HIV protease inhibitors
-
Honda, Y.; Katayama, S.; Kojima, M.; Suzuki, T.; Kishibata, N.; Izawa, K. New approaches to the industrial synthesis of HIV protease inhibitors. Org. Biomol. Chem., 2004, 2, 2061-2070.
-
(2004)
Org. Biomol. Chem
, vol.2
, pp. 2061-2070
-
-
Honda, Y.1
Katayama, S.2
Kojima, M.3
Suzuki, T.4
Kishibata, N.5
Izawa, K.6
-
15
-
-
79961126418
-
Highly Regioselective and Efficient Synthesis of Aminoepoxides by Ring Closure of Aminohalohydrins Mediated by KF-Celite
-
Pace, V.; Hoyos, P.; Sinisterra, J. V.; Alcántara, A. R.; Holzer, W. Highly Regioselective and Efficient Synthesis of Aminoepoxides by Ring Closure of Aminohalohydrins Mediated by KF-Celite. Synlett, 2011, 1831-1834.
-
(2011)
Synlett
, pp. 1831-1834
-
-
Pace, V.1
Hoyos, P.2
Sinisterra, J.V.3
Alcántara, A.R.4
Holzer, W.5
-
16
-
-
85171845929
-
Ein Verfahren zur Überführung von Carbonsäuren in ihre höheren Homologen bzw. deren Derivate
-
Arndt, F.; Eistert, B. Ein Verfahren zur Überführung von Carbonsäuren in ihre höheren Homologen bzw. deren Derivate. Ber. Dtsch. Chem. Ges., 1935, 68, 200-208.
-
(1935)
Ber. Dtsch. Chem. Ges
, vol.68
, pp. 200-208
-
-
Arndt, F.1
Eistert, B.2
-
18
-
-
0000709206
-
Organic Synthesis with.alpha.-Diazo Carbonyl Compounds
-
Ye, T.; McKervey, M. A. Organic Synthesis with.alpha.-Diazo Carbonyl Compounds. Chem. Rev., 1994, 94, 1091-1160.
-
(1994)
Chem. Rev
, vol.94
, pp. 1091-1160
-
-
Ye, T.1
McKervey, M.A.2
-
19
-
-
70350034042
-
New Syntheses of Diazo Compounds
-
G. New Syntheses of Diazo Compounds. Angew. Chem. Int. Ed., 2009, 48, 8186-8195.
-
(2009)
Angew. Chem. Int
, vol.48
, pp. 8186-8195
-
-
-
20
-
-
0036857594
-
Development of a Continuous Process for the Industrial Generation of Diazomethane
-
Proctor, L. D.; Warr, A. J. Development of a Continuous Process for the Industrial Generation of Diazomethane. Org. Proc. Res. Dev., 2002, 6, 884-892.
-
(2002)
Org. Proc. Res. Dev
, vol.6
, pp. 884-892
-
-
Proctor, L.D.1
Warr, A.J.2
-
21
-
-
78650878711
-
Preparation of a,b-Unsaturated Diazoketones Employing a Horner-Wadsworth-Emmons Reagent
-
Pinho, V. D.; Burtoloso, A. C. B. Preparation of a,b-Unsaturated Diazoketones Employing a Horner-Wadsworth-Emmons Reagent. J. Org. Chem., 2011, 76, 289-292.
-
(2011)
J. Org. Chem
, vol.76
, pp. 289-292
-
-
Pinho, V.D.1
Burtoloso, A.C.B.2
-
22
-
-
77955666187
-
Improved Arndt-Eistert Synthesis of a-Diazoketones Requiring Minimal Diazomethane in the Presence of Calcium Oxide as Acid Scavenger
-
Pace, V.; Verniest, G.; Sinisterra, J. V.; Alcántara, A. R.; De Kimpe, N. Improved Arndt-Eistert Synthesis of a-Diazoketones Requiring Minimal Diazomethane in the Presence of Calcium Oxide as Acid Scavenger. J. Org. Chem., 2010, 75, 5760-5763.
-
(2010)
J. Org. Chem
, vol.75
, pp. 5760-5763
-
-
Pace, V.1
Verniest, G.2
Sinisterra, J.V.3
Alcántara, A.R.4
de Kimpe, N.5
-
23
-
-
1442275482
-
One-Carbon Chain Extension of Esters to a-Chloroketones: A Safer Route without Diazomethane
-
Wang, D.; Schwinden, M. D.; Radesca, L.; Patel, B.; Kronenthal, D.; Huang, M.-H.; Nugent, W. A. One-Carbon Chain Extension of Esters to a-Chloroketones: A Safer Route without Diazomethane. J. Org. Chem., 2004, 69, 1629-1633.
-
(2004)
J. Org. Chem
, vol.69
, pp. 1629-1633
-
-
Wang, D.1
Schwinden, M.D.2
Radesca, L.3
Patel, B.4
Kronenthal, D.5
Huang, M.-H.6
Nugent, W.A.7
-
24
-
-
37049068037
-
The first direct preparation of chiral functionalised ketones and their synthetic uses
-
Barluenga, J.; Baragana, B.; Alonso, A.; Concellon, J. M. The first direct preparation of chiral functionalised ketones and their synthetic uses. J. Chem. Soc., Chem. Commun., 1994, 969-970.
-
(1994)
J. Chem. Soc., Chem. Commun
, pp. 969-970
-
-
Barluenga, J.1
Baragana, B.2
Alonso, A.3
Concellon, J.M.4
-
25
-
-
0001430378
-
High Diastereoselective Synthesis of Threo or Erythro Aminoalkyl Epoxides from.alpha
-
Barluenga, J.; Baragana, B.; Concellon, J. M. High Diastereoselective Synthesis of Threo or Erythro Aminoalkyl Epoxides from.alpha. Amino Acids. J. Org. Chem., 1995, 60, 6696-6699.
-
(1995)
Amino Acids. J. Org. Chem
, vol.60
, pp. 6696-6699
-
-
Barluenga, J.1
Baragana, B.2
Concellon, J.M.3
-
26
-
-
0001414444
-
Novel Cleavage of Propargylamines by Reaction with Organolithium Compounds
-
Barluenga, J.; Canteli, R.-M.; Flórez, J. Novel Cleavage of Propargylamines by Reaction with Organolithium Compounds. J. Org. Chem., 1996, 61, 3646-3649.
-
(1996)
J. Org. Chem
, vol.61
, pp. 3646-3649
-
-
Barluenga, J.1
Canteli, R.-M.2
Flórez, J.3
-
27
-
-
0033574487
-
Preparation and Synthetic Applications of Enantiopure (2S,3S)- or (2R,3S)-2-Halomethyl-1,2-epoxyalkan-3-amines
-
For an alternative approach based on the use of Weinreb amides as the electrophiles, see: Pace, V.; Holzer, W.; Verniest, G.; Alcántara, A. R.; De Kimpe, N. Adv. Synth. Catal. 2013, in press, DOI: 10.1002/adsc.201201043
-
Barluenga, J.; Baragana, B.; Concellon, J. M. Preparation and Synthetic Applications of Enantiopure (2S,3S)- or (2R,3S)-2-Halomethyl-1,2-epoxyalkan-3-amines. J. Org. Chem., 1999, 64, 2843-2846. For an alternative approach based on the use of Weinreb amides as the electrophiles, see: Pace, V.; Holzer, W.; Verniest, G.; Alcántara, A. R.; De Kimpe, N. Adv. Synth. Catal. 2013, in press, DOI: 10.1002/adsc.201201043
-
(1999)
J. Org. Chem
, vol.64
, pp. 2843-2846
-
-
Barluenga, J.1
Baragana, B.2
Concellon, J.M.3
-
28
-
-
33746907049
-
Organolithium Reagents in Pharmaceutical Asymmetric Processes
-
Wu, G.; Huang, M. Organolithium Reagents in Pharmaceutical Asymmetric Processes. Chem. Rev., 2006, 106, 2596-2616.
-
(2006)
Chem. Rev
, vol.106
, pp. 2596-2616
-
-
Wu, G.1
Huang, M.2
-
29
-
-
79952574474
-
Highly regioselective control of 1,2-addition of organolithiums to a,b-unsaturated compounds promoted by lithium bromide in 2-methyltetrahydrofuran: A facile and eco-friendly access to allylic alcohols and amines
-
Pace, V.; Castoldi, L.; Hoyos, P.; Sinisterra, J. V.; Pregnolato, M.; Sánchez-Montero, J. M. Highly regioselective control of 1,2-addition of organolithiums to a,b-unsaturated compounds promoted by lithium bromide in 2-methyltetrahydrofuran: a facile and eco-friendly access to allylic alcohols and amines. Tetrahedron, 2011, 67, 2670-2675.
-
(2011)
Tetrahedron
, vol.67
, pp. 2670-2675
-
-
Pace, V.1
Castoldi, L.2
Hoyos, P.3
Sinisterra, J.V.4
Pregnolato, M.5
Sánchez-Montero, J.M.6
-
30
-
-
78149276981
-
1,3-dichloroacetone
-
Pace, V. 1,3-dichloroacetone. Synlett, 2010, 2825-2826.
-
(2010)
Synlett
, pp. 2825-2826
-
-
Pace, V.1
-
31
-
-
34547481476
-
Effective Monoallylation of Anilines Catalyzed by Supported KF
-
Pace, V.; Martínez, F.; Fernández, M.; Sinisterra, J. V.; Alcántara, A. R. Effective Monoallylation of Anilines Catalyzed by Supported KF. Org. Lett., 2007, 9, 2661-2664.
-
(2007)
Org. Lett
, vol.9
, pp. 2661-2664
-
-
Pace, V.1
Martínez, F.2
Fernández, M.3
Sinisterra, J.V.4
Alcántara, A.R.5
-
32
-
-
78649935295
-
Celite-Supported Reagents in Organic Synthesis: An Overview
-
Pace, V.; Sinisterra, J. V.; Alcántara, A. R. Celite-Supported Reagents in Organic Synthesis: An Overview. Curr. Org. Chem., 2010, 14, 2384-2408.
-
(2010)
Curr. Org. Chem
, vol.14
, pp. 2384-2408
-
-
Pace, V.1
Sinisterra, J.V.2
Alcántara, A.R.3
-
33
-
-
84855967092
-
Highly chemoselective synthesis of aryl allylic sulfoxides through calcium hypobromite oxidation of aryl allylic sulfides
-
Pace, V.; Castoldi, L.; Holzer, W. Highly chemoselective synthesis of aryl allylic sulfoxides through calcium hypobromite oxidation of aryl allylic sulfides. Tetrahedron Lett., 2012, 53, 967-972.
-
(2012)
Tetrahedron Lett
, vol.53
, pp. 967-972
-
-
Pace, V.1
Castoldi, L.2
Holzer, W.3
-
34
-
-
73349121622
-
Highly Efficient Synthesis of New α-Arylamino- α'-chloropropan-2-ones via Oxidative Hydrolysis of Vinyl Chlorides Promoted by Calcium Hypochlorite
-
Pace, V.; Martínez, F.; Fernández, M.; Sinisterra, J. V.; Alcántara, A. R. Highly Efficient Synthesis of New α-Arylamino- α'-chloropropan-2-ones via Oxidative Hydrolysis of Vinyl Chlorides Promoted by Calcium Hypochlorite. Adv. Synth. Cat., 2009, 351, 3199-3206.
-
(2009)
Adv. Synth. Cat
, vol.351
, pp. 3199-3206
-
-
Pace, V.1
Martínez, F.2
Fernández, M.3
Sinisterra, J.V.4
Alcántara, A.R.5
-
35
-
-
84865177747
-
A straightforward and general access to α-phthalimido- α'-substituted propan-2-ones
-
Pace, V.; Holzer, W. A straightforward and general access to α-phthalimido- α'-substituted propan-2-ones. Tetrahedron Lett., 10.1016/j.tetlet. 2012, 1007-1045.
-
(2012)
Tetrahedron Lett., 10.1016/j.tetlet
, pp. 1007-1045
-
-
Pace, V.1
Holzer, W.2
-
36
-
-
0036882396
-
Irreversible Inhibitors of Serine, Cysteine, and Threonine Proteases
-
Powers, J. C; Asgian, J. L.; Ekici, Ö. D.; James, K. E. Irreversible Inhibitors of Serine, Cysteine, and Threonine Proteases. Chem. Rev., 2002, 102, 4639-4750.
-
(2002)
Chem. Rev
, vol.102
, pp. 4639-4750
-
-
Powers, J.C.1
Asgian, J.L.2
Ekici, Ö.D.3
James, K.E.4
-
37
-
-
0034628448
-
Protease Inhibitors: Current Status and Future Prospects
-
Leung, D.; Abbenante, G.; Fairlie, D. P. Protease Inhibitors: Current Status and Future Prospects. J. Med. Chem., 2000, 43, 305-341.
-
(2000)
J. Med. Chem
, vol.43
, pp. 305-341
-
-
Leung, D.1
Abbenante, G.2
Fairlie, D.P.3
-
38
-
-
0343433408
-
Cysteine Proteases and Their Inhibitors
-
Otto, H.-H.; Schirmeister, T. Cysteine Proteases and Their Inhibitors. Chem. Rev., 1997, 97, 133-172.
-
(1997)
Chem. Rev
, vol.97
, pp. 133-172
-
-
Otto, H.-H.1
Schirmeister, T.2
-
39
-
-
0035543093
-
The Depth of Chemical Time and the Power of Enzymes as Catalysts
-
Wolfenden, R.; Snider, M. J. The Depth of Chemical Time and the Power of Enzymes as Catalysts. Acc. Chem. Res., 2001, 34, 938-945.
-
(2001)
Acc. Chem. Res
, vol.34
, pp. 938-945
-
-
Wolfenden, R.1
Snider, M.J.2
-
40
-
-
0001244705
-
Direct Evidence for the Presence of Histidine in the Active Center of Chymotrypsin*
-
Schoellmann, G.; Shaw, E. Direct Evidence for the Presence of Histidine in the Active Center of Chymotrypsin*. Biochemistry, 1963, 2, 252-255.
-
(1963)
Biochemistry
, vol.2
, pp. 252-255
-
-
Schoellmann, G.1
Shaw, E.2
-
41
-
-
0000700968
-
Evidence for an Active-Center Histidine in Trypsin through Use of a Specific Reagent, 1-Chloro-3-tosylamido-7-amino-2-heptanone, the Chloromethyl Ketone Derived from Na-Tosyl-L-lysine*
-
Shaw, E.; Mares-Guia, M.; Cohen, W. Evidence for an Active-Center Histidine in Trypsin through Use of a Specific Reagent, 1-Chloro-3-tosylamido-7-amino-2-heptanone, the Chloromethyl Ketone Derived from Na-Tosyl-L-lysine*. Biochemistry, 1965, 4, 2219-2224.
-
(1965)
Biochemistry
, vol.4
, pp. 2219-2224
-
-
Shaw, E.1
Mares-Guia, M.2
Cohen, W.3
-
42
-
-
0017253438
-
Polypeptide halomethyl ketones bind to serine proteases as analogs of the tetrahedral intermediate. X-ray crystallographic comparison of lysine- and phenylalanine-polypeptide chloromethyl ketone-inhibited subtilisin
-
Poulos, T. L.; Alden, R. A.; Freer, S. T.; Birktoft, J. J.; Kraut, J. Polypeptide halomethyl ketones bind to serine proteases as analogs of the tetrahedral intermediate. X-ray crystallographic comparison of lysine- and phenylalanine-polypeptide chloromethyl ketone-inhibited subtilisin. J. Biol. Chem., 1976, 251, 1097-1103.
-
(1976)
J. Biol. Chem
, vol.251
, pp. 1097-1103
-
-
Poulos, T.L.1
Alden, R.A.2
Freer, S.T.3
Birktoft, J.J.4
Kraut, J.5
-
43
-
-
0017324541
-
Reaction of serine proteases with halomethyl ketones
-
William B. Jakoby, M. W., Ed. Academic Press
-
Powers, J. C, Reaction of serine proteases with halomethyl ketones. In Methods Enzymol, William B. Jakoby, M. W., Ed. Academic Press: 1977, 46, pp 197-208.
-
(1977)
Methods Enzymol
, vol.46
, pp. 197-208
-
-
Powers, J.C.1
-
44
-
-
0003723604
-
-
Barrett, A. J.; Salvensen, G. Eds.; Elsevier: Amsterdam
-
Powers, J. C; Harper, J. W., Proteinase Inhibitors. Barrett, A. J.; Salvensen, G. Eds.; Elsevier: Amsterdam, 1985.
-
(1985)
Proteinase Inhibitors
-
-
Powers, J.C.1
Harper, J.W.2
-
45
-
-
0021879888
-
Mammalian chymotrypsin-like enzymes. Comparative reactivities of rat mast cell proteases, human and dog skin chymases, and human cathepsin G with peptide 4-nitroanilide substrates and with peptide chloromethyl ketone and sulfonyl fluoride inhibitors
-
Powers, J. C; Tanaka, T.; Harper, J. W.; Minematsu, Y.; Barker, L.; Lincoln, D.; Crumley, K. V.; Fraki, J. E.; Schechter, N. M. Mammalian chymotrypsin-like enzymes. Comparative reactivities of rat mast cell proteases, human and dog skin chymases, and human cathepsin G with peptide 4-nitroanilide substrates and with peptide chloromethyl ketone and sulfonyl fluoride inhibitors. Biochemistry, 1985, 24, 2048-2058.
-
(1985)
Biochemistry
, vol.24
, pp. 2048-2058
-
-
Powers, J.C.1
Tanaka, T.2
Harper, J.W.3
Minematsu, Y.4
Barker, L.5
Lincoln, D.6
Crumley, K.V.7
Fraki, J.E.8
Schechter, N.M.9
-
46
-
-
0019320457
-
Substrate specificity of two chymotrypsin-like proteases from rat mast cells. Studies with peptide 4-nitroanilides and comparison with cathepsin G
-
Yoshida, N.; Everitt, M. T.; Neurath, H.; Woodbury, R. G.; Powers, J. C. Substrate specificity of two chymotrypsin-like proteases from rat mast cells. Studies with peptide 4-nitroanilides and comparison with cathepsin G. Biochemistry, 1980, 19, 5799-5804.
-
(1980)
Biochemistry
, vol.19
, pp. 5799-5804
-
-
Yoshida, N.1
Everitt, M.T.2
Neurath, H.3
Woodbury, R.G.4
Powers, J.C.5
-
47
-
-
0034615120
-
Structure-activity relationship studies of chloromethyl ketone derivatives for selective human chymase inhibitors
-
Hayashi, Y.; Iijima, K.; Katada, J.; Kiso, Y. Structure-activity relationship studies of chloromethyl ketone derivatives for selective human chymase inhibitors. Bioorg. Med. Chem. Lett., 2000, 10, 199-201.
-
(2000)
Bioorg. Med. Chem. Lett
, vol.10
, pp. 199-201
-
-
Hayashi, Y.1
Iijima, K.2
Katada, J.3
Kiso, Y.4
-
48
-
-
0028968184
-
Crystal Structures of Recombinant Rat Cathepsin B and a Cathepsin B-Inhibitor Complex
-
Jia, Z.; Hasnain, S.; Hirama, T.; Lee, X.; Mort, J. S.; To, R.; Huber, C. P. Crystal Structures of Recombinant Rat Cathepsin B and a Cathepsin B-Inhibitor Complex. J. Biol. Chem., 1995, 270, 5527-5533.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 5527-5533
-
-
Jia, Z.1
Hasnain, S.2
Hirama, T.3
Lee, X.4
Mort, J.S.5
To, R.6
Huber, C.P.7
-
49
-
-
0017138215
-
Binding of chloromethyl ketone substrate analogs to crystalline papain
-
Drenth, J.; Kalk, K. H.; Swen, H. M. Binding of chloromethyl ketone substrate analogs to crystalline papain. Biochemistry, 1976, 15, 3731-3738.
-
(1976)
Biochemistry
, vol.15
, pp. 3731-3738
-
-
Drenth, J.1
Kalk, K.H.2
Swen, H.M.3
-
50
-
-
0030889913
-
Structure of Recombinant Human CPP32 in Complex with the Tetrapeptide Acetyl-Asp-Val-Ala-Asp Fluoromethyl Ketone
-
Mittl, P. R. E.; Di Marco, S.; Krebs, J. F.; Bai, X.; Karanewsky, D. S.; Priestle, J. P.; Tomaselli, K. J.; Grütter, M. G. Structure of Recombinant Human CPP32 in Complex with the Tetrapeptide Acetyl-Asp-Val-Ala-Asp Fluoromethyl Ketone. J. Biol. Chem., 1997, 272, 6539-6547.
-
(1997)
J. Biol. Chem
, vol.272
, pp. 6539-6547
-
-
Mittl, P.R.E.1
Di Marco, S.2
Krebs, J.F.3
Bai, X.4
Karanewsky, D.S.5
Priestle, J.P.6
Tomaselli, K.J.7
Grütter, M.G.8
-
51
-
-
0022398321
-
Synthesis of peptide fluoromethyl ketones and the inhibition of human cathepsin B
-
Rasnick, D. Synthesis of peptide fluoromethyl ketones and the inhibition of human cathepsin B. Anal. Biochem., 1985, 149, 461-465.
-
(1985)
Anal. Biochem
, vol.149
, pp. 461-465
-
-
Rasnick, D.1
-
52
-
-
0026715161
-
Peptidyl fluoromethyl ketones as inhibitors of cathepsin B: Implication for treatment of rheumatoid arthritis
-
Ahmed, N. K.; martin, L. A.; Watts, L. M.; Palmer, J.; Thornburg, L.; Prior, J.; Esser, R. E. Peptidyl fluoromethyl ketones as inhibitors of cathepsin B: Implication for treatment of rheumatoid arthritis. Biochem. Pharmacol, 1992, 44, 1201-1207.
-
(1992)
Biochem. Pharmacol
, vol.44
, pp. 1201-1207
-
-
Ahmed, N.K.1
Martin, L.A.2
Watts, L.M.3
Palmer, J.4
Thornburg, L.5
Prior, J.6
Esser, R.E.7
-
53
-
-
0022632034
-
Inactivation of Calpain I and Calpain II by Specificity-Oriented Tripeptidyl Chloromethyl Ketones
-
Sasaki, T.; Kikuchi, T.; Fukui, I.; Murachi, T. Inactivation of Calpain I and Calpain II by Specificity-Oriented Tripeptidyl Chloromethyl Ketones. J. Biochem., 1986, 99, 173-179.
-
(1986)
J. Biochem
, vol.99
, pp. 173-179
-
-
Sasaki, T.1
Kikuchi, T.2
Fukui, I.3
Murachi, T.4
-
54
-
-
0038337815
-
The Calpain System
-
Goll, D. E.; Thompson, V. F.; Li, H.; Wei, W.; Cong, J. The Calpain System. Physiol. Rev., 2003, 83, 731-801.
-
(2003)
Physiol. Rev
, vol.83
, pp. 731-801
-
-
Goll, D.E.1
Thompson, V.F.2
Li, H.3
Wei, W.4
Cong, J.5
-
55
-
-
79955458657
-
The calpain system and cancer
-
Storr, S. J.; Carragher, N. O.; Frame, M. C; Parr, T.; Martin, S. G. The calpain system and cancer. Nat. Rev. Cancer, 2011, 11, 364-374.
-
(2011)
Nat. Rev. Cancer
, vol.11
, pp. 364-374
-
-
Storr, S.J.1
Carragher, N.O.2
Frame, M.C.3
Parr, T.4
Martin, S.G.5
-
56
-
-
0029950794
-
Potent fluoromethyl ketone inhibitors of recombinant human calpain I
-
Chatterjee, S.; Josef, K.; Wells, G.; Iqbal, M.; Bihovsky, R.; Mallamo, J. P.; Ator, M. A.; Bozyczko-Coyne, D.; Mallya, S.; Senadhi, S.; Siman, R. Potent fluoromethyl ketone inhibitors of recombinant human calpain I. Bioorg. Med. Chem. Lett., 1996, 6, 1237-1240.
-
(1996)
Bioorg. Med. Chem. Lett
, vol.6
, pp. 1237-1240
-
-
Chatterjee, S.1
Josef, K.2
Wells, G.3
Iqbal, M.4
Bihovsky, R.5
Mallamo, J.P.6
Ator, M.A.7
Bozyczko-Coyne, D.8
Mallya, S.9
Senadhi, S.10
Siman, R.11
-
57
-
-
0034618635
-
Caspases as Targets for Anti-Inflammatory and Anti-Apoptotic Drug Discovery
-
Talanian, R. V.; Brady, K. D.; Cryns, V. L. Caspases as Targets for Anti-Inflammatory and Anti-Apoptotic Drug Discovery. J. Med. Chem., 2000, 43, 3351-3371.
-
(2000)
J. Med. Chem
, vol.43
, pp. 3351-3371
-
-
Talanian, R.V.1
Brady, K.D.2
Cryns, V.L.3
-
58
-
-
0032078217
-
Caspases: Key mediators of apoptosis
-
Thornberry, N. A. Caspases: key mediators of apoptosis. Chem. Biol, 1998, 5, R97-R103.
-
(1998)
Chem. Biol
, vol.5
-
-
Thornberry, N.A.1
-
59
-
-
0036931366
-
Caspases: Keys in the Ignition of Cell Death
-
Denault, J.-B.; Salvesen, G. S. Caspases: Keys in the Ignition of Cell Death. Chem. Rev., 2002, 102, 4489-4500.
-
(2002)
Chem. Rev
, vol.102
, pp. 4489-4500
-
-
Denault, J.-B.1
Salvesen, G.S.2
-
60
-
-
0012299811
-
The three-dimensional structure of caspase-8: An initiator enzyme in apoptosis
-
Blanchard, H.; Kodandapani, L.; Mittl, P. R. E.; Marco, S. D.; Krebs, J. F.; Wu, J. C; Tomaselli, K. J.; Grütter, M. G. The three-dimensional structure of caspase-8: an initiator enzyme in apoptosis. Structure, 1999, 7, 1125-1133.
-
(1999)
Structure
, vol.7
, pp. 1125-1133
-
-
Blanchard, H.1
Kodandapani, L.2
Mittl, P.R.E.3
Marco, S.D.4
Krebs, J.F.5
Wu, J.C.6
Tomaselli, K.J.7
Grütter, M.G.8
-
61
-
-
1242293893
-
Dipeptidyl aspartyl fluoromethylketones as potent caspase-3 inhibitors: SAR of the P2 amino acid
-
Wang, Y.; Huang, J.-C; Zhou, Z.-L.; Yang, W.; Guastella, J.; Drewe, J.; Cai, S. X. Dipeptidyl aspartyl fluoromethylketones as potent caspase-3 inhibitors: SAR of the P2 amino acid. Bioorg. Med. Chem. Lett., 2004, 14, 1269-1272.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 1269-1272
-
-
Wang, Y.1
Huang, J.-C.2
Zhou, Z.-L.3
Yang, W.4
Guastella, J.5
Drewe, J.6
Cai, S.X.7
-
62
-
-
5344245984
-
Dipeptidyl aspartyl fluoromethylketones as potent caspase inhibitors: SAR of the N-protecting group
-
Cai, S. X.; Guan, L.; Jia, S.; Wang, Y.; Yang, W.; Tseng, B.; Drewe, J. Dipeptidyl aspartyl fluoromethylketones as potent caspase inhibitors: SAR of the N-protecting group. Bioorg. Med. Chem. Lett., 2004, 14, 5295-5300.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 5295-5300
-
-
Cai, S.X.1
Guan, L.2
Jia, S.3
Wang, Y.4
Yang, W.5
Tseng, B.6
Drewe, J.7
-
63
-
-
13944256153
-
Dipeptidyl aspartyl fluoromethylketones as potent caspase inhibitors: Peptidomimetic replacement of the P2 α-Amino acid by a a-hydroxy acid
-
Wang, Y.; Guan, L.; Jia, S.; Tseng, B.; Drewe, J.; Cai, S. X. Dipeptidyl aspartyl fluoromethylketones as potent caspase inhibitors: peptidomimetic replacement of the P2 α-Amino acid by a a-hydroxy acid. Bioorg. Med. Chem. Lett., 2005, 15, 1379-1383.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 1379-1383
-
-
Wang, Y.1
Guan, L.2
Jia, S.3
Tseng, B.4
Drewe, J.5
Cai, S.X.6
-
64
-
-
33750352001
-
A Novel QSAR Model for Evaluating and Predicting the Inhibition Activity of Dipeptidyl Aspartyl Fluoromethylketones
-
Afantitis, A.; Melagraki, G.; Sarimveis, H.; Koutentis, P. A.; Markopoulos, J.; Igglessi-Markopoulou, O. A Novel QSAR Model for Evaluating and Predicting the Inhibition Activity of Dipeptidyl Aspartyl Fluoromethylketones. QSAR Comb. Sci., 2006, 25, 928-935.
-
(2006)
QSAR Comb. Sci
, vol.25
, pp. 928-935
-
-
Afantitis, A.1
Melagraki, G.2
Sarimveis, H.3
Koutentis, P.A.4
Markopoulos, J.5
Igglessi-Markopoulou, O.6
-
65
-
-
33845278829
-
New inhibitors of cysteine proteinases. Peptidyl acyloxymethyl ketones and the quiescent nucleofuge strategy
-
Smith, R. A.; Copp, L. J.; Coles, P. J.; Pauls, H. W.; Robinson, V. J.; Spencer, R. W.; Heard, S. B.; Krantz, A. New inhibitors of cysteine proteinases. Peptidyl acyloxymethyl ketones and the quiescent nucleofuge strategy. J. Am. Chem. Soc, 1988, 110, 4429-4431.
-
(1988)
J. Am. Chem. Soc
, vol.110
, pp. 4429-4431
-
-
Smith, R.A.1
Copp, L.J.2
Coles, P.J.3
Pauls, H.W.4
Robinson, V.J.5
Spencer, R.W.6
Heard, S.B.7
Krantz, A.8
-
66
-
-
0025908898
-
Peptidyl (acyloxy)methyl ketones and the quiescent affinity label concept: The departing group as a variable structural element in the design of inactivators of cysteine proteinases
-
Krantz, A.; Copp, L. J.; Coles, P. J.; Smith, R. A.; Heard, S. B. Peptidyl (acyloxy)methyl ketones and the quiescent affinity label concept: the departing group as a variable structural element in the design of inactivators of cysteine proteinases. Biochemistry, 1991, 30, 4678-4687.
-
(1991)
Biochemistry
, vol.30
, pp. 4678-4687
-
-
Krantz, A.1
Copp, L.J.2
Coles, P.J.3
Smith, R.A.4
Heard, S.B.5
-
67
-
-
0028793210
-
Effect of interleukin-1 beta converting enzyme inhibitor on acute myelogenous leukemia progenitor proliferation
-
Estrov, Z.; Black, R.; Sleath, P.; Harris, D.; Van, Q.; LaPushin, R.; Estey, E.; Talpaz, M. Effect of interleukin-1 beta converting enzyme inhibitor on acute myelogenous leukemia progenitor proliferation. Blood, 1995, 86, 4594-4602.
-
(1995)
Blood
, vol.86
, pp. 4594-4602
-
-
Estrov, Z.1
Black, R.2
Sleath, P.3
Harris, D.4
Van, Q.5
LaPushin, R.6
Estey, E.7
Talpaz, M.8
-
68
-
-
0031044283
-
In vitro and in vivo studies of ICE inhibitors
-
Livingston, D. J. In vitro and in vivo studies of ICE inhibitors. J. Cell. Biochem., 1997, 64, 19-26.
-
(1997)
J. Cell. Biochem
, vol.64
, pp. 19-26
-
-
Livingston, D.J.1
-
69
-
-
33644857269
-
Exploring the Sn Binding Pockets in Gingipains by Newly Developed Inhibitors: Structure-Based Design, Chemistry, and Activity
-
Bialas, A.; Grembecka, J.; Krowarsch, D.; Otlewski, J.; Potempa, J.; Mucha, A. Exploring the Sn Binding Pockets in Gingipains by Newly Developed Inhibitors: Structure-Based Design, Chemistry, and Activity. J. Med. Chem., 2006, 49, 1744-1753.
-
(2006)
J. Med. Chem
, vol.49
, pp. 1744-1753
-
-
Bialas, A.1
Grembecka, J.2
Krowarsch, D.3
Otlewski, J.4
Potempa, J.5
Mucha, A.6
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