-
1
-
-
0024808080
-
Folylpolyglutamate synthesis and role in the regulation of one-carbon metabolism
-
Shane, B. Folylpolyglutamate synthesis and role in the regulation of one-carbon metabolism. Vitam. Horm. 1989, 45, 263-335.
-
(1989)
Vitam. Horm.
, vol.45
, pp. 263-335
-
-
Shane, B.1
-
2
-
-
0035103620
-
Current understanding of methotrexate pharmacology and efficacy in acute leukemias. Use of newer antifolates in clinical trials
-
Longo-Sorbello, G. S. A.; Bertino, J. R. Current understanding of methotrexate pharmacology and efficacy in acute leukemias. Use of newer antifolates in clinical trials. Haematologica 2001, 86, 121-127.
-
(2001)
Haematologica
, vol.86
, pp. 121-127
-
-
Longo-Sorbello, G.S.A.1
Bertino, J.R.2
-
4
-
-
0344708478
-
Anticancer antifolates: Current status and future directions
-
McGuire, J. J. Anticancer antifolates: Current status and future directions. Curr. Pharm. Design 2003, 9, 2593-2613.
-
(2003)
Curr. Pharm. Design
, vol.9
, pp. 2593-2613
-
-
McGuire, J.J.1
-
5
-
-
14844342386
-
DNA and RNA synthesis: Antifolates
-
Kompis, I. M.; Islam, K.; Then, R. L. DNA and RNA synthesis: Antifolates. Chem. Rev. 2005, 105, 593-620.
-
(2005)
Chem. Rev.
, vol.105
, pp. 593-620
-
-
Kompis, I.M.1
Islam, K.2
Then, R.L.3
-
6
-
-
0000026685
-
Methotrexate-a review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in rheumatoid-arthritis and other immunoregulatory disorders
-
Markham, A.; Faulds, D. Methotrexate-a review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in rheumatoid-arthritis and other immunoregulatory disorders. Clin. Immunother. 1994, 1, 217-244.
-
(1994)
Clin. Immunother.
, vol.1
, pp. 217-244
-
-
Markham, A.1
Faulds, D.2
-
7
-
-
0002079516
-
Folates in biological materials
-
Blakley, R. L., Benkovic, S. J., Eds.; Wiley: New York
-
Cossins, E. A. Folates in biological materials. In Folates and Pterins Biochemistry and Chemistry of Folates; Blakley, R. L., Benkovic, S. J., Eds.; Wiley: New York, 1984; pp 1-59.
-
(1984)
Folates and Pterins Biochemistry and Chemistry of Folates
, pp. 1-59
-
-
Cossins, E.A.1
-
8
-
-
0000083882
-
Pteroylpolyglutamates: Biosynthesis, degradation and function
-
Blakley, R. L., Benkovic, S. J., Eds.; Wiley: New York
-
McGuire, J. J.; Coward, J. K. Pteroylpolyglutamates: biosynthesis, degradation and function. In Folates and Pterins Biochemistry and Chemistry of Folates; Blakley, R. L., Benkovic, S. J., Eds.; Wiley: New York, 1984; pp 135-190.
-
(1984)
Folates and Pterins Biochemistry and Chemistry of Folates
, pp. 135-190
-
-
McGuire, J.J.1
Coward, J.K.2
-
9
-
-
0035476729
-
Transport of methotrexate (MTX) and folates by multidrug resistance protein (MRP) 3 and MRP1: Effect of polyglutamylation on MTX transport
-
Zeng, H.; Chen, Z. S.; Belinsky, M. G.; Rea, P. A.; Kruh, G. D. Transport of methotrexate (MTX) and folates by multidrug resistance protein (MRP) 3 and MRP1: Effect of polyglutamylation on MTX transport. Cancer Res. 2001, 61, 7225-7232.
-
(2001)
Cancer Res.
, vol.61
, pp. 7225-7232
-
-
Zeng, H.1
Chen, Z.S.2
Belinsky, M.G.3
Rea, P.A.4
Kruh, G.D.5
-
10
-
-
0016194956
-
Isolation and biochemical characterization of folate deficient mutants of Chinese-hamster cells
-
McBurney, M. W.; Whitmore, G. F. Isolation and biochemical characterization of folate deficient mutants of Chinese-hamster cells. Cell 1974, 2, 173-182.
-
(1974)
Cell
, vol.2
, pp. 173-182
-
-
McBurney, M.W.1
Whitmore, G.F.2
-
11
-
-
0346252232
-
Folylpolyglutamate synthetase as a target for therapeutic intervention
-
McGuire, J. J.; Coward, J. K. Folylpolyglutamate synthetase as a target for therapeutic intervention. Drugs Future 2003, 28, 967-974.
-
(2003)
Drugs Future
, vol.28
, pp. 967-974
-
-
McGuire, J.J.1
Coward, J.K.2
-
12
-
-
0037455808
-
Loss of folylpoly-γ-glutamate synthetase activity is a dominant mechanism of resistance to polyglutamylation-dependent novel antifolates in multiple human leukemia sublines
-
Liani, E.; Rothem, L.; Bunni, M. A.; Smith, C. A.; Jansen, G.; Assaraf, Y. G. Loss of folylpoly-γ-glutamate synthetase activity is a dominant mechanism of resistance to polyglutamylation-dependent novel antifolates in multiple human leukemia sublines. Int. J. Cancer 2003, 103, 587-599.
-
(2003)
Int. J. Cancer
, vol.103
, pp. 587-599
-
-
Liani, E.1
Rothem, L.2
Bunni, M.A.3
Smith, C.A.4
Jansen, G.5
Assaraf, Y.G.6
-
13
-
-
0024285812
-
Dihydrofolate synthetase and folylpolyglutamate synthetase-direct evidence for intervention of acyl phosphate intermediates
-
Banerjee, R. V.; Shane, B.; McGuire, J. J.; Coward, J. K. Dihydrofolate synthetase and folylpolyglutamate synthetase-direct evidence for intervention of acyl phosphate intermediates. Biochemistry 1988, 27, 9062-9070.
-
(1988)
Biochemistry
, vol.27
, pp. 9062-9070
-
-
Banerjee, R.V.1
Shane, B.2
McGuire, J.J.3
Coward, J.K.4
-
14
-
-
0035958480
-
Phosphinic acid pseudopeptides analogous to glutamyl-γ-glutamate: Synthesis and coupling to pteroyl azides leads to potent inhibitors of folylpoly-γ-glutamate synthetase
-
Valiaeva, N.; Bartley, D.; Konno, T.; Coward, J. K. Phosphinic acid pseudopeptides analogous to glutamyl-γ-glutamate: synthesis and coupling to pteroyl azides leads to potent inhibitors of folylpoly-γ-glutamate synthetase. J. Org. Chem. 2001, 66, 5146-5154.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 5146-5154
-
-
Valiaeva, N.1
Bartley, D.2
Konno, T.3
Coward, J.K.4
-
15
-
-
0037299779
-
Potent inhibition of human folylpolyglutamate synthetase by a phosphinic acid mimic of the tetrahedral reaction intermediate
-
McGuire, J. J.; Haile, W. H.; Valiaeva, N.; Bartley, D.; Guo, J. X.; Coward, J. K. Potent inhibition of human folylpolyglutamate synthetase by a phosphinic acid mimic of the tetrahedral reaction intermediate. Biochem. Pharmacol. 2003, 65, 315-318.
-
(2003)
Biochem. Pharmacol.
, vol.65
, pp. 315-318
-
-
McGuire, J.J.1
Haile, W.H.2
Valiaeva, N.3
Bartley, D.4
Guo, J.X.5
Coward, J.K.6
-
16
-
-
23644459646
-
A stereoselective synthesis of phosphinic acid phosphapeptides corresponding to glutamyl-γ-glutamate and incorporation into potent inhibitors of folylpoly-γ-glutamyl synthetase
-
Bartley, D. M.; Coward, J. K. A stereoselective synthesis of phosphinic acid phosphapeptides corresponding to glutamyl-γ-glutamate and incorporation into potent inhibitors of folylpoly-γ-glutamyl synthetase. J. Org. Chem. 2005, 6757-6774.
-
(2005)
J. Org. Chem.
, pp. 6757-6774
-
-
Bartley, D.M.1
Coward, J.K.2
-
17
-
-
0041305877
-
Membrane transport of folates
-
Matherly, L. H.; Goldman, D. Membrane transport of folates. Vitam. Horm. 2003, 66, 403-456.
-
(2003)
Vitam. Horm.
, vol.66
, pp. 403-456
-
-
Matherly, L.H.1
Goldman, D.2
-
18
-
-
0019276096
-
Prodrugs and site-specific drug delivery
-
Stella, V. J.; Himmelstein, K. J. Prodrugs and site-specific drug delivery. J. Med. Chem. 1980, 23, 1276-1282.
-
(1980)
J. Med. Chem.
, vol.23
, pp. 1276-1282
-
-
Stella, V.J.1
Himmelstein, K.J.2
-
19
-
-
0021035382
-
Studies on prodrugs. 1. Preparation and characterization of acyloxyallylester of ampicillin
-
Sakamoto, F.; Ikeda, S.; Tsukamoto, G. Studies on prodrugs. 1. Preparation and characterization of acyloxyallylester of ampicillin. Chem. Pharm. Bull. 1983, 31, 2698-2707.
-
(1983)
Chem. Pharm. Bull.
, vol.31
, pp. 2698-2707
-
-
Sakamoto, F.1
Ikeda, S.2
Tsukamoto, G.3
-
20
-
-
0021256508
-
Studies on prodrugs. 2. Preparation and characterization of (5-substituted 2-oxo-1,3-dioxolen-4-yl)methyl esters of ampicillin
-
Sakamoto, F.; Ikeda, S.; Tsukamoto, G. Studies on prodrugs. 2. Preparation and characterization of (5-substituted 2-oxo-1,3-dioxolen-4-yl) methyl esters of ampicillin. Chem. Pharm. Bull. 1984, 32, 2241-2248.
-
(1984)
Chem. Pharm. Bull.
, vol.32
, pp. 2241-2248
-
-
Sakamoto, F.1
Ikeda, S.2
Tsukamoto, G.3
-
21
-
-
0021738056
-
Studies on prodrugs. 3. A convenient and practical preparation of ampicillin prodrugs
-
Ikeda, S.; Sakamoto, F.; Kondo, H.; Moriyama, M.; Tsukamoto, G. Studies on prodrugs. 3. A convenient and practical preparation of ampicillin prodrugs. Chem. Pharm. Bull. 1984, 32, 4316-4322.
-
(1984)
Chem. Pharm. Bull.
, vol.32
, pp. 4316-4322
-
-
Ikeda, S.1
Sakamoto, F.2
Kondo, H.3
Moriyama, M.4
Tsukamoto, G.5
-
22
-
-
0343026463
-
Prodrugs for improved ocular drug delivery
-
Jarvinen, T.; Jarvinen, K. Prodrugs for improved ocular drug delivery. Adv. Drug Deliv. Rev. 1996, 19, 203-224.
-
(1996)
Adv. Drug Deliv. Rev.
, vol.19
, pp. 203-224
-
-
Jarvinen, T.1
Jarvinen, K.2
-
23
-
-
0035172949
-
AS-924, a novel, orally active, bifunctional prodrug of ceftizoxime: Physicochemical properties, oral absorption in animals, and antibacterial activity
-
Mori, N.; Kodama, T.; Sakai, A.; Suzuki, T.; Sugihara, T.; Yamaguchi, S.; Nishijima, T.; Aoki, A.; Toriya, M.; Kasai, M.; Hatano, S.; Kitagawa, M.; Yoshimi, A.; Nishimura, K. AS-924, a novel, orally active, bifunctional prodrug of ceftizoxime: Physicochemical properties, oral absorption in animals, and antibacterial activity. Int. J. Antimicrob. Ag. 2001, 18, 451-461.
-
(2001)
Int. J. Antimicrob. Ag.
, vol.18
, pp. 451-461
-
-
Mori, N.1
Kodama, T.2
Sakai, A.3
Suzuki, T.4
Sugihara, T.5
Yamaguchi, S.6
Nishijima, T.7
Aoki, A.8
Toriya, M.9
Kasai, M.10
Hatano, S.11
Kitagawa, M.12
Yoshimi, A.13
Nishimura, K.14
-
25
-
-
0346958512
-
Design of ester prodrugs to enhance oral absorption of poorly permeable compounds: Challenges to the discovery scientist
-
Beaumont, K.; Webster, R.; Gardner, I.; Dack, K. Design of ester prodrugs to enhance oral absorption of poorly permeable compounds: challenges to the discovery scientist. Curr. Drug. Metab. 2003, 4, 461-485.
-
(2003)
Curr. Drug. Metab.
, vol.4
, pp. 461-485
-
-
Beaumont, K.1
Webster, R.2
Gardner, I.3
Dack, K.4
-
26
-
-
0015535262
-
Comparison of ampicillin and hetacillin pharmacokinetics in man
-
Jusko, W. J.; Lewis, G. P. Comparison of ampicillin and hetacillin pharmacokinetics in man. J. Pharm. Sci. 1973, 62, 69-76.
-
(1973)
J. Pharm. Sci.
, vol.62
, pp. 69-76
-
-
Jusko, W.J.1
Lewis, G.P.2
-
27
-
-
0018604964
-
Pharmacokinetics of ampicillin and its prodrugs bacampicillin and pivampicillin in man
-
Ehrnebo, M.; Nilsson, S. O.; Boreus, L. O. Pharmacokinetics of ampicillin and its prodrugs bacampicillin and pivampicillin in man. J. Pharmacokinet. Biopharm. 1979, 7, 429-451.
-
(1979)
J. Pharmacokinet. Biopharm.
, vol.7
, pp. 429-451
-
-
Ehrnebo, M.1
Nilsson, S.O.2
Boreus, L.O.3
-
28
-
-
0019987806
-
Pharmacokinetics of bacmecillinam and pivmecillinam in volunteers
-
Josefsson, K.; Bergan, T.; Magni, L.; Pring, B. G.; Westerlund, D. Pharmacokinetics of bacmecillinam and pivmecillinam in volunteers. Eur. J. Clin. Pharmacol. 1982, 23, 249-252.
-
(1982)
Eur. J. Clin. Pharmacol.
, vol.23
, pp. 249-252
-
-
Josefsson, K.1
Bergan, T.2
Magni, L.3
Pring, B.G.4
Westerlund, D.5
-
29
-
-
0029001172
-
Clinical pharmacokinetics of newer cephalosporins
-
Klepser, M. B.; Marangos, M. N.; Patel, K. B.; Nicolau, D. P.; Quintiliani, R.; Nightingale, C. H. Clinical pharmacokinetics of newer cephalosporins. Clin. Pharmacokinet. 1995, 28, 361-384.
-
(1995)
Clin. Pharmacokinet.
, vol.28
, pp. 361-384
-
-
Klepser, M.B.1
Marangos, M.N.2
Patel, K.B.3
Nicolau, D.P.4
Quintiliani, R.5
Nightingale, C.H.6
-
30
-
-
0030842430
-
Anti-human immunodeficiency virus (HIV) activity, safety, and pharmacokinetics of adefovir dipivoxil (9-2-(bis-pivaloyloxymethyl)- phosphonylmethaxyethyl adenine) in HIV-infected patients
-
Barditch-Crovo, P.; Toole, J.; Hendrix, C. W.; Cundy, K. C.; Ebeling, D.; Jaffe, H. S.; Lietman, P. S. Anti-human immunodeficiency virus (HIV) activity, safety, and pharmacokinetics of adefovir dipivoxil (9-2-(bis-pivaloyloxymethyl)- phosphonylmethaxyethyl adenine) in HIV-infected patients. J. Infect. Dis. 1997, 176, 406-413.
-
(1997)
J. Infect. Dis.
, vol.176
, pp. 406-413
-
-
Barditch-Crovo, P.1
Toole, J.2
Hendrix, C.W.3
Cundy, K.C.4
Ebeling, D.5
Jaffe, H.S.6
Lietman, P.S.7
-
31
-
-
0032997095
-
Clinical pharmacokinetics of the antiviral nucleotide analogues cidofovir and adefovir
-
Cundy, K. C. Clinical pharmacokinetics of the antiviral nucleotide analogues cidofovir and adefovir. Clin. Pharmacokinet. 1999, 36, 127-143.
-
(1999)
Clin. Pharmacokinet.
, vol.36
, pp. 127-143
-
-
Cundy, K.C.1
-
32
-
-
0029025272
-
Phosphinyl acid-based bisubstrate analogue inhibitors of ras farnesyl-protein transferase
-
Patel, D. V.; Gordon, E. M.; Schmidt, R. J.; Weller, H. N.; Young, M. G.; Zahler, R.; Barbacid, M.; Carboni, J. M.; Gullobrown, J. L.; Hunihan, L.; Ricca, C.; Robinson, S.; Seizinger, B. R.; Tuomari, A. V.; Manne, V. Phosphinyl acid-based bisubstrate analogue inhibitors of ras farnesyl-protein transferase. J. Med. Chem. 1995, 38, 435-442.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 435-442
-
-
Patel, D.V.1
Gordon, E.M.2
Schmidt, R.J.3
Weller, H.N.4
Young, M.G.5
Zahler, R.6
Barbacid, M.7
Carboni, J.M.8
Gullobrown, J.L.9
Hunihan, L.10
Ricca, C.11
Robinson, S.12
Seizinger, B.R.13
Tuomari, A.V.14
Manne, V.15
-
33
-
-
0035734121
-
Continuing therapy for childhood acute lymphoblastic leukaemia: Clinical and cellular pharmacology of methotrexate, 6-mercaptopurine and 6-thioguanine
-
Estlin, E. J. Continuing therapy for childhood acute lymphoblastic leukaemia: Clinical and cellular pharmacology of methotrexate, 6-mercaptopurine and 6-thioguanine. Cancer Treat. Rev. 2001, 27, 351-363.
-
(2001)
Cancer Treat. Rev.
, vol.27
, pp. 351-363
-
-
Estlin, E.J.1
-
34
-
-
0020683340
-
Studies of formation and efflux of methotrexate polygkutamates with cultured hepatic cells
-
Goldman, I. D.; Chabner, B. A. Bertino, J. R., Eds; Plenum Press: New York
-
Galivan, J.; Balinska, M. Studies of formation and efflux of methotrexate polygkutamates with cultured hepatic cells. In Folyl and Antifolyl Polyglutamates, Goldman, I. D.; Chabner, B. A. Bertino, J. R., Eds; Plenum Press: New York, 1983; pp 235-246.
-
(1983)
Folyl and Antifolyl Polyglutamates
, pp. 235-246
-
-
Galivan, J.1
Balinska, M.2
-
35
-
-
0015827958
-
Studies on uptake of synthetic conjugated folates by human marrow cells
-
Hoffbran, Av.; Tripp, E.; Houlihan, C. M.; Scott, J. M. Studies on uptake of synthetic conjugated folates by human marrow cells. Blood 1973, 42, 141-146.
-
(1973)
Blood
, vol.42
, pp. 141-146
-
-
Hoffbran, A.1
Tripp, E.2
Houlihan, C.M.3
Scott, J.M.4
-
36
-
-
0026391210
-
Secretion of γ-glutamyl hydrolase in vitro
-
O'Connor, B. M.; Rotundo, R. F.; Nimec, Z.; McGuire, J. J.; Galivan, J. Secretion of γ-glutamyl hydrolase in vitro. Cancer Res. 1991, 51, 3874-3881.
-
(1991)
Cancer Res.
, vol.51
, pp. 3874-3881
-
-
O'Connor, B.M.1
Rotundo, R.F.2
Nimec, Z.3
McGuire, J.J.4
Galivan, J.5
-
37
-
-
0033622009
-
Glutamyl hydrolase: Pharmacological role and enzymatic characterization
-
Galivan, J.; Ryan, T. J.; Chave, K.; Rhee, M.; Yao, R.; Yin, D. Z. Glutamyl hydrolase: Pharmacological role and enzymatic characterization. Pharmacol. Ther. 2000, 85, 207-215.
-
(2000)
Pharmacol. Ther.
, vol.85
, pp. 207-215
-
-
Galivan, J.1
Ryan, T.J.2
Chave, K.3
Rhee, M.4
Yao, R.5
Yin, D.Z.6
-
38
-
-
0020598269
-
Transport of methotrexate in Chinese-hamster ovary cells-a mutant defective in methotrexate uptake and cell binding
-
Flintoff, W. F.; Nagainis, C. R. Transport of methotrexate in Chinese-hamster ovary cells-a mutant defective in methotrexate uptake and cell binding. Arch, Biochem. Biophys. 1983, 223, 433-440.
-
(1983)
Arch, Biochem. Biophys.
, vol.223
, pp. 433-440
-
-
Flintoff, W.F.1
Nagainis, C.R.2
-
39
-
-
0029084385
-
Isolation of human cDNAs that restore methotrexate sensitivity and reduced folate carrier activity in methotrexate transport-defective Chinese-hamster ovary cells
-
Wong, S. C.; Proefke, S. A.; Bhushan, A.; Matherly, L. H. Isolation of human cDNAs that restore methotrexate sensitivity and reduced folate carrier activity in methotrexate transport-defective Chinese-hamster ovary cells. J. Biol. Chem. 1995, 270, 17468-17475.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 17468-17475
-
-
Wong, S.C.1
Proefke, S.A.2
Bhushan, A.3
Matherly, L.H.4
-
40
-
-
0016809717
-
Methotrexate analogues. 6. Replacement of glutamic-acid by various amino-acid esters and amines
-
Chaykovsky, M.; Brown, B. L.; Modest, E. J. Methotrexate analogues. 6. Replacement of glutamic-acid by various amino-acid esters and amines. J. Med. Chem. 1975, 18, 909-912.
-
(1975)
J. Med. Chem.
, vol.18
, pp. 909-912
-
-
Chaykovsky, M.1
Brown, B.L.2
Modest, E.J.3
-
41
-
-
26444508495
-
Synthesis of (6R)- and (6S)-5,10-dideazatetrahydrofolate oligo-γ-glutamate: Kinetics of multiple glutamate ligations catalyzed by folylpoly-γ-glutamate synthetase
-
Tomsho, J. W.; McGuire, J. J.; Coward, J. K. Synthesis of (6R)- and (6S)-5,10-dideazatetrahydrofolate oligo-γ-glutamate: kinetics of multiple glutamate ligations catalyzed by folylpoly-γ-glutamate synthetase. Org. Biomol. Chem. 2005, 3, 3388-3398.
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 3388-3398
-
-
Tomsho, J.W.1
McGuire, J.J.2
Coward, J.K.3
-
42
-
-
0027385182
-
The synthesis of C3-methyl, C3-decarboxy-zaragozic acid-A-A potent squalene synthase inhibitor
-
Kuo, C. H.; Plevyak, S. P.; Biftu, T.; Parsons, W. H.; Berger, G. D. The synthesis of C3-methyl, C3-decarboxy-zaragozic acid-A-A potent squalene synthase inhibitor. Tetrahedron Lett. 1993, 34, 6863-6866.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 6863-6866
-
-
Kuo, C.H.1
Plevyak, S.P.2
Biftu, T.3
Parsons, W.H.4
Berger, G.D.5
-
43
-
-
0001602650
-
Preparation and reactivity of highly functionalized organometallics at the alpha psition of oxygen or nitrogen
-
Knochel, P.; Chou, T. S.; Jubert, C.; Rajagopal, D. Preparation and reactivity of highly functionalized organometallics at the alpha psition of oxygen or nitrogen. J. Org. Chem. 1993, 58, 588-599.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 588-599
-
-
Knochel, P.1
Chou, T.S.2
Jubert, C.3
Rajagopal, D.4
-
44
-
-
0016174444
-
7,8-Dihydropteroyl oligo-γ-L-glutamates-synthesis and kinetic studies with purified dihydrofolate-reductase from mammalian sources
-
Coward, J. K.; Parameswaran, K. N.; Cashmore, A. R.; Bertino, J. R. 7,8-Dihydropteroyl oligo-γ-L-glutamates-synthesis and kinetic studies with purified dihydrofolate-reductase from mammalian sources. Biochemistry 1974, 13, 3899-3903.
-
(1974)
Biochemistry
, vol.13
, pp. 3899-3903
-
-
Coward, J.K.1
Parameswaran, K.N.2
Cashmore, A.R.3
Bertino, J.R.4
-
45
-
-
0021128805
-
Mild arbuzov reactions of phosphonous acids
-
Thottathil, J. K.; Przybyla, C. A.; Moniot, J. L. Mild arbuzov reactions of phosphonous acids. Tetrahedron Lett. 1984, 25, 4737-4740.
-
(1984)
Tetrahedron Lett.
, vol.25
, pp. 4737-4740
-
-
Thottathil, J.K.1
Przybyla, C.A.2
Moniot, J.L.3
-
46
-
-
0028578656
-
The Chemistry of Phosphapeptides-investigations on the synthesis of phosphonamidate, phosphonate, and phosphinate analogues of glutamyl-γ- glutamate
-
Malachowski, W. P.; Coward, J. K. The Chemistry of Phosphapeptides- investigations on the synthesis of phosphonamidate, phosphonate, and phosphinate analogues of glutamyl-γ-glutamate. J. Org. Chem. 1994, 59, 7625-7634.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 7625-7634
-
-
Malachowski, W.P.1
Coward, J.K.2
-
47
-
-
0021180954
-
Preparation of phosphinic acids-michael additions of phosphonous acids esters to conjugated systems
-
Thottathil, J. K.; Ryono, D. E.; Przybyla, C. A.; Moniot, J. L.; Neubeck, R. Preparation of phosphinic acids-michael additions of phosphonous acids esters to conjugated systems. Tetrahedron Lett. 1984, 25, 4741-4744.
-
(1984)
Tetrahedron Lett.
, vol.25
, pp. 4741-4744
-
-
Thottathil, J.K.1
Ryono, D.E.2
Przybyla, C.A.3
Moniot, J.L.4
Neubeck, R.5
-
48
-
-
0025292853
-
A versatile route to substituted phosphinic acids
-
Boyd, E. A.; Corless, M.; James, K.; Regan, A. C. A versatile route to substituted phosphinic acids. Tetrahedron Lett. 1990, 31, 2933-2936.
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 2933-2936
-
-
Boyd, E.A.1
Corless, M.2
James, K.3
Regan, A.C.4
-
49
-
-
0035812795
-
Triethylborane-initiated room-temperature radical addition of hypophosphites to olefins: Synthesis of monosubstituted phosphinic acids and esters
-
Deprele, S.; Montchamp, J. L. Triethylborane-initiated room-temperature radical addition of hypophosphites to olefins: synthesis of monosubstituted phosphinic acids and esters. J. Org. Chem. 2001, 66, 6745-6755.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 6745-6755
-
-
Deprele, S.1
Montchamp, J.L.2
-
50
-
-
0027367934
-
Synthesis of L-(+)-selenomethionine
-
Koch, T.; Buchardt, O. Synthesis of L-(+)-selenomethionine. Synthesis 1993, 1065.
-
(1993)
Synthesis
, pp. 1065
-
-
Koch, T.1
Buchardt, O.2
-
51
-
-
0021912292
-
Methotrexate analogues. 25. Chemical and biological studies on the γ-tert-butyl esters of methotrexate and aminopterin
-
Rosowsky, A.; Freisheim, J. H.; Bader, H.; Forsch, R. A.; Susten, S. S.; Cucchi, C. A.; Frei, E. Methotrexate analogues. 25. Chemical and biological studies on the γ-tert-butyl esters of methotrexate and aminopterin. J. Med. Chem. 1985, 28, 660-667.
-
(1985)
J. Med. Chem.
, vol.28
, pp. 660-667
-
-
Rosowsky, A.1
Freisheim, J.H.2
Bader, H.3
Forsch, R.A.4
Susten, S.S.5
Cucchi, C.A.6
Frei, E.7
-
52
-
-
0007653096
-
Solution of a classical problem-tautomerism and isomerism in α-methylglutaconic acid series
-
Kagan, J.; Tolentino, L.; Ettlinger, M. G. Solution of a classical problem-tautomerism and isomerism in α-methylglutaconic acid series. J. Org. Chem. 1975, 40, 3085-3093.
-
(1975)
J. Org. Chem.
, vol.40
, pp. 3085-3093
-
-
Kagan, J.1
Tolentino, L.2
Ettlinger, M.G.3
-
53
-
-
31544458351
-
Cleavage of N-carbobenzyloxy group in neutral and basic media-neighboring-group participation of carbamate moiety
-
Coward, J. K.; Lok, R. Cleavage of N-carbobenzyloxy group in neutral and basic media-neighboring-group participation of carbamate moiety. J. Org. Chem. 1973, 38, 2546-2548.
-
(1973)
J. Org. Chem.
, vol.38
, pp. 2546-2548
-
-
Coward, J.K.1
Lok, R.2
-
54
-
-
26444495633
-
Design, synthesis, and activity of analogues of phosphinothricin as inhibitors of glutamine synthetase
-
Berlicki, L.; Obojska, A.; Forlani, G.; Kafarski, P. Design, synthesis, and activity of analogues of phosphinothricin as inhibitors of glutamine synthetase. J. Med. Chem. 2005, 48, 6340-6349.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 6340-6349
-
-
Berlicki, L.1
Obojska, A.2
Forlani, G.3
Kafarski, P.4
-
55
-
-
85004388152
-
2) and its application to gas-chromatographic analysis of fatty-acids
-
2) and its application to gas-chromatographic analysis of fatty-acids. Chem. Pharm. Bull. 1981, 29, 1475-1478.
-
(1981)
Chem. Pharm. Bull.
, vol.29
, pp. 1475-1478
-
-
Hashimoto, N.1
Aoyama, T.2
Shioiri, T.3
-
56
-
-
0030872001
-
A convenient route for monodealkylation of diethyl phosphonates
-
Krawczyk, H. A convenient route for monodealkylation of diethyl phosphonates. Synthetic Commun. 1997, 27, 3151-3161.
-
(1997)
Synthetic Commun.
, vol.27
, pp. 3151-3161
-
-
Krawczyk, H.1
-
57
-
-
17844363456
-
Transesterification of trialkyl phosphates from alkyl bromides
-
Lherbet, C.; Castonguay, R.; Keillor, J. W. Transesterification of trialkyl phosphates from alkyl bromides. Tetrahedron Lett. 2005, 46, 3565-3567.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 3565-3567
-
-
Lherbet, C.1
Castonguay, R.2
Keillor, J.W.3
-
58
-
-
0032509931
-
Synthesis of phosphonate analogues of CMP-Neu5Ac determination of α(2-6)-sialyltransferase inhibition
-
Muller, B.; Martin, T. J.; Schaub, C.; Schmidt, R. R. Synthesis of phosphonate analogues of CMP-Neu5Ac determination of α(2-6)- sialyltransferase inhibition. Tetrahedron Lett. 1998, 39, 509-512.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 509-512
-
-
Muller, B.1
Martin, T.J.2
Schaub, C.3
Schmidt, R.R.4
-
59
-
-
0032126162
-
Mechanism-based inhibition of human folylpolyglutamate synthetase: Design, synthesis, and biochemical characterization of a phosphapeptide mimic of the tetrahedral intermediate
-
Tsukamoto, T.; Haile, W. H.; McGuire, J. J.; Coward, J. K. Mechanism-based inhibition of human folylpolyglutamate synthetase: Design, synthesis, and biochemical characterization of a phosphapeptide mimic of the tetrahedral intermediate. Arch. Biochem. Biophys. 1998, 355, 109-118.
-
(1998)
Arch. Biochem. Biophys.
, vol.355
, pp. 109-118
-
-
Tsukamoto, T.1
Haile, W.H.2
McGuire, J.J.3
Coward, J.K.4
-
60
-
-
17944379996
-
Glutamyl-γ-boronate inhibitors of bacterial Glu-tRNAGln amidotransferase. Bioorg
-
Decicco, C. P.; Nelson, D. J.; Luo, Y.; Shen, L.; Horiuchi, K. Y.; Amsler, K. M.; Foster, L. A.; Spitz, S. M.; Merrill, J. J.; Sizemore, C. F.; Rogers, K. C.; Copeland, R. A.; Harpel, M. R. Glutamyl-γ-boronate inhibitors of bacterial Glu-tRNAGln amidotransferase. Bioorg. Med. Chem. Lett. 2001, 11, 2561-2564.
-
(2001)
Med. Chem. Lett.
, vol.11
, pp. 2561-2564
-
-
Decicco, C.P.1
Nelson, D.J.2
Luo, Y.3
Shen, L.4
Horiuchi, K.Y.5
Amsler, K.M.6
Foster, L.A.7
Spitz, S.M.8
Merrill, J.J.9
Sizemore, C.F.10
Rogers, K.C.11
Copeland, R.A.12
Harpel, M.R.13
-
61
-
-
13744254341
-
The synthesis of diaminopimelic acid containing peptidoglycan fragments using metathesis cross coupling
-
Chowdhury, A. R.; Boons, G.-J. The synthesis of diaminopimelic acid containing peptidoglycan fragments using metathesis cross coupling. Tetrahedron Lett. 2005, 46, 1675-1678.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 1675-1678
-
-
Chowdhury, A.R.1
Boons, G.-J.2
-
62
-
-
0025743182
-
Novel ring contractions via 2,3 Wittig type rearrangements-synthesis of 2-deoxy-2-methylenebicyclomycin
-
Williams, R. M.; Sabol, M. R.; Kim, H. D.; Kwast, A. Novel ring contractions via 2,3 Wittig type rearrangements-synthesis of 2-deoxy-2-methylenebicyclomycin. J. Am. Chem. Soc. 1991, 113, 6621-6633.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 6621-6633
-
-
Williams, R.M.1
Sabol, M.R.2
Kim, H.D.3
Kwast, A.4
-
63
-
-
31544459713
-
-
note
-
The fact that the tris-POM ester, 2d, is slightly more cytotoxic in a transport-deficient (R2) cell line than the free acid, 2c, may indicate that the prodrug ester enters the cell more effectively than the parent isopeptide. Subsequent intracellular hydrolysis would then occur as described.
-
-
-
-
64
-
-
31544441550
-
-
Antitumor methotrexate diesters for oral administration JP 63227588
-
Saito, T.; Iwazawa, H.; Nakajima, S.; Fujita, H. Antitumor methotrexate diesters for oral administration JP 63227588; Chem. Abstr. 1989, 110, 154322.
-
(1989)
Chem. Abstr.
, vol.110
, pp. 154322
-
-
Saito, T.1
Iwazawa, H.2
Nakajima, S.3
Fujita, H.4
-
65
-
-
37049060814
-
Some novel penicillin derivatives
-
Jansen, A. B. A.; Russell, T. J. Some novel penicillin derivatives. J. Chem. Soc. 1965, 2127-2132.
-
(1965)
J. Chem. Soc.
, pp. 2127-2132
-
-
Jansen, A.B.A.1
Russell, T.J.2
-
66
-
-
0029000897
-
Bisubstrate inhibitors of farnesyltransferase-a novel class of specific inhibitors of ras transformed-cells
-
Manne, V.; Yan, N.; Carboni, J. M.; Tuomari, A. V.; Ricca, C. S.; Brown, J. G.; Andahazy, M. L.; Schmidt, R. J.; Patel, D.; Zahler, R.; Weinmann, R.; Der, C. J.; Cox, A. D.; Hunt, J. T.; Gordon, E. M.; Barbacid, M.; Seizinger, B. R. Bisubstrate inhibitors of farnesyltransferase-a novel class of specific inhibitors of ras transformed-cells. Oncogene 1995, 10, 1763-1779.
-
(1995)
Oncogene
, vol.10
, pp. 1763-1779
-
-
Manne, V.1
Yan, N.2
Carboni, J.M.3
Tuomari, A.V.4
Ricca, C.S.5
Brown, J.G.6
Andahazy, M.L.7
Schmidt, R.J.8
Patel, D.9
Zahler, R.10
Weinmann, R.11
Der, C.J.12
Cox, A.D.13
Hunt, J.T.14
Gordon, E.M.15
Barbacid, M.16
Seizinger, B.R.17
-
67
-
-
0002714675
-
Rapid chromatographic technique for preparative separations with moderate resolution
-
Still, W. C.; Kahn, M.; Mitra, A. Rapid chromatographic technique for preparative separations with moderate resolution. J. Org. Chem. 1978, 43, 2923-2925.
-
(1978)
J. Org. Chem.
, vol.43
, pp. 2923-2925
-
-
Still, W.C.1
Kahn, M.2
Mitra, A.3
-
68
-
-
0001556055
-
Synthesis of 6-hydroxymethylypteridines
-
Baugh, C. M.; Shaw, E. Synthesis of 6-hydroxymethylypteridines. J. Org. Chem. 1964, 29, 3610-3612.
-
(1964)
J. Org. Chem.
, vol.29
, pp. 3610-3612
-
-
Baugh, C.M.1
Shaw, E.2
-
69
-
-
84982399781
-
Pteridines. 69. Synthesis and reactivity of 2,4-diamino-6-(hydroxymethyl) pteridine
-
Boyle, P. H.; Pfleiderer, W. Pteridines. 69. Synthesis and reactivity of 2,4-diamino-6-(hydroxymethyl)pteridine. Chem. Ber. 1980, 113, 1514-1523.
-
(1980)
Chem. Ber.
, vol.113
, pp. 1514-1523
-
-
Boyle, P.H.1
Pfleiderer, W.2
-
70
-
-
33947488464
-
A new synthesis of p-methylaminobenzoyl-L-glutamic acid
-
Fu, S.-C. J.; Reiner, M. A new synthesis of p-methylaminobenzoyl-L- glutamic acid. J. Org. Chem. 1965, 30, 1277-1278.
-
(1965)
J. Org. Chem.
, vol.30
, pp. 1277-1278
-
-
Fu, S.-C.J.1
Reiner, M.2
-
71
-
-
0000949520
-
Preparation of tert-butyl esters of free amino acids
-
Roeske, R. Preparation of tert-butyl esters of free amino acids. J. Org. Chem. 1963, 28, 1251-1253.
-
(1963)
J. Org. Chem.
, vol.28
, pp. 1251-1253
-
-
Roeske, R.1
-
72
-
-
0001622541
-
1-Hydroxy-3-amino-2-piperidone (delta-N-hydroxycycloornithine) derivatives-key intermediates for the synthesis of hydroxamate-based siderophores
-
Kolasa, T.; Miller, M. J. 1-Hydroxy-3-amino-2-piperidone (delta-N-hydroxycycloornithine) derivatives-key intermediates for the synthesis of hydroxamate-based siderophores. J. Org. Chem. 1990, 55, 1711-1721.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 1711-1721
-
-
Kolasa, T.1
Miller, M.J.2
-
73
-
-
0005366264
-
The reversible esteriflcation of carboxylic acids with isobutene and trimethylethylene-quantitative studies and synthetic applications
-
Altschul, R. The reversible esteriflcation of carboxylic acids with isobutene and trimethylethylene-quantitative studies and synthetic applications. J. Am. Chem. Soc. 1946, 68, 2605-2609.
-
(1946)
J. Am. Chem. Soc.
, vol.68
, pp. 2605-2609
-
-
Altschul, R.1
-
74
-
-
0038748474
-
Synthesis and biological evaluation of thiol-based inhibitors of glutamate carboxypeptidase II: Discovery of an orally active GCP II inhibitor
-
Majer, P.; Jackson, P. F.; Delahanty, G.; Grella, B. S.; Ko, Y. S.; Li, W. X.; Liu, Q.; Maclin, K. M.; Polakova, J.; Shaffer, K. A.; Stoermer, D.; Vitharana, D.; Wang, E. Y.; Zakrzewski, A.; Rojas, C.; Slusher, B. S.; Wozniak, K. M.; Burak, E.; Limsakun, T.; Tsukamoto, T. Synthesis and biological evaluation of thiol-based inhibitors of glutamate carboxypeptidase II: Discovery of an orally active GCP II inhibitor. J. Med. Chem. 2003, 46, 1989-1996.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 1989-1996
-
-
Majer, P.1
Jackson, P.F.2
Delahanty, G.3
Grella, B.S.4
Ko, Y.S.5
Li, W.X.6
Liu, Q.7
Maclin, K.M.8
Polakova, J.9
Shaffer, K.A.10
Stoermer, D.11
Vitharana, D.12
Wang, E.Y.13
Zakrzewski, A.14
Rojas, C.15
Slusher, B.S.16
Wozniak, K.M.17
Burak, E.18
Limsakun, T.19
Tsukamoto, T.20
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