-
1
-
-
0030066361
-
10-propargyl-5,8-dideazafolic Acid (ICI 198583)
-
10-propargyl-5,8-dideazafolic Acid (ICI 198583). J. Med. Chem. 1996, 39, 73-85.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 73-85
-
-
Bavetsias, V.1
Jackman, A.L.2
Kimbell, R.3
Gibson, W.4
Boyle, F.T.5
Bisset, G.M.F.6
-
2
-
-
0028090282
-
10-propargyl-5,8-dideazafolic Acid (ICI 198583)
-
10-propargyl-5,8-dideazafolic Acid (ICI 198583). J. Med. Chem. 1994, 37, 3294-3302.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3294-3302
-
-
Bisset, G.M.F.1
Bavetsias, V.2
Thornton, T.J.3
Pawelczak, K.4
Calvert, A.H.5
Hughes, L.R.6
Jackman, A.L.7
-
3
-
-
0025933916
-
10-propargyl-5,8-dideazafolic acid (ICI 198583)
-
10-propargyl-5,8-dideazafolic acid (ICI 198583). Biochem. Pharmacol. 1991, 42, 1885-1895.
-
(1991)
Biochem. Pharmacol.
, vol.42
, pp. 1885-1895
-
-
Jackman, A.L.1
Newell, D.R.2
Gibson, W.3
Jodrell, D.I.4
Taylor, G.A.5
Bishop, J.A.6
Hughes, L.R.7
Calvert, A.H.8
-
4
-
-
0025820445
-
Quinazoline Antifolate Thymidylate Synthase Inhibitors: Heterocyclic Benzoyl Ring Modifications
-
Marsham, P. R.; Hughes, L. R.; Jackman, A. L.; Hayter, A. J.; Oldfield, J.; Wardleworth, J. M.; Bishop, J. A. M.; O'Connor, B. M.; Calvert, A. H. Quinazoline Antifolate Thymidylate Synthase Inhibitors: Heterocyclic Benzoyl Ring Modifications. J. Med. Chem. 1991, 34, 1594-1605.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 1594-1605
-
-
Marsham, P.R.1
Hughes, L.R.2
Jackman, A.L.3
Hayter, A.J.4
Oldfield, J.5
Wardleworth, J.M.6
Bishop, J.A.M.7
O'Connor, B.M.8
Calvert, A.H.9
-
5
-
-
0025997350
-
ICI D1694, a Quinazoline Antifolate Thymidylate Synthase Inhibitor That is a Potent Inhibitor of L1210 Tumour Cell Growth in Vitro and in Vivo; a New Agent for Clinical Study
-
Jackman, A. L.; Taylor, G. A.; Gibson, W.; Kimbell, R.; Brown, M.; Calvert, A. H.; Judson, I. R.; Hughes, L. R. ICI D1694, A Quinazoline Antifolate Thymidylate Synthase Inhibitor That is a Potent Inhibitor of L1210 Tumour Cell Growth In Vitro and In Vivo; A New Agent for Clinical Study. Cancer Res. 1991, 51, 5579-5586.
-
(1991)
Cancer Res.
, vol.51
, pp. 5579-5586
-
-
Jackman, A.L.1
Taylor, G.A.2
Gibson, W.3
Kimbell, R.4
Brown, M.5
Calvert, A.H.6
Judson, I.R.7
Hughes, L.R.8
-
6
-
-
0029164564
-
ZD1694 (Tomudex): A New Thymidylate Synthase Inhibitor with Activity in Colorectal Cancer
-
Jackman, A. L.; Farrugia, D. C.; Gibson, W.; Kimbell, R.; Harrap, K. R.; Stephens, T. C.; Azab, M.; Boyle, F. T. ZD1694 (Tomudex): A New Thymidylate Synthase Inhibitor With Activity in Colorectal Cancer. Eur. J. Cancer 1995, 31A, 1277-1282.
-
(1995)
Eur. J. Cancer
, vol.31 A
, pp. 1277-1282
-
-
Jackman, A.L.1
Farrugia, D.C.2
Gibson, W.3
Kimbell, R.4
Harrap, K.R.5
Stephens, T.C.6
Azab, M.7
Boyle, F.T.8
-
7
-
-
84952541174
-
A Convenient Synthesis of t-Butyl Esters of Amino Acids
-
Csanady, G.; Medzihradszky, K. A Convenient Synthesis of t-Butyl Esters of Amino Acids. Org. Prep. Proced. Int. 1988, 20, 180-184.
-
(1988)
Org. Prep. Proced. Int.
, vol.20
, pp. 180-184
-
-
Csanady, G.1
Medzihradszky, K.2
-
8
-
-
0002840747
-
Synthesis of 9-Fluorenylmethyloxycarbonyl-Protected N-Alkyl Amino Acids by Reduction of Oxazolidinones
-
Freidinger, R. M.; Hinkle, J. S.; Perlow, D. S.; Arison, B. H. Synthesis of 9-Fluorenylmethyloxycarbonyl-Protected N-Alkyl Amino Acids by Reduction of Oxazolidinones. J. Org. Chem. 1983, 48, 77-81.
-
(1983)
J. Org. Chem.
, vol.48
, pp. 77-81
-
-
Freidinger, R.M.1
Hinkle, J.S.2
Perlow, D.S.3
Arison, B.H.4
-
9
-
-
0000811321
-
The Mixed Carbonic Anhydride Method of Peptide Synthesis
-
Gross, E., Meienhofer, J., Eds.; Academic Press: New York
-
Meienhofer, J. The Mixed Carbonic Anhydride Method of Peptide Synthesis. In The Peptides, Analysis, Synthesis, Biology; Gross, E., Meienhofer, J., Eds.; Academic Press: New York, 1985; Vol. 1, pp 264-309.
-
(1985)
The Peptides, Analysis, Synthesis, Biology
, vol.1
, pp. 264-309
-
-
Meienhofer, J.1
-
10
-
-
0019839154
-
Methotrexate Analogues. 14. Synthesis of New γ-Substituted Derivatives As Dihydrofolate Reductase Inhibitors and Potential Anticancer Agents
-
Rosowsky, A.; Forsch, R.; Uren, J.; Wick, M. Methotrexate Analogues. 14. Synthesis of New γ-Substituted Derivatives As Dihydrofolate Reductase Inhibitors and Potential Anticancer Agents. J. Med. Chem. 1981, 24, 1450-1455.
-
(1981)
J. Med. Chem.
, vol.24
, pp. 1450-1455
-
-
Rosowsky, A.1
Forsch, R.2
Uren, J.3
Wick, M.4
-
11
-
-
0842322097
-
Synthesis of Nonproteinogenic Amino Acids Part 2: Preparation of a Synthetic Equivalent of the γ Anion Synthon for Asymmetric Amino Acid Synthesis
-
Baldwin, J. E.; North, M.; Flinn, A.; Moloney, M. G. Synthesis of Nonproteinogenic Amino Acids Part 2: Preparation of a Synthetic Equivalent of the γ Anion Synthon for Asymmetric Amino Acid Synthesis. Tetrahedron 1989, 45, 1453-1464.
-
(1989)
Tetrahedron
, vol.45
, pp. 1453-1464
-
-
Baldwin, J.E.1
North, M.2
Flinn, A.3
Moloney, M.G.4
-
12
-
-
0000515942
-
Synthesis of 4-Substituted Prolines as Conformationally Constrained Amino Acid Analogues
-
Koskinen, A. M. P.; Rapoport, H. Synthesis of 4-Substituted Prolines as Conformationally Constrained Amino Acid Analogues. J. Org. Chem. 1989, 54, 1859-1866.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 1859-1866
-
-
Koskinen, A.M.P.1
Rapoport, H.2
-
13
-
-
0021087845
-
Methotrexate Analogues. 20. Replacement of Glutamate by Longer-Chain Amino Diacids: Effects on Dihydrofolate Reductase Inhibition, Cytotoxicity, and in Vivo Antitumour Activity
-
Rosowsky, A.; Forsch, R.; Uren, J.; Wick, M.; Kumar, A. A.; Freisheim, J. H. Methotrexate Analogues. 20. Replacement of Glutamate by Longer-Chain Amino Diacids: Effects on Dihydrofolate Reductase Inhibition, Cytotoxicity, and in Vivo Antitumour Activity. J. Med. Chem. 1983, 26, 1719-1724.
-
(1983)
J. Med. Chem.
, vol.26
, pp. 1719-1724
-
-
Rosowsky, A.1
Forsch, R.2
Uren, J.3
Wick, M.4
Kumar, A.A.5
Freisheim, J.H.6
-
14
-
-
5544250773
-
Preparation of tert-Butyl Esters of Free Amino Acids
-
(a) Taschner, E.; Chimiak, A.; Bator, B.; Sokolowska, T. Preparation of tert-Butyl Esters of Free Amino Acids. Justus Liebigs Ann. Chem. 1961, 646, 133-136.
-
(1961)
Justus Liebigs Ann. Chem.
, vol.646
, pp. 133-136
-
-
Taschner, E.1
Chimiak, A.2
Bator, B.3
Sokolowska, T.4
-
15
-
-
0003803058
-
-
Bodanszky, M., Bodanszky, A., Eds.; Springer-Verlag: Berlin
-
(b) The Practice of Peptide Synthesis; Bodanszky, M., Bodanszky, A., Eds.; Springer-Verlag: Berlin, 1984; pp 48-49.
-
(1984)
The Practice of Peptide Synthesis
, pp. 48-49
-
-
-
16
-
-
0028937684
-
Convenient Preparation of α-tert-Butyl N-Blocked Glutamates Through γ-Allyl Ester Protection
-
Bavetsias, V.; Bisset, G. M. F.; Jarman, M. Convenient Preparation of α-tert-Butyl N-Blocked Glutamates Through γ-Allyl Ester Protection. Synth. Commun. 1995, 25, 947-958.
-
(1995)
Synth. Commun.
, vol.25
, pp. 947-958
-
-
Bavetsias, V.1
Bisset, G.M.F.2
Jarman, M.3
-
17
-
-
0025014627
-
PyBOP®: A New Peptide Coupling Reagent Devoid of Toxic By-Product
-
Coste J.; Le-Nguyen, D.; Castro, B. PyBOP®: A New Peptide Coupling Reagent Devoid of Toxic By-Product. Tetrahedron Lett. 1990, 31, 205-208.
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 205-208
-
-
Coste, J.1
Le-Nguyen, D.2
Castro, B.3
-
18
-
-
0026010908
-
PyBOP® and PyBroP: Two Reagents for the Difficult Coupling of the α,α-Dialkyl Amino Acid, Aib
-
and references cited therein
-
Frerot, E.; Coste, J.; Pantaloni, A.; Dufour, M.; Jouin, P. PyBOP® and PyBroP: Two Reagents for the Difficult Coupling of the α,α-Dialkyl Amino Acid, Aib. Tetrahedron 1991, 47, 259-270 and references cited therein.
-
(1991)
Tetrahedron
, vol.47
, pp. 259-270
-
-
Frerot, E.1
Coste, J.2
Pantaloni, A.3
Dufour, M.4
Jouin, P.5
-
19
-
-
0023156568
-
Synthesis of (pGlu-5, MePhe-8, Sar-9) Substance P (5-11) (DiMe-C7) Using a Polyacrylamide Resin and Biological Activity on Guinea Pig Ileum and Tracheal Smooth Muscle
-
Calas, B.; Michelot, R.; Lecaer, J. P.; Cave, A.; Parello, J.; Potier, P. Synthesis of (pGlu-5, MePhe-8, Sar-9) Substance P (5-11) (DiMe-C7) Using a Polyacrylamide Resin and Biological Activity on Guinea Pig Ileum and Tracheal Smooth Muscle. Int. J. Pept. Protein Res. 1987, 29, 170-176.
-
(1987)
Int. J. Pept. Protein Res.
, vol.29
, pp. 170-176
-
-
Calas, B.1
Michelot, R.2
Lecaer, J.P.3
Cave, A.4
Parello, J.5
Potier, P.6
-
20
-
-
0018398601
-
S-Cis and s-Trans Isomerism of the His-Pro Peptide Bond in Angiotensin and Thyroliberin Analogues
-
Liakopoulou-Kyriakides, M.; Galardy, R. E. s-Cis and s-Trans Isomerism of the His-Pro Peptide Bond in Angiotensin and Thyroliberin Analogues. Biochemistry 1979, 18, 1952-1957.
-
(1979)
Biochemistry
, vol.18
, pp. 1952-1957
-
-
Liakopoulou-Kyriakides, M.1
Galardy, R.E.2
-
21
-
-
0022500826
-
10-Propargyl-5,8-dideazafolic Acid (CB 3717): Development, Characterisation and Cross-Resistance Studies
-
10-Propargyl-5,8-dideazafolic Acid (CB 3717): Development, Characterisation and Cross-Resistance Studies. Cancer Res. 1986, 46, 2810-2815.
-
(1986)
Cancer Res.
, vol.46
, pp. 2810-2815
-
-
Jackman, A.L.1
Alison, D.L.2
Calvert, A.H.3
Harrap, K.R.4
-
22
-
-
0023699993
-
10-Propargyl-5,8-dideazafolic Acid (CB 3717) Polyglutamates in L1210 Cells in Vitro
-
10-Propargyl-5,8-dideazafolic Acid (CB 3717) Polyglutamates in L1210 Cells in Vitro. Biochem. Pharmacol. 1988, 37, 4047-4054.
-
(1988)
Biochem. Pharmacol.
, vol.37
, pp. 4047-4054
-
-
Sikora, E.1
Jackman, A.L.2
Newell, D.R.3
Calvert, A.H.4
-
23
-
-
0024997423
-
10-propargyl-5,8-dideazafolic Acid and Related Compounds in Murine (L1210) and Human (W1L2) Systems in Vitro and L1210 in Vivo
-
10-propargyl-5,8-dideazafolic Acid and Related Compounds in Murine (L1210) and Human (W1L2) Systems in Vitro and L1210 in Vivo. Cancer Res. 1990, 50, 5212-5218.
-
(1990)
Cancer Res.
, vol.50
, pp. 5212-5218
-
-
Jackman, A.L.1
Taylor, G.A.2
O'Connor, B.M.3
Bishop, J.A.4
Moran, R.G.5
Calvert, A.H.6
-
24
-
-
0021174011
-
Transport of the Antitumour Antibiotic CI-920 in L1210 Leukemia Cells by the Reduced Folate Carrier System
-
Fry, D. W.; Besserer, J. A.; Boritzki, T. J. Transport of the Antitumour Antibiotic CI-920 in L1210 Leukemia Cells by the Reduced Folate Carrier System. Cancer Res. 1984, 44, 3366-3370.
-
(1984)
Cancer Res.
, vol.44
, pp. 3366-3370
-
-
Fry, D.W.1
Besserer, J.A.2
Boritzki, T.J.3
-
25
-
-
0027130695
-
The in Vivo Metabolic Stability of Dipeptide Analogues of the Quinazoline Antifolate, ICI 198583
-
Mice
-
Jodrell, D. I.; Gibson, W.; Bisset, G. M. F.; Boyle, F. T.; Judson, I. R.; Jackman, A. L. The In Vivo Metabolic Stability of Dipeptide Analogues of the Quinazoline Antifolate, ICI 198583, In Mice. Biochem. Pharmacol. 1993, 46, 2229-2234.
-
(1993)
Biochem. Pharmacol.
, vol.46
, pp. 2229-2234
-
-
Jodrell, D.I.1
Gibson, W.2
Bisset, G.M.F.3
Boyle, F.T.4
Judson, I.R.5
Jackman, A.L.6
-
26
-
-
0029031286
-
Mechanisms of Acquired Resistance to the Quinazoline Inhibitor ZD1694 (Tomudex) in One Mouse and Three Human Cell Lines
-
(a) Jackman, A. L.; Kelland, L. R.; Kimbell, R.; Brown, M.; Gibson, W.; Aherne, G. W.; Hardcastle, A.; Boyle, F. T. Mechanisms of Acquired Resistance to the Quinazoline Inhibitor ZD1694 (Tomudex) in One Mouse and Three Human Cell Lines. Br. J. Cancer 1995, 71, 914-924.
-
(1995)
Br. J. Cancer
, vol.71
, pp. 914-924
-
-
Jackman, A.L.1
Kelland, L.R.2
Kimbell, R.3
Brown, M.4
Gibson, W.5
Aherne, G.W.6
Hardcastle, A.7
Boyle, F.T.8
-
27
-
-
0028788352
-
Quinazoline Thymidylate Synthase Inhibitors: Methods for Assessing the Contribution of Polyglutamation to Their in Vitro Activity
-
(b) Jackman, A. L.; Kimbell, R.; Brown, M.; Brunton, L.; Boyle, F. T. Quinazoline Thymidylate Synthase Inhibitors: Methods for Assessing the Contribution of Polyglutamation to Their in Vitro Activity. Anti-Cancer Drug Des. 1995, 10, 555-572.
-
(1995)
Anti-Cancer Drug Des.
, vol.10
, pp. 555-572
-
-
Jackman, A.L.1
Kimbell, R.2
Brown, M.3
Brunton, L.4
Boyle, F.T.5
-
28
-
-
0028802315
-
Quinazoline-based Thymidylate Synthase Inhibitors: Relationship between Structural Modifications and Polyglutamation
-
Jackman, A. L.; Kimbell, R.; Brown, M.; Brunton, L.; Bisset, G. M. F.; Bavetsias, V.; Marsham, P.; Hughes, L. R.; Boyle, F. T. Quinazoline-based Thymidylate Synthase Inhibitors: Relationship Between Structural Modifications and Polyglutamation. Anti-Cancer Drug Des. 1995, 10, 573-589.
-
(1995)
Anti-Cancer Drug Des.
, vol.10
, pp. 573-589
-
-
Jackman, A.L.1
Kimbell, R.2
Brown, M.3
Brunton, L.4
Bisset, G.M.F.5
Bavetsias, V.6
Marsham, P.7
Hughes, L.R.8
Boyle, F.T.9
-
29
-
-
0028096247
-
A Strategy for the Design of Membrane-Permeable Folylpoly-γ-glutamate Synthetase Inhibitors: "Bay-Regio"-Substituted 2-Desamino-2-methyl-5,8-dideazafolate Analogs
-
Sanghani, P. C.; Jackman, A.; Evans, V. R.; Thornton, T.; Hughes, L.; Calvert, A. H.; Moran, R. G. A Strategy for the Design of Membrane-Permeable Folylpoly-γ-glutamate Synthetase Inhibitors: "Bay-Regio"-Substituted 2-Desamino-2-methyl-5,8-dideazafolate Analogs. Mol. Pharmacol. 1994, 45, 341-351.
-
(1994)
Mol. Pharmacol.
, vol.45
, pp. 341-351
-
-
Sanghani, P.C.1
Jackman, A.2
Evans, V.R.3
Thornton, T.4
Hughes, L.5
Calvert, A.H.6
Moran, R.G.7
-
30
-
-
0001023731
-
N-Methylamino Acids in Peptide Synthesis. II. A New Synthesis of N-Benzyloxycarbonyl, N-Methylamino Acids
-
McDermott, J. R.; Benoiton, N. L. N-Methylamino Acids in Peptide Synthesis. II. A New Synthesis of N-Benzyloxycarbonyl, N-Methylamino Acids. Can. J. Chem. 1973, 51, 1915-1919.
-
(1973)
Can. J. Chem.
, vol.51
, pp. 1915-1919
-
-
McDermott, J.R.1
Benoiton, N.L.2
|