-
1
-
-
0021260057
-
The potential of nucleoside analogs as inhibitors of retroviruses and tumors
-
Robins, R. K. The potential of nucleoside analogs as inhibitors of retroviruses and tumors. Pharm. Res. 1984, 11-18.
-
(1984)
Pharm. Res
, pp. 11-18
-
-
Robins, R.K.1
-
2
-
-
0033567430
-
Role of antimetabolites of purine and pyrimidine nucleotide metabolism in tumor cell differentiation
-
Hatse, S.; De Clercq, E.; Balzarini, J. Role of antimetabolites of purine and pyrimidine nucleotide metabolism in tumor cell differentiation. Biochem. Pharmacol. 1999, 58, 539-555.
-
(1999)
Biochem. Pharmacol
, vol.58
, pp. 539-555
-
-
Hatse, S.1
De Clercq, E.2
Balzarini, J.3
-
4
-
-
0033736202
-
-
Wagner, C. R.; Iyer, V. V.; McIntee, E. J. Pronucleotides: Toward the in vivo delivery of antiviral and anticancer nucleotides. Med. Res. Rev. 2000, 20, 417-451.
-
Wagner, C. R.; Iyer, V. V.; McIntee, E. J. Pronucleotides: Toward the in vivo delivery of antiviral and anticancer nucleotides. Med. Res. Rev. 2000, 20, 417-451.
-
-
-
-
5
-
-
0034597614
-
Synthesis and biological activity of novel 5-fluoro-2′-deoxyuridine phosphoramidate prodrugs
-
Freel Meyers, C. L.; Hong, L.; Joswig, C.; Borch, R. F. Synthesis and biological activity of novel 5-fluoro-2′-deoxyuridine phosphoramidate prodrugs. J. Med. Chem. 2000, 43, 4313-4318.
-
(2000)
J. Med. Chem
, vol.43
, pp. 4313-4318
-
-
Freel Meyers, C.L.1
Hong, L.2
Joswig, C.3
Borch, R.F.4
-
6
-
-
0034597608
-
Activation mechanisms of nucleoside phosphoramidate prodrugs
-
Freel Meyers, C. L.; Borch, R. F. Activation mechanisms of nucleoside phosphoramidate prodrugs. J. Med. Chem. 2000, 43, 4319-4327.
-
(2000)
J. Med. Chem
, vol.43
, pp. 4319-4327
-
-
Freel Meyers, C.L.1
Borch, R.F.2
-
7
-
-
0035818889
-
Synthesis and biological studies of novel nucleoside phosphoramidate prodrugs
-
Tobias, S. C.; Borch, R. F. Synthesis and biological studies of novel nucleoside phosphoramidate prodrugs. J. Med. Chem. 2001, 44, 4475-4480.
-
(2001)
J. Med. Chem
, vol.44
, pp. 4475-4480
-
-
Tobias, S.C.1
Borch, R.F.2
-
8
-
-
3142752643
-
Synthesis and biological evaluation of a cytarabine phosphoramidate prodrug
-
Tobias, S. C.; Borch, R. F. Synthesis and biological evaluation of a cytarabine phosphoramidate prodrug. Mol. Pharmaceutics 2004, 1, 112-116.
-
(2004)
Mol. Pharmaceutics
, vol.1
, pp. 112-116
-
-
Tobias, S.C.1
Borch, R.F.2
-
9
-
-
0025325071
-
Evaluation of the antitumor activity of gemcitabine (2′,2′-difluoro-2′-deoxycytidine)
-
Hertel, L. W.; Boder, G. B.; Kroin, J. S.; Rinzel, S. M.; Poore, G. A.; Todd, G. C.; Grindey, G. B. Evaluation of the antitumor activity of gemcitabine (2′,2′-difluoro-2′-deoxycytidine). Cancer Res. 1990, 50, 4417-4422.
-
(1990)
Cancer Res
, vol.50
, pp. 4417-4422
-
-
Hertel, L.W.1
Boder, G.B.2
Kroin, J.S.3
Rinzel, S.M.4
Poore, G.A.5
Todd, G.C.6
Grindey, G.B.7
-
10
-
-
0029584109
-
Preclinical characteristics of gemcitabine
-
Plunkett, W.; Huang, P.; Gandhi, V. Preclinical characteristics of gemcitabine. Anti-Cancer Drugs 1995, 6 Suppl. 6, 7-13.
-
(1995)
Anti-Cancer Drugs
, vol.6
, Issue.SUPPL. 6
, pp. 7-13
-
-
Plunkett, W.1
Huang, P.2
Gandhi, V.3
-
11
-
-
0028799108
-
Gemcitabine: Metabolism, mechanisms of action, and self-potentiation
-
Plunkett, W.; Huang, P.; Xu, Y. Z.; Heinemann, V.; Grunewald, R.; Gandhi, V. Gemcitabine: Metabolism, mechanisms of action, and self-potentiation. Semin. Oncol. 1995, 22, 3-10.
-
(1995)
Semin. Oncol
, vol.22
, pp. 3-10
-
-
Plunkett, W.1
Huang, P.2
Xu, Y.Z.3
Heinemann, V.4
Grunewald, R.5
Gandhi, V.6
-
12
-
-
0030915362
-
Gemcitabine: Future prospects of single-agent and combination studies
-
van Moorsel, C. J.; Peters, G. J.; Pinedo, H. M. Gemcitabine: Future prospects of single-agent and combination studies. Oncologist 1997, 2, 127-134.
-
(1997)
Oncologist
, vol.2
, pp. 127-134
-
-
van Moorsel, C.J.1
Peters, G.J.2
Pinedo, H.M.3
-
13
-
-
34547572902
-
Clinical activity of gemcitabine as a single agent and in combination
-
Peters, G. J, Ed, Humana Press, Inc, Totowa, NJ
-
Kroep, J. R.; Peters, G. J.; Nagourney, R. A. Clinical activity of gemcitabine as a single agent and in combination. In Cancer Drug Discovery and Development: Deoxynucleoside Analogs in Cancer Therapy; Peters, G. J., Ed.; Humana Press, Inc.: Totowa, NJ, 2006; pp 253-287.
-
(2006)
Cancer Drug Discovery and Development: Deoxynucleoside Analogs in Cancer Therapy
, pp. 253-287
-
-
Kroep, J.R.1
Peters, G.J.2
Nagourney, R.A.3
-
14
-
-
0023783698
-
Comparison of the cellular pharmacokinetics and toxicity of 2′,2′- difluorodeoxycytidine and 1-β-D-arabinofuranosylcytosine
-
Heinemann, V.; Hertel, L. W.; Grindey, G. B.; Plunkett, W. Comparison of the cellular pharmacokinetics and toxicity of 2′,2′- difluorodeoxycytidine and 1-β-D-arabinofuranosylcytosine. Cancer Res. 1988, 48, 4024-4031.
-
(1988)
Cancer Res
, vol.48
, pp. 4024-4031
-
-
Heinemann, V.1
Hertel, L.W.2
Grindey, G.B.3
Plunkett, W.4
-
15
-
-
0031834417
-
Regulation of deoxycytidine kinase by deoxycytidine and deoxycytidine 5′-triphosphate in whole leukemia and tumor cells
-
Heinemann, V.; Schulz, L.; Issels, R. D.; Wilmanns, W. Regulation of deoxycytidine kinase by deoxycytidine and deoxycytidine 5′-triphosphate in whole leukemia and tumor cells. Adv. Exp. Med. Biol. 1998, 431, 249-253.
-
(1998)
Adv. Exp. Med. Biol
, vol.431
, pp. 249-253
-
-
Heinemann, V.1
Schulz, L.2
Issels, R.D.3
Wilmanns, W.4
-
16
-
-
0034470702
-
The role of deoxycytidine kinase in gemcitabine cytotoxicity
-
van der Wilt, C. L.; Kroep, J. R.; Bergman, A. M.; Loves, W. J.; Alvarez, E.; Talianidis, I.; Eriksson, S.; van Groeningen, C. J.; Pinedo, H. M.; Peters, G. J. The role of deoxycytidine kinase in gemcitabine cytotoxicity. Adv. Exp. Med. Biol. 2000, 486, 287-290.
-
(2000)
Adv. Exp. Med. Biol
, vol.486
, pp. 287-290
-
-
van der Wilt, C.L.1
Kroep, J.R.2
Bergman, A.M.3
Loves, W.J.4
Alvarez, E.5
Talianidis, I.6
Eriksson, S.7
van Groeningen, C.J.8
Pinedo, H.M.9
Peters, G.J.10
-
17
-
-
0036462584
-
Determinants of resistance to 2′,2′-difluorodeoxycytidine (gemcitabine)
-
Bergman, A. M.; Pinedo, H. M.; Peters, G. J. Determinants of resistance to 2′,2′-difluorodeoxycytidine (gemcitabine). Drug Resist. Updates 2002, 5, 19-33.
-
(2002)
Drug Resist. Updates
, vol.5
, pp. 19-33
-
-
Bergman, A.M.1
Pinedo, H.M.2
Peters, G.J.3
-
18
-
-
0036023450
-
Role of deoxycytidine kinase (dCK) activity in gemcitabine's radioenhancement in mice and human cell lines in vitro
-
Gregoire, V.; Rosier, J. F.; De Bast, M.; Bruniaux, M.; De Coster, B.; Octave-Prignot, M.; Scalliet, P. Role of deoxycytidine kinase (dCK) activity in gemcitabine's radioenhancement in mice and human cell lines in vitro. Radiother. Oncol. 2002, 63, 329-338.
-
(2002)
Radiother. Oncol
, vol.63
, pp. 329-338
-
-
Gregoire, V.1
Rosier, J.F.2
De Bast, M.3
Bruniaux, M.4
De Coster, B.5
Octave-Prignot, M.6
Scalliet, P.7
-
19
-
-
0030606020
-
Nucleoside and nucleobase transport systems of mammalian cells
-
Griffith, D. A.; Jarvis, S. M. Nucleoside and nucleobase transport systems of mammalian cells. Biochim. Biophys. Acta 1996, 1286, 153-181.
-
(1996)
Biochim. Biophys. Acta
, vol.1286
, pp. 153-181
-
-
Griffith, D.A.1
Jarvis, S.M.2
-
21
-
-
0029557153
-
The influence of BIBW22BS, a dipyridamole derivative, on the antiproliferative effects of 5-fluorouracil, methotrexate and gemcitabine in vitro and in human tumour xenografts
-
Jansen, W. J.; Pinedo, H. M.; van der Wilt, C. L.; Feller, N.; Bamberger, U.; Boven, E. The influence of BIBW22BS, a dipyridamole derivative, on the antiproliferative effects of 5-fluorouracil, methotrexate and gemcitabine in vitro and in human tumour xenografts. Eur. J. Cancer 1995, 31A, 2313-2319.
-
(1995)
Eur. J. Cancer
, vol.31 A
, pp. 2313-2319
-
-
Jansen, W.J.1
Pinedo, H.M.2
van der Wilt, C.L.3
Feller, N.4
Bamberger, U.5
Boven, E.6
-
22
-
-
33845373700
-
Allyloxycarbonyl group: A versatile blocking group for nucleoside synthesis
-
Hayakawa, Y.; Kato, H.; Uchiyama, M.; Kajino, H.; Noyori, R. Allyloxycarbonyl group: A versatile blocking group for nucleoside synthesis. J. Org. Chem. 1986, 51, 2400-2402.
-
(1986)
J. Org. Chem
, vol.51
, pp. 2400-2402
-
-
Hayakawa, Y.1
Kato, H.2
Uchiyama, M.3
Kajino, H.4
Noyori, R.5
-
23
-
-
0000584361
-
A convenient way to N- allyloxycarbonyl protected adenosine and cytidine derivatives
-
Heidenhain, S. B.; Hayakawa, Y. A convenient way to N- allyloxycarbonyl protected adenosine and cytidine derivatives. Synlett 1998, 853-854.
-
(1998)
Synlett
, pp. 853-854
-
-
Heidenhain, S.B.1
Hayakawa, Y.2
-
24
-
-
3142683066
-
A novel method for the preparation of nucleoside triphosphates from activated nucleoside phosphoramidates
-
Wu, W.; Freel Meyers, C. L.; Borch, R. F. A novel method for the preparation of nucleoside triphosphates from activated nucleoside phosphoramidates. Org. Lett. 2004, 6, 2257-2260.
-
(2004)
Org. Lett
, vol.6
, pp. 2257-2260
-
-
Wu, W.1
Freel Meyers, C.L.2
Borch, R.F.3
-
25
-
-
0012910966
-
A novel method for the preparation of nucleoside diphosphates
-
Meyers, C. L.; Borch, R. F. A novel method for the preparation of nucleoside diphosphates. Org. Lett. 2001, 3, 3765-3768.
-
(2001)
Org. Lett
, vol.3
, pp. 3765-3768
-
-
Meyers, C.L.1
Borch, R.F.2
-
26
-
-
0037016739
-
Mutation of residue 33 of human equilibrative nucleoside transporters 1 and 2 alters sensitivity to inhibition of transport by dilazep and dipyridamole
-
Visser, F.; Vickers, M. F.; Ng, A. M.; Baldwin, S. A.; Young, J. D.; Cass, C. E. Mutation of residue 33 of human equilibrative nucleoside transporters 1 and 2 alters sensitivity to inhibition of transport by dilazep and dipyridamole. J. Biol. Chem. 2002, 277, 395-401.
-
(2002)
J. Biol. Chem
, vol.277
, pp. 395-401
-
-
Visser, F.1
Vickers, M.F.2
Ng, A.M.3
Baldwin, S.A.4
Young, J.D.5
Cass, C.E.6
-
27
-
-
0028067217
-
Development and molecular characterization of a 2′,2′-difluorodeoxycytidine- resistant variant of the human ovarian carcinoma cell line A2780
-
Ruiz van Haperen, V. W.; Veerman, G.; Eriksson, S.; Boven, E.; Stegmann, A. P.; Hermsen, M.; Vermorken, J. B.; Pinedo, H. M.; Peters, G. J. Development and molecular characterization of a 2′,2′-difluorodeoxycytidine- resistant variant of the human ovarian carcinoma cell line A2780. Cancer Res. 1994, 54, 4138-4143.
-
(1994)
Cancer Res
, vol.54
, pp. 4138-4143
-
-
Ruiz van Haperen, V.W.1
Veerman, G.2
Eriksson, S.3
Boven, E.4
Stegmann, A.P.5
Hermsen, M.6
Vermorken, J.B.7
Pinedo, H.M.8
Peters, G.J.9
-
28
-
-
0025878872
-
Comparison of the sulforhodamine B protein and tetrazolium (MTT) assays for in vitro chemosensitivity testing
-
Keepers, Y. P.; Pizao, P. E.; Peters, G. J.; van Ark-Otte, J.; Winograd, B.; Pinedo, H. M. Comparison of the sulforhodamine B protein and tetrazolium (MTT) assays for in vitro chemosensitivity testing. Eur. J. Cancer 1991, 27, 897-900.
-
(1991)
Eur. J. Cancer
, vol.27
, pp. 897-900
-
-
Keepers, Y.P.1
Pizao, P.E.2
Peters, G.J.3
van Ark-Otte, J.4
Winograd, B.5
Pinedo, H.M.6
-
29
-
-
0032902787
-
Differential methotrexate resistance in childhood T- versus common/preB-acute lymphoblastic leukemia can be measured by an in situ thymidylate synthase inhibition assay, but not by the MTT assay
-
Rots, M. G.; Pieters, R.; Kaspers, G. J.; van Zantwijk, C. H.; Noordhuis, P.; Mauritz, R.; Veerman, A. J.; Jansen, G.; Peters, G. J. Differential methotrexate resistance in childhood T- versus common/preB-acute lymphoblastic leukemia can be measured by an in situ thymidylate synthase inhibition assay, but not by the MTT assay. Blood 1999, 93, 1067-1074.
-
(1999)
Blood
, vol.93
, pp. 1067-1074
-
-
Rots, M.G.1
Pieters, R.2
Kaspers, G.J.3
van Zantwijk, C.H.4
Noordhuis, P.5
Mauritz, R.6
Veerman, A.J.7
Jansen, G.8
Peters, G.J.9
-
30
-
-
0002831066
-
Pretreatment deoxycytidine kinase levels predict in vivo gemcitabine sensitivity
-
Kroep, J. R.; Loves, W. J.; van der Wilt, C. L.; Alvarez, E.; Talianidis, I.; Boven, E.; Braakhuis, B. J.; van Groeningen, C. J.; Pinedo, H. M.; Peters, G. J. Pretreatment deoxycytidine kinase levels predict in vivo gemcitabine sensitivity. Mol. Cancer Ther. 2002, 1, 371-376.
-
(2002)
Mol. Cancer Ther
, vol.1
, pp. 371-376
-
-
Kroep, J.R.1
Loves, W.J.2
van der Wilt, C.L.3
Alvarez, E.4
Talianidis, I.5
Boven, E.6
Braakhuis, B.J.7
van Groeningen, C.J.8
Pinedo, H.M.9
Peters, G.J.10
|