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Chemical Research in Toxicology
|
October 20, 1998
A monofunctional derivative of melphalan: preparation, DNA alkylation products, and determination of the specificity of monoclonal antibodies that recognize melphalan-DNA adducts
M J Tilby, H McCartney, K A Gould, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
July 13, 2001
In vitro and in vivo properties of novel nucleoside transport inhibitors with improved pharmacological properties that potentiate antifolate activity
P G Smith, H D Thomas, H C Barlow, et al.
British Journal of Cancer
|
September 1, 1999
Potentiation of the cytotoxicity of thymidylate synthase (TS) inhibitors by dipyridamole analogues with reduced alpha1-acid glycoprotein binding
N J Curtin, K J Bowman, R N Turner, et al.
Chemical Research in Toxicology
|
December 22, 1998
Identification of novel metabolites of butadiene monoepoxide in rats and mice
K A Richardson, M M Peters, R H Megens, et al.
Journal of Medicinal Chemistry
|
November 7, 2000
Resistance-modifying agents. 9. Synthesis and biological properties of benzimidazole inhibitors of the DNA repair enzyme poly(ADP-ribose) polymerase
A W White, R Almassy, A H Calvert, et al.
British Journal of Cancer
|
October 27, 2005
Preclinical pharmacokinetics and metabolism of a novel prototype DNA-PK inhibitor NU7026
B P Nutley, N F Smith, A Hayes, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 31, 2000
Resistance-modifying agents. Part 7: 2,6-disubstituted-4,8-dibenzylaminopyrimido[5,4-d]pyrimidines that inhibit nucleoside transport in the presence of alpha1-acid glycoprotein (AGP)
H C Barlow, K J Bowman, N J Curtin, et al.
Journal of Medicinal Chemistry
|
November 7, 2000
Resistance-modifying agents. 8. Inhibition of O(6)-alkylguanine-DNA alkyltransferase by O(6)-alkenyl-, O(6)-cycloalkenyl-, and O(6)-(2-oxoalkyl)guanines and potentiation of temozolomide cytotoxicity in vitro by O(6)-(1-cyclopentenylmethyl)guanine
R J Griffin, C E Arris, C Bleasdale, et al.
Journal of Medicinal Chemistry
|
August 24, 2000
Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles
C E Arris, F T Boyle, A H Calvert, et al.
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Showing results (31-40 of 39) with videos related to
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You have reached the last page of results.
This site can display upto 39 results.
Chemical Research in Toxicology
|
October 20, 1998
A monofunctional derivative of melphalan: preparation, DNA alkylation products, and determination of the specificity of monoclonal antibodies that recognize melphalan-DNA adducts
M J Tilby, H McCartney, K A Gould, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
July 13, 2001
In vitro and in vivo properties of novel nucleoside transport inhibitors with improved pharmacological properties that potentiate antifolate activity
P G Smith, H D Thomas, H C Barlow, et al.
British Journal of Cancer
|
September 1, 1999
Potentiation of the cytotoxicity of thymidylate synthase (TS) inhibitors by dipyridamole analogues with reduced alpha1-acid glycoprotein binding
N J Curtin, K J Bowman, R N Turner, et al.
Chemical Research in Toxicology
|
December 22, 1998
Identification of novel metabolites of butadiene monoepoxide in rats and mice
K A Richardson, M M Peters, R H Megens, et al.
Journal of Medicinal Chemistry
|
November 7, 2000
Resistance-modifying agents. 9. Synthesis and biological properties of benzimidazole inhibitors of the DNA repair enzyme poly(ADP-ribose) polymerase
A W White, R Almassy, A H Calvert, et al.
British Journal of Cancer
|
October 27, 2005
Preclinical pharmacokinetics and metabolism of a novel prototype DNA-PK inhibitor NU7026
B P Nutley, N F Smith, A Hayes, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 31, 2000
Resistance-modifying agents. Part 7: 2,6-disubstituted-4,8-dibenzylaminopyrimido[5,4-d]pyrimidines that inhibit nucleoside transport in the presence of alpha1-acid glycoprotein (AGP)
H C Barlow, K J Bowman, N J Curtin, et al.
Journal of Medicinal Chemistry
|
November 7, 2000
Resistance-modifying agents. 8. Inhibition of O(6)-alkylguanine-DNA alkyltransferase by O(6)-alkenyl-, O(6)-cycloalkenyl-, and O(6)-(2-oxoalkyl)guanines and potentiation of temozolomide cytotoxicity in vitro by O(6)-(1-cyclopentenylmethyl)guanine
R J Griffin, C E Arris, C Bleasdale, et al.
Journal of Medicinal Chemistry
|
August 24, 2000
Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles
C E Arris, F T Boyle, A H Calvert, et al.
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