Page last updated: 2024-08-21

quinazolines and Leukemia L5178

quinazolines has been researched along with Leukemia L5178 in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's4 (66.67)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dedhar, S; Freisheim, JH; Goldie, JH; Hynes, JB2
Boyle, FT; Jackman, AL; McCloskey, ML; Smith, MN; Stephens, TC; Waterman, SE1
Bartlett, CA; Boritzki, TJ; Hillard, JA; Howland, EF; Johnston, AL; Kosa, M; Margosiak, SA; Morse, CA; Shetty, BV; Webber, S1
Aherne, GW; Boyle, FT; Brunton, L; Jackman, AL; Jansen, G; Kimbell, R; Smith, MN; Stephens, TC; Wardleworth, JM1
Brown, SL; Kim, JH; Kim, SH1

Other Studies

6 other study(ies) available for quinazolines and Leukemia L5178

ArticleYear
Inhibition of a methotrexate-insensitive dihydrofolate reductase from L5178Y cells by substituted triazines and quinazolines.
    Biochemical pharmacology, 1983, Mar-01, Volume: 32, Issue:5

    Topics: Animals; Cells, Cultured; Folic Acid Antagonists; Leukemia L5178; Leukemia, Experimental; Methotrexate; Mice; Quinazolines; Triazines

1983
Use of murine L5178Y lymphoma thymidine kinase mutants for in vitro and in vivo antitumour efficacy evaluation of novel thymidylate synthase inhibitors.
    Advances in experimental medicine and biology, 1993, Volume: 338

    Topics: Animals; Antineoplastic Agents; Cell Survival; Drug Screening Assays, Antitumor; Folic Acid; Folic Acid Antagonists; Leukemia L5178; Mice; Mice, Inbred DBA; Mutation; Quinazolines; Structure-Activity Relationship; Thiophenes; Thymidylate Synthase; Tumor Cells, Cultured

1993
AG337, a novel lipophilic thymidylate synthase inhibitor: in vitro and in vivo preclinical studies.
    Cancer chemotherapy and pharmacology, 1996, Volume: 37, Issue:6

    Topics: Administration, Oral; Animals; Antimetabolites, Antineoplastic; Cell Cycle; Enzyme Inhibitors; Folic Acid Antagonists; Growth Inhibitors; Humans; Leukemia L1210; Leukemia L5178; Mice; Quinazolines; Rats; Solubility; Thymidylate Synthase

1996
Cellular pharmacology and in vivo activity of a new anticancer agent, ZD9331: a water-soluble, nonpolyglutamatable, quinazoline-based inhibitor of thymidylate synthase.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 1997, Volume: 3, Issue:6

    Topics: Animals; Antineoplastic Agents; Biological Transport; Cell Division; Female; Humans; Kinetics; Leucovorin; Leukemia L1210; Leukemia L5178; Methotrexate; Mice; Mice, Inbred DBA; Quinazolines; Thymidylate Synthase; Tumor Cells, Cultured; Tumor Stem Cell Assay

1997
The potentiation of radiation response in human colon carcinoma cells in vitro and murine lymphoma in vivo by AG337 (Thymitaq), a novel thymidylate synthase inhibitor.
    International journal of radiation oncology, biology, physics, 1998, Nov-01, Volume: 42, Issue:4

    Topics: Animals; Antimetabolites, Antineoplastic; Cell Survival; Drug Therapy, Combination; Enzyme Inhibitors; HT29 Cells; Humans; Leukemia L5178; Male; Mice; Mice, Inbred DBA; Quinazolines; Thymidylate Synthase

1998
Further studies on substituted quinazolines and triazines as inhibitors of a methotrexate-insensitive murine dihydrofolate reductase.
    Biochemical pharmacology, 1986, Apr-01, Volume: 35, Issue:7

    Topics: Animals; Cell Line; Chemical Phenomena; Chemistry; Leukemia L5178; Methotrexate; Mice; Quinazolines; Tetrahydrofolate Dehydrogenase; Triazines

1986