Paper
Thymidine 5'-O-pivaloate. A prodrug derivative of thymidine with potential applications in high-dose methotrexate therapy.
Published May 1, 1979 · W. Ensminger, A. Rosowsky
Biochemical pharmacology
Q1 SJR score
4
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
Thymidine 5'-O-pivaloate shows potential in preventing toxicity from high-dose methotrexate therapy, with increased survival in leukemic mice treated with high-dose MTX.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
Thymidine rescue of high-dose methotrexate in humans.
Thymidine is an effective rescue agent for high-dose methotrexate in humans, with mucositis and myelosuppression being the major toxicities, and DNA synthesis recovery occurring 24 hours after starting rescue.
1978·72citations·Stephen B. Howell et al.·Cancer research
Cancer research
Enhancement of the therapeutic effectiveness of methotrexate and protection of normal proliferating tissues with purines and pyrimidines.
Methotrexate treatment combined with purine and pyrimidine protection can be more effective and protect normal proliferating tissues in tumor-bearing mice than conventional treatment.
1977·43citations·K. Harrap et al.·Chemico-biological interactions
Chemico-biological interactions
The prevention of methotrexate toxicity by thymidine infusions in humans.
Thymidine infusions significantly protect against methotrexate toxicity in metastatic cancer patients, offering significant protection and preventing bone marrow dysfunction during MTX infusions.
1977·107citations·W. Ensminger et al.·Cancer research
Cancer research
Blood thymidine level and iododeoxyuridine incorporation and reutilization in DNA in mice given long-acting thymidine pellets.
Long-acting thymidine pellets can effectively suppress iododeoxyuridine incorporation and reutilization in DNA, potentially benefiting cancer research.
1976·16citations·D. Lee et al.·Cancer research
Cancer research
The reversal of methotrexate cytotoxicity to mouse bone marrow cells by leucovorin and nucleosides.
Leucovorin can reverse methotrexate toxicity to mouse bone marrow cells, while nucleosides show noncompetitive rescue, potentially impacting chemotherapeutic protocols.
1976·172citations·H. Pinedo et al.·Cancer research
Cancer research
Enzyme pattern directed chemotherapy. The effects of combinations of methotrexate, 5-fluorodeoxyuridine and thymidine on rat hepatoma cells in vitro.
Combinations of methotrexate and 5-fluorodeoxyuridine show summation in slow-growing hepatomas, but less than additive in rapidly growing lines due to competing enzyme patterns.
1976·35citations·R. Jackson et al.·Biochemical pharmacology
Biochemical pharmacology
Methotrexate inhibition of CCRF-CEM cultures of human lymphoblasts.
Methotrexate inhibition of human lymphoblast growth is due to the inhibition of dihydrofolate reductase, not thymidine deficiency.
1975·20citations·D. Roberts et al.·European journal of cancer
European journal of cancer
METHOTREXATE‐THYMIDINE TREATMENT OF MURINE LEUKEMIA *
Thymidine protects mice with leukemia L1210 from methotrexate toxicity without impairing antitumor activity, increasing the therapeutic index of methotrexate by three-fold.
1975·8citations·M. Tattersall et al.·Annals of the New York Academy of Sciences
Annals of the New York Academy of Sciences
Deoxyribonucleoside Triphosphates in Human Cells: Changes in Disease and Following Exposure to Drugs
Deoxyribonucleoside triphosphate concentrations in human cells can be altered by diseases and certain drugs, with folinic acid potentially reversing these effects.
1975·52citations·M. Tattersall et al.·European Journal of Clinical Investigation
European Journal of Clinical Investigation
Citations
A convenient protection for 4-oxopyrimidine moieties in nucleosides by the pivaloyl group
The pivaloyl group provides rapid and efficient protection for the N3 position of thymidine and uridine, with excellent regioselectivity for sugar or thymine moiety, depending on the amines used.
2010·4citations·M. Sobkowski·Collection of Czechoslovak Chemical Communications
Collection of Czechoslovak Chemical Communications
Syntheses and Biological Evaluation of 5′-O-Myristoyl Derivatives of Thymidine against Human Immunodeficiency Virus
5′-O-(12-Azidododecanoyl)thymidine exhibited moderate anti-HIV activity against T4 lymphocytes, with a partition coefficient in the 4.6-4.8 range being optimal for anti-HIV activity.
1997·7citations·K. Parang et al.·Antiviral Chemistry and Chemotherapy
Antiviral Chemistry and Chemotherapy
Selective pivaloylation of 2-acetamido-2-deoxy sugars.
Selective pivaloylation of 2-acetamido-2-deoxy sugars, their methyl glycosides, and N-acetyl-d-muramic acid methyl -glycosides can produce various structures and acylation orders.
1988·17citations·D. Ljevakovic et al.·Carbohydrate research
Carbohydrate research