Cited by 184Folate and B Vitamins ResearchColorectal Cancer Treatments and StudiesCancer therapeutics and mechanisms

From methotrexate to pemetrexed and beyond. A review of the pharmacodynamic and clinical properties of antifolates

Walling, Jackie·2006·Investigational New Drugs

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Crossref · 10.1007/s10637-005-4541-1

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352 of 352 references verified0 citation errors · 0 not checkable

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  • Aminopterin is the precursor of methotrexate and pemetrexed, folate analogues that inhibit one-carbon transfer reactions required for de novo nucleotide synthesis.

    “Aminopterin is the precursor of the currently used drugs methotrexate and pemetrexed, both of which are folate analogues that inhibit one-carbon transfer reactions required for de novo nucleotide synthesis (Figure 1, Figure 2a)(Walling, 2006).”

    From Targeting Metabolism for Cancer Therapy (2017) · cites this paper as Walling, 2006

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Authors
Walling, J.
Affiliations
University of Bristol (GB)
Corresponding author
Walling, Jackie
Venue
Investigational New Drugs
Published
2006-01
Volume
24
Issue
1
Pages
37-77
ISSN
  • 0167-6997 (ISSN-L)
  • 1573-0646
OpenAlex
W1993777583
Cited by
182
References
353
Citations by year
2026: 4 · 2025: 7 · 2024: 9 · 2023: 4 · 2022: 11 · 2021: 15 · 2020: 12 · 2019: 10 · 2018: 7 · 2017: 7 · 2016: 8 · 2015: 17 · 2014: 9 · 2013: 7 · 2012: 8
FWCI
1.55
Type
journal article
Language
en
Open access
closed
Locations
  • Investigational New Drugs (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Rheumatology › Folate and B Vitamins Research
  • Health Sciences › Medicine › Oncology › Colorectal Cancer Treatments and Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cancer therapeutics and mechanisms
Keywords
antifolate, methotrexate, pemetrexed, pharmacodynamics, clinical properties
MeSH terms
Pemetrexed, Antineoplastic Agents, Antineoplastic Combined Chemotherapy Protocols, Biological Transport, Folic Acid Antagonists, Glutamates, Guanine, Humans, Methotrexate, Neoplasms, Randomized Controlled Trials as Topic, Clinical Trials, Phase II as Topic, Clinical Trials, Phase III as Topic, Drug Resistance, Neoplasm

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