Page last updated: 2024-10-26

ethoxyresorufin and Benign Neoplasms

ethoxyresorufin has been researched along with Benign Neoplasms in 1 studies

ethoxyresorufin: structure

Research Excerpts

ExcerptRelevanceReference
"These data indicate that cancer patients treated with DTIC who possess any of the CYP1A1-T461N and I462V variants or the CYP1A2-F186L, D348N, I386F, R431W, and R456H variants are likely to have decreased prodrug activation, and hence may respond less favorably to DTIC treatment compared with individuals with wild-type CYP1A alleles."1.43Impaired dacarbazine activation and 7-ethoxyresorufin deethylation in vitro by polymorphic variants of CYP1A1 and CYP1A2: implications for cancer therapy. ( Korprasertthaworn, P; Lewis, BC; Miners, JO, 2016)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lewis, BC1
Korprasertthaworn, P1
Miners, JO1

Other Studies

1 other study available for ethoxyresorufin and Benign Neoplasms

ArticleYear
Impaired dacarbazine activation and 7-ethoxyresorufin deethylation in vitro by polymorphic variants of CYP1A1 and CYP1A2: implications for cancer therapy.
    Pharmacogenetics and genomics, 2016, Volume: 26, Issue:10

    Topics: Antineoplastic Agents, Alkylating; Catalysis; Cytochrome P-450 CYP1A1; Cytochrome P-450 CYP1A2; Daca

2016