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1,10-Phenanthroline-4,7-diol | CAS:3922-40-5
1,10-Phenanthroline-4,7-diol
  • Name:1,10-Phenanthroline-4,7-diol
  • CAS:3922-40-5
  • Synonyms:
  • Molecular Formula:C12H8N2O2
  • Molecular Weight:212.20
  • EINESC:223-493-6

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Safety

Symbol(GHS) Xi
Hazard Codes R36/37/38
SDS/MSDS S26;S36

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Peer-Reviewed Papers
New bis(pyridyl)methane derivatives from 4-hydroxy-2-pyridones: synthesis and antitumoral activity.Maria Teresa Cocco et al.European journal of medicinal chemistry, 38(1), 37-47 (2003-02-21) Pharmacokinetics of 5-fluorouracil in elderly Japanese patients with cancer treated with S-1 (a combination of tegafur and dihydropyrimidine dehydrogenase inhibitor 5-chloro-2,4-dihydroxypyridine).K Fujita et al.Drug metabolism and disposition: the biological fate of chemicals, 37(7), 1375-1377 (2009-04-25) [Presynaptic effects of aminopyridines on the neuromuscular junction of vertebrates].J Molgó et al.Journal de pharmacologie, 16 Suppl 2, 109-144 (1985-01-01) Sample preparation and estimation of plasma concentration of 3-deazauridine by high-performance liquid chromatography.K T Lin et al.Therapeutic drug monitoring, 5(4), 491-496 (1983-01-01) Synthesis and antitumour activity of 4-hydroxy-2-pyridone derivatives.M T Cocco et al.European journal of medicinal chemistry, 35(5), 545-552 (2000-07-12) Effects of pyrimidine nucleoside phosphorylase inhibitors on hepatic fluoropyrimidine elimination in the rat.F P LaCreta et al.Cancer research, 49(10), 2567-2573 (1989-05-15) Structure-activity relationship of ligands of dihydrouracil dehydrogenase from mouse liver.F N Naguib et al.Biochemical pharmacology, 38(9), 1471-1480 (1989-05-01) Synthesis of diazaphenoxathiin nucleosides from 3-deazauridine and their chemical properties.M Kaneko et al.Nucleic acids symposium series, (12)(12), 13-16 (1983-01-01) Oxyfunctionalization of pyridine derivatives using whole cells of Burkholderia sp. MAK1.Jonita Stankevičiūtė et al.Scientific reports, 6, 39129-39129 (2016-12-17) Quantitative proteomics reveals reduction of endocytic machinery components in gliomas.Dominik P Buser et al.EBioMedicine, 46, 32-41 (2019-07-25)
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