3 Some Pyrimidines of Biological and Medicinal Interest—I
References (929)
- et al.
J. Biol. Chem.
(1948) - et al.
J. Biol. Chem.
(1950) - et al.
J. Biol. Chem.
(1952) - et al.
J. Biol. Chem.
(1950) Am. J. Clin. Nutr.
(1955)J. Biol. Chem.
(1963)- et al.
J. Pharm. Sci.
(1965) - et al.
Biochim. Biophys. Acta
(1961) - et al.
Clin. Chim. Acta
(1965) - et al.
J. Pharm. Sci.
(1965)
J. Org. Chem.
Brit. J. Pharmacol.
Brit. Med. J.
J. Biol. Chem.
Public Health Rept (SUPHS
Am. J. Ophthalmol.
Hakko Kogaku Zasshi
Chem. Abstr.
Trans. N.Y. Acad. Sci.
Nature
Naturwissenschqften
J. Org. Chem.
Proc. Roy. Australian Chem. Inst.
Giorn. Fis. Chim. Storia Nat. (Pavia), decada seconda.
Compt. Rend.
Compt. Rend.
Bull. Soc. Chim. France
Chem. Ber.
Nature
Ann. N.Y. Acad. Sci.
Proc. 5th Intern. Congr. Biochem. Moscow, 1961
Rev. Franc. Etudes Clin. Biol.
J. Med. Pharm. Chem.
Proc. Soc. Exptl Biol. Med.
Cancer Chemotherapy Rept.
J. Biol. Chem.
Advan. Enzymol.
Mol. Pharmacol.
J. Med. Chem.
J. Biol. Chem.
Biochemistry
Ann. Trop. Med. Parasitol.
Ann. Trop. Med. Parasitol.
Brit. J. Pharmacol.
Brit. J. Pharmacol.
Proc. Soc. Exptl Biol. Med.
Nature
Brit. J. Pharmacol.
J. Am. Chem. Soc.
Chem. Abstr.
Cited by (80)
Transition-metal catalyzed modification of nucleosides
2018, Palladium-Catalyzed Modification of Nucleosides, Nucleotides and OligonucleotidesCare for vesicant injuries—Not just historic footnotes
2017, Burns OpenCitation Excerpt :Approximately 90% of patients recover from their ocular injuries, although some can have lingering photosensitivity and conjunctivitis [34]. With regard to the chemical implicated in the current case report, 2,4,6-trichloropyrimidine, a literature search on the subject yielded few returns, both from 50 or more years ago [19,35]. One case series described some hypersensitivity-like reactions following repeat exposures to the chemical.
Synthesis, structural elucidation, microbial, antioxidant and nuclease activities of some novel divalent M(II) complexes derived from 5-fluorouracil and L-tyrosine
2017, Journal of Saudi Chemical SocietyCitation Excerpt :The pyrimidine nitrogen base analogues of uracil, cytosine and thymine are useful to kill or retard the cancer cells in living organisms. Mostly, 5-fluorouracil (Trade name: Adrucil, Carac) is used to kill or destroy the tumor cells [9,36] in colon, rectum, breast, stomach and pancreas cells. In addition, it inhibits and stimulates incorporation of amino acids into nucleoprotein, bacterial cell wall synthesis and thymidine into DNA, respectively [9].
Synthesis, structural elucidation, biological, antioxidant and nuclease activities of some 5-Fluorouracil-amino acid mixed ligand complexes
2015, Spectrochimica Acta - Part A: Molecular and Biomolecular SpectroscopyCitation Excerpt :Their derivatives are the basic building units of nucleic acids, RNA and DNA [3–5]. Recently, the compounds containing pyrimidine moiety have been investigated widely for the design and synthesis of various drugs in clinical, biological, pharmacological, medicinal and therapeutical fields [6]. These compounds were found to have wide range of applications like antibacterial, fungicidal, antitumor, antiviral, anti-inflammatory, antipyretic, antimitotic, antimetabolites, antithyroidal and surface anaesthesia activities [7–9].