Results 1 to 10 of about 68,708 (233)

Studies in pyrimidine metabolism [PDF]

open access: greenJournal of Biological Chemistry, 1920
By partial hydrolysis of yeast nucleic acid, preparations containing pyrimidines as the only nitrogenous constituents were prepared and administered to rabbits. Uracil nucleoside when administered per os, subcutaneously or intraperitoneally caused an increased excretion of urea often much more than enough to account for the nitrogen administered.
Darrell M. Wilson
openalex   +6 more sources

A Search for Interstellar Pyrimidine [PDF]

open access: yesMon.Not.Roy.Astron.Soc.345:650,2003, 2003
We have searched three hot molecular cores for submillimeter emission from the nucleic acid building-block pyrimidine. We obtain upper limits to the total pyrimidine (beam-averaged) column densities towards Sgr B2(N), Orion KL and W51 e1/e2 of 1.7E+14 cm^{-2}, 2.4E+14 cm^{-2} and 3.4E+14 cm^{-2}, respectively.
H. C. Huang   +6 more
arxiv   +5 more sources

Pyrimidines: A New Versatile Molecule in the Drug Development Field, Scope, and Future Aspects [PDF]

open access: yesPharmaceuticals
Pyrimidine is a moiety that occurs in living organisms and has a variety of significant biological properties in pharmacology. Due to the easy handling of synthesis, easily available precursor, and less duration for the reaction, for the synthesis, not ...
Katharigatta N. Venugopala, Vinuta Kamat
doaj   +2 more sources

Review on the Synthesis and Therapeutic Potential of Pyrido[2,3-d], [3,2-d], [3,4-d] and [4,3-d]pyrimidine Derivatives

open access: yesPharmaceuticals, 2022
The objective of this review is to list the structures composed of a pyridopyrimidine moiety which have shown a therapeutic interest or have already been approved for use as therapeutics.
Joana F. Campos   +2 more
doaj   +1 more source

The study of the apoptogenic effect of pyrimidine derivatives on murine leukemia cells [PDF]

open access: yesArchive of Oncology, 2005
BACKGROUND: In the light of the recent findings concerning the role of apoptosis and of tumor cell enzymes in cancer chemotherapy, the interest in pyrimidine derivatives has greatly increased.
Gorneva Galina   +3 more
doaj   +1 more source

Facile preparation and conversion of 4,4,4-trifluorobut-2-yn-1-ones to aromatic and heteroaromatic compounds

open access: yesBeilstein Journal of Organic Chemistry, 2021
The concise preparation of 4,4,4-trifluorobut-2-yn-1-ones by the oxidation of the readily accessible corresponding propargylic alcohols as well as their utilization as Michael acceptors for the construction of aromatic and heteroaromatic compounds are ...
Takashi Yamazaki   +3 more
doaj   +1 more source

REVIEW OF PYRIMIDINE DERIVATIVES AS PHARMACOLOGICALLY ACTIVE COMPOUNDS

open access: yesJuvenis Scientia, 2022
Pyrimidine derivatives represent an extensive class of organic compounds that contain in their structure a six-membered heterocycle with two nitrogen atoms at positions 1 and 3.
A. S. Chiriapkin
doaj   +1 more source

A New Class of Uracil–DNA Glycosylase Inhibitors Active against Human and Vaccinia Virus Enzyme

open access: yesMolecules, 2021
Uracil–DNA glycosylases are enzymes that excise uracil bases appearing in DNA as a result of cytosine deamination or accidental dUMP incorporation from the dUTP pool. The activity of Family 1 uracil–DNA glycosylase (UNG) activity limits the efficiency of
Inga R. Grin   +10 more
doaj   +1 more source

A New Pyrimidine Schiff Base with Selective Activities against Enterococcus faecalis and Gastric Adenocarcinoma

open access: yesMolecules, 2021
Enterococcus faecalis is known as a significant nosocomial pathogen due to its natural resistance to many antibacterial drugs. Moreover, it was found that E. faecalis infection causes inflammation, production of reactive oxygen species, and DNA damage to
Marcin Stolarczyk   +6 more
doaj   +1 more source

Annellation of Triazole and Tetrazole Systems onto Pyrrolo[2,3-d]pyrimidines: Synthesis of Tetrazolo[1,5-c]-pyrrolo[3,2-e]-pyrimidines and Triazolo[1,5-c]pyrrolo-[3,2-e]pyrimidines as Potential Antibacterial Agents

open access: yesMolecules, 2002
Syntheses of several novel 4-chloropyrrolo[2,3-d]pyrimidines (1), 4-hydrazinopyrrolo[2,3-d]pyrimidines (2) and 3-amino-4-iminopyrrolo[2,3-d]pyrimidines (7) and their use in the synthesis of tetrazolo[1,5-c]pyrrolo[3,2-e]pyrimidines (3) and triazolo[1,5-c]
Rina D. Shah, Chaitanya G. Dave
doaj   +1 more source

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