Results 231 to 240 of about 121,011 (315)

DEGRADATION OF SUBSTITUTED PYRIMIDINE NUCLEOSIDES BY ESCHERICHIA COLI AND BACILLUS SUBTILIS

open access: hybrid, 1954
Irving J. Slotnick   +2 more
openalex   +1 more source

S‐Methyl Methanethiosulfonate, the Main Human Metabolite of S‐Methyl‐L‐Cysteine Sulfoxide, Alters Energy Metabolism in Prostate Cancer Cells

open access: yesMolecular Nutrition &Food Research, EarlyView.
In this study, we show that the sulfur compound commonly found in cruciferous and allium vegetables and the main human metabolite of S‐methyl‐L‐cysteine sulfoxide, called S‐methyl methanethiosulfonate (MMTSO), alters energy metabolism in DU145 prostate cancer cells.
Gemma Beasy   +8 more
wiley   +1 more source

Pyrimidine Derivatives. I

open access: bronze, 1951
Masaiti Yanagita, SEIGO FUKUSHIMA
openalex   +2 more sources

A Universal Method for the Synthesis of new Heterocyclic Systems: Pyrimido[2,1‐f][1,2,4]triazines

open access: yesChemistryOpen, EarlyView.
The synthesis of pyrimido[2,1‐f][1,2,4]triazines opens up new prospects for the synthesis of many new unique heterocyclic systems. The construction of these two cycles on any other cycles and heterocycles leads to completely new heterocyclic systems. Abstract The synthesis of pyrimido[2,1‐f][1,2,4]triazines was performed in four steps.
Samvel N. Sirakanyan   +7 more
wiley   +1 more source

A Systematic Review of Synthetic and Anticancer and Antimicrobial Activity of Quinazoline/Quinazolin‐4‐one Analogues

open access: yesChemistryOpen, EarlyView.
Quinazoline represents an important class of heterocycles with diverse medicinal and pharmacological significance. This review systematically examines scholarly efforts toward understanding different synthetic pathways emphasizing the role of metal and non‐metal catalysts including some miscellaneous reagents employed in the synthesis of quinazoline ...
Neha Manhas   +4 more
wiley   +1 more source

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