Results 121 to 130 of about 68,807 (327)

Zur Kenntniss der Pyrimidine [PDF]

open access: green, 1897
Siegfried Ruhemann, A. S. Hemmy
openalex   +1 more source

PYRIMIDINE NUCLEOSIDES AS PRECURSORS OF PYRIMIDINES IN POLYNUCLEOTIDES [PDF]

open access: yesJournal of Biological Chemistry, 1950
E. Hammarsten   +5 more
openaire   +1 more source

Synthesis and Metal‐Ion Binding Properties of Duplexes Containing Thymine Analogs with 1,2‐Diamine Groups

open access: yesChemBioChem, EarlyView.
The findings of thermal denaturation experiments indicate that duplexes containing thymine analogues with 1,2‐ethylenediamine side chains show stabilizing effects with six metal ions (e.g., Cu(II), Ni(II), Zn(II), Co(II), Cd(II)). The 1,2‐diamine side chain demonstrated to be useful as a new metal‐ion binding site. Thymidine analogue with a 1,2‐diamino
Takahiro Atsugi   +3 more
wiley   +1 more source

Synthesis and Antioxidant Activities of Novel Pyrimidine Acrylamides as Inhibitors of Lipoxygenase: Molecular Modeling and In Silico Physicochemical Studies

open access: yesMolecules
The pyrimidine ring is present in various biomolecules such as DNA and RNA bases, aminoacids, vitamins, etc. Additionally, many clinically used drugs including methotrexate and risperidone contain the pyrimidine heterocyclic scaffold as well.
Michail Saragatsis, Eleni Pontiki
doaj   +1 more source

Purine Chemistry in the Early RNA World at the Origins of Life: From RNA and Nucleobases Lesions to Current Key Metabolic Routes

open access: yesChemBioChem, EarlyView.
In the nascent processes of the beginnings and evolution of life, nucleobases and especially purines, ribonucleos(t)ides and primitive RNAs have been continuously modified. A RNA‐peptide world and key metabolic pathways probably have emerged from the corresponding chemical modifications resulting from adenine deamination, purine alkylation and ...
Jean‐Luc Décout   +1 more
wiley   +1 more source

Serendipitous Identification of Azine Anticancer Agents Using a Privileged Scaffold Morphing Strategy

open access: yesMolecules
The use of privileged scaffolds as a starting point for the construction of libraries of bioactive compounds is a widely used strategy in drug discovery and development.
Silvia Cesarini   +13 more
doaj   +1 more source

An Indole Dearomatization Strategy for the Synthesis of Pseudo‐Natural Products

open access: yesChemBioChem, Accepted Article.
The indole moiety is a privileged fragment that frequently populates existing bioactive compound collections. We describe the development of an indole‐dearomatization sequence and its application for library expansion of a collection of indole‐containing pseudo‐NPs.
Joseph G.F. Hoock   +13 more
wiley   +1 more source

Photo‐Promoted Nitrogen‐Centered Radical Mediated Intermolecular Aminative Carbonylation of Tertiary Allyl Alcohols to Access β‐Amino Ketones through (Hetero)Aryl Migration

open access: yesChemistryEurope, EarlyView.
A photocatalyzed aminative carbonylation of unactivated alkenes mediated by nitrogen radicals has been developed. Various β‐aminoketones were produced effectively from allyl alcohols containing different aromatic heterocycles. Abstract Carbon monoxide, as a crucial C1 synthon, has been widely used in the difunctionalization of alkenes.
Ming Hou   +4 more
wiley   +1 more source

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