Results 71 to 80 of about 68,963 (231)

Synthesis, Characterization and Docking Study of Novel Pyrimidine Derivatives as Anticancer Agents

open access: yesIndonesian Journal of Chemistry, 2020
New compounds 5 and 9 using DNA bases e.g. Adenine 1 and Guanine 6 derivatives have been synthesized. The use of simple methods to synthesize compounds 5 and 9 were done using pyrimidine as an alternative DNA base ring.
Manal Mohamed Talaat El-Saidi   +5 more
doaj   +1 more source

Engineered Peptide Self‐Assembled Nanofibers for Enhanced STING Activation: A Promising Nanodelivery Platform for Immunotherapy of Pediatric Solid Tumors

open access: yesAdvanced Science, EarlyView.
An engineered peptide self‐assembled nanofiber platform, designed to replicate STING–cGAMP binding motifs, facilitates pH‐responsive cytosolic delivery of cGAMP, enhances the endoplasmic reticulum with high efficiency, and robustly activates the STING pathway.
Yubin He   +6 more
wiley   +1 more source

Guanidinium phenylarsonate–guanidine–water (1/1/2) [PDF]

open access: yes, 2010
In the structure of the title compound, CH6N3+·C6H6AsO3−·CH5N3·2H2O, the phenylarsonate anion participates in two R22(8) cyclic hydrogen-bonding interactions, one with a guanidinium cation, the other with a guanidine ...
Urs D. Wermuth   +3 more
core   +1 more source

Dry‑Contact Trimming for All‑Perovskite Tandem Solar Cells via Solid‑Solution Homogenization

open access: yesAdvanced Energy Materials, EarlyView.
Narrow‐bandgap Sn–Pb perovskites are promising bottom absorbers for all‐perovskite tandems but suffer from Sn‐rich surfaces and depth‐dependent lattice/compositional inhomogeneity. Layered‐perovskite‐assisted dry‐contact trimming removes Sn‐rich surface species and reconfigures the Sn–Pb absorber, enabling efficient charge collection, reduced voltage ...
Woocheol Han   +10 more
wiley   +1 more source

Quantification of guanidine in environmental samples using benzoin derivatization and LC-MS analysis

open access: yesMethodsX
The recent discovery of guanidine-dependent riboswitches in many microbes raised interest in the biological function and metabolism of this nitrogen-rich compound.
Richard Gruseck   +4 more
doaj   +1 more source

Exploring 3D-QSAR to identify potential small molecule for treating Alzheimer disease: A case study with b-secretase inhibitors [PDF]

open access: yesScripta Medica
Background/Aim: One of the most common neurological conditions that results in dementia is Alzheimer disease. The current treatment options for Alzheimer disease include acetylcholinesterase (AChE) and -methyl-D-aspartate (NMDA) inhibitors, but there is ...
More Uttam A.   +9 more
doaj   +1 more source

Modification of the existing maximum residue level for dodine in honey

open access: yesEFSA Journal
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Arysta Lifescience Benelux Srl submitted a request to the competent national authority in Spain to modify the existing maximum residue level (MRL) for the active substance dodine ...
European Food Safety Authority (EFSA)   +10 more
doaj   +1 more source

Synthesis of rigidified flavin–guanidinium ion conjugates and investigation of their photocatalytic properties

open access: yesBeilstein Journal of Organic Chemistry, 2009
Flavin chromophores can mediate redox reactions upon irradiation by blue light. In an attempt to increase their catalytic efficacy, flavin derivatives bearing a guanidinium ion as oxoanion binding site were prepared.
Harald Schmaderer   +2 more
doaj   +1 more source

A Mild and Regioselective Ring-Opening of Aziridines with Acid Anhydride Using TBD or PS-TBD as a Catalyst

open access: yesMolecules, 2015
The ring-opening of N-tosylaziridines with various acid anhydrides catalyzed by 5 mol % of 1,5,7-triazabicyclo[4,4,0]dec-5-ene (TBD) afforded the corresponding β-amino esters in excellent yields under mild reaction conditions. Polymer-supported catalyst,
Satoru Matsukawa, Yasutaka Mouri
doaj   +1 more source

Breaking the Ceiling of Boron-Boron Bonds: Understanding and Fine-Tuning Basicity in Diborane(4) Complexes. [PDF]

open access: yesJ Comput Chem
Diborane(4) can form strong complexes with one or two nitrogen bases, and still behave as a boron base. Complexed with two nitrogen bases, diborane(4) may reach very high proton affinities, overcoming that of the typical 1,8‐bis(dimethylamino)naphthalene super sponge. However, understanding basicity trends is not straightforward, due to the loss of the
Yáñez M   +3 more
europepmc   +2 more sources

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