Results 51 to 60 of about 8,352 (265)

Oxy-imino saccharidic derivatives as a new structural class of aldose reductase inhibitors endowed with anti-oxidant activity

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2020
Aldose reductase is a key enzyme in the development of long term diabetic complications and its inhibition represents a viable therapeutic solution for people affected by these pathologies.
Felicia D'Andrea   +10 more
doaj   +1 more source

Oxidation of aliphatic hydroxylamines in aqueous solutions [PDF]

open access: yes, 1977
The effects of pH, buffer constituents, duration of storage, presence of air, heavy metal ions, extracting solvents and various additives and cofactors on the aerial oxidation of some aliphatic primary and secondary hydroxylamines were investigated ...
A Rashid Purkaystha   +2 more
core   +1 more source

Stabilized Bi(III) Sites Direct *NH2OH Pathway for Efficient Cyclohexanone Oxime Electrosynthesis

open access: yesAdvanced Materials, EarlyView.
The electron‐buffering effect stabilizes Bi3+ sites under electroreductive conditions, preserving a favorable interfacial water configuration that sustains the selective *NH2OH pathway and enables efficient cyclohexanone oxime electrosynthesis. ABSTRACT Coupling electrocatalytic nitrite reduction reaction (NO2−RR) with cyclohexanone conversion enables ...
Zichao Xi   +8 more
wiley   +1 more source

Irreversible Rearrangement of Silyl Groups between Oxygen and Nitrogen in Tris(silyl)hydroxylamines [PDF]

open access: yes, 2016
Diorganofluorosilylation of 1,2-bis(trimethylsilyl)hydroxylamines at low temperatures gives exclusively O-(diorganofluorosilyl)-N,N-bis(trimethylsilyl)hydroxylamines 1a,b.
Thomas Müller (3554)   +2 more
core   +1 more source

ZDHHC9‐Mediated Palmitoylation of ACSL4 Drives Ferroptosis in Diabetes Mellitus–Induced Erectile Dysfunction

open access: yesAdvanced Science, EarlyView.
ABSTRACT Diabetes mellitus‐induced erectile dysfunction (DMED) is a highly prevalent complication among diabetic patients; however, its underlying pathogenic mechanisms remain incompletely understood. Metabolic disorder is a hallmark of diabetes, yet its precise contribution to DMED progression is not well defined.
Wanyang Guo   +14 more
wiley   +1 more source

Improvement of film quality and solar cell properties of perovskite by the addition of N-benzylhydroxylamine

open access: yesApplied Physics Express
In this study on perovskite solar cells (PVSCs), we incorporate N-benzylhydroxylamine (N-BzHoA) as an additive into the precursor solution. The addition of N-BzHoA suppressed the formation of unwanted PbI _2 and δ-phase perovskite without affecting the ...
Keisuke Nagasawa   +8 more
doaj   +1 more source

Synthetic Chameleon Turns into Oximes, Nitrones, and Hydroxylamines when Exposed to Blue Light [PDF]

open access: yesACS Omega
Michaela Marčeková   +5 more
doaj   +2 more sources

Nitrones and oxaziridines. XXII. Preparation and cyclization of some δ,ε-unsaturated hydroxylamines [PDF]

open access: yes, 1978
Four δ,ε-unsaturated hydroxylamines have been prepared by reduction of the related oximes by sodium cyanoborohydride. Only two of these-those containing terminal olefinic groups-undergo spontaneous cyclization to N-hydroxypyrrolidines, which can be ...
JE Doyle, DSC Black
core   +1 more source

SMAD4 Palmitoylation Drives a Metabolic‐Transcriptional Circuit to Promote Tumorigenesis and Confers Radiosensitivity in Pancreatic Cancer

open access: yesAdvanced Science, EarlyView.
This study identifies palmitoylation as a novel regulatory modification of SMAD4, mediated by ZDHHC22/APT2. It activates fatty acid synthesis, creating a self‐reinforcing SMAD4–FASN–palmitate feedback loop that drives pancreatic cancer growth and enhances radiotherapy sensitivity.
Yang Wang   +16 more
wiley   +1 more source

Palladium catalyzed N-arylation of hydroxylamines [PDF]

open access: yes, 2009
Over the past decade modified Ullmann couplings and palladium-catalyzed arylations of nitrogen contg. compds. (Buchwald-Hartwig aminations) have emerged as powerful tools in synthetic chem. Interestingly, despite their biol.
Tomkinson, Nicholas C. O.   +1 more
core  

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