“Click Chemistry”: An Emerging Tool for Developing a New Class of Structural Motifs against Various Neurodegenerative Disorders
A Manoharan, J Jayan, TM Rangarajan, K Bose… - ACS …, 2023 - ACS Publications
Click chemistry is a set of easy, atom-economical reactions that are often utilized to combine
two desired chemical entities. Click chemistry accelerates lead identification and …
two desired chemical entities. Click chemistry accelerates lead identification and …
Click chemistry in the electrochemical systems: Toward the architecture of electrochemical (bio) sensors
KE Sekhosana, SA Majeed, U Feleni - Coordination Chemistry Reviews, 2023 - Elsevier
Click chemistry is considered one of the most powerful tools used to design a variety of
compounds or complexes including biomolecules, polymers, organometallics, organics …
compounds or complexes including biomolecules, polymers, organometallics, organics …
Determination and the pharmacokinetic study of tigecycline by fluorescence strategy with F, N codoping carbon dots as probe
R Cai, C Miao, L Zhang, Y Zhou, Y Liu, C Zheng… - Sensors and Actuators B …, 2022 - Elsevier
Tigecycline (TIGE) plays a significant role in the management of complex and serious
bacterial infection. The monitoring of TIGE content in plasma and the further application in …
bacterial infection. The monitoring of TIGE content in plasma and the further application in …
Synthesis of novel hybrid quinoxaline containing triazole and acetamide moieties by azide-alkyne click chemistry: Experimental and theoretical characterization
Heterocyclic compounds bearing triazole and quinoxaline possess significant
pharmacological activities. Herein, a new quinoxaline derivative containing 1, 2, 3-triazole …
pharmacological activities. Herein, a new quinoxaline derivative containing 1, 2, 3-triazole …
4‐Azido‐7‐nitrobenzoxadiazole as innovative clickable fluorescence probe for trace and selective quantification of ethinylestradiol in human plasma
Quantification of ethinylestradiol (EE) in biological matrices is challenging as it is a very
potent drug with a very low Cmax (75 pg. ml− 1). Despite the high sensitivity of fluorometric …
potent drug with a very low Cmax (75 pg. ml− 1). Despite the high sensitivity of fluorometric …
Synthesis, design, in silico, in vitro and in vivo (streptozotocin-induced diabetes in mice) biological evaluation of novels N-arylacetamide derivatives
S Mortada, W Guerrab, M Missioui, N Salhi… - Journal of …, 2024 - Taylor & Francis
The organic compounds 2-chloro-N-(aryl) acetamide (Ps13–Ps18) and 2-azido-N-(aryl)
acetamide (148–153) were synthesized and analyzed using 1 H, 13C NMR. The acute oral …
acetamide (148–153) were synthesized and analyzed using 1 H, 13C NMR. The acute oral …
Synthesis and crystal structure of 2-azido-N-phenylacetamide, C8H8N4O
Synthesis and crystal structure of 2-azido-N-phenylacetamide, C8H8N4O Skip to content Should
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Theoretical study on the luminescent and reaction mechanism of dansyl‐based fluorescence probe for detecting hydrogen sulfide
H Li, Y Wang, S Pan, C Wang, Y Liu… - Journal of …, 2025 - Wiley Online Library
The photophysical and photochemical properties of the sulfonyl azide‐based fluorescent
probe DNS–Az and its reduction product DNS by hydrogen sulfide (H2S) have been …
probe DNS–Az and its reduction product DNS by hydrogen sulfide (H2S) have been …
[HTML][HTML] Ligand assisted CuAAC labelling and RP-HPLC analysis of zidovudine and Retrovir using propargyl-Fmoc probe
P Kasza, K Pociecha, K Wójcik-Pszczoła… - European Journal of …, 2022 - Elsevier
The extensive application of zidovudine (ZDV) as a stand-alone anti-HIV drug and a
component in antiviral combination therapies, has made its analysis important both in the …
component in antiviral combination therapies, has made its analysis important both in the …
[PDF][PDF] Crystal structure and Hirshfeld surface analysis of 2-azido-N-(4-fluorophenyl) acetamide
M Missioui, W Guerrab, A Alsubari… - Acta …, 2022 - journals.iucr.org
The asymmetric unit of the title compound, C8H7FN4O, consists of two independent
molecules differing in the orientation of the azido group. Each molecule forms N—H⋯ O …
molecules differing in the orientation of the azido group. Each molecule forms N—H⋯ O …