Recent progress in cyclic aryliodonium chemistry: syntheses and applications
X Peng, A Rahim, W Peng, F Jiang, Z Gu… - Chemical …, 2023 - ACS Publications
Hypervalent aryliodoumiums are intensively investigated as arylating agents. They are
excellent surrogates to aryl halides, and moreover they exhibit better reactivity, which allows …
excellent surrogates to aryl halides, and moreover they exhibit better reactivity, which allows …
The importance of sulfur-containing motifs in drug design and discovery
Introduction Sulfur-containing functional groups are privileged motifs that occur in various
pharmacologically effective substances and several natural products. Various functionalities …
pharmacologically effective substances and several natural products. Various functionalities …
Phenylazothiazoles as visible-light photoswitches
A novel class of photoswitches based on a phenylazothiazole scaffold that undergoes
reversible isomerization under visible-light irradiation is reported. The photoswitch, which …
reversible isomerization under visible-light irradiation is reported. The photoswitch, which …
[HTML][HTML] An overview of the synthesis and antimicrobial, antiprotozoal, and antitumor activity of thiazole and bisthiazole derivatives
Thiazole, a five-membered heteroaromatic ring, is an important scaffold of a large number of
synthetic compounds. Its diverse pharmacological activity is reflected in many clinically …
synthetic compounds. Its diverse pharmacological activity is reflected in many clinically …
A review of progress in histone deacetylase 6 inhibitors research: structural specificity and functional diversity
XH Zhang, Qin-Ma, HP Wu, MY Khamis… - Journal of medicinal …, 2021 - ACS Publications
Histone deacetylases (HDACs) are essential for maintaining homeostasis by catalyzing
histone deacetylation. Aberrant expression of HDACs is associated with various human …
histone deacetylation. Aberrant expression of HDACs is associated with various human …
Thiazole-based thiosemicarbazones: Synthesis, cytotoxicity evaluation and molecular docking study
SM Gomha, HA Abdelhady, DZH Hassain… - Drug design …, 2021 - Taylor & Francis
Introduction Hybrid drug design has developed as a prime method for the development of
novel anticancer therapies that can theoretically solve much of the pharmacokinetic …
novel anticancer therapies that can theoretically solve much of the pharmacokinetic …
Rationalizing the therapeutic potential of apigenin against cancer
Background Despite the remarkable advances made in the diagnosis and treatment of
cancer during the past couple of decades, it remains the second largest cause of mortality in …
cancer during the past couple of decades, it remains the second largest cause of mortality in …
[HTML][HTML] Valosin-containing protein (VCP)/p97: a prognostic biomarker and therapeutic target in cancer
S Costantini, F Capone, A Polo, P Bagnara… - International journal of …, 2021 - mdpi.com
Valosin-containing protein (VCP)/p97, a member of the AAA+ ATPase family, is a molecular
chaperone recruited to the endoplasmic reticulum (ER) membrane by binding to membrane …
chaperone recruited to the endoplasmic reticulum (ER) membrane by binding to membrane …
[HTML][HTML] Development and therapeutic potential of 2-aminothiazole derivatives in anticancer drug discovery
SR Alizadeh, SM Hashemi - Medicinal Chemistry Research, 2021 - Springer
Currently, the development of anticancer drug resistance is significantly restricted the clinical
efficacy of the most commonly prescribed anticancer drug. Malignant disease is widely …
efficacy of the most commonly prescribed anticancer drug. Malignant disease is widely …
Recent advances in microbial toxin-related strategies to combat cancer
It is a major concern to treat cancer successfully, due to the distinctive pathophysiology of
cancer cells and the gradual manifestation of resistance. Specific action, adverse effects and …
cancer cells and the gradual manifestation of resistance. Specific action, adverse effects and …