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[HTML][HTML] The importance of the pyrazole scaffold in the design of protein kinases inhibitors as targeted anticancer therapies
The altered activation or overexpression of protein kinases (PKs) is a major subject of
research in oncology and their inhibition using small molecules, protein kinases inhibitors …
research in oncology and their inhibition using small molecules, protein kinases inhibitors …
Current scenario of pyrazole hybrids with in vivo therapeutic potential against cancers
Z Xu, Y Zhuang, Q Chen - European Journal of Medicinal Chemistry, 2023 - Elsevier
Chemotherapeutics occupy a pivotal role in the medication of different types of cancers, but
the prevalence and mortality rates of cancer remain high. The drug resistance and low …
the prevalence and mortality rates of cancer remain high. The drug resistance and low …
Exploring small-molecule inhibitors targeting MAPK pathway components: Focus on ERK, MEK1, and MEK2 kinases in cancer treatment
Mitogen-activated protein kinases (MAPKs), also known as extracellular signal regulated
kinases (ERKs), are found in numerous signal transduction pathways and are triggered by …
kinases (ERKs), are found in numerous signal transduction pathways and are triggered by …
Heterocycles in breast cancer treatment: The use of pyrazole derivatives
S Ardevines, E Marqués-López… - Current Medicinal …, 2023 - benthamdirect.com
Among the aromatic heterocycle rings, pyrazole–a five-membered ring with two adjacent
nitrogen atoms in its structure has been postulated as a potent candidate in the …
nitrogen atoms in its structure has been postulated as a potent candidate in the …
Ultrasound-assisted synthesis of 1, 5-disubstituted pyrazoles via HFIP-mediated cascade cyclization of enaminones with aryl hydrazine
A simple and efficient metal-free strategy has been developed for the synthesis of 1, 5-
disubstituted pyrazole derivatives by using 1, 1, 1, 3, 3, 3-hexafluoro-2-propanol (HFIP) …
disubstituted pyrazole derivatives by using 1, 1, 1, 3, 3, 3-hexafluoro-2-propanol (HFIP) …
Structure–Activity Relationship Studies on Highly Functionalized Pyrazole Hydrazones and Amides as Antiproliferative and Antioxidant Agents
M Lusardi, MG Signorello, E Russo, D Caviglia… - International Journal of …, 2024 - mdpi.com
Aminopyrazoles represent interesting structures in medicinal chemistry, and several
derivatives showed biological activity in different therapeutic areas. Previously reported 5 …
derivatives showed biological activity in different therapeutic areas. Previously reported 5 …
Design, synthesis, and antiproliferative activities of novel thiazolyl-pyrazole hybrid derivatives
In this study, a series of derivatives of thiazolyl-pyrazole hybrid structures were designed to
search for new heterocyclic compound-based antitumor agents. The designed target …
search for new heterocyclic compound-based antitumor agents. The designed target …
Pyrazole, Pyrazoline, and Fused Pyrazole Derivatives: New Horizons in EGFR‐Targeted Anticancer Agents
Pyrazole and its derivatives remain popular heterocycles in drug research, design, and
development. Several drugs include the pyrazole scaffold, such as ramifenazone …
development. Several drugs include the pyrazole scaffold, such as ramifenazone …
Design, synthesis, biological evaluation, in silico ADME prediction and molecular docking of pyrazole-benzamides as multitargeting protien kinase inhibitors
In the present study, N-(1-(2-bromobenzoyl)-4-cyano-1H-pyrazol-5-yl) halogenated
benzamides (5a-h) were prepared and evaluated for their in vitro anticancer activity against …
benzamides (5a-h) were prepared and evaluated for their in vitro anticancer activity against …
Visible light-promoted green and sustainable approach for one-pot Synthesis of 4, 4'-(arylmethylene) bis (1H-pyrazol-5-ols), In Vitro Anticancer Activity, and Molecular …
A Gupta, S Iqbal, Roohi, MK Hussain, MR Zaheer… - ACS …, 2022 - ACS Publications
A visible light-promoted, efficient, green, and sustainable strategy has been adopted to
unlatch a new pathway toward the synthesis of a library of medicinally important 4, 4 …
unlatch a new pathway toward the synthesis of a library of medicinally important 4, 4 …