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Recent updates on thienopyrimidine derivatives as anticancer agents
Thienopyrimidine derivatives hold a unique place between fused pyrimidine compounds.
They are important and widely represented in medicinal chemistry as they are structural …
They are important and widely represented in medicinal chemistry as they are structural …
Recent advances and future directions on small molecule VEGFR inhibitors in oncological conditions
A Thakur, M Rana, A Mishra, C Kaur, CH Pan… - European Journal of …, 2024 - Elsevier
ABSTRACT “A journey of mixed emotions” is a quote that best describes the progress chart
of vascular endothelial growth factor receptor (VEGFR) inhibitors as cancer therapeutics in …
of vascular endothelial growth factor receptor (VEGFR) inhibitors as cancer therapeutics in …
Design and synthesis of novel hexahydrobenzo[4,5]thieno[2,3‐d]pyrimidine derivatives as potential anticancer agents with antiangiogenic activity via VEGFR‐2 …
SE Seif, Z Mahmoud, WW Wardakhan… - Drug Development …, 2023 - Wiley Online Library
Abstract New thieno [2, 3‐d] pyrimidine derivatives were designed and synthesized. The
National Cancer Institute (NCI) evaluated the synthesized novel compounds against a panel …
National Cancer Institute (NCI) evaluated the synthesized novel compounds against a panel …
Exploring a novel thiazole derivatives hybrid with fluorinated-indenoquinoxaline as dual inhibitors targeting VEGFR2/AKT and apoptosis inducers against …
Hepatocellular carcinoma (HCC) ranks as the third most prevalent reason for cancer-related
death on a global scale. Tyrosine kinase inhibitors (TKIs) continue to be the primary …
death on a global scale. Tyrosine kinase inhibitors (TKIs) continue to be the primary …
Design and synthesis of novel quinazolinone-based derivatives as EGFR inhibitors with antitumor activity
Abstract Nineteen new quinazolin-4 (3 H)-one derivatives 3a–g and 6a–l were designed
and synthesised to inhibit EGFR. The antiproliferative activity of the synthesised compounds …
and synthesised to inhibit EGFR. The antiproliferative activity of the synthesised compounds …
An expeditious FeCl 3-catalyzed cascade 1, 4-conjugate addition/annulation/1, 5-H shift sequence for modular access of all-pyrano-moiety-substituted chromenes
X He, R Li, PY Choy, J Duan, Z Yin, K Xu, Q Tang… - Chemical …, 2022 - pubs.rsc.org
ortho-Alkynyl quinone methides are well-known four-atom synthons for direct [4+ n]
cycloaddition in constructing useful oxa-heterocyclic compounds owing to their high …
cycloaddition in constructing useful oxa-heterocyclic compounds owing to their high …
Dependence on linkers' flexibility designed for benzenesulfonamides targeting discovery of novel hCA IX inhibitors as potent anticancer agents
Herein we reported the design and synthesis of two series comprising twenty-two
benzenesulfonamides that integrate the s-triazine moiety. Target compounds successfully …
benzenesulfonamides that integrate the s-triazine moiety. Target compounds successfully …
An overview of RAF kinases and their inhibitors (2019-2023)
OM Hashem, AI Shahin, MA Al Hindawi… - European Journal of …, 2024 - Elsevier
Protein kinases (PKs) including RAF, performs a principal role in regulating countless
cellular events such as cell growth, differentiation, and angiogenesis. Overexpression and …
cellular events such as cell growth, differentiation, and angiogenesis. Overexpression and …
Design, synthesis, anticancer, and antibacterial evaluation of some quinazolinone‐based derivatives as DHFR inhibitors
Two series of quinazolinone derivatives were designed and synthesized as dihydrofolate
reductase (DHFR) inhibitors. All compounds were evaluated for their antibacterial and …
reductase (DHFR) inhibitors. All compounds were evaluated for their antibacterial and …
Design, synthesis, anticancer evaluation, and in silico studies of some thieno[2,3‐d]pyrimidine derivatives as EGFR inhibitors
Abstract New series of 20 thieno [2, 3‐d] pyrimidine derivatives have been synthesized. The
National Cancer Institute evaluated all the newly synthesized compounds for their …
National Cancer Institute evaluated all the newly synthesized compounds for their …