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Thiazole-containing compounds as therapeutic targets for cancer therapy
In the last few decades, considerable progress has been made in anticancer agents
development, and several new anticancer agents of natural and synthetic origin have been …
development, and several new anticancer agents of natural and synthetic origin have been …
DHFR inhibitors: reading the past for discovering novel anticancer agents
Dihydrofolate reductase inhibitors are an important class of drugs, as evidenced by their use
as antibacterial, antimalarial, antifungal, and anticancer agents. Progress in understanding …
as antibacterial, antimalarial, antifungal, and anticancer agents. Progress in understanding …
An overview on synthetic 2-aminothiazole-based compounds associated with four biological activities
M Farouk Elsadek, B Mohamed Ahmed… - Molecules, 2021 - mdpi.com
Amongst sulfur-and nitrogen-containing heterocyclic compounds, the 2-aminothiazole
scaffold is one of the characteristic structures in drug development as this essential …
scaffold is one of the characteristic structures in drug development as this essential …
Synthesis, spectroscopic, X-ray diffraction, antimicrobial and antitumor studies of Ni (II) and Co (II) complexes derived from 4-acetyl-5, 6-diphenyl-3 (2H)-pyridazinone …
Reactions of the Schiff base ligand derived from 4-acetyl-5, 6-diphenyl-3 (2H)-pyridazinone
and ethylenediamine with Ni (II) and Co (II) using different metal salts; NO 3−, AcO−, ClO 4 …
and ethylenediamine with Ni (II) and Co (II) using different metal salts; NO 3−, AcO−, ClO 4 …
Dihydrofolate reductase inhibitors: Patent landscape and phases of clinical development (2001–2021)
Introduction Dihydrofolate reductase (DHFR) plays an important role in the biosynthesis of
amino acid and folic acid. It participates by reducing dihydrofolate to tetrahydrofolate, in the …
amino acid and folic acid. It participates by reducing dihydrofolate to tetrahydrofolate, in the …
Dihydrofolate reductase (DHFR) inhibitors: a comprehensive review
Background: Dihydrofolate reductase (DHFR) is an indispensable enzyme required for the
survival of most prokaryotic and eukaryotic cells as it is involved in the biosynthesis of …
survival of most prokaryotic and eukaryotic cells as it is involved in the biosynthesis of …
A review of small-molecule inhibitors of one-carbon enzymes: SHMT2 and MTHFD2 in the spotlight
CR Cuthbertson, Z Arabzada… - ACS Pharmacology & …, 2021 - ACS Publications
Metabolic reprogramming is a key hallmark of cancer and shifts cellular metabolism to meet
the demands of biomass production necessary for abnormal cell reproduction. One-carbon …
the demands of biomass production necessary for abnormal cell reproduction. One-carbon …
An insight into synthetic strategies and recent developments of dihydrofolate reductase inhibitors
The dihydrofolate reductase (DHFR) is a significant target in cancer, microbial infection,
fungal infection, malaria, leishmaniasis, and tuberculosis, among other diseases. The DHFR …
fungal infection, malaria, leishmaniasis, and tuberculosis, among other diseases. The DHFR …
Detecting protein-protein interaction based on protein fragment complementation assay
T Wang, N Yang, C Liang, H Xu, Y An… - Current Protein and …, 2020 - ingentaconnect.com
Proteins are the most critical executive molecules by responding to the instructions stored in
the genetic materials in any form of life. More frequently, proteins do their jobs by acting as a …
the genetic materials in any form of life. More frequently, proteins do their jobs by acting as a …
New quinazolinone‐based derivatives as DHFR/EGFR‐TK inhibitors: synthesis, molecular modeling simulations, and anticancer activity
Abstract New 2‐mercapto‐quinazolin‐4‐one analogs were synthesized and tested for their
in vitro anticancer activity, dihydrofolate reductase (DHFR) inhibition, and epidermal growth …
in vitro anticancer activity, dihydrofolate reductase (DHFR) inhibition, and epidermal growth …