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Efficient synthesis and molecular docking analysis of quinazoline and azole hybrid derivatives as promising agents for anti-cancer and anti-tuberculosis activities
Molecular docking is a computational method based on bioinformatics that simulates the
interaction dynamics of molecules such as ligands and receptors, predicting their binding …
interaction dynamics of molecules such as ligands and receptors, predicting their binding …
Synthetic and Medicinal Perspective of 1, 2, 4‐Triazole as Anticancer Agents
Cancer is still one of the leading causes of death worldwide. Many researchers are working
to design and develop heterocyclic‐based drugs with the potential to treat cancer at various …
to design and develop heterocyclic‐based drugs with the potential to treat cancer at various …
Repositioning of acefylline as anti-cancer drug: Synthesis, anticancer and computational studies of azomethines derived from acefylline tethered 4-amino-3-mercapto …
Novel azomethines derived from acefylline tethered triazole hybrids (7a-k) have been
synthesized and evaluated against human liver cancer cell line (Hep G2) using MTT assay …
synthesized and evaluated against human liver cancer cell line (Hep G2) using MTT assay …
Molecular hybrids integrated with imidazole and hydrazone structural motifs: Design, synthesis, biological evaluation, and molecular docking studies
In the present work, a series of compounds containing imidazole and hydrazone structural
frameworks were synthesized and characterized using various spectral techniques …
frameworks were synthesized and characterized using various spectral techniques …
Exploring the synthetic potential of epoxide ring opening reactions toward the synthesis of alkaloids and terpenoids: a review
Epoxides are oxygen containing heterocycles which are significantly employed as crucial
intermediates in various organic transformations. They are considered highly reactive three …
intermediates in various organic transformations. They are considered highly reactive three …
Synergistic biomedical potential and molecular docking analyses of coumarin–triazole hybrids as tyrosinase inhibitors: design, synthesis, in vitro profiling, and in silico …
The tyrosinase enzyme has a vital role in the browning of vegetables and fruits and the
biosynthesis of melanin. In this work, we synthesized a diverse library of coumarin–triazole …
biosynthesis of melanin. In this work, we synthesized a diverse library of coumarin–triazole …
Structure-Based Virtual Screening of Furan-1,3,4-Oxadiazole Tethered N-phenylacetamide Derivatives as Novel Class of hTYR and hTYRP1 Inhibitors
Human tyrosinase (hTYR) is a key and rate-limiting enzyme along with human tyrosinase-
related protein-1 (hTYRP1), which are among the most prominent targets of inhibiting hyper …
related protein-1 (hTYRP1), which are among the most prominent targets of inhibiting hyper …
Update on novel synthetic approaches towards the construction of carbazole nuclei: a review
The carbazole scaffold is a significant entity in organic compounds due to its variety of
biological and synthetic applications. Traditionally, carbazole skeletons have been …
biological and synthetic applications. Traditionally, carbazole skeletons have been …
Discovery of novel 1, 2, 4-triazole tethered β-hydroxy sulfides as bacterial tyrosinase inhibitors: synthesis and biophysical evaluation through in vitro and in silico …
In this study, a series of 1, 2, 4-triazole-tethered β-hydroxy sulfide scaffolds 11a–h was
synthesized in good to remarkable yields (69–90%) through the thiolysis of oxiranes by the …
synthesized in good to remarkable yields (69–90%) through the thiolysis of oxiranes by the …
Exploring innovative strategies for identifying anti-breast cancer compounds by integrating 2D/3D-QSAR, molecular docking analyses, ADMET predictions, molecular …
Breast cancer is a crucial global health issue, representing the most frequent cancer and a
major cause of cancer-related mortality of women. The difficulty of treating this disease is …
major cause of cancer-related mortality of women. The difficulty of treating this disease is …