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Recent advances in 1, 2, 4‐triazole scaffolds as antiviral agents
SA El‐Sebaey - ChemistrySelect, 2020 - Wiley Online Library
In recent years, severe viral infections have emerged, and antiviral chemotherapeutic agents
are not adequately effective in curing these infections, leading to serious human diseases …
are not adequately effective in curing these infections, leading to serious human diseases …
Exploring the chemistry and therapeutic potential of triazoles: a comprehensive literature review
Triazole is a valuable platform in medicinal chemistry, possessing assorted pharmacological
properties, which could play a major role in the common mechanisms associated with …
properties, which could play a major role in the common mechanisms associated with …
Design and antiproliferative and antioxidant activities of furan-based thiosemicarbazides and 1, 2, 4-triazoles: their structure-activity relationship and SwissADME …
Y Sicak - Medicinal Chemistry Research, 2021 - Springer
Due to the limited number of drugs in current clinical use, the diverse biological applications
of furan have encouraged the preparation of a wide variety of thiosemicarbazide and triazole …
of furan have encouraged the preparation of a wide variety of thiosemicarbazide and triazole …
Antiviral activity of 1, 2, 4-triazole derivatives (microreview)
NV Simurova, OI Maiboroda - Chemistry of heterocyclic compounds, 2021 - Springer
Antiviral activity of 1,2,4-triazole derivatives (microreview) | Chemistry of Heterocyclic
Compounds Skip to main content Advertisement Springer Nature Link Account Menu Find a …
Compounds Skip to main content Advertisement Springer Nature Link Account Menu Find a …
Biological activity and molecular docking studies of some N‐phenylsulfonamides against cholinesterases and carbonic anhydrase isoenzymes
In this research, a series of N‐phenylsulfonamide derivatives (1‐12) were designed,
synthesized, and investigated for their inhibitory potencies against carbonic anhydrase …
synthesized, and investigated for their inhibitory potencies against carbonic anhydrase …
Recent advances in triazole-benzenesulfonamide hybrids and their biological activities
Hybridization is the process of fusion of two or more existing moieties to make a single
molecule. Triazoles and benzenesulfonamides are the useful pharmacological agents …
molecule. Triazoles and benzenesulfonamides are the useful pharmacological agents …
Recent advances in biological active sulfonamide based hybrid compounds part B: Two-component sulfonamide hybrids
Sulfonamide compounds, also known as sulfa drugs, are a significant class of synthetic
bacteriostatic antimicrobials and were the primary source of therapy against bacterial …
bacteriostatic antimicrobials and were the primary source of therapy against bacterial …
Chiral thioureas containing naphthalene moiety as selective butyrylcholinesterase inhibitors: Design, synthesis, cholinesterase inhibition activity and molecular …
Butyrylcholinesterase (BChE), which plays a role in the regulation of acetylcholine (ACh) as
well as cholinergic type neurotransmission, also has non-cholinergic functions such as …
well as cholinergic type neurotransmission, also has non-cholinergic functions such as …
[HTML][HTML] Multi-omics studies towards novel modulators of influenza A virus–host interaction
Human influenza A viruses (IAVs) cause global pandemics and epidemics. These viruses
evolve rapidly, making current treatment options ineffective. To identify novel modulators of …
evolve rapidly, making current treatment options ineffective. To identify novel modulators of …
Synthesis of novel chiral metal complexes derived from chiral thiosemicarbazide ligands as potential antioxidant agents
Two new chiral thiosemicarbazide ligands and their Cu (II), Ni (II), Pd (II), and Zn (II)
complexes were synthesized and characterized by nuclear magnetic resonance (NMR)(only …
complexes were synthesized and characterized by nuclear magnetic resonance (NMR)(only …