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Structure-activity relationship (SAR) study and design strategies of nitrogen-containing heterocyclic moieties for their anticancer activities
The present review article offers a detailed account of the design strategies employed for the
synthesis of nitrogen-containing anticancer agents. The results of different studies describe …
synthesis of nitrogen-containing anticancer agents. The results of different studies describe …
Coumarin heterocyclic derivatives: chemical synthesis and biological activity
FG Medina, JG Marrero, M Macías-Alonso… - Natural product …, 2015 - pubs.rsc.org
Coumarin heterocyclic derivatives: chemical synthesis and biological activity - Natural Product
Reports (RSC Publishing) DOI:10.1039/C4NP00162A Royal Society of Chemistry View PDF …
Reports (RSC Publishing) DOI:10.1039/C4NP00162A Royal Society of Chemistry View PDF …
DYRK1A inhibitors for disease therapy: Current status and perspectives
Dual-specificity tyrosine phosphorylation-regulated kinase 1 A (DYRK1A) is a conserved
protein kinase that plays essential roles in various biological processes. It is located in the …
protein kinase that plays essential roles in various biological processes. It is located in the …
A review: Biologically active 3, 4-heterocycle-fused coumarins
The combination of heterocycles offers a new opportunity to create novel multicyclic
compounds having improved biological activity. Coumarins are ubiquitous natural …
compounds having improved biological activity. Coumarins are ubiquitous natural …
[HTML][HTML] Marine pyrrole alkaloids
K Seipp, L Geske, T Opatz - Marine Drugs, 2021 - mdpi.com
Nitrogen heterocycles are essential parts of the chemical machinery of life and often reveal
intriguing structures. They are not only widespread in terrestrial habitats but can also …
intriguing structures. They are not only widespread in terrestrial habitats but can also …
Imitation of β-lactam binding enables broad-spectrum metallo-β-lactamase inhibitors
J Brem, T Panduwawala, JU Hansen, J Hewitt… - Nature Chemistry, 2022 - nature.com
Carbapenems are vital antibiotics, but their efficacy is increasingly compromised by metallo-
β-lactamases (MBLs). Here we report the discovery and optimization of potent broad …
β-lactamases (MBLs). Here we report the discovery and optimization of potent broad …
The azaindole framework in the design of kinase inhibitors
This review article illustrates the growing use of azaindole derivatives as kinase inhibitors
and their contribution to drug discovery and innovation. The different protein kinases which …
and their contribution to drug discovery and innovation. The different protein kinases which …
Anticancer properties of lamellarins
C Bailly - Marine Drugs, 2015 - mdpi.com
In 1985 the first lamellarins were isolated from a small oceanic sea snail. Today, more than
50 lamellarins have been inventoried and numerous derivatives synthesized and tested as …
50 lamellarins have been inventoried and numerous derivatives synthesized and tested as …
Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) inhibitors as potential therapeutics
DB Jarhad, KK Mashelkar, HR Kim… - Journal of medicinal …, 2018 - ACS Publications
Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) is a member of an
evolutionarily conserved family of protein kinases that belongs to the CMGC group of …
evolutionarily conserved family of protein kinases that belongs to the CMGC group of …
DYRK1A in neurodegeneration and cancer: Molecular basis and clinical implications
Protein kinases are one of the most studied drug targets in current pharmacological
research, as evidenced by the vast number of kinase-targeting agents enrolled in active …
research, as evidenced by the vast number of kinase-targeting agents enrolled in active …