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Benzimidazole based derivatives as anticancer agents: Structure activity relationship analysis for various targets
G Satija, B Sharma, A Madan, A Iqubal… - Journal of …, 2022 - Wiley Online Library
Benzimidazole, the benzo derivative of imidazole, is a class of bicyclic aromatic organic
compound consisting of six‐membered benzene ring fused to five‐membered imidazole at 4 …
compound consisting of six‐membered benzene ring fused to five‐membered imidazole at 4 …
Recent advances of benzimidazole as anticancer agents
S Venugopal, B Kaur, A Verma… - Chemical Biology & …, 2023 - Wiley Online Library
Cancer is the second leading cause of death globally, with 9.6 million deaths yearly. As a life‐
threatening disease, it necessitates the emergence of new therapies. Resistance to current …
threatening disease, it necessitates the emergence of new therapies. Resistance to current …
Design, synthesis, molecular modeling, DFT, ADME and biological evaluation studies of some new 1, 3, 4-oxadiazole linked benzimidazoles as anticancer agents and …
Breast cancer is the most frequent female cancer and second cause of cancer-related
deaths among women around the world. Two thirds of breast cancer patients have hormone …
deaths among women around the world. Two thirds of breast cancer patients have hormone …
Recent advance in the development of N-heterocyclic derivatives as anti-SARS-CoV-2 inhibitors: A review
The pandemic caused by COVID-19 hinders everything on earth, including physical and
mental health, daily life and the global economy. Currently, there are no defined drugs and …
mental health, daily life and the global economy. Currently, there are no defined drugs and …
Receptor-based pharmacophore modeling, molecular docking, synthesis and biological evaluation of novel VEGFR-2, FGFR-1, and BRAF multi-kinase inhibitors
HT Abdel-Mohsen, MA Ibrahim, AM Nageeb… - BMC chemistry, 2024 - Springer
A receptor-based pharmacophore model describing the binding features required for the
multi-kinase inhibition of the target kinases (VEGFR-2, FGFR-1, and BRAF) were …
multi-kinase inhibition of the target kinases (VEGFR-2, FGFR-1, and BRAF) were …
Benzimidazole hybrids as anticancer drugs: An updated review on anticancer properties, structure–activity relationship, and mechanisms of action (2019–2021)
LS Feng, WQ Su, JB Cheng, T **ao, HZ Li… - Archiv der …, 2022 - Wiley Online Library
Cancer, characterized by a deregulation of the cell cycle which mainly results in a
progressive loss of cellular differentiation and uncontrolled cellular growth, remains a …
progressive loss of cellular differentiation and uncontrolled cellular growth, remains a …
New benzimidazole-triazole derivatives as topoisomerase i inhibitors: design, synthesis, anticancer screening, and molecular modeling studies
In this study, we designed, synthesized, and evaluated a series of 1, 2, 4-triazole
benzimidazoles for their cytotoxic effects against the A549, C6, and NIH3T3 cell lines …
benzimidazoles for their cytotoxic effects against the A549, C6, and NIH3T3 cell lines …
A panoramic review of benzimidazole derivatives and their potential biological activity
H Hernández-López… - Mini Reviews in …, 2022 - benthamdirect.com
The therapeutic potential of the benzimidazole nucleus has been recognized since 1944,
and it is an important heterocycle system due to its presence in a wide range of bioactive …
and it is an important heterocycle system due to its presence in a wide range of bioactive …
Design, synthesis, and molecular modeling studies of a novel benzimidazole as an aromatase inhibitor
In this study, a series of novel 1, 3, 4-oxadiazole-benzimidazole derivatives were designed
and synthesized. Their cytotoxic activities against five cancer cell lines, including A549, MCF …
and synthesized. Their cytotoxic activities against five cancer cell lines, including A549, MCF …
Synthesis, characterization, biological evaluation, and molecular docking studies of new 1, 3, 4-oxadiazole-thioether derivative as antioxidants and cytotoxic agents
DG Shiferaw, B Kalluraya - Heliyon, 2024 - cell.com
Oxadiazoles and their derivatives with thioether functionalities represent a new and exciting
class of physiologically active heterocyclic compounds. Several molecules with these …
class of physiologically active heterocyclic compounds. Several molecules with these …