Design, synthesis and molecular modeling studies of few chalcone analogues of benzimidazole for epidermal growth factor receptor inhibitor in search of useful …
In the present investigation, few 3-(substitutedphenyl)-1-[2-(1-hydroxy-ethyl)]-1H-
benzimidazol-1-yl) prop-2-en-1-ones are EGFR antagonist are designed, by molecular …
benzimidazol-1-yl) prop-2-en-1-ones are EGFR antagonist are designed, by molecular …
Synthesis, molecular docking, in silico ADME, and EGFR kinase inhibitor activity studies of some new benzimidazole derivatives bearing thiosemicarbazide, triazole …
Epidermal growth factor receptor (EGFR), one of the important targets in the development of
the anticancer compound, is a member of the ErbB receptor tyrosine kinase receptor family …
the anticancer compound, is a member of the ErbB receptor tyrosine kinase receptor family …
Design, In Silico Molecular Docking, and ADMET Prediction of Amide Derivatives of Chalcone Nucleus as EGFR Inhibitors for the Treatment of Cancer
S Patil, V Randive, I Mahadik… - Current Drug Discovery …, 2024 - ingentaconnect.com
Background: Cancer is a devastating disease. Many studies have shown that the primary
causes of the aggressive and resistant types of cancer are the overexpression of receptors …
causes of the aggressive and resistant types of cancer are the overexpression of receptors …
Synthesis, antitumor evaluation and molecular modeling study of novel benzimidazoles and pyrazinobenzimidazoles
AAB Mohameda, FA Badriab, AR Maaroufa… - Journal of Applied …, 2017 - japsonline.com
Some novel benzimidazole and pyrazinobenzimidazole derivatives 5-8 was designed for
evaluation of their in vitro cytotoxicity studies using MTT-based assay against three cancer …
evaluation of their in vitro cytotoxicity studies using MTT-based assay against three cancer …
[HTML][HTML] Molecular docking based screening of novel designed chalcone series of compounds for their anti-cancer activity targeting EGFR kinase domain
Epidermal growth factor receptors (EGFR) are critical for the growth of many tumors and
expressed at high levels in about one third of epithelial cancers. Hence, blockade of the …
expressed at high levels in about one third of epithelial cancers. Hence, blockade of the …
Newly designed 2-(aminomethyl) benzimidazole derivatives as possible tyrosine kinase inhibitors: synthesis, characterization, preliminary cytotoxic evaluation and in …
SQ Al-Sultan, MH Mohammed… - Chemical Review and …, 2024 - chemrevlett.com
Benzimidazole is an isostere of purine nucleosides so; it is widely used as a basic nucleus
in the development of different anticancer agents. Receptor tyrosine kinases (RTK) was …
in the development of different anticancer agents. Receptor tyrosine kinases (RTK) was …
Computational and molecular docking studies of new benzene sulfonamide drugs with anticancer and antioxidant effects
HS Mohamed, MA Abdelgawad… - Current Organic …, 2023 - ingentaconnect.com
Background: The studies on the potential usage of benzene sulfonamide derivatives as
anticancer agents are limited. benzene sulfonamide derivatives are currently used as …
anticancer agents are limited. benzene sulfonamide derivatives are currently used as …
Molecular Modeling of some 1, 3, 4-Oxadiazole Derivatives as EGFR Inhibitors for the Treatment of Cancer
SM Patil, SV Bhandari, VA Patil… - Letters in Drug …, 2024 - benthamdirect.com
Background: Cancer is a group of illnesses characterised by the impartial increase and
unfolding of somatic cells. A variety of natural compounds, such as curcumin, zingiberine …
unfolding of somatic cells. A variety of natural compounds, such as curcumin, zingiberine …
[PDF][PDF] Novel series of 1, 5 Benzothiazepine skeleton based compounds as anti-cancer agents–In silico and MTT assay based study
CH Rao, MM Prasada - Journal of PeerScientist, 2018 - researchgate.net
A novel series of Benzothiazepine derivatives were designed and evaluated for epidermal
growth factor receptor (EFGR) inhibitory potential by using various computational tools along …
growth factor receptor (EFGR) inhibitory potential by using various computational tools along …
Synthesis, ADMET predictions, molecular docking studies, and in-vitro anticancer activity of some benzoxazines against A549 human lung cancer cells
Objectives This study aims to synthesize a series of benzoxazines (1–5) to be examined as
an epidermal growth factor receptor (EGFR) inhibitor by in-silico study. The overexpression …
an epidermal growth factor receptor (EGFR) inhibitor by in-silico study. The overexpression …