The lipophilic bullet hits the targets: medicinal chemistry of adamantane derivatives

L Wanka, K Iqbal, PR Schreiner - Chemical reviews, 2013 - ACS Publications
A simple, primary amine bearing a C10H15 alkyl residue was found to display potent anti-
Influenza A properties in 1964. 1 Soon thereafter, antiviral activity of this amine was found …

Role of CCK/gastrin receptors in gastrointestinal/metabolic diseases and results of human studies using gastrin/CCK receptor agonists/antagonists in these diseases

MJ Berna, RT Jensen - Current topics in medicinal chemistry, 2007 - ingentaconnect.com
In this paper, the estabished and possible roles of CCK1 and CCK2 receptors in
gastrointestinal (GI) and metabolic diseases are reviewed and available results from human …

Progress in developing cholecystokinin (CCK)/gastrin receptor ligands that have therapeutic potential

MJ Berna, JA Tapia, V Sancho, RT Jensen - Current opinion in …, 2007 - Elsevier
Gastrin and cholecystokinin (CCK) are two of the oldest hormones and within the past 15
years there has been an exponential increase in knowledge of their pharmacology, cell …

Molecular mechanisms in therapy of acid-related diseases

JM Shin, O Vagin, K Munson, M Kidd, IM Modlin… - Cellular and molecular …, 2008 - Springer
Inhibition of gastric acid secretion is the mainstay of the treatment of gastroesophageal reflux
disease and peptic ulceration; therapies to inhibit acid are among the best-selling drugs …

3D-QSAR modeling and molecular docking studies on a series of 2, 4, 5-trisubstituted imidazole derivatives as CK2 inhibitors

A Goudzal, A El Aissouq, H El Hamdani… - Journal of …, 2023 - Taylor & Francis
Protein case in kinase II alpha subunit (CK2) plays an imperative function in treating cancer
disease. Herein, we have performed a three-dimensional quantitative structure activity …

Nonpeptidic ligands for peptide-activated G protein-coupled receptors

JS Blakeney, RC Reid, GT Le, DP Fairlie - Chemical reviews, 2007 - ACS Publications
There are some 850 human G protein-coupled receptors (GPCRs) currently known
(http://bioinformatics2. biol. uoa. gr), making this the most abundant family of well …

[HTML][HTML] Enantioselective N-Heterocyclic Carbene-Catalyzed Annulation Reactions with Imidazolidinones

EOB McCusker, KA Scheidt - Angewandte Chemie (International …, 2013 - ncbi.nlm.nih.gov
The development of efficient strategies for the stereoselective construction of privileged
heterocyclic systems is an important objective in chemical synthesis and pharmaceutical …

[HTML][HTML] EGFR, HER2 target based molecular docking analysis, in vitro screening of 2, 4, 5-trisubstituted imidazole derivatives as potential anti-oxidant and cytotoxic …

R Guda, G Kumar, R Korra, S Balaji, G Dayakar… - … of Photochemistry and …, 2017 - Elsevier
In our endeavor towards the development of potent molecules for cancer diseases, we have
designed and synthesized a series of 2, 4, 5-trisubstituted imidazole derivatives (B1–B24) …

Scaffold Hopping with Molecular Field Points:  Identification of a Cholecystokinin-2 (CCK2) Receptor Pharmacophore and Its Use in the Design of a Prototypical Series of …

CMR Low, IM Buck, T Cooke, JR Cushnir… - Journal of medicinal …, 2005 - ACS Publications
A new molecular modeling approach has been used to derive a pharmacophore of the
potent and selective cholecystokinin-2 (CCK2) receptor antagonist 5 (JB93182), based on …

Application of 2,4,5‐tris(2‐pyridyl)imidazole as 'turn‐off' fluorescence sensor for Cu(II) and Hg(II) ions and in vitro cell imaging

A Bhattacharya, S Mahata, A Bandyopadhyay… - …, 2022 - Wiley Online Library
Abstract The 2, 4, 5‐tris (2‐pyridyl) imidazole (L) molecule has been evaluated as a probe
for dual sensing of Hg2+ and Cu2+ ions in EtOH/HEPES buffer medium (5 mM, pH= 7.34, 1 …