21 articles for I Khan
The following articles (labelled with PubMed ID or TBD) are for your review
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Synthesis of benzimidazole based thiadiazole and carbohydrazide conjugates as glycogen synthase kinase-3ß inhibitors with anti-depressant activity.

Jamia Hamdard (Hamdard University)
Quinazolines and quinazolinones as ubiquitous structural fragments in medicinal chemistry: An update on the development of synthetic methods and pharmacological diversification.

Quaid-I-Azam University
Synthetic approaches, functionalization and therapeutic potential of quinazoline and quinazolinone skeletons: the advances continue.

University of Nottingham
Recent advances in the structural library of functionalized quinazoline and quinazolinone scaffolds: synthetic approaches and multifarious applications.

Quaid-I-Azam University
Active compounds from a diverse library of triazolothiadiazole and triazolothiadiazine scaffolds: synthesis, crystal structure determination, cytotoxicity, cholinesterase inhibitory activity, and binding mode analysis.

Quaid-I-Azam University
Synthesis, crystal structure and biological evaluation of some novel 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines.

Quaid-I-Azam University
Triazolothiadiazoles and triazolothiadiazines--biologically attractive scaffolds.

Quaid-I-Azam University
Exploration of the structure-activity relationship of the diaryl anilide class of ligands for translocator protein--potential novel positron emitting tomography imaging agents.

Ge Healthcare
[¹¿?¿F]GE-180: a novel fluorine-18 labelled PET tracer for imaging Translocator protein 18 kDa (TSPO).

Ge Healthcare
Discovery and molecular docking of quinolyl-thienyl chalcones as anti-angiogenic agents targeting VEGFR-2 tyrosine kinase.

University of The Punjab
Synthesis, antioxidant activities and urease inhibition of some new 1,2,4-triazole and 1,3,4-thiadiazole derivatives.

Quaid-I-Azam University
Developing new hybrid scaffold for urease inhibition based on carbazole-chalcone conjugates: Synthesis, assessment of therapeutic potential and computational docking analysis.

Quaid-I-Azam University
An overview on the synthetic and medicinal perspectives of indenopyrazoles.

Csir-Indian Institute of Chemical Technology
Exploration of the structure-activity relationship of a novel tetracyclic class of TSPO ligands-potential novel positron emitting tomography imaging agents.

Ge Healthcare
Developing hybrid molecule therapeutics for diverse enzyme inhibitory action: Active role of coumarin-based structural leads in drug discovery.

Abbottabad University of Science and Technology
Natural and synthetic bioactive inhibitors of glycogen synthase kinase.

Jamia Hamdard (Hamdard University)
6,7-unsaturated-7-carbamoyl substituted morphinan derivative

Shionogi
Pharmacology of the urotensin-II receptor antagonist palosuran (ACT-058362; 1-[2-(4-benzyl-4-hydroxy-piperidin-1-yl)-ethyl]-3-(2-methyl-quinolin-4-yl)-urea sulfate salt): first demonstration of a pathophysiological role of the urotensin System.

Actelion Pharmaceuticals
Behaviroal, pharmacological, and molecular characterization of an amphibian cannabinoid receptor.

Oregon State University