18 articles for A Khan
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Quaternary Indolizidine and Indolizidone Iminosugars as Potential Immunostimulating and Glycosidase Inhibitory Agents: Synthesis, Conformational Analysis, Biological Activity, and Molecular Docking Study.
Savitribai Phule Pune University (Formerly University of Pune)
Design and synthesis of new barbituric- and thiobarbituric acid derivatives as potent urease inhibitors: Structure activity relationship and molecular modeling studies.
The Islamia University of Bahawalpur
Synthesis of novel derivatives of oxindole, their urease inhibition and molecular docking studies.
Universiti Teknologi Mara Puncak Alam Campus
Synthesis of diethyl 4-substituted-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylates as a new series of inhibitors against yeasta-glucosidase.
University of Karachi
Synthesis and in vitro urease inhibitory activity of N,N'-disubstituted thioureas.
University Karachi
Methylenebissantin: a rare methylene-bridged bisflavonoid from Dodonaea viscosa which inhibits Plasmodium falciparum enoyl-ACP reductase.
University of Karachi
Synthesis, antioxidant activities and urease inhibition of some new 1,2,4-triazole and 1,3,4-thiadiazole derivatives.
Quaid-I-Azam University
Identification of a butyrophenone analog as a potential atypical antipsychotic agent: 4-[4-(4-chlorophenyl)-1,4-diazepan-1-yl]-1-(4-fluorophenyl)butan-1-one.
Florida A&M University
The neuroprotective action of JNK3 inhibitors based on the 6,7-dihydro-5H-pyrrolo[1,2-a]imidazole scaffold.
University College London
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
α-Geminal disubstituted pyrrolidine iminosugars and their C-4-fluoro analogues: Synthesis, glycosidase inhibition and molecular docking studies.
Savitribai Phule Pune University (Formerly University of Pune)
Non-peptide macrocyclic histone deacetylese (HDAC) inhibitors and methods of making and using thereof
Georgia Tech Research
Pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use
F. Hoffmann-La Roche
Synthesis and biological evaluation of thienopyrrolizines, a new family of CDK/GSK-3 inhibitors.
UniversitÉ