What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Enzyme
- Biochemistry
His primary areas of investigation include Stereochemistry, Organic chemistry, Enzyme, Acarbose and IC50.
His research in Stereochemistry intersects with topics in In vitro, Urease and Oxadiazole.
The Oxadiazole study which covers Active site that intersects with In silico.
The study incorporates disciplines such as Combinatorial chemistry, Antibacterial activity and Nuclear chemistry in addition to Organic chemistry.
His research investigates the connection between Enzyme and topics such as Chemical synthesis that intersect with issues in Nitro compound and Oxazolone.
His Acarbose research includes elements of Substituent, α glucosidase, Structure–activity relationship and Molecular Docking Simulation.
His most cited work include:
- Biochemical Basis of Flour Properties in Bread Wheats. I. Effects of Variation in the Quantity and Size Distribution of Polymeric Protein (453 citations)
- Regional Distribution of Neuritic Plaques in the Nondemented Elderly and Subjects With Very Mild Alzheimer Disease (245 citations)
- Neurofibrillary Tangles in Nondemented Elderly Subjects and Mild Alzheimer Disease (184 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Stereochemistry, Organic chemistry, Enzyme, In vitro and Combinatorial chemistry.
His research integrates issues of Structure–activity relationship, Acarbose, Active site, IC50 and In silico in his study of Stereochemistry.
His Active site study frequently draws parallels with other fields, such as Oxadiazole.
Alkyl and Catalysis are among the areas of Organic chemistry where Khalid Mohammed Khan concentrates his study.
Enzyme is a subfield of Biochemistry that Khalid Mohammed Khan studies.
His research on In vitro also deals with topics like
- Urease and related Docking,
- Proton NMR which is related to area like Carbon-13 NMR.
He most often published in these fields:
- Stereochemistry (39.31%)
- Organic chemistry (21.38%)
- Enzyme (24.60%)
What were the highlights of his more recent work (between 2017-2021)?
- Stereochemistry (39.31%)
- Enzyme (24.60%)
- In vitro (23.11%)
In recent papers he was focusing on the following fields of study:
Khalid Mohammed Khan spends much of his time researching Stereochemistry, Enzyme, In vitro, Active site and Structure–activity relationship.
His Stereochemistry study incorporates themes from IC50 and Aryl.
His studies in Enzyme integrate themes in fields like Indole test and Combinatorial chemistry.
His In vitro research incorporates elements of Thiourea, Inhibitory postsynaptic potential, Molecular model, In silico and Urease.
His Active site research includes themes of Hydrazide, Ligand, Oxadiazole, Phenacyl and α glucosidase inhibitory.
As part of the same scientific family, he usually focuses on Structure–activity relationship, concentrating on Nuclear chemistry and intersecting with Nanoparticle, Cytotoxic T cell, DPPH and Antioxidant.
Between 2017 and 2021, his most popular works were:
- Synthesis, α-glucosidase inhibition and molecular docking study of coumarin based derivatives (51 citations)
- Quinazoline and quinazolinone as important medicinal scaffolds: a comparative patent review (2011-2016). (49 citations)
- Oxindole based oxadiazole hybrid analogs: Novel α-glucosidase inhibitors. (32 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Enzyme
- Biochemistry
Stereochemistry, Enzyme, In vitro, Structure–activity relationship and Active site are his primary areas of study.
His Stereochemistry study combines topics from a wide range of disciplines, such as Acarbose, IC50, Aryl and In silico.
His Enzyme research integrates issues from Glycoside, Molecule, Oxadiazole and Benzimidazole.
He interconnects Molecular model and Carbon-13 NMR in the investigation of issues within In vitro.
His Structure–activity relationship research is multidisciplinary, relying on both Thiourea, Docking, Molecular Docking Simulation, Butyrylcholinesterase and Urease.
His Active site research incorporates themes from Tryptamine and Ligand.
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