Katy Kellett

Katy Kellett
University of California, San Diego | UCSD · Skaggs School of Pharmacy and Pharmaceutical Sciences

PhD Pharmaceutical Chemistry

About

11
Publications
1,597
Reads
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144
Citations
Additional affiliations
May 2014 - September 2014
University of Southern Mississippi
Position
  • Researcher

Publications

Publications (11)
Article
Full-text available
We investigate the binding of native β-cyclodextrin (β-CD) and eight novel β-CD derivatives with two different guest compounds, using isothermal calorimetry and 2D NOESY NMR. In all cases, the stoichiometry is 1:1 and binding is exothermic. Overall, modifications at the 3′ position of β-CD, which is at the secondary face, weaken binding by several...
Preprint
We investigate the binding of native β-cyclodextrin (β-CD) and eight novel β-CD derivatives with two different guest compounds, using isothermal calorimetry (ITC) and 2D NOESY NMR. In all cases, the stoichiometry is 1:1 and binding is exothermic. Overall, modifications at the 3’ position of β-CD, which is at the secondary face, weaken binding by se...
Article
Substituted cyclodextrins (CDs) have many applications, but synthetic challenges have limited the derivatives that can routinely be accessed. In particular, although there is considerable interest in selective derivatization at the 2- and 3-hydroxyls on the secondary face, since bulky guest molecules are most likely to project through this larger a...
Preprint
We have described simple, high-yield, protocols, which require only commonly accessible equipment, to synthesize a wide range of β-CD derivatives mono-substituted at the secondary face. These derivatives may be useful in their own right, and they are also scaffolds for further modification, and examples of the far broader array of derivatives that...
Article
Full-text available
Researchers developing software to predict the binding constants of small molecules for proteins have, in recent years, turned to host–guest systems as simple, computationally tractable model systems to test and improve these computational methods. However, taking full advantage of this strategy requires aqueous host–guest systems that probe a grea...
Preprint
We have described simple, high-yield, protocols, which require only commonly accessible equipment, to synthesize a wide range of β-CD derivatives mono-substituted at the secondary face. These derivatives may be useful in their own right, and they are also scaffolds for further modification, and examples of the far broader array of derivatives that...
Article
Objectives: A method was developed to analyze St John's wort (Hypericum perforatum L.) herb and preparations using inductively coupled plasma-optical emission spectroscopy (ICP-OES) to determine the quantity of 11 elements (Al, B, Ba, Ca, Cu, Fe, Mg, Mn, Ni, Sr and Zn). Methods: This study includes the evaluation of digestion acids and calibrati...
Article
An anthracene molecular probe has been synthesised and shown to target mephedrone, a stimulant drug from the cathinone class of new psychoactive substances (NPS). A protocol has been developed to detect mephedrone via the probe using NMR spectroscopy in a simulated street sample containing two of the most common cutting agents, benzocaine and caffe...
Article
Using current research and real-life scenarios to motivate students to understand chemistry principles is a key strategy in learning and teaching. An illustration of psychoactive drugs referred to as “legal highs” used in the U.K. and Europe is presented to highlight key chemistry principles and relate the importance of chemistry research in health...
Article
Using current research and real-life scenarios to motivate students to understand chemistry principles is a key strategy in learning and teaching. An illustration of psychoactive drugs referred to as " legal highs " used in the U.K. and Europe is presented to highlight key chemistry principles and relate the importance of chemistry research in heal...

Questions

Questions (2)
Question
I am trying to see if it is possible to incorporate this into a device, as opposed to having to carry out a freebase extraction before using a potential microfluidic device. 
Question
have about 10 receptor sites with one ligand and want to develop a pharmacophore model using schrodinger software. Has anyone every done this? or know if it is easily possible.

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