Not exact matches
David Sinclair of Harvard Medical School in Boston and colleagues at the biotech firm BIOMOL Research Laboratories in Plymouth Meeting, Pennsylvania,
screened a
library of compounds for
molecules that trigger SIRT1 activity.
In this study, the researchers
screened a
library of 200,000 small
molecule compounds to identify potential inhibitors of Ebola virus RNA synthesis.
Today, the pharmaceutical industry
screens synthetic chemical
libraries of thousands of
molecules to find one that may have a medicinal effect, said Parekkadan, who joined Rutgers» School of Engineering in January.
In one case, the researchers
screened a small -
molecule compound
library and identified compounds that bind tightly to NUCB1, an otherwise little - known protein that showed strong interactions with the arachidonoyl probes.
They identified AM404 as a potential antiviral agent by
screening the National Institutes of Health Clinical Collection, a
library of small
molecules that have been used clinically in humans, using a high - throughput
screening system.
Nikolas Jorstad and Matt Wilken, graduate students in Reh's lab,
screened a
library of small
molecules to find one that could reopen access to the genetic code in the adult mouse.
To test DDX3's druggability, the team chose to design its own small
molecule rather than
screen libraries of
molecules already created.
The process of drug discovery has been dominated in recent years by the
screening of large
libraries of structurally diverse small
molecules for effects on target proteins associated with disease.
Such projects involve developing and optimizing assays for automation,
screening a large compound
library, and characterizing each small -
molecule probe.
We are going to
screen a larger
library of chemicals to identify
molecules that either boost or weaken NMD, which should help develop better and more targeted drugs for treating ALS, muscular dystrophy and cystic fibrosis.»
Scientists at the Centers for Disease Control and Prevention (CDC) also contributed by performing initial
screening of the Gilead Sciences compound
library to find
molecules with promising antiviral activity.
«We're now working with our colleagues in Sanford - Burnham's Conrad Prebys Center for Chemical Genomics to
screen a large chemical
library — a collection of around 300,000 compounds — to find
molecules that bind to these newly discovered HNF - 4α sites,» Rastinejad said.
The MSC is a core facility providing the use of high throughput
screening technology (HTS), as well as expertise and reagents, necessary for the
screening of the
library of small
molecules for biologically active compounds in a variety of readout systems.
The facility maintains a small
molecule library of ~ 100,000 drug - like small
molecules for high - throughput
screening and provides access to liquid handling robotics and a multilabel plate reader.
Our current works have focused on
screening the chemical
libraries to identify and further characterize small
molecules that can control stem cell fate in various systems.
UniChem supports the integration of high - throughput
screening data on small
molecules with chemical
libraries and chemical resources for drug discovery and optimization.
The course gives a broad introduction to high throughput
screening (HTS) that is technique used to identify biologically active small organic
molecules through
screening of compound
libraries with the help of robust test systems and advanced instrumentation.
The identification of disease signatures will enable
screens of small
molecule libraries to delineate molecular targets that modulate these disease signatures and identify new diagnostic and therapeutic leads for schizophrenia and bipolar disorder.
With Jan Stichel at Annette Beck - Sickinger's lab, Leipzig University, Germany and David Weaver, head of the high - throughput
screening facilities at Vanderbilt University, I will be
screening Vanderbilt's
library of small
molecules for potential allosteric modulators of the human Y4 receptor.
Another key contribution made to the field is Schreiber's formal planning of diversity - oriented synthesis (DOS), which involves the creation of diverse
libraries of small
molecules for biological
screening.
Once the Vanderbilt small
molecule library has been
screened for potential modulators of the Y4 receptor, I will use the results to design efficient and accurate descriptors that can be used with artificial neural networks to predict activity at the Y4 receptor based on a small
molecule's structural properties.
Using this information, we will then take advantage of recent advances in the quantification of assembly to
screen candidate small -
molecule libraries for enhanced activity in assembly acceleration, inhibition, and misdirection.
Phenotypic
screening of small
molecule libraries using iPSC - based models to identify novel drug candidates and disease mechanisms.
The team
screened a small
molecule compound
library and identify a drug, which they call CLP257.