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Molsoft to Evaluate Novel Scaffolds for PDF Inhibitor Program |
South San Francisco and La Jolla, CA (October 21, 2002)
Molsoft LLC, a La Jolla based company providing new, breakthrough technologies
in computational chemistry and biology, and GeneSoft Pharmaceuticals Inc., a
specialty pharmaceutical company headquartered in South San Francisco,
announced that they have signed a collaborative agreement to evaluate
inhibitors of peptide deformylase (PDF), an essential bacterial metalloenzyme
and novel antibiotic target.
GeneSoft is developing PDF inhibitors under a broad-based antimicrobial
metalloenzyme research and development collaboration with UK-based British
Biotech, a leader in the field of metalloenzyme inhibition.
Under its agreement with GeneSoft, Molsoft will use its proprietary ICM
flexible docking technology to evaluate novel chemistries for PDF inhibition.
Molsoft ICM allows accurate prediction of docking geometries and in silico
selection of drug candidates from millions of compounds. Molsoft will deliver
the results of the docking procedure to GeneSoft.
"This collaboration represents an ideal opportunity to apply state-of-the-art
docking technology to an exciting target (PDF) where structural information is
available," said Heinz Moser, Chief Technical Officer and Vice-President of
Chemistry at GeneSoft. "Evaluating novel scaffolds in silico prior to making a
synthetic commitment will greatly improve our efficiency in optimizing PDF
inhibitors. We believe that this enzyme is an excellent target for Molsoft's
technology."
"We are very excited about this project and look forward to advancing
GeneSoft's research and development objectives through a lasting, collaborative
relationship," said Maxim Totrov, Ph.D., Principal Scientist and Scientific
Co-founder at Molsoft. "Based on our previous successes using Molsoft's
advanced technology for flexible receptor docking, we expect GeneSoft and
British Biotech will gain invaluable insight into the factors that help improve
the affinities of the metal binding groups, thus facilitating their
antibacterial therapeutic initiative."
About Molsoft LLC
Molsoft LLC is a leading provider of software products and contract research
services to the pharmaceutical and biotechnology companies. Founded in 1994 by
Prof. Ruben Abagyan, Molsoft offers expertise, knowledge and technology to
client organizations for computational structural genomics, large scale 3D
modeling, characterization of newly discovered proteins, characterization and
prioritization of targets for drug discovery, prediction of binding pockets,
validation of pocket models via flexible receptor-ligand docking,
structure-based drug design, virtual ligand screening for rational drug design,
structure-focused combinatorial library design and structure-based vaccine
design.
Molsoft is located in La Jolla, California. www.molsoft.com
About GeneSoft Pharmaceuticals Inc.
GeneSoft, founded in 1998, is a specialty pharmaceutical company focused on
discovering, developing and marketing novel anti-infective products. Genesoft
believes that the recent emergence of drug-resistant infectious organisms calls
for the design of new therapies with novel mechanisms of action. GeneSoft
currently has a portfolio of lead compounds in clinical and pre-clinical
development. GeneSoft's first oral antibiotic, Factive, is in late stage
clinical development. BB-83698, a novel-mode-of-action antibiotic for the
treatment of drug resistant infections being developed with British Biotech,
entered Phase I trials in October 2002. Several other drug candidates are
expected to enter clinical trials in the next 24 months.
GeneSoft is located in South San Francisco, California. www.genesoft.com
About British Biotech
British Biotech is a research and development stage pharmaceuticals company
aiming to develop and commercialize specialist drugs for serious illnesses,
including cancer, acute thrombotic diseases, inflammatory disease and bacterial
infections. It currently has four products in patient trials, including the PDF
inhibitor BB-83698 (the first-ever clinical evaluation of a PDF inhibitor),
supplemented by focused, collaborative drug discovery research programs.
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