July 3, 2007 (Press Release) --
LITMUS LLC, a leading global technology innovations company, today announces that Dr. Bill W. Massey has been appointed as President of its wholly owned subsidiary, LITMUS Molecular Design (“LMD”).
LMD is dedicated to the discovery and development of new molecular entities for the pharmaceutical, chemical and materials science industries. LMD’s technology dramatically improves the efficiency and predictive accuracy of the discovery and development process thereby substantially reducing the associated time and costs. Consequently LMD is able to generate significant value for users of its technology in their commercialization of new molecular entities.
LMD creates new molecular entities designed to have specified desired properties and characterizes the activity of existing molecules through the use of LITMUS Spectral Modeling, the application of its patented, cutting edge methodology called Spectral Data Activity Relationship (SDAR). The method uses computer modeling techniques to predict the properties that a molecular structure will exhibit based solely on spectral analysis (LITMUS Spectral Modeling). This removes the need to physically create the molecule and exhaustively test for which individual properties it possesses. LMD can also screen existing molecules for desirable, or undesirable, activity. As all of these capabilities are assessed in silico (on the computer), the time and cost are greatly reduced. Developed by scientists at the U.S. Food and Drug Administration (FDA)’s National Center for Toxicological Research, LITMUS Spectral Modeling can predict a wide range of a given molecular structure’s scientifically important properties, including chemical reactivity, carcinogenicity, biological activity, receptor-binding affinity, toxicity, metabolism, absorption, and chemical and physical properties. LMD owns the worldwide license on LITMUS Spectral Modeling.
Dr. Massey has had a successful 15 year career in the pharmaceutical industry, spanning a variety of areas including pre-clinical research, clinical research, regulatory affairs, marketing, and business operations/planning. He has held senior management positions at Astra Merck Inc., Quintiles Central Nervous System (CNS) Therapeutics Inc., Scirex Corporation, and AstraZeneca plc. He has actively managed the preparation and submission of a number of original investigational new drug and product marketing applications, and has leadership experience in international drug development programs in the cardiovascular and CNS therapeutic areas. Dr. Massey received his PhD from the Department of Pharmacology and Interdisciplinary Toxicology of the University of Arkansas for Medical Sciences. He currently holds two adjunct faculty appointments in pharmacology, at the University of Arkansas for Medical Sciences, and psychiatry, at the University of Mississippi Medical Center.
LMD is dedicated to the discovery and development of new molecular entities for the pharmaceutical, chemical and materials science industries. LMD’s technology dramatically improves the efficiency and predictive accuracy of the discovery and development process thereby substantially reducing the associated time and costs. Consequently LMD is able to generate significant value for users of its technology in their commercialization of new molecular entities.
LMD creates new molecular entities designed to have specified desired properties and characterizes the activity of existing molecules through the use of LITMUS Spectral Modeling, the application of its patented, cutting edge methodology called Spectral Data Activity Relationship (SDAR). The method uses computer modeling techniques to predict the properties that a molecular structure will exhibit based solely on spectral analysis (LITMUS Spectral Modeling). This removes the need to physically create the molecule and exhaustively test for which individual properties it possesses. LMD can also screen existing molecules for desirable, or undesirable, activity. As all of these capabilities are assessed in silico (on the computer), the time and cost are greatly reduced. Developed by scientists at the U.S. Food and Drug Administration (FDA)’s National Center for Toxicological Research, LITMUS Spectral Modeling can predict a wide range of a given molecular structure’s scientifically important properties, including chemical reactivity, carcinogenicity, biological activity, receptor-binding affinity, toxicity, metabolism, absorption, and chemical and physical properties. LMD owns the worldwide license on LITMUS Spectral Modeling.
Dr. Massey has had a successful 15 year career in the pharmaceutical industry, spanning a variety of areas including pre-clinical research, clinical research, regulatory affairs, marketing, and business operations/planning. He has held senior management positions at Astra Merck Inc., Quintiles Central Nervous System (CNS) Therapeutics Inc., Scirex Corporation, and AstraZeneca plc. He has actively managed the preparation and submission of a number of original investigational new drug and product marketing applications, and has leadership experience in international drug development programs in the cardiovascular and CNS therapeutic areas. Dr. Massey received his PhD from the Department of Pharmacology and Interdisciplinary Toxicology of the University of Arkansas for Medical Sciences. He currently holds two adjunct faculty appointments in pharmacology, at the University of Arkansas for Medical Sciences, and psychiatry, at the University of Mississippi Medical Center.

LITMUS LLC, a leading global technology innovations company, today announces that Dr. Bill W. Massey has been appointed as President of its wholly owned subsidiary, LITMUS Molecular Design (“LMD”).
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