PPT-Antibacterial Drug Discovery
Author : olivia-moreira | Published Date : 2017-03-15
and Machine Learning Michael Charlton ChEMBL Physical Property Analysis Ebejer et al J Cheminformatics extracted data from Chembl and assigned an antibacterial
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Antibacterial Drug Discovery: Transcript
and Machine Learning Michael Charlton ChEMBL Physical Property Analysis Ebejer et al J Cheminformatics extracted data from Chembl and assigned an antibacterial class Antibacterial . HOW should this drug be taken This drug is usually used in combination with other agents to treat MAC The dose of ciprofloxacin is 500 to 750 mg twice daily If ciprofloxacin is prescribed to treat another infection the dose may be different Also the By Andreas Dr Lorenz M.Mayr Drug Discovery World Summer 2006 Miniaturisation ofassay developmentand screening In recent years we have seen a strong increase in the number of chemicalcompounds and mole an Industrial Process. How are drugs . discovered and developed?. Dr Steve Carney, s.carney@elsevier.com. Managing Editor, . Drug Discovery Today. What’s my background?. First degree in Biochemistry. Elliot Young. Honey. Background. Background. Background. Background. Background. +. Background. Methodology. 3 honeys compared:. Processed. Unprocessed. 10+ UMF Manuka. Honey’s antibacterial qualities tested against . – . get ready for the show. Weidong Zhang. Pfizer. 1. Outline. Overview of omics technology. Application of omics in drug discovery. Case studies from pre-clinical to phase II/III. 2. 3. Omics provide paramount view of biological cascade. Properties: . Optimizing Pharmacokinetics and Safety During Drug . Discovery. ACS Short Course. Li Di and Edward H. Kerns. Introduction to Drug-Like Properties. Few research compounds will become drugs because they lack sufficient pharmacokinetics (PK) and safety. Distinguished University Professor Lecture. Presented on January 29, 2015 by Paul Erhardt, PhD. UT DUP and Director of the Center for Drug Design and Development (CD3). paul.erhardt@utoledo.edu. 1. Outline. Please Sign Up:. . Name. . Email (. Onyen. is fine, or …). . Are You . ENRolled. ?. Dept. & Advisor (Lab?). . Tentative Title (“????” Is OK). . When:. Next Week, Early, Oct., Nov., Late. Additional copies are available from Office of Communications Division of Drug Information Center for Drug Evaluation and Research Food and Drug Administration 10001 New Hampshire Ave Hillandale Bldg Tchemical entitiessrn KarlsdttirM Sc thesis University of IcelandFacultyof Pharmaceutical SciencesSchool of Health SciencesThe origin of FDA approved natural product new chemical entitiessrn Karlsdtti . ……………………………………………………………………………………………………………………………………………………………………………………………………………………………………………. Gerald J. Wyckoff. Training modes. Are we training . genomicists. to deal with the right problems?. Are the training modalities we’re using proper?. What questions should we be looking at?. Problems in Drug Discovery. linking diseases, drivers, targets and drugs. via multi-omics, clinical, imaging and perturbation data fusion. Nathalie Pochet, Ph.D.. Assistant Professor, Harvard Medical School. Associate Scientist, Brigham and Women’s Hospital. 1. Dr. Abd El Raheim Donia. Generally,. . a drug . can be . defined . as a . substance that . induces . a response . within the human . body.. Dr. Abd El Raheim Donia. 2. FDA Definition . of a . Drug.
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