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  2. Drug design - Wikipedia

    en.wikipedia.org/wiki/Drug_design

    The phrase "drug design" is similar to ligand design (i.e., design of a molecule that will bind tightly to its target). [6] Although design techniques for prediction of binding affinity are reasonably successful, there are many other properties, such as bioavailability, metabolic half-life, and side effects, that first must be optimized before a ligand can become a safe and effictive drug.

  3. Medicinal chemistry - Wikipedia

    en.wikipedia.org/wiki/Medicinal_chemistry

    It also includes the study of existing drugs, their biological properties, and their quantitative structure-activity relationships (QSAR). [1] [2] Medicinal chemistry is a highly interdisciplinary science combining organic chemistry with biochemistry, computational chemistry, pharmacology, molecular biology, statistics, and physical chemistry.

  4. Goodman & Gilman's The Pharmacological Basis of Therapeutics

    en.wikipedia.org/wiki/Goodman_&_Gilman's_The...

    While teaching jointly in the Yale School of Medicine's Department of Pharmacology, Goodman and Gilman began developing a course textbook that emphasized relationships between pharmacodynamics and pharmacotherapy, introduced recent pharmacological advances like sulfa drugs, and discussed the history of drug development.

  5. Pharmacology - Wikipedia

    en.wikipedia.org/wiki/Pharmacology

    The study of pharmacology overlaps with biomedical sciences and is the study of the effects of drugs on living organisms. Pharmacological research can lead to new drug discoveries, and promote a better understanding of human physiology. Students of pharmacology must have a detailed working knowledge of aspects in physiology, pathology, and ...

  6. List of benzimidazole opioids - Wikipedia

    en.wikipedia.org/wiki/List_of_benzimidazole_opioids

    The structure-activity relationship of the drug class has been explored to a reasonable extent. The optimal substitution pattern is fairly tightly defined (i.e. N,N-diethyl on the amine nitrogen, 4-ethoxy on the benzyl ring and 5-nitro on the benzimidazole ring), but even derivatives incorporating only some of these features are still potent opioids.

  7. Classical pharmacology - Wikipedia

    en.wikipedia.org/wiki/Classical_pharmacology

    Forward (classical) and reverse pharmacology approaches in drug discovery. In the field of drug discovery, classical pharmacology, [1] also known as forward pharmacology, [2] [3] [4] or phenotypic drug discovery (PDD), [5] relies on phenotypic screening (screening in intact cells or whole organisms) of chemical libraries of synthetic small molecules, natural products or extracts to identify ...

  8. Drug discovery - Wikipedia

    en.wikipedia.org/wiki/Drug_discovery

    The elucidation of the chemical structure is critical to avoid the re-discovery of a chemical agent that is already known for its structure and chemical activity. Mass spectrometry is a method in which individual compounds are identified based on their mass/charge ratio, after ionization. Chemical compounds exist in nature as mixtures, so the ...

  9. Pharmacotherapy - Wikipedia

    en.wikipedia.org/wiki/Pharmacotherapy

    Pharmacotherapy, also known as pharmacological therapy or drug therapy, is defined as medical treatment that utilizes one or more pharmaceutical drugs to improve ongoing symptoms (symptomatic relief), treat the underlying condition, or act as a prevention for other diseases (prophylaxis).