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  2. High-throughput screening - Wikipedia

    en.wikipedia.org/wiki/High-throughput_screening

    High-throughput screening (HTS) is a method for scientific discovery especially used in drug discovery and relevant to the fields of biology, materials science [1] and chemistry. [ 2 ] [ 3 ] Using robotics , data processing/control software, liquid handling devices, and sensitive detectors, high-throughput screening allows a researcher to ...

  3. Chemogenomics - Wikipedia

    en.wikipedia.org/wiki/Chemogenomics

    Chemogenomics Staubli robot retrieves assay plates from incubators. Chemogenomics, or chemical genomics, is the systematic screening of targeted chemical libraries of small molecules against individual drug target families (e.g., GPCRs, nuclear receptors, kinases, proteases, etc.) with the ultimate goal of identification of novel drugs and drug targets. [1]

  4. Verseon - Wikipedia

    en.wikipedia.org/wiki/Verseon

    Nano Magazine noted the platform has produced “multiple chemically diverse clinical candidates…unlikely to be found through any other method” for every one of its drug programs. [7] Currently, most drugs are discovered using the high-throughput screening method. [8]

  5. Chemical library - Wikipedia

    en.wikipedia.org/wiki/Chemical_library

    In drug discovery high-throughput screening, it is desirable to screen a drug target against a selection of chemicals that try to take advantage of as much of the appropriate chemical space as possible. The chemical space of all possible chemical structures is extraordinarily large. Most stored chemical libraries do not typically have a fully ...

  6. Hit to lead - Wikipedia

    en.wikipedia.org/wiki/Hit_to_lead

    Hit to lead (H2L) also known as lead generation is a stage in early drug discovery where small molecule hits from a high throughput screen (HTS) are evaluated and undergo limited optimization to identify promising lead compounds.

  7. Virtual screening - Wikipedia

    en.wikipedia.org/wiki/Virtual_screening

    Virtual screening (VS) is a computational technique used in drug discovery to search libraries of small molecules in order to identify those structures which are most likely to bind to a drug target, typically a protein receptor or enzyme.

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