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ADME Bioanalytical

Essential Capabilities in Support of Drug Discovery and Development

The bioavailability of any molecule depends on its absorption, metabolism and distribution in humans. To support both lead optimization and candidate selection, SCYNEXIS provides rapid generation of reliable ADMET and pharmacokinetic (PK) data on compounds in discovery through NDA filing. SCYNEXIS rapidly screens for properties such as metabolic stability and cytotoxicity to prioritize and differentiate lead series based on those key ADMET parameters.

Lead optimization projects can also be guided by plasma stability studies, permeability assays and metabolite identification. In support of preclinical and clinical development, SCYNEXIS performs analyses of compounds in various matrices according to current GLP guidelines. In addition, SCYNEXIS can customize protocols and reports based on therapeutic areas and customer’s specifications.

In Vitro ADMET Capabilities

  • Cytochrome P450 Isozyme Assays
    • Human Recombinant
    • Microsome-Based Assays
  • Metabolic Stability
    • Rodent, Dog and Human
    • Hepatocytes and Microsomes
  • Cytotoxicity and Cell-Based Assays
    • Variety of Tissue Cell Lines
    • Variety of Endpoints
    • Client-Specific Assays
    Bioanalytical Capabilities
  • Sample Preparation
    • Tissue Extraction
    • Microtiter and Online SPE
    • Liquid Handlers
  • Triple-Quadrupole MS
  • Tandem-MS (MRM and SRM) Quantitation
  • LC-NMR
  • PD Studies
  • N-in-1 PK Screening
  • Metabolite ID
  • GLP-Compliant Studies