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Plataforma de Cribado de Fármacos y Farmacogenómica

REACT-EU PROJECT
CONVENIO DE COLABORACIÓN ENTRE A AXENCIA GALEGA DE INNOVACIÓN E A UNIVERSIDADE DE SANTIAGO DE COMPOSTELA PARA REGULAR AS CONDICIÓNS DA AXUDA DESTINADA Á ACTUALIZACIÓN E AMPLIACIÓN DA PLATAFORMA INNOPHARMA DA USC
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Las infraestructuras de alta capacidad de INNOPHARMA ofrecen un conjunto de servicios que cobren todas las etapas del proceso de descubrimiento temprano de fármacos, desde la identificación de dianas hasta la evaluación preliminar de seguridad y toxicidad. La plataforma está disponible tanto para servicios a la carta como para proyectos complementarios de colaboración en el descubrimiento de fármacos.

 

  • Drug discovery program design

    • Candidate Target Profile definition
    • Feasibility/druggability assessment
    • Screening cascade design
    • Identification of hits, leads and candidates

    Assay development, miniaturization, and automation

    • Target-based assays
    • Phenotypic assays
    • Deconvolution assays
    • Custom assays

    De-risking programs

    • Drug discovery programs up to proof of concept stage

    Chemical compound libraries

    • Compounds selected in silico based on biological and structural diversity
    • Proprietary compounds
    • Drug repurposing libraries
    • Target-focused sub-libraries

    Pharmacogenomics studies

    • Biomarkers identification
    • Identification of novel therapeutic targets

    In vitro preliminary ADME-Tox and safety

    • Cytochrome P450 induction and inhibition
    • Cytotoxicity
    • hERG channel
    • Chemical, microsomal and plasma stability
    • Plasma protein binding
    • Permeability assay
    • P-glycoprotein
    • Genotoxicity

    Customized assay development

    • Target engagement
    • Phenotypic assays
    • Deconvolution assays
  • From INNOPHARMA we are constantly developing new tests and implementing new technologies, so if you have any interest in any test or technology not included in this list, please contact us

    COVID-19

    • IN VITRO ASSAYS

     


    ACE2 activity
    TMPRSS2 activity
    Furin activity

    TARGET-BASED

    • GPCRs
    Radioligand Assays

     


    Adenosine

     


    A1
    A2A
    A2B
    A3
      Dopamine

     


    D1
    D2
    D3
    D4
    D5
    Histamine

     


    H1
    H2
    H3
     
    Adrenergic:

     


    α1
    α2
    α2C
    β1
    β2
    β3
    Serotonin

     


    5-HT1A   5-HT1B   5-HT1D
    5-HT2A  5-HT2B  5- HT2C
    5-HT5A   5-HT6   5-HT7
      Cannabinoid:

     


    CB1
    CB2
    Muscarinic:

     


    M1
    M2
    M3
    M4
    M5
                 
    Second Messengers

     


    Arachidonic acid metabolism
    Nitric oxide synthase
    Inositol phosphate
    Calcium mobilization
      Isolated Organ Assays

     


    Adenosine: A1 A2A A2B
    Adrenergic: α1 α2 β1
    Histamine: H1 H2
    Muscarinic: M1 M2 M3
    Serotonin: 5-HT2A 5-HT2B 5-HT3 5-HT4
    Beta-Arrestin Translocation - BRET

     


    Mu-opioid
    CX3CR1
    • TRANSPORTERS

     


    Radioligand Assays

     


    Dopamine (DAT)
    Noradrenaline (NAT)
    Serotonin (5-HTT)
    • NUCLEAR RECEPTORS

     


    Radioligand Assays

     


    Estrogen receptors (ER)
    Androgen receptor (AR)
    Progesterone receptor (PR)
    Glucocorticoid receptor (GR)
    Peroxisome proliferator-activated receptors (PPAR)
    Prostanoid receptors (PR)
    Functional assays

     


    Androgen receptor (AR)
    Glucocorticoid receptor (GR)

     

    • ENZYMES

     


    Kinase profiling >  250 functional assays
    Phosphodiesterases: 15 activity assays
    Phosphatases
    Beta-secretase
    Acetylcholinesterase  
    Monoamine oxidases: MAO-A, MAO-B
    Epigenetic enzymes    
    • ION CHANNELS

     


    Voltage-gated

     


    Calcium
    Potasium
    Sodium
    hERG
    Membrane ligand-gated

     


    NMDA
    GABAA
    5-HT3

    PHENOTYPIC ASSAYS

    • CELL VIABILITY AND CYTOTOXICITY IN 20+ HUMAN CELL LINES
    • MORPHOLOGICAL PROFILING BY HIGH-CONTENT IMAGING (CELL PAINTING)
    • PHENOTYPIC PROFILING BY LABEL-FREE DYNAMIC MASS REDISTRIBUTION-BASED ASSAYS
    • TARGET-DECONVOLUTION STRATEGIES
    • IN VITRO TRANSLATIONAL DISEASE-RELATED ASSAYS

     


    Neurological and neurodegenerative diseases

     


    Neurite outgrowth
    α-synuclein aggregation
    Metabolic- disease

     


    Adipocyte assay

    PRELIMINARY ADME-Tox AND SAFETY ASSAYS

    • CITOTOXICITY
    Cell Lines

     


    Cancer cell lines

     


    Human ovarian carcinoma: A2780, A2780cis, NCI-ADR/RES
    Human cervix carcinoma: HeLa 229
    Human breast carcinoma: MCF-7, T47D, MDA-MB-231, Hs578T
    Human lung carcinoma: NCI-H460, A549
    Human glioblastoma: SF268
    Human colon carcinoma: CACO-2, HT-29, HCT116
    Human liver carcinoma: Hep-G2
    Human neuroblastoma: SH-SY5Y
    Human acute myeloid leukemia: HL-60
    Human pancreatic carcinoma: CFPAC-1
    Human prostate carcinoma: LNCaP, PC3
    Human osteosarcoma: U2OS
    Other cell lines

     


    Human lung fibroblasts: MRC-5
    Porcine kidney cell line: LLC-PK1
         
    Cell Viability Technologies

     


    Crystal violet
    MTT reduction
    Sulforhodamine B
    ATP production
         
    • CYTOCHROME INDUCTION AND INHIBITION

     


    Recombinant P450 (1A2, 2C9, 2C19, 2D6, 3A4)
    • hERG
       
    • CHANNEL PERMEABILITY ASSAYS

     


    CACO-2 (6-well, 24-well and 96-well formats)
    • P-GLYCOPROTEIN SUBSTRATE
       
    • SOLUBILITY ASSAYS

     


    Aqueous solubility (pH-dependent)
    • MICROSOMAL STABILITY

     


    In several species
    • PLASMA PROTEIN BINDING

     


    In several species
    • PLASMA STABILITY

     


    In several species
    • GENOTOXICITY

     


    Micronucleus assay
         

    CUSTOMIZED ASSAYS

    • AD-HOC ASSAY DEVELOPMENT AND SCREENING

     


    Target engagement
    Phenotypic assays
    Target deconvolution strategies
  • The Innopharma Platform has state-of the art equipment for carrying out assay development projects and screening campaigns with different technological approaches

    • Radioactivity (Filtration and SPA)
    • Absorbance
    • Fluorescence intensity and polarization
    • Luminescence
    • FRET and Homogeneous Time-Resolved Fluorescence
    • BRET
    • Alphascreen
    • Fluorescence Lifetime Imaging
    • Automated patch-clamp
    • Label free (Dynamic Mass Redistribution)
    • Automated mobility shift (Lab on a chip)
    • High Content Screening
    • UPLC-MS/MS
    • Genome wide and candidate gene association studies
    • Next Generation Sequencing
Los contenidos de esta página se actualizaron el 10.09.2024.