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- Metabolic soft spot analysis in liver microsomes, hepatocytes and other in vitro systems
- GSH-trapping of reactive metabolites in liver microsomes
- Comparative metabolism across species in liver microsomes, hepatocytes and other in vitro systems
- Biotransformation of slowly metabolized drugs in 3D hepatocyte spheroid culture
- ADME studies in mice, rats, dogs, monkeys, and other animal species
- Metabolite profiling and identification in plasma, urine, feces, bile and tissue samples from pharmacokinetics, pharmacology, toxicology, and clinical studies
- Comparative metabolite profiling in plasma of human and Tox species for MIST evaluation
- Radiolabeled mass balance and ADME studies in mice, rats, dogs, monkeys, and other animal species
- QWBA tissue distribution studies in mice and rats
- Human mass balance study
- Profiling and identification of payload-containing components released from an ADC in vitro
- In vitro metabolite profiling and metabolizing enzyme phenotyping of payloads
- Metabolite profiling and identification of payloads in rats, monkeys and other animal species
- ADME study of radiolabeled ADCs and payloads in rats, monkeys and other animals
- Studies of payload release and ADME of other antibody conjugates, including antibody-peptide conjugate (APC), antibody-oligonucleotide conjugate (AOC), and degrader-antibody conjugate (DAC)
- In vitro and in vivo metabolite profiling and identification of peptide-containing therapeutics, including peptide drug conjugate (PDC) and radionuclide drug conjugate (RDC)
- In vitro and in vivo metabolite profiling and identification of oligonucleotides
- Metabolite profiling and identification of proteolysis-targeting chimeras (PROTACs) and small molecule drug conjugates (SMDCs)
- ADME studies of radiolabeled peptide, PDC, oligoneucides, PROTAC and SMDC therapeutics in rats, monkeys and other animal species
- Identification of the role of AO in drug metabolism
- CYP phenotyping in drug discovery
- Phenotyping of other metabolizing enzymes
- Enzyme kinetic studies of metabolite formation
- Definitive CYP enzyme phenotyping
- 在肝微粒体/胞浆/S9、肝细胞和其他体外系统中进行多种属的比较代谢分析
- 在3D肝细胞球(合珀)培养中进行慢代谢药物的生物转化
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