SLC6A19-IN-4 is an allosteric-competitive and orally active B 0 AT1 inhibitor. SLC6A19-IN-4 inhibits both human and mouse B 0 AT1 with IC 50 values of 513 nM and 295 nM, respectively. SLC6A19-IN-4 exhibits excellent metabolic stability. SLC6A19-IN-4 significantly increases urinary phenylalanine (Phe) excretion and reduces plasma Phe levels through dual inhibition of B 0 AT1 in both the intestine (reducing absorption) and kidney (promoting excretion) in vivo. SLC6A19-IN-4 can be used for phenylketonuria (PKU) and other disorders involving SLC6 -family transporters research.
Products | Products > Disease Areas > Metabolic or Endocrine Disease | Products > Disease Areas > Amino Acid/Protein Metabolism | Products > Disease Areas > Phenylketonuria | Products > Signaling Pathways > Membrane Transporter/Ion Channel | Products > Research Areas > Metabolic Disease | Products > Signaling Pathways > Amino acid Transporter
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