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ChemicalBook--->CAS DataBase List--->1646682-14-5

1646682-14-5

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    1. 1646682-14-5 Structure

      1646682-14-5 Structure
      IdentificationBack Directory
      [Name]

      FD-IN-1
      [CAS]

      1646682-14-5
      [Synonyms]

      FD-IN-1
      Benzeneacetic acid, 2-[[3'-[(1S)-1-amino-2-hydroxyethyl][1,1'-biphenyl]-3-yl]methoxy]-
      (S)-2-(2-((3'-(1-amino-2-hydroxyethyl)-[1,1'-biphenyl]-3-yl)methoxy)phenyl)acetic acid
      [Molecular Formula]

      C23H23NO4
      [MDL Number]

      MFCD32067952
      [MOL File]

      1646682-14-5.mol
      [Molecular Weight]

      377.43
      Chemical PropertiesBack Directory
      [Boiling point ]

      629.4±55.0 °C(Predicted)
      [density ]

      1.251±0.06 g/cm3(Predicted)
      [storage temp. ]

      Store at -20°C
      [solubility ]

      Soluble in DMSO
      [form ]

      Solid
      [pka]

      4.14±0.10(Predicted)
      [color ]

      White to off-white
      Hazard InformationBack Directory
      [Biological Activity]

      FD-IN-1 (Compound 12) is a potent, orally active complement factor D (FD) inhibitor with IC50 of 12 nM.It also inhibits factor XIa (FXIa) and tryptase β2 with IC50 of 7.7 and 6.5 μM, respectively.
      [in vitro]

      FD-IN-1 (Compound 12) exhibits functional inhibition of AP activation (IC 50 =0.26 μM) in vitro in a membrane attack complex (MAC) deposition assay using 50% human whole blood (WB).

      [in vivo]

      FD-IN-1 (Compound 12) demonstrates systemic suppression of AP activation in a lipopolysaccharide-induced alternative complement pathway (AP) activation model as well as local ocular suppression in intravitreal injection-induced AP activation model in mice expressing human FD.
      FD-IN-1 (Compound 12) exhibits high oral bioavailability (C57BL6 mice 83%, Beagle dogs 70%) following oral administration (mice and dogs 10 mg/kg).
      FD -IN-1 (Compound 12) exhibits terminal elimination half-lives (C57BL6 mice 1.6 h and Beagle dogs 3.8 h) following intravenous administration (mice and dogs 1 mg/kg).

      b>

      table>
      Animal Model: Human FD knock-in mice
      Dosage: 3 and 10 mg/kg
      Administration: Oral gavage
      Result: The AP pathway was fully inhibited for up to 10 h at the 10 mg/kg dose.
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