반응 #73866

ord-fc9cf28c0b3845f1a9bead206d3c31ee

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타for 15 minutes
  2. 2
    기타at 37° C.
  3. 3
    workup.ADDITIONit was quickly added on a glass fiber
  4. 4
    여과filter plate (Multiscreen FB, Millipore inc.) coated with 0.05% Brij 35
  5. 5
    여과filtered under reduced pressure
  6. 6
    여과The glass fiber filter
  7. 7
    세척was washed with 200 μL of ice-
  8. 8
    온도cooled 50 mM Tris-HCl (pH=7.6) twice
  9. 9
    여과repeatedly filtered under reduced pressure
  10. 10
    workup.ADDITIONa vial containing 4 mL of Ecoscint A (National Diagnostics inc.)
  11. 11
    여과The residual radioactivity on the glass fiber filter

실험 절차

5-HT2A receptor binding assay was performed in reference to a method described by Hirose et al. (Japan. J. Pharmacol., 53, 321-329, 1990). After a reaction in a total volume of 200 μL of 50 mM Tris-HCl (pH=7.6) buffer solution containing 50 μL of [3H]-ketanserin (final concentration 1 nM), 1 μL of test drug in DMSO, and 149 μL of human 5-HT2A receptor-expressing CHO cell membrane sample, human 5-HT2A receptor binding activity of [3H]-ketanserin was measured. The reaction solution let stand for 15 minutes at 37° C., and then it was quickly added on a glass fiber filter plate (Multiscreen FB, Millipore inc.) coated with 0.05% Brij 35 and filtered under reduced pressure. The glass fiber filter was washed with 200 μL of ice-cooled 50 mM Tris-HCl (pH=7.6) twice, repeatedly filtered under reduced pressure, and then transferred to a vial containing 4 mL of Ecoscint A (National Diagnostics inc.). The residual radioactivity on the glass fiber filter was measured by a liquid scintillation counter. Nonspecific binding was measured in the presence of 10 μM of MDL-100907, and [3H]-ketanserin binding inhibition rate in the presence of 1 nM or 10 nM of test drug was determined. The results are shown in Tables 8 to 13.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08541585B2uspto-grants-2013_09