Reaktion #3749

ord-dcc14ee6b9974d65bb8d7fa919a98560

Reaktionsgleichung

CCNC(=O)[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O
[3H]NECA
Nc1ncnc2c1ncn2[C@]1(C2CCCCC2)O[C@H](CO)[C@@H](O)[C@H]1O
cyclohexyl-adenosine
[Cl-].[Cl-].[Mg+2]
MgCl2
Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Adenosine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengen/ml adenosine deaminase, 100 μl of test compounds at various concentrations over the range of 10-10M to 10-4M
  2. 2
    workup.ADDITIONdiluted with assay buffer (50 mM Tris-HCl, pH 7.7) and 0.2 μl of membrane suspension (5 mg wet weight)
  3. 3
    FiltrationEach tube is filtered through GF/B glass fiber filters
  4. 4
    WaschenThe filters are rinsed two times with 5 ml of the ice-cold buffer
  5. 5
    workup.ADDITIONis added

Vorschrift

Incubation tubes, in triplicate, receive 100 μl of [3H]NECA (94 nM in the assay), 100 μl of 1 μM cyclohexyl-adenosine (CHA), 100 μl of 100 mM MgCl2, 100 μl of 1 IU/ml adenosine deaminase, 100 μl of test compounds at various concentrations over the range of 10-10M to 10-4M diluted with assay buffer (50 mM Tris-HCl, pH 7.7) and 0.2 μl of membrane suspension (5 mg wet weight), in a final volume of 1 ml of 50 mM Tris-HCl, pH 7.7. Incubations are carried out at 25° C. for 60 minutes. Each tube is filtered through GF/B glass fiber filters using a vacuum. The filters are rinsed two times with 5 ml of the ice-cold buffer. The membranes on the filters are transferred to scintillation vials to which 8 ml of Omnifluor with 5% Protosol is added. The filters are counted by liquid scintillation spectrometry.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05734052uspto-grants-1998_03