Reacción #1005988

ord-f919ac1c64034673b0bb16bc29acf326

Ecuación de reacción

C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)CO
11-deoxycorticosterone
CS(C)=O
DMSO
C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)CO
corticosterone

Disolventes

Condiciones de reacción

Temperatura
32°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONA suspension of fission yeast (S. pombe PE1) with a cell density of 3·107 cells/ml
  2. 2
    Otrowas prepared on a freshly grown culture
  3. 3
    OtroThe enzyme reaction
  4. 4
    OtroThe test was quenched
  5. 5
    Extracciónby extracting the sample with 500 μl of EtOAc
  6. 6
    OtroAfter centrifugation (10,000 g, 2 min), the EtOAc phase was removed
  7. 7
    Otroevaporated to dryness
  8. 8
    OtroThe reaction of the substrate

Procedimiento

A suspension of fission yeast (S. pombe PE1) with a cell density of 3·107 cells/ml was prepared on a freshly grown culture using fresh EMMG (pH 7.4) as modified according to Ehmer et al. (Ehmer, P. B. et al., 1. Steroid. Biochem. Mol. Biol. 81, 173-179 (2002)). 492.5 μl of this cell suspension was admixed with 5 μl of inhibitor solution (50 μM of the compound to be tested in ethanol or DMSO) and incubated at 32° C. for 15 min. Controls were admixed with 5 μl of ethanol. The enzyme reaction was started by adding 2.5 μl of 11-deoxycorticosterone (20 μM, containing 1.25 nCi of [4-14C]11-deoxycorticosterone in Ethanol), followed by horizontal shaking at 32° C. for 6 h. The test was quenched by extracting the sample with 500 μl of EtOAc. After centrifugation (10,000 g, 2 min), the EtOAc phase was removed and evaporated to dryness. The residue was taken up in 10 μl of chloroform. The reaction of the substrate to form corticosterone was analyzed by HPTLC (see below).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09271963B2uspto-grants-2016_03