Steroids 1996-05-01

Synthesis of N-acetylcysteine conjugates of catechol estrogens.

E Suzuki, R Iwasaki, J Goto, Y Matsuki, T Nambara

Index: Steroids 61(5) , 296-301, (1996)

Full Text: HTML

Abstract

The synthesis of N-acetylcysteine conjugates of 2-hydroxyestrone (2-OHE1) and 4-hydroxyestrone (4-OHE1) is described. The reaction of estrone 2,3-quinone with N-acetylcysteine provided 2-OHE1 and its C-4 and C-1 thioether conjugates in a ratio of 1:1, while estrone 3,4-quinone with N-acetylcysteine gave 4-OHE1 and its C-2 thioether conjugate as a sole product. Their structures were characterized by inspection of NMR spectra, chemical derivatization (methylation and acetylation), and comparison with the reactivity of 4-bromoestrone 2,3-quinone or 2-bromoestrone 3,4-quinone toward N-acetylcysteine.


Related Compounds

  • 4-hydroxyestrone

Related Articles:

Improved profiling of estrogen metabolites by orbitrap LC/MS.

2015-07-01

[Steroids 99 , 84-90, (2015)]

Redox cycling of catechol estrogens generating apurinic/apyrimidinic sites and 8-oxo-deoxyguanosine via reactive oxygen species differentiates equine and human estrogens.

2010-08-16

[Chem. Res. Toxicol. 23(8) , 1365-73, (2010)]

Menstrual cycle effects on urinary estrogen metabolites.

1999-11-01

[J. Clin. Endocrinol. Metab. 84(11) , 3914-8, (1999)]

The effects of steroidal estrogens in ACI rat mammary carcinogenesis: 17beta-estradiol, 2-hydroxyestradiol, 4-hydroxyestradiol, 16alpha-hydroxyestradiol, and 4-hydroxyestrone.

2004-10-01

[J. Endocrinol. 183(1) , 91-9, (2004)]

In vitro generation of peroxynitrite by 2- and 4-hydroxyestrogens in the presence of nitric oxide.

2001-05-01

[Chem. Res. Toxicol. 14(5) , 547-54, (2001)]

More Articles...