Steroids 1997-04-01

Estrone sulfonates as inhibitors of estrone sulfatase.

N M Howarth, A Purohit, M J Reed, B V Potter

文献索引:Steroids 62(4) , 346-50, (1997)

全文:HTML全文

摘要

In our continuing quest to design efficient inhibitors of estrone sulfatase activity and to assess the recognition of estrone sulfate surrogates by estrone sulfatase, we synthesized and evaluated several sulfonate derivatives of 5,6,7,8-tetrahydronaphth-2-ol and estrone. 5,6,7,8-Tetrahydronaphth-2-methanesulfonate (11), and 5,6,7,8-tetrahydronaphth-2-(p-toluene)sulfonate (12) were found not to inhibit estrone sulfatase activity; estrone-3-methane-sulfonate (5), estrone-3-ethanesulfonate (6), estrone-3-butanesulfonate (7), and estrone-3-[(+)10-camphor]sulfonate (8) all weakly inhibited estrone sulfatase, and the best inhibitor, from this class of compounds, was estrone-3-(p-toluene)sulfonate (9). At 10 microM, it inhibited estrone sulfatase activity by 91%. These results emphasize some of the requirements needed for high-affinity binding to the enzyme.


相关化合物

  • 5,6,7,8-四氢-2-萘...

相关文献:

Photodegradation of the steroid hormones 17beta-estradiol (E2) and 17alpha-ethinylestradiol (EE2) in dilute aqueous solution.

2008-11-01

[Chemosphere 73(8) , 1216-23, (2008)]

An electron spin resonance study of o-semiquinones formed during the enzymatic and autoxidation of catechol estrogens.

1984-11-25

[J. Biol. Chem. 259(22) , 14018-22, (1984)]

Non-radiative depletion of the excited electronic states of 9-cyanoanthracene in presence of tetrahydronaphthols.

2003-02-01

[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 59(3) , 525-35, (2003)]

更多文献...