Mechanisms of hydrolysis of phenyl- and benzyl 4-nitrophenyl-sulfamate esters-Reference-Cited by-同舟云学术

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Mechanisms of hydrolysis of phenyl- and benzyl 4-nitrophenyl-sulfamate esters

Published:2011 Issue:2 Volume:9 Page:523-530
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Spillane William J.,Thea Sergio,Cevasco Giorgio,Hynes Michael J.,McCaw Cheryl J. A.,Maguire Neil P.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2011/OB/C0OB00362J

Reference46 articles.

1. Carbonic anhydrase inhibitors. Interaction of the antitumor sulfamate EMD 486019 with twelve mammalian carbonic anhydrase isoforms: Kinetic and X-ray crystallographic studies

2. Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with bis-sulfamates

3. Recent Developments of Steroid Sulfatase Inhibitors as Anti-Cancer Agents

4. Inhibition of steroid sulfatase activity and cell proliferation in ZR-75-1 and BT-474 human breast cancer cells by KW-2581 in vitro and in vivo

5. Novel D-ring modified steroid derivatives as potent, non-estrogenic, steroid sulfatase inhibitors with in vivo activity

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