HNO and NO Release from a Primary Amine-Based Diazeniumdiolate As a Function of pH-Reference-Cited by-同舟云学术

HNO and NO Release from a Primary Amine-Based Diazeniumdiolate As a Function of pH

Published:2011-03-15 Issue:8 Volume:50 Page:3262-3270
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Salmon Debra J.¹,Torres de Holding Claudia L.¹,Thomas Lynta¹,Peterson Kyle V.¹,Goodman Gens P.¹,Saavedra Joseph E.²,Srinivasan Aloka³,Davies Keith M.⁴,Keefer Larry K.³,Miranda Katrina M.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of Arizona, Tucson, Arizona 85721, United States

2. Basic Research Program, SAIC-Frederick, National Cancer Institute at Frederick, Frederick, Maryland 21702, United States

3. Laboratory of Comparative Carcinogenesis, National Cancer Institute at Frederick, Frederick, Maryland 21702, United States

4. Department of Chemistry, George Mason University, Fairfax, Virginia 22030, United States

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic101736e

Reference50 articles.

1. Nitroxyl anion exerts redox-sensitive positive cardiac inotropy in vivo by calcitonin gene-related peptide signaling

2. Nitroxyl affords thiol-sensitive myocardial protective effects akin to early preconditioning

3. Evidence for nitroxyl in the catalase-mediated bioactivation of the alcohol deterrent agent cyanamide

4. Nitroxyl inhibits breast tumor growth and angiogenesis

5. The chemistry of nitroxyl (HNO) and implications in biology

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