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Diazeniumdiolated carbamates: A novel class of nitric oxide donors

  1. Author:
    Nandurdikar, R. S.
    Maciag, A. E.
    Cao, Z.
    Keefer, L. K.
    Saavedra, J. E.
  2. Author Address

    [Nandurdikar, Rahul S.; Keefer, Larry K.] NCI, Drug Design Sect, Biol Chem Lab, Frederick, MD 21702 USA. [Maciag, Anna E.; Cao, Zhao; Saavedra, Joseph E.] NCI, Basic Sci Program, SAIC Frederick Inc, Frederick, MD 21702 USA.;Nandurdikar, RS (reprint author), NCI, Drug Design Sect, Biol Chem Lab, Frederick, MD 21702 USA;nandurdikarr@mail.nih.gov saavedjo@mail.nih.gov
    1. Year: 2012
    2. Date: Mar
  1. Journal: Bioorganic & Medicinal Chemistry
    1. 20
    2. 6
    3. Pages: 2025-2029
  2. Type of Article: Article
  3. ISSN: 0968-0896
  1. Abstract:

    We report an indirect method for synthesis of previously inaccessible diazeniumdiolated carbamates. Synthesis involves use of previously reported triisopropylsilyloxymethylated isopropylamine diazeniumdiolate (TOM-ylated IPA/NO). These novel diazeniumdiolated carbamate prodrugs upon activation release nitric oxide (NO) similar to their secondary amine counterparts. They are also efficient sources of intracellular NO. These prodrugs may have potential applications as therapeutic NO-donors. (C) 2012 Elsevier Ltd. All rights

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External Sources

  1. DOI: 10.1016/j.bmc.2012.01.046
  2. WOS: 000301201100023

Library Notes

  1. Fiscal Year: FY2011-2012
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