Synthesis and Cytotoxic Activity of Halogen-Containing Dinitromethyl-1,3,5-triazine Derivatives

Гидаспов, А. А.; Бахарев, В. В.; Kachanovskaya, E. V.; Kosareva, E. A.; Galkina, M. V.; Ekimova, E. V.; Yakunina, N. G.; Bulychev, Yu. N.

doi:10.1023/b:phac.0000048901.45151.7f

Pharmaceutical Chemistry Journal

2004

DOI: 10.1023/b:phac.0000048901.45151.7f

|View full text |Cite

Synthesis and Cytotoxic Activity of Halogen-Containing Dinitromethyl-1,3,5-triazine Derivatives

А. А. Гидаспов

В. В. Бахарев

E. V. Kachanovskaya

et al.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

Mentioning

Contrasting

Year Published

2009

2023

Publication Types

Select...

Article5

Relationship

Self Cite1

Independent4

Authors

Journals

Cited by 5 publications

(1 citation statement)

References 1 publication

Supporting

Mentioning

Contrasting

Order By: Relevance

“…In continuation of our investigations [13][14][15][16][17] in this field of chemistry, we published a preliminary report on possible preparation of model nitrolic acid of the 1,3,5 triazine series. 18 In the present work, a synthetic scheme that allows designing 1,3,5 triazinenitrolic acids is described in detail, and data on NO release (detected as the nitrite anion) upon transformations of these compounds at dif ferent рН are also presented.…”

mentioning

confidence: 99%

1,3,5-Triazinenitrolic acids. Synthesis and NO-releasing properties

et al. 2009

Self Cite

View full text Add to dashboard Cite

Reactions of salts of 1,3,5 triazine dinitromethyl derivatives with nitrogen dioxide that result mainly in 1,3,5 triazinenitrolic acids are investigated. The behavior of nitrolic acid in electroreduction at a mercury drop electrode at various pH was studied; oxygen was shown to accelerate the process. The promoting effect of nitrolic acids on the activity of soluble guanylate cyclase of human platelets was shown. The studied nitrolic acids are active donors of nitric oxide, a universal and important regulator of cell metabolism functions. NO releasing proper ties of furoxans are investigated.At present it is reliably established that nitric oxide (NO) is an intra and intercellular second messenger (neurotransmitter). It plays a key role in regulation of the major biological processes of cardiovascular, gastroen teric, urinogenital, respiratory, central and peripheral ner vous systems. Chemical, biochemical, and pharmaceuti cal aspects of action of nitric oxide donors are considered in detail in recent reviews. 1-8It is known that the formation of NO in an organism in insufficient quantities leads to a number of serious consequences. In this connection, one of the most actively developing now directions 1-6 is the search for various compounds that can serve as NO generators, i.e., xenobiotics, that are transformed with its formation. At present a number of drugs the activity of which is reason ably connected with their ability to liberate NO in vivo is employed in medical practice.The substances containing S , O , N , and C nitroso and nitro groups, viz., diazeniumdiolates, furoxans, NO metal complexes, etc., 6 are related to the compounds showing properties of nitric oxide donors. Among the found NO donors, high efficiency of some oximes 4,6 is noted.Nitrolic acids, RC(=NOH)NO 2 , containing the oxime and nitro groups at the same carbon atom, are interesting class of potential prodrugs. Antithrombotic and hypoten sive activity 9 was shown for some nitrolic acids. Ophthal mologic effects of imidazolenitrolic acids were recently described. 10,11 On the basis of a structure of the nitrolic acids it is logical to suppose that they are capable to gen erate nitric oxide. It is established, for example, that some nitrolic acids decompose with formation of HNO even at room temperature. 5 The basic analytical methods that allow identifi cation of NO are described in detail in a review. 7 The colorimetric method that quantifies the nitrite ion, a marker of NO formation, is one of the most common methods (see Ref. 8). It is this method that is employed in the present work.A review 12 on development of the synthesis methods and the reactivity of mono , di , and trinitromethyl derivatives of 1,3,5 triazines has recently been published.

show abstract

mentioning

confidence: 99%

1,3,5-Triazinenitrolic acids. Synthesis and NO-releasing properties

et al. 2009

Self Cite

View full text Add to dashboard Cite

show abstract

Chemistry of (dinitromethyl)azines

Бахарев

Гидаспов

Parfenov

2017

Chem Heterocycl Comp

View full text Add to dashboard Cite

Synthesis and structure elucidation of novel 5-dinitromethyl-7-alkylamino-1,2,4-triazolo[4,3-a]-1,3,5-triazines

Golovina

Бахарев

Головин

et al. 2013

Tetrahedron Letters

View full text Add to dashboard Cite

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

customersupport@researchsolutions.com

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

Synthesis and Cytotoxic Activity of Halogen-Containing Dinitromethyl-1,3,5-triazine Derivatives

Cited by 5 publications

References 1 publication

1,3,5-Triazinenitrolic acids. Synthesis and NO-releasing properties

1,3,5-Triazinenitrolic acids. Synthesis and NO-releasing properties

Chemistry of (dinitromethyl)azines

Synthesis and structure elucidation of novel 5-dinitromethyl-7-alkylamino-1,2,4-triazolo[4,3-a]-1,3,5-triazines

Contact Info

Product

Resources

About