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Usp. Khim., 2011, Volume 80, Issue 2, Pages 182–198 (Mi rcr43)  

This article is cited in 12 scientific papers (total in 12 papers)

Exogenous nitric oxide donors in the series of C-nitro compounds

V. G. Granik, N. B. Grigoriev

Centre for Medicinal Chemistry, All-Russian Research Chemical-Pharmaceutical Institute, Moscow

Abstract: The published data on nitrogen(II) oxide donors related to C-nitro compounds are generalized and described systematically. The key classes of these compounds and the possible mechanisms of their transformations under hydrolytic conditions and in living organisms are considered. The attention is focused on C-nitro compounds as potential medicinal agents for treating a broad range of diseases (cardiovascular diseases, tuberculosis, cancer, etc.).

Full text: http://www.uspkhim.ru/.../paper_rus.phtml?journal_id=rc&paper_id=4135

English version:
Russian Chemical Reviews, 2011, 80:2, 171–186

Bibliographic databases:

Document Type: Article
Received: 13.01.2010

Citation: V. G. Granik, N. B. Grigoriev, “Exogenous nitric oxide donors in the series of C-nitro compounds”, Usp. Khim., 80:2 (2011), 182–198; Russian Chem. Reviews, 80:2 (2011), 171–186

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    Citing articles on Google Scholar: Russian citations, English citations
    Related articles on Google Scholar: Russian articles, English articles

    This publication is cited in the following articles:
    1. V. G. Granik, N. B. Grigoriev, “ChemInform Abstract: Exogenous Nitric Oxide Donors in the Series of C-Nitro Compounds”, ChemInform, 42:34 (2011), no  crossref
    2. Julia Kozhukh, Juliana Fedoce Lopes, Hélio F. Dos Santos, Stephen J. Lippard, “Reactions of Organozinc Thiolates with Nitrosonium Ion:C-Nitroso Formation by Possible Transnitrosation”, Organometallics, 2012, 1211120807  crossref  isi  scopus
    3. Belen'kii L.I. Evdokimenkova Yu.B., “The Literature of Heterocyclic Chemistry, Part XII, 2010-2011”, Advances in Heterocyclic Chemistry, Vol 111, Adv. Heterocycl. Chem., 111, ed. Katritzky A., 2014, 147–274  crossref  isi  scopus
    4. Konstantinova L.S., Amelichev S.A., Zlotin S.G., Struchkova M.I., Godovikova T.I., Rakitin O.A., “[1,4]Dithiino[2,3-C:5,6-C `]Bis[1,2,5]Oxadiazole Di-N-Oxide: Synthesis and Oxidation To Mono- and Bis-S-Oxides”, Mendeleev Commun., 25:5 (2015), 339–340  crossref  isi  elib  scopus
    5. Chistyakov V.A., Semenyuk Yu.P., Morozov P.G., Prazdnova E.V., Chmykhalo V.K., Kharchenko E.Yu., Kletskii M.E., Borodkin G.S., Lisovin A.V., Burov O.N., Kurbatov S.V., “Synthesis and Biological Properties of Nitrobenzoxadiazole Derivatives as Potential Nitrogen(II) Oxide Donors: Sox Induction, Toxicity, Genotoxicity, and Dna Protective Activity in Experiments Using Escherichia Coli-Based Lux Biosensors”, Russ. Chem. Bull., 64:6 (2015), 1369–1377  crossref  mathscinet  isi  scopus
    6. Bakharev V.V., Parfenov V.E., Gidaspov A.A., Selezneva E.V., Baymuratov M.R., Averkiev B.B., Sheremetev A.B., “A Simple and Convenient Method For the Synthesis of 1,3,5-Triazine-Nitrolic Acids. The First X-Ray Investigation of Z-Isomeric Nitrolic Acid”, Heterocycl. Commun., 22:1 (2016), 7–10  crossref  isi  scopus
    7. Ogurtsov V.A., Shastin A.V., Zlotin S.G., Rakitin O.A., “Short and efficient synthesis of 1-(2-oxido-1,2,5-oxadiazol-3-yl)alkyl nitrates by unconventional nitrooxylation of 3-alkyl-1,2,5-oxadiazole 2-oxides”, Tetrahedron Lett., 57:36 (2016), 4027–4030  crossref  isi  scopus
    8. Orlov N.V., “Rational design of complex molecular structures starting from readily available precursors”, Russ. Chem. Bull., 65:6 (2016), 1418–1440  crossref  isi  scopus
    9. Ogurtsov V.A. Shastin A.V. Zlotin S.G. Rakitin O.A., “Unusual Transformation of 3-Alkylfuroxans Into 3-(Nitrooxyalkyl)Furoxans on Treatment With a Mixture of Nitric and Sulfuric Acids”, Russ. Chem. Bull., 65:12 (2016), 2901–2906  crossref  isi
    10. Makhova N.N. Rakitin O.A., “Furoxans Fused With Heterocycles as Promising Donors and Precursors For Nitric Oxide Donors (Microreview)”, Chem. Heterocycl. Compds., 53:8 (2017), 849–851  crossref  isi  scopus
    11. Konstantinova L.S. Knyazeva E.A. Gatilov Yu.V. Zlotin S.G. Rakitin O.A., “Nitro Derivatives of 2,1,3-Benzothiadiazole 1-Oxides: Synthesis, Structural Study, and No Release”, Russ. Chem. Bull., 67:1 (2018), 95–101  crossref  isi  scopus
    12. Obruchnikova N.V. Novikov R.A. Zlotin S.G. Dorovatovskii P.V. Khrustalev V.N. Rakitin O.A., “Synthesis and Structural Investigation of 4,4-Dimethyl-[3,3-Bi(1,2,5-Oxadiazole)] 5,5-Dioxide”, Russ. Chem. Bull., 67:11 (2018), 2044–2048  crossref  isi  scopus
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