Abstract:
Oximes of quinuclidin-3-ones give NO under mild biomimetic oxidative conditions and activate soluble guanylate cyclase.
Document Type:
Article
Language: English
Citation:
L. N. Koikov, N. V. Alekseeva, N. B. Grigoriev, V. I. Levina, K. F. Turchin, T. Ya. Filipenko, I. S. Severina, I. K. Ryaposova, V. G. Granik, “Oximes of quinuclidin-3-ones as nitric oxide donors”, Mendeleev Commun., 6:3 (1996), 94–96
Linking options:
https://www.mathnet.ru/eng/mendc4928
https://www.mathnet.ru/eng/mendc/v6/i3/p94
This publication is cited in the following 6 articles:
Peng George Wang, Ming Xian, Xiaoping Tang, Xuejun Wu, Zhong Wen, Tingwei Cai, Adam J. Janczuk, “Nitric Oxide Donors: Chemical Activities and Biological Applications”, Chem. Rev., 102:4 (2002), 1091
V. I. Levina, A. V. Danilov, N. B. Grigor'ev, “Polarographic detection of nitric oxide during the oxidation of some nitrogen-containing organic compounds by potassium ferricyanide”, Pharm Chem J, 32:4 (1998), 226
N. V. Alekseeva, L. N. Koikov, K. F. Turchin, “Condensation of N-ethylpiperid-4-one with benzaldehyde”, Chem Heterocycl Compd, 34:9 (1998), 1070
L. N. Koikov, N. V. Alekseeva, E. A. Lisitza, E. S. Krichevsky, N. B. Grigoriev, A. V. Danilov, I. S. Severina, N. V. Pyatakova, V. G. Granik, “Oximes, amidoximes and hydroxamic acids as nitric oxide donors”, Mendeleev Commun., 8:4 (1998), 165–168
L. N. Koikov, N. V. Alekseeva, N. B. Grigor'ev, V. I. Levina, K. F. Turchin, T. Ya. Filipenko, M. D. Mashkovskii, M. É. Kaminka, V. B. Nikitin, G. N. Engalycheva, M. I. Kalinkina, V. G. Granik, I. S. Severina, I. K. Ryaposova, “Search for no donors. Part I. 3-Quinuclidone oximes”, Pharm Chem J, 31:5 (1997), 243
L. N. KOIKOV, N. V. ALEKSEEVA, N. B. GRIGOR'EV, V. I. LEVINA, K. F. TURCHIN, T. YA. FILIPENKO, I. S. SEVERINA, I. K. RYAPOSOVA, V. G. GRANIK, “ChemInform Abstract: Oximes of Quinuclidin‐3‐ones as Nitric Oxide Donors.”, ChemInform, 27:38 (1996)
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