Azanone (HNO) interaction with Hemeproteins and metalloporphyrins
Azanone (HNO), also called nitroxyl, is a highly reactive compound, with interesting yet poorly understood biological properties. Like its closely related sibling NO, its main biological targets are heme proteins, although significant differences in their reactivity and pharmacological effects are o...
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| 040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
| 100 | 1 | |a Doctorovich, F. | |
| 245 | 1 | 0 | |a Azanone (HNO) interaction with Hemeproteins and metalloporphyrins |
| 260 | |c 2012 | ||
| 270 | 1 | 0 | |m Doctorovich, F.; Departamento de Química Inorgánica, Analítica y Química Física, INQUIMAE-CONICET, Buenos Aires, Argentina |
| 506 | |2 openaire |e Política editorial | ||
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| 520 | 3 | |a Azanone (HNO), also called nitroxyl, is a highly reactive compound, with interesting yet poorly understood biological properties. Like its closely related sibling NO, its main biological targets are heme proteins, although significant differences in their reactivity and pharmacological effects are observed. Due to its high reactivity, azanone studies rely on the use of donors, molecules that therefore offer interesting therapeutic perspectives. In this review, we firstly describe the pharmacological potential of azanone, the chemistry of the available donors, and the main biological relevant HNO reactions with special focus on heme proteins and metalloporphyrins (Fe, Mn, and Co). Finally, we present evidence concerning the endogenous . in vivo azanone production hypothesis, and how the recent porphyrin-based developed methods for its detection may contribute to solve this key physiological question. © 2012 Elsevier Inc. |l eng | |
| 536 | |a Detalles de la financiación: UBACYT X065, UBACyT2010-12 | ||
| 536 | |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica, PICT-07-1650, PICT 2006-2396, CONICET PIP1207 | ||
| 536 | |a Detalles de la financiación: This work was financially supported by the University of Buenos Aires UBACYT X065 and UBACyT2010-12 to MAM, Agencia Nacional de Promoción Científica y Tecnológica (PICT 2006-2396 and PICT-07-1650) and CONICET PIP1207. M. A. M. and F. D. are members of CONICET. | ||
| 593 | |a Departamento de Química Inorgánica, Analítica y Química Física, INQUIMAE-CONICET, Buenos Aires, Argentina | ||
| 593 | |a Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pab. II (1428), Buenos Aires, Argentina | ||
| 690 | 1 | 0 | |a AZANONE |
| 690 | 1 | 0 | |a COBALT |
| 690 | 1 | 0 | |a HEME |
| 690 | 1 | 0 | |a HNO |
| 690 | 1 | 0 | |a IRON |
| 690 | 1 | 0 | |a KINETICS |
| 690 | 1 | 0 | |a MANGANESE |
| 690 | 1 | 0 | |a MYOGLOBIN |
| 690 | 1 | 0 | |a NITROSYL |
| 690 | 1 | 0 | |a NITROXYL |
| 690 | 1 | 0 | |a NITROXYL ANION |
| 690 | 1 | 0 | |a NO |
| 690 | 1 | 0 | |a NOS |
| 690 | 1 | 0 | |a OXIDATION |
| 690 | 1 | 0 | |a PORPHYRIN |
| 690 | 1 | 0 | |a PROTEIN |
| 690 | 1 | 0 | |a REDUCTIVE NITROSYLATION |
| 690 | 1 | 0 | |a RUTHENIUM |
| 700 | 1 | |a Bikiel, D.E. | |
| 700 | 1 | |a Pellegrino, J. | |
| 700 | 1 | |a Suárez, S.A. | |
| 700 | 1 | |a Martí, M.A. | |
| 773 | 0 | |d 2012 |g v. 64 |h pp. 97-139 |p Adv. Inorg. Chem. |x 08988838 |t Advances in Inorganic Chemistry | |
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