Ru360
Names | |
---|---|
IUPAC name
azanide;formic acid;ruthenium(5+);trichloride;hydrate
| |
Other names
Ru360; (μ)[(HCO2)(NH3)4Ru]2OCl3; Obftar
| |
Identifiers | |
| |
3D model (JSmol)
|
|
ChemSpider | |
PubChem CID
|
|
| |
| |
Properties | |
C2H26Cl3N8O5Ru2 | |
Molar mass | 550.77 g·mol−1 |
Appearance | Reddish brown solid |
deoxygenated H2O | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Ru360 is an oxo-bridged dinuclear ruthenium ammine complex with an absorption spectrum maximum at 360 nm. It is an analog of ruthenium red, a well-known effective inhibitor of the mitochondrial calcium uniporter.[1]
Ru360 was discovered after scientists found that commercial preparations of ruthenium red were often less than 20% pure, and that the crude mixture produced a stronger inhibition than the purified product.[2] This component was later isolated and its structure determined,[1] Ru360 has structural formula (μ-O)[(HCO2)(NH3)4Ru]2Cl3, that is, an oxygen-linked chain only two octahedral ruthenium–ammine units rather than the three of ruthenium red. One of the ruthenium atoms is in a +3 oxidation state, and the other in a +4 oxidation state. In addition to the four ammonia ligands, each ruthenium also has one formate group and there are a total of three chloride ions to balance the charge. In solution, chloride or hydroxide groups displace the formates.[1]
Since Ru360 inhibits the flow of calcium into mitochondria, which can prevent the opening of the mitochondrial permeability transition pore, it has been investigated as a therapeutic treatment for stroke and heart attack.[3]
References[]
- ^ a b c Ying, W. L.; Emerson, J.; Clarke, M. J.; Sanadi, D. R. (1991-05-21). "Inhibition of mitochondrial calcium ion transport by an oxo-bridged dinuclear ruthenium ammine complex". Biochemistry. 30 (20): 4949–4952. doi:10.1021/bi00234a016. ISSN 0006-2960. PMID 2036363.
- ^ Broekemeier, K. M.; Krebsbach, R. J.; Pfeiffer, D. R. (1994-10-12). "Inhibition of the mitochondrial Ca2+ uniporter by pure and impure ruthenium red". Molecular and Cellular Biochemistry. 139 (1): 33–40. doi:10.1007/bf00944201. ISSN 0300-8177. PMID 7531818. S2CID 516473.
- ^ García-Rivas, G. de J.; Carvajal, K.; Correa, F.; Zazueta, C. (2006-12-01). "Ru360, a specific mitochondrial calcium uptake inhibitor, improves cardiac post-ischaemic functional recovery in rats in vivo". British Journal of Pharmacology. 149 (7): 829–837. doi:10.1038/sj.bjp.0706932. ISSN 0007-1188. PMC 2014682. PMID 17031386.
- Ruthenium complexes
- Ion channel blockers