Ruthenium red: Difference between revisions
Added reference for usage in plant research |
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{{Chembox |
{{Chembox |
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| verifiedrevid = 464384628 |
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| Name = Ammoniated ruthenium oxychloride |
| Name = Ammoniated ruthenium oxychloride |
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| ImageFile = Ruthenium red cation.svg |
| ImageFile = Ruthenium red cation.svg |
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| ImageSize = |
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| ImageSize = |
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| IUPACName = |
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| OtherNames = |
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| Section1 = {{Chembox Identifiers |
| Section1 = {{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 7827798 |
| ChemSpiderID = 7827798 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = CIBHIQPXTCXIRW-UHFFFAOYSA-H |
| StdInChIKey = CIBHIQPXTCXIRW-UHFFFAOYSA-H |
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| CASNo_Ref = {{cascite|changed|CAS}} |
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| CASNo = 11103-72-3 |
| CASNo = 11103-72-3 |
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| UNII_Ref = {{fdacite|changed|FDA}} |
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| UNII = KU6M163B0R |
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| PubChem = 9548875 |
| PubChem = 9548875 |
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| ChEMBL_Ref = {{ebicite|changed|EBI}} |
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| ChEMBL = |
| ChEMBL = 2068405 |
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| SMILES = [Ru+5].[Ru+5].[Ru+4].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].O.O.N.N.N.N.N.N.N.N.N.N.N.N.N.N |
| SMILES = [Ru+5].[Ru+5].[Ru+4].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].O.O.N.N.N.N.N.N.N.N.N.N.N.N.N.N |
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}} |
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| Section2 = {{Chembox Properties |
| Section2 = {{Chembox Properties |
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| Ru |
| Ru=3 | Cl=6 | N=14 | H=42 | O=2 |
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| MolarMass = |
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| BoilingPt = |
| BoilingPt = |
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| Solubility = }} |
| Solubility = }} |
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| Section3 = {{Chembox Hazards |
| Section3 = {{Chembox Hazards |
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| MainHazards = |
| MainHazards = |
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| FlashPt = |
| FlashPt = |
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| AutoignitionPt = }} |
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The inorganic dye '''ammoniated ruthenium oxychloride''', also known as ''' |
The inorganic dye '''ammoniated [[ruthenium]] oxychloride''', also known as '''ruthenium red''', is used in [[histology]] to [[staining|stain]] [[aldehyde]] [[fixation (histology)|fixed]] [[mucopolysaccharides]]. |
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Ruthenium |
Ruthenium red (RR) has also been used as a pharmacological tool to study specific cellular mechanisms. Selectivity is a significant issue in such studies as RR is known to interact with many proteins.<ref>{{cite journal | pmid = 21671873 | volume=11 | issue=17 | title=TRPV4 agonists and antagonists | year=2011 | journal=Curr Top Med Chem | pages=2216–26 | last1 = Vincent | first1 = F | last2 = Duncton | first2 = MA | doi=10.2174/156802611796904861}}</ref> These include mammalian ion channels ([[CatSper1]], [[TASK]], [[RyR1]], [[RyR2]], [[RyR3]], [[TRPM6]], [[TRPM8]], [[TRPV1]], [[TRPV2]], [[TRPV3]], [[TRPV4]], [[TRPV5]], [[TRPV6]], [[TRPA1]], [[mCa1]], [[mCa2]], [[CALHM1]]<ref>{{cite journal | last1 = Ma | first1 = Z | last2 = Siebert | first2 = AP | last3 = Cheung | first3 = KH | last4 = Lee | first4 = RJ | last5 = Johnson | first5 = B | last6 = Cohen | first6 = AS | last7 = Vingtdeux | first7 = V | last8 = Marambaud | first8 = P | last9 = Foskett | first9 = JK | year = 2012 | title = Calcium homeostasis modulator 1 (CALHM1) is the pore-forming subunit of an ion channel that mediates extracellular Ca<sup>2+</sup> regulation of neuronal excitability | journal = Proc Natl Acad Sci USA | volume = 109 | issue = 28| pages = E1963–71 | pmid = 22711817 | doi=10.1073/pnas.1204023109 | pmc=3396471| bibcode = 2012PNAS..109E1963M | doi-access = free }}</ref><ref>{{cite journal | last1 = Dreses-Werringloer | first1 = U | last2 = Vingtdeux | first2 = V | last3 = Zhao | first3 = H | last4 = Chandakkar | first4 = P | last5 = Davies | first5 = P | last6 = Marambaud | first6 = P | year = 2013 | title = CALHM1 controls Ca<sup>2+</sup>-dependent MEK/ERK/RSK/MSK signaling in neurons | journal = J Cell Sci | volume = 126| issue = Pt 5| pages = 1199–206| pmid = 23345406 | doi = 10.1242/jcs.117135 | pmc = 4481642 }}</ref>) [[TRPP3]],<ref name="DeCaen 2013">{{Cite journal |
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| last1 = Decaen | first1 = P. G. |
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Ann NY Acad Sci 1998 853: 130-148 [http://www.annalsnyas.org/cgi/content/abstract/853/1/130]</ref> |
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| last2 = Delling | first2 = M. |
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| last3 = Vien | first3 = T. N. |
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⚫ | RR has been used on plant material since 1890 for staining pectins, |
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| last4 = Clapham | first4 = D. E. |
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| title = Direct recording and molecular identification of the calcium channel of primary cilia |
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| doi = 10.1038/nature12832 |
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| journal = Nature |
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| volume = 504 |
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| issue = 7479 |
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| pages = 315–318 |
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| year = 2013 |
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| pmid = 24336289 |
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| pmc = 4073646 |
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| bibcode = 2013Natur.504..315D |
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}}</ref> a plant ion channel, [[Calcium ATPase|Ca<sup>2+</sup>-ATPase]], [[Mitochondrial calcium uniporter|mitochondrial Ca<sup>2+</sup> uniporter]],<ref>{{cite journal | last1 = Hajnóczky | first1 = G | last2 = Csordás | first2 = G | last3 = Das | first3 = S | last4 = Garcia-Perez | first4 = C | last5 = Saotome | first5 = M | last6 = Sinha Roy | first6 = S | last7 = Yi | first7 = M | year = 2006 | title = Mitochondrial calcium signalling and cell death: approaches for assessing the role of mitochondrial Ca<sup><sup>2+</sup></sup> uptake in apoptosis | journal = Cell Calcium | volume = 40 | issue = 5–6| pages = 553–60 | doi=10.1016/j.ceca.2006.08.016 | pmid=17074387 | pmc=2692319}}</ref> [[tubulin]], [[myosin light-chain phosphatase]], and Ca<sup>2+</sup> binding proteins such as [[calmodulin]]. Ruthenium red displays nanomolar potency against several of its binding partners (e.g. TRPV4, [[ryanodine]] receptors,...). For example, it is a potent inhibitor of intracellular [[calcium]] release by ryanodine receptors (Kd ~20 nM).<ref>{{cite journal | last1 = Tripathy | first1 = Le Xu Ashutosh | last2 = Pasek | first2 = Daniel A. | last3 = Meissner | first3 = Gerhard | year = 1998 | title = Potential for Pharmacology of Ryanodine Receptor/Calcium Release Channels | url = http://www.annalsnyas.org/cgi/content/abstract/853/1/130 | journal = Ann NY Acad Sci | volume = 853 | issue = 1 | pages = 130–148 | doi = 10.1111/j.1749-6632.1998.tb08262.x | pmid = 10603942 | bibcode = 1998NYASA.853..130T | s2cid = 86436194 | access-date = 2006-10-22 | archive-date = 2008-04-23 | archive-url = https://web.archive.org/web/20080423065203/http://www.annalsnyas.org/cgi/content/abstract/853/1/130 | url-status = dead }}</ref> As a TRPA1 blocker, it assists in reducing the airway inflammation caused by [[pepper spray]]. |
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⚫ | RR has been used on plant material since 1890 for staining [[pectins]], [[mucilage]]s, and [[Natural gum|gums]]. RR is a stereoselective stain for pectic acid, insofar as the staining site occurs between each monomer unit and the next adjacent neighbor.<ref>Mariani Colombo P, Rascio N. "Ruthenium red staining for electron microscopy of plant material". ''Journal of Ultrastructure Research'' Volume 60, Issue 2, August 1977, Pages 135–139</ref> |
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==References== |
==References== |
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<references/> |
<references/> |
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{{Transient receptor potential channel modulators}} |
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[[Category:Staining dyes]] |
[[Category:Staining dyes]] |
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[[Category:Ruthenium |
[[Category:Ruthenium complexes]] |
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[[Category:Ammine complexes]] |
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[[de:Rutheniumrot]] |
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[[it:Rosso di Rutenio]] |
Latest revision as of 19:02, 22 September 2023
Identifiers | |
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3D model (JSmol)
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.228.922 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
Cl6H42N14O2Ru3 | |
Molar mass | 786.34 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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The inorganic dye ammoniated ruthenium oxychloride, also known as ruthenium red, is used in histology to stain aldehyde fixed mucopolysaccharides.
Ruthenium red (RR) has also been used as a pharmacological tool to study specific cellular mechanisms. Selectivity is a significant issue in such studies as RR is known to interact with many proteins.[1] These include mammalian ion channels (CatSper1, TASK, RyR1, RyR2, RyR3, TRPM6, TRPM8, TRPV1, TRPV2, TRPV3, TRPV4, TRPV5, TRPV6, TRPA1, mCa1, mCa2, CALHM1[2][3]) TRPP3,[4] a plant ion channel, Ca2+-ATPase, mitochondrial Ca2+ uniporter,[5] tubulin, myosin light-chain phosphatase, and Ca2+ binding proteins such as calmodulin. Ruthenium red displays nanomolar potency against several of its binding partners (e.g. TRPV4, ryanodine receptors,...). For example, it is a potent inhibitor of intracellular calcium release by ryanodine receptors (Kd ~20 nM).[6] As a TRPA1 blocker, it assists in reducing the airway inflammation caused by pepper spray.
RR has been used on plant material since 1890 for staining pectins, mucilages, and gums. RR is a stereoselective stain for pectic acid, insofar as the staining site occurs between each monomer unit and the next adjacent neighbor.[7]
References
[edit]- ^ Vincent, F; Duncton, MA (2011). "TRPV4 agonists and antagonists". Curr Top Med Chem. 11 (17): 2216–26. doi:10.2174/156802611796904861. PMID 21671873.
- ^ Ma, Z; Siebert, AP; Cheung, KH; Lee, RJ; Johnson, B; Cohen, AS; Vingtdeux, V; Marambaud, P; Foskett, JK (2012). "Calcium homeostasis modulator 1 (CALHM1) is the pore-forming subunit of an ion channel that mediates extracellular Ca2+ regulation of neuronal excitability". Proc Natl Acad Sci USA. 109 (28): E1963–71. Bibcode:2012PNAS..109E1963M. doi:10.1073/pnas.1204023109. PMC 3396471. PMID 22711817.
- ^ Dreses-Werringloer, U; Vingtdeux, V; Zhao, H; Chandakkar, P; Davies, P; Marambaud, P (2013). "CALHM1 controls Ca2+-dependent MEK/ERK/RSK/MSK signaling in neurons". J Cell Sci. 126 (Pt 5): 1199–206. doi:10.1242/jcs.117135. PMC 4481642. PMID 23345406.
- ^ Decaen, P. G.; Delling, M.; Vien, T. N.; Clapham, D. E. (2013). "Direct recording and molecular identification of the calcium channel of primary cilia". Nature. 504 (7479): 315–318. Bibcode:2013Natur.504..315D. doi:10.1038/nature12832. PMC 4073646. PMID 24336289.
- ^ Hajnóczky, G; Csordás, G; Das, S; Garcia-Perez, C; Saotome, M; Sinha Roy, S; Yi, M (2006). "Mitochondrial calcium signalling and cell death: approaches for assessing the role of mitochondrial Ca2+ uptake in apoptosis". Cell Calcium. 40 (5–6): 553–60. doi:10.1016/j.ceca.2006.08.016. PMC 2692319. PMID 17074387.
- ^ Tripathy, Le Xu Ashutosh; Pasek, Daniel A.; Meissner, Gerhard (1998). "Potential for Pharmacology of Ryanodine Receptor/Calcium Release Channels". Ann NY Acad Sci. 853 (1): 130–148. Bibcode:1998NYASA.853..130T. doi:10.1111/j.1749-6632.1998.tb08262.x. PMID 10603942. S2CID 86436194. Archived from the original on 2008-04-23. Retrieved 2006-10-22.
- ^ Mariani Colombo P, Rascio N. "Ruthenium red staining for electron microscopy of plant material". Journal of Ultrastructure Research Volume 60, Issue 2, August 1977, Pages 135–139