Structure via PubChem · Public domain (PubChem)
In the Vinony graph
Within Vinony's link graph, ruthenium red is referenced by 576 other articles, and connects out to hepoxilin, Onion and Allium sativum.
Vinony files it under Ammine complexes, Chembox having GHS data and ECHA InfoCard ID from Wikidata.
Its subject is documented across 8 Wikipedia language editions.
Chemical data
- Formula
- Cl6H46N14O2Ru3
- Molecular weight
- 790.4 g/mol
- IUPAC name
- azane;tris(ruthenium(2+));hexachloride;dihydrate
- SMILES
- N.N.N.N.N.N.N.N.N.N.N.N.N.N.O.O.[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Ru+2].[Ru+2].[Ru+2]
- InChIKey
- JQJSTVUROJELSR-UHFFFAOYSA-H
- Polar surface area
- 16 Ų
- H-bond donors
- 16
- H-bond acceptors
- 22
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
5,013 papers- Ruthenium red: Blocker or antagonist of TRPV channels?Cell calcium · 2024
- Ruthenium red and the bacterial glycocalyx.Biotechnic & histochemistry : official publication of the Biological Stain Commission · 1999
- Ruthenium red as a capsaicin antagonist.Life sciences · 1991
- Ruthenium red attenuates acute pancreatitis by inhibiting MCU and improving mitochondrial function.Biochemical and biophysical research communications · 2022
- Ruthenium red as a tool to study calcium channels, neuronal death and the function of neural pathways.Neurochemistry international · 1997
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Has use
- dye
Show 1 more fact
- chemical formula
- Cl₆H₄₆N₁₄O₂Ru₃
Sources (2)
via Wikidata · CC0