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Tricarbonyldichlororuthenium(II) dimer (CORM-2) 22594-69-0

Tricarbonyldichlororuthenium(II) dimer (CORM-2) 22594-69-0

CAS No.: 22594-69-0

Tricarbonyldichlororuthenium(II) dimer is a pharmacological donor that releases CO. The CO released by Tricarbonyldichlo
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This product is for research use only, not for human use. We do not sell to patients.

Tricarbonyldichlororuthenium(II) dimer is a pharmacological donor that releases CO. The CO released by Tricarbonyldichlororuthenium(II) dimer prevents oxidative damage to the gastric mucosa caused by ischemia/reperfusion (I/R), improves gastric blood flow (GBF), and reduces DNA oxidation and inflammatory responses at the systemic level.

Physicochemical Properties


Molecular Formula C6H6CL4O6RU2
Molecular Weight 512.01
Exact Mass 511.654
CAS # 22594-69-0
PubChem CID 10951331
Appearance Off-white to yellow solid powder
Melting Point 208ºC (dec.)
LogP 1.51
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 6
Rotatable Bond Count 0
Heavy Atom Count 18
Complexity 12.8
Defined Atom Stereocenter Count 0
InChi Key JYHHJVKGDCZCCL-UHFFFAOYSA-J
InChi Code

InChI=1S/6CO.4ClH.2Ru/c6*1-2;;;;;;/h;;;;;;4*1H;;/q;;;;;;;;;;2*+2/p-4
Chemical Name

carbon monoxide;dichlororuthenium
HS Tariff Code 2934.99.9001
Storage

Powder-20°C 3 years

4°C 2 years

In solvent -80°C 6 months

-20°C 1 month

Note: Please store this product in a sealed and protected environment (e.g. under nitrogen), avoid exposure to moisture and light.
Shipping Condition Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

Biological Activity


References

[1]. Oxidative gastric mucosal damage induced by ischemia/reperfusion and the mechanisms of its prevention by carbon monoxide-releasing tricarbonyldichlororuthenium (II) dimer. Free Radic Biol Med. 2019 Dec; 145:198-208.


Solubility Data


Solubility (In Vitro) DMSO: 30 mg/mL (58.59 mM)
H2O: < 0.1 mg/mL
Solubility (In Vivo) Solubility in Formulation 1: ≥ 3 mg/mL (5.86 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 30.0 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL.
Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution.

Solubility in Formulation 2: ≥ 3 mg/mL (5.86 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 30.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 1.9531 mL 9.7654 mL 19.5309 mL
5 mM 0.3906 mL 1.9531 mL 3.9062 mL
10 mM 0.1953 mL 0.9765 mL 1.9531 mL
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.