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Safety Information

SML2991

Sigma-Aldrich

Ru265

≥95% (HPLC), powder, mitochondrial calcium uniporter inhibitor

Synonym(s):

Ru2(μ-N)(NH3)8Cl2]Cl3, trans,trans-Octaamminedichloro-μ-nitridodi-Ruthenium(3+) trichloride, Nitride, ruthenium complex

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About This Item

Empirical Formula (Hill Notation):
Cl5H24N9Ru2
CAS Number:
Molecular Weight:
529.66
UNSPSC Code:
12352200
NACRES:
NA.77

product name

Ru265, ≥95% (HPLC)

Quality Level

Assay

≥95% (HPLC)

form

powder

color

white to dark beige

solubility

H2O: 2 mg/mL, clear

storage temp.

2-8°C

SMILES string

Cl[Ru](N)(N)(N)(N)n[Ru](N)(N)(N)(N)Cl

Biochem/physiol Actions

Ru265 is a non-cytotoxic, aqueous soluble nitrido-bridged dinuclear Ru(IV) complex that acts as a selective mitochondrial calcium uniporter (MCU) inhibitor via a manner distinct from the oxo-bridged Ru360. Ru265 selectively reduces 100 μM histamine-induced mitochondrial [Ca2+] (mCa2+), but not cytosolic [Ca2+] (cCa2+) transient (50 ?M; HeLa) by blocking MCU-mediated mCa2+ uptake at a >10-fold greater potency as Ru360 (IC50 ~2.6 nM vs. 30 nM; HEK293T) without effecting mCa2+ efflux or membrane potential (ΔΨm). Ru265 (50 μM) protects neonatal rat ventricular myocytes from hypoxia/reoxygenation injury by preventing mPTP opening and mCa2+ overload.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

SML2991-BULK:
SML2991-VAR:
SML2991-BULK-CR:
SML2991-25MG:
SML2991-5MG:


Certificates of Analysis (COA)

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Joshua J Woods et al.
Angewandte Chemie (International ed. in English), 59(16), 6482-6491 (2020-02-11)
The mitochondrial calcium uniporter (MCU) is the ion channel that mediates Ca2+ uptake in mitochondria. Inhibitors of the MCU are valuable as potential therapeutic agents and tools to study mitochondrial Ca2+ . The best-known inhibitor of the MCU is the

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