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[(η(6)-p-cymene)Ru(o-C6H4(PPh2)2)Cl]PF6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

209854-76-2

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209854-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209854-76-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,8,5 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 209854-76:
(8*2)+(7*0)+(6*9)+(5*8)+(4*5)+(3*4)+(2*7)+(1*6)=162
162 % 10 = 2
So 209854-76-2 is a valid CAS Registry Number.

209854-76-2Downstream Products

209854-76-2Relevant academic research and scientific papers

Organometallic ruthenium and iridium phosphorus complexes: Synthesis, cellular imaging, organelle targeting and anticancer applications

Li, JuanJuan,Tian, Zhenzhen,Zhang, Shumiao,Xu, Zhishan,Mao, Xudong,Zhou, Yumin,Liu, Zhe

, (2019)

The use of metal complexes containing phosphorus ligands as anticancer agents has not been well studied. In this work, eight novel half-sandwich IrIII and RuII compounds with P^P-chelating ligands have been synthesized and fully characterized, and alongside two crystal structures were reported. All eight complexes displayed highly potent antiproliferative activity, up to nine times more potent than the clinical anticancer drug cisplatin towards A549 lung cancer cells. Complex Ir1, which has a simpler structure and highly potent antiproliferative activity, was selected to investigate in further mechanistic studies. No hydrolysis and nucleobase binding occurred for complex Ir1. In order to elucidate subcellular localization, the self-luminescence of the complex Ir1 was utilized. Ir1 can specifically target lysosomes and facilitate excessive production of reactive oxygen species, resulting in lysosomal membrane permeabilization in A549 cells. Release of cathepsin B and changes in the mitochondria membrane potential also contributed to the observed cytotoxicity of Ir1, which demonstrated an anticancer action mechanism that was different from that of cisplatin. The favorable results from biological and chemical research demonstrated that these types of complexes hold significant theranostic potential.

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