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Pd((C6H5)C3N2(CH3)2(O)NCH(C6H4O))Cl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119016-74-9

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119016-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119016-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,1 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119016-74:
(8*1)+(7*1)+(6*9)+(5*0)+(4*1)+(3*6)+(2*7)+(1*4)=109
109 % 10 = 9
So 119016-74-9 is a valid CAS Registry Number.

119016-74-9Downstream Products

119016-74-9Relevant academic research and scientific papers

Synthesis, characterization, cytotoxicity, and molecular docking studies of ampyrone-based transition metal complexes

Azam, Mohammad,Wabaidur, Saikh Mohammad,Alam, Mahboob,Khan, Zahid,Alanazi, Ibrahim O.,Al-Resayes, Saud I.,Moon, Il Soo,Rajendra

, p. 65 - 71 (2021)

A novel series of mononuclear transition metal complexes, [Cu(L)Cl] 1, [Zn(L)Cl] 2, [Pd(L)Cl] 3, [Cd(L)I] 4, [Pt(L)Cl] 5, and [Hg(L)Cl] 6, was constructed from a pyrazole-derived Schiff ligand, HL, and characterized by physicochemical and spectroscopic methods. Fourier-transform infrared (FT-IR) spectral data showed the studied ligand to be tridentate and coordinated to the metal ions via ONO donor atoms, whereas powder X-ray diffraction (PXRD) analysis revealed the crystalline nature of all the complexes. The in vitro cytotoxicity of the studied ligand and its complexes were tested by the 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay against the human colorectal cancer cell lines HCT116 and HT29. The results suggested that the HCT116 cell line is highly sensitive to complex 1 with a half-maximal inhibitory concentration (IC50) of 45.6?μM, while both cell lines tolerated complexes 2 and 4 better in comparison with HL. In addition, complex 1 with significant anticancer activity was analyzed by molecular docking studies to explore its binding efficacy to the cyclin-dependent kinase?2 active site.

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