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2-Anthracenesulfonic acid, 1-amino-4-([1,1'-biphenyl]-4-ylamino)-9,10-dihydro-9,10-dioxo-, monosodium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65012-06-8

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65012-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65012-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,1 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65012-06:
(7*6)+(6*5)+(5*0)+(4*1)+(3*2)+(2*0)+(1*6)=88
88 % 10 = 8
So 65012-06-8 is a valid CAS Registry Number.

65012-06-8Downstream Products

65012-06-8Relevant academic research and scientific papers

Development of 1-Amino-4-(phenylamino)anthraquinone-2-sulfonate Sodium Derivatives as a New Class of Inhibitors of RANKL-Induced Osteoclastogenesis

Lee, Chia-Chung,Chen, Chun-Liang,Liu, Fei-Lan,Chiou, Chung-Yu,Chen, Tsung-Chih,Wu, Cheng-Chi,Sun, Wei-Hsin,Chang, Deh-Ming,Huang, Hsu-Shan

, p. 342 - 355 (2016/05/19)

A series of 1-amino-4-(phenylamino)anthraquinone-2-sulfonate sodium derivatives was synthesized and evaluated for osteoclast inhibition using a TRAP-staining assay. Among them, two compounds, LCCY-13 and LCCY-15, dose-dependently suppressed receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclast formation. Moreover, the cytotoxicity assay on RAW264.7 cells suggested that the inhibition of osteoclastic bone resorption by these compounds was not a result of their cytotoxicity. Further, the inhibitory activities of compounds LCCY-13 and LCCY-15 were further confirmed by including specific inhibition of NFATc1 expression levels in nuclei using an immunofluorescent analysis. In addition, LCCY-13 and LCCY-15 also significantly attenuated the bone resorption activity of osteoclasts according to a pit formation assay. Thus, a new class of 1-amino-4-(phenylamino)anthraquinone-2-sulfonate sodium compounds might be considered as an essential lead structure for the further development of anti-resorptive agents.

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