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4-[(2,5-dimethylphenyl)thio]anthra[1,2-c][1,2,5]thiadiazol-6,11-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1472629-71-2

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1472629-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1472629-71-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,7,2,6,2 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1472629-71:
(9*1)+(8*4)+(7*7)+(6*2)+(5*6)+(4*2)+(3*9)+(2*7)+(1*1)=182
182 % 10 = 2
So 1472629-71-2 is a valid CAS Registry Number.

1472629-71-2Downstream Products

1472629-71-2Relevant academic research and scientific papers

Ring fusion strategy for synthesis and lead optimization of sulfur-substituted anthra[1,2-c[[1,2,5]thiadiazole-6,11-dione derivatives as promising scaffold of antitumor agents

Lee, Yu-Ru,Chen, Tsung-Chih,Lee, Chia-Chung,Chen, Chun-Liang,Ahmed Ali, Ahmed Atef,Tikhomirov, Alexander,Guh, Jih-Hwa,Yu, Dah-Shyong,Huang, Hsu-Shan

, p. 661 - 676 (2015)

A series of sulfur-substituted anthra[1,2-c][1,2,5]thiadiazole-6,11-diones were synthesized and evaluated using the cell proliferations, apoptosis and NCI-60 cell panel assays. Also, the signaling pathways that account for their activities were investigated. Compounds 2, 3, 4a, 4d, 4f, 4i, 4k, 5b, 5c, 5d, 5f, 5g, 6b, 6c, 6d, 6e, 6g, 7a and 7g were selected by NCI. Among the tested compounds, 6g appeared to be the most active compound of this series that not only induced apoptosis in DU-145 cancer cells but also attenuated the ERK1/2 and p38 signaling pathways. All test compounds exhibited diverse cytostatic and cytotoxic activities that warrant further development as potential anticancer agents.

HETEROCYCLIC FUSED ANTHRAQUINONE DERIVATIVES, MANUFACTURING METHOD AND PHARMACEUTICAL COMPOSITION USING THEREOF

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Paragraph 0101 - 0105, (2013/11/06)

A heterocyclic fused anthraquinone derivatives, which is represented by a formula (I): wherein R1 is a substituent being one selected from a group consisting of hydrogen, halogens, aminoalkyl group, sulfoalkyl group, haloalkyl group, piperazino

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