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3-(phenylsulfonyl)-4-(4-((S)-2-(2-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienylthio)benzamido)propanoyloxy)but-2-ynyloxy)-1,2,5-oxadiazol-2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1229581-58-1

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1229581-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1229581-58-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,9,5,8 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1229581-58:
(9*1)+(8*2)+(7*2)+(6*9)+(5*5)+(4*8)+(3*1)+(2*5)+(1*8)=171
171 % 10 = 1
So 1229581-58-1 is a valid CAS Registry Number.

1229581-58-1Downstream Products

1229581-58-1Relevant academic research and scientific papers

Synthesis and evaluation of nitric oxide-releasing derivatives of farnesylthiosalicylic acid as anti-tumor agents

Ling, Yong,Ye, Xiaolei,Ji, Hui,Zhang, Yihua,Lai, Yisheng,Peng, Sixun,Tian, Jide

experimental part, p. 3448 - 3456 (2010/10/03)

Novel furoxan-based nitric oxide (NO)-releasing derivatives (11a-p) of farnesylthiosalicylic acid (FTA) were synthesized. Compounds 11d, 11f, 11k, and 11m-o displayed anti-tumor activities superior to FTA and sorafenib in most cancer cells tested. Analysis of six compounds revealed that 11d, 11f, 11n, 11o, and 11p, but not 11a that had low anti-tumor activity, produced high levels of NO, associated with their strong anti-tumor activity. Furthermore, the anti-tumor activity of 11f was partially mimicked by the furoxan moiety, but reduced by pre-treatment with hemoglobin. Importantly, treatment with 11f inhibited Ras-related signaling in cancer cells. Apparently, the high anti-tumor activity of 11f was attributed to the synergic effect of high levels of NO production and inhibition of Ras-related signaling in cancer cells. Our findings suggest that the furoxan/FTA hybrids may hold greater promise as therapeutic agents for the intervention of human cancers.

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