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(E)-1-(2,5-dihydroxyphenyl)-3-(4-nitrophenyl)prop-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107915-59-3

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107915-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107915-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,1 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107915-59:
(8*1)+(7*0)+(6*7)+(5*9)+(4*1)+(3*5)+(2*5)+(1*9)=133
133 % 10 = 3
So 107915-59-3 is a valid CAS Registry Number.

107915-59-3Downstream Products

107915-59-3Relevant academic research and scientific papers

Synthesis, antihyperglycemic activity and computational studies of antioxidant chalcones and flavanones derived from 2,5 dihydroxyacetophenone

Tajammal, Affifa,Batool, Majda,Ramzan, Ayesha,Samra, Malka M.,Mahnoor, Idrees,Verpoort, Francis,Irfan, Ahmad,Al-Sehemi, Abdullah G.,Munawar, Munawar Ali,Basra, Muhammad Asim R.

, p. 512 - 520 (2017)

Chronic exposure of supraphysiologic glucose concentration to cells and tissues resulted in glucose toxicity which causes oxidative stress. Antioxidants have promising effect in suppressing the oxidative stress in the pathogenesis of diabetes mellitus (DM

Cytotoxic 2',5'-dihydroxychalcones with unexpected antiangiogenic activity.

Nam, Nguyen-Hai,Kim, Yong,You, Young-Jae,Hong, Dong-Ho,Kim, Hwan-Mook,Ahn, Byung-Zun

, p. 179 - 187 (2007/10/03)

A series of 2',5'-dihydroxychalcones were synthesized and evaluated for cytotoxicity against tumor cell lines and human umbilical venous endothelial cells (HUVEC). It was found that chalcones with electron-withdrawing substituents on the B ring exhibited potent cytotoxicity against a variety of tumor cell lines while compounds with electron-releasing groups were less potent in general. Those compounds with B ring replaced by extended or heteroaromatic rings exhibited significant bioactivity. Several compounds were shown to have marked cytotoxic selectivity towards HUVECs. Especially, among the synthesized compounds, 2-chloro-2',5'-dihydroxychalcone (2-3) showed the highest selectivity index up to 66 in comparison to HCT116 cells. This compound also exhibited strong inhibitory effects on the HUVEC tube formation in an in vitro model. When administered into BDF1 mice bearing Lewis lung carcinoma cells at 50 mg kg(-1) day(-1), 2-3 was found to inhibit the growth of tumor mass by 60.5%.

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