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(E)-3-(benzo[d][1,3]dioxol-5-yl)-1-(2-hydroxy-5-methylphenyl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16635-71-5

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16635-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16635-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16635-71:
(7*1)+(6*6)+(5*6)+(4*3)+(3*5)+(2*7)+(1*1)=115
115 % 10 = 5
So 16635-71-5 is a valid CAS Registry Number.

16635-71-5Downstream Products

16635-71-5Relevant academic research and scientific papers

Discovery of 2′-hydroxychalcones as autophagy inducer in A549 lung cancer cells

Wang, Fang-Wu,Wang, Sheng-Qing,Zhao, Bao-Xiang,Miao, Jun-Ying

, p. 3062 - 3070 (2014)

A series of 2′-hydroxychalcone derivatives was synthesized and the effects of all the compounds on growth of A549 lung cancer cell were investigated. The results showed that all compounds had inhibitory effects on the growth of A549 lung cancer cells and compound 2-7 possessed the highest growth inhibitory effect and induced autophagy of A549 lung cancer cells.

SAR Studies and Biological Characterization of a Chromen-4-one Derivative as an Anti- Trypanosoma brucei Agent

Borsari, Chiara,Santarem, Nuno,MacEdo, Sara,Jiménez-Antón, María Dolores,Torrado, Juan J.,Olías-Molero, Ana Isabel,Corral, María J.,Tait, Annalisa,Ferrari, Stefania,Costantino, Luca,Luciani, Rosaria,Ponterini, Glauco,Gul, Sheraz,Kuzikov, Maria,Ellinger, Bernhard,Behrens, Birte,Reinshagen, Jeanette,Alunda, José María,Cordeiro-Da-Silva, Anabela,Costi, Maria Paola

supporting information, p. 528 - 533 (2019/04/25)

Chemical modulation of the flavonol 2-(benzo[d][1,3]dioxol-5-yl)-chromen-4-one (1), a promising anti-Trypanosomatid agent previously identified, was evaluated through a phenotypic screening approach. Herein, we have performed structure-activity relationsh

CDK inhibitors having flavone structure

-

, (2008/06/13)

The present invention relates to a novel flavone derivative, pharmaceutically acceptable salt, hydrate, solvate and isomer thereof which is useful as an inhibitor against Cyclin Dependent Kinase (CDK), a process for preparation thereof, and a composition of anti-cancer agent or agent for treating neurodegenerative disease comprising this compound as an active ingredient.

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