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(Z)-1-(3,4,5-trimethoxy)phenyl-2-(3'-hydroxy-4'-ethoxy)phenylethylene Fmoc-glycinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1015697-75-2

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1015697-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1015697-75-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,5,6,9 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1015697-75:
(9*1)+(8*0)+(7*1)+(6*5)+(5*6)+(4*9)+(3*7)+(2*7)+(1*5)=152
152 % 10 = 2
So 1015697-75-2 is a valid CAS Registry Number.

1015697-75-2Relevant academic research and scientific papers

THE PREPARTION AND THE USE OF ETHOXY COMBRETASTATINS AND THEIR PRODRUGS

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Page/Page column 13; 20, (2009/06/27)

The invention disclosed a total synthesis process of novel ethoxy combretastatins and their prodrugs. Combretastatins are chemically modified by ethoxy substituted on the 4'-position of their B aryl ring and are converted to be their soluble prodrugs of phosphate or their inner salt of phosphorylcholine by modifying the hydroxyl on the 3'-position of their B aryl ring. Similarly, 3'-amino combretastatin is 4'-ethoxy chemically modified and further side chain of amino acid can be introduced to the amino to form soluble prodrug of amino acidamide. The structure of the said compound is showed as formula (I). Ethoxy combretastatins possess potent tubulin polymerization inhibitory activity and can be used for the treatment of inhibiting tumor or neovascular.

PREPARATION AND THE USE OF ETHOXY COMBRETASTATINS AND THEIR PRODRUGS

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Page/Page column 9-10; fig.2, (2009/07/17)

The invention disclosed a total synthesis process of novel ethoxy combretastatins and their prodrugs. Combretastatins are chemically modified by ethoxy substituted on the 4′-position of their B aryl ring and are converted to be their soluble prodrugs of phosphate or their inner salt of phosphorylcholine by modifying the hydroxyl on the 3′-position of their B aryl ring. Similarly, 3′-amino combretastatin is 4′-ethoxy chemically modified and further side chain of amino acid can be introduced to the amino to form soluble prodrug of amino acidamide. The structure of the said compound is showed as formula (I). Ethoxy combretastatins possess potent tubulin polymerization inhibitory activity and can be used for the treatment of inhibiting tumor or neovascular.

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