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2-Propen-1-one, 1-(1-methyl-1H-indol-3-yl)-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27664-05-7

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27664-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27664-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,6 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27664-05:
(7*2)+(6*7)+(5*6)+(4*6)+(3*4)+(2*0)+(1*5)=127
127 % 10 = 7
So 27664-05-7 is a valid CAS Registry Number.

27664-05-7Downstream Products

27664-05-7Relevant academic research and scientific papers

Synthesis, antioxidant activity and DFT study of some novel N-methylated indole incorporating isoxazole moieties

Jani Matilda,Abbs Fen Reji

, p. 244 - 248 (2020/01/08)

A novel series of indolyl isoxazole derivatives were synthesized and the structure of the products is confirmed on the basis of IR, 1H NMR, MS and analytical data. The synthesized compounds were evaluated for their antioxidant and anticancer ac

Structural requirement of arylindolylpropenones as anti-bladder carcinoma cells agents

Martel-Frachet, Véronique,Kadri, Malika,Boumendjel, Ahcne,Ronot, Xavier

experimental part, p. 6143 - 6148 (2011/10/31)

Chalcones have been identified as interesting compounds with cytotoxicity, anti-inflammatory and antioxidant properties. In the present study, we report the synthesis and evaluation of new 1-(N-methylindolyl)-3-phenylpropenones as anti-cancer agents acting on bladder carcinoma cell line. Among the 15 investigated molecules, three of them inhibit the growth of bladder cancer cells with IC50 values less than 4 μM after 48 h of treatment. To investigate their mode of action, cell cycle analyses were performed. The most active compounds induce high accumulation at the G2+M phase as assessed by flow cytometry. The structure-activity relationship drawn from the present study highlights the importance of the substitution pattern of the phenyl ring and provides valuable information for further development of this class of compounds as novel anti-cancer chemotherapeutic agents.

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