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N-(3-chloro-3-phenylpropyl)-9,10-dihydro-9-oxoacridine-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1250437-83-2

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1250437-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1250437-83-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,0,4,3 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1250437-83:
(9*1)+(8*2)+(7*5)+(6*0)+(5*4)+(4*3)+(3*7)+(2*8)+(1*3)=132
132 % 10 = 2
So 1250437-83-2 is a valid CAS Registry Number.

1250437-83-2Downstream Products

1250437-83-2Relevant academic research and scientific papers

Design, synthesis and evaluation of substituted N-(3-arylpropyl)-9,10- dihydro-9-oxoacridine-4-carboxamides as potent MDR reversal agents in cancer

Velingkar,Dandekar

, p. 504 - 510 (2012/01/06)

A novel class of molecules with structure N-(3-arylpropyl)-9,10-dihydro-9- oxoacridine-4-carboxamides (20-29) were designed by generating a pharmacophore for potent MDR reversal activity using phase drug design software. The designed molecules were synthesized by a novel synthesis route and evaluated for their inhibitory effects on the transport activity of P-glycoprotein (P-gp) by standard Hoechst 33342 assay method. Based on the pIC50 values of ten title compounds screened, three compounds exhibited better activity as compared to Verapamil used as standard.

Microwave-assisted synthesis and evaluation of substituted aryl propyl acridone-4-carboxamides as potential chemosensitizing agents for cancer

Velingkar, Vinaykumar S.,Dandekar, Vikrant D.

, p. 268 - 275 (2013/01/10)

A novel class of compounds with structure Aryl propyl acridone-4- carboxamides were synthesized by conventional and microwave (MW) irradiation methods and evaluated for their inhibitory effects on the transport activity of P- glycoprotein (P-gp) by standard Hoechst 33342 assay method. The title compounds with phenoxy substitution exhibited better activity.

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