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N,1-dibenzyl-2-imino-5-oxo-1,5-dihydro-2H-dipyrido[1,2-a:2',3'-d]pyrimidine-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

615273-28-4

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615273-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 615273-28-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,5,2,7 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 615273-28:
(8*6)+(7*1)+(6*5)+(5*2)+(4*7)+(3*3)+(2*2)+(1*8)=144
144 % 10 = 4
So 615273-28-4 is a valid CAS Registry Number.

615273-28-4Downstream Products

615273-28-4Relevant academic research and scientific papers

Novel iminodipyridinopyrimidine analogs, its enantiomers, its diastereomers or its pharmaceutically acceptable salt and antiviral composition against hepatitis C virus containing the same as an active ingredient

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Paragraph 0119; 0132-0135; 0137, (2019/04/06)

The present invention relates to a novel iminodipyridinopyrimidine analogue, an enantiomer thereof, a diastereomer thereof or pharmaceutically acceptable salt thereof, and an antiviral composition for hepatitis C virus containing the same as an active com

Characterization and structure-activity relationship study of iminodipyridinopyrimidines as novel hepatitis C virus inhibitor

Park, Dong-Sik,Jo, Eunji,Choi, Jihyun,Lee, MyungEun,Kim, Soohyun,Kim, Hee-Young,Nam, Jiyon,Ahn, Sujin,Hwang, Jong Yeon,Windisch, Marc Peter

, p. 65 - 73 (2017/09/20)

Upon high-throughput screening of synthetic small molecule libraries with the infectious hepatitis C virus (HCV) cell culture system, we identified an iminodipyridinopyrimidine (IDPP) scaffold. IDPP did not inhibit HCV replication, but exhibited very potent inhibitory activity on early and late steps of HCV life cycle. Applying an intensive structure-activity relationship (SAR) study, a promising IDPP Lead compound (12c) with excellent potency (EC50 = 10 nM), high safety margin (SI > 2000), and an acceptable stability in human and rat liver microsomes (t1/2 >60 min) was identified. Overall, our results suggest that the IDPP scaffold could be used for the development of novel HCV interventions.

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