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4-{3-[4-(6-chloropyridazin-3-yl)piperazin-1-yl]propoxy}benzoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124437-35-0

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124437-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124437-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,3 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 124437-35:
(8*1)+(7*2)+(6*4)+(5*4)+(4*3)+(3*7)+(2*3)+(1*5)=110
110 % 10 = 0
So 124437-35-0 is a valid CAS Registry Number.

124437-35-0Downstream Products

124437-35-0Relevant academic research and scientific papers

PYRIDAZINE DERIVATIVES AND USE THEREOF AS MEDICAMENTS FOR TREATING MICRORNA VIRAL INFECTION

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Paragraph 0054, (2013/06/27)

Disclosed are pyridazine derivatives represented by formula I or pharmaceutically acceptable salts or hydrates thereof, pharmaceutical compositions comprising the compounds, and the use of the compounds in preparing the medicaments for treating and/or preventing diseases or disorders associated with viral infections. The compounds represented by formula I have antiviral activity, especially anti-microRNA viral activity. Symbols in the compounds represented are described in the specification.

Pharmacophore-based design, synthesis, and biological evaluation of novel chloro-pyridazine piperazines as human rhinovirus (HRV-3) inhibitors

Wang, Hongliang,Xiao, Junhai,Gao, Dapeng,Zhang, Xian,Yan, Hui,Gong, Zehui,Sun, Tinmin,Li, Song

, p. 1057 - 1059 (2011/03/21)

A series of chloro-pyridazine piperazines were developed based on the structure of human rhinovirus (HRV) capsid-binding inhibitors with proven activity using a pharmacophore model. A preliminary evaluation demonstrated potent activity against HRV-3 with low cytotoxicity. A docking analysis indicated that 8a could fit into, and form tight interactions (e.g., H-bonds, σ-π effect) with the active site in VP1.

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