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AKOS BBS-00005670 is a chemical compound identified by its unique AKOS catalog number. It is a specific substance that has been cataloged for research and industrial applications, though without additional context or a chemical name, it's challenging to provide a detailed summary. Typically, such compounds are used in various fields like pharmaceuticals, materials science, or chemical research. For a comprehensive understanding of its properties, applications, and safety data, one would need to refer to the manufacturer's technical specifications or a detailed chemical database.

5361-23-9

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5361-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5361-23-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5361-23:
(6*5)+(5*3)+(4*6)+(3*1)+(2*2)+(1*3)=79
79 % 10 = 9
So 5361-23-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H10ClN3O3S/c15-10-6-4-9(5-7-10)13(19)17-14(22)16-11-2-1-3-12(8-11)18(20)21/h1-8H,(H2,16,17,19,22)

5361-23-9Upstream product

5361-23-9Downstream Products

5361-23-9Relevant academic research and scientific papers

Quinazolines as adenosine receptor antagonists: SAR and selectivity for A2B receptors

Webb, Thomas R.,Lvovskiy, Dmitriy,Kim, Soon-Ai,Ji, Xiao-Duo,Melman, Neli,Linden, Joel,Jacobson, Kenneth A.

, p. 77 - 85 (2007/10/03)

We have recently reported the discovery of numerous new compounds that are selective inhibitors of all of the subtypes of the adenosine receptor family via a pharmacophore database searching and screening strategy. During the course of this work we made the unexpected discovery of a potent A2B receptor antagonist, 4-methyl-7-methoxyquinazolyl-2-(2′-amino-4′-imidazolinone) (38, CMB 6446), which showed selectivity for this receptor and functioned as an antagonist, with a binding Ki value of 112 nM. We explored the effects of both substituent- and ring-structural variations on the receptor affinity in this series of derivatives, which were found to be mostly non-selective adenosine receptor ligands with Ki values in the micromolar range. Since no enhancement of A2B receptor affinity of 38 was achieved, the previously reported pharmacophore-based searching strategy yielded the most potent and selective structurally-related hit in the database originally searched.

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