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5-(2,4-dichlorophenyl)-3-(pyridin-2-yl)-1,2,4-oxadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

339103-05-8

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339103-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 339103-05-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,1,0 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 339103-05:
(8*3)+(7*3)+(6*9)+(5*1)+(4*0)+(3*3)+(2*0)+(1*5)=118
118 % 10 = 8
So 339103-05-8 is a valid CAS Registry Number.

339103-05-8Downstream Products

339103-05-8Relevant academic research and scientific papers

NOVEL OXADIAZOLE COMPOUND AND COMPOSITION FOR PREVENTING OR TREATING DIABETES COMPRISING THE SAME

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Paragraph 0056-0060, (2021/01/28)

The present invention relates to a novel oxadiazole compound represented by chemical formula 1 and a composition for preventing or treating diabetes comprising the same.

Discovery and characterization of AZD9272 and AZD6538 - Two novel mGluR5 negative allosteric modulators selected for clinical development

Raboisson, Patrick,Breitholtz-Emanuelsson, Anna,Dahlloef, Henrik,Kers, Annika,Minidis, Alexander B. E.,Nordmark, Anna,Stroem, Peter,Terelius, Ylva,Wensbo, David,Edwards, Louise,Isaac, Methvin,Jarvie, Keith,Slassi, Abdelmalik,Wilson, Julie M.,Xin, Tao,Heaton, William L.,Sheehan, Susan M.,McLeod, Donald A.

, p. 6974 - 6979,6 (2020/09/02)

AZD9272 and AZD6538 are two novel mGluR5 negative allosteric modulators selected for further clinical development. An initial high-throughput screening revealed leads with promising profiles, which were further optimized by minor, yet indispensable, structural modifications to bring forth these drug candidates. Advantageously, both compounds may be synthesized in as little as one step. Both are highly potent and selective for the human as well as the rat mGluR5 where they interact at the same binding site than MPEP. They are orally available, allow for long interval administration due to a high metabolic stability and long half-lives in rats and permeate the blood brain barrier to a high extent. AZD9272 has progressed into phase I clinical studies.

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