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Phenol, 4-(3-phenyl-5-isoxazolyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22439-71-0

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22439-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22439-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,3 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22439-71:
(7*2)+(6*2)+(5*4)+(4*3)+(3*9)+(2*7)+(1*1)=100
100 % 10 = 0
So 22439-71-0 is a valid CAS Registry Number.

22439-71-0Relevant academic research and scientific papers

Synthesis of some novel substituted phenylisoxazol phenoxy 2-methylpropanoic acids and there in vivo hypolipidemic activity

Mokale, Santosh N.,Dube, Pritam N.,Nevase, Manjusha C.,Sakle, Nikhil S.,Shelke, Vishakha R.,Bhavale, Swati A.,Begum, Afreen

, p. 422 - 428 (2016/02/19)

The novel series of phenylisoxazol phenoxy 2-methylpropanoic acid derivatives were synthesized and evaluated for their in vivo hypolipidemic activity by triton WR-1339-induced hyperlipidemia in rats. The newly synthesized compounds 5a and 5i showed significant decrease in the serum TCH, TG, LDL and VLDL along with an increase in serum HDL levels as compared to standard drug Fenofibrate. The treated groups also showed significant decrease in the atherogenic index, TC:HDL risk ratios compared to cholesterol-induced hyperlipidemic control group. These molecules indeed have the potential to be developed as antihypolipidemic molecules.

Synthesis and in-vivo hypolipidemic activity of some novel substituted phenyl isoxazol phenoxy acetic acid derivatives

Mokale, Santosh N.,Nevase, Manjusha C.,Sakle, Nikhil S.,Dube, Pritam N.,Shelke, Vishakha R.,Bhavale, Swati A.,Begum, Afreen

, p. 2155 - 2158 (2014/05/06)

The present study was undertaken to evaluate in-vivo hypolipidemic activity of a novel series of 2-methyl-2-(substituted phenyl isoxazol)phenoxyacetic acid derivatives by triton induced hyperlipidemia in rats. The newly synthesized compounds 5a, 5d and 5g showed significant decrease in the serum TCH, TG, LDL and VLDL along with an increase in serum HDL levels as compared to standard drug Fenofibrate. The treated groups also showed significant decrease in the atherogenic index and increase in % protective activity compared to control group.

Synthesis and structure-activity relationships of 3,5-diarylisoxazoles and 3,5-diaryl-1,2,4-oxadiazoles, novel classes of small molecule interleukin-8 (IL-8) receptor antagonists

Weidner-Wells, Michele A.,Henninger, Todd C.,Fraga-Spano, Stephanie A.,Boggs, Christine M.,Matheis, Michele,Ritchie, David M.,Argentieri, Dennis C.,Wachter, Michael P.,Hlasta, Dennis J.

, p. 4307 - 4311 (2007/10/03)

A novel series of 3,5-diarylisoxazole and 3,5-diaryl-1,2,4-oxadiazole IL-8 inhibitors has been identified. These compounds exhibit activity in an IL-8 binding assay as well as in a functional assay of IL-8 induced elastase release from neutrophils. In add

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