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(S)-ethyl 2-(4-bromo-3-methyl-phenoxy)-3-phenylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1416332-63-2

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1416332-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1416332-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,3,3 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1416332-63:
(9*1)+(8*4)+(7*1)+(6*6)+(5*3)+(4*3)+(3*2)+(2*6)+(1*3)=132
132 % 10 = 2
So 1416332-63-2 is a valid CAS Registry Number.

1416332-63-2Relevant academic research and scientific papers

New 2-(aryloxy)-3-phenylpropanoic acids as peroxisome proliferator- activated receptor α/γ dual agonists able to upregulate mitochondrial carnitine shuttle system gene expression

Laghezza,Pochetti,Lavecchia,Fracchiolla,Faliti,Piemontese,Di Giovanni,Iacobazzi,Infantino,Montanari,Capelli,Tortorella,Loiodice

, p. 60 - 72 (2013)

The preparation of a series of 2-(aryloxy)-3-phenylpropanoic acids, resulting from the introduction of different substituents into the biphenyl system of the previously reported peroxisome proliferator-activated receptor α/γ (PPARα/γ) dual agonist 1, allowed the identification of new ligands with higher potency on PPARα and fine-tuned moderate PPARγ activity. For the most promising stereoisomer (S)-16, X-ray and calorimetric studies in PPARγ revealed, at high ligand concentration, the presence of two molecules simultaneously bound to the receptor. On the basis of these results and docking experiments in both receptor subtypes, a molecular explanation was provided for its different behavior as a full and partial agonist of PPARα and PPARγ, respectively. The effects of (S)-16 on mitochondrial acylcarnitine carrier and carnitine-palmitoyl-transferase 1 gene expression, two key components of the carnitine shuttle system, were also investigated, allowing the hypothesis of a more beneficial pharmacological profile of this compound compared to the less potent PPARα agonist fibrates currently used in therapy.

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