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4-Piperidinamine, N-[4-(2,2-dimethoxyethyl)phenyl]-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

392630-77-2

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392630-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 392630-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,2,6,3 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 392630-77:
(8*3)+(7*9)+(6*2)+(5*6)+(4*3)+(3*0)+(2*7)+(1*7)=162
162 % 10 = 2
So 392630-77-2 is a valid CAS Registry Number.

392630-77-2Relevant academic research and scientific papers

HETEROCYCLIC BETA-3 ADRENERGIC RECEPTOR AGONISTS

-

, (2008/06/13)

This invention provides compounds of Formula I having the structure U, V, W, X, and Y are as defined hereinbefore, or a pharmaceutically acceptable salt thereof, which are useful in treating or inhibiting metabolic disorders related to insulin resistance or hyperglycemia (typically associated with obesity or glucose intolerance), atherosclerosis, gastrointestinal disorders, neurogenetic inflammation, glaucoma, ocular hypertension and frequent urination; and are particularly useful in the treatment or inhibition of type II diabetes.

4-Aminopiperidine ureas as potent selective agonists of the human β3-Adrenergic receptor

Ashwell, Mark A,Solvibile Jr., William R,Han, Stella,Largis, Elwood,Mulvey, Ruth,Tillet, Jeffrey

, p. 3123 - 3127 (2007/10/03)

The preparation and structure-activity relationships (SARs) of potent agonists of the human β3-adrenergic receptor (AR) derived from a 4-aminopiperidine scaffold are described. Examples combine human β3-AR potency with selectivity over human β1-AR and/or human β2-AR agonism. Compound 29s was identified as a potent (EC50 = 1 nM) and selective (greater than 400-fold over β1- with no β2-AR agonism) full β3-AR agonist with in vivo activity in a transgenic mouse model of thermogenesis.

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