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4-[(2,2-DIMETHYLPROPANOYL)AMINO]NICOTINIC ACID, also known as Laropiprant, is a pharmaceutical compound characterized by its role as a nicotinic acid receptor antagonist. It is specifically designed to inhibit prostaglandin D2 (PGD2), thereby reducing the vasodilatory effects associated with niacin treatment. This selective inhibition of the prostaglandin D2 receptor subtype 1 (DP1) helps in mitigating the flushing side effect in patients undergoing treatment for primary hypercholesterolemia or mixed dyslipidemia with niacin. Laropiprant, available in oral tablet form, is metabolized primarily by the liver and is typically administered under medical supervision.

125867-31-4

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125867-31-4 Usage

Uses

Used in Pharmaceutical Industry:
4-[(2,2-DIMETHYLPROPANOYL)AMINO]NICOTINIC ACID is used as a pharmaceutical compound for the treatment of primary hypercholesterolemia or mixed dyslipidemia. It serves as an adjunct to niacin therapy, specifically to reduce the incidence of flushing, a common side effect of niacin treatment. By inhibiting the prostaglandin D2 receptor subtype 1 (DP1), Laropiprant effectively diminishes the vasodilatory effects of niacin, thus improving patient comfort and compliance during treatment.
Additionally, as a nicotinic acid receptor antagonist, 4-[(2,2-DIMETHYLPROPANOYL)AMINO]NICOTINIC ACID may have potential applications in other areas of medicine where modulation of prostaglandin D2 signaling is beneficial. However, further research and clinical trials would be necessary to explore and validate these potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 125867-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,6 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 125867-31:
(8*1)+(7*2)+(6*5)+(5*8)+(4*6)+(3*7)+(2*3)+(1*1)=144
144 % 10 = 4
So 125867-31-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O3/c1-11(2,3)10(16)13-8-4-5-12-6-7(8)9(14)15/h4-6H,1-3H3,(H,14,15)(H,12,13,16)

125867-31-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,2-dimethylpropanoylamino)pyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-pivaloylaminopyridine-3-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:125867-31-4 SDS

125867-31-4Relevant academic research and scientific papers

Synthesis of ortho-substituted aminopyridines. Metalation of pivaloylamino derivatives

Estel,Linard,Marsais,Godard,Queguiner

, p. 105 - 112 (2007/10/02)

The three isomeric pivaloylaminopyridines were lithiated in more than 80% yields. Aminopyridine derivatives were treated by 2.5-3 equivalents of the complex BuLi-TMEDA at -10° in diethyl ether. Reaction of the lithiated species with various electrophiles afforded a number of ortho-substituted pivaloylaminopyridines in good yields. Secondary pyridine alcohols were oxidized to the corresponding aminopyridyl ketones. Pyridopyrimidines, benzonaphthyridines as well as an analogue of the natural antitumor alkaloid ellipticine has been synthesized showing the versatility of the method.

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