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[4-(2-Methyl-pyridin-4-yl)-phenyl]-acetic acid is a chemical compound characterized by its molecular formula C15H13NO2. It is a derivative of phenylacetic acid, featuring a substituted pyridine ring that contributes to its unique structural properties. [4-(2-Methyl-pyridin-4-yl)-phenyl]-acetic acid is of interest in pharmaceutical research due to its potential therapeutic applications, which are currently being explored.

1243245-69-3

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1243245-69-3 Usage

Uses

Used in Pharmaceutical Research:
[4-(2-Methyl-pyridin-4-yl)-phenyl]-acetic acid is used as a research compound for its potential therapeutic applications. Its structural properties, including the presence of a substituted pyridine ring, make it a promising candidate for the development of new drugs.
Used in Anti-inflammatory and Analgesic Drug Development:
In the field of drug development, [4-(2-Methyl-pyridin-4-yl)-phenyl]-acetic acid is utilized as a lead compound for the creation of anti-inflammatory and analgesic medications. Studies have indicated that derivatives of phenylacetic acid, including [4-(2-Methyl-pyridin-4-yl)-phenyl]-acetic acid, have demonstrated anti-inflammatory and analgesic effects, which are valuable for treating various conditions associated with pain and inflammation.
Further research is necessary to fully understand the potential uses and benefits of [4-(2-Methyl-pyridin-4-yl)-phenyl]-acetic acid, as its therapeutic applications are still being investigated. As it stands, the compound holds promise for contributing to advancements in pharmaceuticals, particularly in the areas of pain management and inflammation control.

Check Digit Verification of cas no

The CAS Registry Mumber 1243245-69-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,3,2,4 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1243245-69:
(9*1)+(8*2)+(7*4)+(6*3)+(5*2)+(4*4)+(3*5)+(2*6)+(1*9)=133
133 % 10 = 3
So 1243245-69-3 is a valid CAS Registry Number.

1243245-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-(2-methylpyridin-4-yl)phenyl)acetic acid

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:1243245-69-3 SDS

1243245-69-3Relevant academic research and scientific papers

With Wnt signal path to inhibit the active heterocyclic compounds (by machine translation)

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, (2017/08/15)

The invention relates to a signal path with Wnt inhibiting activity of a heterocyclic compound, including the compound and its pharmaceutically acceptable salt, various isotope, various isomers or various crystal structure, having the general formula I of the structure shown in: the invention relates to a compound and its joint application composition can effectively inhibit the Wnt signal path, can be used for the treatment or prevention of a disorder associated with a Wnt signal path. (by machine translation)

Design, synthesis, and evaluation of potent Wnt signaling inhibitors featuring a fused 3-ring system

Xu, Zhixiang,Li, Jiajun,Wu, Yiyuan,Sun, Zhijian,Luo, Lusong,Hu, Zhilin,He, Sudan,Zheng, Jiyue,Zhang, Hongjian,Zhang, Xiaohu

, p. 154 - 165 (2015/12/04)

The Wnt signaling pathway is a critical developmental pathway which operates through control of cellular functions such as proliferation and differentiation. Aberrant Wnt signaling has been linked to the formation and metastasis of tumors. Porcupine, a member of the membrane-bound O-acyltransferase family of proteins, is an important component of the Wnt pathway. Porcupine catalyzes the palmitoylation of Wnt proteins, a process needed for their secretion and activity. Here we report a novel series of compounds obtained by a scaffold hybridization strategy from a known porcupine inhibitor class. The leading compound 59 demonstrated subnanomolar inhibition of Wnt signaling in a paracrine cellular assay. Compound 59 also showed excellent chemical, plasma and liver microsomal stabilities. Furthermore, compound 59 exhibited good pharmacokinetic profiles with 30% oral bioavailability in rat. Collectively, these results strongly support further optimization of this novel scaffold to develop better Wnt pathway inhibitors.

N- (HETERO)ARYL, 2- (HETERO)ARYL-SUBSTITUTED ACETAMIDES FOR USE AS WNT SIGNALING MODULATORS

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Page/Page column 44; 45, (2010/09/18)

The present invention relates to compounds of formulae 1 and 2 and methods for modulating the Wnt signaling pathway using these compounds, wherein A1, A2, B, Y and Z all represent rings.

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