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1H-BenziMidazole, 2-[4-[2-(2-phenyl-1H-benziMidazol-1-yl)-2-(4-piperidinyl)ethoxy]phenyl]-1-(phenylMethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1440754-12-0

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1440754-12-0 Usage

Molecular Structure

1H-Benzimidazole, 2-[4-[2-(2-phenyl-1H-benzimidol-1-yl)-2-(4-piperidinyl)ethoxy]phenyl]-1-(phenylmethyl)has a complex molecular structure containing benzimidazole, phenyl, piperidine, and ethoxy groups.

Aromatic System

The compound is characterized by a large aromatic system, which contributes to its stability and potential pharmacological activities.

Benzimidazole Group

The presence of the benzimidazole group provides a stable, planar structure that can participate in various chemical reactions and interactions.

Phenyl Group

The phenyl group contributes to the compound's aromaticity and can influence its solubility, stability, and pharmacokinetic properties.

Piperidine Group

The piperidine group is a nitrogen-containing, heterocyclic structure that can participate in hydrogen bonding and coordination with other molecules, potentially affecting the compound's pharmacological activity.

Ethoxy Group

The ethoxy group is an alkoxy substituent that can influence the compound's solubility, stability, and lipophilicity, which may be important for its pharmacokinetic properties and bioavailability.

Medicinal Chemistry Applications

Due to its structural features and potential pharmacological activities, 1H-Benzimidazole, 2-[4-[2-(2-phenyl-1H-benzimidol-1-yl)-2-(4-piperidinyl)ethoxy]phenyl]-1-(phenylmethyl)has potential applications in medicinal chemistry and drug design.

Further Study and Analysis

The specific properties and potential uses of 1H-BenziMidazole, 2-[4-[2-(2-phenyl-1H-benziMidazol-1-yl)-2-(4-piperidinyl)ethoxy]phenyl]-1-(phenylMethyl)- would require further study and analysis to fully understand its potential in drug development and therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1440754-12-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,0,7,5 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1440754-12:
(9*1)+(8*4)+(7*4)+(6*0)+(5*7)+(4*5)+(3*4)+(2*1)+(1*2)=140
140 % 10 = 0
So 1440754-12-0 is a valid CAS Registry Number.

1440754-12-0Downstream Products

1440754-12-0Relevant academic research and scientific papers

Structure guided design and kinetic analysis of highly potent benzimidazole inhibitors targeting the PDEδ prenyl binding site

Zimmermann, Gunther,Schultz-Fademrecht, Carsten,Küchler, Philipp,Murarka, Sandip,Ismail, Shehab,Triola, Gemma,Nussbaumer, Peter,Wittinghofer, Alfred,Waldmann, Herbert

, p. 5435 - 5448 (2014/07/08)

K-Ras is one of the most frequently mutated signal transducing human oncogenes. Ras signaling activity requires correct cellular localization of the GTPase. The spatial organization of K-Ras is controlled by the prenyl binding protein PDEδ, which enhances Ras diffusion in the cytosol. Inhibition of the Ras-PDEδ interaction by small molecules impairs Ras localization and signaling. Here we describe in detail the identification and structure guided development of Ras-PDEδ inhibitors targeting the farnesyl binding pocket of PDEδ with nanomolar affinity. We report kinetic data that characterize the binding of the most potent small molecule ligands to PDEδ and prove their binding to endogenous PDEδ in cell lysates. The PDEδ inhibitors provide promising starting points for the establishment of new drug discovery programs aimed at cancers harboring oncogenic K-Ras.

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