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1-[2-(phenylsulfanyl)ethyl]piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69967-27-7

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69967-27-7 Usage

Chemical class

Piperidine derivatives

Structure

Contains a piperidine ring and a phenylsulfanyl ethyl group

Known as

N-PEP

Potential pharmaceutical applications

Inhibitor of the dopamine transporter

Investigated for

Treatment of cocaine addiction

Researched for

Neuroprotective and neurotrophic properties

Relevance to neurodegenerative diseases

Parkinson's and Alzheimer's disease

Check Digit Verification of cas no

The CAS Registry Mumber 69967-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,6 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69967-27:
(7*6)+(6*9)+(5*9)+(4*6)+(3*7)+(2*2)+(1*7)=197
197 % 10 = 7
So 69967-27-7 is a valid CAS Registry Number.

69967-27-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-phenylsulfanylethyl)piperidine,hydrochloride

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

More Details:69967-27-7 SDS

69967-27-7Downstream Products

69967-27-7Relevant academic research and scientific papers

Aniline-Based Inhibitors of Influenza H1N1 Virus Acting on Hemagglutinin-Mediated Fusion

Leiva, Rosana,Barniol-Xicota, Marta,Codony, Sandra,Ginex, Tiziana,Vanderlinden, Evelien,Montes, Marta,Caffrey, Michael,Luque, F. Javier,Naesens, Lieve,Vázquez, Santiago

, p. 98 - 118 (2018/02/10)

Two series of easily accessible anilines were identified as inhibitors of influenza A virus subtype H1N1, and extensive chemical synthesis and analysis of the structure-activity relationship were performed. The compounds were shown to interfere with low pH-induced membrane fusion mediated by the H1 and H5 (group 1) hemagglutinin (HA) subtypes. A combination of virus resistance, HA interaction, and molecular dynamics simulation studies elucidated the binding site of these aniline-based influenza fusion inhibitors, which significantly overlaps with the pocket occupied by some H3 HA-specific inhibitors, indicating the high relevance of this cavity for drug design.

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