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(4-(piperidin-1-ylsulfonyl)phenyl)methanamine is a chemical compound characterized by its molecular formula C13H20N2O2S. It is a versatile building block in the synthesis of pharmaceutical compounds and organic molecules due to its structural features, including a piperidine ring, a sulfonyl group, and an amine group. These attributes make it a promising candidate for medicinal chemistry and drug discovery, with potential applications in the development of new medications for various diseases and conditions.

205259-71-8

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205259-71-8 Usage

Uses

Used in Pharmaceutical Industry:
(4-(piperidin-1-ylsulfonyl)phenyl)methanamine is used as a building block or intermediate for the synthesis of various pharmaceutical compounds and organic molecules. Its unique structural features, including the piperidine ring, sulfonyl group, and amine group, contribute to its versatility in medicinal chemistry and drug discovery.
Used in Drug Discovery:
(4-(piperidin-1-ylsulfonyl)phenyl)methanamine is used as a potential candidate for the development of new medications. Its structural components make it suitable for the treatment of various diseases and conditions, offering a promising avenue for research and development in the pharmaceutical industry.
Used in Research Laboratories:
(4-(piperidin-1-ylsulfonyl)phenyl)methanamine is utilized in research laboratories for the development of new drugs and therapeutic agents. Its unique structural elements provide a foundation for exploring novel chemical entities and potential therapeutic interventions in various medical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 205259-71-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,2,5 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 205259-71:
(8*2)+(7*0)+(6*5)+(5*2)+(4*5)+(3*9)+(2*7)+(1*1)=118
118 % 10 = 8
So 205259-71-8 is a valid CAS Registry Number.

205259-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-piperidin-1-ylsulfonylphenyl)methanamine

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:205259-71-8 SDS

205259-71-8Relevant academic research and scientific papers

Structure-activity relationship studies in substituted sulfamoyl benzamidothiazoles that prolong NF-κB activation

Shukla, Nikunj M.,Chan, Michael,Lao, Fitzgerald S.,Chu, Paul J.,Belsuzarri, Masiel,Yao, Shiyin,Nan, Jason,Sato-Kaneko, Fumi,Saito, Tetsuya,Hayashi, Tomoko,Corr, Maripat,Carson, Dennis A.,Cottam, Howard B.

, (2021/07/19)

In the face of emerging infectious diseases, there remains an unmet need for vaccine development where adjuvants that enhance immune responses to pathogenic antigens are highly desired. Using high-throughput screens with a cell-based nuclear factor κB (NF-κB) reporter assay, we identified a sulfamoyl benzamidothiazole bearing compound 1 that demonstrated a sustained activation of NF-κB after a primary stimulus with a Toll-like receptor (TLR)-4 agonist, lipopolysaccharide (LPS). Here, we explore systematic structure–activity relationship (SAR) studies on compound 1 that indicated the sites on the scaffold that tolerated modification and yielded more potent compounds compared to 1. The selected analogs enhanced release of immunostimulatory cytokines in the human monocytic cell line THP-1 cells and murine primary dendritic cells. In murine vaccination studies, select compounds were used as co-adjuvants in combination with the Food and Drug Administration approved TLR-4 agonistic adjuvant, monophosphoryl lipid A (MPLA) that showed significant enhancement in antigen-specific antibody titers compared to MPLA alone. Additionally, our SAR studies led to identification of a photoaffinity probe which will aid the target identification and mechanism of action studies in the future.

VACCINE ADJUVANT

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Page/Page column 78, (2020/06/10)

Compounds useful as an adjuvant, e.g., formulas (I)-(VI) and uses thereof, for example, with immunogenic moieties or other adjuvants, are provided.

Identification of amides derived from 1H-pyrazolo[3,4-b]pyridine-5- carboxylic acid as potent inhibitors of human nicotinamide phosphoribosyltransferase (NAMPT)

Zheng, Xiaozhang,Bair, Kenneth W.,Bauer, Paul,Baumeister, Timm,Bowman, Krista K.,Buckmelter, Alexandre J.,Caligiuri, Maureen,Clodfelter, Karl H.,Feng, Yezhen,Han, Bingsong,Ho, Yen-Ching,Kley, Nikolai,Li, Hong,Liang, Xiaorong,Liederer, Bianca M.,Lin, Jian,Ly, Justin,O'Brien, Thomas,Oeh, Jason,Oh, Angela,Reynolds, Dominic J.,Sampath, Deepak,Sharma, Geeta,Skelton, Nicholas,Smith, Chase C.,Tremayne, Jarrod,Wang, Leslie,Wang, Weiru,Wang, Zhongguo,Wu, Hongxing,Wu, Jiansheng,Xiao, Yang,Yang, Guangxing,Yuen, Po-Wai,Zak, Mark,Dragovich, Peter S.

, p. 5488 - 5497 (2013/10/01)

Potent, 1H-pyrazolo[3,4-b]pyridine-containing inhibitors of the human nicotinamide phosphoribosyltransferase (NAMPT) enzyme were identified using structure-based design techniques. Many of these compounds exhibited nanomolar antiproliferation activities a

AMIDO-BENZYL SULFONE AND SULFOXIDE DERIVATIVES

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Page/Page column 146; 147, (2013/09/12)

The present invention relates to certain amido-benzyl sulfoxide and sulfone compounds, pharmaceutical compositions comprising such compounds, and methods of treatment using such compounds.

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