Welcome to LookChem.com Sign In|Join Free
  • or
9-Octadecenamide, N-[2-hydroxy-1-(hydroxymethyl)ethyl]-, (9Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72809-08-6

Post Buying Request

72809-08-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

72809-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72809-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,0 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72809-08:
(7*7)+(6*2)+(5*8)+(4*0)+(3*9)+(2*0)+(1*8)=136
136 % 10 = 6
So 72809-08-6 is a valid CAS Registry Number.

72809-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1,3-dihydroxypropan-2-yl)octadec-9-enamide

1.2 Other means of identification

Product number -
Other names 2-(oleamido)propane-1,3-diol

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:72809-08-6 SDS

72809-08-6Downstream Products

72809-08-6Relevant academic research and scientific papers

A novel class of cationic and non-peptidic small molecules as hits for the development of antimicrobial agents

Jiménez, Aranza,García, Pablo,De La Puente, Sofia,Madrona, Andrés,Camarasa, María José,Pérez-Pérez, María-Jesús,Quintela, José-Carlos,García-del Portillo, Francisco,San-Félix, Ana

, (2018/07/10)

Cationic and non-peptide small molecules containing a total of six positive charges arranged on one side and a long aliphatic tail on the other have been synthesized and tested against Gram-positive and Gram-negative bacteria. The positive charges have be

Novel polyphenols that inhibit colon cancer cell growth affecting cancer cell metabolisms

Gómez de Cedrón, Marta,Vargas, Teodoro,Madrona, Andrés,Jiménez, Aranza,Pérez-Pérez, María-Jesús,Quintela, José-Carlos,Reglero, Guillermo,San-Félix, Ana,Ramírez de Molina, Ana

, p. 377 - 389 (2018/07/31)

New series of polyphenols with a hydrophilic galloyl-based head and a hydrophobic N-acyl tail, linked through a serinol moiety, have been synthesized and tested against colon cancer cell growth. Our structure activity relationship studies revealed that galloyl moieties are essential for growth inhibition. Moreover, the length of the N-acyl chain is crucial for the activity. Introduction of a (Z) double bond in the acyl chain increased the anticancer properties. Our findings demonstrate that 16, the most potent compound within this series, has inhibitory effects on colon cancer cell growth and metabolism (glycolysis and mitochondrial respiration) at the same time that it activates 59AMP-activated kinase (AMPK) and induces apoptotic cell death. Based on these results, we propose that 16 might reprogram colon cancer cell metabolism through AMPK activation. This might lead to alterations on cancer cell bioenergy compromising cancer cell viability. Importantly, these antiproliferative and proapoptotic effects are selective for cancer cells. Accordingly, these results indicate that 16, with an unsaturated C18 chain, might be a useful prototype for the development of novel colon cancer cell growth inhibitors affecting cell metabolism.

Design and synthesis of lipids for the fabrication of functional lipidic cubic-phase biomaterials

Osornio, Yazmin M.,Uebelhart, Peter,Bosshard, Silvan,Konrad, Fabian,Siegel, Jay S.,Landau, Ehud M.

, p. 10583 - 10595 (2013/02/22)

A series of novel lipids with designed functionalities were synthesized. These lipids are based on conjugation of α-amino acids and their esters, cationic, anionic, neutral, and photochromic moieties to the lipophilic 9-cis octadecenyl chains by amide, ester, thioester, or amine bonds. Because of the plasticity of lipidic cubic phases, it is envisaged that when mixed with monooleoyl-rac-glycerol (monoolein, MO) and water at appropriate proportions, they would assemble to form bicontinuous lipidic cubic phases (LCPs) that exhibit the well-known material properties of LCPs such as phase stability, optical transparency, and chemical permeability. Moreover, due to the nature and position of the functionality at the headgroup region, we envision them to perform as functional materials by design.

Compositions and methods for enrichment of neural stem cells using ceramide analogs

-

Page/Page column 24, (2008/12/04)

The present invention provides compositions and methods for human neural cell production. More particularly, the present invention provides cellular differentiation methods employing amphiphilic lipid compounds, preferably ceramide analogs of the β-hydroxyalkylamine type and optionally employing an essentially serum free MEDII conditioned medium for the generation of human neural cells from pluripotent human cells. The methods alternatively comprise modulating apoptosis by modifying the levels of PAR-4, with or without the presence of amphiphilic lipid compounds and optionally employing MEDII conditioned medium. The methods alternatively encompass modulating apoptosis by modulating the intracellular concentration of endogenous lipid second messengers, such as ceramide.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 72809-08-6