Welcome to LookChem.com Sign In|Join Free
  • or
2-(3-trifluoromethylphenyl)octahydropyrrolo<3,4-c>pyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86732-26-5

Post Buying Request

86732-26-5 Suppliers

Recommended suppliers

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

86732-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86732-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,3 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86732-26:
(7*8)+(6*6)+(5*7)+(4*3)+(3*2)+(2*2)+(1*6)=155
155 % 10 = 5
So 86732-26-5 is a valid CAS Registry Number.

86732-26-5Downstream Products

86732-26-5Relevant academic research and scientific papers

4-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)- N -(4-methoxypyridin-2-yl) piperazine-1-carbothioamide (ML267), a potent inhibitor of bacterial phosphopantetheinyl transferase that attenuates secondary metabolism and thwarts bacterial growth

Foley, Timothy L.,Rai, Ganesha,Yasgar, Adam,Daniel, Thomas,Baker, Heather L.,Attene-Ramos, Matias,Kosa, Nicolas M.,Leister, William,Burkart, Michael D.,Jadhav, Ajit,Simeonov, Anton,Maloney, David J.

supporting information, p. 1063 - 1078 (2014/03/21)

4′-Phosphopantetheinyl transferases (PPTases) catalyze a post-translational modification essential to bacterial cell viability and virulence. We present the discovery and medicinal chemistry optimization of 2-pyridinyl-N-(4-aryl)piperazine-1-carbothioamides, which exhibit submicromolar inhibition of bacterial Sfp-PPTase with no activity toward the human orthologue. Moreover, compounds within this class possess antibacterial activity in the absence of a rapid cytotoxic response in human cells. An advanced analogue of this series, ML267 (55), was found to attenuate production of an Sfp-PPTase-dependent metabolite when applied to Bacillus subtilis at sublethal doses. Additional testing revealed antibacterial activity against methicillin-resistant Staphylococcus aureus, and chemical genetic studies implicated efflux as a mechanism for resistance in Escherichia coli. Additionally, we highlight the in vitro absorption, distribution, metabolism, and excretion and in vivo pharmacokinetic profiles of compound 55 to further demonstrate the potential utility of this small-molecule inhibitor.

Synthesis and Carbon-13 NMR Study of 2-Benzyl, 2-Methyl, 2-Aryloctahydropyrrolopyrroles and the 1,2,3,5-Tetrahydropyrrolopyrrole Ring System

Ohnmacht, Cyrus J.,Draper, Clyde W.,Dedinas, Robert F.,Loftus, Philip,Wong, J. J.

, p. 321 - 329 (2007/10/02)

2-Benzyl, 2-phenyl, 2-(3-methoxyphenyl) and 2-(3-trifluoromethylphenyl)octahydropyrrolopyrrole (9a, 9b, 9c and 9d, respectively) were prepared in five steps from 1-benzylpyrrole-3,4-dicarboxylic acid (2). 2-Methyloctahydropyrrolopyrrole (9'a

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 86732-26-5