Fields, Francisco R. et al. published their research in ACS Pharmacology & Translational Science in 2020 | CAS: 26662-94-2

(2R,9Z)-1-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)-3-(palmitoyloxy)propan-2-yl oleate (cas: 26662-94-2) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Computed Properties of C39H76NO8P

Synthetic Antimicrobial Peptide Tuning Permits Membrane Disruption and Interpeptide Synergy was written by Fields, Francisco R.;Manzo, Giorgia;Hind, Charlotte K.;Janardhanan, Jeshina;Foik, Ilona P.;Carmo Silva, Phoebe Do;Balsara, Rashna D.;Clifford, Melanie;Vu, Henry M.;Ross, Jessica N.;Kalwajtys, Veronica R.;Gonzalez, Alejandro J.;Bui, Tam T.;Ploplis, Victoria A.;Castellino, Francis J.;Siryaporn, Albert;Chang, Mayland;Sutton, J. Mark;Mason, A. James;Lee, Shaun. And the article was included in ACS Pharmacology & Translational Science in 2020.Computed Properties of C39H76NO8P The following contents are mentioned in the article:

The ribosomally produced antimicrobial peptides of bacteria (bacteriocins) represent an unexplored source of membrane-active antibiotics. We designed a library of linear peptides from a circular bacteriocin and show that pore-formation dynamics in bacterial membranes are tunable via selective amino acid substitution. We observed antibacterial interpeptide synergy indicating that fundamentally altering interactions with the membrane enables synergy. Our findings suggest an approach for engineering pore-formation through rational peptide design and increasing the utility of novel antimicrobial peptides by exploiting synergy. This study involved multiple reactions and reactants, such as (2R,9Z)-1-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)-3-(palmitoyloxy)propan-2-yl oleate (cas: 26662-94-2Computed Properties of C39H76NO8P).

(2R,9Z)-1-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)-3-(palmitoyloxy)propan-2-yl oleate (cas: 26662-94-2) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Computed Properties of C39H76NO8P

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics