The invention relates to new peptide nucleic acid monomers and peptide nucleic acid oligomers comprising a dialkylamine side chain substituted with phosphonic acid ester group(s) or phosphonic acid group(s), and to the uses thereof.
A cellulose acylate film comprising at least one cellulose acylate, at least one sterol derivative represented by formula (1), and at least one saccharide derivative and/or at least one oligomer plasticizer is disclosed. R
1
, R
2
and R
3
represents a hydrogen atom, a hydroxyl group or a substituent represented by -L-R*, provided that at least one of them represents the substituent represented by -L-R*; L represents a single bond or a divalent connecting group selected from the group consisting of —O—, —CO—, —CONR
6
—, —CH
2
— and a combination thereof, R* represents a substituted or unsubstituted aromatic ring group, heterocyclic group or alkyl group; R
4
represents a carboxyl group or —CHR
7
—CH(CH
3
)
2
; R
5
represents a hydrogen atom or a methyl group.
ANTIMICROBIAL PEPTIDE DERIVATIVE AND USE THEREOF
申请人:SI CHUAN UNIVERSITY
公开号:US20190216939A1
公开(公告)日:2019-07-18
The invention relates to the field of biomedicine and particularly to a hydrophobically modified antimicrobial peptide and a use thereof. The technical problem to be solved by the invention is to provide a hydrophobically modified antimicrobial peptide, the hydrophobic modification is to couple a hydrophobic fragment at the nitrogen terminal of the antimicrobial peptide. The invention further provides a micelle prepared from the hydrophobically modified antimicrobial peptide, and use of the hydrophobically modified antimicrobial peptide and the micelle in preparing antimicrobial drugs, nucleic acid transporter, immune adjuvant and the like. Due to small molecular weight, the antimicrobial peptide of the invention can be conveniently synthesized by Fmoc solid phase polypeptide, and coupled to a hydrophobic fragment by the chemical synthesis method in a simple and feasible way.