Total Synthesis and Structure-Activity Relationships Study of Odilorhabdins, a New Class of Peptides Showing Potent Antibacterial Activity

被引:21
|
作者
Sarciaux, Matthieu [1 ]
Pantel, Lucile [1 ]
Midrier, Camille [2 ]
Serri, Marine [1 ]
Gerber, Cristelle [1 ]
de Figueiredo, Renata Marcia [2 ]
Campagne, Jean-Marc [2 ]
Villain-Guillot, Philippe [1 ]
Gualtieri, Maxime [1 ]
Racine, Emilie [1 ]
机构
[1] Nosopharm, 110 Allee Charles Babbage,Espace Innovat 2, F-30000 Nimes, France
[2] Univ Montpellier, CNRS, ENSCM Ecole Natl Super Chim, UMR 5253,ICGM, 8 Rue Ecole Normale, F-34296 Montpellier 5, France
关键词
L-THREONINE ALDOLASE; DRUG DISCOVERY; AMINO-ACID; NATURAL-PRODUCTS; RESISTANCE; DERIVATIVES; REAGENT; HEXAFLUOROPHOSPHATE; ENTEROBACTERIACEAE; ANTIBIOTICS;
D O I
10.1021/acs.jmedchem.8b00790
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The spread of antibiotic-resistant pathogens is a growing concern, and new families of antibacterials are desperately needed. Odilorhabdins are a new class of antibacterial compounds that bind to the bacterial ribosome and kill bacteria through inhibition of the translation. NOSO-95C, one of the first member of this family, was synthesized for the first time, and then a structure-activity relationships study was performed to understand which groups are important for antibacterial activity and for inhibition of the bacterial translation. Based on this study an analogue showing improved properties compared to the parent compound was identified and showed promising in vitro and in vivo efficacy against Enterobacteriaceae.
引用
收藏
页码:7814 / 7826
页数:13
相关论文
共 50 条
  • [1] Structure-activity relationships of antibacterial peptides
    Ciulla, Maria Gessica
    Gelain, Fabrizio
    MICROBIAL BIOTECHNOLOGY, 2023, 16 (04): : 757 - 777
  • [2] Structure-activity relationships in cyclic β-sheet antibacterial peptides
    Kondejewski, LH
    Jelokhani-Niaraki, M
    Hancock, REW
    Hodges, RS
    PEPTIDES: FRONTIERS OF PEPTIDES SCIENCE, 1999, : 152 - 153
  • [3] Lebetin Peptides, a Potent Platelet Aggregation Inhibitors: Chemical Synthesis, Biological Activity and Structure-Activity Relationships.
    Mosbah, A.
    Marrakchi, N.
    Ganzalez, M. J.
    Giralt, E.
    El Ayeb, M.
    Bertin, D.
    Gigmes, D.
    Floc'h, M. Baudy
    Darbon, H.
    Mabrouk, K.
    JOURNAL OF PEPTIDE SCIENCE, 2012, 18 : S143 - S143
  • [4] NEW CLASS OF POTENT MONOAMINE OXIDASE INHIBITORS - CHEMISTRY AND STRUCTURE-ACTIVITY RELATIONSHIPS OF AMINOALKYLHYDRAZINES
    BIEL, JH
    MITCHELL, TF
    DRUKKER, AE
    HORITA, A
    CONWAY, AC
    NUHFER, PA
    JOURNAL OF ORGANIC CHEMISTRY, 1961, 26 (09): : 3338 - &
  • [5] Synthesis and structure-activity relationships in a novel class of herbicides
    Mitchell, G
    Barnes, NJ
    Cox, JM
    Matthews, IR
    Pearson, DPJ
    Smith, SC
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1999, 217 : U63 - U63
  • [6] Total synthesis and initial structure-activity relationships of longicatenamycin A
    von Nussbaum, Franz
    Anlauf, Sonia
    Freiberg, Christoph
    Benet-Buchholz, Jordi
    Schamberger, Jens
    Henkel, Thomas
    Schiffer, Guido
    Haebich, Dieter
    CHEMMEDCHEM, 2008, 3 (04) : 619 - 626
  • [7] Structure-activity relationships of antiarrhythmic peptides
    Dhein, S
    Grover, R
    Piecha, D
    Tudyka, T
    Kruesemann, K
    Klaus, W
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1998, 357 (04) : R101 - R101
  • [8] Structure-activity relationships of nitrofuran derivatives with antibacterial activity
    Pires, JR
    Giesbrecht, A
    Gomes, SL
    do-Amaral, AT
    MOLECULAR MODELING AND PREDICTION OF BIOACTIVITY, 2000, : 290 - 291
  • [9] Synthesis and novel structure-activity relationships of potent sansalvamide A derivatives
    Otrubova, K
    Styers, TJ
    Pan, PS
    Rodriguez, R
    McGuire, KL
    McAlpine, SR
    CHEMICAL COMMUNICATIONS, 2006, (09) : 1033 - 1034
  • [10] Antibacterial activity and structure-activity relationships of berberine analogs
    Iwasa, K
    Kamigauchi, M
    Ueki, M
    Taniguchi, M
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1996, 31 (06) : 469 - 478