[EN] BROAD SPECTRUM PRO-QUORUM-SENSING MOLECULES AS INHIBITORS OF VIRULENCE IN VIBRIOS [FR] MOLÉCULES DE DÉTECTION DE QUORUM À LARGE SPECTRE COMME INHIBITEURS DE VIRULENCE DE VIBRIONS
[EN] HETEROCYCLE ANALOGS OF CAI-1 AS AGONISTS OF QUORUM SENSING IN VIBRIO<br/>[FR] ANALOGUES HÉTÉROCYCLIQUES DE CAI-1 EN TANT QU'AGONISTES DE LA DÉTECTION DU QUORUM CHEZ VIBRIO
申请人:UNIV PRINCETON
公开号:WO2015026796A1
公开(公告)日:2015-02-26
A structurally distinct and potent series of synthetic small molecule activators of Vibrio cholerae quorum sensing have been chemically synthesized. The small molecule activators reduce virulence in V. cholerae. Acyl pyrrole molecules displayed strong potency and stability, particularly l-(1H-pyrrol-3-yl)decan-l-one.
BROAD SPECTRUM PRO-QUORUM-SENSING MOLECULES AS INHIBITORS OF VIRULENCE IN VIBRIOS
申请人:THE TRUSTEES OF PRINCETON UNIVERSITY
公开号:US20150126474A1
公开(公告)日:2015-05-07
Using a whole-cell high-throughput screen, eleven molecules were identified that activate
V. cholerae
quorum sensing (QS). Eight molecules are receptor agonists and three molecules are antagonists of LuxO, the central NtrC-type response regulator that controls the global
V. cholerae
QS cascade. Pro-QS molecules are used for the development of novel anti-infectives.
HETEROCYCLE ANALOGS OF CAI-1 AS AGONISTS OF QUORUM SENSING IN VIBRIO
申请人:BASSLER Bonnie L.
公开号:US20160200678A1
公开(公告)日:2016-07-14
A structurally distinct and potent series of synthetic small molecule activators of
Vibrio cholerae
quorum sensing have been chemically synthesized. The small molecule activators reduce virulence in
V. cholerae
. Acyl pyrrole molecules displayed strong potency and stability, particularly 1-(1H-pyrrol-3-yl)decan-1-one.
Heterocycle analogs of CAI-1 as agonists of quorum sensing in vibrio
申请人:The Trustees of Princeton University
公开号:US10285978B2
公开(公告)日:2019-05-14
A structurally distinct and potent series of synthetic small molecule activators of Vibrio cholerae quorum sensing have been chemically synthesized. The small molecule activators reduce virulence in V. cholerae. Acyl pyrrole molecules displayed strong potency and stability, particularly 1-(1H-pyrrol-3-yl)decan-1-one.