US2005250841A1PendingUtilityA1
Autoinducer molecule
Est. expiryAug 9, 2013(expired)· nominal 20-yr term from priority
Inventors:James PearsonKendall M. GrayLuciano PassadorKenneth TuckerAnatol EberhardBarbara H. IglewskiEverett P. Greenberg
Y02A50/30C12N 1/38A61K 31/4015A61K 31/382A61K 31/366A61K 31/381Y10S435/874Y10S435/875
44
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Claims
Abstract
Autoinducer molecules, e.g., N-(3-oxododecanoyl)homoserine lactone, for Pseudomonas aeruginosa are described. The molecules regulate gene expression in the bacterium. Therapeutic compositions and therapeutic methods involving analogs and/or inhibitors of the autoinducer molecules also are described. The molecules are useful for treating or preventing infection by Pseudomonas aeruginosa.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . An autoinducer molecule comprising a molecule of the formula:
wherein n is 2 or 3; Y is O, S, or NH; X is O, S, or NH; and R is a C 11 -C 14 acyl moiety that may be substituted or a moiety having at least seven members containing a ring structure that may be substituted; the molecule being able to regulate the activity of the LasR protein of Pseudomonas aeruginosa.
3 - 4 . (canceled)
5 . The autoinducer molecule of claims 2 wherein R is a C 12 acyl moiety.
6 - 7 . (canceled)
8 . The autoinducer molecule of claim 2 wherein R contains a heterocyclic ring structure.
9 . The autoinducer molecule of claim 8 wherein the heterocyclic ring structure has five to seven ring members.
10 . The autoinducer molecule of claim 9 wherein the heterocyclic ring structure contains oxygen.
11 . The autoinducer molecule of claim 2 wherein R contains a carbocyclic ring structure.
12 . The autoinducer of claim 11 wherein the carbocyclic ring structure is a fused ring system.
13 . The autoinducer molecule of claim 2 wherein the molecule is purified from the native source.
14 . The autoinducer molecule of claim 13 wherein the native source is the culture media of Pseudomonas aeruginosa.
15 . The autoinducer molecule of claim 2 wherein the molecule is synthesized by chemical means.
16 . The autoinducer molecule of claim 2 wherein the molecule is an optically active isomer.
17 . The autoinducer molecule of claim 16 wherein the isomer is the L-isomer.
18 . The autoinducer molecule of claim 16 wherein the isomer is the D-isomer.
19 - 20 . (canceled)
21 . An analog of an autoinducer molecule comprising a molecule of the formula
wherein n is 2 or 3; Y is O, S, or NH; X is O, S, or NH; and R is a C 11 -C 14 acyl moiety that may be substituted or a moiety having at least seven members containing a ring structure that may be substituted; that affects the activity of the LasR protein.
22 . The analog of claim 21 wherein the analog inhibits the autoinducer activity of the N-(3-oxododecanoyl)homoserine lactone.
23 . The analog of claim 21 wherein the analog synergistically enhances the autoinducer activity of N-(3-oxododecanoyl)homoserine lactone.
24 . The analog of claim 21 , wherein the analog is an agonist of the LasR protein of Pseudomonas aeruginosa.
25 . The analog of claim 21 , wherein the analog is an antagonist of the LasR protein of Pseudomonas aeruginosa.
26 - 43 . (canceled)
44 . A composition comprising an autoinducer molecule of the formula:
wherein n is 2 or 3; Y is O, S, or NH; X is O, S, or NH; and R is a C 11 -C 14 acyl moiety that may be substituted or a moiety having at least seven members containing a ring structure that may be substituted; the molecule being able to regulate the activity of the LasR protein of Pseudomonas aeruginosa ; and a pharmaceutically acceptable carrier.Cited by (0)
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