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Antimicrobial compounds

a technology of antimicrobial compounds and compounds, applied in the field of antimicrobial compounds, can solve the problems of poor efficacy of current treatments against cystic stages of parasites, cornea infection, etc., and achieve the effect of reducing the rate at which an enzyme catalyses the production of a particular compound from a particular substra

Inactive Publication Date: 2011-10-06
UNIV OF STRATHCLYDE
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The proposed solution effectively inhibits the growth or causes death of Acanthamoeba, potentially reducing the need for prolonged and arduous treatments and minimizing residual infections, offering a new avenue for treating Acanthamoeba-related diseases.

Problems solved by technology

Current treatments are poorly effective against the cystic stages of the parasite and allow residual infection.
Corneal transplantation is often necessary due to extensive damage caused by the parasites prior to diagnosis.
Residual cysts remaining after treatment can result in infection of transplanted corneas (Seal, 2003).

Method used

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  • Antimicrobial compounds
  • Antimicrobial compounds
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Examples

Experimental program
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Embodiment Construction

[0073]The present invention will now be described by way of example and with reference to the figures which show:

[0074]FIG. 1. Glyphosate inhibition of A. castellanii over a 96 hr period as determined by percent alamarBlue reduction relative to untreated control cultures.

[0075]FIG. 2. The cDNA sequence of A. castellanii DHQS and partial EPSP synthase.

[0076]FIG. 3. The predicted amino acid sequence of A. castellanii DHQS and partial EPSP synthase.

[0077]FIG. 4. Partial cDNA sequence of A. castellanii chorismate synthase.

[0078]FIG. 5. Partial cDNA for DAHP synthase sequence from A. castellanii.

[0079]FIG. 6. Partial cDNA for Tryptophan synthase Beta subunit from A. castellanii.

[0080]FIG. 7. Partial gDNA for Anthranilate synthase from A. castellanii.

[0081]FIG. 8. Partial gDNA for DAHP from A. polyphaga

[0082]FIG. 9. The cDNA sequence of A. polyphaga DHQS and partial EPSP synthase.

[0083]FIG. 10. Partial gDNA sequence of DHQS, EPSP synthase and Shikimate kinase from A. castellanii.

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Abstract

The present invention relates to compounds that modulate the shikimate pathway and / or a pathway branching from the shikimate pathway in members of the Amoebida Order. In particular these compounds may be useful in the treatment or prevention of diseases caused or contributed to by members of the Amoebida Order.

Description

CROSS REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation of U.S. application Ser. No. 11 / 908,377, filed Feb. 29, 2008, which is a U.S. National Stage Application of PCT / GB2006 / 000875, filed Mar. 13, 2006, which claims priority to GB 0504998.9, filed Mar. 11, 2005, the contents of each application are fully incorporated by reference herein.FIELD OF THE INVENTION[0002]The present invention relates to compounds that modulate the shikimate pathway and / or a pathway branching from the shikimate pathway in the Amoebida. In particular such compounds may be useful in the treatment or prevention of diseases caused or contributed to by members of the Amoebida Order.BACKGROUND OF THE INVENTION[0003]Acanthamoeba are normally free-living protozoa found throughout the environment. Acanthamoeba are responsible for Acanthamoeba keratitis and granulomatous Acanthamoeba encephalitis (GAE) in humans (Cohen et al., 1985; Culbertson et al., 1966). Acanthamoeba keratitis is normally...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A01N43/90A01N41/06A01N43/54A01N37/52A01N43/68A01N43/64A01P1/00A61L12/08C12Q1/18C12Q1/68
CPCA61L12/08C12Q1/6893C12Q1/18A61P33/04
Inventor ROBERTS, CRAIG WILLIAMROBERTS, FIONAHENRIQUEZ, FIONA LUISAINGRAM, PAUL RICHARD
Owner UNIV OF STRATHCLYDE