Literature DB >> 17970221

Programs to facilitate tuberculosis drug discovery: the tuberculosis antimicrobial acquisition and coordinating facility.

R C Goldman1, B E Laughon, R C Reynolds, J A Secrist, J A Maddry, M-A Guié, A C Poffenberger, C A Kwong, S Ananthan.   

Abstract

There is a real need to discover new drugs that are active on drug-resistant tuberculosis (TB), and for drugs that will shorten the time of therapy. Large pharmaceutical companies have traditionally led the quest for discovering and developing new antiinfective agents but this is not the case when it comes to diseases like tuberculosis that primarily occur in resource restricted countries. Throughout the world many research groups are actively engaged in the scientific discovery of new TB drugs. Unfortunately, most research laboratories do not have the necessary safety facilities or resources for all facets of TB drug discovery. The Tuberculosis Antimicrobial Acquisition and Coordinating Facility (TAACF) was established in order to make comprehensive testing services available at no cost to research laboratories with an interest in discovering new TB drugs. The TAACF is a consortium of contracts managed and funded by the National Institute of Allergy and Infectious Diseases (National Institutes of Health, Bethesda, MD) as a resource to support preclinical drug discovery and development. The core of the TAACF is the Southern Research Institute, Birmingham, AL, which supports compound acquisition, storage, medicinal chemistry, and high throughput assays. Other collaborating groups provide biological data on antimycobacterial activity and cytotoxicity, preliminary in vivo toxicity, oral bioavailability and efficacy in animal models, specialty testing (such as activity against non-replicating persistent bacteria), and assistance in technology transfer for developing comprehensive promotional packages and facilitating partnerships with pharmaceutical companies for drug development. The TAACF program and recent progress that has been publicly disclosed by suppliers is reviewed. There are many aspects promising of the program that will not be discussed due to confidentially.

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Year:  2007        PMID: 17970221     DOI: 10.2174/187152607781001790

Source DB:  PubMed          Journal:  Infect Disord Drug Targets        ISSN: 1871-5265


  13 in total

1.  Structure-activity relationship of new anti-tuberculosis agents derived from oxazoline and oxazole benzyl esters.

Authors:  Garrett C Moraski; Mayland Chang; Adriel Villegas-Estrada; Scott G Franzblau; Ute Möllmann; Marvin J Miller
Journal:  Eur J Med Chem       Date:  2010-01-14       Impact factor: 6.514

2.  High-throughput screening for inhibitors of Mycobacterium tuberculosis H37Rv.

Authors:  Subramaniam Ananthan; Ellen R Faaleolea; Robert C Goldman; Judith V Hobrath; Cecil D Kwong; Barbara E Laughon; Joseph A Maddry; Alka Mehta; Lynn Rasmussen; Robert C Reynolds; John A Secrist; Nice Shindo; Dustin N Showe; Melinda I Sosa; William J Suling; E Lucile White
Journal:  Tuberculosis (Edinb)       Date:  2009-09-15       Impact factor: 3.131

3.  6-Oxo and 6-thio purine analogs as antimycobacterial agents.

Authors:  Ashish K Pathak; Vibha Pathak; Lainne E Seitz; William J Suling; Robert C Reynolds
Journal:  Bioorg Med Chem       Date:  2013-02-04       Impact factor: 3.641

4.  In vitro evaluation of tetrazoles as a novel class of Antimycobacterium tuberculosis agents.

Authors:  P B Mohite; V H Bhaskar
Journal:  Adv Pharm Bull       Date:  2012-02-15

5.  2-[4-(4-Methoxyphenylcarbonyloxy)benzylidene]-6-dimethylaminomethyl cyclohexanone hydrochloride: a Mannich base which inhibits the growth of some drug-resistant strains of Mycobacterium tuberculosis.

Authors:  S Das; U Das; B Bandy; D K J Gorecki; J R Dimmock
Journal:  Pharmazie       Date:  2010-11       Impact factor: 1.267

6.  SQ109 targets MmpL3, a membrane transporter of trehalose monomycolate involved in mycolic acid donation to the cell wall core of Mycobacterium tuberculosis.

Authors:  Kapil Tahlan; Regina Wilson; David B Kastrinsky; Kriti Arora; Vinod Nair; Elizabeth Fischer; S Whitney Barnes; John R Walker; David Alland; Clifton E Barry; Helena I Boshoff
Journal:  Antimicrob Agents Chemother       Date:  2012-01-17       Impact factor: 5.191

7.  Predictive models for anti-tubercular molecules using machine learning on high-throughput biological screening datasets.

Authors:  Vinita Periwal; Jinuraj K Rajappan; Abdul Uc Jaleel; Vinod Scaria
Journal:  BMC Res Notes       Date:  2011-11-18

8.  Antituberculosis activity of the molecular libraries screening center network library.

Authors:  Joseph A Maddry; Subramaniam Ananthan; Robert C Goldman; Judith V Hobrath; Cecil D Kwong; Clinton Maddox; Lynn Rasmussen; Robert C Reynolds; John A Secrist; Melinda I Sosa; E Lucile White; Wei Zhang
Journal:  Tuberculosis (Edinb)       Date:  2009-09-26       Impact factor: 3.131

9.  Discovery and validation of new antitubercular compounds as potential drug leads and probes.

Authors:  Robert C Goldman; Barbara E Laughon
Journal:  Tuberculosis (Edinb)       Date:  2009-08-28       Impact factor: 3.131

10.  Assessment of the Efficacy of New Anti-Tuberculosis Drugs.

Authors:  Denis A Mitchison; Geraint R Davies
Journal:  Open Infect Dis J       Date:  2008-12
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