Miscellaneous applications of ferrocene‐based peptides/amides

B Lal, A Badshah, AA Altaf, N Khan… - Applied Organometallic …, 2011 - Wiley Online Library
This article provides a critical review of the different applications of ferrocene‐based
peptides/amides in biological as well as in non‐biological systems. Ferrocene‐based …

Synthesis and Structure− Activity Studies of Biphenyl Analogues of the Tuberculosis Drug (6 S)-2-Nitro-6-{[4-(trifluoromethoxy) benzyl] oxy}-6, 7-dihydro-5 H-imidazo …

BD Palmer, AM Thompson, HS Sutherland… - Journal of medicinal …, 2010 - ACS Publications
A series of biphenyl analogues of the new tuberculosis drug PA-824 was prepared, primarily
by coupling the known (6 S)-2-nitro-6, 7-dihydro-5 H-imidazo [2, 1-b][1, 3] oxazin-6-ol with …

Synthesis, Reduction Potentials, and Antitubercular Activity of Ring A/B Analogues of the Bioreductive Drug (6S)-2-Nitro-6-{[4-(trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5H …

AM Thompson, A Blaser, RF Anderson… - Journal of medicinal …, 2009 - ACS Publications
The nitroimidazooxazine S-1 (PA-824) is a new class of bioreductive drug for tuberculosis. A
series of related bicyclic nitroheterocycles was synthesized, designed to have a wide range …

Current nanotechnological strategies for effective delivery of bioactive drug molecules in the treatment of tuberculosis

M Kaur, T Garg, G Rath, A Goyal - Critical Reviews™ in …, 2014 - dl.begellhouse.com
Tuberculosis (TB) has gone from being a forgotten disease to a modern and recrudescent
pathology from past decades. Some clinical problems and challenges associated with …

Synthesis and structure− activity relationships of antitubercular 2-nitroimidazooxazines bearing heterocyclic side chains

HS Sutherland, A Blaser, I Kmentova… - Journal of medicinal …, 2010 - ACS Publications
Recently described biphenyl analogues of the antituberculosis drug PA-824 displayed
improved potencies against M. tuberculosis but were poorly soluble. Heterobiaryl analogues …

Rising standards for tuberculosis drug development

TS Balganesh, PM Alzari, ST Cole - Trends in pharmacological sciences, 2008 - cell.com
Development of new drugs to treat tuberculosis (TB) faces even more constraints than the
development of therapeutic agents for other diseases. This is due, in part, to intrinsic …

Supramolecular assembly of rifampicin and PEGylated PAMAM dendrimer as a novel conjugate for tuberculosis

R Ahmed, M Aucamp, N Ebrahim… - Journal of Drug Delivery …, 2021 - Elsevier
Introduction The study aimed to develop and explore the efficiency of a surface-modified 4.0
G PAMAM dendrimer as a novel delivery system for the anti-tuberculosis (TB) drug …

An Exploratory Review of the Potential of Lytic Proteins and Bacteriophages for the Treatment of Tuberculosis

S Mtimka, P Pillay, L Kwezi, OJ Pooe, TL Tsekoa - Microorganisms, 2024 - mdpi.com
Tuberculosis (TB) is a highly prevalent infectious disease that causes more than 1.5 million
deaths a year. More than 25% of TB deaths occur in Africa, and TB is South Africa's leading …

Synthesis and antimycobacterial activity of a series of ferrocenyl derivatives

GM Maguene, J Jakhlal, M Ladyman, A Vallin… - European journal of …, 2011 - Elsevier
In this work we reported the synthesis and evaluation of Mycobacterium tuberculosis
activities in vitro of a series of twenty five ferrocenyl derivatives: ferrocenyl amides derived …

Structure–Activity Relationships for Amide-, Carbamate-, And Urea-Linked Analogues of the Tuberculosis Drug (6S)-2-Nitro-6-{[4-(trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5H …

A Blaser, BD Palmer, HS Sutherland… - Journal of Medicinal …, 2012 - ACS Publications
Analogues of clinical tuberculosis drug (6 S)-2-nitro-6-{[4-(trifluoromethoxy) benzyl] oxy}-6, 7-
dihydro-5 H-imidazo [2, 1-b][1, 3] oxazine (PA-824), in which the OCH2 linkage was …