Miscellaneous applications of ferrocene‐based peptides/amides
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 …
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 …
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 …
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
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 …
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 …
improved potencies against M. tuberculosis but were poorly soluble. Heterobiaryl analogues …
Rising standards for tuberculosis drug development
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 …
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
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 …
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
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 …
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 …
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 …
dihydro-5 H-imidazo [2, 1-b][1, 3] oxazine (PA-824), in which the OCH2 linkage was …