[HTML][HTML] Inosine pranobex: a key player in the game against a wide range of viral infections and non-infectious diseases
J Sliva, CN Pantzartzi, M Votava - Advances in therapy, 2019 - Springer
Inosine pranobex (IP), commonly known as inosine acedoben dimepranol, isoprinosine and
methisoprinol, has been proven to positively impact the host's immune system, by enhancing …
methisoprinol, has been proven to positively impact the host's immune system, by enhancing …
[HTML][HTML] Recent therapeutic approaches for the management of tuberculosis: Challenges and opportunities
Tuberculosis is a highly contagious disease spread by Mycobacterium tuberculosis. It is
responsible for highest numbers of death and soon will surpass the deaths caused by HIV …
responsible for highest numbers of death and soon will surpass the deaths caused by HIV …
High-throughput screening for inhibitors of Mycobacterium tuberculosis H37Rv
S Ananthan, ER Faaleolea, RC Goldman, JV Hobrath… - Tuberculosis, 2009 - Elsevier
There is an urgent need for the discovery and development of new antitubercular agents that
target new biochemical pathways and treat drug resistant forms of the disease. One …
target new biochemical pathways and treat drug resistant forms of the disease. One …
Preparation and antitubercular activities in vitro and in vivo of novel Schiff bases of isoniazid
MJ Hearn, MH Cynamon, MF Chen, R Coppins… - European journal of …, 2009 - Elsevier
Structural modification of the frontline antitubercular isonicotinic acid hydrazide (INH)
provides lipophilic adaptations (3–46) of the drug in which the hydrazine moiety of the …
provides lipophilic adaptations (3–46) of the drug in which the hydrazine moiety of the …
[HTML][HTML] The war against tuberculosis: A review of natural compounds and their derivatives
M Maiolini, S Gause, J Taylor, T Steakin, G Shipp… - Molecules, 2020 - mdpi.com
Tuberculosis (TB), caused by the bacterial organism Mycobacterium tuberculosis, pose a
major threat to public health, especially in middle and low-income countries. Worldwide in …
major threat to public health, especially in middle and low-income countries. Worldwide in …
Innovative therapeutic approaches based on nanotechnology for the treatment and management of tuberculosis
Tuberculosis (TB), derived from bacterium named Mycobacterium tuberculosis, has become
one of the worst infectious and contagious illnesses in the world after HIV/AIDS. Long-term …
one of the worst infectious and contagious illnesses in the world after HIV/AIDS. Long-term …
6-Cyano analogues of bedaquiline as less lipophilic and potentially safer diarylquinolines for tuberculosis
AST Tong, PJ Choi, A Blaser… - ACS medicinal …, 2017 - ACS Publications
Bedaquiline (1) is a new drug for tuberculosis and the first of the diarylquinoline class. It
demonstrates excellent efficacy against TB but induces phospholipidosis at high doses, has …
demonstrates excellent efficacy against TB but induces phospholipidosis at high doses, has …
Experimental tuberculosis: the role of comparative pathology in the discovery of improved tuberculosis treatment strategies
RJ Basaraba - Tuberculosis, 2008 - Elsevier
The use of laboratory animals is critical to the discovery and in vivo pre-clinical testing of
new drugs and drug combinations for use in humans. M. tuberculosis infection of mice, rats …
new drugs and drug combinations for use in humans. M. tuberculosis infection of mice, rats …
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 …