Back to Search Start Over

An insight into the discovery, clinical studies, compositions, and patents of macozinone: A drug targeting the DprE1 enzyme of Mycobacterium tuberculosis

Authors :
Mohd. Imran
Shah Alam Khan
Syed Mohammed Basheeruddin Asdaq
Mazen Almehmadi
Osama Abdulaziz
Mehnaz Kamal
Mohammed Kanan Alshammari
Lojain Ibrahim Alsubaihi
Khansa Hamza Hussain
Abrar Saleh Alharbi
A. Khuzaim Alzahrani
Source :
Journal of Infection and Public Health, Vol 15, Iss 10, Pp 1097-1107 (2022)
Publication Year :
2022
Publisher :
Elsevier, 2022.

Abstract

Decaprenyl-phosphoryl-ribose 2′-epimerase (DprE1) inhibitors are an innovative and futuristic orally active group of antituberculosis agents. A few DprE1 inhibitors are in the clinical trial for tuberculosis (TB), including macozinone. This review highlights the discovery, developmental status, clinical studies, patents, and prospects of macozinone (MCZ). The patent and non-patent literature search was done by entering keywords such as macozinone; MCZ; PBTZ169; PBTZ-169 in Pubmed, Espacenet, Patentscope, and the USPTO databases. However, data on Sci-Finder was searched using CAS registry number: 1377239–83–2. MCZ clinical trial studies were retrieved from the clinicaltrials.gov database using the exact keywords. The chemical structure of MCZ was disclosed in 2009. Accordingly, patents/patent applications published from 2009 to June 12, 2022, have been discussed herein. MCZ and MCZ hydrochloride salt patents were granted in 2014 and 2019, respectively, in the USA. The patent literature and the clinical trial studies suggest capsule, tablet, and suspension formulations of crystalline MCZ and its hydrochloride salt as the possible and prospective dosage forms to treat TB. Some combinations of MCZ with other drugs (chloroquine, telacebec, tafenoquine, TBI-166, and sanfetrinem) with improved anti-TB efficacy have been documented. Based on the literature covered in this review article on the clinical studies and patents applied/granted to MCZ, it can be inferred that MCZ seems to be a promising DprE1 inhibitor and could help to tackle the emerging dilemma of drug-resistant either as a monotherapy or in combination with additional anti-TB agents. Furthermore, the authors anticipate the development of new combinations, salts, and polymorphs of MCZ as anti-TB agents shortly. This review article might prove beneficial to the scientific community as it summarizes chemistry, pharmacology and provides an update on the clinical studies and patents/patent applications of one of the emerging anti-TB drugs in one place.

Details

Language :
English
ISSN :
18760341
Volume :
15
Issue :
10
Database :
Directory of Open Access Journals
Journal :
Journal of Infection and Public Health
Publication Type :
Academic Journal
Accession number :
edsdoj.59494c5bfdad4d92abcca5d6089def84
Document Type :
article
Full Text :
https://doi.org/10.1016/j.jiph.2022.08.016