Areas of Application
Low-molecular compounds
with antituberculosis action
Advantages
The developed compounds act
on the strains of Mycobacterium tuberculosis
that are stable to known commercial
antituberculosis drugs, in particular,
isoniazid, rifampin, and ofl oxacin
Specifi cation
Chemical names:3-isopropoxybenzaldehyde
thiosemicarbazone (1) and N’-[1E)-1-methyl-1H-
pyrrol-2-yl)methylene]isonicotinic hydrazide
(2). The compounds inhibit the growth
of Mycobacterium tuberculosis in aerobic
conditions with MIC = 0.79 μM (compound 1)
and 0.39 μM (compound 2); the compounds
are not cytotoxic with respect to cellular line
of human liver HepG2; penetrate through
the monolayer of Caco-2 cells, which is in vitro
model of the mucous membrane of human
small intestine for predicting drug absorption;
the binding with proteins of blood plasma
makes up 86.8 and 42.1 for compounds
1 and 2, respectively
Stage of Development.
Suggestion for Commercialization
IRL2, TRL2
Seeking partners for preclinical/clinical trials.
The ready offering can be proposed
to pharmaceutical corporations
IPR Protection
IPR2
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