Antimycobacterial activity of novel hydrazide-hydrazone derivatives with 2H-chromene and coumarin scaffold

VT Angelova, V Valcheva, NG Vassilev… - Bioorganic & Medicinal …, 2017 - Elsevier
This study reports the synthesis of new 2H-chromene or coumarin based acylhydrazones,
which were evaluated for their in vitro antimycobacterial activity against reference strain …

Multi-target antitubercular drugs

J de Oliveira Viana, HM Ishiki… - Current Topics in …, 2018 - ingentaconnect.com
Tuberculosis is an infectious disease caused by Mycobacterium tuberculosis, which has
high levels of mortality worldwide and has already gained resistance to first-and second-line …

Preparation, biological evaluation and molecular docking study of imidazolyl dihydropyrimidines as potential Mycobacterium tuberculosis dihydrofolate reductase …

NC Desai, AR Trivedi, VM Khedkar - Bioorganic & medicinal chemistry …, 2016 - Elsevier
A series of novel dihydropyrimidine derivatives bearing an imidazole nucleus at C-4 position
were synthesized in excellent yields via Biginelli multi-component reaction. The newly …

Artificial neural network methods applied to drug discovery for neglected diseases

L Scotti, H Ishiki, F JB Mendonca Junior… - … chemistry & high …, 2015 - ingentaconnect.com
Among the chemometric tools used in rational drug design, we find artificial neural network
methods (ANNs), a statistical learning algorithm similar to the human brain, to be quite …

Antimycobacterial activity generated by the amide coupling of (−)-fenchone derived aminoalcohol with cinnamic acids and analogues

I Slavchev, GM Dobrikov, V Valcheva, I Ugrinova… - Bioorganic & Medicinal …, 2014 - Elsevier
Aminoethyl substituted 2-endo-fenchol prepared from (−)-fenchone was used as scaffold for
the synthesis of series of 31 amide structures by N-acylation applying cinnamic acids and …

Synthesis, antibacterial activity and molecular docking studies of new pyrazole derivatives

A Cetin, H Kurt - letters in drug design & discovery, 2020 - ingentaconnect.com
Background: The pyrazole structure is an important heterocyclic structure and plays critical
roles in agriculture, industrial and medicine. Furthermore, compounds containing pyrazole …

Pyrazinamide and Pyrazinoic acid derivatives directed to mycobacterial enzymes against tuberculosis

M Fidelis Corrêa… - Current Protein and …, 2016 - ingentaconnect.com
Tuberculosis (TB) is an infectious diseases responsible for thousands of deaths worldwide.
Due to the use of antimycobacterial drugs, TB prevalence seemed to be controlled, but with …

The Literature of Heterocyclic Chemistry, Part XIII, 2012–2013

LI Belen'kii, YB Evdokimenkova - Advances in Heterocyclic Chemistry, 2015 - Elsevier
A systematized review of reviews and monographs published in 2012–2013 on all aspects
of heterocyclic chemistry is given.

Development of Antitubercular Agents Through Hybridization Strategies, Future Challenges and Perspectives

S Kantevari, A Jallapally, AD Tangutur… - Microbial …, 2017 - api.taylorfrancis.com
Tuberculosis (TB) is one the most prevalent endemic lung infection caused by the pathogen
Mycobacterium tuberculosis (Mtb). In spite of the availability of various combinations of …

[PDF][PDF] (Z)-3-(4-(benzo [d] thiazol-2-ylthio) phenyl)-5-(substituted-benzylidene)-2-(pyridine-4-yl) thiazolidine-4-one as antitubercular agent: Their microwave assisted …

VM Patel, NB Patel - Chemistry & Biology Interface, 2017 - cbijournal.com
Present work describe the synthesis of a new series of (Z)-3-(4-(benzo [d] thiazol-2-ylthio)
phenyl)-5-benzylidene-2-(pyridine-4-yl) thiazolidine-4-one (4a-j) from 3-(4-(benzo [d] thiazol …