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 …
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 …
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 …
were synthesized in excellent yields via Biginelli multi-component reaction. The newly …
Artificial neural network methods applied to drug discovery for neglected diseases
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 …
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 …
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 …
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 …
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.
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 …
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 …
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 …
phenyl)-5-benzylidene-2-(pyridine-4-yl) thiazolidine-4-one (4a-j) from 3-(4-(benzo [d] thiazol …