Natural and synthetic coumarins as potential anticancer agents

J Klenkar, M Molnar - Journal of chemical and pharmaceutical research, 2015 - croris.hr
Sažetak Coumarins, natural or synthetic, due to their wide range of biological activities, have
become an interesting subject of investigation for many researchers. Coumarin scaffold has …

Synthesis of 1, 2-benzisoxazole tethered 1, 2, 3-triazoles that exhibit anticancer activity in acute myeloid leukemia cell lines by inhibiting histone deacetylases, and …

N Ashwini, M Garg, CD Mohan, JE Fuchs… - Bioorganic & medicinal …, 2015 - Elsevier
Triazole-based heterocycles have previously been shown to possess significant anticancer
activity in various tumor models. In the present study, we attached a 1, 2, 3-triazole moiety to …

X-box–binding protein 1 and innate immune responses of human cystic fibrosis alveolar macrophages

BA Lubamba, LC Jones, WK O'Neal… - American journal of …, 2015 - atsjournals.org
Rationale: Alveolar macrophages (AMs) play a key role in host defense to inhaled bacterial
pathogens, in part by secreting inflammatory mediators. Cystic fibrosis (CF) airways exhibit a …

Novel synthetic bisbenzimidazole that targets angiogenesis in Ehrlich ascites carcinoma bearing mice

R Roopashree, CD Mohan, TR Swaroop… - Bioorganic & medicinal …, 2015 - Elsevier
Cancer is a leading cause of death in developed countries and second cause in developing
countries. Herein we are reporting the synthesis of novel bisbenzimidazole derivatives and …

Screening of quinoline, 1, 3-benzoxazine, and 1, 3-oxazine-based small molecules against isolated methionyl-tRNA synthetase and A549 and HCT116 cancer cells …

H Bharathkumar, CD Mohan, S Rangappa… - Organic & …, 2015 - pubs.rsc.org
Elevated activity of methionyl-tRNA synthetase (MRS) in many cancers renders it a possible
drug target in this disease area, as well as in a series of parasitic diseases. In the present …

Development of novel triazolo-thiadiazoles from heterogeneous “green” catalysis as protein tyrosine phosphatase 1B inhibitors

CP Baburajeev, C Dhananjaya Mohan, H Ananda… - Scientific reports, 2015 - nature.com
Condensed-bicyclic triazolo-thiadiazoles were synthesized via an efficient “green” catalyst
strategy and identified as effective inhibitors of PTP1B in vitro. The lead compound, 6-(2 …

Synthesis and characterization of novel oxazines and demonstration that they specifically target cyclooxygenase 2

V Srinivas, CD Mohan, CP Baburajeev… - Bioorganic & Medicinal …, 2015 - Elsevier
In the present study, we used solution combustion synthesis-bismuth oxide (Bi 2 O 3) as
catalyst for the simple and efficient synthesis of 1, 2-oxazine based derivatives of 6-fluoro-3 …

Pharmacological evaluation of hybrid thiazolidin-4-one-1, 3, 5-triazines for NF-κB, biofilm and CFTR activity

JK Srivastava, NT Awatade, HR Bhat, A Kmit… - RSC …, 2015 - pubs.rsc.org
Cystic fibrosis (CF) is a monogenetic disease caused mostly by the F508del mutation, a
deletion of phenylalanine at position 508 of the CF transmembrane conductance regulator …

A Nano-MgO and ionic liquid-catalyzed 'green'synthesis protocol for the development of adamantyl-imidazolo-thiadiazoles as anti-tuberculosis agents targeting sterol …

S Anusha, B Cp, CD Mohan, J Mathai, S Rangappa… - PLoS …, 2015 - journals.plos.org
In this work, we describe the 'green'synthesis of novel 6-(adamantan-1-yl)-2-substituted-
imidazo [2, 1-b][1, 3, 4] thiadiazoles (AITs) by ring formation reactions using 1-(adamantan-1 …

Synthesis, characterization and in vitro evaluation of novel enantiomerically-pure sulphonamide antimalarials

S Anusha, A Sinha, CPB Rajeev, TTT Chu… - Organic & …, 2015 - pubs.rsc.org
Malaria parasites are currently gaining drug-resistance rapidly, across countries and
continents. Hence, the discovery and development of novel chemical scaffolds, with superior …